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Anyone have experience with Multiple System Atrophy (MSA)?
Brain & Nervous System | Last Active: 3 hours ago | Replies (56)Comment receiving replies
When we finally ended up at a neurologist's office, and after several visits, the Dr. handed me a sticky note with: Multiple System Atrophy-C...the other Spinocerebellar Ataxia (SCA Type 3). I did the research and his symptoms clearly led to MSA-C. There is also MSA-P, which resembles more parkinsonian symptoms, i.e. stiffness, tremors, etc. Talk to people and do your research, these are all "tricky" diseases.
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Hi Shelley, How are things going with your husband. I got the Syn-one test now waiting on the results (3 weeks to come back). Did you guys decide on having a Syn-One or not? All my symptoms continue and none have gone away, and I take that as a very bad sign. I hope the rash has abated, and at least that misery is gone. Praying you both are given comfort and strength in this horrible illness. Have you found any other sites to visit for support? Not much out there a few FB pages.