Working towards a cure for Glanzmann's 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's Thrombasthenia (GT).

As a 501(c)(3) non-profit, our primary goal is to fund research aimed at finding a cure for Glanzmann's 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's 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 young girl posing for a photo.

Faces of GT

Luísa

August of 2006 was a month we were waiting for with a great deal of excitement. 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 C-section. She was brought to me soon after, but would not stop…

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 an amazing community in the GT family. I was born and raised in Brooklyn, NY where I was diagnosed with Glanzmann’s Thrombasthenia at Weill Cornell Medical Center in 1988 at one year old. Since that time, I have been managed closely by…

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. She weighed just over 7 pounds and was considered a healthy newborn, aside from a couple purplish spots on her chest. She established her personality from the start, betraying the nurses promises that Amelie would sleep soundly through her first night outside her…

In our News section, we keep you updated with the latest developments in Glanzmann's Thrombasthenia research and treatment. Stay informed about the strides we're making in our mission to cure GT.

Rare Disease Day & Glanzmann Thrombasthenia Awareness Day: Why Awareness Matters

February 9, 2025

Every year, Rare Disease Day (February 28) and Glanzmann Thrombasthenia Awareness Day (March 1) provide an opportunity to shine a light on conditions that often go unnoticed. With over 300 million people worldwide living with a rare disease, awareness is the first step toward progress—whether it’s in research, treatment, or support for those affected. One…

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