posted
After writing every Ly,me site I could find, the EPA, one news station, and my old hospital administrator where I THOUGHT I still had insurance-things are in motion.
Turns the small clinic with my new "heallth care professional', had also been leading my new insurance carrier on kind of a goose chase not providing me or them with phone numbers or my po box to receive myninsurance cards/plan/ect.
I have 3 months to take the whole lot before a review board, but getting a new LLDr was most important I can no longer speak-have to type or try to write, but he's great!
If anyone wants to read about possibilities, p#rasites, GMO's, Lyme/Morgellons, and more-*********and enjoy my goofy pix too-
I'm kind of like that freeway accident you just gotta look at-now I have hope it's a temp look, tings will change, and eventually I'll have hair again and possible eyesight and yes-Ill say it-SPELLCHECK!
**edited info for funding site**
Breaking up the text for easier reading for many here -
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/