MS Books
Dr. Timothy L. Vollmer
Chairman, Division of Barrow Neurology

Director, Barrow NeuroImmunology Program

Barrow Neurological Institute
St. Joseph's Hospital and Medical Center
My Educational Video on MS and MS Trials
Produced by MD Health Channel
Executive Editor.....Anne-Merete Robbs
CEO..............Stan Swartz
FREE e-mail alerts on your MS meds!
We were 1st in AZ to alert MS patients of the Tysabri's deaths..plus they received Dr. Vollmer's Tysabri video below:

Timothy L. Vollmer M.D.
Director, Barrow NeuroImmunology Program
Barrow Neurological Institute
St. Joseph's Hospital and Medical Center


MS treatment news:

"Dr. Vollmer is close to a MS cure..but..he needs you to help by joining a trial!"
Stan Swartz, CEO, The MD Health Channel

"Plus...You'll receive all medication and study based procedures at
NO CHARGE"

.

MS Can Not
Rob You of Joy
"I'm an M.D....my Mom has MS and we have a message for everyone."
- Jennifer Hartmark-Hill MD
Beverly Dean

"I've had MS for 2 years...this is the most important advice you'll ever hear."
"This is how I give myself a painless injection."
Heather Johnson

"A helpful tip for newly diagnosed MS patients."
"Important advice on choosing MS medication "
Joyce Moore

"MY EDUCATIONAL VIDEO ON MS"
For Broadband Users Runtime: 4:17 WMV
 
"THE VOLUNTARY SUSPENSION OF TYSABRI BY BIOGEN IDEC AND ELAN"
For Broadband Users Runtime: 4:17 WMV
 
Timothy L. Vollmer M.D.
Director, Barrow NeuroImmunology Program
Barrow Neurological Institute
St. Joseph's Hospital and Medical Center

"I FEEL GOOD ABOUT FINDING A CURE FOR MS"
Runtime: 54 sec
Runtime: 54 sec
Susan N. Rhodes
Multiple Sclerosis Research
Barrow Neurological Institute

"I'M PRESIDENT OF THE NATIONAL MS SOCIETY..
I WANT TO HELP YOU!"
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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Thursday

 

My Story: A Photographic Essay on Life with Multiple Sclerosis (Paperback) - click on "Best Price" to buy for $11.85

REVIEW: Ameila Davis is a documentary photographer, diagnosed with MS in 1998.

Though titled "My Story", this book is really "their stories". In this book, she uses her trained eye to illustrate 32 essays personally portraying the lives of men and women with Multiple Sclerosis.

They range from 17 to 70, across a spectrum of ethnicities, genders, occupations, socio-economic backgrounds and family circumstances.

Through her book, Amelia captures the unique approach each person has used to frame their chronic disease with, not only a positive attitude, but with a positive approach to life.

She also includes the caregivers ... those frequently forgotten in the struggle with MS and all chronic disease.

Her essays help others to see, through the stories of real people, the different possible treatments and therapies and the techniques for coping (such as exercise, yoga, creative activities and competitive sports).

Her photographs capture the people behind these essays, putting a real face, a personal face, on what is often discussed in impersonal, clinical terms. You don't just read their story; you are drawn into a human connection with them.

This is a book to buy and read. And it is also a book to buy and display, a coffee table book.

Discussing MS with friends and family can be difficult. Chronic disease can create a "distance", a separation. This book can help to bridge that gap.

As someone picks up this book to browse and becomes captured by the photographs, it can crack the door to an open conversation about MS, about what it means and about how lives continue after diagnosis.