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You Are Not Alone: Two mothers’ perspectives on the TS community

Thank you to Charlotte Regen and Carolyn Baldwin for sharing their stories and their insight into raising children with TS and finding a supportive community with NJCTS.

NJCTS is committed to supporting individuals and families affected by Tourette Syndrome (TS) and associated disorders. We provide a continuum of services, support, and education for families; outreach and training for medical and educational professionals; and advocacy for collaborative research for better treatments and a cure for TS.

Your first step is to call us at 908.575.7350 or email us at info@njcts.org. If you are calling/emailing outside of normal business hours, please let us know the best time to call you back. A family intake coordinator will get back to you ASAP.

Family Welcome Page

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NJCTS Resource Room

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