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  • Kerri your experience sounds very similar to mine
    atypical lesions muscle twitches atrophy , though Im not as bad as you.
    They say poss MS for me too but as you say it doesnt feel right and i too am struggling with the als question . Here is my email [email protected] if you want to chat as we both seem to be in same nowhere land which is frightening I know best wishes margaret England
    Kerri, that was a very nice post you did.
    I really hope things work out for you. It's terribly difficult, being unwell, let alone not being sure of what's going on. We all expect instant answers nowadays, and immediate treatment. Us humans are just not that clever yet. Maybe one day. Bless you and do keep in touch, when you have news.
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