Arhive etichetă | Rife cancer

dr Virginia Livingston, MD un fals sau Geniul Medical?

De Alan Cantwell , MD
Los Angeles, CA 16 iulie 2006

cancerul este cea mai înfricoșătoare boală umană, iar cauza ei rămâne evazivă. Prin urmare, pare de neconceput că descoperirea unei cauze germen de cancer ar provoca o astfel de ostilitate în rândul instituției de cancer. Dar, într-adevăr, credința într-un germen de cancer a fost dintotdeauna erezie științifică.

În lunga istorie a cercetării în domeniul cancerului, un medic nu a fost niciodată mai deschis și controversat decât Virginia Wuerthele-Caspe Livingston (1906-1990). Timp de mai mult de 40 de ani, ea a susținut ideea revoluționară că bacteriile au cauzat cancer și a elaborat un tratament pentru a încerca să lupte împotriva acestor microbi prin IMUNOterapie.

La șaisprezece ani de la moartea ei, ea este acum uitată, dar este încă condamnată de organizații atât de puternice, cum ar fi Societatea Americană pentru Cancer – și pe lista neagră a Quackwatch – o corporație nonprofit dedicată combaterii „fraudei, miturilor, erorilor „…pina si a sucului de morcov as putea adauga si nu glumesc.

CERCETAREA CANCERULUI LIVINGSTON

Începând cu sfârșitul anilor 1940, Livingston a reușit să dezvolte/izoleze bacterii din tumori de cancer; și când ea și asociații ei au injectat bacterii de cancer în animale de laborator, unele au dezvoltat cancer. Alte animale au dezvoltat boli degenerative și proliferative, iar unele animale au rămas sănătoase. Livingston credea că „imunitatea” gazdei a fost un factor important pentru a determina dacă cancerul se va dezvolta.

Virginia Livingston MD (1906-1990)

În 1969, într-o întâlnire la Academia de Științe din New York, Livingston și colegii ei au sugerat că cancerul a fost cauzat de o bacterie extrem de neobișnuită, pe care ea a numit-o criptocide progenitoare – greacă pentru „ucigașul ascendent al strămoșilor”. Cu toate acestea, Livingston a afirmat că elementele microbului erau prezente în fiecare celulă umană. Datorită proprietăților sale biochimice, ea credea că organismul a fost responsabil pentru inițierea vieții și pentru vindecarea țesuturilor – și pentru uciderea noastră cu cancer și alte infirmități. Criticii acestei cercetări au continuat să insiste că nu există un astfel de lucru ca un germen/bacterie de cancer.

Incercand sa foloseasca o varietate de modalitati (dieta, suplimente, antibiotice, precum si metode traditionale) pentru a trata cancerul, a folosit un vaccin „autogen” derivat din bacteriile cancerului proprii ale pacientului gasite in urina si sange. Livingston a explicat că nu era un vaccin anti-cancer, ci un vaccin care să stimuleze și să îmbunătățească propriul sistem imunitar al pacientului.Administrarea acestui vaccin neaprobat a provocat o furie în instituția de cancer și, eventual, au fost întreprinse acțiuni în justiție împotriva ei și a Clinicii Livingston-Wheeler din San Diego. În ciuda tuturor problemelor sale legale, ea a continuat să vadă pacienții până la moartea ei la 83 de ani.

În martie 1990, anul morții ei, un articol extrem de important despre terapia Livingston-Wheeler a apărut în revista American Cancer Society sponsored by CA: Journal of Cancer for Physicians. (Nici un autor nu a fost enumerat.) Raportul a recomandat pacientilor sa stea departe de clinica San Diego si a afirmat: tratamentul lui Livingston-Wheeler se bazeaza pe convingerea ca cancerul este cauzat de o bacterie pe care a denumit criptocide Progenitor. tehnicile au arătat că nu există niciun astfel de organism și că Livingston-Wheeler a confundat, în mod evident, mai multe tipuri diferite de bacterii, atât rare, cât și comune, pentru un microb unic. În ciuda cercetărilor sârguincioase pentru izolarea unui microorganism cauzator de cancer, niciunul nu a fost gasit ; in timp ce multi oncologi si-au exprimat speranta ca intr-o zi un vaccin va fi dezvoltat impotriva cancerului, cauza (cauzele) cancerului trebuie sa fie determinata/e inainte ca cercetarea poate să fie îndreptata spre dezvoltarea unui vaccin.Rațiunea pentru alte fațete ale terapiei cancer Livingston-Wheeler este similar defectuoasă. nu exista nici o dovada din care rezultă ca ,cancerul rezulta dintr-un sistem imunitar defect, că o dietă cu alimente întregrale restabilește deficiențele sistemului imunitar, că acidul abscisic încetinește creșterea tumorii sau că cancerul este transmis la om de către pui „. (Raportul complet este on-line la: http://caonline.amcancersoc.org/cgi/reprint/40/2/103)
BACTERIA CAZATOARE DE CANCER

Recunoașterea bacteriilor producătoare de boli a permis științelor medicale să iasă din epoca întunecată în epoca medicinei moderne. La sfârșitul secolului al XIX-lea, când bacteriile s-au dovedit a fi provocatoare de boli cum ar fi tuberculoza (TB), sifilisul și lepra, unii medici suspectați că cancerul la om ar putea avea o cauză similară.

Ideea că bacteriile provoacă cancer este considerată absurdă de majoritatea medicilor. Cu toate acestea, în ciuda viziunii antagoniste a Societății Americane de Cancer și a științei medicale, există dovezi ample în literatura de specialitate publicată, care sugerează că „microbii cancerului” cauzează cancer.

Forme coccoide cu dimensiuni variabile intracelulare în cancerul de sân.
Acid-rapid pata; Mărire x1000, în ulei .

Conform rapoartelor de la Livingston și de la alți cercetători, cancerul este cauzat de bacterii pleomorfe, de celule perete deficitar – wall deficient cells . Diferitele forme ale organismului variază în funcție de formele submicroscopice asemănătoare virusului, până la mărimea bacteriilor, drojdiilor și ciupercilor. În cultură și în țesut, formele bacteriene sunt variabile „acid-rapide” (având o calitate a colorării ca bacteriile TuBerculoza). Aceste bacterii sunt omniprezente și există în sângele și țesuturile tuturor ființelor umane (încă o „erezie”). În absența unui răspuns imun protector, aceste bacterii cu deficit de perete celular pot deveni patogene și favorizează dezvoltarea cancerului, boala autoimună, SIDA și anumite alte boli cronice de etiologie necunoscută.

Inutil să spun că toată această cercetare a căzut pe urechile moarte deoarece bacteriile au fost în totalitate excluse ca si cauză a tuturor cancerelor în primii ani ai secolului al XX-lea. Astfel, bacteriile observate în cancer au fost pur și simplu respinse , catalogate in elemente de degenerare celulară sau ca invadatori ai țesutului slăbit de cancer sau ca „contaminanți” de origine de laborator.

STAȚIE DE VIAȚĂ ȘI CRIPTOCIDE PROGENITOARE

Începând cu anul 1950, într-o serie de lucrări și cărți, Livingston și colegii săi au susținut că microbul cancerului a fost un imitator excelent al cărui forme pleomorfice ce seamănă cu stafilococi, difteride, ciuperci, virusuri și incluziuni de celule gazdă. Cu toate acestea, dacă germenul a fost studiat cu atenție în toate etapele sale de tranziție, acesta ar putea fi identificat ca un singur agent.Ea a fost prima care a sugerat că pete-stains acide-rapide au fost cheia pentru identificarea microbului de cancer în țesut și în cultură; și, de asemenea, a demonstrat apariția sa în sângele bolnavilor de cancer, prin utilizarea microscopiei cu câmp închis – darkfield – si dr robert o young si gastons naessens au observat similar cu microscop darkfield.

