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….

Two individuals with glanzmann's thrombasthenia and their companion stand side by side.

Faces of GT

Dan Beyer

Hi. My name is Daniel Beyer, but my friends call me Dan. As a child, I spent half of my life in the hospital until about the age of twelve. From twelve to my mid-thirties, I did not have many problems. When I hit my late thirties, early forties, I began having more problems. In…

A woman with glanzmann's thrombasthenia holding up a drawing of a caricature.

Faces of GT

Karen “Kaytee”

My story is long but since I am one of the oldest diagnosed Glanzmann’s Thrombasthenia patients in the United States. I must be upfront that my history is not a nice one, but I have learned in life, everyone’s life is not all peaches and cream. It is also taken from a couple of e-mails…

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.

Rare Disease Day & Glanzmann Thrombasthenia Awareness Day: Why Awareness Matters

February 9, 2025

Every year, Rare Disease Day (February 28) and Glanzmann Thrombasthenia Awareness Day (March 1) provide an opportunity to shine a light on conditions that often go unnoticed. With over 300 million people worldwide living with a rare disease, awareness is the first step toward progress—whether it’s in research, treatment, or support for those affected. One…

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.