i live in DC now but am originally from Buffalo and believe i contracted Lyme as a child.
there is not a lot of awareness about it there i don't think. glad to see there is a support group, and i will remember you if i ever move back (which western new yorkers have a habit of doing)!
also do you have any recommendations for LLMD's? i really want a hometown friend of mine to get a lyme test, as she displays many of the same symptoms as i have.
Posts: 35 | From Washington, dc | Registered: Jul 2007
| IP: Logged |
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/