Beruflich Dokumente
Kultur Dokumente
"Virusfiltrate, die als Ursache von Encephalitis angenommen wurden zeigten runde Formen
- einzeln und paarweise - blass pink und kleiner als bei Polio unter Rifes Beleuchtung" hier
"Rifes spezielle Beleuchtung zeigt die filtrierten Organismen in verschiedenen
charakteristischen Farben.. keine 2 Formen haben dieselbe Farbe..
eine Form hatte 2 Farben: am Ende/in der Mitte -> 2 Frequenzen bentigt" hier
"Tuberkulose-Bazillen erschienen grn, Lepra rubinrot, E.coli mahagoni, der BX violettrot" hier
"wo wir nun eine Maschine haben, die 2 Frequenzen gleichzeitig erzeugen kann wre es einfach
alle Formen der Tuberkulose - die Bazillen und die Muchschen Granula (Dr. Hans Christian Much)
zu behandeln.. Dr. Milbank Johnson an Rife 1935" hier
"Rife beobachtete, da sich Tuberkelbazillen bei Bestrahlung mit der entsprechenden
Frequenz aufl sten und daraus Viren entstanden.. diese konnte er mit der N hrl sung vermehren
und dann die entsprechende Frequenz zum Aufl sen der Viren finden" hier
"Rife studierte Lepra.. isolierte Virus und fand Frequenz dagegen..
ein Arzt in Dayton Ohio testete diese mit groem Erfolg bei mehreren Personen mit Fupilz" hier
"jedes Pathogen hat eine andere chemische Zusammensetzung und damit eine
andere molekulare Eigenfrequenz und bentigt somit zur Zerstrung eine andere Frequenz" hier
"wenn die richtige Frequenz erreicht wurde lsten sich tdliche Organismen wie Tuberkulose,
Typhus, Lepra, Maul- und Klauenseuche und andere im Mikroskopfeld auf" hier
"eine gesunde Zelle hat eine Frequenz, die sich im Krankheitsfall ndert" hier
"Insgesamt fand Rife 14 Frequenzen, mit denen er alle gefundenen Viren- und Bakterienarten
aufl sen konnte, einschlie lich der damit in Zusammenhang stehenden Pilzarten" hier
"Rife war ein brillianter und beharrlicher Wissenschaftler..
wo die erforderliche Technologie nicht existierte, erfand er sie einfach:
+ die ersten Mikrodissektoren, Mikromanipulatoren und
+ ultravioletten berlagerungsmikroskope" hier
"jede biochemische Komponente ozilliert in in ihrem ureigenen Frequenzmuster..
Rife identifizierte mittels Spektroskop-Mikroskopen die energetische Signatur,
die jeder Krankheit eigen ist.." hier
"Rife isolierte die Muster, modifizierte sie und setzte sie gegen die Mikroben ein,
die sie erzeugt hatten.. jede Krankheit durch Frequenzen besiegen..
destruktive Resonanz zerstrt nur Erreger mit dem genau gleichen Oszillationsmuster..
deshalb ist die Rife-Therapie eine der wenigen,
von denen keine einzige Nebenwirkung bekannt ist" hier vgl. Albert Abrams Oszilloclast..
"Der F-Scan reizt den Krper mit Frequenzen von 1-2.999.999Hz.. stellt Resonanzen fest" hier
"Rifes Werk so erstaunlich, da die Regierung ihm 14 Vertrge anbot praktische
Anwendungsverfahren fr seine Entdeckung spezifischer Frequenzen zu entwickeln" hier
"Eliminierung der Krankheiten in der Geflgelindustrie:
Rife behandelte ganze Schar Kken und befreite sie von allen Krankheiten" hier
"20.11.1931: Bankett mit 44 der geachtetsten
Autoritten der Medizin unter dem Motto 'Das Ende aller Krankheiten' " hier
"Rife erhielt von Regierungsseite 14 Auszeichnungen fr seine wissenschaftlichen
Entdeckungen und einen medizinischen Grad ehrenhalber der Universitt Heidelberg" hier
"Rifes Entdeckungen wurden dem
+ Smithsonian-Institut in Washington und dem
"Rife stellte fest, da er bei neutralem ph-Wert keine Kultur anlegen konnte..
Rife dachte, da der Krper bei neutralem pH keine Krankheiten entwickeln knne" hier
Claude Bernard: "die Mikrobe ist nichts, das Milieu, in dem sie lebt, ist alles"
"Gaston Naessens hat viele von Rifes Entdeckungen besttigt und
16 Wandlungsphasen skizziert, die Rife die prmodale Identitt nennt..
Naessens nennt sie Somatiden" hier
"Naessens nahm Videos auf von den 16 verschiedenen Wandlungsformen des BX-Krebsvirus..
die beweglichen BX und BY Krebsviren klar sichtbar.. sehen so aus wie Rife sie beschrieb" hier
"im gesunden Blut sind nur die in Symbiose lebenden 3 ersten Entwicklungsstadien der Mikrobe zu
finden..
- im kranken Tumorgewebe mit saurem pH-Wert entwickeln sich pilzhnliche Formen
- im kranken alkalischen Venenblut bakterienhnliche Form" hier
"die bakterien- und pilz-hnlichen Entwicklungsformen
- rauben dem Krper wesentliche Nhrstoffe
- vergiften ihn mit ihren toxischen Stoffwechselprodukten" hier
"BY-Krebsvirus verursacht Sarkom-Krebs, nachdem es lngere Zeit UV-Licht ausgesetzt war" hier
"Rife suchte nach Methoden die BX-Viren zu zerstren..
Viren blhten auf unter Bestrahlung bestimmter Elemente..
Radium/Cobat-60 -> schlafende Viren wurden bsartig" hier
"Pathogene ca. 2000x empfindlicher als Krperzellen
-> durch elektr. Impulse zerstrbar ohne dem Patienten zu schaden" hier
"Rifes tragbares Gert richtete weniger Energie auf den Patienten als ein heutiger
Farbfernseher. Entscheidend sind Frequenz und Timing der Energieimpulse" hier
"11.780.000Hz fr BX und 11.430.000 fr BY" hier
"Das Rife-Frequenzinstrument ttet 'normale' Karzinom-Krebszelle indem
es die vielen Tausend BX-Krebsviren, die in ihr wohnen, platzen lsst.." hier
"Rife benutzte (anfangs) 2 Oszillatoren
+ fr das Durchdringungsfeld und
+ die Zertrmmerungsfrequenz.. ein Frequenzpaar pro Pathogen" hier
"die Frequenz mit dem Trger wird einer Rhre hnlich einer Rntgenrhre zugefhrt,
die mit einem anderem Gas gefllt ist.. wirkt als Richtantenne" hier
"Rife experimentierte mit verschiedenen Gasen und stellte fest, da Helium das
Bombardement besser als jedes andere Gas wie z.B. Argon od. Krypton vertrug.." hier
"Platinelektrode in heliumgefllter Quarzrhre.. 17x durchdringender als Rntgen" hier
"bei der Supraleitung werden 2 Elektronen mit unterschiedlichem Spin magnetisch gekoppelt..
der Strom fliet nur als Cooper Paar.. fr einzelne Elektronen ist das supraleitende Material
ein perfekter Isolator.. Licht=beschleunigte Cooper Paare mit Oszillationsenergie..
Cooper Paare knnen in gerader Linie beschleunigt werden.. Strahl..
Strahl ggf. schneller als Lichtgeschwindigkeit.. Tesla ma bis zu 157%..
Cooper Paare im Vakuum erzeugt, beschleunigt, fokussiert.. TV-Gert.. hnlich Rntgenrhre..
Rife nutzte schwache, perfekt getimte Sinuswellenpulse.. TV-Gert umbauen.. Pulse 1ns" hier
"Schaukel funktioniert durch korrekt getimtes Anschieben.. Impuls im richtigen Moment zufhren..
chemische Bindungen verhalten sich analog.. -> gepulste Cooper Paare zur Therapie effektiver als
Sinus..
auch zur Diagnose genutzt.. Probe angepingt -> charakteristische Resonanzen hren" hier
"Dr. Lee de Forest berwachte Design und Zusammenbau vieler Oszillatorbauteile des Rife-Systems.
W.D. Coolidge selbst (General Electric) sandte hunderte Rntgenrhren, die von
Rife und seinen Techikern mit einer Mischung aus Wasserstoff und Helium gefllt und
getestet wurden, damit sie nur die gewnschten Elektroimpulsstrahlen projezierten" hier
"gelegentlich funktionierte ein System pltzlich nicht.. atmosphrische Vernderungen?
der Abstimmkondensator des RF-Oszillators lag in Reihe mit der Plasmarhre..
-> die Frequenz hing somit von der Kapazitt des Patienten und vom Wetter ab" hier
"Die Frequenzinstrumente wurden stetig verbessert von der frhen Version 1920
zu den klinischen Versionen von 1934-38 und weiter in den 50er Jahren
bis Rife sagte sie seien unfehlbar und einfach zu bedienen" hier
"verschiedene Erreger konnten nebeneinander aufgereiht werden. Wenn man die ResonanzFrequenz des einen traf wurde er zerstrt, whrend die anderen unbeeinflusst blieben" hier
"Metallschrnke (Alu) schtzten Viren nicht vor der Strahlung.. bis zu 8 Meilen" hier
"Rifes Personal wurde den Frequenzen ausgesetzt..
es gab keine Krankheiten, nicht einmal eine Erkltung..
nach einer gewissen Zeit trug Rife bei der Arbeit mit den Viren nur noch selten Handschuhe..
weder er, noch seine Techniker bekamen je eine der Krankheiten" hier
"durch das Abtten der Erreger werden Toxine frei, die die elektr. Bluteigenschaften ndern
-> spezielle Elektrolyte ntig, um Herzattacken/Schlaganflle durch reduz. Zetapotential und
resultierende Verklumpungen zu vermeiden" hier
"Forschungskomitee der Universitt Sdkalifornien 1934.. rzte, Pathologen:
16 Krebspatienten.. nach 3 Monaten 14 vollstndig genesen..
Behandlung leicht verndert.. letzte 2 in 4 Wochen ebenfalls gesund" hier RifeRay #4
"Rife's normale Krebsbehandlung war 3 Minuten alle 3 Tage.." hier
"bei Krebs erzeugte Rifes Frequenzgenerator mglicherweise wiederholt Pakete von
11.780.000 oder 23.560.000 Lichtpulsen pro Sekunde.. diese Lichtpulse erzeugten im Krper
ultra low intensity Ultraschall mit einer Frequenz von 11.780.000 oder 23.560.000Hz,
was der mechanischen Resonanzfrequenz des BX-Krebsvirus entspricht" hier
"Dr. Milbank Johnson wandte Rifes Therapie an..
konnte viele Flle von Krebsheilung dokumentieren.." hier
"ein Original BeamRay-Gert von 1939 wurde gefunden.. mit Sinusfrequenzen, kein Rechteck..
(aber Gating und harmonischer Trger: Anm. Weisser)
Dr. Milbank Johnson schrieb am 4.11.1936, da sie ein neues Frequenzband gefunden
htten, das das Glas im Labor zerbrach.. die Frequenz fr den BX-Virus lag bei 21275Hz
und damit Faktor 10 ber den Crane/Stafford-Frequenzen aus den 50er Jahren" hier
"Dr. Yale lebte in San Diego, nicht weit von Rifes Labor.. er beschaffte sich ein Frequenzgert
und begann Krebspatienten zu behandeln.. 1940 berichtete er ber einige Ergebnisse
seiner 10-jhrigen Erfahrung.. die Ergebnisse seien einzigartig und unglaublich gewesen..
mit Rifes Ray sei die Krebsmasse in einem Zehntel der Zeit verschwunden - ohne Rckflle" hier
"am 28.5.1937 schrieb Dr. Milbank Johnson an Dr. Joseph D. Heitger ber 8 Monate
Arbeit an grauem Star: stellten in den meisten Fllen die volle Sehfhigkeit her..
wir wissen nicht warum das geht.. es ist jedoch eine Tatsache, gesttzt durch viele Flle" hier
"kleinere portable Gerte wurden hergestellt fr den Einsatz in Arztpraxen..
bei ordnungsgemem Einsatz gab es Erfolgsberichte.. nie gab es negative Berichte" hier
"Halsentzndung durch Streptokokken (strep throat) in 1 Sitzung behandelbar..
spezielles Gurgelmittel um die resultierenden Toxine zu beseitigen" hier
hier
"1950 trafen sich Crane und Rife und 2-3 Jahre spter John Marsh.. Marshs Frau hatte
Unterleibskrebs..
Rife gab ihnen ein altes rhrenbestcktes BeamRay-Gert, das Vern Thompson reparierte..
nach einigen Sitzungen verschwanden die Schmerzen und sie wurde gesund.." hier
"Marsh und Crane wollten mit Rife zusammenarbeiten und wieder Frequenzgerte bauen.. Rife
missfiel
der harmonische Trger und sie entfernten das Gating.. es dauerte Jahre, bis das erste Gert
funktionierte,
indem sie den Audiofrequenzen Harmonische zufgten -> Rechteckfrequenzen..
Hoylands Frequenzen wurden fr das AZ-58 Ray Tube-Gert (2.2/4.8MHz sinusfrmiger Trger)
und die Pad-Gerte (kein Trger, Handzylinder/Fuplatten) um den Faktor 10 heruntergesetzt.." hier
"Dr. Stafford nutzte das AZ-58 5 Jahre fr seine Patienten.. teilweise unglaublich gute Resultate..
bei Krebs funktionierte es nicht wie erwartet: mglicherweise Frequenzen falsch oder nur fast richtig..
sieht so aus, als ob es die Kombination der Sinusfrequenzen mit dem harmonischen Trger + Gating
(wie bei Hoylands BeamRay-Gert) war, das die korrekte Funktion ermglichte.." hier
"wissenschaftliche Studien: Audiofrequenzen dringen nur in das Bindegewebe um die Zellen..
je nher bei 1 MHz, umso strker das Eindringvermgen in die Zelle.." hier
"die wichtigsten Rife/Crane-Frequenzen.. mit der hchsten beginnen.. je 3-5min..
nicht mit zuviel Strom.. max 12V.. 9V besonders gut geeignet..
max. 7-10 Frequenzen.. max 3x pro Woche.. vorher/nachher viel reines Wasser..
+ 10000Hz harmonisiert Nervensystem
+ 5000Hz schmerzlindernd, blutreinigend
+ 2127Hz (besser 2130.14Hz?) Karzinom: Brust-, Prostatakrebs, Lungenkrebs, Magen-, Darmkrebs..
+ 2008Hz (besser 2007.51Hz?) Sarkom: Krebs an Knochen, Knorpel, Muskel-, Fettgewebe
+ 880Hz Streptokokken -> Scharlach, Rheuma, Meningitis..
+ 787Hz anti-entzndlich
+ 728Hz Staphylokokken" hier
"Rife beobachtete die Polarisation von Mikroorganismen.. Teile richten sich zu den Polen hin aus..
keiner der Teile wrde einzeln fr sich wachsen..
zusammen ergbe sich eine Mikroorganismusstruktur.. Aspekt weiblich/mnnlich" hier
Rifes Stimme auf Tonband hier
Rifes Labor auf Video hier
Rifes Laborhandbuch und John Marsh's Sammlung hier
Historie von Rifes Frequenzgerten und Frequenzen hier
wichtiger Artikel ber Ultramikroskope, Nanobakterien, heilende Strahlen.. Literaturverzeichnis hier
"Dan Tracy`s EMEM-Gert: kleinere Spule mit Ferritkern an Verstrker..
manche Tumoren verschwanden in nur 2 Wochen.." hier
"EMEM3/EMEM3D zahlreiche Spontanremissionen von Krebs berichtet" hier
"Fred Walter: Bare-Rife-Gert alle 3 Tage..
Tumorverkleinerung - Adenosarkom der Brust - auf 1/3 in einer Woche bei Katze" hier
"'Doug' speiste Frequenzen in kleine Spule unter seinem Mikroskoptrger..
entdeckte Lyme-Frequenzen" hier
"Veja-Gert: Ankopplung der Rife-Frequenzen optisch im IR- bis Rot-Bereich..
-> Frequenzen ber die Haut aufgenommen und im K rper weitergeleitet.." hier
"Michael Prescott's 'Do it yourself'-Versuche mit einfachen Gerten:
+ TASCO Microscope 100x, 200x, 300x
+ Mikroskopschlitten mit Elektroden
+ FLEXCAM, Videokamera, Framegrabber ber PC, Videorekorder
Czip
Rzip
Ezip
Lzip
Bzip
Rzip
Ezip
Rzip
R-
zip
Czip
Ezip
Rzip
Lzip
Clark: "Heilung aller fortgeschrittenen Krebsarten" ..21Tages-Programm.. ganzheitlicher Ansatz.. Tumore reduziert..
Blutchemie normalisiert.. viele Fallbeispiele mit Beweisbildern..
macht Mut..
Clark: "The cure for HIV and AIDS. With 68 Case Histories"
sehr gute Kritik.. engl. Fassung..
Allergien, Energie
"Eine Leberreinigung ist anzuraten, da durch den Tod der Parasiten und Bakterien eine erhhte
Belastung auf Darm, Leber und Nieren zukommt.
Wenn man die Leber von Gallensteinen befreit, hat das eine auerordentlich gnstige Wirkung auf die
Verdauung, und dies ist wiederum die Grundlage Ihrer allgemeinen Gesundheit.
Sie knnen erwarten, da Sie mit jeder Leberreinigung weniger Allergien haben werden. Sie
knnen sich sogar von Schmerzen in der Schulter, im Oberarm und im oberen Rcken befreien. Sie
haben mehr Energie und Ihr Wohlbefinden steigert sich deutlich." S.595
Asthma
"Asthma steht in allen Fllen mit Ascarislarven (Spulwurm) in Zusammenhang. In den meisten Fllen
sind auch Bakterien vorhanden. Beim ersten Anzeichen von Husten setzen Sie am besten einen
Zapper ein.
Hunde, Katzen, Schweine und Pferde sind Trger von Ascaris. Man kann sich von Asthma befreien,
indem man sich vom Spulwurm befreit." S.165
Alzheimer
"Bei dieser Krankheit knnen Aluminium, Quecksilber, FCKW, Thallium und Cadmium vorhanden
sein. Bei allen Alzheimer-Kranken werden erhhte Alminiumwerte festgestellt. Dies ist zweifellos ein
Faktor der wirklichen Krankheitsursache. Entfernen Sie alle Aluminiumquellen und machen Sie dann
einen Therapeuten ausfindig (Therapeutenliste), der mit Hilfe der Chelattherapie das Aluminium aus
Ihrem Gehirn beseitigen kann. Nehmen Sie Liponsure ein (100mg 2-3 mal tglich).Tten Sie die Egel
mit dem Zapper ab. Fhren Sie baldmglichst eine Nierenkur durch." S.315
Autismus
"Bei autistischen Kindern wird stets eine Bleibelastung beobachtet. Auch Quecksilber kann von der
Mutter auf das Kind bertragen werden. Hufige Parasiten wie Ascaris, Hakenwurm, Strongyloides
und Trichinen dringen leicht in das Gehirn ein. Wenn sich die Parasiten einmal einen Weg zum Gehirn
gebahnt haben, ist es schwierig sie wieder zu vertreiben. Wenn Blei und Parasiten mehrere Wochen
ferngehalten wurden, heilt der Pfad zum Gehirn. Fr eine Heilung ist eine vollstndige Sanierung
(Zappen, Parasitenkur, Leberkur usw.) durchzufhren." S.308
Bluthochdruck
"Bluthochdruck (Hypertonie) zhlt zu den Krankheiten, die oft ohne Arzneimittel beseitigt werden
knnen. Die vordringlichste Manahme besteht darin kein Koffein mehr zu sich zu nehmen. Bei
unseren Untersuchungen haben wir fast immer Cadmium gefunden. Die Toxizitt von Cadmium, da
heit sein Zusammenhang mit Bluthochdruck, ist seit langem bekannt.
