ALS - Lou Gehrig's Disease

Posted by seema73 @seema73, Dec 13, 2011

My father just got diagnosed with ALS and I am devastated. There is no cure and I don't know how long he will have. It is slowly ravaging his body. I am still at the acceptance part. I would love to speak with anyone going through similar circumstances.

Interested in more discussions like this? Go to the Brain & Nervous System Support Group.

@johnbishop

Hi @rivermaya34, I was hoping they might be helpful but thought you may have already seen them. You might want to start a new discussion specifically for ALS-4 to see if others like you may be searching and see it on Connect and join in the discussion.

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I think I will do that @johnbishop . Took me a while to find this specific discussion, and didn't see any others that were type specific...Which group do I start it under?

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@rivermaya34

I think I will do that @johnbishop . Took me a while to find this specific discussion, and didn't see any others that were type specific...Which group do I start it under?

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I think the same group as this one - Brain & Nervous System

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