coiling your eyes - Stacey

[Guest guest]

Hi Stacey,

I haven't coiled my eyes yet - I've been a bit frightened of doing that. What frequencies did you use, and how long did you coil? Also, how close did you put the coil to your face? Did you have a cloth over your face, and have the coil in contact with it? Did you position the coil so that the hole was over your eyes? I haven't asked any of these questions yet.

- Jane

Subject: Re: Losing eye sight, has this happened to any one else, terrifyingTo: Lyme_and_Rife Date: Wednesday, March 3, 2010, 5:55 PM

I've had temporary loss of color vision and flashing lights and the more common ones such as floaters, spots etc (not to mention eye paralysis and some other unsettling eye related events). I've found eye symptoms (and ear symptoms) to be extremely treatable with rife (coil), I rarely have any eye symptoms anymore and it used to be like a fireworks show some nights. I've found so far that Lyme, Babesia and Bartonella contribute to my eye stuff (by my flares with the coil).BTW, I've only been treating for Babesia for about a month or two and but after having a few big flares from it my hair loss has slowed down. Tell your daughter to hang in there, I've found out it is amazing how the body can recover from this disease. I'm still really tired a lot and my flares from the coil can be bad, but I'm knocking off symptoms and I had many (many, many) and was in excruciating pain with severe

neurological (now more moderate) problems.I personally would err on the side my current treatment isn't working if I were starting to lose my vision. I can't think of ever experiencing "new" symptoms when I treatment is working and the disease is under control (both when on antibiotics and when I switched to rife), just flares of current or past symptoms. Maybe others on the board have gotten new symptoms from effective treatement, I don't know.*Info not attended to treat or diagnose*>> My daughter is familiar with the extreme sensitivities to light, floaters, > etc. Basically all that comes with lyme. She is now losing her sight very > quickly. Up close she can see fine but sitting in

a car, looking out the > window she can't make out much of anything, can tell if a person is maybe a > man or woman, can't read any signs, etc. It is getting worse. She is doing > the KPU protocol, and the Vit D. Could it be the protocol? Could it be Lyme, > coinfections. She doesn't herx from anything anymore. Is this an entirely > different disease. This is terrifying, and she has had alot of hair loss as > well. Maybe she took the wrong thyroid test, can't remember which one it > was now. It seems that there is always a new low to sink to these days. Would > greatly appreciate hearing from any one with ideas, or is walking this > path. If you are there or have been there do you end up blind, permanent loss > of vision? If recovered how long does it take to recover and what did you > do to get there. Thanks,

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