Alle Flle von Bluthochdruck, die ich behandelt habe, konnten durch eine Beseitigung von Cadmium
und anderer Schadstoffe und eine anschlieende Nierenreinigung geheilt werden." S.250
Candida
"Der hufigste beim Menschen vorkommende Hefepilz ist Candida albicans. Das Immunsystem kann
den Hefepilz beseitigen, wenn es nicht geschwcht ist. Alle Formen von Pilzbefall, knnen in
derselben Weise behandelt werden.
* Entziehen Sie dem Pilz Feuchtigkeit und Zucker
* Entziehen Sie den Erregern Eisen
* Strken Sie Ihre Abwehrkrfte
Tten Sie Candida tglich mit dem Zapper ab. Die Lugol-Lsung erreicht den Pilz nur an der
Oberflche. Wenn jedoch die oberste Schicht abgettet ist, knnen Sie die darunterliegende
erreichen. Es erfordert etwa einen Monat tgliche Behandlung, um die Erkrankung zu kurieren." S.289
Depressionen
"Die Ursache von Depressionen ist, da das Gehirn nicht mehr genug Neurotransmitter herstellen
kann oder deren Gleichgewicht gestrt ist. Bei allen meinen Patienten mit einer klinischen Depression
fand ich kleine Rundwrmer im Gehirn. Leiden Sie unter Depressionen , verwenden Sie den Zapper,
um sofort die Rundwrmer anzutten. Wenn auerdem Lsungsmittel und Toxine im Gehirn
Arrhythmien und Mitralsegelprolaps geheilt. Es kann jedoch ebenso eine bakterielle Infektion
vorliegen." S.179
Multiple Sklerose
"ist eine Erkrankung des Gehirns und der Wirbelsule. Die Ursache von MS sind Egel, die in das
Gehirn oder die Wirbelsule eindringen. Tten Sie diese sofort mit dem Zapper ab. Im Gehirn knnen
sich diese Egel nur vermehren wenn Lsungsmittel vorhanden sind.
Bei MS-Patienten fanden wir immer Xylol und Toluol im Gehirn. Xylol und Toluol sind industrielle
Lsungsmittel, die in Farben und Verdnnungsmitteln Verwendung finden. Ein weiteres mit Multiple
Sklerose zusammenhngendes Umweltgift ist Quecksilber aus Zahnmetall. Man kann die
Quecksilberausscheidung erhhen, indem man eine Nieren- und Leberkur durchfhrt. Auf alle Flle
knnen Sie ein weiteres Fortschreiten der Krankheit aufhalten, indem Sie Ihr Gebi und Ihre
Umgebung sanieren und Ihre Ernhrung umstellen. Wenn die Krankheit nicht zu weit fortgeschritten
ist, ist sie oft heilbar." S.244
Nieren
"Oft hngt ein Nierenproblem mit einem Herzproblem zusammen. Wird der meiste Harn nachts
ausgeschieden, sind die Nieren nicht gesund. Wenden Sie die Nierenkruter an, aber nur die halbe
Dosis. Nach ca. 6 Wochen verliert der Harn seinen strengen Geruch (kein Ammoniak, kein Azeton und
keine Bakterien) und sieht klar aus. Weil Wasser und Schlacken den Krper rascher verlassen
knnen, ist weniger Druck seitens des Herzens erforderlich, um Blut durch die Nieren zu pressen.
Dies entlastet auch das Herz. Herz und Nieren arbeiten zusammen." S.369
Prostatitis
"Wenn Sie den Harn nicht vollstndig entleeren knnen und daher hufig auf Toilette mssen, auch
nachts, dann ist an Druck auf die Harnrhre durch eine vergrerte Prostata zu denken. Restharn ist
oft auch Ursache fr Blasen und Niereninfekte.
Die Prostata zieht Giftstoffe an, insbesondere Nickel. Eine bedeutende Nickelquelle ist Zahnmetall,
wo es zum Hrten von Gold dient. Nickel dient zum Anfertigen von Brcken, Kronen und ist
Bestandteil von Amalgam. Essen und kochen Sie nicht mehr mit Metallgertschaften.
Prostataprobleme jeglicher Art hren auf, wenn die Bakterien gezappt werden, die Nierenreinigung
durchgefhrt wird, die Zhne saniert werden und das Darmprogramm eingehalten wird." S.154
Rheuma
"Wenn die Gelenke nicht nur schmerzen, sondern auch entzndet und geschwollen sind, ist meist im
Blut der sogenannte Rheumafaktor nachzuweisen. In diesem Fall sind die Gelenke von Rundwrmern
befallen: Ascaris, Ankylostoma, Strongyloides und Trichinella. Fhren Sie das Zahnprogramm durch
und anschlieend das Nieren- und Leberprogramm.
Mglicherweise klingen Ihre Schmerzen unmittelbar nach dem Zappen ab, doch sollten Sie das
komplette Programm durchfhren. Stellen Sie Ihre Ernhrung um. Senken Sie die
Phosphataufnahme, und fhren Sie mehr Calcium zu. Fhren Sie das Kruterprogramm gegen
Parasiten durch und zappen Sie regelmig." S.108
(herausgeschrieben 7.2001 Dr. Matthias Weisser)
Dies ist eine reine Hinweis-Seite, sie ersetzt keine rztliche Beratung !
"jede Krankheit lt sich aufhalten.. die Regeneration des Krpers wird
den Rest bernehmen" Baklayan
"Die Heilkrfte des Krpers sind unvorstellbar gro.. selbst Krebs, MS, Polio
oder Blindheit sind heilbar,
wenn die Patienten nur richtig atmen und ihr Lymphsystem aktivieren" West
"die Gesundheit baut sich sogar bei schwersten Krebs- u. HerzKreislauferkrankungen wieder auf" Schatalova S.18
"Krebszellen entstanden aus gesunden Zellen, denen wiederholt der Sauerstoff
entzogen wurde..
kehren in embryonalen Urzustand und Grungsstoffwechsel zurck.. Otto
Warburg 1926..
vergren Glukose statt Sauerstoff zu verbrennen.. weier Zucker Hauptnahrung
der Krebszellen" hier
"Experimente der Amerikaner Illmensee und Mintz 1975/77 widersprechen der
These,
da Gendefekte fr die Krebsentstehung hauptverantwortlich sind" hier
"Krebszellen verhalten sich, als ob eine embryonale Gensequenz reaktiviert
wurde" hier
"manche Zellen knnen trotz eisiger Klte berleben: Embryonen, Spermien,
Krebszellen" hier
"damit eine Zelle gefhrlich entartet
mssen mindestens 5-6 Regulationssysteme gestrt werden" Robert A. Weinberg MIT
-> Ansatz Dr. Smit
"Pekar fand heraus, dass jeder Tumor ein ber seinen Durchmesser
hinausgehendes.. ver ndertes elektrisches Feld hat.. ist nicht automatisch
verschwunden, wenn man den Tumor operativ entfernt..
erkl rt ..die hohe R ckfallquote nach Operationen" Pekar
"Lymphknoten befallen heit.. da sie ihre Arbeit tun..
verhindern Krebsausbreitung.. das Immunsystem entfernen?" Lorraine Day
"Bestrahlung mit Radioisotopen baut vorhandene Energiedepots ab, zerstrt
die zarte Substanz der magnetischen Felder (Spin der Elektronen).. unerllich
fr den Energietransport.." Budwig S.96
"Alan Cantwell: massive Dosis Antibiotika.. massive Bestrahlung/Chemo..
Krebs tot,
die auslsende Mikrobe immer noch durch Autopsie nachweisbar" Lynes: "The
Cancer Cure That Worked!" S.125
entzogen..
mit Marihuana belkeit whrend Chemotherapie am besten in den Griff
bekommen" Herer/Brckers
"Nachweismethode fr Tumorbildungen im Anfangsstadium (rntgenologisch
noch nicht nachweisbar)..
sicherer und einfacher als Rntgen.. seit 1953" Budwig (siehe auch 10. Diagnostik)
"Menschen in Not merken und fhlen, wo Wahrheit herrscht" Budwig
"in chirurgischer Klinik in Helsinki 90% Erfolge bei Anwendung der Budwigschen
Erkenntnisse" Budwig
"Krebskranke sollten die freie Wahl haben welche Therapie sie whlen knnen..
die Krankenkassen die Anwendung einer naturgemen Therapie im Interesse
der Patienten finanzieren" Budwig
"die Medizin der Zukunft ist Licht.. Augen=bester Zugangsweg zu den
inneren Organen" Liberman
wird Krebs verursacht durch einen Mangel an Chemotherapie oder
Bestrahlung?
rufen Chemotherapie und Bestrahlung Krebs hervor?
warum nehmen wir es dann dagegen?
Die Ursache von Krebs ist bekannt.. mind. 65% aller Krebsarten knnten
vermieden werden durch
eine nderung von Ernhrung und Lebensweise (Harvard School of Public
Health) Lorraine Day
und warum unternehmen wir nichts
dagegen?
"Wer heilt, hat recht"
"bei Chemo-/Strahlentherapie.. keine Unterscheidung zwischen Krebszellen und gesunden Zellen..
beide werden angegriffen.. die tdliche Phase des Krebs beginnt mit
dem Befall anderer Organe durch Krebszellen (Metastase).." hier
"Forschungen haben gezeigt, da eine Kombination aus
Vitamin C und den natrlichen Aminosuren Lysin, Prolin.. Extrakt aus grnem Tee
die Invasion der Krebszellen aufhalten kann..
die Kombination aus Vitamin C.. Lysin, Prolin, Polyphenol
verhinderte die Ausbreitung vollstndig.. Dickdarm-, Lungen-, Haut- und Brustkrebs.." hier
"Petersilie gegen Metastasen.. erstaunliche Ergebnisse.. nicht mit chemischen "Bomben",
sondern.. Mimosin.. Teilung fast ganz stoppen.. besser noch Apigenin
- eine Substanz aus der heimischen Petersilie.. Knoblauch, Zwiebel?, MSM?" hier
"Allicin gibt Knoblauch scharfen Geruch/Geschmack..
fr Tumorzellen/Mikroorganismen schdlich..
gelungen Krebstumore bei Musen gezielt zu zerstren" hier
"melanomapositive Zellen in der Blutbahn nach Operation..
potentielle Krebszellen aus Blut isolieren, auf Bsartigkeit untersuchen..
fr therapeutische Zwecke kultivieren.. durch mehrere Therapiezyklen Blutbahn von
melanomapositiven Zellen befreit" S.95 Kbler: "Krebs wird heilbar" hier
"Studie University San Franzisco Medical School: 120 Krebspatienten im Endstadium:
Gruppe A konventionelle Chemo/Bestrahlung, Gruppe B keine bzw. alternative Therapie..
berlebensrate in B viel besser.. Studie von Medien ignoriert.." hier
durchschnittliche Lebenserwartung bei Krebs..
mit aggressiver Therapie 3.5 Jahre, ohne aggressive Therapie >12 Jahre..
"viele leiden unter den schrecklichen Nebenwirkungen der Krebsmedikamente: belkeit, Brechreiz,
Haarausfall, Impotenz, Blut- und Organschden, schwere psychische Symptome.. Zweitkrebse..
Sterilitt, Minderwuchs, Lernschwierigkeiten, Schwerhrigkeit, Lungenfibrose, Hepatitis,
Leberzirrhose,
Niereninsuffizienz.. 4 von 10 Kindern leiden an Langzeitfolgen" rztliche Praxis 51, 25.6.94 hier
"Crystin Schiff, 4.. bsartiger Hirntumor.. Operation, 6 Monate Strahlen-/Chemotherapie als angeblich
einziges Heilmittel.. schwerste Nebenwirkungen.. mit Burzinski's Antineoplaston-Therapie tumorfrei
innerhalb Monaten.. gestorben tumorfrei wegen Hirnschadens als Ergebnis Chemo/Bestrahlung.."
hier
"berlebensrate mit Chemotherapie nur 3%" New England Journal of Medicine 1986 gilt auch fr
2001 hier
"Wendet Ihr Arzt Chemo an, weil er wei, da es wirkt oder weil er
dem Behandlungsprotokoll zu folgen hat, dessen Miachtung ihn teuer zu stehen kommen knnte?
..wrde er Mitglieder seiner eigenen Familie damit behandeln?" hier
"Brusttumor: Operation/Wiederaufbau 12-15000$, Chemotherapie 4-5000$.. und immer noch nicht
gesund..
diese Maschine schrumpft Tumor, bis er weg ist.. zerstrt Erreger im Krper fr weniger als 2-300$..
die amerikanische Krebsgesellschaft warnt.. nur Placebo-Effekt.." hier
"Chemotherapie und Strahlentherapie heilen nicht.. zerstren auch Zellen des Immunsystems..
das bentigt wird um gesund zu werden.. und es spter zu bleiben..
besser das Immunsystem durch natrliche Therapien aufbauen..
Immunsystem ttet dann Krebszellen ohne Nebenwirkungen.. heilt gleichzeitig Krper" hier
befallene Lymphknoten entfernen? ..sind Teil des Immunsystems.. wenn sie befallen sind,
so heit das, da sie ihre Arbeit tun.. verhindern Krebsausbreitung.. Immunsystem entfernen? hier
"Jede zweite Frau leidet nach einer Brustkrebs- und Armlymph-Amputation an einem
(oft sehr schmerzhaften) Lymphdem und Strungen der Lymphzirkulation" hier
"Jeder Krebs ist das Ergebnis eines nicht richtig funktionierenden Immunsystems..
alle Krebsarten reagieren auf die Wiederherstellung des Immunsystems durch natrliche
Methoden" hier
Brustkrebs im Endstadium.. keine Chemo/OP/Bestrahlung/Medikamente.. geheilt.. hier
Histologie: Infiltrierendes
Karzinom der Brust
Krebstheorien/heilende Effekte:
* Lorraine Day: Krebs=nicht richtig funktionierendes Immunsystem.. alle Krebsarten
reagieren auf Wiederherstellung Immunsystem durch natrliche Methoden hier
* Julius Cohnheim: Krebs aus abgesprengten Zellen embryonalen Ursprungs entwickelt
hier
* John Beard: 1902 Lancet 1:1758: Krebszellen gleichen trophoblastischen
Embryonalzellen.. sorgen dafr, da sich Embryo in Gebrmutter einnisten kann..
wachsen aggressiv/chaotisch.. teilen sich schnell.. gewinnen Energie aus Zuckergrung..
unterdrcken Immunsystem der Mutter.. produzieren humanes Choriongonadotropin
hCG.. als Tumormarker anerkannt.. Wucherung stoppt erst, wenn Embryo ab 7. Woche
Pankreasenzyme erzeugt.. ohne diese Enzyme bsartigster Tumor: Choriocarcinom..
Einnahme von Pankreasenzymen hier
* Robert O. Becker: Krebszelle ungengend dedifferenziert.. vermehrt sich ungehemmt,
kann sich nicht spezialisieren.. Zelle voll dedifferenzieren.. Silberionen als Mittel zur
Dedifferenzierung.. positive Ladung stoppt Zellteilung.. insbesondere bei Krebszellen..
liegt am Silber.. bei anderen Materialien verstrktes Tumorwachstum.. Petrieschale mit
Silberelektroden.. pos. Strom.. Silberionen.. wandelt Krebszelle in primitive Zelle, die in
Organzelle redifferenziert.. Hautkrebs umgewandelt Haley: 'Poltics in Healing' Kap.9
D* Robert O. Becker: Zusammenhang niedriger Silberanteil <-> Krankheiten..
zip
durchschnittlich 0.001%.. bei Absinken Fehlfunktion des Immunsystems.. kolloidales
Silber kann Krebszellen in normale Zellen rckverwandeln hier
* Gary Smith: Silbermangel wahrscheinlich einer der Hauptgrnde, da Krebs existiert
und sich so schnell in Industrielndern vermehrt hier
* Maes: Elektrosmog: 80mV entfernt.. Brusttumor verkleinerte sich in 3 Mon. auf 1/10 hier
* Prof. Pappas: Energiemangel der Zelle -> Notprogramm zur Reproduktion.. hier Jan.02
Zellpotential zu klein -> Gerte wie Dan's Enhancer, Zapper, Blitze.. heben dies wieder an
vgl. meine eigenen Messungen vom messbaren Verhalten eines Kondensators
* Ulmer: in allen Organismen Wassermolekle, welche stetig aus Erdmagnetfeld
Energie produzieren wo bleibt diese Energie wenn das Erdmagnetfeld schwcher wird?
hier
* Seitz: durch Magnetfelder knnen Zellmembranen von Tumorzellen zerrissen werden..
