Gavin R Stevens Foundation

Gavin R Stevens Foundation

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Our mission is to raise awareness and increase funding for research to find a treatment and cure for

Gavin R. Stevens Foundation 12/30/2017

Gavin R. Stevens Foundation Gavin Stevens, was born with a very rare genetic retina condition called Leber's Congenital Amaurosis (LCA). There is no cure, YET. Research is promising, and reminds us to move forward with fundraising for a cure. There are only 150 individuals in the United States with this genetic mutation condit...

Support Gavin R Stevens Foundation by shopping at AmazonSmile. 11/27/2017

Support Gavin R Stevens Foundation by shopping at AmazonSmile. When you shop at AmazonSmile, Amazon will donate to Gavin R Stevens Foundation. Support us every time you shop.

Timeline photos 07/03/2017

A huge thank you to the Lions Club! They asked Gavin to perform for them as they celebrate their 100th year! We met Lions from around the whole world - They were also so kind to donate a $10,000 check to the Gavin R Stevens Foundation, so we can keep moving LCA research in the right direction!

Little Big Shots Kid Sees More Than Most 03/17/2017

Little Big Shots Kid Sees More Than Most Seven year old Gavin was born with (LCA) Lebers Congenital Amaourosis, but Gavin doesn't allow his age or blindness get in the way of his awesomeness.[VIDEO]

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Address


PO Box 2108
Chino, CA
91708