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Resources for Myofascial Pain Syndrome? (CMP)?
Hello readers,
I have the syndrome (which is now looked upon as a neuromuscular disease). I've made some progress in researching this disease, and am steadily looking to improve my knowledge and resources. So here is the question:
- Do you personally know of any websites that delve into the topic? Any Blogs?
- Most importantly, has anyone seen any groups (be it Facebook or otherwise) where people like me can share findings and facts?
Finally, I do have some information to share - if you are a fellow patient like me you might have questions, and I'll gladly share what pieces of the puzzle I've gathered with you so far. Some of it was discovered as recently as 2011 and beyond. I'll also add that I'm not opposed to starting an online support and info-exchange group with some like-minded people. If anyone would like to get in touch with me privately my business email is akadarauch@horizon.csueastbay.edu
1 Answer
- ?Lv 78 years agoFavorite Answer
No sir I do not have that information, And I guess no one else cared to answer. Sometimes I think questions are simply put here to amuse or confuse us out here. But I cant help but feel pain when I read someone needs help and I cry if I cannot help them. I hope you found what you need with your individual efforts.
