posted
I was diagnosed with "possible" Lymes in WI 15-20 years ago in WI,my home for 50 years. This was after a 3rd case of Bell's Palsy. I received the month long oral antibiotic. No more Bell's Palsy, but other symptoms led to a diagnosis of Fibromayalgia. Now I'm learning that these symptoms, especially the muscle pain and fatigue, could be from the Lymes. I would really like to find a specialist near Raleigh, NC!
Posts: 3 | From Cary, NC | Registered: Apr 2010
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Siciliano
Frequent Contributor (1K+ posts)
Member # 15920
posted
Hi, Debbeejo and WELCOME to our lyme site. We're glad you came to us for help.
I have sent you a private message (pm), click on the flashing envelope.
Also, check out our great "Medical Questions" forum where you can ask all the questions you might have and our wonderful, knowledgeable members will answer them. Just read some of the threads and you'll see just how informative they are!
-------------------- I'm sorry but I am no longer accepting any private messages due to my own battle with lyme. Posts: 3897 | From New Hampshire | Registered: Jun 2008
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emla999/Lyme
Frequent Contributor (1K+ posts)
Member # 12606
posted
Hello and and welcome!!
I also sent you a private message with a couple of names.
Posts: 1223 | From U.S.A | Registered: Jul 2007
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