HealingWell
Search Close Search
☰

Has anyone tried rife frequencies for treatment?

Support Forums
>
Lyme Disease
✚ New Topic ✚ Reply
❬ ❬ Previous Thread |Next Thread ❭ ❭
Posted 11/6/2014 9:32 PM (GMT 0)
Finding these a lot on Youtube. I've been listening to a few of them to see if they help or not, and sure enough, they do which makes me all more suspcious that I have lymes!
Posted 11/7/2014 4:21 AM (GMT 0)
I just ordered the GB4000 rife machine. We will see if it works or not. There are actually several stories on the Internet of successful treatment with the GB4000... Probably more success stories than with other rife machines. There is an amp that you can attach to boost the output. Some people are done treatment after a few rounds on high power although they said the die off and herxing was rather intense. Should be good for deep tissue penetration.
Posted 11/7/2014 7:26 AM (GMT 0)
Hi LymePickle,

How'd you get 90% recovered? Do you have a post where you talked about your treatment? Hope that Rife works ;)
Posted 11/7/2014 9:29 AM (GMT 0)
My husband had an ALS diagnosis and his symptoms stopped progressing after using Rife technology. We had to drive an hour to a place that had the machines - along with other devices employing this alternative modality- and he only used it maybe 8 times to see the difference. The place runs by donation only. I talked to many people who experimented with the machines and the success stories, especially with cancer, are remarkable. In fact I talked to several people who had stage 4 cancer and after using the machines for as long as they felt they needed they survived....and one of them was diagnosed 14 years ago! We do plan to go back after Toby has had a chance to heal with the brain injury from his fall. I think you need to be consistent with it's use. Please post any positive results with the machine. We have not invested in one, but maybe at some point we will. It is hard to travel frequently for treatment.
Posted 11/7/2014 8:18 PM (GMT 0)
Hey Healthydude,

I see you were asking what I did to get to 90%?

Well patience, persistance, and I kept rotating my treatments.

I'm sure you are wondering what the most helpful thing I did was? Well back in March-May, I did an antibiotic combo of minocycline+tinidazole+septra DS+ plaquenil. And that was rather powerful. And resolved my neurolyme issue rather quickly actually. But the tinidazole is a rather toxic medication. I think you should be aware of the risks.

ONE Thing I would suggest about tinidazole. Is don't use it at the doses recommended by an LLMD. They told me to take 1 gram a day which is just too much. I found it works at doses of only 250 mg a day. Or 250 mg every second day, or 250 mg dose twice a day. I did 500 mg twice a day, and that is simply too high of a dose. My LLMD may have been trying to induce me with cancer.
Posted 11/10/2014 4:30 PM (GMT 0)
I wanted to share 2 links I have used which seem to be helping:

Lyme's Disease Rife:
http://youtu.be/OYAxHZid_Jk?list=UU-qmilt_DHLB_xTE8rIEPUg

Bartonella Rife
http://youtu.be/D_nmFKxck3o?list=UU-qmilt_DHLB_xTE8rIEPUg

Hope this helps some of you! I'll listen to this 2-3 times a day (Morning, afternoon and night)
✚ New Topic ✚ Reply