These, da sich Krebs in einem krftigen Magnetfeld nicht entwickeln kann hier
* Liberman: Wasser in Krebszellen/geschdigten Zellen anders strukturiert.. z.B. durch
Kiva-Licht so umstrukturieren, dass es gesunden Zellen entspricht hier
* Banik/Landone: hartes Wasser versiegelt jede Zelle mit einem Film -> Sauerstoff kann
nicht durch -> neue Zellen, die mit weniger Sauerstoff auskommen=Krebszellen,
destilliertes Wasser befreit die Zellen -> Sauerstoff kann wieder durch hier
* Karl S. Trincher: Tumore durch Zerstrung Wasserstruktur in der Zelle.. im
intrazellulren Wasser.. Herd aus "nicht lebendem Wasser" innerhalb des "lebenden"
quasikristallinen energetisierten Zellwassers.. wirkt als permanenter Reiz auf die Zelle
sich zu teilen hier
* George Lakhovsky: in krebsfreien Drfern keine Wasserleitungen/-rohre.. Karzinome,
als rtliche Brunnen stillgelegt und stattdessen Wasserleitungen.. lange Rohre..
biologisch totes Wasser -> Energetisierung hier
* George Lakhovsky: Pflanze mit Krebs: 1 Leiterschleife aus Kupfer herum, 30cm
Durchmesser, sammelt kosmische Energie, gibt an Pflanze ab, Tumoren verschwanden
hier
* Gianni Dotto: Energiezufuhr an DNA durch Dotto-Ring.. kombinierter Thomson-PeltierEffekt erzeugt oszillierendes Magnetfeld..10 gauss in der Mitte.. induktive Energie..
gesunde Zellen aufgeladen, parasitte Krebszellen nehmen keine Ladung an.. am Ende
des Zellzyklus verschwindet Tumor hier
* Dr. Aschoff: durch energieloses Leitungswasser, radioaktive Belastung, geopathische
Strzonen nehmen magnet. Krfte im Krper ab.. bei Krebs hat Blut Magnetismus
verloren.. natrlicher Spin Elektronen im Blut verndert -> Energetisierung ntig, Nahrung
und Wasser sollen magnetisch sein hier Maes S.203
* Louis Claude Vincent: pH, rH2, R-Wert bestimmen Qualitt von Blut, Speichel, Urin
eindeutig.. charakteristische Bereiche fr Viren, Mikroben, Krebs, etc.. Hring S.60f
* Schreiber: Zetapotential in lebenden Systemen immer negativ, wenn zerstrt ballen sich
Zellen zusammen -> Viskositt Blut nimmt zu -> Zellen knnen Stoffaustausch nicht mehr
bewerkstelligen hier
* Medical Tribune 1966: unterschiedl. Verhalten Normalzellen <-> Krebs-/Leukmiezellen
im Magnetfeld.. Maes S.203
* Dr. Cone: Depolarisation der Zelle als signifikanter Faktor Tumorwachstum.. Maes
S.203
* Dr. Clark: PCB's als Isolator, reduzieren Zapperstrom hier
* Dr. Udo Erasmus: Fette als Isolatoren der Nerven, Zellen und Membranen hier
* Weisser: Kurzschlu der Zellen bei Fettmangel? (vgl. Dr. Erasmus) -> Verlust
Magnetismus, Energiemangel -> Krebs.. Na-Ka-Pumpe: Na- u. Kaliumionen unterschiedl.
elektr. Potentiale, ber Zellwand hinweg -> gesunde Zelle 60 mV bei Zellwandungsdicke
100 (Isolator).. Enzym Aldosteron wandelt Natrium <-> Kalium.. bei Mangel? hier
* Matthias Leisen: Germanium, Blei, Arsen, Eisen, Samarium, Zink und Zinn als
energetische od. stoffliche Schlacken im Krper von Krebskranken.. Schlacken mit
bestimmten Pflanzen lsen/entfernen.. Gleiches lst Gleiches.. Tee als D4-D6-Lsung der
in den Pflanzen enthaltenen Elemente.. Schllkraut enthlt As, Bi, Cs, Ci, Fe, Ge, Gra,
K, Co, Li, Na, Pb, Sn, Sm, S, Si, V, Zr, Zn.. Riegeltee.. Peter Jentschura-Basenkur Der
freie Arzt 9/10 11.03 S.57
* Weisser: Krebs wg. Bi-Mangel? Bi mit Supraleitung in Verbindung gebracht.. Bi
enthalten in Schllkraut, Kamille, Zinnkraut, Lwenzahn, Fuchskreuzkraut, Papayabltter,
Spitzwegerich, Walnussbltter, Bohnenkraut, Basilikum, Labkraut, Lapachorinde
Jentschura: Die Basenkur
* Seitz: Magnetfeld Ionen.. geordnet/neu ausgerichtet.. Zellmembranpotential..
verbessert.. Photonenemission der DNA beeinflut und damit interzellulre
Kommunikation, Zellstoffwechsel.. Ionenflu gefrdert.. Hormone/Enzyme..
Geschwulstgewebe: elektr. Potential herabgesetzt..
Magnetismus -> im Gewebe elektr. Felder erzeugen -> el. Potential steigt an..
These, da sich Krebs in einem krftigen Magnetfeld nicht entwickeln kann hier
* Prof. E. Zeidler: Unterschied gesundes Gewebe <-> Tumor-Gewebe: Spin.. Maes S.203
* Prof. F.A. Popp: magnetische Funktionen im Organismus ohne Energieaufwand..
magnetisch ausgerichtete Krperzellen geben kleinste Lichtsignale ab (Maes S.203)
Stoffwechsel emittiert Lichtquanten/Biophotonen.. fr Kommunikation zwischen den
Zellen.. bei Krebs Intensitt und Ordnungszustand (Kohrenz) der Photonenemission
vermindert.. Zellen von induzierten Tumoren hatten Lichtkontakt weitgehend verloren..
hier
* Klinghardt: Omega-6-Fettsuren Distel-/Sonnenblumenl, Nachtkerzenl -> ab/umgebaut zu Prostaglandinen.. Prostaglandine verantwortlich fr interzellulre
Kommunikation=von Zelle zu Zelle hier
* W.F. Koch: Viren/Antibiotika reagieren mit Aminogruppen z.B. Kreatinin.. bilden
Polymere die die Atmungskette beeintrchtigen -> Hypoxie -> Prparate mit hohem
Redoxpotential, um Hypoxie zu berwinden.. homopathisch aufbereitete D6/D9
Carbonylgruppen-haltige Substanzen (z.B. Glyoxale, Chinone).. Methylglyoxal
photoverstrkend bei 300nm.. Photonen fr Zellkommunikation hier
* F. Batmanghelidj: Untersuchungen haben gezeigt, da viele Krebspatienten einen
niedrigen Salzspiegel aufweisen.. zuwenig Salz fhrt dazu, da in einigen Zellen Sure
entsteht.. hoher Suregehalt kann DNA-Struktur schdigen.. Salz wichtig fr
hydroelektrische Energie der Zellen.. lokale Energiequelle.. fr Kommunikation
Nervenzellen.. fr Absorption Nahrung.. Wasserkur.. hier hier
* F. Batmanghelidj: Wassermangel + ineffiziente Lieferung Rohstoffe -> Rckverwandlung
bestimmter Zellen in frhere primitive Form.. primitive Zellen besitzen aggressive
'eigenntzige' Gene.. Zellgrenzen berwuchern.. krebsartige Geschwulstbildung, die in
einer Umgebung ohne Sauerstoff bestens gedeihen kann.. S.115 hier
* idw 2.5.03: Krebspatienten haben in Organen weniger Anti-Oxydantien (Beta-Carotin,
Lycopin) als gesunde Personen.. Nachweis durch Raman-Resonanz-Spektroskopie an
der Haut.. kostengnstig.. Klinik fr Dermatologie FU Berlin
* J. Stockwell: Beta-Carotin, Selen, Vitamin E (wichtigste Antioxidantien) -> weniger
Magenkrebs.. wenn man freie Radikale vermindert und Gewebe mit genug reinem
Sauerstoff versorgt, hat Krebs keine Chance hier
* Lange-Ernst: Unser Immunsystem S.78f: durch Vitamin C, E, Beta-Karotin, Selen wre
Krebsrisiko auf 1/5 zu drosseln.. 95% der Bevlkerung bentigen Anhebung Versorgung
* Pauling/Rath: Kombination aus Vitamin C, Lysin, Prolin, Extrakten grner Tee kann
Invasion durch Krebszellen aufhalten.. Lehrvideo, wie Krebs entsteht hier
* Jon Brooks: Vitamin C kann Krebs heilen.. bis 100g/Tag, jede Stunde 1 Teelffel.. bei
zuviel -> Durchfall.. hier
* Waltraut Fryda: bsartige Tumoren durch Adrenalinmangel.. gehufter Stress fhrt zur
Erschpfung des adrenalinproduzierenden Systems.. Anregung der Adrenalinproduktion
fhrt bei Ratten dazu da Impftumoren gar nicht angehen.. vorhandene maligne
Vernderungen verschwinden spurlos.. Fryda S.9,12
* Erich Klemke: krpereigenen krebsheilenden Mechanismus aktivieren: Defekt bei der
ATP-Produktion der Mitochondrien beheben durch Vitamin B1, Carnitin, Liponsure..
H2O2-Produktion der Mitochondrien.. Kalbsbries enthlt Tumosteron.. hier
* Walter Binder: Zusammenhang Krebsentstehung und Sauerstoffmangel wahrscheinlich..
Notmanahme vorzeitige Teilung.. beschleunigte Zellwucherung.. Exodus Mitochondrien
als Selbstrettungsaktion? hier
* Prof. Wendt: zuviel Eiwei (Fleisch, Molkereiprodukte) -> Ablagerungen -> behinderte
Versorgung der Zellen mit Sauerstoff, Nhr- und Vitalstoffen Opitz S.95
* Weisser: Krebs als Eiweispeicherkrankheit, wg. Mangel an Verdauungsenzymen, die
Fett, Strke und Eiwei (Fleisch..) spalten? daher Dr. Kelley's Erfolge mit pankreatischen
Enzymen? Krebs durch zellwandangreifendes Enzym.. hnlich Aids.. 50-100uA blocken
Enzym.. ist das der Mechanismus der Elektrotherapie?
* Otto Warburg: Krebs bei Senkung Sauerstoff in Zellumgebung um 35% (Nobelpreis
1931) krankmachende Mikroorganismen bentigen wenig Sauerstoff -> bleiben bei
Sauerstoffmangel im Gewebe brig, vermehren sich rasch.. je mehr sich Krebszellen
vermehren, umso mehr Energie fr normale Zellen verloren.. Viren/Pathogene/Krebs
verschwinden bei ausreichend angehobener Sauerstoffkonzentration in den
umgebenden Krperflssigkeiten, normale Zellen erholen sich.. Energie aus Glukose..
normale Zelle braucht Sauerstoff dazu, Krebszelle nicht.. Krebszelle braucht so nur 1/15
der Energie einer normalen Zelle zur Zuckerverarbeitung.. Krebszellen leben vom
Zucker.. Milchsure als Abfallprodukt.. viel Appetit auf Zucker -> hufiger Krebs..
Zuckerverzicht! hier hier
* John Ott: 'Risikofaktor Kunstlicht' ..an Krebsforschungsinstituten in Bethesda und
Chicago nachgewiesen: durch UV-B-Licht Krebsschutzstoffe entwickelt.. durch UV-B der
Kalzium-, Kohlehydrat- und Phosphor-Stoffwechsel im Krper gesteuert.. durch UV-BLicht Negativ-Ionen erzeugt.. ausgeatmetes CO2 in Sauerstoff umgewandelt..
* Gianni Dotto: Amygdalin (Vitamin B17) dreht Ebene des polarisierten Lichts strker links
als kristalliner Zucker nach rechts.. unter dem Einflu von UV-Sonnenlicht Ebene nach
links gedreht, korrekter Orbitalspin der Phosphat-Base wiederhergestellt.. DNAReparatureffekt proportional zur verfgbaren UV-Lichtmenge.. bei Menschen induktive
Energie effektiver und unkomplizierter hier
* Johanna Budwig: denaturierte/toxische Fette z.B. durch Behandlung mit berhitztem
Ktxt
Pzip
Czip
Dzip
Czip
B1zip
"Das Blut gibt Aufschlu ber den Grad der Erkrankung und Hinweise, wie weit die
Heilung fortgeschritten ist.." Budwig2
B1zip
"Am fruchtbarsten: Kranke abends nach oder morgens vor Beginn der Sprechstunde..
frisch entnommenes Blut sofort untersuchen.. Zweiphasen-Kontrast-Mikroskop.. Blut nach
10 Minuten unbrauchbar -> wiederholt Blutproben entnehmen.. von der gleichen
B1Blutprobe 1 Tropfen auf Papierstreifen zur Herstellung papyrographischer
zip
Hmatogramme.. Ernhrungsumstellung.. Erfolg und Fortschritt feststellen.. Vergleiche
der mikroskopischen Untersuchung mit der papierchromatographischen interessant"
Budwig2
"zeigte sich, da die im Blute der Krebskranken beschriebenen Lebewesen im Laufe der
Ernhrungstherapie mit l-Eiwei-Kost verschwinden, wie auch im Papyrogramm der
B1gelb-grne Fleck verschwand, der auf Sauerstoffnot/Dysfunktion durch Fehlen der
zip
Atmungsfermente durch Fehlen der ungesttigten Fettsuren hinweist" Budwig2
"Heinz-Spagyrik Blutkristallanalyse: ganzheitliche Diagnose-/Therapie: 1 Blutprobe
-> Erkrankung/Belastung aller wichtigen Organe (frh-)erkennen: entzndlich/degenerativ,
bakteriell/viral/mykotisch, Giftstoffe, Umweltbelastungen
-> Analogien Kristallstrukturen Blut <-> Kristallstrukturen Lebensmittel -> Ditempfehlung
-> hochwirksames individuelles krpereigenes Arzneimittel aus Blut/Urin: "Homodot"
-> steigert Abwehr, keine herkmmlichen Nebenwirkungen
Neurodermitis, Psoriasis, chron. degenerative Prozesse z. B. Bewegungsapparat,
Stillstand
z. B. bei MS, Prkanzerosen, kleine maligne Vernderungen, Minderverbrauch von
Schmerzmitteln, verbesserte Lebensqualitt, Cholesterinstoffwechsel, Arteriosklerose, M.
Bechterew, Durchblutungsstrungen, virale, bakterielle und mykotische Prozesse" hier
"Ursache von Krebs u.a. Mikroparasiten.. Krebs als Endstadium dieser Mikroparasiten..
Diagnose im Frhstadium.. Therapie entdeckt.. systematisch unterdrckt/verschwiegen..
Buch/Video Wollenberg/Blasig: 'Der Krebs-Bankrott'" hier
"Bei einem gesunden (bzw. nicht infizierten) Menschen sieht man ausschlielich tote,
vertrocknete Zellen. Ist der Patient infiziert zeigt sich reges Leben in den toten Blutzellen.
Aus den Zellen kommen tausende von Parasiten und bewegen sich quicklebendig in alle
Richtungen. Die Menge der Parasiten korrelierte stets mit dem Schweregrad der
Symptomatik der Patienten: Je krnker ein Patient ist, desto mehr Parasiten im Blut" hier
"Hulda Regehr Clark: mikroparasitre Krebstheorie.. Ausbreitung in Kombination mit
bestimmten Lsemitteln im Krper.. Nachweis mit Frequenz-Resonanzgert.. Entgiftung,
Parasitenkur.. Buch 'Die Heilung aller Krebsarten' " hier
Kzip
Kzip
"Peyton Rous: filterte 1911 aus einem Muskeltumor mit der sehr hohen Filterfeinheit von
K120 Nanometern ein Extrakt, mit dem er wieder Krebs erzeugen konnte.. vermutete in
zip
diesem Extrakt ein Virus.." hier Rous Sarkom-Virus -> Nobelpreis 1966!
"Prof. Dr. Enderlein: 1925.. "Die Bakterien-Cyclogenie" erster mikroskopischer Nachweis
von Blutparasiten in Lebendblut mit Dunkelfeldmikroskopie.. Erreger durchlaufen
Kverschiedene Entwicklungsstadien.. Pleomorphismus.. heute bekannt bei Malaria..
zip
Enderlein entwickelte Reihe von Medikamenten aus Schimmelpilzkulturen.. Erreger in die
niederen Entwicklungsstadien zerfallen lassen.." hier
"Dr. Wilhelm von Brehmer: entdeckte 1928 im Blut Erreger 'Siphonospora polymorpha v.
Brehmer', der einhergehend mit Steigerung des pH-Wertes Krebs hervorruft..
verschiedene Entwicklungsstadien.. Bremer: 'Krebs -Eine Erregerkrankeit' 1932 in
KFachzeitschrift 'Fortschritte der Medizin'.. Erreger lie sich regelmig bei Kranken
zip
nachweisen.. isolieren, zchten, damit wieder Krebs hervorrufen.. Besttigung 1934 in
'Die Medizinische Welt' verffentlicht.." hier
"Dr. Rife und Dr. Kendall zeigten erfolgreich die Isolation des BX-Krebsvirus vor 50
Pathologen.. derselbe Virus trat bei jedem menschlichen Krebsfall auf" hier
"Dr. Wilhelm Reich: bei Krebspatienten degenerierten die Bione in T-Bazillen (T von
Tod).. injiziert in Muse verursachten sie Krebs - wie Rifes BX-Formen" hier
Reich: "The Cancer Biopathy"
"Dr. Virginia Livingston-Wheeler: fand krebserregende Organismen 1947.. verffentlicht
August 1948 im New York Microscopical Society Bulletin.. Artikel Dez. 1950 im American
Journal of Medical Sciences ber Kulturen von menschlichen/Tiertumoren.. am 10. Sept.
1953 berichtete die Washington Post ber die Entdeckungen von Dr. Wheelers Team.."
hier
"Johanna Budwig: 1953.. im nativen Blut der Krebskranken strichfrmige Gebilde wie
aufgesetzte Stecknadeln an roten Blutkrperchen.. wurmartige Gebilde.. schwer zu
fotografieren, besser Film.. Lebewesen, im Zweiphasen-Kontrast-Mikroskop genau als
solche zu erkennen.. Eigenbewegung.. beschnuppern sich nhernde Elemente.. bisher
nur im Blute Krebskranker, nicht bei Zuckerkranken.. Erreger als Lebewesen betrachtet,
die sich erst im pathologischen Milieu des Blutes entwickeln knnen.. ganze Knuel von
Lebewesen hnlich Oxyuren/kleine Madenwrmer im frischen Blute Krebskranker"
Budwig2
"Dr. Elmer Pierre Nemes: Litraonics-Mikroskop=Nemescope zeigt innere Struktur von
Atomen/Moleklen und Energiebnder in Farbe.. extrem hohe Vergrerung.. Bilder von
Blutzellen.. 1955 Zusammenhang zwischen Krebs und Virus aufgezeigt" hier
"Dr. Irene Diller: isolierte kleine runde Organismen aus Tumoren, Sarkomen und aus
dem Blut von Leukmiepatienten.. injiziert in Muse wuchsen Tumoren.." hier
Diller: "Tumor Incidence in ICR-Albino and C37/B16JNicr Male Mice Injected with cultured
forms from Mouse Malignant Tissues" S.507 Growth, vol.38, 1974
"Dr. Florence B. Seibert: isolierte pleomorphische Mikroben aus Blut und Tumoren
B1zip
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Dzip
Rzip
Bzip
Bzip
hier
"befallene Lymphknoten.. sind Teil des Immunsystems..
verhindern Krebsausbreitung.. das Immunsystem entfernen?" hier
"Im Karzinom.. Umweltgifte aller Art.. vom Immunsystem erkannt/eingekapselt.
Das sind also die Metastasen" Kanne "Tumoren als Ausweg des K rpers, um
Quecksilber zu speichern, um es nicht ins Gehirn kommen zu lassen?" Klinghardt
"Lymphknoten befallen heit.. da sie ihre Arbeit tun..
verhindern Krebsausbreitung.. das Immunsystem entfernen?" Lorraine Day
"in Brusttumor nur sehr wenige Zellen in der Lage neue Krebsherde zu erzeugen..
Bestrahlung/Chemo tten vorwiegend instabile mutierte aber harmlose Krperzellen ab..
Cdie Schrumpfung des Tumors=nicht der Schlssel zum Erfolg.. wenige Zellen reichen aus,
zip
um neue Metastasen zu setzen.. zehntausende der anderen Krebszellen erzeugten
keinen neuen Tumor.. Dr. Clarke, Ann Arbor Universitt von Michigan" hier
"Rife suchte nach Methoden die BX-Viren zu zerstren.. die Viren blhten auf unter
Bestrahlung bestimmter Elemente.. Radium/Cobat-60.. schlafende Viren wurden
bsartig..
Rife behauptete, da er Bestrahlung im Organgewebe bis 6 Monate danach feststellen
konnte und bis 2 Jahre nach Radium-Therapie.." hier
"Alan Cantwell: massive Dosis Antibiotika.. massive Bestrahlung/Chemo.. Krebs tot, die
auslsende Mikrobe immer noch durch Autopsie nachweisbar" S.125 Lynes: "The Cancer
Cure That Worked!"
"Chirurg beseitigt ein Symptom, Verursachung bleibt zurck.. Bio-Elektrotherapie
vermeidet gg. chirurgischem Vorgehen die lebensentscheidende
Metastasierung/Rezidiv" Pekar hier
Czip
Bzip
Zeitraum hat der Krper den ganzen Haarboden leergerumt.. alle dort befindlichen
Spurenelemente/Mineralstoffe zwecks Sure- und Giftneutralisierung
verbraucht/geopfert.. Zelltod bewirkt Flut von Harnsure/Harnstoffen in den
Krperflssigkeiten.. Harnsureanstieg fhrt zu erneutem Angriff auf
Haarboden/Haarwuchs bei denjenigen Therapierten, deren Haarwuchs bislang
standgehalten hatte und vernichtet ihn jetzt mit zeitlichem Verzug.." Vortrag Jentschura
hier
"Analgetika, Morphium.. Gerson war der Meinung da man bei Krebs vor allem entgiften
mu.. unmglich zu entgiften und gleichzeitig Medikamente und Gifte zuzufhren..
