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To all of you I want to say thank you and Merry Christmas. I hope that as the...
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Slow but relentless progression of PLS
Submitted by mrs70 on Fri, 03/10/2017 - 15:26
Hi, I just found this site today and am glad to have found you.
I was diagnosed with PLS in 1998. So, I have been living with it a long time. It's been slow, but...
if there is a law in nature that x number of people must be diagnosed with als i am glad
it was me an not another young person with small children (that always brings a tear) my
wife of 55 years and i have been truely blessed. children grown and secure in their
careers. two good and rewarding...
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This description is based on research up to June 2009.
Functional/somatoform neurological disorders are mental illnesses and adaptations that cause real physical symptoms, but without an addressable physical cause. The one I'm going to be talking about mostly is conversion, because I know it...
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Hi everyone...
I've been lurking in the ALS forum since before I was diagnosed in April 2010 to see what the scoop was on ALS. I've got the picture now and don't like it much, but there's no use complaining.
At this point, I'm still walking and talking, so I consider myself fortunate. I've...
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Hi Everyone,
My husband Joe is going to the Dr on tuesday for a consult for a peg. He really needs the peg. When he was first Dx they said he should make up his mind before he reaches 50% on his FVC test. That has a long time come and gone. He said flat out no peg. Now he is having such...
Hello, My name is Brian I am 37 years old and a father of four children. I am currently a police officer and life is good. However a month and a half ago I began getting what I thought was flu like symptoms (Aching just plain feeling like crap) After On the third day I began feeling a little...