Perseverance = Real Heros: 173 stories
Dr. Timothy L. Vollmer
Chairman, Division of Barrow Neurology

Director, Barrow NeuroImmunology Program

Barrow Neurological Institute
St. Joseph's Hospital and Medical Center
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Timothy L. Vollmer M.D.
Director, Barrow NeuroImmunology Program
Barrow Neurological Institute
St. Joseph's Hospital and Medical Center
HERO'S - PERSEVERANCE: 154 PATIENT STORIES
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"MS Can Not
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"I'm an M.D....my Mom has MS and we have a message for everyone."
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Beverly Dean
"I've had MS for 2 years...this is the most important advice you'll ever hear."
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"A helpful tip for newly diagnosed MS patients."
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Joyce Moore
"OUR TEAM IS WORKING ON A CURE FOR MS"
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Susan N. Rhodes
Multiple Sclerosis Research
Barrow Neurological Institute
"'The 2006 Barrow Neurological Institute at St. Joseph's Hospital MS "Walk on the Wild Side" raised more than $460,000 with 3,500 walkers! Click on the blue link above to view photos"

Chris Uithoven
President
National Multiple Sclerosis Society
Arizona Chapter
"THE MS SOCIETY OFFERS MANY PROGRAMS TO HELP...EVERYTHING FROM PILATES & SUPPORT GROUPS TO HORSEBACK RIDING"
Jerry Turner
Program Director
National Multiple Sclerosis Society
Arizona Chapter
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OUR MySpace FRIEND CARRIE: A HERO FOR HELPING OTHERS WITH HER GROUP: "MS 20 SOMETHING"



I have been diagnosed since I was 22

















































Hi Stan,

Thanks for The MS News Channel!

I feel lucky to help the newly diagnosed and the people who have been diagnosed forever find out information.

For many people it seems like being dxed with MS is scary to terrifying. I hope that my site can make it a little less scary and help put a face on the disease.

I think it is crucial for people who are dxed with MS realize that they are the same person they were before the diagnoses and they most likely have been living with this disease for awhile.

I think the words of advice that I have for the newly dxed is for them to realize that they are the same person they were before the diagnosing.

I think that it is important for people who are newly dxed to find support for dealing with the disease. Family and friends can be a great support, but I think that it helps to have someone else who has been dxed. There is understanding that happens, in my opinon, with people who deal with MS everyday.

:-)
Carrie



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