I would love to hear experiences from anyone who has treated with photon therapy whose symptoms were (hopefully were and not are) predominantly CNS issues. Was photon treatment effective for your CNS malfunction?
Oh, and the odd thing is, I have had very little cognitive dysfunction - word retrieval was a little weird early on in my illness, but that has passed.
Even the slightest stress, inflames all of these symptoms. I'm talking stupid, minor stress - it sends my CNS into a tailspin, like it just can't handle it.
Of course, as with all things Lyme, there are other symptoms. Fatigue is there, but not dibilitating - I can live with it. No debilitating pain outside of the constant neck pain. But, the symptoms I do have are miserable. Never ever feel even close to "normal," not ever.
Before I jump in with both feet with another treatment - besides oral/IV abx, supps, detox - I've tried rifing too (I need to prioritize where I put my $$), I would love to hear if anyone with these types of symptoms, has used photon treatment with success.
Yes, I have treated both Bart and Babs rather aggressively.
Thanks for input! TS
Posts: 566 | From West Coast | Registered: May 2008
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Hmmm.....no one?
Posts: 566 | From West Coast | Registered: May 2008
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sixgoofykids
Honored Contributor (10K+ posts)
Member # 11141
posted
Sorry, didn't see it.
I had a lot of CNS symptoms. BAD pain. I had really bad cognitive function. It was a lot better by the time I went to Germany, but still not totally normal.
At one point I had light/sound sensitivity, but I think that was not a problem when I left.
I don't know if this is really a helpful answer. When I got rid of borrelia, the symptoms it caused went away, too. Then I could focus on healing things like my digestive tract and rebalancing my musculature/skeleton.
-------------------- sixgoofykids.blogspot.com Posts: 13449 | From Ohio | Registered: Feb 2007
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posted
We have most of the symptoms above that you mentioned. We just got the PE-1 and are going to begin treatment soon. I will try to keep you posted. I'm certainly counting on it helping with the CNS symptoms.
Many of the other PE-1 threads have given me hope. Search "PE-1" on here for more. I wish you all the best!
Posts: 63 | From Millersville, PA | Registered: Jul 2010
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feelfit
Frequent Contributor (1K+ posts)
Member # 12770
posted
Tickssuck, Sent you a PM- follow through!
Posts: 3975 | From usa | Registered: Aug 2007
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GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
Look for Toxic Heavy Metals - theeeeee major CNS disturbance. I know because I suffered from it for several years. Be sure you read my post on Rife and Photons, and be prepared before you do.
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
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17hens
Frequent Contributor (1K+ posts)
Member # 23747
I had these before Bart/Babesia treatment and they started to dissipate with treatment. Then we had to stop treatment (hubby lost his job & med. coverage) and they started coming back.
So I had them again (although not as bad as earlier) before going to Germany.
Since Germany, they are all but completely gone.
I have done ONLY Bionic 880 - slowly!! and coffee enemas. I take a multi, a probiotic and iodine. Oh, and B when I can afford it, magnesium when I feel I need it but that's not much anymore, and yes, some adrenal support. Tonic water too.
My infections are being overpowered, my immune system is strengthening, parasites are leaving (I'm shocked that they are leaving more rapidly with this protocol than when I was on anti-parasitics), and my adrenals are getting back to normal (hopefully the whole way back! we'll see).
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