When the next 75 years start with the impact you’ve already made 🙏

Families got answers. Kids built independence. Caregivers felt supported. Research & advocacy moved forward.

We can’t thank you enough.

💙💛 #ForwardTogether #MDA75

🚨 Registration is OPEN! 🚨
Join us March 8–11, 2026 in Orlando for the #MDAConference, the leading global event for neuromuscular care & research. 🌍🧬

🔗 Register now: www.mdaconference.org

#MDA #MuscularDystrophy #neuromuscular

How do you raise the standard of care? You make it law.

Thanks to the MD-Care Act, more people with neuromuscular disease now have access to the care they need.

Join us in making an impact: MDA75.org. 💙💛

#MDA75 #MuscularDystrophy #ALS #Neuromuscular

Dr. Jeni Stepanek calls herself a welcome mat.

But not because she is walked on - because she invites others in and celebrates their stories. Stories defined by purpose and potential.

Watch her story and share yours at #75YearsStrong!

💙💛

#MDA75
#MuscularDystrophy #Neuromuscular

In 1986, Dr. Lou Kunkel cracked the genetic code of dystrophin, the gene behind Duchenne and Becker muscular dystrophies. This breakthrough paved the way for lifesaving treatments and gene therapies that are transforming lives today. 💛💙

Donate today: MDA75.org

Sometimes, going the distance for others starts by going the distance yourself. Literally. See how disability advocate & travel blogger Cory Lee helps others see the world—and share your own story at #75YearsStrong!
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#75YearsStrong #MDA75 #MuscularDystrophy #Neuromuscular #Travel #Adventure

📺 One nation, one mission. In 1971, the first national MDA Telethon hit the airwaves—bringing America together to fight neuromuscular disease. Millions watched, donated, and changed lives.

💙 Be part of the next historic moment. Donate today: MDA75.org 💛

#MDA75 #ALS #MuscularDystrophy

ALS influencer Brooke Eby’s perspective? You can endure anything if you make it funny. See how she’s tackling ALS and share your own story! 💙💛

#MDA75 #EndALSwithMDA #EndALS #ALS #MuscularDystrophy #Neuromuscular #ALSawarenessMonth #75YearsStrong

Every kid deserves a summer of fun. In 1955, we launched #MDA Summer Camp,a place where kids with neuromuscular disease could experience friendship, adventure, and freedom without limits. 75 years later, the magic continues. Help make summers more unforgettable. Donate today: MDA75.org

🌟 Not even muscular dystrophy could stop country musician Bradley Walker from becoming a star. Watch his story of hope and share yours at #75YearsStrong. 💙💛 #75YearsStrong #MDA75 #MuscularDystrophy #ALS #Neuromuscular

Summer fun can change the world. Just ask #MDA Camp Counselor Devin Jensen. His work with campers living with neuromuscular disease has changed their lives —and changed his too.

Watch his story and share yours! 💙💛

#75YearsStrong #MDA75 #SummerCamp #MuscularDystrophy #Neuromuscular

In 1953, the first MDA Care Centers opened—transforming life with neuromuscular disease forever. Today, our impact spans 150+ centers nationwide—helping families every day. Be part of the next breakthrough.

Donate today: MDA75.org 💙💛 #HealthcareHeroes #MDA75 #ALS #MuscularDystrophy

When hope wasn't enough, they took action. In just two months, these unstoppable families changed the future of #neuromuscular disease forever. The first breakthrough in our 75-year journey that defined MDA.

Donate now at MDA75.org. 💙💛

#MDA75 #ALS #MuscularDystrophy

75 years of hope, progress, & action 💙💛 #MDA’s new PSA, Legacy. Impact. Momentum., celebrates the families, researchers, clinicians, advocates, volunteers, donors, & partners who’ve shaped the fight against #neuromuscular disease.

🎥 Watch the PSA: www.mda.org/press-releas...

MDA75.org #MDA75