WHO WE ARE
RP Hope is a place the public can visit to find information about Retinitis Pigmentosa (RP), a rare genetic disease that leads to blindness. We serve to educate the public and RP patients on this disease.
A world where treatments for RP are operative, effective, and accessible to all patients.
Caity as student teacher in Nepal, 2019
Funds raised will go toward medical research grants. Grants will be awarded to those conducting research into treatments for non-syndromic retinitis pigmentosa.
MED REVIEW BOARD
Carin Elam - Europe & U.S.
Cate Elam - Europe
Judy & Mark Jordan - US