Working towards a cure for Glanzmann 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 Thrombasthenia (GT).

As a 501(c)(3) non-profit, our primary goal is to fund research aimed at finding a cure for Glanzmann 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 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 woman with glanzmann's thrombasthenia wearing ripped jeans and a white top.

Faces of GT

Dezirya

Dezirya Merritt was born in Sept 2000 on her expected due date, and I was so happy I had finally gotten a girl. I had three boys prior. Well, the doctor noticed she was jaundiced and ordered the unique lamp for her, and like usual, we were discharged and on our way home. We were…

Two women standing in front of a sign that says forever sisters, one of whom has Glanzmann's thrombasthenia.

Faces of GT

Jyll

Hi, my name is Jyll, and I was born on 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 bo, rn my umbilical cord would not stop bleeding. After three weeks, it was cauterized….

A man with a beard and glasses is taking a selfie in front of a sign.

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 forgive me. When I was 1. year old, my mother noticed bleeding from my…

In our News section, stay updated on Glanzmann Thrombasthenia research and treatment progress. Explore our Blog for personal stories and insights from those living with GT.

In the News

Glanzmann Thrombasthenia Support Group Marks 18 Years of Connection and Announces Next Chapter for the GRF

October 6, 2025

Today, the Glanzmann Thrombasthenia Support Group proudly celebrates its 18th anniversary, marking nearly two decades of compassion, connection, and shared purpose among patients and families affected by Glanzmann Thrombasthenia (GT). What began as a small online gathering of individuals seeking understanding has evolved into a global community where members exchange advice, share personal experiences, and…

Our Blog

Staying Safe on the Trail: The Road Less Traveled

June 30, 2025

By Elizabeth G. Harvey Can you embrace outdoor adventures with Glanzmann Thrombasthenia (GT) or a bleeding disorder? I used to think the answer was a resounding NO! Live safely. Avoid potential harm at all costs. But doesn’t your soul crave overcoming challenges and being thrilled? For those of us living with a platelet disorder, even…

Our Resources section is a comprehensive guide for anyone seeking information about Glanzmann Thrombasthenia. From frequently asked questions to detailed information for doctors, we aim to provide a wealth of knowledge for those dealing with GT.