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

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…

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

Luísa

August of 2006 was a month we were waiting for with a great deal of excitement. It would be the month of the birth of our first daughter, Luisa. After some complications and 14 hours of labor, Luisa came to this world through C-section. She was brought to me soon after, but would not stop…

Help us on Amazon Smile Today!

November 30, 2020

Hi everyone and happy holidays! With cyber Monday upon us here is a great and easy way to help donate funding for a cure for GT.   Sign in to smile.amazon.com on your desktop or mobile phone. From your desktop, go to Your Account and select the option to Change your Charity. Or, from your…