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Art for a Cause

Giving back to the Tourette's community

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See my product line here...

About Art for a Cause

Art for a Cause is an advocacy-driven project and merchandise line that aims to inspire empathy, challenge misconceptions, and encourage more open-minded conversations around neurodiversity and mental health.

 

We donate to and collaborate with organizations within the Tourette Syndrome community. 

Daytime Buffalo: Tourette's Awareness Month 2025

Speaking with Chelsea Lovell on WIVB Daytime Buffalo about my advocacy oriented merch line: Art For a Cause and the fundraiser Power & Purpose: A Night For Tourette's. May 1st, 2025

Power & Purpose: A Night For Tourette's

May 10th, 2025

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From Left: Isabella Constantino, Baylen Dupree, Greg Lawrence- President of The Ryan Lawrence Foundation at Power & Purpose: A Night For Tourette's 

I had the wonderful opportunity to talk with Chelsea Lovell on WIVB  Daytime Buffalo about my journey with Tourette Syndrome and the many beautiful connections I've made along the way. We spoke about art and advocacy, including my fundraiser appearance in Washington, D.C. on May 10, 2025! 

 

I'm so grateful to have been connected with the Ryan Lawrence Foundation, Baylen Dupree, and an amazing group of women entrepreneurs who put this event together, and to be reminded of what it means to turn compassion into action. 

 

This journey started over 15 years ago being chosen along with three other teens for ABC Prime Time special on TS and finding support and empowerment through the wonderful people of the Tourette Association of America.  

 

That advocacy continues now through Art for a Cause and the fundraiser Power & Purpose: A Night For Tourette's.

 

Thank you for all of your support!

The Ryan Lawrence Foundation

​​In collaboration with The Ryan Lawrence Foundation, part of the proceeds from this line go to raising awareness and funding the creation of a new Tourette Syndrome Research and Treatment Clinic at the Toronto Western Hospital.

 

Read more about their foundation below!

Ryan Lawrence Foundation

Ryan Lawrence was a spirited individual who had more strength than the average individual. Whether it was school, sports or accepting and coping with his life with Tourette's, he lived with unimaginable stress each day.

 

Ryan passed on at 21 years old due to complications from Tourette's syndrome and undiagnosed cardiomyopathy, but his strength and love has been passed on to help us create a foundation and act on his behalf to support research, treatment and advocacy for Tourette's Syndrome.

- Ryan Lawrence Foundation Website

Learn how you can donate to or participate with the foundation here!

Letters For Hope

Being a teenager is a lot for anyone, let alone a teenager with a very visible disability. I started high school with an influx of symptoms and stress that only increased with the rigorous coursework. 

My local Tourette's Association chapter provided support during this very difficult time. Because of some very dedicated teachers and members of the TS community, I was able to get the help I needed from my school to get through the year. I was encouraged and empowered by the incredible people who helped me advocate for myself and for the resources I needed to succeed.

The following year, I wanted to give back to the association that had given me so much.

I started a line of cards I called "Letters for Hope." It consisted of different variations of Buffalo art and holiday cards which I sold at craft fairs, local TSA events, and to individuals such as Joanne Faletta, conductor of the Buffalo Philharmonic Orchestra.

Proceeds from these cards went to the Tourette Syndrome Association of Greater NY, to help provide support and resources for other kids with TS. This card line was part of what inspired me to create my current collection of Tick products that I hope will benefit many more people with TS. 

"Tourette Syndrome is a neurodevelopmental disorder that affects children, adolescents and adults. The condition is characterized by sudden, involuntary movements and/or sounds called tics. Tics can range from mild/inconsequential to moderate and severe, and are disabling in some cases."
 

- Tourette Syndrome Association of America

Do you or someone you know have TS?
Looking for support?

Find support and communtity in your area and see how you can become a part of your local Tourette Association. 

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