Hi Dennis,
Welcome aboard. Please feel free to tell us your story, ask any questions - and like Jeff said - we've all had one symptom or another. Hopefully we can help you with some questions you may have. Or at least offer support!
Hugs
Linda in Bothell, WA
-------------- Original message --------------
From: jeff bernier <[EMAIL PROTECTED]>
HI DENNIS!!!WELCOME TO THE LIST,IF YOUR LOOKING FOR ANSWERS YOUR IN THE RIGHT PLACE,EVERYONE ON HERE HAS JUST ABOUT EVERY SYMPTOM YOU CAN THINK OF.THIS IS A HUGE FAMILY AND WE ALL SUPPORT EACHOTHER,PLEASE TELL US SOME MORE ABOUT YOURSELF AND WHEN YOU WERE DX WITH TM\MS,PLEASE DONT BE AFRAID TO VENT YOUR FRUSTRATION ON HERE, WE ALL UNDERSTAND.JUST A QUICK WORD OF ADVICE FIND A GOOD DOCTOR THAT UNDERSTANDS THE DISEASE AND ITS PROCESS,MOST NEURO'S DONT HAVE A CLUE WHEN IT COMES TO TM.JEFFCENTRAL NYUSA
dennis rabalais <[EMAIL PROTECTED]> wrote:I AM A NEW SUBSCRIBER. MY NAME IS DENNIS RABALAIS. I AM A C3-L5 QUAD. IS THERE ANY STUDIES FOR ME TO BE AWARE OF? THANKS.
DIPLOMACY DOES NOT
WORK WHEN DEALING WITH
NUT'S HELL BENT ON
DESTROYING US.
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