Working toward a cure for Glanzmann Thrombasthenia and providing hope and help for those living with GT today.

Glanzmann's Research Foundation is a 501(c)(3) nonprofit dedicated to supporting people and families affected by Glanzmann Thrombasthenia. We provide trusted information about GT symptoms, diagnosis, treatment, bleeding management, and ongoing research while connecting patients, families, caregivers, and healthcare professionals with resources and community support.

Our mission is to improve life with Glanzmann Thrombasthenia today while supporting research toward better treatments and, ultimately, a cure.

Faces of GT

Our Faces of GT section shares real stories from people and families living with Glanzmann Thrombasthenia (GT) worldwide. Explore their experiences with diagnosis, bleeding, treatment, daily life, and the challenges and successes that come with living with this rare bleeding disorder.

A woman with glasses holding a glass of wine.

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 as hemophilia. He died as a result of having undergone a splenectomy – supposedly, at that time, the cure-alll to severe bleeding problems!! He was…

A woman in a black hijab is posing for a photo, embodying diversity and inclusion.

Faces of GT

Yosra

My name is Yosra, but I’m known as Tanja in the Group. I’m 24 years old! I was diagnosed with Glanzmann’s when I was six months old. 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 bruises…

Faces of GT

Altaf Khaji

My name is Altaf, and I am from India. I was born with Glanzmann Thrombasthenia, although I was not diagnosed until I was 12 years old. Living with GT has brought many challenges throughout my life, especially frequent gum bleeding. Over the years, I have learned how to manage these challenges and better understand my…