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…

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 black and white running top walking through tall grass.

Faces of GT

Pauline Gauthier

Diagnosed with Glanzmann Thrombasthenia at Six Months Old My name is Pauline, and I was born in France in 1993, where I still live today. At six months old, I was diagnosed with Glanzmann Thrombasthenia (GT)—a rare platelet disorder that prevents blood from clotting properly. As a child, I faced many challenges due to frequent…

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

Apollo Hospitals Navi Mumbai Achieves Landmark Success in Robotic Hysterectomy for Patient with Rare, Life-Threatening Bleeding Disorder

March 5, 2026

NAVI MUMBAI, 5 MARCH 2026 (SACHIN MURDESHWAR 8108510506): For years, every menstrual cycle for 37-year-old Ms. Neelam meant a medical emergency. Due to a rare and life-threatening bleeding disorder, she required blood transfusions almost every month just to manage the severe blood loss caused by her periods. Doctors at Apollo Hospitals Navi Mumbai have now…

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.