A call to Rife owners If you own one please let me know., page 2
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reply posted on 9-6-2009 @ 01:17 AM by titorite
Wow look at that. I missed some replies while I was away from the net a few months back.

I doubt we can get the anon poster to speak more about his or her rife unit but maybe ElizabethRI could speak more about her experiences. Or maybe you the reader have a Rife unit you could talk about.

I had never heard of the BCX211 or BCX411 but here is a
Link I think mine would be more closely related to the 211 model...Mine also cost less. I think if I could do it over I might go with this 411 style instead.... I know I sure would like to hear more personal experiences about it.

For the record I do not have much experience with the Beam Ray version of the Rife Machine but my audio unit does interfere with analog transmission... I am not really sure of the technical reason why but it does not bother me in the least.

To date the two biggest diseases I have seen this unit of mine cure is Multiple Myeloma and Melanoma, two different forms of cancer. I have also seen it treat many other types of diseases.

So who else has a Rife Machine?



reply posted on 15-7-2009 @ 05:08 PM by mcduff53
reply to post by titorite



Dear Titorite:

I WISH I had a Rife machine, and I know it is not "snake oil", although I can see why people might believe that who have not done any research into the subject. My father, who is deceased, was a doctor, and he would certainly have said so. I would have tried to set him straight, if he had only lived long enough. A Rife machine might have cured him.

(I see that this thread is over a year old, and I do not know if there are any ATS rules relevant to that. If I am breaking rules, please forgive me, yes, let me know, but don't be too hard on me! I'm reading the Freshman Forum thread...)

Would you mind telling me where you are? Hmm, probably I should be be able to look up your profile, and I shall do so, as soon as I figure out how to do so.

I am looking for info on CFS, or CFIDS/ME, as I prefer to call it. I am on disability, not by choice. And I have a 15 year old daughter who is pretty ill with it. And a husband who essentially doesn't believe in it. And I've been thinking about writing a book about it, because the whole experience has been so unbelievable.

I was also trying to find a way to ask Jim Marrs about it, relating to Gulf War Syndrome and such. On his forum he suggests starting a thread, but either that's not his wish any longer, or I haven't earned the privilege of beginning a thread.

mcduff53
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