November 12, 2022
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The Syngap Soiree Host Committee is rallying behind Jansen Jones, recently diagnosed with SYNGAP1, a rare, presently incurable, neurodevelopmental genetic disorder caused by a single gene mutation. On behalf of the SynGAP Research Fund (SRF), we are planning an evening to educate the community on SYNGAP1 and raise funds to benefit research into groundbreaking drug and gene therapies. Please save the date and stay tuned for more details to follow! For more information on SYNGAP1, please visit syngapresearchfund.org. With your support, we hope to ignite Sparks of Hope.