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.

helena-lopes-PGnqT0rXWLs-unsplash

Faces of GT

Yosra

My name is Yosra but I’m known as Tanja in the Group. I’m 24 years old! I’ve been diagnosed with Glanzmann’s when I was 6 Months. Since my illness is hereditary, my older cousin has the Glanzmann’s so my mom had an idea about it. And when I was a baby mom found some bruises…

Faces of GT

Vincenzo

Sono Anna e questa è la storia di Vincenzo un ragazzo GT , nato il 12 dicembre del 2005 a Napoli in Italia. Alla nascita dopo un lungo travaglio Vincenzo è nato con un parto naturale , senza complicazioni, presentava una grande ecchimosi alla schiena , petecchie in tutto il corpo , anche negli occhi…

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…

Rare Across America

January 4, 2021

Join us for Rare Across America this February and March to meet your new and re-elected legislators, share your story, and make rare diseases a priority in the 117th Congress. Haz clic aquí para obtener información en español y para registrarte. WHEN February 22 – March 5, 2021 (Virtual Congressional meetings on March 3rd and…