not important, but curious...hair loss

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trying to stay positive

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Joined
Sep 17, 2007
Messages
313
Reason
CALS
Diagnosis
08/2007
Country
US
State
Illinois
City
Chicago area
Hey everyone, this is not especially important, but I am curious none the less. My husband says that he has noticed accelerated hair loss on his head since his symptoms first appeared 2 & 1/2 years ago. Has anyone else noticed this phenomenom or is this just his excuse for going bald?:mrgreen:
 
My mom's hair also got rather thin during her battle with this terrible disease. My mom battled with bulbar. I am not sure if hair loss is related to the disease. I have not heard anyone else bring this up.
Anne
 
Hubby's hair is thinning also. Who knows if it is related to ALS or not...
 
Same here. Think I brought it up on another thread. Strange....
 
Could Be Thyroid Or Hormonal Inherited Cant Blame Everything On Als Lol
 
Mine fell out long before the ALS. One thing for sure though, it may not grow on your head but it sure will grow wild on your butt and in your ears and nose.
AL.
 
:-D That is old age, AL. :-D
 
Does that mean you ladies are having the same problems? LOL
al.
 
Yes, we do. The nose keeps growing while everything else shrinks. And although the hair on our heads gets thinner, it grows out of our ears and nose and even a few sprigs on the chin. That's old age, my friend!:-D
 
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