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 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…

A young girl posing for a photo.

Faces of GT

Luísa

August 2006 was a month we were excited about. It would be the month of the birth of our first daughter, Luisa. After some complications and 14 hours of labor, Luisa came to this world through a C-section. She was brought to me soon after but would not stop crying. My mom opened the blanket…

A group of people sitting on a bench with a baby affected by glanzmann's thrombasthenia.

Faces of GT

Peter Zdziarski

Glanzmann Thrombasthenia (GT) is a rare bleeding disorder that has shaped my life in many ways. I was diagnosed with Glanzmann Thrombasthenia at just eight months old. Over the years, I have learned how to navigate the challenges of this condition, and I want to share my experience to help others in the GT community. Life…

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.