<div>LGMD2L is a devastating rare disease that destroys muscle. No treatments exist. At the LGMD2L Foundation we have a plan to change that.
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<div>With our partner Cure Rare Disease, we have started working on a gene therapy. This therapy will be a one-time infusion that replaces the damaged gene, allowing sufferers a chance of a normal life instead of slowly losing the strength to walk and care for themselves.
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<div>With your help, we already raised $25,000 that has paid to develop tools needed to develop and test this gene therapy. That work is underway now at Virginia Commonwealth University. Then we raised $100,000 to develop the actual treatment candidate. Now we're asking for your support to help cover the last milestone before human trials, the studies on its safety and effectiveness. 
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<div>Both the LGMD2L Foundation and CRD are nonprofits, and 100% of donations will go to pay for the costs of developing the treatment.
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<div>Read more here: <a href="https://www.businesswire.com/news/home/20260302184269/en/Cure-Rare-Disease-and-LGMD2L-Foundation-Announce-Multi-Year-Partnership-to-Develop-Gene-Therapy-for-Anoctamin-5-Related-Disease" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.businesswire.com/news/home/20260302184269/en/Cure-Rare-Disease-and-LGMD2L-Foundation-Announce-Multi-Year-Partnership-to-Develop-Gene-Therapy-for-Anoctamin-5-Related-Disease</a>
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Help us cure a rare and devastating muscle disease, LGMD2L

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Platform is iOS

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Help us cure a rare and devastating muscle disease, LGMD2L

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