posted
can you pls pm me if you know someone.
Posts: 47 | From usa | Registered: Nov 2011
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ktkdommer
Frequent Contributor (1K+ posts)
Member # 29020
posted
Many in Florida have to travel out of state. It is not a state rich in Lyme education.
Have you tried the sunshine state Lyme forum for information?
Repost if you are willing to travel.
My sister in Florida can get cheap flights north. She will start seeing a doc in Cleveland.
Many of the LLMD's will let you phone consult in between appointments.
-------------------- 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
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posted
Thanks for responding KT. This is for my friend who lives in FL. I live in NY and have an llmd. She may have to travel up here. It seems so many people in FL have it but they don't know about lyme. I hope many people become aware of it this month.
Posts: 47 | From usa | Registered: Nov 2011
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posted
There are many doctors treating TBD in Florida and the majority of people on our Facebook Sunshine group are not going out of state. We actually had a few members who were treating out of state and are now treating in Florida.
Things are starting to change in Florida for the better.
Posts: 671 | From Fort Myers, Florida | Registered: Jun 2009
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