Have you been diagnosed with LGMD2D/R3? Join our patient registry.

LGMD2D Foundation
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    • About Our Foundation
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  • More
    • Home
    • About Us
      • About Our Foundation
      • Meet Our Team
      • What is LGMD2D/R3?
      • LGMD2D Awareness Video
    • Patient Registry
    • Patient Resources
    • Support by Donating
    • LGMD2D Research
    • LGMD2D Events
      • Hope in Motion Virtual 5k
      • 2025 Golf Tournament
      • 2026 Golf Tournament
    • Contact Us
    • LGMD Press Release
LGMD2D Foundation
  • Home
  • About Us
    • About Our Foundation
    • Meet Our Team
    • What is LGMD2D/R3?
    • LGMD2D Awareness Video
  • Patient Registry
  • Patient Resources
  • Support by Donating
  • LGMD2D Research
  • LGMD2D Events
    • Hope in Motion Virtual 5k
    • 2025 Golf Tournament
    • 2026 Golf Tournament
  • Contact Us
  • LGMD Press Release

Join Our Fight Against LGMD2D/R3.

Raising awareness for a cure.

Raising awareness for a cure.Raising awareness for a cure.Raising awareness for a cure.
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Our Mission

To accelerate the development of treatments and a cure for LGMD2D/R3 by funding critical research, advancing clinical trials, and leveraging our global patient registry to drive progress. 

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About LGMD2D/R3

 Limb-Girdle Muscular Dystrophy Type 2D/R3 is a severe, progressive muscle-wasting disease caused by mutations in the alpha-sarcoglycan (SGCA) gene.

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Patient Registry

Free to join, the International LGMD2D Patient Registry is critical to driving research forward. As the only global database for LGMD2D/R3 patients, it directly supports the development of future treatments. 

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Your support will change lives.

Your generous donation will help support awareness, advocacy, and research to find effective treatments or a cure for LGMD2D/R3.


We accept grants and donations from Fidelity Charitable, Schwab Charitable, Vanguard Charitable, and all major DAF sponsors. 


Donate below or email info@lgmd2d.org for more information.

Pay with PayPal or a debit/credit card

LGMD Advocacy Partners

Cure SCG - Sarcoglycanopathy
Coalition to cure Calpain 3
The Dion Foundation
The Speak Foundation
LGMD Awareness Foundation
  • Cure SCG - Sarcoglycanopathy
  • Coalition to cure Calpain 3
  • The Dion Foundation
  • The Speak Foundation
  • LGMD Awareness Foundation
  • Cure SCG - Sarcoglycanopathy
  • Coalition to cure Calpain 3

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Sign up to stay up to date with updates and progress within the LGMD2D/R3 community.

LGMD2D Foundation

Copyright © 2026 LGMD2D Foundation - All Rights Reserved. LGMD2D Foundation is a 501(c)(3), EIN # 46-4128016. Est. 2013.

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Support LGMD2D/R3 Warriors

There are currently no approved treatments or a cure for LGMD2D/R3. The incredible warriors fighting this disease around the world need your support. Please consider making a donation—no dollar is too small, and every dollar goes directly toward raising awareness, advocating for families, and driving the development of life-changing treatments. Join us in this critical mission. Your support truly makes a difference. 

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