What a thrilling night it was at the New Jersey Center for Tourette Syndrome 20th Anniversary Gala! More than 170 members of our community gathered at the Bridgewater Marriott on Thursday, October 17, to celebrate a remarkable journey together. With the theme “Keeping the Faith,” NJCTS honored inspiring founder, Faith Rice, and presented the Faith W. Rice Legacy Award to her successor, Patricia Phillips, who sadly passed in March. Both the Rice and Phillips families were in attendance for the event. The event raised more than $80,000 for Tourette Syndrome education, advocacy, and research.
The evening was a whirlwind of excitement, featuring a delightful cocktail reception, a silent and live auction, and dinner. Attendees were deeply moved by a presentation from NJCTS Youth Advocates, both past and present, who shared a heartfelt video of their parents reflecting on the profound impact our organization has had on their lives.
“We are tremendously grateful to everyone who came out to support our 20th Anniversary Gala,” said NJCTS Executive Director Hilary Kruchowy. “Your presence and generosity not only honor the legacy of Faith Rice but also empower our mission to continue making a difference in the lives of those we serve.”
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A dedicated committee of volunteers, led by the Chair Donna Tischfield, worked tirelessly for an entire year to craft a truly magical evening. Emcee, the talented Michael Leopold from The UpTIC, brought energy to the night, while professional auctioneer Chris Ward skillfully raised tens of thousands through the live auction and paddle raise.
The ambiance was enhanced by the enchanting music of harpist Sara Henya during cocktail hour and the captivating sounds of The Jarrett Walser Quartet in the ballroom.
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"We are so grateful to everyone who made this unforgettable celebration possible!" said Kruchowy.
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About NCTS:
New Jersey Center for Tourette Syndrome and Associated Disorders is a non-profit organization whose mission is to ensure children and adults with Tourette Syndrome and associated disorders are empowered and accepted through education, advocacy and research. Our focus is on providing high quality educational programs to the public, medical professionals, and teachers; advocating for individuals and families impacted by the disorder; and supporting ongoing and new research into the causes and treatments of Tourette Syndrome.
