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! ❤️