canefan17
Frequent Contributor (5K+ posts)
Member # 22149
posted
She was recently diagnosed with Multiple Sclerosis and tomorrow she wants to meet up and ask me questions (as she heard I've researched Lyme/MS and their potential relation)
Any key points to bring up? I'd love to print her off some info or LLMDs with evidence of Lyme in MS patients. Anyone have any info?
Or even better... anyone here diagnosed with MS only to later test positive for Lyme and treat and get better?
What should she do first? Get with an LLMD and get tested? What if false test? Etc etc
-------------------- 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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