The 2026 #MDAconference agenda is LIVE! 🧬Join global leaders in #neuromuscular research, care & advocacy March 8-11 in Orlando FL. View tracks, speakers & sessions: www.mda.org/press-releas...

#NeuromuscularResearch #GeneticMedicine #RareDisease #ClinicalCare#RareDiseaseshtag/ClinicalCare" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#ClinicalCarehtag/GeneticMedicine" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GeneticMedicineg/NeuromuscularResearch" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#NeuromuscularResearch

💡The Muscular Dystrophy Association @mda.org advances research, care & advocacy for 300+ neuromuscular conditions. 💙

Learn more: https://bit.ly/47gnMR3

#RareAdvocacySpotlight #RareSky #MDAStrong #MuscularDystrophyAssociation

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

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