Spotlight on Leber congenital amaurosis (LCA) 👁️‍🗨️ LCA isn’t caused by just one gene—mutations in at least 25 different genes can lead to this disease. That’s what makes diagnosing and treating LCA so complex—and why genetic testing is a crucial first step in unlocking answers. Learn more about LCA on our website at: https://bit.ly/4l3aPha Video Description: Dark blue background with the Foundation Fighting Blindness and Spotlight on Leber Congenital Amaurosis logos top-left. Text below that

Spotlight on Leber congenital amaurosis (LCA) 👁️‍🗨️ “For so long, I believed research would help someone else, but not me. Now I’m living it.” Meet Lindsey Rambo: mom, runner, educator, and the first participant in the groundbreaking Opus Genetics gene therapy trial for LCA5. After decades of uncertainty and vision loss, Lindsey’s story is one of real hope and real progress. From spotting her kids playing in the yard for the first time to inspiring others through advocacy—Lindsey is lighting t