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  • Hi Bergwijn,

    You sound a lot like my dad. I was positive he had ALS, and at least so far, it does not look like he actually does.

    He also has had a plethora of cervical spine issues and I was in fact able to get him in to see a neuro & get an EMG. They basically said they're sure it is his spine.

    His twitching is also localized to bicep&tricep area too. Very similar!

    Cheers
    I
    ItsTough
    Awesome! In the FB group with "support" in the name, search for a video posted by "OG Dee"

    Do your tricep twitches look like that? As you may see from my comment on there, its pretty much exactly what my dad has!
    I
    ItsTough
    Also, the BFS subreddit is good! (r/BFS)

    A bit of a different demographic I think
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    Bergwijn
    Yeah I am in both, kind of sticking to the cervical radiculopathy group on fb for now. Those bfs folks on reddit are nice and I do think I have that to some degree. But my symptoms match so many in the cr group it has been nice to go in there and post comments.
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