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 people sitting on a bench with a baby affected by glanzmann's thrombasthenia.

Faces of GT

Peter Zdziarski

Glanzmann Thrombasthenia (GT) is a rare bleeding disorder that has shaped my life in many ways. I was diagnosed with Glanzmann Thrombasthenia at just eight months old. Over the years, I have learned how to navigate the challenges of this condition, and I want to share my experience to help others in the GT community. Life…

A white person icon on a green background representing glanzmann's thrombasthenia.

Faces of GT

Denise Kurta

One day, I was on the Internet and came upon the GT website. When I looked at a group picture on the site, I gasped. I could tell who had GT from the tell-tale bruises they had. For the first time in my life, I saw other people just like me! My name is Denise…

A white person icon on a green background representing glanzmann's thrombasthenia.

Faces of GT

Michela Golia

Hi, I’m a 51-year-old woman with Glanzmann thrombasthenia. I was diagnosed at 6, after the death of my older brother, who had the same condition as me but was mistaken for hemophilia. Relatively quiet childhood with various hematomas throughout the body. At 13, I started hospitalization due to bleeding from menstruation. I took endless transfusions…

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

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Glanzmann Thrombasthenia Support Group Marks 18 Years of Connection and Announces Next Chapter for the GRF

October 6, 2025

Today, the Glanzmann Thrombasthenia Support Group proudly celebrates its 18th anniversary, marking nearly two decades of compassion, connection, and shared purpose among patients and families affected by Glanzmann Thrombasthenia (GT). What began as a small online gathering of individuals seeking understanding has evolved into a global community where members exchange advice, share personal experiences, and…

Our Blog

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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.