Working towards a cure for Glanzmann 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 Thrombasthenia (GT).

As a 501(c)(3) non-profit, our primary goal is to fund research aimed at finding a cure for Glanzmann 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 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 with glasses holding a glass of wine.

Faces of GT

Joy

I was born in 1944 and named for the great Joy that my parents were feeling. Five years earlier, they had lost their first son to what doctors put down as hemophilia. He died as a result of having undergone a splenectomy – supposedly, at that time, the cure-alll to severe bleeding problems!! He was…

A white person icon on a green background representing glanzmann's thrombasthenia.

Faces of GT

Sandra Fox

MY GT JOURNEY. I am now 74 years old and living in Australia. This meant I had a long time, 64 years actually, till I was diagnosed with GT. Until the,n I was “just one of those women who bleed”. My periods lasted 10 days, y,s, and even on the pi,  ll, they lasted 7…

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

Faces of GT

Pauline Gauthier

Diagnosed with Glanzmann Thrombasthenia at Six Months Old My name is Pauline, and I was born in France in 1993, where I still live today. At six months old, I was diagnosed with Glanzmann Thrombasthenia (GT)—a rare platelet disorder that prevents blood from clotting properly. As a child, I faced many challenges due to frequent…

In our News section, stay updated on Glanzmann Thrombasthenia research and treatment progress. Explore our Blog for personal stories and insights from those living with GT.

In the News

Honoring the Women of the Glanzmann Thrombasthenia Community on International Women’s Day

March 8, 2025

Today, on International Women’s Day, we celebrate the remarkable women in the Glanzmann Thrombasthenia (GT) community. From patients to mothers, sisters, caregivers, and advocates, these women embody strength, resilience, and unwavering dedication. The Strength of GT Patients Women living with Glanzmann Thrombasthenia face unique challenges daily. They show immense courage, from navigating spontaneous bleeding episodes…

Our Blog

Bruises & Barbells: Lifting with a Bleeding Disorder

March 9, 2025

By Pauline Gth & Peter Zdziarski Can you lift weights with Glanzmann Thrombasthenia (GT) or a bleeding disorder? The answer is yes—with the proper precautions. Strength training offers significant benefits, including muscle growth, joint support, and overall health, but those with GT, hemophilia, or Von Willebrand disease must approach it differently. Whether you’re new to…

Our Resources section is a comprehensive guide for anyone seeking information about Glanzmann Thrombasthenia. From frequently asked questions to detailed information for doctors, we aim to provide a wealth of knowledge for those dealing with GT.