Oricine își acordă timp să citească rapoartele lui Livingston în literatura medicală va recunoaște repede că este o om de știință de cercetare credibilă, care s-a aliat cu alți experți – și cu siguranță nu a fost doctorul vrăjitor prezentat de criminali. Realizările sale în microbiologia cancerului se regăsesc și în cărțile sale autobiografice: Cancer, New Breakthrough (1972); Microbiologia cancerului (1977); și Cucerirea Cancerului (1984). Cercetările sale au fost confirmate de alți oameni de știință, cum ar fi microbiologul Eleanor Alexander-Jackson, citologul celular Irene Diller, biochimistul Florența Seibert și dermatologul Alan Cantwell, printre altii.

Bacteriile intracellulare in cancerul de prostata.
Acid-rapid pata; mărire x1000, în ulei.

MICROBUL CANCERULUI ȘI PLEOMORFISMUL BACTERIAL

Microbiologii au rezistat mult timp ideea de pleomorfism bacterian și nu recunosc sau nu acceptă diferitele forme de creștere și ciclul de viață al bacteriilor propuse de diverșii lucrători/cercetatori în domeniul microbilor. Majoritatea bacteriologilor nu acceptă ideea că o bacterie se va schimba de la un cocus la o tijă sau la o ciupercă. În funcție de mediul înconjurător, microbul în faza cu deficiență de perete celular poate atinge dimensiuni mari, chiar mai mari decât cel al unei celule roșii din sânge. Alte forme sunt submicroscopice și de dimensiuni ale virusului. Studiile microscopice electronice și fotografiile culturilor filtrate (fără bacterii) ale microbilor de cancer prezintă elemente de mărime ale virusului pt microbul de cancer, care pot reveni la microbi cu dimensiuni bacteriene.

Microbii de cancer s-au adaptat la viața omului și a animalelor prin existența unei stări de deficit de perete de tip mycoplasma sau de celulă. În secțiunile de țesut ale cancerului colorate pentru bacterii cu pată specială acidă rapidă, microbul poate fi văzut ca un coccus rotund variat de aciditate rapidă (albastru, roșu sau violet) sau ca granule abia vizibile. La măriri de o mie de ori (în ulei), aceste forme pot fi observate atât în interiorul cât și în afara celulelor.

Studiul atent și observația micilor forme rotunde de coccoid în țesutul canceros indică faptul că se pot mări progresiv până la dimensiunea așa-numitelor corpuri Russell, care sunt bine-cunoscute de patologi. Corpurile Russell pot atinge dimensiunea globulelor roșii și chiar mai mari.
William Russell a fost un patolog scoțian bine respectat, care în 1890 a raportat pentru prima dată constatarea „paraziților cancerului” în țesutul tuturor cancerelor pe care le-a studiat. Cu toate acestea, patologii moderni neagă că organismele lui Russell sunt de origine microbiană. Pentru mai multe informații despre corpurile lui Russell și despre „parazitul cancerului” lui Russell (și relația sa intimă cu microbii cancerului), Google: indiciul uitat la cauza bacteriană a cancerului; sau accesați: http://www.joimr.org/phorum/read.php?f=2&i=50&t=50 .

EXTINDEREA BACTERIILOR CONFIRMATE ÎN CANCER

Odată ce bacteriile au fost eliminate ca o cauză a cancerului acum un secol, a devenit dogmă și imposibil de schimbat opinia medicală. În această epocă actuală a științei medicale, s-ar crede imposibil ca experții în boli infecțioase și patologii să nu recunoască bacteriile în cancer. Cu toate acestea, bacteriile pot apărea în continuare în bolile în care au fost inițial trecute cu vederea.
Când o boală pulmonară nouă și mortală a izbucnit printre legionarii din Philadelphia în iulie 1976, două sute douăzeci și doi de persoane s-au îmbolnăvit și treizeci și patru au murit. Cauza bolii plămânului ucigaș a rămas un mister medical de peste cinci luni, până când Joe McDade de la Legea Dermatologică a CDC a detectat bacterii neobișnuite la cobai infectați experimental cu țesut pulmonar din legionarii morți. Modificarea ulterioară a metodelor de cultură bacteriană a permis în cele din urmă izolarea bacteriilor cauzale și trecută cu vederea, cunoscută acum ca Legionella pneumophila.

Nodul limfatic care prezintă limfom Hodgkin. Săgeată punct
la forme rotunde de coccoide rotunde și la corpuri mai mari Russell.
Gram stain; mărire x1000, în ulei.

Un alt exemplu de cercetare în domeniul dogmelor este oferită de studii recente care demonstrează că bacteriile (Helicobacter pylori) sunt o cauză obișnuită a ulcerelor de stomac, care uneori pot duce la cancer la stomac și la limfom. Timp de un secol, medicii au refuzat să creadă că bacteriile au cauzat ulcere deoarece credeau că bacteriile nu pot trăi în mediul acid al stomacului. În 2005, Premiul Nobel pentru Medicină a fost acordat a doi cercetători australieni pentru descoperirea lor din 1982. Aceste bacterii de stomac au putut fi detectate numai prin utilizarea de pete de țesut special. CDC afirmă acum că H. pylori provoacă mai mult de 90% din ulcere duodenale și 80% ulcere gastrice. Aproximativ două treimi din populația lumii este infectată cu acești microbi.

În ultimii patru ani s-au raportat cazuri de bacterii nou descoperite în boala ganglionară gravă; în limfomul Hodgkin; în cancerul gurii; și în cancerul de prostată, pentru a numi doar câteva.

Toate aceste studii dovedesc că bacteriile se pot aprinde în bolile unde se așteaptă cel mai puțin. Un astfel de avertisment este adecvat pentru medici care cred că știu totul despre cancer și neaa toate aspectele legate de cercetarea microbilor de cancer.

STUDIU MICROBI CANCERULUI

Livingston nu a susținut niciodată că a fost descoperitorul microbului cancerului. În scrierile sale, ea a acordat întotdeauna credit unor oameni de știință, unele datează din secolul al XIX-lea, care au încercat să dovedească faptul că bacteriile cauzează cancer. Unii dintre acești cercetători remarcabili includ studiile de lungă durată ale microbilor de cancer ale obstetricianului scoțian James Young, medicului din Chicago, John Nuzum, chirurgului din Montana, James Scott, cercetătorului psihiatru Wilhelm Reich, microscopului Raymond Royal Rife și alții prea numeroși.
Această cercetare în domeniul microbilor de cancer a fost explorată în cărțile mele Cancer Microbe: Killerul ascuns în cancer, SIDA și alte boli imune [1990] și în patru femei împotriva cancerului: bacterii, cancer și originea vieții [2005] povestea lui Livingston, Alexander-Jackson, Diller și Seibert – patru oameni de știință remarcabili care au încercat să aducă microbii de cancer în atenția unei instituții medicale dezinteresate. Am fost privilegiat să întâlnesc toate aceste femei remarcabile, care mi-au influențat în mare măsură propria cercetare în domeniul cancerului.

