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Bill Woods

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@william-woodschoa-org

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    Bill Woods replied to the topic Clinical trials in the forum Using our Forums 6 months ago

    Hi thee, I don’t know where you are writing from, but I would think that every ‘certified’ ALS Center can point you in the right direction. I URGE you to find one, as we ALL benefit by as much participation in clin trials as possible. There are MANY out there, some simple with others quite complex. IF you have any difficulty finding one through…[Read more]

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    Bill Woods replied to the topic Riluzole side effect in the forum Living With ALS 8 months ago

    Stomach problems on Riluzole are most common, like 1/3 of patients. I tried EVERYTHING including proton pump inhibitors to no avail. The the nurse practicioner recommended Pepsid Complete : it worked like a charm, now only occasional stomach aches . Hope this helps!

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    Bill Woods became a registered member 1 year ago

    • Profile picture of Dagmar Munn
      Dagmar Munn replied 1 year ago

      Hello Bill,

      Welcome to the forum! I am one of the forum moderators and a person living with ALS: I was diagnosed in 2010.

      If there is anything specific you would like to see discussed on the forum, feel free to post a new topic in any of our forums or jump in on an existing topic. You can also search for past topics or discussions by typing a…[Read more]

    • Profile picture of Amanda
      Amanda replied 1 year ago

      Hello Bill, and welcome to the ALS forum. I’m Amanda, one of the co-moderators of the forum. We are happy you have joined our online community. You will find that the ALS forum is made up of people with different associations with ALS. My family has an extensive history of ALS and we know that we have a genetic mutation in the SOD1 gene. I lost m…[Read more]

    • Profile picture of Amanda
      Amanda replied 1 year ago

      Hello Bill, and welcome to the ALS forum. I’m Amanda, one of the co-moderators of the forum. We are happy you have joined our online community. You will find that the ALS forum is made up of people with different associations with ALS. My family has an extensive history of ALS and we know that we have a genetic mutation in the SOD1 gene. I lost m…[Read more]

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