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 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…

A young girl with glanzmann's thrombasthenia is smiling while sitting on a couch.

Faces of GT

Amelie Iavicoli

Amelie was born on November 13, 2012, at 11:12 in the evening. Aside from a couple of purplish spots on her chest, she weighed just over 7 pounds and was considered a healthy newborn. She established her personality from the start, betraying the nurse’s promises that Amelie would sleep soundly through her first night outside…

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

A vintage typewriter with a paper titled 'News', symbolizing journalism and communication.

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

Group of hikers silhouetted against a vibrant sunset, enjoying an adventurous outdoor trek.

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.