With help from Dutch Bros., MDA is fighting to end ALS
Thanks in part to Dutch Bros. generous support, MDA is currently funding 38 active ALS grants, with a total funding commitment of $9.6 million.
Thanks in part to Dutch Bros. generous support, MDA is currently funding 38 active ALS grants, with a total funding commitment of $9.6 million.
Heading off to college and wondering how to find a personal care assistant? Megan Crowley, who lives with Pompe disease, shares her tips.
Accessible travel blogger, Curb Free With Cory Lee, shares his thoughts on Morgan’s Inspiration Island.
Alicia Miro, whose son lives with MD, shares why she runs the Marine Corps Marathon with MDA Team Momentum and why you should too.
Erin Brady Worsham, who lives with ALS, offers the idea that life in her garden may not be all too different from our own lives.
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.
Doug McCullough often hears that he is inspiring. His response: “OK, thanks. But what have I inspired you to do?”
Ralph Yaniz reflects on the milestones of being a father with a neuromuscular disease just in time for Father’s Day.
Chris Anselmo, who lives with Miyoshi myopathy, shares a letter to his dad and all MDA dads this Father’s Day.
When Chris Anselmo, who lives with Miyoishi myopathy, learned that Pete Frates’, the creator of the ALS Ice Bucket Challenge was facing challenges paying his medical bills, he felt compelled to share his story.