This Is MS Multiple Sclerosis Community: Knowledge & Support
Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
I am new to the site but not to MS. I was diagnosed 20 years ago. The last 2 years have been hard as I am basically at home. I tried BetaSeron and Avonex but had very bad side effects so I am not on any CRAB medications.
Finally, I have learnt how to work this websight. Sorry to hear you are stuck at home. I have been too. Do you have friends? Family? I find that friends and family find it hard to be emotionally supportive long term. The best thing would be an M.S. group maybe even meeting in you house. P.S.As I couldn't read or watch T.V. I used audio recordings and actually listened to the radio!
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