The Patient Advisory Board (PAB) has six members who represent the diversity of the Tourette Syndrome (TS) community. Their role is to bring their lived and professional experiences to bear in ensuring community responsive implementation of our studies during monthly meetings. This group of volunteers care deeply about you and want to make sure you can benefit from this study. Our current members are:

Laura Beljaars 

PAB Member

I'm from the Netherlands and got diagnosed with Tourette's at the age of 11. I've been working with researchers to implement the patient's perspective for a while now and I'm very excited about this project! I have my masters in education and work in my own business where we help parents, kids, adults, teachers etc. who deal with Tourette's. I love baking cakes and making improvements around my house, and I'm currently preparing for the birth of my son!

Sara Hamilton

PAB Member

Sara Hamilton is a passionate advocate of the Tourette and neurodiversity communities. As a dedicated volunteer for the TAA, Sara has presented at National Conferences and Education Workshops, and she has served as a strategic consultant and facilitator at Research Summits and Leadership Sessions. Sara has also been a Board member and volunteer for several nonprofits and educational institutions, including the Masonic Institute for the Developing Brain. Her daughter, Jane, was diagnosed with Tourette as a child; she spent her young adulthood advocating for others with neurological differences by becoming a TAA Youth Ambassador and Rising Leader, and she is now pursuing a degree in neuroscience.

Praveena Hook 

PAB Member

Living in Minnesota, I've embraced the beautiful landscapes and communities, but also faced challenges when my son was diagnosed with Tourette Syndrome at the age of 9. In a region where resources and support for TS are limited, advocating for my son has become my passion and purpose. I aim to create a more inclusive and supportive environment for individuals with TS, ensuring that my son and others like him can reach their full potential with the right support they need.

Ellie Jarvie 

PAB Member

I am an adult with Tourette who lives in Madison WI. I have been involved in the Tourette Syndrome community since the mid 1980's. My motivation for being on the Patient Advisory Board is to share what I have learned from others, my own lived experience and my professional experience to improve the lives of people with tics.

Elise Minkin 

PAB Member

Thomas White

PAB Member

Tom writes, edits, researches, and ghostwrites professionally for a number of startup/F500 executives, VCs, and institutional fund managers; advises and consults on web3/growth/storytelling/customer psychology for a number of different international startups and funds; and pens a free weekly newsletter on books and behavior, psychology and philosophy: www.whitenoise.email. In light of his battle with Tourette, he works tirelessly to spread awareness, hope, and positivity.