Displaying 101–110 of 114 resources results
Apr 21, 2014
There’s nothing like a sense of urgency to turn what seems like a crazy idea into reality.
Dec 12, 2013
The driving force behind the Foundation’s considerable advances covers those, as well as other compelling subjects, during a 27-minute Q&A.
Dec 2, 2013
Moira Shea describes her experience with acupuncture.
Oct 20, 2013
For those with night blindness, a symptom of many retinal diseases, most notably retinitis pigmentosa, or RP, navigating a trick-or-treating throng can be, well, a nightmare.
Sep 6, 2013
His name is Battle. He’s an Arabian, stands more than 15 hands (or 5 feet) tall and weighs 1,000 pounds. He’s been with Alice Bartlett since his birth 26 years ago, and she’s been riding him since he was 2.
Alice, by the way, is legally blind.
Jun 30, 2013
Rollie and Sandie Purvis, parents of two sons with choroideremia, describe their sons’ film project, “Driving Blind.”
May 24, 2013
By Rich Shea
Apr 10, 2013
Foundation Board Member Moira Shea describes her life with a retinal disease.
Mar 22, 2013
Author Shawn Maloney describes his journey with RP.
Dec 20, 2012
Stem-cell-based therapies – including those derived from a patient’s blood or skin – are among the many cutting-edge approaches to treatments the Foundation has funded for decades.