ALS and Water fast
 

Hi, I hope i am doing this right as my P.C skills are not good. I am considering sending my ex-wife Julie to Dr. Scotts facility in Ohio for a medically supervised water fast. She was diagnosed last year with an apparently slow progressing form of ALS. They think she has been showing symptoms for about 4 years. She is, at this point, using a cane but getting along pretty well, still drives and is totally ambulatory.

Does anyone have any information on extended water fasts and ALS?

Thank You,
Robert

Robert,

Hello and welcome to NeuroTalk. Great to see you have come to be with us. You will find a great number of caring, supporting members here willing to help each other as they can.

I have listed the link to our ALS forum, there will many there to help you out.

http://neurotalk.psychcentral.com/forum6.html

Again welcome, looking forward to seeing you around.

Darlene:hug:

Hi, Robert! :Wave-Hello: Welcome to NeuroTalk!

I'm afraid that I've never heard of this, it sounds interesting. Please follow the link offered by Darlene, I'm sure you'll find more folks "in the know" about this treatment. Feel free to join in anywhere. :)