Entgiftung und Schmerztherapie gleichzeitig verblffend einfach.. Kaffeeeinlufe" hier
Gzip
B1zip
Szip
Gzip
"Pilz Agaricus Blazei Murill.. strkt Immunsystem.. baut rasch Giftstoffe aus Chemo/Strahlentherapie ab.." Blasig 23.10.03 hier hier
"reduzierte Lymphzirkulation nach OP am Arm.. schwierig Narben aufzulsen und
Zirkulation wieder herzustellen.. dauert Jahre.. Gerson-Therapie" hier
"Lymphstauungen nach Brust-OP -> kleine Eigenbluttherapie, 15min Magnetfeld/Tag..
Besserung der Beschwerden um 50%.. Leukozyten 3000 -> 5100" S.73 Hanusch
"bei Stauungen/Schwellungen nach Entfernen lokaler Lymphknoten hilft
Magnetfeldtherapie
hervorragend, weil sie Mikrozirkulation/Muskelkontraktionen untersttzt" S.95 Hanusch
"Leisten-Lymphknoten-OP, 2x Chemo mit Haarausfall/Mdigkeit.. Bein geschwollen,
Schmerzen in Leiste -> 5-20min Magnetfeld/Tag in Rundspule.. nach 3 Wochen
berraschend schnelle Gesundung.. patholog. Laborwerte um die Hlfte gefallen" S.74
Hanusch
"Pflanze Astragalus membranaceus (chin. Tragant) enthlt Asparagin, Calcyosin,
Formononetin, Astragaloside, Kumatakenin, Sterole.. stimuliert Immunsystem..
antikanzerogen.. nach Chemotherapie gg. Nebenwirkungen" Internet ebay
"Aminosure Cystein hilft bei Entgiftung.. schtzt Krper vor Strahlenschdigungen.. wirkt
am besten mit Selen u. Vitamin E" hier
"Aminosure Histidin schtzt Krper vor Strahlungsschden, hilft Blutdruck senken,
Schwermetalle ausleiten (Chrom, Nickel).. Aids" hier
"grne Grassfte schtzen nachweislich vor radioaktiven Strahlenschden wie
Rntgenstrahlen.. nur bei regelmiger tglicher Zufuhr" S.20 Simonsohn:
"Gerstengrassaft"
Herer/Brckers: "Die Wiederentdeckung der Nutzpflanze Cannabis Marihuana Hanf" bei
Aids, Tumoren.. als Antibrechmittel bei Chemotherapie, als Appetitanreger.. Erleichterung
bei Stre und Migrne.. fr Schlaf und Entspannung.. Strkung Immunsystem..
"Akupressur + Akupunktur gegen postoperative belkeit/Brechreiz, belkeit bei
Chemotherapie" S.119 Milton: "Verbotene Wissenschaften"
Gzip
"Dotto-Ring=induktive Spule.. ldt Zellen auf.. sehr hilfreich bei Strahlenschden durch
Bestrahlung, Kobalt, Linearbeschleuniger.." Dotto
-> Schmerzen hier
"Knochenmetastasen nach Brust-OP, starke Rckenschmerzen -> Magnetfeld,
Sauerstoffionenbehandlung -> Schmerzmittel deutlich reduziert -> gute geistige
Regsamkeit, Blutwerte besserten sich erheblich" S.73f Hanusch
"Reflexpunkte mit RS 45 bzw. Druck stimulieren: bis 2 Tage vor Exitus ohne
Spritze/Medikamente.. Metastasen bildeten sich zurck, Beweglichkeit stieg.. starke
Schmerzen nach 1 Einzelimpuls fr 5h verschwunden" Dr. Smit
Kzip
"Wo die Sonne nicht hinkommt, ist der Doktor nicht fern" Liberman S.164
"Schlafsttte: Wenn man auf einer Wasserader liegt, kann der Krper nicht
regenerieren.
vgl. Rife (Wayne).. mit den Frequenzen, die blockiert sind bis das Signal stehen
bleibt..
"die Medizin der Zukunft ist Licht.. Augen=bester Zugangsweg zu den
inneren Organen" Liberman
"Lakhovsky: alle lebenden Zellen haben elektr. Eigenschaften.. erzeugen
Oszillationen und reagieren darauf..
Pflanze mit Tumor.. 30cm Cu-Ring herum fngt kosmische Energie ein..
heilsame Resonanz.. Pflanze immer robuster.. Tumor fllt ab.. offener
Kupferarmreif, Lakhovskyspulen gegen Krankheiten" Lakhovsky
"Meryl S. Rose 1948: Nierentumor auf Salamander bertragen.. breitet sich aus,
fhrt zum Tod..
vollstndige Heilung, falls Bein mitten im Tumor abgetrennt ->
Regenerationsstrom fr Bein und Rckbildung des Tumors" Becker: "The Body
Electric" S.217f
Tzip
Tzip
Czip
Kzip
Kzip
Kzip
Dzip
Dzip
Dzip
D-
zip
Tzip
Lzip
Ctxt
Ezip
Rzip
Bzip
B1zip
Rzip
zusammenstellt" hier
"Ergebnisse mit Bares Rife-Gert (Batyah-Projekt)" hier
Barry Lynes: "The Cancer Cure That Worked: 50 Years of
Suppression" ber Royal Rife, der mit elektr. Verfahren um 1930
bei Krebs fast 100% Heilung erzielte.. Labor zerstrt.. damit
heilende rzte aus der rztekammer ausgeschlossen.. Heilgerte
zerstrt.. Unterlagen ber Heilerfolge systematisch vernichtet..
Wissen unterdrckt.. Bestseller mit besten Kritiken..
die Krebstherapie, die funktionierte!
Barry Lynes: "The healing of Cancer: The Cures, The Cover-Ups
and the Solution Now!" interessant zu lesen, viele Quellen.. hier
"Bestrahlung verndert DNA.. Zellmembranschden.. Rifes
Frequenzen gegen BX wrden evtl. nicht wirken.. Bestrahlung
knnte Krebszelle erzeugen die Rife nicht heilt" hier
"malignes Melanom.. rechter Fu amputiert.. Rezidiv im Stumpf..
Dr. Stafford -> Vorschlag Rife/Crane 880Hz (Streptococcus),
2008Hz (Sarcoma), 2128Hz (Carcinoma) je 5min ber Herz..
728Hz (Staphylococcus) 10min ber Herz.. 800+1550Hz (TB) je
5min.. destilliertes Wasser, Welche's Grape, reiner Orangensaft
(nur Flssigkeit).. Ernhrung.. 1959" S.273 'Blast It' hier
Waynes Erfolge mit Rife hier . . . probieren Sie es nicht selbst
mit der Steckdose!!
* 70-80 Brustkebs geheilt Diagnose ber 3 Freq, wenn instabil:
Tumor,bsartig,Metastasen
* Dutzende Mnner Prostata-, Dickdarm-, Hirnkrebs, Hodkgin, HIV
* Axel 70.. Dickdarmkrebs.. keine Chemo/Bestrahlung..
lebenslang knstl. Darmausgang angedroht.. 11x Rife-Generator..
beim letzten Mal blieb Freq. auf Anzeige stabil.. Chirurg konnte
Tumor nicht mehr finden..
* Williams 77.. Prostatakrebs.. PSA 40 -> 25.. Maschine wirkt..
* Hirntumor.. 12 Frequenzen.. zu 75% schrumpft er und
verschwindet..
* Sal 71.. Nierenkrebs.. Metastasen in Lunge..
Chemo/Bestrahlung/alternativ..
* Wayne 19.. Hodgkin Lymphknoten befallen.. inoperabel.. 3x
Chemo.. wchst genauso weiter.. zustzlich Rife-Frequenzen.. 1
Jahr.. verschwunden..
Fe in gereinigtem Wasser.. el. Spannung dazwischen.. 220V DC
fast ohne Strom!.. Vibrationsenergie der Frequenzen.. Beine
zittern.. kein Problem.. selbe Elektrizitt wie im Krper.. Jack
Nicklaus.. Arnold Palmer.. Rife Function Alternator.. alles im
Krper elektrisch gesteuert, bis auf Zhne/Finger-/Fungel, die
auch nach Tod weiterwachsen.. alle Molekle vibrieren.. el.
Resonanzfrequenz zerstrt Viren/Bakterien wie Ella Fitzgeralds
Stimme das Glas.. Rifes Maschine heilt und diagnostiziert (vgl. FScan).. wenn Freq. herumspringt ist etwas nicht i.O.. Diagnose
stimmt mit rztl. Diagnosen zusammen.. Krper hat 122
Frequenzen.. jede wirkt auf einen speziellen Teil.. Frequenzlisten..
"Wundermaschine" aus Deutschland.. wirkt nicht bei jedem.. bei
Lungenkrebs 26 Freq..
Rzip
Pzip
Bzip
Tzip
Tzip
Breast (Brust)
(Bronchial)
Liver (Leber)
Liver (Leber)
Liver (Leber)
Liver and Biliary (Leber)
Cervical (Gebrmutter)
Stomach (Magen)
Neural? Insulinomas?
Majority of Non-Hogkins
Lymphoma
Hairy-cell Leukemia (Leukmie)
A Typ Leukemia Japan (Leukmie)
Burketts Lymphoma, naso
pharyngeal (Rachen)
Kaposis Sarcoma, Myeloma
Bladder (Blase)
HMTV?
462, 852, 1582
Hepatitis B Virus
Hepatitis B Virus
Hepatitis C Virus
Liver Flukes
Human Papilloma Virus
HPV16/18
Helicobacter Pylori
Polyomavirus BK und JC
Epstein Barr Virus
Retrovirus HTLV-2
HTLV-1
Epstein Barr Virus
Kaposis Sarcoma Herpes
Virus
Schistosomiasis
Czip
Dzip
Dzip
Dzip
Kzip
Maes: "Elektrosmog,
Baubiologie - praktis
Jeder 3. umweltkran
Wohn-/Schlafbereich
von Hochspannungs
mehr Wohngifte als a
Straenkreuzungen.
mit geballter Kompet
lesbar..
Klaus-Ulrich Hoffman
Immunsystem 2. Die
der Wahrheit " ..Ursa
Behandlungsmglich
Darstellung.. interess
Gesunde und Kranke
Klaus-Ulrich Hoffman
Immunsystem 3. Kre
Medizin. Behandlung
..biologisch sanfte Al
Lebensqualitt, Gesu
Selbsthilfegruppe M
des Krebsproblems
Andere Hilfen und Ta
2 90537 Feucht DM
Batmanghelidj: "Was
Umlernbuch." Wirkun
Alterungsprozesse..
Kopfschmerzen.. Du
Krper an Wasser m
Wassers klar und ve
einleuchtend.. Wass
Krankheiten ohne M
auch bei Krebs.. we
Campbell: "Hydrogen
medizinisches Wund
Stockburger: "OzonDurchblutungsstrun
Schmerzen, Hauterk
Herstellung.. Hinweis
Behandlungstechnik
Eigenblutbehandlung
Extremittenbegasun
rektale Begasung.. o
Olivenl..
Dehmlow, Jungmann
Sauerstoff-Therapien
wissenschaftliche Gr
Handbuch zu allen w
Sauerstofftherapien.
Eigenblutbestrahlu
Oxidationstherapie (H
Therapie.. degenera
Durchblutungsstrun
Sauerstoffmangelzus
Diabetes.. Mglichke
Hobday: "Sonnenlich
Huser heilen/beuge
Brustkrebs, Herzerkr
Wundheilung..
Moermann, Breuss:
andere scheinbar un
natrlichen Mitteln
und ihre abwehrstrk
Forman, Niederwiese
Gtter." fr Heilzwec
Lapachobaumes.. be
Blutzucker.. Diabete
Blutkrperchen.. fhr
Geschwre, Asthma
immunstimulierende
Krebsheilmittel pat
Teegetrnke, Speise
Schweppe, Schwarz
Lapacho." Heiltee zu
Krankheiten/Beschw
Zucker.. Anwendung
Lapacho-Entgiftung
Simonsohn: "Gersten
Ergnzungsmittel un
hervorragendes Nh
im Krper erhht.. An
weie Haare wieder
Gesundheitselixier..
Green
Blank,Streibel,Amelu
"Diagnose: 'Damit m
DANKE!'" ..krpereig
und Abtransport aller
Enzymmangel als Kr
mit Regulat.. Erfolge
Schmerzen, Mdigke
Durchblutungsstru
Pilzen, Kopfhautjuck
Arthrose, Schlaganfa
Parodontose, Akne,
Jopp: "Risikofaktor V
Auswirkung - Verme
gengt nicht.. die Su
frischem Obst und G
nehmen 40-80% der
das Minimum der fr
Mengen an Vitamine
Zivilisationserkranku
abgesichert durch 10
wissenschaftliche St
sachlich und ntzli
Burgerstein, Schurga
"Burgersteins Handb
unschlagbar! Die "B
Ernhrungsbchern.
Erfolgsberichte bei A
Herzrhytmusstrung
Diabetes, Nierenvers
bergewicht, Depres
Immunschwche, Pr
Nhrstoffmanko der
ergnzen.. sehr vers
Chance fr aufgesch
Hippokratischen Eid
Pearsall: "Heilung au
Lebensenergie, die
erstaunliche Heilproz
Hay: "Gesundheit fr
ist nichts anderes als
Harmonie und des V
Ausfhrlicher als 'He
Pechatschek: "Kohlb
der Natur" enorme H
Stoffe aus dem Kr
soviel Vitamin C wie
Salben...
Leonhardt: "Noni" ..
bei den Einwohnern
verwendet ..Bluthoch
Verdauungsproblem
Immunsystems
Simonsohn: "Papaya
Wunderfrucht" ..bein
groem, entzndung
Wirkspektrum.. eines
Lebensmittel
Pies: "Olivenblatt-Ex
jahrtausendaltes Hei
Gesundheit: Olivenb
Blattextrakt wirksam
bei Parasiten.. Pilzen
verbessert Blutflu.
Fasching: "Teepilz K
Stoffwechselerkrank
Leiden.. sogar Krebs
Eigenschaften..
Sanders: "Leben ! Ic
gesund" hervorrage
wertvolle Schriftstck
in die Hnde fallen u
noch ehrlicher mit sic
Informationen zur Au
hervorragendes Buc
Bestseller..
Herer/Brckers: "Die
Nutzpflanze Cannab
Wirkung bei Asthma,
Muskelkrmpfe, Rc
Rheuma, multiple Sk
Antibrechmittel bei C
Appetitanreger, Depr
antibakterielle Wirku
Lungen, zur Behand
Lungenemphysemen
Migrne, fr Schlaf u
Hanfsamen (indisch
Grundnahrungsmitte
Glanz der Haut, Haa
Arterien, Strkung d
Akne, trockene Haut
Clark: "Heilverfahren
Fallgeschichten gehe
elektronischer Gert
bzw. deren Beseitigu
Wollenberg/Blasig: "D
eine Infektionskrankh
umfassend beschrieb
gibt es hier
K. Windstosser: "Pol
und Krpergewebe a
Krebsgeschehens. E
ihrer Beobachtung u
Jahrhunderten mit ei
Hans A. Nieper" fast
Gebiet angefhrt mit
jeden Anfnger auf d
notwendig.. reiche Q
Weigel: "SANUM-Th
und ergnzende Ma
..medizinisch-ganzhe
Prof. Enderleins.. wie
SANUM-Mittel eindru
Ergebnisse bei einer
Erkrankungen erzielt
der Praxis fr die Pra
Therapieplne durch
Brehmer: "Siphonosp
Br."..Beweisfhrung
Semmelweis-Verlag.
Robert O. Becker, Se
Electromagnetism an
Life"..Einflu elektrom
Krper.. Regenerier
Experimente und F
interessant.. einfach
der Hand zu legen..
Bachler: "Erfahrunge
To provide you with some serious background information on the subject, here is an extract from a
paper entitled:
"Dr. Rife and the Death of the Cancer Industry"
The Possible Genetic Cause of the Great Majority of Cancer Cases that are Microbe Induced
In 1931, after seven years of attempting to isolate a microbe cause of cancer from over 20.000 cancer
tissue samples, Dr. Royal Raymond Rife did just that. Rife's 1931 discovery of a cancer microbe finally
reached general public notice in 1944. That year a article entitled The New Microscopes was
published both in the February issue of The Journal of the Franklin Institute and in the 1944 Annual
Report of the Board of Directors of the Smithsonian Institution.
Rife's work was not then and has not yet been appreciated by microbiology. because microbiology has
a large blind spot, both in its physical visual view of the living microworld and in its conceptual view of
the structure and life cycles of the living microworld. If you wish to look at living cells, the best research
optical microscopes generally available throughout the world only reach about three thousand power.
These microscopes in general cannot detect viruses, unless a fluorescence technique like Rife's
fluorescence technique is used. These microscopes give very limited structural detail about living cell
organelles. If the biologist wants detailed structural information about some cell structure, they use an
electron microscope. However, the electron microscope picture is the picture of a dead, often highly
degraded and distorted structure. This is because the sample preparation process, which produces a
sample that can withstand the conditions of high vacuum and bombardment by a high energy electron
beam has degraded and distorted the original living structure. So at best you end up with a distorted
snap shot of a non living structure.
I do not mean to denigrate the great and marvelous contributions made by the electron microscope. I
have considerable personal experience with the use and operation of scanning electron microscopes
and I hold them and transmission electron microscopes with high regard. I particularly appreciate the
immense contributions made to the understanding of micro cell structure by the massive ultra high
resolution transmission electron microscopes such as can be found at the University of Colorado at
IBoulder,CO. . However, all this not withstanding. I also know the electron microscopes' limitations,
both physically and in its actual use by researchers. If you have a interest in understanding biological
microstructure, go to the trouble of going to a good research library and look up the Feb. 1944 issue of
The Journal of the Franklin Institute or the 1944 Annual Report of the Board of Directors of the
Smithsonian Institution. In the RE. Seidel and M. Elizabeth Winter article, The New Microscopes, look
at the photographic plates. Note the high quality resolution comparable to that of current electron
microscope photographs. The photograph of the typhoid bacillus was taken with the Rife Universal
Microscope at 23,000 power and then photographically enlarged to 300,000 power. Note that this
photograph has the resolution commonly found in todays high resolution electron microscope pictures
of bacteria. Further note that the resolution in this print is not as good as the resolution on the negative
it came from do to the limitations in printing pictures in 1944 and even today. As was explained in
technical detail in Appendix A, Rife had discovered an optical assembly configuration that effectively
suppressed all Fraunhofer diffraction phenomenon. while at the same time he made the organism light
itself by a natural fluorescence phenomenon. This fluorescence phenomenon was achieved by
illuminating the specimen with an intense narrow wavelength band of light. The particular band of light
was unique to each microbe. Also note that this is a photograph of an intact living bacterium. If you are
familiar with current microbiology. you know that little if any time is spent by the great majority of
researchers watching and studying live microbes. Except for spot optical microscope checks to make
sure live cultures are as they should be or are as assumed they should be. research is carried out by
biochemical techniques the results of which are interpreted in the light of past perceived research
results. In short actually very little live observation on microbe life cycles are carried out by
researchers anywhere on the entire planet.
