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 a blue dress.

Faces of GT

Sherry Crutchfield

Hi, my name is Sherry Crutchfield, my husband and I live in Fernandina Beach, FL. I aa 54 years old with GT. I have never known anyone but me with this disorder until I found this current site of Helen Smith’s. I am from the small town of Roysto, Ga. I was diagnosed at six…

A woman in a blue and orange top standing in front of bushes.

Faces of GT

Cassandra Peel

Hi, everyone! I’m Cassandra, and I am very thankful to have found such a fantastic community in the GT family. I was born and raised in Brooklyn, N, Y, where I was diagnosed with Glanzmann Thrombasthenia at Weill Cornell Medical Center in 1988 at one year old. Since then, top specialists have managed me closely,…

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.