ktkdommer
Frequent Contributor (1K+ posts)
Member # 29020
posted
I'm sorry no one is helping. I have only heard once through a post that Dr. S. is good. Have you tried this contact- Brenda Morency Minnesota Lyme Association www.mnlyme.com? Hopefully, someone will come through with some help. Where are you in MN? Could you go to WI?
-------------------- 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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He was a speaker at a recent lyme support meeting and I have to say I was really impressed with him.
That being said I made the decision to go out of state for treatment (east coast) for myself and my son and am glad I did (we were not seeing dr S).
If you can't go out of state I would say he is probably your best bet, we just don't have many doctors in this state that are willing/able to help us.
Posts: 448 | From minnesota | Registered: Feb 2010
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