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Month: January 2020

Happy New Year! Looking back on the last decade, we have made significant strides towards greater understanding, awareness and acceptance of Tourette Syndrome and co-occurring conditions. We continue to extend our footprint across the country with more national events including the Funders Breakfast in New York City, new webinars, increased provider education programming and an expanded Centers of Excellence program. 2020 is also monumental as it marks the return of our biennial National Conference.
On March 4, in Washington, D.C., the Tourette Association of America will advocate for the most pressing issues facing the TS community on National Advocacy Day. Youth Ambassadors, TAA staff, volunteers, and community members will head to Capitol Hill to speak with elected officials on policy affecting the community. Youth Ambassadors and a Support Group Leader share their experiences from past Advocacy Day events and what it was like to #Rally4Tourette.
As part of O, The Oprah Magazine’s December 2019 issue featuring women who live with chronic health conditions, Nikki Burdine shared her story and experiences with Tourette Syndrome. "In my case, I’m no longer embarrassed about having Tourette. I just don’t want it to be a distraction from my job or a reason for people to treat me differently. The truth is, everyone is battling something. My struggle is just a little more obvious.” - Nikki