This powerful video was created by patients and families living with LGMD2D/R3 — to raise awareness, amplify their voices, and accelerate the urgency for treatment.  

LGMD2D (Limb-Girdle Muscular Dystrophy Type 2D/R3) is a rare, progressive neuromuscular disease that weakens the muscles needed for mobility, independence, and everyday life. 

There are currently no approved treatments. Every day without progress matters.  

In this short but impactful film, individuals and families share their lived experiences, the challenges they face, and their hope for a future where effective therapies exist. Their stories highlight the medical need as well as the strength, resilience, and determination of the LGMD2D community.  

🌟 Help us raise awareness. Help us push for action. 🌟 

Please share this video, learn more, and stand with those affected by LGMD2D. Together, we can bring urgency, visibility, and momentum to the fight for LGMD2D treatments.