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.

Two men named Patrick walking in a park with backpacks.

Faces of GT

Patrick Muls

Hey! I’m Patrick from Belgium. I was born in 1958. I was diagnosed with GT when I was still an infant. This has influenced my life ever since. No dangerous sports like football (soccer) or so. As the son of a fighter pilot, I also wanted to fly jets but knew that dream would never…

Two women standing in front of a sign that says forever sisters, one of whom has Glanzmann's thrombasthenia.

Faces of GT

Jyll

Hi, my name is Jyll, and I was born on March 24, 1973, in Toledo, Ohio. I was so glad to have found this website through Kaytee, one of my GT sisters because I’m not alone anymore! When I was bo, rn my umbilical cord would not stop bleeding. After three weeks, it was cauterized….

A young girl posing for a photo.

Faces of GT

Luísa

August 2006 was a month we were excited about. It would be the month of the birth of our first daughter, Luisa. After some complications and 14 hours of labor, Luisa came to this world through a C-section. She was brought to me soon after but would not stop crying. My mom opened the blanket…

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.