Working towards a cure for Glanzmann's Thrombasthenia, & providing hope & help for the present.
Faces of GT
Our Faces of GT section showcases the stories of individuals living with Glanzmann's Thrombasthenia, offering a glimpse into their lives and experiences. We believe that sharing these stories can help foster understanding and empathy for those affected by GT.
Faces of GT
Pauline Gauthier
My name is Pauline, I was born in France in 1993 and I still live in France. I was diagnosed with GT at 6 months (diagnosis not being possible, at the time, before 6 months). I had many problems with GT as a child. I had a gastrointestinal hemorrhage when I was 3 years old….
Faces of GT
Peter Zdziarski
Below is an update to Peter’s story, originally written by his mom when he was 14 years old. You can find his original story at the bottom of this page. Update – 2020 Hi everyone, I’ve come a long way since 14 years old. I am now turning 28 and doing great. The older I…
Faces of GT
Cassandra Peel
Hi, everyone! I’m Cassandra, and I am very thankful to have found such an amazing community in the GT family. I was born and raised in Brooklyn, NY where I was diagnosed with Glanzmann’s Thrombasthenia at Weill Cornell Medical Center in 1988 at one year old. Since that time, I have been managed closely by…
In our News section, we keep you updated with the latest developments in Glanzmann's Thrombasthenia research and treatment. Stay informed about the strides we're making in our mission to cure GT.
In the News
Resilience with Glanzmann’s Thrombasthenia: Robie’s Story
In this podcast, host Taylor and guest Robie share a heartfelt conversation about Glanzmann’s Thrombasthenia, a rare genetic bleeding disorder. They discuss Robie’s journey, struggles, surgeries, and life lessons. The dialogue covers adapting to the disorder, family decisions, and not letting it limit one’s life. Want to Sponsor the Podcast? Contact Us Here Have GT?…
Our Resources section is a comprehensive guide for anyone seeking information about Glanzmann's Thrombasthenia. From frequently asked questions to detailed information for doctors, we aim to provide a wealth of knowledge for those dealing with GT.