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Lyme Disease Support Group
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01/24/2008 13:53
RebeccaLynn
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Does anyone know of an LLMD in Tennesee? If not, in one of the surrounding states?

I don't understand why Tennessee doctors keep telling me that there is no lyme disease in Tennessee?

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01/24/2008 15:07
Julie4848
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Love when they say that...My god Lyme is everywhere...Jerks

Julie

Lyme will not win, we will and we WILL…

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01/25/2008 05:44
jaime1978
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yeah, according to most regular ducs, it's nowhere... HA. I know of a few in PA if that's too far for you to travel, please PM me and I will tell you how to find another closer to you ...there may be one in tenn. I don't know.
Please do not take anything I say as medical advice. I am not a doctor.

~lyme disease support group leader~
please pm me with any special concerns
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02/02/2008 10:07
ConnieD
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hi rebecca lynn, I'm new to this kind of communcication. Ihope this info helps. I live in Tennessee and I have lyme and coinfections(babesia, erhlichia, bartonella) plus I had two viruses as a result of compromised immune syste. I was misdiagnosed for the last 10 years. My doctors dismissed my symptoms and referred me to a psychiatrist. You can just imagine my frustration. Just when I was feeling pretty helpless, fate matched us to a doctor in Atlanta ,GA. He is an MD who has an alternative clinic. He has treated hundreds of lyme disease patients with great success. I am one of the successes. It took about 8 months to begin to reclaim my life, but it was worth it! I am feeling so much better! I have discontinued all of my prescription medicine including pain pills! It may seem a little awkward to take the alternative route, but I read a lot of books and I did a lot of research on the internet and found that conventional medicine did not have the success rate that I was looking for.(I also did not want to risk infection with an IV antibiotic...our bodies are infected enough.. I'm sure you can identify.) My husband and I made the 3.5 hour trip many times over the summer and it was worth it! Good luck and good health. If you have any questions, I will be happy to answer them. sincerely, lymie(I did not know of a good username, I may change it in the future).

Post edited by: lymie, at: 03/28/2008 10:51

Please do not take anything I say as medical advice. I am not a doctor.

Open your mind to the possibilities available to you.

An attitude of gratitude is good 'medicine,' too.

~Lyme Disease Support Group Leader~
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