Working towards a cure, and providing hope and help for the present.

Glanzmann’s Research Foundation exists to provide information and support to patients, family, and healthcare providers affected by the rare inherited blood clotting disorder Glanzmann’s Thrombasthenia (GT).

We are a a 501(c)3 non-profit with the goal of funding research to find a cure.

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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 pardon me. When I was 1.5 yrs old my mother noticed bleeding from my…

Faces of GT

Joy

I was born in 1944 and named for the great Joy that my parents were feeling. Five years earlier they had lost their first son to what doctors put down to haemophilia. He died as a result of having undergone a splenectomy – supposedly, at that time, the cure all to severe bleeding problems!! He…

Faces of GT

Dan Beyer

Hi. My name is Daniel Beyer, but my friends call me Dan. As a child, I spent half of my life in the hospital until about the age of twelve. From twelve to my mid-thirties, I did not have many problems. When I hit my late thirties, early forties, I began having more problems. In…

Shirt Fundraiser

July 31, 2020

We are excited to announce a great way to help raise funds for finding a cure for Glanzmann’s Thrombasthenia. Starting now, Showpony has launched a GT shirt! This shirt is only available for the next 7 days. Help us spread awareness for GT by wearing this limited edition T and sharing this link with your…