Hey @mda.org in your 60 second ad for #MDA75 you tout accomplishments, yet never mention or show Jerry Lewis, the man who put the organization's name on the map and helped raise hundreds of millions of dollars. The only Telethon picture you posted excluded Jerry. Why?

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

Inspired by his uncle and cousin who lived with muscular dystrophy, Zack has volunteered at MDA Summer Camp for the last 14 years.

He says the community gives him strength, but it’s his commitment that makes us stronger. Thank you, Zack!

💙💛 #ForwardTogether #MDA75 #MDAVolunteer

This year, thousands of families found answers, care & hope because of you.

From research to camp memories, your support goes beyond numbers — it changes lives.

💙💛 #ForwardTogether #MDA75

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

A former Muscular Dystrophy Association employee talks layoffs and donation discrepancies, while major national sponsors seem to have severed ties with the organization. My latest in Medium.

#mda #musculardystrophyassociation #nonprofit #MDA75

medium.com/@despinakarr...

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!
💙💛
#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

Congrats to Kathy Mathews for winning the MDA Legacy Award for her tireless work on the Dystroglycanopathies and other rare NMDs. #MDA75

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