Stories of Hope
A triathlete with her sights set on the Paralympic Games of 2016, Erin Scala dreams of the day her vision will be restored but has not let RP get in her way.
Since the 3-year-old’s diagnosis with LCA, his parents, Jennifer and Jason, have been focused on giving him a sighted future.
The comedy writer and performer, who has Stargardt disease, has become an unexpected source of support for others grappling with vision loss.
The story of how the Argus II retinal prosthesis—recently approved by the FDA—shed light on one Englishman’s life after decades of darkness.
How Meghan Downing, an 11-year-old with Stargardt disease, helps support the Foundation while continuing to surf, swim and, yes, play dodge ball.
Their two children were born legally blind. But Chris and Doug Day are confident that, with the Foundation’s support, their kids will lead fulfilling lives. That’s why they’ve joined thousands of families across the country doing their part to raise aware
One Foundation benefactor, who’s also affected, knows the value of planning ahead.
Diagnosed last year with Stargardt disease, Gracie Nash is as active as any 7-year-old. Her parents, meanwhile, are encouraged by the great research strides supported by the Foundation.
Affected by Usher syndrome, Rachel Weeks has both limited hearing and sight. But that doesn’t keep her from running, swimming and biking competitively – again and again.
Brooke James has had more than a glimpse of what it means to be blind in certain parts of the world. And she can assure you, it’s scary.