Working towards a cure for Glanzmann's 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's Thrombasthenia (GT).

As a 501(c)(3) non-profit, our primary goal is to fund research aimed at finding a cure for Glanzmann's 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'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.

Two women standing in front of a sign that says forever sisters, one of whom has Glanzmann's thrombasthenia.

Faces of GT

Jyll

Hi, my name is Jyll and I was born March 24, 1973 in Toledo, Ohio. I was so glad to have found this website through Kaytee, one of my GT sisters because I’m not alone anymore! When I was born my umbilical cord would not stop bleeding. After three weeks it was cauterized. I was…

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 I came upon the GT web site. 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…

A young boy wearing an adidas t-shirt standing on a sidewalk at night with glanzmann's thrombasthenia.

Faces of GT

Vincenzo

I am Anna, and this is the story of Vincenzo, a GT boy born on 12 December 2005 in Naples, Italy. At birth, after a long labor, Vincenzo was born with natural birth, without complications; he presented a great bruise on the back, petechiae all over the body, also in the eyes, there were broken…

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.

Rare Disease Day & Glanzmann Thrombasthenia Awareness Day: Why Awareness Matters

February 9, 2025

Every year, Rare Disease Day (February 28) and Glanzmann Thrombasthenia Awareness Day (March 1) provide an opportunity to shine a light on conditions that often go unnoticed. With over 300 million people worldwide living with a rare disease, awareness is the first step toward progress—whether it’s in research, treatment, or support for those affected. One…

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.