posted
I heard of this LLMD through a friend of a friend and would like very much to hear, via Private Message, opinions and patient experiences.
I've been treating for ~3 years with an LLMD in Maryland, but relocated over a year ago to the Midwest.
At the time of my move I thought I was almost done treating, but since it's taking a bit longer I hope to find someone closer so that I don't need to travel back to Maryland 2-3 times per year.
Thanks in advance.
Posts: 455 | From Was in PA, then MD, now in the Midwest | Registered: Nov 2008
| IP: Logged |
ktkdommer
Frequent Contributor (1K+ posts)
Member # 29020
posted
I called her office once for information for my sister's son and the nurse put me through to her. I was able to ask questions. I couldn't believe it. I know that she is ILADS trained and active in the community with Lyme disease awareness. She came highly recommended from an Iowa advocate.
-------------------- Things are never dull. After 3 fighting Lyme, 2 are in remission. Youngest is still sick, age 22. He has new diagnosed Chiari Malformation and Ehlers Danlos Syndrome. Posts: 1366 | From Perrysburg, Ohio | Registered: Nov 2010
| IP: Logged |
posted
Thank you for the replies. I set up an initial appointment for January.
Posts: 455 | From Was in PA, then MD, now in the Midwest | Registered: Nov 2008
| 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/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic