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Lyme Disease Community
This forum is for questions and support regarding What Causes Lyme Disease, Diagnosing Lyme Disease, Joint Pain issues, Living with Lyme Disease, Nervous System issues, Prevention, Risk Factors, Skin Disorders, Symptoms and Treatments.
MS vs LYME
by leesalow, Apr 19, 2008 08:48AM
Thanks Patsy. I think I do have a pretty good set of doctors. With lyme, I have (had) a neuro, a neurosurgeon, a cardiologist and my awesome infectious disease doc. I must give a big shout out to anyone suffering with Lyme disease or symptoms of it. YOU CAN FEEL BETTER. I got my pic line out 2 days ago but started seeing results after 4 weeks. I just feel so much better overall. Thanks for all the thoughts/prayers that many of you sent my way. WE have all disputed if MS is lyme and if lyme is part of MS. It will still be a great debate in my life as I progress. I will have a watchful eye on the lesions- I will insist. Also, in either case I know what to be aware of and look for (but I believe the symptoms will just slap ya in the face). I have had all the symptoms of both for over a year. It's been CRAZY. But on this day, I AM HAPPY. Have a great day to you all and if anyone ever wants to get in touch with me and share experiences/thoughts regarding lyme/ms? or ms/lyme? I am always here and reading comments as well. Off to work I go now. God Bless!
Lisa in MS
Lisa in MS
Member Comments (1)
by patsy10, Apr 19, 2008 05:32PM
To: leesalow
You're welcome. Everyone needs to read this. It will given them hope.
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