This brings us to the other blind spot in biology. Its name is pleomorphism or the ability of a microbe to
change its physical form. During the later half of the 19th century and into the early part of this century,
a sharply fought battle over whether or not some microbes could change their physical form was
waged. Those infavor of monomorphism won out and it became "heresy" to advocate pleomorphism.
After two years of reviewing the research for and against pleomorphism, it is clear that the
monomorphists were wrong. The monomorphists won the argument because they had political
prestige and economic positions of leverage. The monomorphists used optical microscopes and lab
techniques not adequate to determine the issue due to inadequate magnification power, lack of nonlethal staining methods, sheer ignorance, and sloppy to lazy research work. If you go to the trouble of
looking up the Feb. 1944 issue of the Franklin Journal, note that the Rife microscope photograph of
the typhoid bacillus clearly shows the formation of a filter passing form (the original operational
meaning of the word virus) of the typhoid bacillus, in the top end of the bacillus. Rife found that when
this bacillus virus was released by the bacillus, it had a bacterium flagella and was motile. Now all of
this is just plain crazy, if you are a currently trained microbiologist. However, no currently trained
microbiologist owns or uses a Rife type optical microscope which could easily view this and the similar
BX cancer virus, which is also a motile virus (ovoid body with bacterium flagella). The ovoid body
dimensions of the BX cancer virus are 750 angstroms long by 500 angstroms thick. It is propelled by a
proton transport flagella the same as the parent bacterium. This "virus" will easily fit inside the so
called AIDS virus (HIV) outer capsid and is comparable in size to the inner (HIV) capsid. I now ask you
microbiologists reading this: Will this BX cancer "virus" be recognized in a high power electron
microscope photograph for what it is or will it just be considered another piece of degraded cellular
debris in the prepared cancer cell section sample? Much of what you see is what you are trained to
see. How are microbiologists trained to see?
Rife, using his Rife type microscope, had for seven years been able to observe and isolate a microbe
from carcinoma cancer tissue. However, upon injection of concentrations of this microbe into test
animals, no cancer was produced. In 1931, Rife got the idea to expose a sample of card normal breast
cancer tissue to 24 hours of broad band violet to ultraviolet light exposure from a argon gas discharge
tube (see Journal of the Franklin Institute article). A one half centimeter on a side cube of carcinoma
breast cancer tissue was placed into a test tube containing Kendall medium and incubated at 37
degrees centigrade. The test tube was then exposed to 24 hours of argon gas discharge light. The test
tube growth medium was then examined under the Rife Universal microscope. at a magnification of
10.000 diameters. The medium was found to be teeming with animated ovoid microbes 1/15 microns
long and 1/20 microns thick. which Rife eventually named the BX cancer virus. This BX cancer virus
was then carried through fourteen transplants from Kendall Medium to Kendall Medium. The animated
BX cancer virus multiplied and remained of constant form. The fact that the BX cancer virus could
multiply on a sterile non-living growth medium indicated that Rife's BX cancer "virus" was a living
microorganism unlike the currently accepted understanding of a virus as a biological structure
dependent on cellular metabolism to regenerate (multiply) and propagate its existence. From current
knowledge, we must assume that Rife's BX cancer virus contains within its structure, a gnome, DNA
decoding enzymes, protein digestive enzymes, transfer RNA, ribosomes, and associated proteins.
When concentrations of this BX cancer virus were injected into 426 albino rats, all rats developed
cancer tumors at the injection release site in the animal tissue. Further experiments with the BX
cancer virus demonstrated that it can be easily changed from one microbe form to another by means
of altering the media upon which it is grown. Rife found more than six forms, which the BX cancer
virus could be transformed into. These included: 1) BY cancer virus, which caused sarcoma cancer
tumors. 2) Cryptomyces plemorphia fungi, which Rife found implicated in rheumatoid arthritis. 3)
Progenitor cryptocides. 4) Bacillus coli. 5) Bacillus typhosus, and 6) Virus of the bacillus typhosus,
which can be clearly seen in the photograph of the typhoid bacillus appearing in the article The New
Microscopes of Feb.1944.
Rife was not the only researcher to find a microbial cause for cancer. Many others have also. Nor was
Rife the only one to build an optical microscope that could see the BX cancer virus. Currently in
Canada the biologist Gaston Naessens uses an ultraviolet microscope which can easily view the BX
cancer virus in living blood from cancer patients. Naessens' microscope uses an ultraviolet light
source which is first polarized. then focused down and sent through a frequency doubler crystal and
finally sent into a special condenser section for dark field microscopy. Looking at live blood from
cancer patients, Naessens has found and made videos of at least sixteen different forms the BX
cancer virus can be transformed into. I have viewed some of these videos and the anti mated (motile)
BX and BY cancer virues are clearly visible and look just as Rife described them.
As for the other researchers who have found the same microbial cause for cancer as Rife, they have
all been persecuted, while their work has been maimed and discredited by the corrupt higher ruling
circles of what currently passes for legitimate medicine and microbiology. Perhaps a brief review of the
work of one victim is in order.
Dr. Virginia Livingston-Wheeler in 1947, while studying tumors, found the same organism in all of
them. Her findings were published in August 1948 by the New York Microscopical Society Bulletin.
Later in Dec. 1950, Wheeler had an article published in the American Journal of Medical Sciences on
microbes cultures taken from both human and animal tumors. On Sept. 10, 1953 The Washington
Post reported the discoveries of Dr. Wheeler and her team from Rutgers-Presbyterian Hospital
Laboratory which were disclosed at the 6 th International Congress of Microbiology in Rome. They had
found conducive proof of a microbial cause for cancer. When Dr. Wheeler and her group returned from
Rome to Rutgers-Presbyterian Hospital they found that the funds for their laboratory were being cut
off. The laboratory was closed. This was the behind-the-scenes work and doings of Dr. Corneluis P.
Rhoads, the head of Memorial Sloan-Kettering Cancer Center. The fear of the cancer industry elite is
and was immense. If the truth about the true cause of cancer becomes known, a cheap cure will be
found shortly thereafter. This will kill the cancer goose which lays tens of billions of dollars worth of
eggs a year. Is there nothing these scum will not do for their god money? No!
The San Diego Union of July 31st, 1949 reported on the work of Dr. Gruner of Mill University,
Montreal, Canada and Dr. J.E. Heft of Windsor, Canada. They were in agreement with and had
experimental proof that Dr.Royal Raymond Rife's discovery that cancer was caused by a microbe was
correct.
In 1950 Dr. James Hillman of RCA Labs in Princeton, N.J. found the BX cancer virus using an electron
microscope.
For an in-depth documented overview of the massive suppression by allopathic medicine of real
cancer treatment breakthroughs that worked, I recommend you read: 1) The Cancer Cure That
Worked, by Barry Lynes, and 2) The Healing of Cancer, by Barry Lynes. Both books are available
through Marcus Books, P.O. Box 327, Queensville, Ontario, Canada LOG 1 RO. (41 6)-478-2201.
I will now share with you some observations about cancer cells and a classic experiment in which they
are compared to normal cells, which suggests a simple answer to how cells infected with the BX
cancer virus become cancerous. It has long been noted that cancer cells act and appear somewhat
like undifferentiated embryonic cells. Furthermore, cancer cells apparently have mostly an anaerobic
(without oxygen) metabolism. Note that the only time in the normal life cycle of mammalian cells in
which they are of a undifferentiated embryonic nature and also have an apparent appreciable
anaerobic metabolism is the period between the time the female egg, the ovum, has been fertilized in
the fallopian tube and just before a viable placenta has developed in the uterus. Geneticists and
embryologists have shown that the entire development of the fetus from just-fertilized ovum to the fully
developed fetus is governed completely by sequentially read and expressed genetic information.
There is an exceedingly complex genetic interchange and feedback control system in operation. Some
of this genetic code is used only for a short period of time and is then sealed away not to be read or
opened up again in the individuals existence, except during chromosome copying prior to cell division.
Cancer cells act as though they have had some set of embryonic gene sequences reactivated.
However, in the now mature differentiated mammalian cells from which this cancer cell has been
derived, the control system that normally would have deactivated this embryonic gene sequence(s) is
itself long since deactivated. The cancer cell is in a run away catch 22 situation.
It has been found that many genes occur in sequenced sets in which none of the genes in the
sequence can be read and expressed unless the first gene in the sequence has been opened to be
read. Just in front of that first gene there is a DNA code sequence which has to have a promoter
protein bound to it so that the DNA code sequence reading enzyme can temporarily attach to this
promoter protein and then begin reading/translating the DNA code of the gene sequences into
messenger RNA for protein synthesis by ribosomes. For this promoter protein to attach to its DNA
coupling sequence at the beginning of the gene sequence, this sequence must be in the normal BDNA right handed double helix form (see Figures 1 and 3). If the coupling site code sequence or the
DNA code sequence immediately in front of it has a blocking protein attached or is in the form of the
left handed Z-DNA double helix (see Figure 2), the promoter protein can not bind/couple with its DNA
code sequence and therefore the entire sequence of genes will not be read and expressed. The ZDNA double helix form is a very compact form of the double helix. It has no major grove structure like
the B-DNA double helix which allows a promoter protein to physically match up with a specific DNA
code sequence which will manifest itself in the unique molecular structure of the surface of the major
grove for that unique DNA code sequence. The Z-DNA double helix structure gives very little
information about what the DNA code sequence is in its core. For a left handed Z-DNA double helix
associated with a specific DNA code sequence to convert itself into a right handed B-DNA double
helix, so that the promoter protein can attach, the concentrations of various ions in the cell nucleus
must be in certain specific ranges for that specific Z-DNA sequence. The specific concentrations and
ratios of ions in the nucleus is determined by the actions of ion gates and pumps in the cell outer
membrane. These ion gates and pumps are controlled by messenger proteins and compounds from
both inside and outside the cell membrane. What this means is that the cell genetic expression can be
greatly influenced and controlled by the genetic expression of other cells and cell sets (organs). And of
coarse during embryonic development this external cell influence is in dominant control of the whole
cell system of membrane ion gates and pumps.
Now that some of the basic genetic control process has been stated, several questions need to be
asked. Can one or more microbe proteins or chemical compounds be generated and released inside a
mammalian cell by a parasitic microbe? Can these proteins or compounds act as a messenger to
open up or close down cell membrane ion gates or pumps? Can this opening or dosing of ion gates
and or pumps cause a gene sequence which is normally only open during early embryonic
development to open up again and thereby cause the cell to go cancerous? I believe the answer to all
these questions is yes. Of course there are many other possibilities i.e. some of these protein
fragments may act as promoter proteins or combine with and remove blocker proteins, thereby
allowing a promoter protein to attach to a DNA sequence and thereby initiate DNA transcription.
Dr. Robert 0. Becker, M.D. has written a book The Body Electric in which he goes into great detail
about tissue regeneration processes and their electrical and ionic connection to genetic expression. I
will now use information distilled from Becker's book which supports my above suppositions. In 1948
Dr. Meryl S. Rose performed a mile stone experiment on salamanders. Rose transplanted frog kidney
cancer tumor tissue onto a salamander's hind limb. These frog tumors were virus induced. The results
of his experiment, however are the same even if the tumor is carcinogen induced, which was done
later. The transplanted tumors would grow and spread, leading to the salamander's death, if no
intervention was taken. However, if Rose amputated the limb below or through the middle of the
tumor, the salamander would regrow the limb and in the process the tumor(s) would disappear, even if
the tumor had already spread to other body locations. Tissue biopsies of the wound region during
regeneration showed that both salamander cells as well as cancerous frog kidney cells
dedifferentiated into embryonic cell forms during the blastema formation process as the wound healed.
Even more amazing, as the blastema propagated forward, regenerating the limb, both embryonic frog
and embryonic salamander cells of the blastema multiplied (devided). They differentiated into the cell
types needed to form the new limb tissue, i.e. muscle cells, cartilage cells, capillary cells, etc. In later
years researchers such as Becker demonstrated that it was the near unique ability of the salamander's
nervous system to drastically change the ionic environment around blastema cells, along with
hormone secretions from nerve dendrites, which allowed blastema cells to dedifferentiate into
embryonic cells and then to red differentiate into the new cell types of the regenerating limb. Becker
and other researchers were able to get rats to regrow most of, or all of a amputated limb. They
implanted a negative current source that produced a negative electric potential distribution inside the
limb directly behind the amputation site. This closely mimicked what a salamander would have at that
site if it were scaled up to the rats size. To understand what is happening here, you need to know that
in a rat just as in a salamander the myelin sheath cells coating the motor nerve fibers carry an electron
current through collagen fibers which are N-type semi-conductors. This current is deposited mostly
into the body's electrolytic solution surrounding the cells near where the nerve fiber ends. The myelin
sheath cells coating the sensor nerve fibers carry an electron current on their collagen fibers away
from where the sensor nerve fiber ends. The motor nerve fibers are essentially all in the body interior
and the sensor nerve fibers are essentially all on the body surface. As a amputation wound heals over
with skin, surface sensor nerve fibers cover over what is normally a motor nerve fiber region. In a short
period of time the cells under the new forming skin layer can be converted into dedifferentiated
embryonic cells under the influence or control of the external cell membrane ionic environment at the
wound site as determined by the electric currentipotential of the combined sensor and motor nerve
sheaths activity in the wound area ( blastema formation zone). I can not here go into all of the
wonderful detail of Becker's book. However, I hope I have given the reader at least an understanding
of how cancer can possibly come about by a simple change in the ion environment in the cell nucleus.
If you are interested in tissue regeneration or are aserious biologist. I can not recommend Becker's
book enough. Particularly the last chapter, Postcript: Political Science. This chapter with great clarity
and skill, clearly shows why we as a nation need to dismantle all centralized cesspools of corruption
as exemplified by the National Institutes Of Health. The NIH needs to be replaced by regional
institutes which are government funded, but ran and controlled by democratically elected
administrators elected by the research community.
Before ending this appendix, a warning and an explanation of why X-ray radiation should never be
used to treat cancer. Rife was able to isolate the BX cancer virus from cancer tumor tissue samples.
He then exposed these viruses to 24 hours of ultra violet light exposure. This virus obtained in this
manner was 100% effective in inducing cancer in lab animals. His form of the BX cancer virus was
exceedingly virulent. Other researchers who apparently isolated the same BX cancer virus, or a form
of it, and inoculated test animals by similar methods only had approximately 25% cancer induction
rates. A possible simple answer for the discrepancy is that the ultraviolet light from the argon
discharge caused some of the adjacent thimine DNA base codes to dimerize (chemically bond
together). When the DNA reader enzyme which translates the DNA base code into messenger RNA
for protein synthesis comes across a dimerized thimine base code pair, it stops RNA synthesis. The
reader enzyme then breaks into two fragments. One fragment stays at the dimerization site to mark it
and the other fragment initiates a complex set of enzyme reactions to remove the dimerized pair and
replace them with a new undimerized pair. During this repair process the messenger RNA generated
fragment is released. If this messenger RNA fragment contains the genetic RNA base code sequence
for ribosome attachment, it will be read by the ribosomes and a protein fragment will be generated and
released. In particular, if the RNA fragment is fed into a cluster of ribosomes (polyribosomes) which
are located on or associated with the intercellular matrix web intersections, we can expect many
copies of the coded protein fragment to be generated and released Furthermore, since the RNA
fragment does not contain the normal stop synthesis code and message RNA end sequence base
code, the RNA fragment is not likely to be immediately dismantled after polyribosome reading and
protein synthesis like regular messenger RNA is. This fragment is likely to be read over again and
again. Now. if the generated protein fragment happens to be an activator or suppressor of a cell
membrane ion channel or ion pump you have the potential beginnings of a cancer producing situation
as discussed above. This protein fragment(s) might also act as a promoter protein that enables the
DNA reader enzyme to attach to and read a gene sequence. Or this protein fragment may combine
with a blocker protein on a repressor gene at the front of a DNA gene sequence and remove it,
thereby allowing a promoter protein to combine with a DNA sequence and then facilitating attachment
of the DNA reader enzyme (RNA polymerase). All of this is not the normal "plan" of the normal cell
metabolism. An excellent example of this sort of defective protein production and its cancerous
consequences is the genetic disease xeroderma pigmentosum. In it the individual has an inherited
defect in their ability to repair the aforementioned DNA base code dimerization damage. They are
hypersensitive to sun light exposure and develop pre-cancerous and cancerous skin conditions. They
usually die of skin cancer before their twentieth birthday. Now what does this have to do with massive
cellular tissue damage suffered by cancer patients while under going standard allopathic medical Xray treatment for cancer? As stated in Appendix B. Rife's normal treatment for cancer patients was
three minutes of exposure once every three days to his frequency instrument. This frequency
instrument, when treating cancer, probably produced repeating packets of 11,780,000 or 23.560,000
light pulses per second. These light pulses in turn produced ultra low intensity ultra sound in the
patient's body of a frequency of 11.780.000 or 23.560.000 cycles per second, which is the
approximate mechanical structural resonance frequency of the BX cancer viruses. The Bx viruses
disintegrated. In the normal carcinoma cancer cell, there are thousands of BX cancer viruses. When
these BX cancer viruses all disintegrate together at the same time, they release their gnome, digestive
enzymes, ribosomes, assorted proteinslenzymes, etc. into the cell. The cancer cell is overwhelmed,
dies, and promptly disintegrates. When using Rife's cancer treatment method on a cancer patient that
has undergone extensive allopathic medical X-ray damage, there is the high possibility of an
encounter with a new kind of cancer cell which Rife's treatment method won't work on. Allopathic
medical X-ray treatment causes significant ultraviolet light, ionization, and free radical production both
in tumor tissue and adjacent normal tissue. With this ultraviolet light, ionization and free radical
production, there is the associated dimerization of adjacent DNA base code molecular pairs. Both
cancer cells and adjacent non cancer cells suffer significant cell membrane integrity damage from the
X-ray radiation. All of this culminates in the possibility of a heavily radiation damaged BX cancer virus
penetrating the cell membrane of a non cancerous cell and instigating production of cancer causing
protein fragments as discussed above. But its own gnome so badly damaged that it can not propagate
itself. If this were to occur, then a cancer cell could be created which was not infested with the BX
cancer virus and therefore not treatable by Rife's frequency instrument or ultra sound of 11.789,000 or
23.560.000 cycles per second. Of coarse the X-ray radiation alone could generate a cancer cell that
the original Rife's treatment method would not cure.
Well we have skimmed over a lot of technical data in this appendix. however, I hope the reader now
has a conceptual frame work in which to begin questioning the current allopathic medicine approach to
cancer causes, treatments, and cures. Only by honest researchers going back and looking at the
suppressed results of past honest cancer researchers can we hope to find honest valid answers about
cancer causes and cures.
"An important scientific innovation rarely makes its way by gradually winning over and converting its
opponents: it rarely happens that Saul becomes Pual. What does happen is that its opponents
gradually die out and that the growing generation is familiarized with the idea from the beginning."
Max Planck
Taken from: DR. RIFE AND THE DEATH OF THE CANCER INDUSTRY. a paper by physicist Gary
Wade.
