Working towards a cure for Glanzmann's Thrombasthenia, & providing hope & help for the present.
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.
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…
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…
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.
In the News
This Giving Tuesday, Help Us Fund a Cure
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.