Working towards a cure for Glanzmann's Thrombasthenia, & providing hope & help for the present.

Glanzmann's Research Foundation is a dedicated platform providing comprehensive information and support to patients, families, and healthcare providers affected by the rare inherited blood clotting disorder, Glanzmann's Thrombasthenia (GT).

As a 501(c)(3) non-profit, our primary goal is to fund research aimed at finding a cure for Glanzmann's Thrombasthenia. We strive to create a community where individuals affected by GT can find resources, connect with others, and contribute to the fight against this rare condition.

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.

A woman in a black and white running top walking through tall grass.

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….

A group of people sitting on a bench with a baby affected by glanzmann's thrombasthenia.

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…

A woman in a blue and orange top standing in front of bushes.

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.

Resilience with Glanzmann’s Thrombasthenia: Robie’s Story

November 5, 2023

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.