It's not news that
multiple sclerosis drugs are expensive… really expensive. I live
it.
It was 10 years ago this summer that I fell down some stairs
one morning and, by the end of the day, learned that I was living with
multiple sclerosis, a disease I share with more than 400,000 fellow
Americans.
But did you know that Congress can help make the cost
of specialty MS drugs more affordable? Some drug therapies can
cost up to $30,000 each year. With your help, my goal is to send
Congress more than 10,000 email messages by
June 15 about high prescription drug costs.
Please
take a minute to email your members of Congress. Urge them to ease the
financial burden of expensive drugs on people living with MS and their
families.
When I was diagnosed, my neurologist told
me that new MS drugs and technologies were showing promise. But then I
learned that the drugs would cost me more than $800 every month. So I
postponed treatment as long as possible. When I couldn’t walk any more,
I started on an MS therapy. But now this off-patent drug is more than
$2,200 every month and not getting any more affordable… unless we
convince Congress to do something.
Ask
Congress to approve more affordable MS therapies. Simply click here to
send your message today.
Thank you,
Scott
Hanson MS activist, diagnosed in 1998
|
MS stops
people from moving. The National MS Society exists to make sure it
doesn’t. We are a collective of passionate individuals, moving
together to create a world free of MS. JOIN THE
MOVEMENT
Early and
ongoing treatment with an FDA-approved therapy can make a difference
for people with multiple sclerosis. Learn about your options by
talking to your health care professional and contacting the
National MS Society at www.nationalmssociety.org or
1-800-344-4867.
National Multiple Sclerosis Society | 733 Third Avenue | New
York, NY | 10017
|
|