WHO WE ARE

​OUR MISSION

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. 

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OUR VISION

A world where treatments for RP are operative, effective, and accessible to all patients.

YOUR DONATION

Caity as student teacher in Nepal, 2019

VOLUNTEERS

Funds raised will go toward medical research grants. Grants will be awarded to those conducting research into treatments for non-syndromic retinitis pigmentosa.

BOARD

MED REVIEW BOARD

COMMUNICATIONS

Eric Elam

Lyndon Elam

Tim Geistlinger

Kevin Unger

in process

Taylor Nelson

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FUNDRAISING

Carin Elam - Europe & U.S.

Cate Elam - Europe

Judy & Mark Jordan - US

NONPROFIT ADMIN

Carin Elam

Judi Hagen

Drew Elam