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.

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

Faces of GT

Peter Zdziarski

Below is an update to Peter’s story, originally written by his mom when he was 14 years old. You can find his original story at the bottom of this page. Update – 2020 Hi everyone, I’ve come a long way since 14 years old. I am now turning 28 and doing great. The older I…

A woman with Glanzmann's Thrombasthenia wearing a blue dress.

Faces of GT

Sherry Crutchfield

Hi my name is Sherry Crutchfield, my husband and I live in Fernandina Beach Fl. I am a 54 years old with GT. I have never known anyone but me with this disorder until I found this curegt site of Helen Smith’s. I am from the small town of Royston Ga. I was diagnosed at…

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.

2024 #RAREis Global Advocate Grant Recipient

September 5, 2024

We’re honored to announce that we’ve been selected as a 2024 RAREis Global Advocate Grant recipient by Amgen’s RAREis program. This recognition underscores our unwavering commitment to the Glanzmann’s Thrombasthenia community and the rare disease community at large, who inspire us every day with their strength and resilience amid care and research barriers. With this…

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.