The Snow Foundation was represented at the 3rd Annual Wolfram Syndrome Support and Information Day in the UK in November. The conference had numerous speakers ranging from specialized service, therapeutics, developing treatments, urology, psychology and neurology, to name a few. Dr. Fumihiko Urano gave a presentation on patient based therapeutics and Stephanie Snow Gebel spoke about […]
/wp-content/uploads/2016/02/snow-foundation-website.png00The Snow Foundation/wp-content/uploads/2016/02/snow-foundation-website.pngThe Snow Foundation2015-12-22 19:24:512016-02-23 19:26:33Wolfram Syndrome Support and Information Day in the UK
On Tuesday, July 7th at AT&T park, the San Francisco Giants celebrated “Snow Foundation Night” to raise awareness of its mission to find a cure for rare disease, Wolfram syndrome. Prior to the 7:15 p.m. match up between the reigning World Series Champs and the New York Mets, former Giants first baseman and six time Gold Glove winner, […]
/wp-content/uploads/2016/02/snow-foundation-website.png00The Snow Foundation/wp-content/uploads/2016/02/snow-foundation-website.pngThe Snow Foundation2015-06-22 01:51:452016-02-24 01:57:09San Francisco Giants Recognize The Snow Foundation
The Snow Foundation is a voice for rare disease, working towards a cure for Wolfram Syndrome and developing novel therapies for diabetes, vision loss, hearing loss and neurodegeneration.
Rare Diseases...Common Problems
P.O. Box 50224
Clayton, MO 63105