View Single Post
Old 08-07-2007, 07:58 PM
SallyC's Avatar
SallyC SallyC is offline
In Remembrance
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
SallyC SallyC is offline
In Remembrance
SallyC's Avatar
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
Default

Thanks for posting this, Greta. I hope my Daughter, who also has MS,
will feel the same about me. Actually I think she does.



Quote:
Originally Posted by greta View Post
I've only been dx'd for 5.5 years, so I'll give you my mom's experience.

Mom was dx'd originally in 1971 when she had ON a couple months after my birth. She had almost nothing in the way of symptoms for 20 years. In 1990 she started having some numbness in her fingers. She progressed, trying both Avonex and Novantrone, and by 2007 she is in a wheelchair fulltime and at most has decent use of her left hand. She needs assistance with many of her ADLs. She can bear no weight, but she still has a good life, despite all the crap she's been dealt She's an inspiration to me.
__________________
~Love, Sally
.





"The best way out is always through". Robert Frost



~If The World Didn't Suck, We Would All Fall Off~
SallyC is offline   Reply With QuoteReply With Quote