Category: General

Search
The TAA Wisconsin Chapter is hosting a virtual webinar series in place of their annual Tourette Connections conference. The funding for this virtual series is being provided through the Small Grants Program, a program under the TAA’s partnership with the CDC. The Small Grants Program provides funding for TAA Chapters and Support Groups as an opportunity to host outreach and education activities about Tourette Syndrome within their communities. This FREE live webinar series is appropriate for those with tics or Tourette Syndrome, family members, professionals and friends.
december tc
’ve spent a fair amount of time thinking about what I’d like to say to you all this holiday season. To be honest, I’ve struggled to steer clear of being too cliché, too negative, too positive, or too predictable. I’ve struggled with these thoughts because it’s been such an unpredictable time in an uncertain year. When we gathered together in January to plan the year ahead, the TAA team and I could not have imagined a year like 2020. Above anything else, this was a year where our need for one another was highlighted, bold-faced, ENLARGED. We needed to acclimate, pivot, and turn on a dime — that’s something the TAA has done particularly well in the face of COVID-19.
november touretteconnect
“Words matter.” It’s a phrase we hear and use frequently. It’s also something that can be a particularly tricky mine field for those living with Tourette Syndrome (TS) and, more specifically, coprolalia. In October, we shared with you a story out of Indiana where a young man living with TS was asked to leave his college campus as a result of offensive and unnerving phrases he involuntarily uttered. Unfortunately, this isn’t the only incident that has come across my desk in the last few weeks.
jason duika blog header
At age five and half I was diagnosed with Tourette Syndrome, and until I was nineteen, I struggled horribly. I had episodes where I would tic hundreds of times in an afternoon, sometimes over a thousand times in a day. I had ‘coprolalia’, ‘copropraxia’, but my ability to be a mimic, spurred on by my ‘echolalia’, I have found to be of great benefit today. I was bullied a great deal, even beaten up on occasion, and though it was sport for my peers to ostracize me, despite this I had a good attitude, and amazing parents, who allowed me to be creative, explore, and try new things. After a twelve year struggle, my Mother, who never gave up hope for a cure, and never allowed me to give up hope either, discovered a unique balance of homeopathy, exercise, and spirituality that proved just the right thing to help me tip the scales from an unmanageable case of Tourette to a more manageable one.
touretteconnect sept
2020 has certainly proven to be one of the most unpredictable and challenging years for everyone. While the uncertainty of the pandemic may have made us rethink how we support the community, it did not derail us. In fact, by the close of this year the Tourette Association of America will have tripled our virtual offerings, with almost 100 virtual support initiatives – from a free Virtual Conference, weekly webinars, a Virtual Gala and virtual walks around the country. To continue at this pace, we need your financial support.