Submitted by: Judy S. on Mon, 09/19/2022

My son was a young doctor when he was diagnosed with ALS. The
doctors gave him 2-3 years. He lived 11 years, getting progressively worse. He, too used the eye based computer and continued sending medical questions weekly to the doctors studying for the Medical Boards. All doctors in the hospitals answered the questions. He was an amazing person. This is the saddest disease for patients and families. We miss him so.

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