P.S. - It is now empirically known that many types of cancer can be easily and quickly killed by
exposure to pressure square waves of a frequency of approximately 2127 cycles per second. It
appears that one or more of the higher frequency hidden fourier sine wave components. i.e. 3(2127),
5(2127), 7(2127), 9(2127), etc. opens up ion gates on the cancer cells' membrane and radically
changes the ionic conditions inside the cancer cell such that it drops the bi-lipid layer potential
difference below some critical value below which the cancer cell can not recover and it dies.
www.papimi.gr/cancer.htm
No idea presented here for the first time may be expressed or transmitted in any form without ethical
acknowledgement and proper due reference to the Author.
We would like to state a more consistent theory of cancer that we came up to, based
in ten years of experience with the fascinating results obtained after PAP IMI exposures,
and, compare these results, with other theories and methods .
The first assumption concerns the most basic principle of physics, which we have
come to several years ago in association with cancer. The assumption concerns the physical
energy of the cell. Energy in physics, even in universe as a whole, is the most fundamental
and universal concept of cause and effect, which controls every action in the cosmos, between
a donor of the energy -the cause, and a receptor of the energy -the result. We may say, a
system with energy transformed from one form to another or given from a donor to a receptor,
is an alive system. A system with energy but not given and taken between donors and
receptors is a died system. We state below this extremely simple and fundamental principle
for cancer in relation to the physical energy condition of a cell.
We demonstrate the above, with a common example taken from agriculture, and
known practically to all farmers.
Let us suppose, that we have two plants , which we water every day. The plants stay
healthy, but do not produce flowers or seeds to enter into the of reproduction. However, as
soon as, one of the plants is deprived of watering, and as a result is found in a state of stress ,
having less nutrition and energy , then it flowers and reproduces to survive by extension. That
is, as soon as, one of the plants is found in a stressful environment , i.e. without nutrition and
energy, (because of lack of water which acts as the carrier of nutrition), it produces as soon as
possible flowers and seeds, in order to multiply, and obviously, tries to survive as species, via
a large number of successors, following an "instinct" or a survival "program ", deeply
encoded in its DNA by its creator.
This is a general phenomenon of reproduction, known for almost all plants .
The same holds true for an advanced organism , which may secure its food fairly
easier versus a primitive one, which strives every day for food. Indeed, a primitive organism
is in a continuous state of stress , for finding food and energy . In order to counter this and
overtake its daily battle for food and to survive as species, it multiplies very fast and in large
numbers.
On the contrary, an advanced organism or animal multiplies very slowly, and in
fewer numbers. For example, big animals like elephants or humans multiply very, very
slowly, with respect to a smaller animal like a rabbit or a primitive organism for example.
The same is true for a poor, versus a rich, society. Poor couples of primitive societies,
usually tend to have five, ten or more children with respect to rich couples of wealthy
societies, which tend to have one or two children only.
A low energy proliferating cell with limited resources and energy availability, for
any reason, because it is in a toxic environment , or because it is found in a rather
anaerobic (non-oxygenated) environment, which was not intended to be so in the first
place, or because it is surrounded by a tumor, or it is adjacent to a tumor, which lacks
veins and arteries and strives for energy and food, and without possibility of proper
oxygenation, nutrition, or metabolism and therefore energy, causes to the adjacent or
nearby cells, a similar shortage of nutrition and energy .
We can say, proliferating cells in energy crisis, cause a similar "energy crisis" to nearby
cells. In other words, the energy crisis of a smaller area of cells, is diffused or extended to a
broader area, because of the most basic and fundamental principle of physics , the principle
of conservation energy in a limited area.
reactions and
With above conditions and when transmembrane potential drops below 15 mV, it
leads to cell division and eventually cell over population, which enhances and diffuses the
existing energy crisis from the cells to the system., in other words, energy crisis is then
extended and generalized for the system as a whole with the characteristic of low energy and
ischemia for the system itself. We may say, that cells with low energy get into a "panic" state
of feverish multiplication, in order to preserve their species, following an inherent program
encoded in the most fundamental part of their DNA for survival under the emergency of
severe conditions. So, more cells are produced inside the tumor, or more cells are produced
adjacent to the tumor which are found naturally in a low energy or poverty environment,
diffused from the expanding prime energy crisis - prime cancer. Newer cancer cells will
lack even more energy for the same reason. So, we see naturally why the tumor grows or
diffuses to adjacent areas and tissues, a phenomenon known as "cancer diffusion", i.e.,
cancers ability to diffuse to adjacent healthy cells and tissues which is particularly
unexplained today. Obviously, the more those "low energy" cells multiply, the more is the
need for even more energy in the organism as a hole to feed the newborn cells. Therefore,
the energy crisis and the cell starvation expands and expands.
The organism soon becomes a "poor society in a panic crisis situation" as a whole,
lacking even more energy . In such a case, more and more cells will become into a "panic
state" for nutrition and energy and so, we see that cancer thriumphally metastasizes and
generalizes. The organism or person becomes thin, weak and ischemic, with the common
characteristic of energy lack and improper nutrition. Cancer then spreads and
generalizes, with no way for the organism or person to overcome this increasing need of
energy and nutrition.
Apparently, there is no way out of this "energy crisis" when many more new cells
appear, and, the organism (or the person) dies. This is more or less the macroscopic
"scenario" of the cancer phenomenon, omitting numerous details of the cell physiology, and
the details how the organism gradually fails as a whole, because of its growing "starving
cells over population", and the resulting development of this "energy crisis".
The just fertilized egg is stressed to extinction, its survival program encoded in
its DNA is automatically activated and tries to survive by multiplication in large
numbers.
After a number of proliferating cell copies, biologists then remove the cell copies
back to a proper nutrition and energy environment , where proliferation stops and proper
cell development to identical embryos occurs.
The same technique for plants is known for many thousands of years to farmers of this
planet, called "meristomatic" culturing, or plants cloning as we could say today. This old
technique can be found in encyclopedias. Meristomatic culturing or cloning for the plants is
typical for Orchids confirming directly our above hypothesis of multiplication and cancer.
A small piece of a leave of an orchid is cut and removed to a dry isolated air sealed
environment, and is placed on a dry inorganic material like a stone-wool (used in building
industry for sound insulation). Stone-wool has nothing to offer to the piece of leave in the dry
air-sealed environment. The orchid cells are found immediately in a stressed environment
with complete lack of nutrition other than the nutrition was already in serum of the leave.
Soon the cells in the piece of the leave, because the energy and nutrition crisis they face,
multiply and provide a new orchid.
The above example of orchid is in principle common and typical with meristomatic
culturing of other plants and it is in rinciple the same with the modern technique of modern
cloning in Biology.
However, we may question immediately the following:
Why orchid cells when stressed lead to a new orchid and not to cancer?
Similarly, the other way around:
Why cells when stressed lead to cancer and not to a new plant or animal like in
meristomatic culturing or in biological cloning?
The answer is that meristomatic culturing or biological cloning is always processed away of
the main plant or animal, and then a new identical in form and in function plant or animal
develops, according to its DNA description of the cell, regardless of the location. On a
particular location or anatomic position of an organism, cells differentiate, or specialize, or
restrict their DNA function to a specific task. This DNA restriction imposed by the anatomic
position of the organism is what prohibits a multiplying cell on the organism to develop to a
new independent organism as it would have done away of it and away from the particular
anatomic position.
When starving conditions are imposed on an anatomic position of a plant or on an animal,
either the cells will die or the cells with the "restricted by this position DNA" give a "monster
form" multiplication that we call cancer.
It is beyond the scope of this article to discuss and prove the form giving or cell
differentiation factor on an anatomic position of an organism. For the present scope, we may
only call the controlling factor, the etheric archetype or morphogenic ether of the
organism, after Aristoteles who specifically defines the non material and non visible "Ether"
or the "Fifth Essence", as the non material agent that gives form to inorganic and organic
matter. Additionally, we may say that the etheric archetype seems to be in operation in
giving forms to plants, animals, stones, clouds, mountains, the visible craters of the moon, the
recent (late 90's) found galaxy arrangement in the Universe, forms associated with cohesion
forces, forms of the iris of the eye, forms in crystals, ores concentration, forms in dried water,
dried blood, dried saline, ice, all different forms of the very well known, but still unexplained,
snow flakes!... etc.
Cancer has also form. Though cancer is considered as a non controlled multiplication
of cells. We may directly this an exaggeration because cancer is indeed the opposite. It is a
controlled multiplication in a particular volume. Any arbitrary concentration of cancer cells in
a particular volume is subject to immediate fatality, for no metabolism necessary for any kind
of cells, can be supported. For any cells, including cancer cells, an elementary system
providing nutrients and sustaining at least an elementary metabolism is required. Tumors are
known to create an organized net of capillary tubes, arteries and veins that collectively
connect to a main artery for blood supply in humans. Medication for halting an organized
geometric structure called angiogenesis is provided to cancer patients to eliminate their
tumors. So we see that tumors without the differentiated cells to form geometric structures
called angia or arteries can not survive.
The new factor that differentiates and gives the particular form to new born cells and
geometric form to the non- existing before tumor, we may call here the etheric archetype
of the tumor that gives form to it enabling it to survive.
We shall postulate also here that this form factor is also the same as the universal
form-factor called ether by Aristoteles and that is present every where in the Universe, as in
the examples we gave above, indicate.
From the many years of observations and experimentations and for reasons to
understand the rest of this presentation, We shall also state here, as postulates, two basic
principles which govern this non material form of etheric archetype.
1.
2.
The Principle of fractal information for the etheric archetype, i.e., to carry all
the form information to any point irrespectively of the available volume.
We may conclude, that the methods of treating cancer, obviously should be based
on controlling one or more of the factors, governing the above self-sustained
mechanism of lack of energy and shelf-organized proliferation, which is creating
more need for energy, for the induced population growth.
"We consider this category, to be the first category used to control cancer.
We call this category "destructive", because, it is mainly based on means of
destruction (or means for killing cancer cells), which may, or may not be the same
means, which have already caused cancer in the first place, according to the ideas
expressed here.
Immediately, we see that the destruction methods or any cell destruction
processes are cause of cancer too, as cancer itself is a state of emergency for
survival against any destruction and extinction.
1. Surgery
Surgery consists of removing and destroying of a large population of cancer cells, mainly by
mechanical means.
2.
Radiation
Radiation consists of destroying of a large population of such cells, mainly by gamma
radioactivity.
3. Chemotherapy
Chemotherapy is a generic term derived form two Greek words that of chemia for
chemistry and that of therapia for treatment. However, chemotherapy in practice consists in
destroying large population of cancer cells and other cells, by strong toxic substances.
Constructive methods
1. Primarily restoring the missing energy , so the cells do not need to proliferate, and
subsequently become cancer cells.
2. Helping the organism
in lack of energy .
3. Enhancing the immune system, which may limit the number of cancer cells, and thus
limit the energy and nutrition expenditure of the organism .
Preventing self-organization of tumors by the extinction of the etheric archetype associated
with the particular tumors.
Unfortunately, the existing medical methods are not oriented into the constructive
methods of treatment of cancer. On the contrary, constructive methods are called
"alternative" methods. Law excludes them in certain States of USA, even for those medical
cases, that the destructive methods are admitted to offer no hope.
radiation
For example, in certain States of USA, any treatment of cancer other than surgery,
and chemotherapy is considered illegal!
A law, which in its strict sense, obviously contradicts, and interferes with the freedom
of "scientific" method and development.
PAP IMI exposures are assumed to provide magnetic and induced electrical energy
which transform to direct energy to all cells and particular to "energy thirsty" cancer cells,
by increasing the transmembrane potential of the cells, and thus, putting them into a state
which is known not to trigger proliferation. (Nobel Laureate Albert Szent-Gyorgyi, Cone, and
others).
PAP IMI exposure, due to its unique instant power, may cause considerable disturbances
that apparently may disorganizes or may erase the etheric archetype associated with the
tumor. As soon the tumor's etheric archetype is erased, during the PAP IMI pulse pause, the
rest of the body's healthy etheric archetype may be extended or copied in the area, under the
first principle of extendability of etheric archetypes.
In the respect of the principle of the etheric archetype extendability, a rejection has been
reported in many cases along or after PAP IMI exposures, by an "under the tumor growth" of
healthy tissue , to the point that the tumor itself was rejected, in a manner that a "foreign body
" took place. Also, tumor necrosis has been many times observed without ever any
destructive effect on adjacent or any where else healthy tissue.
Apparently, systematic or generalized cancer cases may not be helped by PAP IMI
exposures and the principle of extendabilty, for there will be no healthy area to be copied or
extended to over a local cancerous area. Indeed, systematic or whole body leukemia cancer
were never found to be helped by PAP IMI exposures.
1.
PAP IMI exposures, are assumed to stop cell proliferation by increasing energy
directly in the form of increase of transmembrane potential and also by reestablishing
cell metabolism to normal levels.
2.
PAP IMI exposures are assumed to enhance or excite the immune system, that may
extinguish cancer cells. Also, PAP IMI enhances other vital functions of the body, i.e.,
liver function, lung function, blood and lymph circulation, kidney function, etc, that may
sustain or enhance in general metabolism
3. PAP IMI may erase the etheric archetype associated with the tumor to the point to cause
tumor disorganization and necrosis, as well as to initiate tumor rejection as a "foreign
body rejection" by under the tumor healthy tissue growth.
As secondary actions of PAP IMI exposures in the respect of treating cancer cells with
the above ideas of "cancer being in a state of low biological energy and nutrition", in
general may be considered to be:
blood
Suggested provisions associated with PAP IMI treatments for reestablishing metabolism:
It is an imperative condition that a cancer patient may have availability in all nutrients for
his intended enhancement of metabolism by PAP IMI.
"All cancer patients should be in good and sufficient order with respect to all of their
vital functions that will sustain sufficiently their metabolism with and after PAP IMI
exposures. In this direction, vital function's sufficient restoration or enhancement is
necessary prior to the fulfilment of PAP IMI exposures.
We anticipate to publish in the near future, (see articles on nuclear transmutation on this
presentation) numerous didactic examples and paradigms, more details of how PMF energy
of the kind the PAP IMI devices is producing, increases cell energy, action and vitality, in
the light of the research of biological nuclear transmutations of low energy, made by
the Great French Scientist Louis C. Kervran; as well as in the light of the recent
developments of cold nuclear fusion relating and confirming Louis C. Kervran of low
energy nuclear reactions, which seem to take place particularly in every biological activity
and to be the soul of every living cell.
We believe Louis C. Kervran's findings are the missing link so far, for understanding
properly basic cell physiology, energy and cancer. Such ideas will distinguish the year 2001
and beyond from all previous years.
January 2, 2002
Death by Doctoring
www.whatareweswallowing.freeserve.co.uk/deathbydoctoring1.htm
Every year in the UK, 200,000 people are diagnosed with cancer and 152,500 people
die. [1] In the US, the annual death rate for this disease is approximately 547,000.[2]
These deaths are recorded as cancer deaths, but how many of these deaths are
really attributable to the disease itself? How many deaths should in fact be recorded
as 'death by doctoring'? When we consider that conventional treatment consists
almost entirely of radiation, chemotherapy and the long-term application of toxic
pharmaceuticals, treatments which are all well known for their life-threatening sideeffects, then the question becomes all the more legitimate. On chemotherapy for
instance, note the following:
"Most cancer patients in this country die of chemotherapy. Chemotherapy does not
eliminate breast, colon, or lung cancers. This fact has been documented for over a
decade, yet doctors still use chemotherapy for these tumors." Allen Levin, MD
UCSF The Healing of Cancer, Marcus Books, 1990
The extraordinary evidence to substantiate Levin's observations plus many other
damning statements on conventional cancer treatments are presented for the reader
in the following pages. We examine the much-publicised story of UK media
personality, the late John Diamond, who opted for conventional treatment. What does
his story tell us? John was known for his critical attitude towards many of the more
popular alternative therapies. We look at some aspects of the alternative approach
and ask if his criticisms were entirely undeserved. We hear from those within the
cancer establishment itself who cite the conventional cut, burn and dissolve
techniques as ugly and inhumane and from those who seriously question the
amounts of money being invested in conventional cancer today given the
depressingly low recovery rate. In the UK alone, 2.8billion a year is spent in the
conventional cancer emporium. That's roughly 6,800,000 a day. US spending on
cancer is ten times higher.
We also hear from those who defied conventional wisdom and opted for non-toxic,
non-conventional cancer treatments, with remarkable results. And no, we are not
talking dolphin or pyramid therapy. From the known range of anti-cancer treatments
available, this story focuses on the naturally occurring Vitamin B17, Vitamin C and
the supporting role of nutrition. Vitamin B17 in particular has been attracting a great
deal of attention recently, despite the concerted efforts of the world-wide cancer
establishment to suppress or distort all the positive reporting on this vitamin.
Some may baulk at this accusation. We must realise however, that with global
spending on conventional cancer running into the hundreds of billions of pounds and
dollars annually, any news of a successful anti-cancer treatment extracted from the
simple apricot kernel could do some serious damage to the wealth of the mighty
Cancer Inc. In the following pages, we read the testimonies and evidence in support
of this charge.
But first, by way of introduction to the subject of 'death by doctoring', we travel back
a few hundred years, to the bedside of King Charles II, where fourteen of the highest
physicians in the land are earnestly 'reviving' the king from a stroke.
We can be sure that the physicians gathered around the King's bed were all leaders in
their particular field - royalty and presidents do not settle for anything less. But as
Proust observed, with hindsight, we can now see the hideous error of their
therapeutics. Today, the skull-drops, the ammonia and the pigeon dung have long
since disappeared from the conventional arsenal, but what will we say in a few years'
time when we look back on the 'highly respected' cancer therapeutics of 2002? Will
we dare to venture that there is nothing new under the sun?
ordeal. Kate Law of the Cancer Research Campaign said that John's story helped to
bring cancer out of the closet in Britain. John's writings certainly brought home the
ugliness of conventional treatment. But the more informed in the cancer debate who
have read John's columns and book will have recognised that John's writings,
brilliant though they were, did not bring out the full story of cancer at all.
Death on legs
The side effects from both chemotherapy and radiation itself are extensive. They can
include dizziness, skin discolouration, sensory loss, audio-visual impairment, nausea,
diarrhoea, loss of hair, loss of appetite, leading to malnutrition, loss of sex drive, loss
of white blood cells, permanent organ damage, organ failure, internal bleeding, tissue
loss, cardio-vascular leakage (artery deterioration) to name but a few. Vincristin is a
commonly applied chemotherapy agent. It's side-effects include rapid heart-beat,
wheezing or difficulty breathing, skin rash or swelling fever or chills, infection
unusual bleeding or bruising abdominal or stomach cramps loss of movement or
coordination muscle spasms fits, seizures or convulsions. The full list can be viewed
at
http://healthanswers.telstra.com/drugdata/appco/00070129.asp
Another common drug is Actinomycin - D. The side-effects again are horrendous
and can be viewed at http://www.tirgan.com/actinomy.htm They include hairloss, anemia, low white platelet count, nausea, sickness, diarrhea and liver failure.
Two years ago, Hazel was diagnosed with breast cancer. She described her
chemotherapy as the worst experience of her life. "This highly toxic fluid was being
injected into my veins. The nurse administering it was wearing protective gloves
because it would burn her skin if just a tiny drip came into contact with it. I
couldn't help asking myself "If such precautions are needed to be taken on the
outside, what is it doing to me on the inside?" From 7 pm that evening, I vomited
solidly for two and a half days. During my treatment, I lost my hair by the handful,
I lost my appetite, my skin colour, my zest for life. I was death on legs."
For a graphic visual account of the dangers posed by chemotherapy when making
contact with bare skin, visit chemo spill This page is not for the faint-hearted.
We shall be hearing more from Hazel later, although under very different
circumstances! It seems though that with chemotherapy, we have once again been
visited by King Charles' ammonia treatment, and again being administered by the
highest, most learned physicians in the land. Similarly, on the toxicity of radiation
'therapy', John Diamond noted that it was only when he began his radiation
treatment that he began to feel really ill.
Senior cancer physician Dr. Charles Moertal of the Mayo Clinic in the US stated: "Our
most effective regimens are fraught with risks and side-effects and practical
problems; and after this price is paid by all the patients we have treated, only a
small fraction are rewarded with a transient period of usually incomplete tumour
regressions...." [8]
Dr Ralph Moss is the author of 'The Cancer Industry' - a shocking expose of the world
of conventional cancer politics and practice. Interviewed live on the Laurie Lee show
in 1994, Moss stated: "In the end, there is no proof that chemotherapy actually
extends life in the vast majority of cases , and this is the great lie about
chemotherapy, that somehow there is a correlation between shrinking a tumour
and extending the life of a patient." [9]
Scientists based at McGill Cancer Centre sent a questionnaire to 118 lung cancer
doctors to determine what degree of faith these practicing cancer physicians placed in
the therapies they administered. They were asked to imagine that they had cancer
and were asked which of six current trials they would choose. 79 doctors responded of
which 64 (81%) would not consent to be in any trial containing Cisplatin - one of the
common chemotherapy drugs they were trialling, (currently achieving worldwide
sales of about $110,000,000 a year) and 58 of the 79 (73%) found that all the trials in
question were unacceptable due to the ineffectiveness of chemotherapy and its
unacceptably high degree of toxicity. [10]
the body (external radiation therapy). Radiation may be used before or after
surgery and/or chemotherapy.
After several years, some patients develop another form of cancer as a result of
their treatment with chemotherapy and radiation. Clinical trials are ongoing to
determine if lower doses of chemotherapy and radiation can be used."
The
site
can
be
accessed
http://www.cancerlinksusa.com/kidney/wilm/treatment.htm
at
I needed to go along with it. I kind of went into a trance and although something
didn't feel quite right, I found myself nodding to chemotherapy."
Most definitely, the power imbalance that exists in all doctor-patient relationships,
(whence the term 'shrink' in psychiatry) is a key agent in determining the direction of
treatment. But there is another factor and a contentious one at that...
And they will employ all means possible to disseminate their damaging
disinformation as far and wide as possible in order to protect their own lucrative
market. No department, private or public, is beyond the reach of their all-consuming
influence. Thriller writer John Le Carre spent many years working in the British
Foreign Office and knows the politics of big business very well. His most recent book
The Constant Gardener, focuses on the corrupt nature of the pharmaceutical
industry. In an interview on the subject, Le Carre stated recently:
"Big Pharma is engaged in the deliberate seduction of the medical profession,
country by country, worldwide. It is spending a fortune on influencing, hiring and
purchasing academic judgment to a point where, in a few years' time, if Big Pharma
continues unchecked on its present happy path, unbought medical opinion will be
hard to find." [12]
In opposition to the incessant drive by big business to dominate our health choices,
Dr Matthias Rath (below left) provides a concise summary of the primary ethics of
the merchant's house:
"Throughout the 20th century, the pharmaceutical industry has been constructed by
investors, the goal being to replace effective but non-patentable natural remedies
with mostly ineffective but patentable and highly profitable pharmaceutical drugs.
The very nature of the pharmaceutical industry is to make money from ongoing
diseases. Like other industries, the pharmaceutical industry tries to expand their
market - that is to maintain ongoing diseases and to find new diseases for their
drugs. Prevention and cure of diseases damages the pharmaceutical business and
the eradication of common diseases threatens its very existence.
Therefore, the pharmaceutical industry fights the eradication of any disease at all
costs. The pharmaceutical industry itself is the main obstacle, why today's most
widespread diseases are further expanding including heart attacks, strokes, cancer,
high blood pressure, diabetes, osteoporosis, and many others. Pharmaceutical
drugs are not intended to cure diseases. According to health insurers, over 24,000
pharmaceutical drugs are currently marketed and prescribed without any proven
therapeutic value (AOKMagazine 4/98). According to medical doctors associations,
the known dangerous side-effects of pharmaceutical drugs have become the fourth
leading cause of death after heart attacks, cancer and strokes (Journal of the
American Medical Association, JAMA April 15, 1998 )
Millions of people and patients around the world are defrauded twice: A major
portion of their income is used up to finance the exploding profits of the
pharmaceutical industry. In return, they are offered a medicine that does not even
cure."
A number of organisations are currently spearheading the fight against the
pharmaceutical industries as they seek to legislate against our free use of vitamins
and minerals. If this legislation is passed, it will directly affect YOU in many ways. A
web site address is included at the end of this article which enables you to quickly
and easily register your protest.
Writing in the UK Guardian on Thursday, 7th February, 2002, senior health editor
Sarah Bosely reports that:
"Scientists are accepting large sums of money from drug companies to put their
names to articles endorsing new medicines that they have not written - a growing
practice that some fear is putting scientific integrity in jeopardy." [12a]
These supposed guardians of our health are being paid what to say. Said one
physician in the article, "What day is it today? I'm just working out what drug I'm
supporting today." From top to bottom, the delivery system of 21st century
conventional healthcare is being bought out and taught to think of treatment and
prevention of disease in pharmaceutical terms only.
Aside from the politicking and the big business string-pulling taking place behind the
scenes, our minds are also being washed with the constant froth of emotive,
unfounded, pro-establishment, populist headlines such as Another breakthrough
at UCLA! . (yes.but with mice.) It's in the genes! (another 5 million NOW will
help us to isolate the gene in 2010..perhaps.) Excitement at latest oncology
findings! (Buoyant opening paragraph, descending into the usual mixture of hope
extinguished by caution and the obligatory appeal to the pocket.) Cancer vaccine
close! (Yes, and close since 1975 actually. But please, continue to give generously,
because next time, it could be you!)
And so it goes on. And all the while, the mortality statistics worsen. Yet still, the
money - our money - just keeps on rolling in. On that note, The Campaign Against
Fraudulent Medical Research states: "The next time you are asked to donate to a
cancer organisation, bear in mind that your money will be used to sustain an
industry which has been deemed by many eminent scientists as a qualified failure
and by others, as a complete fraud." [13]
Mammograms!
Thank you to Dr Tim O'Shea for highlighting the following very important
information on the practice of mammography:
"This is one topic where the line between advertising and scientific proof has become
very blurred. As far back as 1976, the American Cancer Society itself and its
government colleague the National Cancer Institute terminated the routine use of
mammography for women under the age of 50 because of its "detrimental"
(carcinogenic) effects. More recently, a large study done in Canada on found that
women who had routine mammograms before the age of 50 also had increased
death rates from breast cancer by 36%. (Miller) Lorraine Day notes the same
findings in her video presentation "Cancer Doesn't Scare Me Any More." The reader
is directed to these sources and should perhaps consider the opinion of other sources
than those selling the procedure, before making a decision.
John McDougall MD has made a thorough review of pertinent literature on
mammograms. He points out that the $5-13 billion per year generated by
mammograms controls the information that women get. Fear and incomplete data
are the tools commonly used to persuade women to get routine mammograms.
What is clear is that mammography cannot prevent breast cancer or even the
spread of breast cancer. By the time a tumor is large enough to be detected by
mammography, it has been there as long as 12 years! It is therefore ridiculous to
advertise mammography as "early detection." (McDougall p 114)
The other unsupportable illusion is that mammograms prevent breast cancer, which
they don't. On the contrary, the painful compression of breast tissue during the
procedure itself can increase the possibility of metastasis by as much as 80%! Dr.
McDougall notes that a between 10 and 17% of the time, breast cancer is a selflimiting non-life-threatening type called ductal carcinoma in situ. This harmless
cancer can be made active by the compressive force of routine mammography.
(McDougall, p105)
Most extensive studies show no increased survival rate from routine screening
mammograms. After reviewing all available literature in the world on the subject,
noted researchers Drs. Wright and Mueller of the University of British Columbia
recommended the withdrawal of public funding for mammography screening,
because the "benefit achieved is marginal, and the harm caused is substantial."
(Lancet, 1 Jul 1995) The harm they're referring to includes the constant worrying
and emotional distress, as well as the tendency for unnecessary procedures and
testing to be done based on results which have a false positive rate as high as 50%."
(New York Times, 14 Dec 1997) [13a]
************
Whilst the remit of this article does not extend to a full exploration of the physical
harm being exacted by some diagnostic methods and drug treatments, or the
corrupting influence that money is exerting over medicine and medical practice, let
the reader be assured that conventional medicine has more than its fair share of
attendant commercial pressures, and especially so in the world of cancer, as we shall
later discover.
I should put my faith in the Bessarabian radish, the desiccated root of which has
been used for centuries by Tartar nomads to cure athlete's foot, tennis elbow and
cancer, as detailed in their book Why Your Doctor Hates You And Wants You To
Die, review copy enclosed."[15]
Notwithstanding the genuine treatments available in the natural cabinet, which we
shall discuss very shortly, a huge number of remedies being sold as 'medicine' today
contain no sensible methodology, yet amazingly, they are selling very well. No better
is this phenomenon illustrated than in the lucrative minor ailments market, where on
a daily basis across the world, untold millions is being spent on pharmacologically
inert mixtures and 'essences', producing truly marvellous results with illnesses from
which we were going to get better anyway.[16]
handling arsenals of nuclear weapons. The result is likely to be unhappy and stands
a decent chance of proving a disaster. Irrational beliefs are always dangerously
corrupting, even when they only relate to the cause and cure of piles." [17]
Reputation is everything
But what relevance does all this have to the debate on treatments for cancer, you
might ask? Where is all of this headed? This has been a necessary diversion firstly,
that we might begin to understand some of the frustrations many reasoned thinkers
have with the issues raised: and secondly, that we might begin to consider the impact
that such weakened thinking has on genuine natural treatments for disease. For
instance, what damage is secondarily being wrought upon the reputation of the
genuine treatments in the cabinet, the ones that can actually heal? Sadly, there is no
clear division between the reputation of much of the unregulated alternative health
industry and that of the many sensible non-conventional treatments available today.
It has all become a horrible blur and is a point of major concern even to the nonorthodox regulatory bodies overseeing the alternative/complementary health
movement. The whole arena is fraught with as much vested interests and
misunderstandings as conventional health, but commentaries drawing such
conclusions even from those concerned bodies sympathetic to the natural approach
are viewed as almost heretical and somehow betraying the brotherhood of the
alternative heirachy.
Critical debate should commence as soon as possible with regard to those 'helping'
therapies that only temporarily distract the seriously ill. In need only of sensible
advice and sensible treatment, these people can very quickly end up worse off in
body, mind and spirit; and last but not least, in pocket, leading very quickly to
derision and a carte blanche dismissal of all the good that genuine natural treatments
have to offer. John Diamond stated that there was as much chance of him going down
the alternative treatment route as there was of the Pope getting drunk on the
communion wine and getting off with a couple of nuns. [18]
Whilst we can perhaps understand some of John Diamond's frustrations, his
comparisons don't exactly aid the cause. Because the truth is that the alternativist's
cabinet is not all 'mumbo-jumbo' by any means. Genuine medicine can be found in
there. Perhaps a name change is in order. Are we alternative? Are we
complementary? But complementary to what? To chemotherapy perhaps? But then
what medicine could possibly complement chemotherapy? Shouldn't there just be
medicine and non-medicine, full stop? Be that as it may, many people are wrongly
assuming that the non-orthodox medical cabinet is barren and not worthy of closer
inspection. The hazy and often crazy information being disseminated on numerous
non-conventional treatments coupled with our innate and nave trust in the
orthodoxy is the reason why thousands of people like John Diamond are staying with,
and relying upon conventional treatments for serious illnesses, including cancer. As a
result, thousands of people like John Diamond are dying, and often in a horrible
fashion.
treatments known to man, the natural extract of the apricot kernel, otherwise known
as Vitamin B17.
"Supporters of Laetrile (vitamin B17) and Essiac, in particular, made so much noise
about their miracle cures that both have been through the research mill on
numerous occasions and found to be useless." [19]
"When we add laetrile to a cancer culture under the microscope," said Burk,
"providing the enzyme glucosidase also is present, we can see the cancer cells
dying off like flies." [20] (glucosidase being the enzyme heavily present in cancerous
cells which triggers the unique cancer-destroying mechanism found in Vitamin B17.
An excellent clinical analysis of this mechanism is found in 'B17 Metabolic Therapy In The Prevention And Control Of Cancer - a concise history of the research into this
vitamin, including many clinical assessments. More details on this book can be found
at the end of this article.) [21] Dr Burk also stated that evidence for Laetrile's
efficacy had been noted in at least five independent institutions in three widely
separated countries of the world. [22]
So who do we trust in this matter? Diamond or Burk? Now we can ask ourselves
whether it was perhaps the fault of some kindly but misguided soul who posted John
Diamond an essay on the benefits of Vitamin B17 mixed with walnut water that
caused him to dismiss B17 so emphatically. Or it could be that John actually trusted
the conventional research reports he had accrued on this vitamin. By examining the
sources from where John Diamond might have got his B17 research 'information', the
ugly features of conventional cancer research move more sharply into focus.
Unable to sit on this information, Moss later called a press conference of his own and,
before a battery of reporters and cameramen, charged that Sloan-Kettering officials
had engineered a massive cover-up. He provided all the supporting documents and
named all the names necessary to validate his case. The following day he was fired for
'failing to carry out his most basic job responsibilities'. [24]
Similarly, in his book 'World Without Cancer', cancer industry researcher Edward Griffin noted
"Every Laetrile study had been tarnished with the same kind of scientific ineptitude, bias and outright deception. Some of these
studies openly admitted evidence of anti-cancer effect but hastened to attribute this effect to other causes. Some were toxicity
studies only, which means that they weren't trying to see if Laetrile was effective, but merely to determine how much of it was
required to kill the patient." [24a]
The 'evidence' supporting John Diamond's claim that Vitamin B17 is useless and even
dangerous is available in abundance in all of the major cancer institutions today. Well
of course it is! We're in the merchant's house, don't forget. As Pat Rattigan, author of
'The Cancer Business' reports:
"The threat to the cancer business from effective therapies was taken very seriously
from the beginning. By the 1940's the Syndicate had 300,000 names on its 'quack'
files. Vitamin B17, being a unique threat due to its simplicity, attracted more
concentrated attacks than all the other treatments put together: fraudulent test
reports; hired, banner-carrying pickets outside clinics; rigged juries; newspaper
character assassinations; dismissal of heretic employees, etc. The FDA,
orchestrating the onslaught, sent out 10,000 posters and hundreds of thousands of
leaflets warning about the dangers of the toxicity of the non-toxic substance.
Earlier, a Congressional Accounting Office had found that 350 FDA employees had
shares in, or had refused to declare an interest in, the pharmaceutical industry."
The American Food and Drug Administration issued one such story about the death
of an eleven month old girl, supposedly from cyanide poisoning due to her apparently
swallowing her father's Vitamin B17 tablets. Cancer specialist and B17 advocate Dr
Harold Manner takes up the story:
'.I was lecturing in Buffalo, New York and...after I had made some strong
statements - a man stood up and said "Dr. Manner, how in the world can you make
statements like that when the FDA is making these other statements?" I reiterated
that the FDA statements were lies. 'He said, "Look at this little girl in upstate New
York, she took her father's Laetrile tablets and died of cyanide poisoning." Just then
a little lady stood up: "Dr. Manner let me answer that question. I think I am entitled
to because I am that little baby's mother. That baby never touched her father's
Laetrile tablets. The doctor, knowing the father was on Laetrile, marked down
"possible cyanide poisoning". At the hospital they used a cyanide antidote and it
was the antidote that killed the child. And yet that statement will continue to appear
even though they know it is a lie." [24b]
The scare stories always focus on the minute amounts of naturally occurring cyanide
found in VitaminB17. But no mention is made in any of these stories of the wondrous
mechanism governing the release of this cyanide. No harm is done to the person
eating this vitamin ( if that were the case, we have consumed enough apricots, apples,
peaches and cherries etc containing B17 to have finished us off long ago.) The cyanide
is released only when cancerous cells are recognised by their high glucosidase
content. B17 cyanide attacks cancer cells specifically. No large amounts of glucosidase
detected means no cyanide release. Rest assured, there is no evidence that vitamin
B17 can kill, unless of course, one is accidentally crushed under a pallet of the stuff!
A further embarrasment for the cancer orthodoxy must surely be the research being
carried out at the Imperial College in London, where researchers are looking at ways
of using naturally-occurring plant cyanide to specifically attack human bowel
tumours. The idea came about after studying the pattern of specific cyanide release in
the almond and cassava fruit which protects them from insect attack. Another one of
those natural wonders just crying out to be heard is at last being listened to by the
orthodoxy perhaps? [24c]
Very sadly, in assessing the deservedness of the 'shady' reputation bestowed upon
Vitamin B17 metabolic therapy, we realise it is entirely unwarranted and that
instead, there has been a sustained attack by the conventional cancer industry on this
treatment, an attack that has carried on in one form or another for the last forty
years. As mentioned earlier, with global spending on conventional cancer running
into the hundreds of billions annually, a naturally-occurring cancer cure of any
description is an unwanted intruder. Dr Moss again, on the money involved in
conventional cancer:
Moss: "About 630,000 people die every year of cancer in the US, and it really is an
epidemic disease. We have got a tremendous industry. Every one of those people
who is getting cancer and dying of it is going to be treated, and these treatments are
extremely expensive. Chemo is tens of thousands, sometimes hundreds of thousands
of dollars. A bone marrow transplant, which is basically another way of giving
chemotherapy, or radiation, can run to about $150,000 per person, and is almost
never effective. It kills about 25% of the patients."
Lee: "Why carry on doing it?"
Moss: " Because of the money, which is tremendous." [25]
When we understand the amounts of money involved, we can begin to understand the in-house desire to sustain a 'fact-creating'
process in support of conventional treatment. Conventional cancer treatment and research is a licence to print money. Most
definitely, conventional interested parties and institutions have colluded in a shameful anti-Vitamin B17 'fact-creating' process,
which in turn has surely led to the early and even unnecessary deaths of thousands upon thousands of people. As for John
Diamond's dismissal of Vitamin B17, he didn't write his comments on B17 as an intentional slur. He wasn't the forked tongue in
this chain of events. He desperately wanted to live. His single paragraph read by thousands was just another example of the
damaging knock-on effect of merchant-speak. Merchant-speak on Vitamin B17 metabolic therapy has exacted a grave injustice
upon this treatment and subsequently, upon all who have been persuaded to think likewise. Let's now hear some testimonies
from those who have not been persuaded by the negative propaganda.
Phillip
Phillip is 64. In April 2001, he was diagnosed with inoperable lung cancer. The
oncologist showed him the x-rays that confirmed the dreaded 'shadows'. He was told
to go home, enjoy his life as best he could and put his affairs in order. A week later, in
a chance conversation at work, Phillip was told about Vitamin B17. Phillip
immediately began taking a combination of Vitamin B17 and Vitamin C. Four months
later, Phillip returned to hospital for a check-up, where a new set of x-rays were
taken. The shadows had completely disappeared. Says Phillip, "I know what I saw
and the doctor couldn't explain it. I'm continuing with my Vitamin B17 regime and
eating about 10 kernels a day." Phillip now pays great attention to his diet and
believes that what we put into our bodies can have a dramatic effect medicinally.
