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Homeless With MS

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    #16
    Hi Scotty, I'm in Canada so have no info on resources but your post made me tear up, a little light "bubbling" happened. It's so sad that you're homeless with this horrible disease, I hope some of the other info that other members have posted helps you along, you must be terrified. Just wanted to send healing thoughts your way, you epitomise the Maya Angelou quote, "I can be changed by what happens to me but I refuse to be reduced by it." Continue to keep reaching out, you'll eventually find some peace, even if it's only inner peace. You have an amazing attitude for all that you're dealing with.
    Jen
    RRMS 2005, Copaxone since 2007
    "I hope to be the person my dog thinks I am."

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      #17
      If anyone is having any trouble contacting local or state MS Society offices.....the main number for NMSS is 1-800-FIGHTMS or 1-800-344-4867

      That number has been my main 'SAFEGUARD' since first symptoms in 1980.
      George aka GTEJrRetha

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