JERRY
LEWIS, MDA REQUEST POSTPONEMENT
OF NEW MEDICARE POLICY FOR POWER WHEELCHAIRS
TUCSON, Ariz., Nov. 1, 2006 —
Jerry Lewis, national chairman of the
Muscular Dystrophy Association (MDA),
has asked U.S. Health and Human Services
Secretary Michael Leavitt to postpone
new Medicare pricing and coverage policies
for power wheelchairs, citing the policies’
negative impact on people with muscular
dystrophy and other severe disabilities.
The new fee schedule, slated to go
into effect Nov. 15, reduces Medicare
reimbursement rates for power mobility
devices by up to 40 percent for some
wheelchairs. In addition, new eligibility
requirements make it harder for people
with severe and progressive disabilities
to qualify for more technologically
complex power wheelchairs that promote
health, safety and independence.
“Although CMS’ original
intention was to combat fraud, CMS (Centers
for Medicare and Medicaid Services)
is itself misleading Americans by claiming
that these new policies will provide
appropriate power wheelchairs for all
Medicare beneficiaries,” Lewis
said in a letter to Leavitt, a copy
of which went to President Bush and
each member of Congress.
He added, “We’re extremely
disappointed by this policy change because
it’s detrimental to people with
disabilities. The new eligibility criteria
will make it very difficult for those
with progressive diseases to receive
power wheelchairs equipped for their
needs.”
Lewis requested that implementation
be delayed until the policy could be
adjusted to better accommodate the needs
of those with severe and progressive
disabilities.
He told Leavitt that he’ll be
willing to travel to Washington to meet
with him, the CMS or any other group
that could repair the problems with
the proposed policies.
“These changes are so drastic
and so detrimental to “my kids”
and other Americans with progressive
diseases that I’m prepared to
drop everything and address this issue
personally,” Lewis said.
Under the new policy, applicants who
can transfer from bed to wheelchair
by standing and pivoting, with or without
assistance, won’t be eligible
for power wheelchairs with more than
basic features. This assessment doesn’t
account for disease progression and
fatigue, crucial factors when determining
the wheelchair needs of a person with
neuromuscular disease, Lewis said.
More complex features such as tilt,
recline, stronger motors, custom headrests,
and ability to navigate uneven terrain
provide wheelchair users with more independence
and safety. For instance, tilt-and-recline
features assist users with self-transfers,
are safer on steep inclines and help
prevent pressure sores.
If chairs have fewer features needed
for independence, the result may be
to force people out of their homes and
into long-term care facilities.
In addition, the new fee schedule places
a greater financial burden on low-income
people with severe disabilities and
the nonprofit organizations that serve
them.
Among its services for people registered
with MDA, the Association provides financial
help toward the purchase and repair
of wheelchairs.
MDA is a voluntary health organization
working to defeat more than 40 neuromuscular
diseases through programs of worldwide
research, comprehensive services, and
far-reaching professional and public
health education. The Association’s
programs are funded almost entirely
by individual private contributors.
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