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They are learning more and more about the origins of MS. Fascinating stuff!

Raingrrl profile image
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neurosciencenews.com/geneti...

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Raingrrl
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starlight5 profile image
starlight5

Thanks for the link!

jimeka profile image
jimeka

Thank you 😊

ahrogers profile image
ahrogers

Interesting article, hopefully it leads to better treatment!

MaryAZ profile image
MaryAZ

Thank you! So much we don’t know. I didn’t have any symptoms until after I had a bad knee replacement in 2011. Downhill from there. Incorrect diagnoses. No, I didn’t have peripheral artery disease. I didn’t need a spinal fusion either. Finally referred myself to neurologist in 2017 who ordered brain and spine MRI which clearly showed many lesions. I wasn’t having relapses, I was just getting worse. Diagnosed with PPMS. No one in my family has MS. I really wish I knew how I got it so I appreciate any and all information.

Sandydemop profile image
Sandydemop

thanks for the very informative article.

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