9th International Wolfram Syndrome Symposium Berkshire, England 22nd-24th October 2024
Invite only! For more information please get in touch with Stephanie@thesnowfoundation.org
Today: June 5, 2026
Invite only! For more information please get in touch with Stephanie@thesnowfoundation.org
Last year all known WS groups were invited to a virtual meeting to discuss the idea of creating a global awareness day for Wolfram Syndrome (WSGAD). The meeting was attended by 7 WS groups from 5 different countries. We have Rare Disease Day which encompasses all rare diseases once year…
Head to the link to listen to it now. https://youtu.be/zQ-WrsgEi3o
Dr. Giulio Frontino and Dr. Maurizio Delvecchio of IRCCS San Raffaele Hospital, Milan, Italy. Unified Care for Diverse Challenges: Crafting National Guidelines for WS from Diagnosis to Care. You can listen to the presentation by following the link provided. https://youtu.be/PssLjWZgsFE
The Snow Foundation is a collective voice for Wolfram syndrome patients, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss and neurodegeneration.
P.O. Box 50224
Clayton, MO 63105
(636) 448-4134
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