sca3 patient being treated as MSA: A doctor... - Ataxia UK

Ataxia UK

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sca3 patient being treated as MSA

Collinhucn profile image
4 Replies

A doctor recomanned me to be administered in hospital to cure my disease for 10 days. What worries me is that he kept talking about mutiple system atrophy (MSA) and I have been diagnosed to be sca3 in genetic test 4 years ago. Has anyone of you had the same experience? l am worried that once I have been in hospital, things may be detiorated faster.

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Collinhucn profile image
Collinhucn
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wobblybee profile image
wobblybee

🙂 Are you having symptoms that can only be treated in hospital? If so this is obviously the best decision.

Collinhucn profile image
Collinhucn in reply to wobblybee

Thank you, wobblybee, for the suggestion. 👍😀

isabelalfaiate profile image
isabelalfaiate

Dear collinhucn,I am not sure but I think you shoould get a second opinion. I have SCA3 and as far as I know there is no cure. Why is he treating you for MSA, it is not the same thing. I am sure the doctor knows better, but if you have been diagnosed with one thing it seems odd to get treatment for something else. I would definitely get a second opinion.

Best wishes

Suebeeee profile image
Suebeeee

I wonder if its a treatment only approved for MSA that has hopes of helping sca3. My family member is going through a similar thing (in USA) - doc proposing IVIG treatment (immunotherapy) that is approved for MSG (Myosthenia Gravis).

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