I am looking for a LLMD in Gainesville, Florida. I would hope that there would be someone at the U of F and Shands Teaching Hospital. I have been suffering w/fibromyalgia since 1994 and an undiagnosed autoimmune disease recently but all my symptoms are that of LD. I live in the woods of north Florida and have always have tick bites. One time in the early 90's my husband and I got into a nest of ticks and I pulled over 100 "seed" ticks off him and he off me. Fibro was diagnosed in both of us a few years later. We thought, how odd that we would both have the same strange illness and symptoms. If any one knows of a doc in Gainesville or the north Florida area, please let me know. I now have hope that maybe my illness can be resolved. Thanks Blayer
Posts: 2 | From Florida | Registered: Apr 2009
| IP: Logged |
bettyg
Unregistered
posted
welcome! check your profile above for florida info
please break up your entire post into short paragraphs for us neuro lyme folks who can not read or comprehend your long, solid paragraph above; see my guidelines please; thank you!
Welcome; i'm so glad you found us!! You've come to the right place for education and support!
Dr. Burrascano's most recent "Diagnostic Hints and 2008 Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @
Betty's suggested POSTING GUIDELINES . many of us have neuro lyme where we can NOT read long solid block text and be able to comprehend and read it as is.
please edit your post by CLICKING PAPER/PENCIL ICON to right of your name. that opens up BOTH subject line and body text.
now please break up your WORDY SENTENCES into one sentence paragraphs. Then hit ENTER KEY ``TWICE`` after each paragraph; we need that space for comprehension.
then go to left hand corner and mark box to receive ALL REPLIES, and click EDIT SEND
we thank you for helping us; otherwise, we will SOB, SCROLL ON BY, since we can't read to help you. If I see posts like this, I SOB them; to hard on me. ------------------------------------------------------
People seeking doctors might be able to get help from their state online information and support group. Nearly 3,400 people belong to state groups. Some of the groups are small but more than 20 of them have 50 or more people and seven have over 100.
The groups are moderated and you have to apply. Most don't allow doctor names, but once on the group, you can ask for doctors in a certain area and ask people to email you privately.
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/