John Diamond again, this time on some nutter with a magical diet:
Now if this cancer 'nutter' was just an isolated case of recovery through diet, his
recovery would not of course constitute proof. But with Vitamin B17 metabolic
therapy, we are seeing tremendous results time after time. Continuing on in the name
of fair dealing.
William
What are we eating?
It is interesting to note that there are cultures today who remain almost entirely
cancer-free. The Abkhasians, the Azerbaijanis, the Hunzas, the Eskimaux and the
Karakorum all live on foodstuffs rich in nitriloside or vitamin B17. Their food consists
variously of buckwheat, peas, broad beans, lucerne, turnips, lettuce, sprouting pulse
or gram, apricots with their seeds and berries of various kinds. Their diet can provide
them with as much as 250-3,000mg of nitriloside a day. The founding father of
Vitamin B17 research, Ernst T Krebs Jr., studied the dietary habits of these tribes.
Krebs stated:
"Upon investigating the diet of these people, we found that the seed of the apricot
was prized as a delicacy and that every part of the apricot was utilized." [27]
The average western diet with its refined, fibreless foods offers less than 2mg of
nitriloside a day. It has also been noted that natives from these tribes, who move into
'civilised' areas and change their diets accordingly, are prone to cancers at the regular
western incidence. [28] An important point to note with B17 content in the apricot
fruit is that the more bitter the taste of the apricot kernal, the richer is the content of
B17. If the kernel does not taste bitter, the B17 content will be quite low. The
necessary advice on this subject is included in detail in the books available on the
following page.
Flora
Flora was diagnosed with stage 4 bowel cancer in 1999.
"Before the operation, they gave me chemotherapy which was devastating. By the
end of the course, I could hardly stand. They then removed the tumour from my
bowel. I was told the cancer had spread to the liver. I was offered further
chemotherapy but declined. I attended Middlesex hospital and had five sessions of
laser treatment to try and contain the liver cancer followed by more chemotherapy.
After the fifth time of trying to contain the cancer, they said that it was beginning to
grow yet again. So I began an organic diet and attended the Dove Clinic for
intensive Vitamin C treatment, with other supplements. It was there that I was told
about Vitamin B17. I added that to my regime. Over a period of time, the cancer
completely disappeared from my liver. It is now February 2002 and I have been one
year clear of cancer. I am maintaining my organic diet and eating about 50
apricot kernels a day. I'm 64, I've returned to work and I feel fine. Treatments such
as these should at least be made known to patients by the NHS."
There are literally thousands of people who can attest to the pharmacological, lifesaving power of Vitamin B17 and its supporting nutritional regime. And the same can
also be said of Vitamin C.
Vitamin C
The all-round benefits of Vitamin C to the human physiology have been known and
utilised for centuries. In terms of its benefits in cancer treatment and prevention, we
read the following from Phillip Day:
"Dr Linus Pauling, often known as the 'Father of Vitamin C' and twice awarded the
Nobel Prize, declared that daily intakes of up to 10g of the vitamin aids anti-cancer
activity within the body. Pauling was largely derided for making these declarations,
but today, large doses of Vitamin C are used by many practitioners for cancer
patients in nutritional therapy, who believe Pauling was right and that the popular
nutrient is indispensable to the body in its fight to regain health from cancer." [31]
Hazel
Hazel had been given a virtual death sentence by her cancer doctor, telling her that
although there was an 86% recovery from her type of breast cancer, she was
unfortunately in the smaller category. As previously noted, Hazel's chemotherapy was
only making her feel terrible, and she decided that if she was going to die, then she
would do so without further conventional treatment. Hazel began a regime of
intravenously administered Vitamin C and supplements including Vitamin B17 and
paid great attention to her diet. She soon began to feel a great deal better. She
regained her weight and her hair and her appetite. About nine months following the
diagnosis, she was troubled with lower back pain and visited her doctor. He suggested
a further scan based on Hazel's lower back pain, which the doctor believed was
possibly the result of her cancer having spread to the base of her spine. Hazel said
there was no way she was going for more chemotherapy or scans which she believes
in themselves can trigger carcinogenic activity. Instead, Hazel supplemented her
Vitamin C regime with a course of Vitamin B17 kernels, as well as maintaining a
sensible diet and staying away from her conventional cancer physician. The blood
count taken by her GP before Christmas read as normal. She feels very healthy and is
in the process of writing a book on her experiences. She feels passionately that people
need to know that there are alternative cancer treatments available and speaks to
groups on this subject.
Let the reader be assured that the recent scare tactics surrounding Vitamin C and its
supposed links to cancer are just another one of those smear campaigns orchestrated
by the merchants. Quite simply, any good news on Vitamin C represents yet another
threat to the pharmaceutical industries' considerable income from conventional
cancer treatments. The full story on the vested interests supporting the author of the
much-publicised
vitamin
C/cancer
story
can
be
found
at
www.whatareweswallowing.freeserve.co.uk/vitc.htm
And finally, we hear from Dr Nicola Hembry of the Dove Clinic, specialising in the
non-conventional approach to cancer care and treatment:
"Nutritional treatments such as high dose vitamin C and B17 (laetrile) have been
known about for years, and there are many success stories from patients lucky
enough to have received and benefited from them. Research shows that levels of
400mg/dl Vitamin C in the blood can kill cancer cells by a pro-oxidative
mechanism, and there is a great deal of data showing that B17 is preferentially toxic
to cancer cells. The trouble is that there is little in the way of well-designed random
control trial data for the use of these substances, and therefore mainstream
medicine rejects them out of hand without even considering the evidence available
or even asking why these trials haven't been carried out. It has to be said that one of
the reasons is a lack of financial incentive because these substances cannot be
patented. Sadly it is the cancer sufferers who lose out. To not even have the choice of
these safer, more natural treatments even when a cancer is deemed incurable and
only palliative chemotherapy or radiotherapy is offered is in my view totally
unacceptable. I have seen many patients experience an improved duration and
quality of life with an integrated approach, and some go on to achieve complete
remission of their disease even when dismissed as incurable by their oncologists."
Treating cancer is not just about getting hold of Vitamin B17 as quickly as possible.
We need to be educated in a whole range of issues. 'Cancer: Why We're Still Dying
To Know The Truth' has been written in an easily readable and easily understood
manner, specifically to inform the general public on all of the key issues pertaining to
natural treatment for cancer. It makes for necessary and fascinating reading!
For those interested in finding out more on the issues raised in this article, just click
on the following titles available from Credence Publications.
Cancer: Why We're Still Dying To Know The Truth A concise account of the
cancer industry and of the good news on vitamin B17 metabolic therapy.
Vitamin B17 Metabolic Therapy - A Clinical Guide A clinical account of
vitamin B17, detailing the landmark research on this most vital of vitamins in the
fight against cancer.
Food For Thought Delicious recipes designed to promote health. A vital
contribution to cancer prevention and recovery. All these titles and more available at
www.credence.org
And finally...
Throughout the writing of this article, I have been acutely aware of three things.
Firstly, of my own slender mortality and that it is only by the grace of God that I have
not had to face a cancer diagnosis of my own. The motivating factor behind the
writing of 'Death by Doctoring' was to inject realism as well as a sense of hope. And
as far as one is able to write about a subject without having personally walked that
particular walk, I hope also that this article has been written with the deserved
sensitivity.
Secondly, Vitamin B17 metabolic therapy and Vitamin C form only part of a much
wider regime of treatments that have proven successful in the treatment of cancer.
These and other treatments are explained in more detail in the above Credence titles.
Thirdly, this site does not accuse all doctors of working towards some vast
medical conspiracy to kill everyone! A doctor wrote to this site recently, under
the impression that Death by Doctoring is propagating this belief.
"I have yet to see single shred of evidence the supports the conspiracy theories that
abound on the web. It doesn't matter whether it's cancer treatment, aspartame, or
even soybeans. Consider this: would any company seek to sell products that kill the
customer? It doesn't make any sense. The scientist who discovered cisplatin [the
drug that 81% of cancer doctors would not administer to themselves] was a professor
of mine in university. I knew his mind and his heart. He wanted to find a cure
because it had devastated someone in his family. While all chemotherapies are
poisons, by extension of your logic, he was creating a product that he knew would
kill his family members. Does that even make sense to you?"
Of course I am not saying that medical professors are intentionally designing
something that would kill. With chemotherapy, what started off as a supposed
saviour, quickly turned into a huge money-spinner, but with devastating
consequences. A lucrative ball had gained too much momentum. And once the
profitability of a drug is recognised, the business decisions at corporate level are often
at complete odds with those lower down at manufacturing and distribution level. As
for those within the industry's 'circle of knowledge' regarding the dangers of today's
pharmaceuticals, very definitely there are key personnel within drug companies who
know exactly the dangers that relate to their products, but who choose to say nothing
in order to preserve income and to protect from litigation. To deny this takes place
would be naive in the extreme. Nicholas Murray Butler was chief spokesman for US
giant JP Morgan and Co. On the subject of 'circles of knowledge', Butler once stated:
Applying this principle to the pharmaceutical industry, further on down the chain of
command, a number of dangerous products are being manufactured and prescribed
today, by a great multitude who are innocently proud to be associated with these
supposedly 'life-saving' medicines. Conventional doctors especially can so easily fall
into the category of 'Butler's 'great multitude'. Working under extreme pressures,
doctors and nurses just do not have room in their day to step off the conventional
treadmill to conduct contrary research. It is far simpler and far more expedient to
dismiss all non-pharmaceutical information as fringe lunacy.
Having said all this, there are many, many dedicated people involved in conventional
health care who are practicing elements of conventional medicine and who are saving
and enhancing lives every day, not least in some methods of diagnosis, pre-emptive
surgery and in acute and emergency medicine. Accident and Emergency units
especially, perform a tremendous job. As with all medicine, may the good continue
and may the bad be open to complete reappraisal.
Finally, I do so wish I'd been given the opportunity to meet John Diamond. Because I
reckon we'd have got on like a house on fire. And who knows what might have
happened as a result?
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star letter
Thank you for reading.
Steven Ransom,
Research Director,
Credence Publications
Please visit http://www.laleva.cc/indexeng.html right now and sign the petition
against the restriction of vitamin and mineral sales. It will only take thirty seconds to
complete and it is so important.
references
Mr Ransom, I share your thoughts and I applaud you for your courage for bringing us 'Death by
Doctoring'. The most dangerous place on planet earth is the hospital - next is the doctor's office followed closely by the dentist's office." Frank D Wiewel, Former Chairman, Pharmacological
and Biological Treatments Committee, Office of Alternative Medicine (OAM) US
National Institutes of Health (NIH)
The violet ray device. This is a small Tesla coil that feeds variously shaped plasma
tubes. Good results have been reported. Currently some are building these with
variable frequency capability. Construction details are at
http://www.royalrife.com/violetray.html. I have built one of these using the 555
circuit and transistor from an EMEM2.
The Rife beam-ray device. Rife fed various frequencies into the electrodes of gas
filled glass phanotron tubes to form an ionized plasma. This was very effective
against the carcinoma and sarcoma viruses and other pathogens. It also stimulated
various tissues to repair themselves - dissolve cataracts, and so on. It is reported that
he fed 500 watts of power into the tube, which was placed within a few inches of the
person being treated. This was a bit more aggressive than the current practice of
using a 100 or so watt unit several feet from the patient. Rife's frequencies ranged
from 160,000 to 12,830,000 Hz and many of these were in the same range as those
researched by Dr. Hulda Clark.
Contact Pad Devices. It is not certain who began using audio frequencies and
applied them to the skin via contact electrodes. Such pad devices are often called
Rife machines, but Rife-Crane or just Crane may be more accurate. A lot has been
said about the effectiveness of such devices, much of it negative. On the other hand,
I have seen these units destroy diseases like herpes quickly, and take care of
mononucleosis in one treatment so that a very sick child was fine the next morning
and ready for school. Many have reported "spontaneous remissions" of cancers. Not
bad by any standard. I am sure that many more stories could be told. The BK-4011
or 4040 can easily be converted to a Crane type of device. Unfortunately some
companies are advertising contact pad devices as "Original Rife Machines"
Dan's Enhancer. Wanting to observe auras, Dan (not the same Dan who built the first
EMEM devices) took a 12000 volt neon sign transformer, two sheets of glass, one
sheet of aluminum foil, a small sheet of copper, and a neon bulb and built the
Enhancer. The unit was found to have biological effects by accident. Hundreds of
these units have been built, and numerous "spontaneous remissions" of many
conditions, including cancer, have been reported. Run times used by those who have
recovered from cancer tend to be in the range of four hours per day. One theory is
that the Enhancer puts out a huge variety of frequencies, and that the person using it
is getting small doses of the ones that they need. It takes a long time so soak up
enough of the desired frequencies. It is also said that the device increases the
voltage across cell membranes, also very desirable. One advantage of this unit is
that it may be effective against conditions where frequencies are not yet known. The
Enhancer cost me about $200 to build, and the test run was a very interesting
experience.
The "Doug" unit. "Doug" had heard that Rife had killed pathogens using various
frequencies. So "Doug" fed frequencies into a small coil under his microscope stage
and discovered Lyme disease frequencies. He then fed these into a 2000W audio
amplifier, and ran the output of that into a large capacitor and coil combination. Using
this setup, he cured himself. Several others used the device for successful breast
cancer cures. They reported that they could feel something happening in the
tumors at 2128Hz. Construction information is available at
http://healthalternative.freeyellow.com.
The EMEM unit. As the 2000 watt amplifiers that "Doug" used are no longer built,
Dan Tracy built a device using a smaller coil with a ferrite core and smaller amplifier.
Results have been good. One Seattle researcher reports that breast cancers often
feel hot when exposed to the device. Some tumors have disappeared in as little
as two weeks.
The "Ray" device. The Crane type units generally have an output control that controls
the output voltage, and thus the current. "Ray" developed a device that puts out 200
volts at constant current of about 1 milliamp. Low currents are used, so that there is
less sensation than when other pad-type devices are used. A woman with breast
cancer borrowed the unit and placed one electrode on each side of her affected
breast. In only one week of treatments, the tumor shrunk to the point where the
mastectomy was cancelled. This device was later successfully with a case of
prostate cancer. One man who has used the Ray device reports 7 consecutive
cancer recoveries and recoveries from everything else it has been used on except
for a case of diabetes. The Ray device is solid state but there are plans for a
vacuum tube version of this device at http://www.royalrife.com/tubeunit.html. The
vacuum tube version has also successfully been used for cancer.
The Beck zapper/plant stimulator/blood cleaner. At one point, Dr. Bob Beck (who
invented the camera strobe) weighed 285 pounds, was confined to a wheelchair, had
very high blood pressure, had very high blood sugar, and had lost most of his hair.
He had previously written articles on Rife-Crane type equipment. In 1991 he heard
about Dr. Stephen Kaali and others at Albert Einstein College and their announced
and patented cure for AIDS. They had found that a mere 50-100uA of electricity at 60
Hz would rid the blood of AIDS. According to the patents, it will also rid the blood of
any other pathogens present. Beck decided that it was not necessary to remove the
blood from the body as per the patents. He would just apply 4 Hz (AC is used to
prevent electrolysis) to a small electrode on each of two pulse points and clean the
blood in the body. He chose the pulse points on the inside of the ankle just below and
behind the ankle bone. (We currently use the radial and ulnar arteries on the same
wrist.) To test for negative effects, he went around for four hours a day for a month
with one electrode on each ankle. He also used his magnetic pulser (see below) on
himself. After a month, he began to effortlessly lose weight. His blood pressure and
blood sugar normalized. His hair grew back. When I visited with him in March of
1996, he weighed 180 pounds and was not using a wheelchair. This unit will clear up
many (possibly all) infections in the blood, and no frequency needs to be known. I
have seen hepatitis C clear up using this device a number of times.
The Beck magnetic pulse generator. The Beck blood cleaner only cleans what is in
the blood that flows past the electrodes. It does not get at the lymph (which may have
little or no circulation) or pathogens that may hang out there. So Beck put a 2.5mh
coil in series with the flash tube of a camera flash. When the test button is pushed, a
powerful magnetic pulse is produced. This produces a small current in any nearby
tissue, dealing with pathogens resident there. It is not only a lymph cleanser; it does
very well on localized infections such as sties or pockets beneath teeth. No frequency
need be known. It also loosens up tight muscles so that chiropractic adjustments
are much easier. The Vivitar 1900 flash has been used as the basis of thousands of
these devices. The coils come from MCM Electronics. Another variety that I call the
super thumpy, uses the same coil, and the small party strobe from Radio Shack.
Construction notes are at http://www.royalrife.com/superthumpy.html. And at
The EMEM2. Dan, who designed the original coil-type EMEM, tried feeding the
output of an audio amplifier into an automotive ignition coil, through a spark plug,
and then into one end of a plasma tube similar to those used in the Bare devices.
The other end of the plasma tube is connected to a ground, and to a plate for contact
with the feet. It is a contact device - the tube (or a small metal plate attached to it)
must be touched for best results. Dan reports that it is more effective against Lyme
and other conditions than was his EMEM coil device. In the latest version, a single
transistor replaced the audio amplifier. There are reported cases of cancer recovery
using this device. One Seattle researcher reports that the EMEM2 using plates for
both feet is more effective for prostatitis than other devices including the EMEM3.
Construction information is available at http://www.royalrife.com/emem2.html.
Bruce Stenulson produces a quality version of this device with some refinements
such as variable output and adjustable spark gap or no gap as some prefer.
The EMEM3. This is similar to the EMEM2 but uses a high pressure helium
phanotron tube. It is more convenient than the EMEM2 in that no contact is made
with the device during use. The current version is called the EMEM3D and uses two
ignition coils for added power. One Seattle man built a "quad" with four coils, and
even an eight coil version. That is the most powerful radiant device that I have
personally seen. Users of EMEM3 and EMEM3D have reported numerous
spontaneous remissions of cancers. One patient with advanced prostate and bone
cancer used an EMEM3 using only 727 Hz. After several months his doctor phoned
me to say that the unit appeared to be doing some good. After a few more months
(one year total) the doctor called to say that the patient is now cancer free. A
radionics saliva test showed high levels of BX, however so the single frequency
was not adequate for that. The EMEM3 also works well without the spark gap.
The Weeks Parker device. Dr. Rife reported the frequency of 11,780,000 Hz as the
frequency that kills the carcinoma/BX virus. Weeks Parker developed an
inexpensive 5-watt unit to produce that frequency. No audio is used. His device has
been used to drive the linear amplifier on a Bare unit. One person with prostate
cancer used this device and I was later able to have a radionics saliva test done. BX
virus levels had dropped to zero. Construction information is at
http://www.geocities.com/weeks_parker.
I have also experimented with a B&K-4040 at 11,780,000Hz for BX and 11,430,000
for BY with good results. Treatment times have to be fairly long.
There is also a person using the Icom IC-718 ham radio transmitter on 11,430,000
and 11,780,000 with very good results. Run times have to be very short, on the
order of 30 seconds due to die-off problems. Two antennas are used instead of a
plasma tube. These frequencies can also easily be modulated with audio if desired. A
plasma tube could be used if desired.
The Bioray. The Bioray (also called the BeamRay) is a computer that produces audio
frequencies, an audio amplifier, and a plasma tube. There have been some good
reports from users. One user reported that she liked hers almost as well as her
EMEM3D, so it must be good!
The F-Scan. This is a major breakthrough. The F-Scan "pings" the body with
frequencies from 1-2,999,999 Hz and detects resonances.