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MDA’s award-winning bimonthly national magazine goes to everyone registered with MDA, as well as to MDA clinics, researchers and subscribers.
Quest publishes articles on all aspects of living with a neuromuscular disease, and updates on research findings. Quest’s circulation is 125,000.


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Quest Vol. 15, No.5  September to October 2008

Game to Get Away

Online games provide an alternate world in which to play, say gamers with neuromuscular diseases. Here’s a primer of terminology, gaming options, social tips and info on how playing may affect muscles. In addition, Kid Quest, page 69, provides Internet gaming safety tips for kids.
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    Home> Publications > QUEST Extra >Volume 12, Number 4, July/August 2005

Reversing Medicare's "in the Home" Policy

Signatures Needed for Congressional Petition

by Kathy Wechsler

While adjusting the coverage guidelines for mobility devices, the Center for Medicare and Medicaid Services (CMS) has neglected to modify Medicare’s “in the home” policy. Medicare will continue refusing to cover mobility devices unless they’re medically necessary for participation in an activity of daily living in the home.

Calling the current policy “discriminatory,” Emily Niederman of the Independence Through Enhancement of Medicare and Medicaid (ITEM) Coalition said, “Let's say you’re able to get around your home with a manual wheelchair, but to go several blocks or to get to work get on the bus, you need a power wheelchair. You’re not going to get that power wheelchair.

“In the end, people aren’t getting the right wheelchairs to help them get into their community.”

Along with the United Spinal Association, the ITEM Coalition is working to reverse Medicare’s “in the home” restriction.

Between now and mid-June, Reps. Jim Langevin (D-R.I.) and Charlie Bass (R-N.H.) are circulating a bipartisan letter in the House of Representatives to be signed by its members and sent to the Secretary of Health and Human Services Michael Leavitt asking for modification of the “in the home” restriction.

Those interested in seeing the policy changed can call their members of Congress and ask them to sign the Langevin/Bass “in the home” policy letter. For more information, visit www.itemcoalition.org or www.rightwheelchair.org.


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