L-CMD Research Foundation is a non-profit organization founded by the parents of a child named Austin after he had been diagnosed with L-CMD (a rare and fatal genetic disease of childhood muscular dystrophy). This non-profit aimed to urgently translate available medical technologies into treatments and ultimately find the cure. This project uses moderated remote user testing to find usability problems throughout the website and provides potential solutions for its navigation, visuals, and content. Also, we hope to encourage more people to donate on the website.