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The primary function of Eye on Jacob is to fund research for treatment and, hopefully, a cure for Usher Syndrome. The secondary mission is to establish support groups for patients and families of patients with Usher Syndrome.
The Eye on Jacob Foundation is a 501 c-3 nonprofit founded by Sonia Desormeaux in 2008. Sonia's youngest son, Jacob, suffers from Ushers Syndrome.
Board of Directors:
We have launched a $5 million campaign to fund research for the next three years to advance discoveries in the treatment and cure for Usher Syndrome. Please share our enthusiasm by making a meaningful financial contribution to Eye on Jacob. You can make a difference to 12,000 children, and this program can make a difference to the world. Donate today.