They are learning more and more about th... - My MSAA Community
They are learning more and more about the origins of MS. Fascinating stuff!
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Raingrrl
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Thanks for the link!
Thank you 😊
Interesting article, hopefully it leads to better treatment!
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.
thanks for the very informative article.
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