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Muscular dystrophy conference honors Nashville volunteers, researchers

The 2022 Muscular Dystrophy Association Clinical & Scientific Conference kicked off on Monday in Nashville. ....

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Three Leading ALS Organizations Celebrate House Passage of ACT for ALS, Call for Swift Senate Action

/PRNewswire/ Today, I AM ALS, The ALS Association and the Muscular Dystrophy Association released the following statement on today s passage of ACT for ALS. ....

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Three Leading ALS Organizations Celebrate House Passage of ACT for ALS, Call for Swift Senate Action

/PRNewswire/ Today, I AM ALS, The ALS Association and the Muscular Dystrophy Association released the following statement on today s passage of ACT for ALS. ....

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Sen. Coons, colleagues continue fight against ALS, neurodegenerative diseases | WITN Channel 22 Wilmington, Delaware

May 26, 2021
ACT for ALS Act endorsed by I AM ALS, ALS Association and Muscular Dystrophy Association
WASHINGTON – On Tuesday, U.S. Senators Chris Coons (D-Del.), co-chair of the Senate ALS Caucus, and Lisa Murkowski (R-Alaska), along with U.S. Representatives Mike Quigley (D-Ill.) and Jeff Fortenberry (R-Neb.) reintroduced the bipartisan, bicameral
Accelerating Access to Critical Therapies for ALS Act (ACT for ALS). This legislation would create the infrastructure necessary to fund early access to promising investigational therapies for patients suffering from fast-progressing rare neurodegenerative and terminal diseases, like ALS.
“Action to support patients with ALS and discover new therapies is incredibly urgent,” ....

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Muscular Dystrophy Association Releases FAQs for the Neuromuscular Disease Community for Access to the COVID-19 Vaccines

Muscular Dystrophy Association Releases FAQs for the Neuromuscular Disease Community for Access to the COVID-19 Vaccines
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