For anyone with mast cell activation syndrome who wants to participate. This is being done by the NIH.
Posts: 13116 | From San Francisco | Registered: May 2006
| IP: Logged |
posted
It is with TMS. They are going to have a meeting at the NIH and they would like to have some survey info.
Posts: 13116 | From San Francisco | Registered: May 2006
| 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/