Hi All, I am new this. I was diagnosed last March with RRMS, I would really like to meet other MSer’s support. Since being diagnosed I kinda buried my head in the sand although I have being following the OMS programme and I am due to start Lemtrada at the end of the month. I feel I only have my partner to talk to about my diagnoses & being brutally honest I think at times it gets to him me rabbiting on, so my new years resolution is to try to go out meet other people……
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