ARCHIVE # 4: 554 ARTICLES (NOV -SEPT 2006)
Dr. Timothy L. Vollmer


Chairman, Division of Neurology

Barrow Neurological Institute
St. Joseph's Hospital and Medical Center
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Timothy L. Vollmer M.D.
Chairman, Division of Neurology
Barrow Neurological Institute
St. Joseph's Hospital and Medical Center


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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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Runtime: 54 sec
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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Friday, November 10, 2006

 
Medicare policy would restrict people's mobility: Daily Chronicle - Opinions

A new, damaging Medicare policy is about to go into effect, largely unnoticed. It will restrict the mobility and independence of people with disabilities in our community, by restricting coverage of power mobility devices.

Many people with multiple sclerosis, spinal injuries, cerebral palsy - even paralyzed veterans - rely on wheelchairs, scooters and other devices to get out of the house, go to work, run errands and simply enjoy life.

The new Medicare restrictions do not take physicians' recommendations for appropriate mobility devices into consideration; instead, they arbitrarily place people with disabilities into lower-quality, more poorly performing mobility devices. The new guidelines do not factor in the effects of disease progression, and it is likely they could result in a person receiving a device that actually exacerbates a person's symptoms. In addition, they significantly reduce reimbursement across all devices, which will severely limit availability even if someone is eligible.

This reverses rehabilitation and limits quality of life - not to mention increasing the burden on caregivers and discouraging manufacturers from providing more-advanced technologies.

When this policy goes into effect on Nov. 15, people with MS and other disabilities in our community will lose their mobility and independence. It's time to move for those who cannot. By calling your local legislators today, you're helping ensure that the people in your community who need power mobility devices will retain their independence.

JACKIE GUTHRIE

Advocacy and outreach manager

National Multiple Sclerosis Society

Greater Illinois Chapter

Chicago