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 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…

Two individuals with glanzmann's thrombasthenia and their companion stand side by side.

Faces of GT

Dan Beyer

Living with a Rare Bleeding Disorder My name is Daniel Beyer, but my friends call me Dan. I was diagnosed with Glanzmann Thrombasthenia (GT) as a child, a rare platelet disorder that prevents blood from clotting properly. For much of my early life, I spent countless days in the hospital, dealing with frequent and severe…

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

Bruises & Barbells: Lifting with a Bleeding Disorder

March 9, 2025

By Pauline Gth & Peter Zdziarski Can you lift weights with Glanzmann Thrombasthenia (GT) or a bleeding disorder? The answer is yes—with the proper precautions. Strength training offers significant benefits, including muscle growth, joint support, and overall health, but those with GT, hemophilia, or Von Willebrand disease must approach it differently. Whether you’re new to…

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.