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 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…

A woman in a blue and orange top standing in front of bushes.

Faces of GT

Cassandra Peel

Hi, everyone! I’m Cassandra, and I am very thankful to have found such a fantastic community in the GT family. I was born and raised in Brooklyn, N, Y, where I was diagnosed with Glanzmann Thrombasthenia at Weill Cornell Medical Center in 1988 at one year old. Since then, top specialists have managed me closely,…

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

In our News section, stay updated on Glanzmann Thrombasthenia research and treatment progress. Explore our Blog for personal stories and insights from those living with GT.

In the News

Honoring the Women of the Glanzmann Thrombasthenia Community on International Women’s Day

March 8, 2025

Today, on International Women’s Day, we celebrate the remarkable women in the Glanzmann Thrombasthenia (GT) community. From patients to mothers, sisters, caregivers, and advocates, these women embody strength, resilience, and unwavering dedication. The Strength of GT Patients Women living with Glanzmann Thrombasthenia face unique challenges daily. They show immense courage, from navigating spontaneous bleeding episodes…

Our Blog

Group of hikers silhouetted against a vibrant sunset, enjoying an adventurous outdoor trek.

Staying Safe on the Trail: The Road Less Traveled

June 30, 2025

By Elizabeth G. Harvey Can you embrace outdoor adventures with Glanzmann Thrombasthenia (GT) or a bleeding disorder? I used to think the answer was a resounding NO! Live safely. Avoid potential harm at all costs. But doesn’t your soul crave overcoming challenges and being thrilled? For those of us living with a platelet disorder, even…

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.