posted
Two years ago, my neurologist convinced me that I have MS and not lyme. I am a gardener in Chester County, PA. I need to make sure this is not lyme because my symptoms seem more like lyme. I am moving to Raleigh, NC in July and just want to start the process to determine what I have as soon as possible since my neurologist wants me to begin the MS shots. Does anyone have recommendations a LLMD that could help me?
-------------------- IgM ++41, IND 31, 34, 39, 83-93 IgG IND 41
"To the world you may be one person, but to one person you may be the world." - unknown Posts: 72 | From NC | Registered: Sep 2011
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pmerv
Frequent Contributor (1K+ posts)
Member # 1504
posted
Please consider joining your own state group in the LymeDisease.org network. Many groups are sizable enough to offer quite a bit of help. Go to http://health.groups.yahoo.com/group/statenamelyme to find how to find your group.
-------------------- Phyllis Mervine LymeDisease.org Posts: 1808 | From Ukiah, California, USA | Registered: Aug 2001
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Dekrator48
Frequent Contributor (5K+ posts)
Member # 18239
posted
PM sent with info for PA.
-------------------- The fibromyalgia I've had for 32 years was an undiagnosed Lyme symptom.
"For I know the plans I have for you", declares the Lord, "plans to prosper you and not to harm you, plans to give you hope and a future". -Jeremiah 29:11 Posts: 6076 | From Pennsylvania, USA | Registered: Nov 2008
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