posted
Opening up my search for good doctor, open to iv,or orals take to finish line. 3 years in treatment, still on full-time pain meds to function, some days that does not help. Feeling hopeless. Sorry if this posted twice, new to site
Posts: 15 | From Maine | Registered: Nov 2011
| IP: Logged |
posted
PM sent with NY and VT info.
Posts: 447 | From Vermont | Registered: Jan 2011
| IP: Logged |
Dekrator48
Frequent Contributor (5K+ posts)
Member # 18239
posted
PA info sent.
-------------------- The fibromyalgia I've had for 32 years was an undiagnosed Lyme symptom.
"For I know the plans I have for you", declares the Lord, "plans to prosper you and not to harm you, plans to give you hope and a future". -Jeremiah 29:11 Posts: 6076 | From Pennsylvania, USA | Registered: Nov 2008
| IP: Logged |
pmerv
Frequent Contributor (1K+ posts)
Member # 1504
posted
Please consider joining your own state group in the LymeDisease.org network. Many groups are sizable enough to offer quite a bit of help. Go to http://health.groups.yahoo.com/group/statenamelyme to find how to find your group.
-------------------- Phyllis Mervine LymeDisease.org Posts: 1808 | From Ukiah, California, USA | Registered: Aug 2001
| 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/