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Senator Andrew Zwicker Visits NJCTS, Engages with Youth Advocates and Presents State Funding
Senator Andrew Zwicker Visits NJ Center for Tourette Syndrome, Engages with Youth Advocates and Presents State Funding
The New Jersey Center for Tourette Syndrome and Associated Disorders, Inc. (NJCTS) was honored to welcome Senator Andrew Zwicker of New Jersey’s 16th Legislative District to its office on August 25. The visit marked an important moment of recognition and support for the organization’s mission, as Senator Zwicker met with youth advocates and presented a ceremonial check representing state funding allocated in the Governor’s budget.
During his visit, Senator Zwicker engaged in a meaningful conversation with four of NJCTS’s outstanding youth advocates: Sofia, Reina, Sree, and Caroline. Each advocate shared personal stories and perspectives on living with Tourette Syndrome and spoke about the positive impact NJCTS has had on their lives. The discussion also included a thoughtful Q&A, giving the youth advocates an opportunity to ask questions and discuss advocacy issues directly with the senator.
“It was inspiring to see young leaders speak so passionately and candidly about their journeys,” said Senator Zwicker. “Their courage and advocacy are exactly what we need to raise awareness and understanding of Tourette Syndrome in our communities and beyond.”
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The ceremonial check presented during the visit reflects the dedicated line item of funding included for NJCTS in the State of New Jersey’s fiscal year 2026 budget. This funding will support the organization’s wide range of programming, education, outreach, and research initiatives that benefit individuals and families affected by Tourette Syndrome across the state.
“This funding represents more than just financial support. It is a recognition of the vital work our team, families, and youth advocates do every day,” said Hilary Kruchowy, Executive Director of NJCTS. “We are deeply grateful to Senator Zwicker and the State of New Jersey for their continued partnership and commitment to our mission.”
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NJ Center for Tourette Syndrome and Associated Disorders, the nation’s first Center of Excellence for Tourette Syndrome, is a not-for-profit organization committed to the advocacy of children and families with Tourette Syndrome, tic disorders, and associated disorders. Dedicated to delivering high quality services to these individuals, the Center recognizes the importance of educating the public, medical professionals, and teachers about the disorder through programs and affiliations with schools, health centers, and universities. To learn more about NJCTS, visit www.njcts.org or call 908.575.7350.
