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 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’s 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 referred to me as the “blueberry muffin baby”. After numerous tests, including a biopsy of one…

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 to haemophilia. He died as a result of having undergone a splenectomy – supposedly, at that time, the cure all to severe bleeding problems!! He…

A woman with glanzmann's thrombasthenia wearing ripped jeans and a white top.

Faces of GT

Dezirya

Dezirya Merritt was born in Sept 2000 on her expected due date, and I was all so happy I had finally gotten a girl. I had three boys prior. Well, the doctor noticed she was jaundiced and ordered the special lamp for her, and like normal, we were discharged and on our way home. We…

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.

This Giving Tuesday, Help Us Fund a Cure

November 22, 2024

Make a Difference in the Lives of Those with Glanzmann’s Thrombasthenia Giving Tuesday is a day for generosity, community, and hope. At the Glanzmann’s Research Foundation (GRF), we’re committed to advancing research for a cure for Glanzmann’s Thrombasthenia (GT), a rare and challenging bleeding disorder. With your support, we can continue funding groundbreaking research and…

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.