De ce este explorarea cercetării bacteriilor în cancer atât de puternic opozata? Poate că reprezintă o amenințare la adresa intereselor bănești implicate în tratamentul stabilit și ortodox pentru cancer. Diverse forme de tratament pentru cancer includ chirurgie, radiații și chimioterapie. Aceste terapii ar putea fi reevaluate dacă s-ar dovedi că, cancerul este o boală infecțioasă.

SUGESTII PENTRU STUDIUL INTERNET ALTERNATIV
Mai multe informații referitoare la cercetarea privind microbii în domeniul cancerului (atât pro și con) pot fi găsite de Google: microbul cancerului; pleomorfismul bacterian; bacterii cu deficit de perete celular; „alan cantwell”;„virginia livingston”; „Eleanor Alexander-Jackson”; precum și alte denumiri și cuvinte-cheie menționate în prezenta comunicare.

Pentru o listă de publicații științifice referitoare la microbiologia cancerului, accesați site-ul PubMed găzduit de Institutul Național de Sănătate (www.ncbi.nlm.nih.gov) și tastați în „Cantwell AR”, „Livingston VW”, ” Alexander-Jackson E „,” Diller IC „,” Seibert FB „etc. în caseta de căutare.

Această comunicare scurtă este puțin probabil să convingă mulți profesioniști din domeniul sănătății că bacteriile cauzează cancer. Cu toate acestea, după patru decenii de studiere a microbilor cancerului în țesuturi canceroase, sunt personal convins că Dr. Virginia Livingston va fi o zi justificată și recunoscută ca fiind una dintre cele mai mari genitive medicale ale secolului al XX-lea.

Ralph W Moss, avocat de cancer și autor al industriei cancerului, notează că trecerea ei in nefiinta a fost „o pierdere majoră pentru lumea cancerului”. În Cancer Chronicles # 6, 1990, scrie: „Virginia Livingston a fost o persoană grozavă și o mare om de știință. Din păcate, ea nu a primit niciodată recunoașterea pe care a meritat-o în timpul vieții sale.“

Acest raport onorează centenarul nașterii sale care are loc la 28 decembrie 2006.

BIBLIOGRAFIE :

Alexander-Jackson E. Un tip specific de microorganisme izolate de cancerul de origine animală și umană: bacteriologia organismului. Creştere. 1954 Mar; 18 (1): 37-51.

Cantwell AR. Variante bacteriene cu deficit de acid celular de tip celular, ca o posibilă cauză a bolii dermatologice. În, Domingue GJ (Ed). Bacterii cu deficit de perete celular. Lectură: Addison-Wesley Publishing Co; 1982. Pp. 321-360.

Cantwell A. Cancer Microbe. Los Angeles: Aries Rising Press; 1990.

Cantwell A. Patru femei împotriva cancerului. Los Angeles: Aries Rising Press; 2005.

Diller IC, Diller WF. Organismele intracelulare cu aciditate rapidă izolate din țesuturi maligne. Trans Amer Micr Soc. 1965; 84: 138-148.

Greenberg DE, Ding L, Zelazny AM, Stoc F, Wong A, Anderson VL, Miller G, Kleiner DE, Tenorio AR, Brinster L, Dorward DW, Murray PR, Holland SM. O bacterie nouă asociată cu limfadenită la un pacient cu boală granulomatoasă cronică. PLoS Pathog. 2006 aprilie 2 (4): e28. Epub 2006 Apr 14.

Hooper SJ, Crean SJ, Lewis MA, Spratt DA, Wade WG, Wilson MJ. Viabilitatea bacteriilor este prezentă în țesutul carcinom cu celule scuamoase orale. J Clin Microbiol. 2006 mai, 44 (5): 1719-25.

Nuzum JW. Producerea experimentală a carcinomului metastazant al sânului câinelui și a epiteliului primar la om prin inocularea repetată a unui micrococcus izolat din cancerul de sân uman. Surg Gynecol Obstet. 1925; 11; 343-352.

Russell W. O adresă pe un organism caracteristic al cancerului. Br Med J. 1890; 2: 1356-1360.

Russell W. Parazitul cancerului. Lancet. 1899; 1: 1138-1141.

Sauter C, Kurrer MO. Bacteriile intracelulare în boala lui Hodgkin și limfomul cu celule B mediastinală sclerozantă: semnul unei etiologii bacteriene? Elveția Med Wkly. 2002 iunie 15; 132 (23-24): 312-5.
Scott MJ. Originea parazitară a carcinomului. Northwest Med. 1925; 24: 162-166.

Seibert FB, Feldmann FM, Davis RL, Richmond IS. Studii morfologice, biologice și imunologice asupra izolatelor din tumorile și sângelui leucemic. Ann NY Acad Sci. 1970 Oct 30; 174 (2): 690-728.

Shannon BA, Garrett KL, Cohen RJ. Legături între Propionibacterium acnes și cancerul de prostată. Viitorul Oncol. 2006 aprilie 2 (2): 225-32. Revizuire.

Wuerthele Caspe-Livingston V, Alexander-Jackson E, Anderson JA, și colab. Proprietățile culturale și patogenitatea anumitor microorganisme obținute din diferite boli proliferative și neoplazice. Amer J Med Sci. 1950; 220; 628-646.

Wuerthele-Caspe Livingston V, Livingston AM. Demonstrarea criptocidelor progenitoare în sângele pacienților cu boli de colagen și neoplazice. Trans NY Acad Sci. 1972; 174 (2): 636-654.

Young J. Descrierea unui organism obținut din creșteri carcinomatoase. Edinburgh Med J. 1921; 27: 212-221.

[Dr. Alan Cantwell este un dermatolog pensionar și autorul CANCER MICROBE și al patrulea FEMEI ÎMPOTRIVA CANCERULUI, ambele disponibile la Aries Rising Press, PO Box 29532, Los Angeles, CA 90029 (www.ariesrisingpress.com ). Email: alancantwell@sbcglobal.net . Rezumatele a 30 de lucrări publicate pot fi găsite pe site-ul PubMed (tip în Cantwell AR). Multe dintre scrierile sale personale pot fi găsite pe www.google.com prin folosirea cuvintelor cheie „alan cantwell” + articole. Cărțile sale sunt de asemenea disponibile pe www.amazon.com și prin Casa Clearing House @ 1-800-431-1579]

RIFE machines cancer treatment

nov.19

CLICK AICI pentru limba ROmana(traducerea “aproximativa” utilizand google translate).

Prior to reading this article it is recomended to read the articles:

“Cancer Causes ” (click here)

How cancer develops over a 24 months period (click here)

Cancer fungus- the link between cancer & microbes (click here) Immune System, alkalinity and cancer microbe

Cancer Theory and Electromedicine Treatments

The link between low immunity in conjunction with acidity-low PH / low oxygen levels that allow cancer and microorganisms to form a symbiotic relation with cancer and develop out of control has been around from :

-Hahnemann, the founder of homeopathy,

-Prof. Enderlein, who spoke of endobionts,

–Prof. Gaston Naesenss,

-Tamara Lebedeva ,

–Dr. Hulda Clark, who sees a intestinal parasites as a cause,

–Dr Tullio Simoncini and

-a number of other well- known researchers, including Dr Robert O Young, Dr Royal Rife, Dr.Matias Rath, Irene Diller , Caste Livingston and many others (click here for more details and scientific research & evidence).

All of these researchers observed the link between cancer and microorganism independently, using different techniques, thus named these microorganisms differently and also proposed & developed different solutions to this problem.

