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L-CMD Research Foundation x 2024

Raising $2,000,000 for rare disease treatments for kids impacted by terminal L-CMD, like Austin.

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$2,002,020

2.5k Supporters

100% of $2,000,000 goal

Mariel Borrel

Fundraiser since Feb 2021

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$3,541

41 supporters

7% of $50,000 goal

Mariel Borrel's Story

Please consider donating to fund crucial gene therapy research for my sweetest nephew Austin, who has a rare, fatal form of congenital (ie present at birth) muscular dystrophy (CMD). 100% of funds are going to urgently fund a research project with a major academic institution. Let’s save Austin and other children with LMNA related muscular dystrophies. We are ready to start the research as soon as we meet our goal of $2 million. It is doable with YOUR support! ❤️

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$2,002,020

2.5k Supporters

100% of $2,000,000 goal

L-CMD Research Foundation

A 501(c)(3) Public Charity

EIN 85-2640499