L-CMD Research Foundation

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.