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
Yosra
My name is Yosra, but I’m known as Tanja in the Group. I’m 24 years old! I was diagnosed with Glanzmann’s when I was six months. Since my illness is hereditary, my older cousin has the Glanzmann’s, so my mom had an idea about it. And when I was a baby, mom found bruises and…
Faces of GT
Amelie Iavicoli
Amelie was born on November 13, 2012 at 11:12 in the evening. She weighed just over 7 pounds and was considered a healthy newborn, aside from a couple purplish spots on her chest. She established her personality from the start, betraying the nurses promises that Amelie would sleep soundly through her first night outside her…
Faces of GT
Sherry Crutchfield
Hi my name is Sherry Crutchfield, my husband and I live in Fernandina Beach Fl. I am a 54 years old with GT. I have never known anyone but me with this disorder until I found this curegt site of Helen Smith’s. I am from the small town of Royston Ga. I was diagnosed at…
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
2024 #RAREis Global Advocate Grant Recipient
We’re honored to announce that we’ve been selected as a 2024 RAREis Global Advocate Grant recipient by Amgen’s RAREis program. This recognition underscores our unwavering commitment to the Glanzmann’s Thrombasthenia community and the rare disease community at large, who inspire us every day with their strength and resilience amid care and research barriers. With this…
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.