Hi Group -
I've had Lyme Disease over 10 years before it was discovered. I was forced to
retired on widow's disability as I became too crippled to get around. Often
room bound, (can't cut the yard any more) I read from substantial research
around the world, abx are just "buying me (and most chronic cases w/no $) a
little time" and will not cure a person in my late stage LD + co-infections.
Spirochetes grow inside like angel hair pasta did you know? They split ever 20
minutes and it takes 1,500 of them end to end to make up an inch. They like to
travel better in the flesh than blood. Far out huh?
MRI's show damage to my myelin, EEG's confirm it. I did go to Mexico in March
of this year for a form of Oxygen therapy, and probably caused a mass execution
of Borellia Burgdorferi (judging from a severe "herx" and a few alleviated
symptoms). However, true to form, the little buggers are still quite plentiful
as evidenced by blood cultures (5 days) and fluorescent staining in May 2000 by
a reputable pathologist. I've heard "through the grape vine" there are a few
happy success stories connected to this CS chatroom. Two Lymies have combined
the CS therapy with the Zappers, and Pulser (Thumpers) winning the war on Lyme
through electrocution! Please don't get shy now! I want to hear all about it.
How far along were the cases? What duration was Zap patrol? Was anyone
crippled like me. I have read of cases worse than me making a comeback, but
it's a lucky thing to be able to afford Ceftin, I.V. Rocephin at 4 gms. a day
etc. What dose on the CS? Which Zapper(s), how long, how bad the herx's and
any other particulars. Please y'all get in touch w/these fabulously fortunate
people and have them share their happy stories with me ASAP, as I'll share
it with 7 more people ..and we'll all get happy and lucky with the availability
of this technology. Thanks much and waiting with happy expectations. Silvia
[email protected]
