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
Thanks guys
[ 06-18-2012, 06:34 PM: Message edited by: canefan17 ]
Posted by LymeXtu (Member # 24590) on :
Check out some articles by Tom Grier, he is a microbiologist from Duluth that was told he had MS.
He was very sick by the time he found out it was actually Lyme disease.
I think he started the support group in Duluth and has written some really good articles.
He is well now ( after treating for Lyme and other infections ) he is doing research and lecturing.