Currently, we gather some data but we need to focus on better identifying the specific data that tells our story and lets people know what we do and the impact it has. Much of our data is qualitative and this project will help us develop the best methods for gathering qualitative as well as quantitative information about our programs. This will be shared with our constituents and will help us communicate our impact to potential funding sources.
The New Jersey Center for Tourette Syndrome is a not-for-profit organization committed to the advocacy of children and families with Tourette Syndrome and its 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 this disorder through programs and affiliations with public schools, health centers, and universities.
To ensure that individuals with Tourette Syndrome are contributing members of their communities and society at large, the Center is committed to leading the development of diagnostic and treatment therapies and actively supporting research for a cure.
(No testimonial has been submitted by Barbara)
(No testimonial has been submitted by Ann)