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 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…

Eva Turek-Jewkes taking a selfie in front of Uluru.

Faces of GT

Eva Turek-Jewkes

Statistically, GT affects one in one million people, making me one of twenty-five people in Australia who suffer from this disease. My medical opinion is that I’m out of options. Today, I wait patiently for a donor in the hope of a bone marrow transplant. Against the backdrop of my immigrant family and relentless cultural…

A group of veterinarians in front of a truck, highlighting glanzmann's thrombasthenia.

Faces of GT

Emily

Hello! I am Emily, a 25-year-old with Glanzmann Thrombasthenia. My journey with GT started when I was only a few hours old. I developed purple marks (later found to be bruises) all over my body. The doctors and nurses called me the “blueberry muffin baby.” After numerous tests, including a biopsy of one of the…

In the News

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.