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  • Hi Laurivi,
    if you click on the ALS/MND Support Groups Forums link at the top, then scroll down to the bottom there is a section there to introduce yourself. I just stumbled onto you wall and saw what you have written, but hardly anyone will see anything there.
    Posting to the forum is the best way to get to know us and we can support you.
    So sorry about your dads diagnosis :( Tillie
    It's mostly in his throat. Difficult swallowing, twitching, gets tired fast, a little drooling, slurring speech, muscle weakness. Extra saliva. And just today noticed his bottom lip just on one side was more in his mouth than the other side.
    Hi everyone. This is my first time on the site. We just found out my dad has PMA. The doctor said its a slower version of ALS. I thought joining this site may help me and my family get through this.
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