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 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’s 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. Quite quiet childhood with various hematomas throughout the body. At 13, I started hospitalization due to bleeding from menstruation. Endless transfusions and tranex…

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 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…

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.

Lauren’s Adoption Journey: Parenthood with Glanzmann’s Thrombasthenia

April 7, 2024

In the latest episode of “Bruised Not Broken: Life with Glanzmann’s Thrombasthenia,” Melissa Zdziarski and guest Lauren Hurley share their heartfelt stories of navigating motherhood while affected by GT. Lauren, a GT patient from Massachusetts, recounts her lifelong battle with Glanzmann’s Thrombasthenia and her determination to become a mother through adoption. The episode explores the…

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.