posted
just wanted to say that my llmd is alway there for me..it is something that has helped me tremedously in getting better and getting me thru bad herxes and also pointing out that I was getting better..we lymies know we lose hope sometimes as we are constantly bombarded by the cytokine storm..your llmd is crucial to your recovery..my last llmd told me we cant kill it so we will keep you on low dose forever...i felt like I was the one to figure things out with the old llmd...anyway just thought I would put that out..
Posts: 593 | From long island ny | Registered: Apr 2006
| IP: Logged |
posted
Unsure.. You are in the Northeast, and Polarblast is in New York. Maybe if you send a PM to Polarblast you can get her dr.s name.
-------------------- Wishing You Showers Of Blessings! Lyme since Fall 1983 = Diagnosed Summer 2008 IV Rocephin 7 weeks Stopped due to drug fever Now doxycycline "For I know the plans I have for you...plans to give you hope and a future." Jeremiah 29:11 Posts: 430 | From Sunny South | Registered: Jul 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/