I.e.

profesor Gaston Naesenss observed these microorganisms around 1950, with the microscope he developed (called somatoscope) and named these microorganisms according to their pleomorphic shapes, from somatids, spores, double spores. etc.; as a solution he developed an immune re- balancer called 714 X to re-balance the immune system.

Dr Royal Rife observed this link between microorganisms and cancer, in 1930, with the powerful microscope he developed and called these microorganism , according to pleomorhpic state they were observed in, but differently, from BX, BY, etc.; Dr Rife developed an electromedicine device for killing these microbes, wich, in 1930 achieved 100% cure rate with terminal cancer patients:

Royal Raymond Rife (1888 – 1971) was a brilliant scientist who developed technologies which are still in use today in the fields of optics, electronics, radiochemistry, biochemistry, ballistics and aviation.

During the 66 years that Rife spent designing and building medical instruments, he worked for Zeiss Optics, the U.S. Government, and several private benefactors.

Using a remarkable new microscope he designed and built, in 1930 Royal R. Rife cultured tissue from a breast cancer sample, in Kendall medium, and isolated a micro-organism.

He followed this experiment with a series of other studies in which he cultured an organism in Kendall media, from tissue taken from a human breast cancer.

He then injected this microorganism into 412 healthy rats, and found that without fail they all developed breast cancer.

Finally, he was then able to isolate the original microorganism from the tumours which grew in the rats. In the process Rife became probably the first person ever to fulfil Koch’s postulants, for cancer causing microbes.

Koch’s Postulants are a set of rules to prove the causation of disease by microorganisms. They state that to prove such causality the microorganism must first be isolated and cultured. It must then be shown to have infected a health animal, and finally the same organism must be recoverable from the now infected animal.

The cancer virus which Rife named Cryptocides Primordiales or the BX virus, was a minute 1/5 micron in length and 1/20 micron in width. It was highly motile, aerobic (requiring free oxygen for its survival) and highly pathogenic.

Rife discovered that while exposing the virus/microorgansims to a temperature of 42C for 24 hours would kill the virus(an additional reason why hyperthermia works), it remained unaffected by exposure to either X-ray, UV or Infra-red waves.

While the discovery of a cancer virus was in itself an incredible feat of scientific endeavour, Rife was to make yet more discoveries destined to rock the scientific status quo.

The BX virus was observed & shown to be a polymorphic (meaning it has/can change in many forms) virus, able to change its states according to the culture in which it was grown.

When a BX virus was cultivated in a different media/ environments, it was seen to change into a BY virus. When the media/ environment was changed yet again it developed into a monococcoid in the monocytes of the blood, and with a further change of media/environment it morphed once again, this time into crytomyces pleomorphia fungi.

At any stage along this journey of polymorphism, the original BX virus could be grown again by adding any one of these forms to the original media/environment.

Everything was documented with film, photographs and meticulous records.

NOTES:

1.The pleomorphism has also been observed and confirmed by other researchers and scientists, independently. using other methods (ie. profesor Gaston Naesenss observed this usign the powerful microscope he developed, called somatoscope and gave these microorganisms different names ).

2. These cancer microorganisms can take up to 16 forms :

In a healthy person, with a strong immune system, these microbes can be found in 3 forms: somatids, spores & double spores (as named by professor Naesenss); These forms are harmless (harmful forms are killed by the immune system)

Once the immune system is weak, if the environment is favorable( acidic , optionally high in sugar) , thse microorganism can take an additional 13 HARMFUL forms and the forms they can be found in/ all shapes & sizes they can take, depend on the environments PH ( acidity/alkalinity/ oxygen level).

Next Dr Rife was able to use a certain frequency of energy produced by a machine he developed that could destroy these cancer causing viruses in the body without harming any normal cells.

Royal Rife’s electromagnetism machine had a 100% cure rate of terminal cancer patients.

All of this was in the 1930s.

Everything was documented with film, photographs and meticulous records.

Rife’s work was vigorously discredited by the conventional medical establishment, and it remains so to this day – as was and is the case with Dr Stanislaw Burzinski , Dr Philip E . Binzel. Dr. William D Kelley, Dr Max Gerson, professor Gaston Naesenss amd all great researchers that made an important contribution in curing cancer using methods that , besides being effective and NO-toxic, cannot be patented – profit cannot be made as with medical drugs .

The AMA(American Medical Association) persecuted Royal Rife to the extreme. His lab was burned down, one of his associates was murdered, his equipment was hunted down and destroyed.

A group in England claimed to obtain a Royal Rife machine that was not destroyed. A website which discussed old versions of the Royal Rife machine and other versions of it, and has a copy of the English report can be found at this web site: http://www.scoon.co.uk/

Also see this web site (this is a vendor and a source of superb information): http://www.rifecranerockwell.com/

There are now thousands of websites devoted this little-known genius and humanitarian, and his amazing contributions to the welfare of us all.

NOTES:

1. Electromedicine devices decribed in this article – Rife machines , mean very gentle electrical devices which are designed to get rid of cancer cells without the need of nutrients!!

These devices use SAFE radio waves , NOT DANGEROUS ionized radiation used in radiotherapy.

2.a. It has been demonstrated many times that if you kill all of the microorganisms inside of a cancer cell, the cancer cell will revert into a normal cell ( as nothing will prevent the cell from restoring it’s normal functions ).

2.b. Some good examples of treatments that kill these microbes inside cancer cells, you can do at home right now:

1) Vitamin C IntraVenously(also extends life),

2) fruit juices (i.e. dark skinned grapes, berries, etc)

3) Treatments using honey as carrier( i.e. turmeric and honey, ginger & honey, cinnamon & honey, etc)

4) All DMSO / All MSM treatments ( similar to honey as carrier treatments but, unlike hoey/ glucose, these CAN be used by patients with severe cachexia – see my book, english/international version),

2.c. One of the most efficient ways to kill these microbes is with electromedicine Rife devices.

Original RIFE devices-High Frequency RF Rife machines were designed especially to kill the pleomorphic microorganisms that can cause cancer.

Do NOT confuse these powerfull electromedical devices with the Zappers (Hulda Clark) or Bob Beck devices.

Rife replica devices will do the job Zappers and Bob Beck devices do (clean the blood and areas such as liver,lymph & dental area from micoorganisms) AND, IN ADDITION , also kill the microbes INSIDE cancer cells, restoring these to normal cells.

They use a Radio Frequency(RF) for killing cancer microbes and another RF as a carrier for the first “cancer killer RF” inside cancer cells .

This allows the cancer cells to revert to normal cells because nothing prevents ATP energy production when microbes are dead.

This is the best and safest way to kill and cure cancer, because there is no dead cancer cells debris in the body( only debris from dead microorganisms, witch is far less toxic ).

There are some other cases where these gentle electromedicine treatments would be highly suggested if one can afford it for the treatment of cancer.

The cases are:

1) The patient cannot eat very much,

2) The patient has significant problems digesting their foods (e.g. they have had stomach or colon surgery),

3) The patient cannot extract nutrients from the foods/supplements they take (e.g. due to significant chemotherapy that damages digestive tract ( as it has fast growing cells)),

4) The cancer is fast-spreading,

5) The cancer has spread throughout the body.

2. d . So how do these devices kill the microbes which are inside of a cancer cell?

It is generally believed that each of the 16 shapes and sizes of the cancer microbe has a different „Mortal Oscillatory Rate” or M.O.R., meaning they have a different frequency at which they vibrate until they explode and die.

Think of a wine glass being shattered by an opera singer. At a certain frequency the glass will shatter.

Likewise, each microbe/microorganism has a specific frequency (i.e. M.O.R.) at which it will „explode” and die.

In theory, this would imply that it would take 16 different frequencies to kill the „cancer microbe.”

Well, it is not that simple.

The Independent Cancer Research Foundation will determine these frequencies if they ever get enough funding. But for now understand that it has been shown by those using electromedicine, by trial and error, that taking some ionized water makes the device more effective.

This makes perfect sense because at the larger sizes and shapes, finding an effective frequency to vibrate them until they explode may be very difficult. This may be exacerbated by the shapes of the larger sizes. Some shapes may prevent a uniform and consistent vibration.

By taking some ionized water the alkalinity inside the cancer cells will go up and the size of the microbes will go down into the mid-size range of the microbe sizes.

However, it has also been shown that when too much ionized water is taken, in conjunction with an alkaline treatment, that the microbe becomes too small to kill by the frequency range of the device.

These conclusions were based on case studies.

Much more research needs to be done in this area, but for now realize that the cardinal rule of using electromedicine is to take a reasonable amount of ionized or alkaline water, but do not be fanatical.

By using moderation the size and shape of the cancer microbe will be in the middle range and it will be easier to kill the microbes by using vibrations. This is a highly theoretical discussion, but the theory coincides with the actual success of the devices.

IMPORTANT NOTE:

Dr Rife observed these cancer microbes can NOT be killed faster than they can spread in an acidic (low PH/ low oxygen ) environment.

Thus, raising cellular alkalinity /cellular oxygen levels (STOPping the spread of cancer) is more important and comes first( these microorganisms are mostly found in the blood and liver in a healthy person but once the cellular PH is low, the acidic cells can be invaded by these microorganisms, if the immune system is weak as well; these microorganisms will NOT develop and spread in an alkaline environment/where the PH is high/high oxygen levels or where the immune system is strong enough; unfortunately strenghtening the immune system is harder as it takes a long time;alkalinity remains your only option for stopping the spread of cancer ).

This can be done safely with the help of an alkaline diet or alkaline water ( both are not needed ; to much alkalinity can make these microorganisms difficult to kill using electromedicine; methods as

Cesium should also be avoided with Rife electromedicine;

Calcium or Ozone/Oxygen therapies, used in conjuction with proteolitic enzymes (protease will digest the protein layer that prevents oxugen & Calcium (as an oxygen carrier) form entering a cancer cell and raise it’s oxygen level/PH might also be sufficient alkalinity – more studies need to be conducted here)

The bottom line with electromedicine protocols the way to maximize the effectiveness of these protocols is to use some alkalinity to put the microbes in the middle size range and stop them from spreading faster than they can be killed, but not use too much alkalinity.

„Moderation” of alkalinity is a good term.

Read this article about alkalinity & microorganisms for more details.

NOTES:

1. More than a hundred experts have tried to replicate Rife’s technology.

More than one of these „machines” Rife was highly effective against cancer!

WARNING :

Most brands of so-called Rife machines available on the market today are completely ineffective for cancer because they either do not have power or not the necessary /corresponding frequency range, carrier wave, etc.

But there are few that are extremely effective :

A research group had sufficient library and money resources to restore some original equipment Rife which were sold and delivered before Dr. Rife to be stopped by the AMA in 1939.

A frequency generator and Plasma amplifier that can transmit Rife’s frequencies using Rife’s original method is decribed in my book .

2. a. Please note that, as I’ve repeatedly stated & you’ve probably noticed, the purpose of this website is to adequately & OBJECTIVELY inform you of your best options, with scientific arguments (information based on scientific studies & confirmed by case studies and clinical trials).

From my point of view, being objective also implies being equidistant. Thus, I do endorse anyone, I do not make any type of recommendations neither when it comes to treatments, nor when it comes to vendors (though many of you have asked me to also mention vendors and brands).

What you decide to do, if you decide to buy something, from who and from where you buy, etc, is ENTIRELY your choice. My purpose is to adequately and objectively inform you of your options in order to ease / help you make a BETTER decision , FASTER.

HOWEVER, you should / MUST ask you vendor if he /she offers support for using this type of machine for cancer, and you should also ask him about results he/she have had – statistics based on case studies/ clinical trials.

As vendors may be reluctant as they cannot offer medical claims (according to the law), I realise it may be difficult to find a good option in this area without doing some heavy research before.

It is why with Rife machines I decided to include some links where you can find some RIFE replicas reported to have worked. But keep in mind this is not an official endorsement. It is just meant to help you with / ease your research .

Rife had a 100% cure rate in 1930. Nowadays, there are very few Rife replicas.

Most of electro-medicine devices sold on the internet as Rife machines do NOT work well enough as they do NOT have enough power or do NOT have the frequencies or do NOT replicate exactly Rife instructions or may even be frauds .(I do not know & I do not have the resources to test every machine or product that claims to be a „miracle” cure for cancer; THE BEST WAY TO KNOW if the product ( drug , supplement, electromedicine device , etc) is working is to

TEST/MONITOR YOUR PROGRESS ON A REGULAR BASIS ).

One type that surely works is described in my book as the developers replicated it according to original Rife documentation and have successively tested it on humans with cancers .

But, once again:

2.b.TEST/MONITOR YOUR PROGRESS ON A REGULAR BASIS

There are many factors to consider, each case is unique, each patient has it’s own cancer characteristics & needs ( type of cancer, stage of cancer , how fast cancer is spreading,cellular PH balance – that cannot be measured, how much cancer has spread, how much he/she has been affected by conventional cancer treatments, ability/inability of the digestive tract to use nutrients from food, physical energy , psychical energy, spiritual energy, willing to live etc.)

No matter what treatment you decide to use you must :

TEST/MONITOR YOUR PROGRESS ON A REGULAR BASIS , in order to see if the treatment is adequate for your case or improvements, modifications or radical chances in treatment plan must be performed.

2.c. Some of these Rife devices(at least the ones I mention in my book) also include energizing protocols (meant to provide energy to your body) but they do not do the same great thing in providing energy such as Photon Devices or Quantum Pulse /Vibe Machines/Bio Pulsers) .

On the other hand , Vibe Machines & Photon Devices ( besides being far more expensive) are best for providing energy to help keep a patient alive but do NOT kill cancer microbes as Rife devices do.

The choice depends on the situation.

A person who can affrod may use both devices. They do NOT conflict.

A RIFE device generating high-Radio Frequency RF (electrode or plasma tube) is synergistic with one or both of the Photon devices.

When people can afford only one of the devices the rule is:

-if the main danger of cancer is lack of energy or a dangerous tumor(life-threatening), buy Photon device .

-if the main danger of the cancer are cancer cells (when tumors are not considered life-threatening), buy RIFE device.

A compromise solution would be to purchase a Rife device that can be used both to energize and as a cancer treatment, but do not neglect a consultation from the Ed Skilling Institute , even without buying a Photon device. Their experience could prove crucial.

Again, it is your decision if / what you buy (if you buy something), according to your personal needs: do you have enough energy and need to kill a fast spreading cancer and rapidly supercharge the immune system with a Rife device, or are you a very weak patient that needs crucial energy ?

3.a.This is the type of machine I bought for my mother. Unfortunately, I didn’t get much time to test it . My mother went into severe cachexia and died very soon after I bought the Rife Replica from Independent Cancer Research Foundation (ICRF) Inc. Thus. instead of using the device to help my mother, it is still in boxes with a layer of dust above them.

