A Look Back at the 2017 Ride for Life
More than 800 Riders + Nearly 1,000 Miles + $1,209,392 Raised = Hope for Kids and Adults with MD, ALS and Related diseases
An expression of the live unlimited spirit, stories and voices of the MDA community
More than 800 Riders + Nearly 1,000 Miles + $1,209,392 Raised = Hope for Kids and Adults with MD, ALS and Related diseases
DMD Families are invited to an Emflaza webinar in partnership with PTC Therapeutics on July 6.
Alan Alderman who lives with ALS encourages others to join the ALS Registry.
Hugo Trevino shares insightful observations about the intersectionality of having a disability and accepting your sexual or gender identity — and how having SMA helped him come out and live proudly as a gay man.
The U.S. Senate introduced its health care reform bill that sets out changes to modify health care coverage of people across the country, including MDA families.
Doug McCullough often hears that he is inspiring. His response: “OK, thanks. But what have I inspired you to do?”
The investigational drug AMO-02 (tideglusib) has received FDA fast track designation for the treatment of DM1.
Recent high school graduate Abbey Umali, a former MDA National Ambassador who lives with CMT, shares her plans for the future.
At the end of 2016 we asked the MDA community about their experiences with air travel. We received more than 2,000 responses. This is what we found.
Air travel is essential to being able to live, work or go to school where you choose—and can determine whether someone can see a specialty provider or participate in a clinical trial that is far from home. MDA believes accessto air travel is essential to living unlimited. That’s why we’re working with policy makers, federal agencies, industry, and other advocacy and disability rights organizations to help improve access to air travel for MDA families.
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