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 man with a beard and glasses is taking a selfie in front of a sign.

Faces of GT

Md. Kaium Ali Jibon

Hi, my name is Md. Kaium Ali, and my nickname is Jibon. I live in Bangladesh with my family. I noticed this website from the Facebook GT support group. I am not good at English, so if I make mistakes, please forgive me. When I was 1. year old, my mother noticed bleeding from my…

A woman in a black and white running top walking through tall grass.

Faces of GT

Pauline Gauthier

Diagnosed with Glanzmann Thrombasthenia at Six Months Old My name is Pauline, and I was born in France in 1993, where I still live today. At six months old, I was diagnosed with Glanzmann Thrombasthenia (GT)—a rare platelet disorder that prevents blood from clotting properly. As a child, I faced many challenges due to frequent…

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,…

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.