3.b.I’ve mentioned this as the ICRF have done a lot of research with replicas of Rifes original devices over the years, they have clinical cases they report they have successively treated and they provide support. The ICRF is one of the premiere alternative cancer treatment research organizations and you can read more about them & support their research: Independent Cancer Research Foundation, Inc.

While I can offer these cancer treatments / protocols for free for anyone who wants this , I cannot guarantee they will work on the devices you buy, even if you buy them from ICRF Inc as each producer has it’s own software installed on the device. All I can say about the protocols I have is that they will work on the device I have, with the sofware version installed on the device I have.

Once again, ask the vendor if he/she offers support for treating cancer before you buy and about clinical cases .I do not endorse and do not make any guarantees for anyone.And test your treatment regularly to monitor you progress.

3.c.

Recent studies indicate that in many cases, the cancer causing microorganism is Helicobacter Pylori, when it gets inside of normal cells or when a cancer cell divides and creates two daughter cancer cells which each have these microbes.

According to Independent Cancer Research Foundation, the evidence that H. Pylori causes cancer is very solid.

For example:

1) It is ubiquitous in the stomach and common in the bloodstream (all humans have some cancer cells at all times),

2) It is known to be a pleomorphic microbe,

3) The most effective herb at killing H. Pylori, turmeric, is also the same herb that is most effective at treating cancer,

4) More than one alternative cancer researcher has come to the same conclusion independently.

But regardless of what the cancer microbe is, it has been known since the 1930s (starting with Royal Rife and many others) that one of the best ways to cure cancer is to kill the microbes which are inside of the cancer cells. In this way the cancer cells will revert into normal cells .

In addition, because just killing these microbes inside cancer cells is less toxic than killing cancer cells, these treatments can be applied SAFELY, in much HIGHER doses that other treatments focused on killing cancer cells ( i.e .: than Vitamin B17 ) , making these a far better (MORE efficient and LESS toxic) option.

This devices used specific square waves for each specific microbe because each microbe has its own resonance frequency (meaning the frequency at which it dies ,just like an opera singer can shatter a crystal glass at proper resonance frequency) .

Fortunately the frequency of cancer microbe is well known (so it can be killed!).

In theory, this device can cure cancer in a single day.

So why does it not heal in a day?

First, the use of this great power would be unpredictable and it could be very dangerous for the patient for several reasons.

It would definitely cause Herxheimer reaction („brain fog” due to extreme detoxification). If you kill every microbe in the body in one day a person could die of Herxheimer reaction.

There are patients with cancer who had a severe Herxheimer reaction (because they allow the body to adapt), and refused to use the Electromedical device again.

This is because detoxification caused by toxins (dead microbes) .

The device is very gentle. Usually, a person will not feel that electromedical device is on !

But abuses must be avoided.

Anyway, do NOT try to use it twice a day, before using the device for at least 10 days.

Start with small doses and gradually increase them as the body adapts(as with every other treatment).

But, even with full power, it will not kill all the microbes in a single day. There are various reasons for this safety feature.

Rife method is a complete cancer treatment , but nutritional protocols are recommended to be added for patients with advanced cancer.

As Photon devices , RIFE devices always come with a nutritional combination of treatments (protocol). Dr. Rife noted that in highly acidic environment cancer spreads faster than it can be killed . Alkalinity IS ESSENTIAL. whatever approach.

Cancer patients always have more problems than cancer cells, especially if they have had chemotherapy and radiation.

Many cancer patients have died without many cancer cells in their body due to damage to healthy cells by chemotherapy and radiation, so nutrition, protection, energy are always critical.

WARNING:

Avoid the RIFE devices , Bob Beck devices and Hulda Clark Zappers while chemotherapy is in the blood. Certain chemotherapy drugs remain in the blood for long periods of time given. While chemotherapy is in the blood one should not use such Electromedical devices.

The reason for this rule is that electro protocols create electroporation. Electroporation „opens” all cells ports, not just cancer cells ports. These devices will allow chemo drugs to enter into numerous non-cancerous cells. They will enter these cells anyway but helping this is NOT a good thing!

More details and more powerful options in my book.

Best of health!

Cristian

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How Stress Causes Cancer

nov.10

click aici pentru textul in limba romana, traducere realizata de Cristina (sa ii multumim si sa ne rugam si pentru mama ei)

CLICK AICI pentru limba ROmana(traducerea „aproximativa” utilizand google translate).

This is a very important article, explaining how cancer occurs in the body over a period a time.It explains the connection between stress (meaning various stress factors), acidity/low PH, fungus , sugar fermentation, hormones & immune system, etc.

Everybody should read carefully this post if he/she wants to have a real chance in PREVENTING, HEALING & KEEEPING CANCER AWAY!

Cancer occurs when the body’s cells become depleted of adrenaline, high in sugar and low in oxygen due to prolonged internal stress (caused by various factors: psychological, physiological , chemical, etc ) .

At a cellular level, these lead to a breaking of the cells oxygen Krebs cycle causing cell „mutation”.

At a systemic level( meaning whole body level) various stress factors (that add up) will eventually cause a weakness in the immune system and the number of cancer cells will grow out of control .

There are a number of factors that create stress on the body’s cells:

Psychological stresses include (and are not limited to):

inescapable shock, repressed emotional pain, grief, trauma, anger, depression , other „bad”/ stressful emotional states that lead to poor sleep ( lack of melatonin ) or prelonged stress, etc. .

Physiological stresses include (and are not limited to):

poor and toxic nutrition, chemicals, toxins,GM(Genetic Modified) foods irradiated foods, radiation( ionized & EMF, NOT moderate sunlight), lack of sunlight and lack fresh air, lack of exercise, a weak or sick organ (i.e: liver or colon or kidney or lung disease) ,parasites, etc.

In the vast majority of those with cancer there exists both a combination of psychological as well as physiological stresses that have contributed to the formation of cancer in the body.

We have simplified into six separate phases, how cancer forms within the body at the cellular level over an 18-24 month period.

Phase 1 – Stress factors weaken the immune system

Phase 1 occurs approximately 18-24 months prior to the cancer diagnosis.

Various stress factors( Psychological and / or

Physiological )

weaken the immune system (every human has cancer cells in his/her body; the immune system is responsible for identifying & killing and keeping the number of caner cells under control ;when the immune system is weak the number of cancer cells might get out/grow out of control )

Thus, the number of cancer cells might get out/grow out of control

This migth be where someone(the cancer personality) experiences an Inescapable Shock or emotional trauma, or anything affecting deep sleep and the production of melatonin within the body (including working at nights, etc).

Melatonin(click here) is necessary for inhibiting cancer cell growth and is the primary hormone responsible for regulating the immune system; in particular production of interleukin-2 (IL-2) which protects against microbial infection and regulates white blood cells (T cells, B cells and Natural Killer NK cells) responsible for immunity.

As discovered by Dr Ryke Geerd Hamer every cancer has a different emotional cause. During this initial phase a part of the emotional reflex centre in the brain slowly breaks down as a result of the specific emotional trauma. Each part of the emotional reflex centre controls and is connected to a different organ of the body, and when this emotion centre starts to break down, so does the organ of the body it controls, to later form cancer, which occurs through a direct and ongoing suppression of the immune system, as outlined below.

The above(lack of melatonin due to Inescapable Shock or emotional trauma) are examples.

ANYTHING that weakens the immune system(any stress factors) can be the start point of cancer.

