I am new here but an 8 year veteran in my dance with MS. Actually...they traced it back to my mid twenties so I guess I am more of a 24 year veteran! Back then they called it "chronic fatigue" then it was "Epstein Barr" then,,, the pins/needles and numbness took over and wha'la... the lesions showed up and my diagnosis was confirmed! I was actually happy to have a definitive answer to the years of struggle.
I don't personally know anyone else with MS so feel pretty alone in this. I hope to change that by coming here. I try to stay as upbeat as possible but as we all know...some days that can be a major challenge. I hope to add something positive to this site as well as find some support.
I don't personally know anyone else with MS so feel pretty alone in this. I hope to change that by coming here. I try to stay as upbeat as possible but as we all know...some days that can be a major challenge. I hope to add something positive to this site as well as find some support.
plenty of support here and awnsers to most (if not all) questions. feel free to ask away or vent, whichever you feel needs done. hope to see you around here more. check with your local office of nmss for support groups near you too. good luck
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