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    #61
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    A story of a man in Montana that was diagnosed with SPS after 7 years of misdiagnosis; his journey. His sounds relatively mild in that he does not need a wheelchair full time, but bad enough as it is.

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      #62
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      This is a. Great website written by the man in Montana on his journey with SPS
      Last edited by Sunshine 2; 07-16-2021, 10:05 AM.

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        #63
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        This is a news story about a man with SPS in Australia who said that MMJ was the only way to combat the spasticity pain

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          #64
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          Three interesting case studies of SPS

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            #65
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            unsolved mysteries that still baffle scientists

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              #66
              Having a very rare disorder must make a person feel quite alone. It's not always comforting to be told you're one in a million.

              SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatiramer acetate since December 2020.

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