Phase 2 – Stress Causes Immune System Shut Down, Bacteria/ Fungus „installs” and „takes over”

Stress factors (the same ones or others ) weaken the immune system further, almost until it’s shutdown.

During phase 2 the immune system almost gets „shut down”.

For example, by a subconscious wanting to die, caused by high stress hormone cortisol levels depleting all-important serotonin/dopamine levels.

An individual experiencing inescapable shock and prolonged stress often feels tired of life and deep down wants out of the never-ending struggle and pain of life, sending subliminal messages to the immune system to shut down

NOTE: This is why wanting to live/ the willing to live is crucial for PREVENTING, HEALING & KEEPING CANCER AWAY.(the immune system must NOT be shut down as the immune system is the one that keeps cancer cells under control, identifies, kills & elimneate parasites in our bodies.

The immune system „shut down” causes somatids, tiny organisms (necessary for life) that live in our blood to pleomorphise into the cancer-fungus.

In a healthy person, where the immune system is functioning properly, these somatids are limited to 3 stages in their life cycle – somatid, spore, double spore.

When the immune system is impaired or suppressed, somatids pleomorphise (or change) into a further 13 stages (16 altogether).

These further 13 stages are pathogenic (harmful) to the body and include viral, bacterial, and yeast-like fungus forms.

Professor Gaston Naessens, who discovered the somatid after inventing the world’s smallest microscope (the Somatoscope) in the 1950’s, discovered that these further 13 stages always progressed over an 18-24 month time period when the body was under severe immunicological stress, which manifested as all types of chronic illness, notably cancer.

Below: The Somatid 16 stage Cycle, as discovered by Professor Gaston Naessens.

Read more about what Professor Gaston Naessens discovered regarding cancer and his solutions to this problem www.cerbe.com .I will write an article on this topic (714x) as well.

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Phase 3 – Stress Depletes Adrenaline, Causing Cell Glucose Levels to Rise

During phase 3 high stress hormone cortisol levels deplete all-important adrenaline levels within the body. There are only limited reserves of adrenaline in the body and when a person is under constant stress these reserves are depleted quickly.

This causes glucose (sugar) levels to rise within normal bodily cells in the following way: Insulin is used to transport glucose into cells and adrenaline is used to transport glucose out of cells to supply energy for general bodily use. When adrenaline reserves are depleted, glucose (sugar) levels increase sharply within the cells – leaving little room for oxygen.

This is why so many cancer patients are weak and lethargic because they have little adrenaline left to convert the glucose in their cells into energy for the body, and their cells subsequently have very little room left to accept oxygen from passing blood.

Phase 4 – Fungus Enter Cells to Feed on Glucose

During phase 4, pathogenic microbes (viral-bacterial-yeast-like-fungus) that thrive in this acidic , high sugar environment, have pleomorphised and established themselves in the weakened part of the body, then enter normal cells to feed on these high glucose levels.

These microbes/fungus/bacteria, once installed in an environment they like ( anaerobic/acidic/low PH, high in sugar) will do many things to protect themselves and the environment they live in, including steal cell energy , secrete a protein coating around its host ( host meaning the cancer cell) that will protect it from the immune system and will intercept more glucose and keep oxygen out of the cell, release mycotoxins, etc. see cancer causes click here

Below are some details about t

hese microbes that do many amazing things to help cancer cells do their damage and protect themselves:

1) Due to a weakened cell membrane, which can be caused by a carcinogen or many other things, a microbe is able to enter inside a normal cell (as Dr. Young stated, the microbe is pleomorphic and this can help the microbe get inside the cell which is still normal at this point),

(Note: the microbe(s) can also get inside a cell during the cell division of a cancer cell. For example, when a cancer cell, which already contains microbes, divides, there will likely be microbes in both cells which result from the cell division.)

2) The microbe, once inside, intercepts the glucose entering the cell (most microbes eat glucose),

3) The microbe excretes “mycotoxins,” dangerous hormones and perhaps a thick slime (mycotoxins are the normal excretions of microbes),

4) Because mycotoxins are very, very acidic, the inside of the cell becomes highly acidic, which is a characteristic of cancer cells (in fact the longer a cell is cancerous, generally the more acidic it becomes),

5) The cell’s mitochondria (which convert glucose into energy) get very little glucose because the microbe has intercepted most of the glucose,

6) What the cell’s mitochondria does get is lots of mycotoxins and other harmful garbage, which it cannot convert into energy,

7) The mitochondria’s energy level (ATP provides the key energy of a cell, but ATP is created by the Krebs Cycle and ETC) plummets because it is living in a sea of filth, meaning the ATP energy drops,

8) Signals are sent to the insulin receptors and glucose receptors on the cell membranes to grab more glucose,

9) More glucose enters the cell (about 15 times to 17 times more), but most of the glucose is intercepted by the microbe (which may be multiplying) and the mitochondria are bathing in an increasingly large sea of mycotoxins, dangerous hormones and possibly slime. Technically, the glucose is normally converted into pyruvate and it is the pyruvate that enters the mitochondria, but without glucose there is less pyruvate.

10) Because there is a limit to how high the activity of these two types of receptors can become there is no way for the mitochondria (and thus the ATP) to get enough glucose/pyruvate and energy,

11) The cell is now officially cancerous because its energy level drops (the ATP energy levels can be compared to the steps of a ladder) and it is defined to be anaerobic.

In this process, two things happen:

First, because of the microbe(s) the break in the Krebs Cycle and ETC are broken as long as the microbe(s) are inside the cell.

Second, each sick cancer cell contains very healthy microbes living inside!! Because the microbe(s) are healthy, and the cell is sick, it makes it very difficult to kill the microbe without killing the cell.

The bottom line in all of this is that the cell’s mitochondria, instead of swimming in a sea of pyruvate (which is made from glucose), are swimming in a sea of highly acidic mycotoxins because the microbes not only steal glucose (and thus pyruvate) from the mitochondria, they excrete highly acidic mycotoxins.

The body’s tissue and cells become highly acidic (low pH) due to the mycotoxins released by the viral-bacterial-yeast-like fungus.

Thus, the ATP prodution in the mitochondria drops to virtually nothing. The cell is forced to survive by using fermentation (of glucose)which creates a very small amount of ATP energy.

Over-acidification of the body also occurs due to fermentation of excess stress hormones in the body, poor diet (low pH value foods), and lack of exercise. (Viruses, bacteria, yeast, mould, fungus, candida and cancer cells thrive in a low pH acidic environment.)

The microbes also modify the cells DNA and create a thick protein coating on the outside of the cells wall which not only attracts glucose but also blocks oxygen.

Phase 5 – Fungus and Cancer form Symbiotic Relationship

During phase 5 viral-bacterial-yeast-like fungus (cancer-fungus) form a symbiotic relationship with newly created cancer / tumour cells:

The cancer-fungus feeds on the high levels of glucose present in the cancer / tumour cell to use for energy in their own reproduction.

The cancer-fungus provides a natural fermentation process in return, fermenting glucose within the cancer / tumour cell, providing energy and a natural growth factor.

The cancer-fungus uses the cancer / tumour cells as a host (like a home/house) for their rich reserves of glucose, and stimulates cancer / tumour cells to propagate more houses.

The result is a mass of tumour cells, or tumour sites.

The cancer-fungus prevents cancer / tumour cells reverting back into normal healthy cells (re-establishing their Oxygen Krebs Cycle), as they continue to release highly acidic waste products called mycotoxins, meaning cancer / tumour cells are literally held hostage to the cancer-fungus that inhabit them.

