I would be honored to play with you
I have ALS/ Lou Gehrig disease, and I use my eyes and IR eye tracking technology to make the moves.
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You are an inspiration
I would be honored to play with you
I would be honored to play with you
ALSUncensored wrote:
If you ever play against me, know that not only do I have to consider my move, but then I have to use my eyes to control a cursor with a dwell timer to move the piece.
It’s actually pretty amazing, although my game is not. But I’m working on it 🍻🏴☠️
It’s actually pretty amazing, although my game is not. But I’m working on it 🍻🏴☠️
Thanks for sharing this.
There are so many negative comments posted on Chess.com about opponents taking too long, making blunders, or simply not being worthy enough to play against other members. Online chess players compete against people from all over the world. Your post should serve as a good reminder that we really never know what our opponent is dealing with on the other side of the computer.
I was diagnosed with bulbar ALS in May 2024. I live in Texas, and I’m 68 years old. I take Nudexta medication to help with the emotional outbursts of laughing and crying. The weakness, slurred speech, and muscle loss progressed quickly. Mobility has been an issue since Dec 26, when I fell and broke my hip, and although I made small strides at first, I felt like my life had been placed on a countdown, as there was no known cure other than the prescription of riluzole medications, vitamins, and therapies. As the disease progressed, my symptoms worsened. With my neurologist's guidance we decided to try other approaches and started the ALS/MND treatment, and it changed everything. Within 5 months, I noticed more strength in my limbs, clearer speech, and I have stopped using feeding tubes. I’m starting to learn how to walk again & I now sleep better. This ALS/MND treatment program gave me back control and hope. we got the treatment from uinehealthcentre. net This is a game changer for people with ALS.
Jul 11, 2025
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#7
stevenwesterrmann wrote:
I was diagnosed with bulbar ALS in May 2024. I live in Texas, and I’m 68 years old. I take Nudexta medication to help with the emotional outbursts of laughing and crying. The weakness, slurred speech, and muscle loss progressed quickly. Mobility has been an issue since Dec 26, when I fell and broke my hip, and although I made small strides at first, I felt like my life had been placed on a countdown, as there was no known cure other than the prescription of riluzole medications, vitamins, and therapies. As the disease progressed, my symptoms worsened. With my neurologist's guidance we decided to try other approaches and started the ALS/MND treatment, and it changed everything. Within 5 months, I noticed more strength in my limbs, clearer speech, and I have stopped using feeding tubes. I’m starting to learn how to walk again & I now sleep better. This ALS/MND treatment program gave me back control and hope. we got the treatment from uinehealthcentre. net This is a game changer for people with ALS.
"uinehealthcentre.net has a very low trust score which indicates that there is a strong likelyhood the website is a scam. Be very careful when using this ..." if im wrong im wrong? google it
It’s actually pretty amazing, although my game is not. But I’m working on it 🍻🏴☠️