Today we are one step closer to a tomorrow without LMNA-related congenital muscular dystrophy Inspired by our beautiful son Austin, our foundation is dedicated to urgently translating available technologies into impactful treatments for L-CMD now. Together we can raise the funds to make it happen ASAP. The more support we raise, the more momentum we have to make our children stronger and give them the chance at full and rich lives.
| Website | https://linktr.ee/lcmd.foundation |
| Employees | 3 (1 on RocketReach) |
| Founded | 2020 |
| Industry | Non-profit Organizations |
| Keywords | Rare Disease Research, Muscular Dystrophy Treatment, Genetic Muscle Disorders, Medical Research Foundation, Rare Disease Foundation, Children's Health Research, Disease Research Funding, Gene Therapy Research, Pharmaceutical Research, Biotechnology Research, Clinical Trials, New Treatments, Medical Breakthroughs, Health Innovation, Charitable Organization |
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L-CMD Research Foundation Questions
Hannah Corman is the President of L-CMD Research Foundation.
1 people are employed at L-CMD Research Foundation.
L-CMD Research Foundation is based in Houston, Texas.
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Hannah Corman
President at L-CMD Research Foundation
Houston, TX, US13
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