It is why these microbes must be killed if you want to revert a cancer cell back into a normal cell( providing that stress factors that made the cell cancerous are also solved)

Also, alkalinity(high PH/high levels of Oxygen) are crucial for making your inner terrain hostile to cancer & cancer bacteria/ microbes/ fungus.

As observed by Dr. Royal Rife(detalis in my book) and most other alternative cancer researchers, cancer canNOT be killed faster than it can spread in a favorable environment (acidic, high in sugar).

There are many ways to increase alkalinity/oxygen leveis (alkaline diet & water, alkaline minerals(CEsium, Calcium) Ozone/ Oxygen therapies ) and one should keep in mind that negative emotions(i.e. : anger, grief) create acidity,whereas positive emotions( i.e.: optimism, self confidence ) create alkalinity.

Phase 6 – Stress Stimulates Tumour Cell Growth / Metastases

During phase 6 elevated levels of norepinephrine and epinephrine (stress hormones) stimulate tumour cells to produce three compounds: MMP-2 and MMP-9 (both matrix metalloproteinases) and the growth compound VEGF (Vascular Endothelial Growth Factor).

Tumour cells make receptors for these stress hormones on their surface, to stimulate these three compounds. MMP-2 and MMP-9 breakdown the scaffolding of tumour cell walls making it easier for microbes inside cancer cells to travel to other parts of the body and establish a new colony where they find a favorable (acidic, high in sugar ) environment , a process known as metastases.

Remenber: once you have a cancer diagnosis( one tumor), your immune system is already weak/”shut down” This means it is very poor at killing new cancer cells and this microbes/fungus/bacteria mentioned above.They can spread via blood more easily, but, as the immune system is weak, and more stress only adds up, new tumors may also occur just as the first tumor occurred (by speculating a weak part of the body / without the spread of microbes)

VEGF causes blood vessels to grow in new tumour cells, cells get the excess sugar and nutrients they need, these micobres thrive in these environment, can multiply and spread more rapidly( in proximity ,causing local tumor growth or at another distant location , metastasis).

Elevated stress hormone norepinephrine and epinephrine levels also increase ATF3 levels in macrophages (immune system cells) taken over by tumor cells, further increasing the rate of metastases.

Other metastasis (tumors in new locations ) can also be caused just by the news of cancer at this stage often becomes a further inescapable shock and the 6 phases begin again with secondary tumour sites forming in different parts or organs of the body.

COMPLETE DETAILS & CLINICAL STUDIES ABOUT THE ABOVE -CLICK HERE

SOLUTIONS :

As you can notice above , it takes time for cancer to develop , cancer is a complex disease and is usually caused by many/a variety of stress factors.

This is why, PREVENTING m CURING & KEEPING CANCER AWAY is complex as well and canNOT be done just by taking a miracle pill or supplement. It is the reason why there is and there will be no such thing as the miracle pill for cancer.

PREVENTING m CURING & KEEPING CANCER AWAY implies switching to an alkaline lifestyle ( this implies many things :

rebalancing & energising your entire body,

willing/wanting to live, getting rid of as many stress factors as possible( both psychological & , and physiological) , getting rid of stress factors and streess hormones, normalizing melatonin levels and getting better sleep.

(re)alkalizing your body (re) balancing it to make it an environment hostile to cancer & cancer microbes, killing these cancer microbes(fungus that live inside cancer cells), strengthening your immune system, etc.)

The solution to PREVENTING , HEALING and KEEPING CANCER AWAY is complex and implies changing to an alkaline lifestyle (i.e. such as promoted by Bill Clinton).

Concrete things to do are:

getting rid of stress factors, including :

adopting an optimistic mental attitude & strong DESIRE TO LIVE, emotional support from the loved ones, trust in GOD;
getting rid of chemicals in the environment you live in ( air, water, food, etc .as much as possible);
avoiding GM food and irradiated food;
avoiding radiation( ionized, EMF, etc) as much as possible;
getting rid of toxins & heavy metals within(detox & chelation );
etc.

ENERGIZING & re balancing your body( ensure you SURVIVE during & after treatment ) including:

getting more sunshine on your skin for crucial ENERGY & vitamin D,
doing some/ moderate physical exercise in a clean , oxygenated environment to pump lymph system for detox, push oxygen into cells, increase internal antioxidants levels such as gluthatione, regulate production of melatonin and other hormones responsible for feeling well ( as much as you fell it is good for you as to make you feel better, from a simple walk in the park , walking your dog, etc do NOT overwork / do NOT put too much stress on your body )
re – hydrating with energy rich water (alkaline ionized water ) & energy rich foods (rich in healthy fats)
getting adequate sleep & rest at night for vital melatonin
using electromedical devices for energy (especially advanced patients, as described in my book)
etc.

(re)alkalizing your body (re) balancing to make it an environment hostile to cancer & cancer microbes:

adopting an alkaline diet (including supplementing with alkaline minerals such as Cesium or Calcium , akaline water, etc)
killing these cancer microbes(fungus that live inside cancer cells) – alkalinity will kill part of them, many natural substances will kill most ( Colloidal SILVER, grape juice, turmeric, etc, especially when used in a treatment using honey as carrier); RIFE electromedicine achieved 100% cure rate at killing this microbes & healing cancer when used in conjuction with an alkaline treatment(environment) ( as described in my book ) NOTE: as observed by Royal Rife, these microbes and cancer cannot be killed faster than it can spread in a favorable environment( acidic . high in sugar).thus, alkalinity is vital.
using Ozone / Oxygen therapies to raise cells oxygen levels & strengthen the immune system
strengthening your immune system(nutritional, electromedical)
etc.

Of course. various supplements can be added and some could prove vital on the short term(i.e.: vitamin C for extending life and keeping a patient alive, Cesium for creating alkalinity fast, hidrazine sulphate for patients with cachexia, etc).

But, keep in mind, these will only help on the short term (will solve a specific issue such as keep a patient alive or help create alkalinity fast, etc. On the long term, the only solution is an alkaline lifestyle; I personal know Stage IV cancer patients that went into remmision after following a Cesium therapy (as described in my book as well ), went into remission only after a couple of months and when they returned to their old habits and lifestyle cancer returned; just alkalinity(i.e: cesium, calcium, baking soda, diet, ozone/ oxygen) is not enough- microbes can just go into one of their self preservation states; just killing cancer cells/microbes is not enough – they can spread faster in an acid environment; strengthening the immune system takes time; etc. ; plus, many other specific situations & complications can occur (i.e. cachexia, lack of energy ,malnutrition, pain, etc) ).THUS:

On the long term, getting rid of cancer for good can be done only by doing as many sinergic things to Energize, Re- Balance & Strenghthen your Body , Mind and Immune System to make it a machine „immune to cancer”.

Some of these things were mentioned above.

I’ve written a complete chapter on this topic in my book.

For more details read this article click here.

Also read CANCER SURVIVOR PROGRAM-click here

One should also keep in mind there is no such thing as perfection in real life.Be reasonable and do whatever you can . Use common sense, do what you can/ what is up to you. Even if you make mistakes, mistakes are part of being human. Do not worry to much about them. But try not to be superficial in order to maximize your healing chances.

Monitor your progress on a regular basis to see id what you are currently doing is strong enough or needs improvements

I will be back with more articles on things to do to survive and beat your cancer.

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Complete details in my book.

Best of health,

Cristian