feeling be no see em

GinniferLynne

Well-known member
Karen,

I really don't know if there is significance to seeing them, or not seeing them.

When Jenifer Estess was diagnosed, she said her legs and arms looked like "waves at Jones' beach).

I've read other stories of people with ALS that couldn't see or feel them, but they were detected on an EMG (they went to the doc for other symptoms).

I've also read stories of people with ALS that could BARELY see them.

I think it is way important on the company the twitches keep (weakness, atrophy, etc.)

Ginny
 

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