Working towards a cure, and providing hope and help for the present.

Glanzmann’s Research Foundation exists to provide information and support to patients, family, and healthcare providers affected by the rare inherited blood clotting disorder Glanzmann’s Thrombasthenia (GT).

We are a a 501(c)3 non-profit with the goal of funding research to find a cure.

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Faces of GT

Sandra Fox

MY GT JOURNEY. I am now 74 years old and living in Australia. This meant I had a long time, 64 years actually till I was diagnosed with GT. Until then I was “just one of those women who bleed”. My periods lasted 10 days and even on the pill they lasted 7 days. I…

Faces of GT

Denise Kurta

One day I was on the internet and I came upon the GT web site. When I looked at a group picture on the site I gasped, I could tell who had GT from the tell tale bruises they had. For the first time in my life I saw other people just like ME! My…

Faces of GT

Michela Golia

Salve, sono una donna di 51 anni con tromboastenia di glanzmann. Ho avuto la diagnosi a 6 anni, dopo la morte di mio fratello maggiore che aveva la mia stessa patologia ma scambiavano per emofilia. L’infanzia abbastanza tranquilla con vari ematomi in tutto il corpo. All’età di 13 anni ho cominciato con i ricoveri in…

Shirt Fundraiser

July 31, 2020

We are excited to announce a great way to help raise funds for finding a cure for Glanzmann’s Thrombasthenia. Starting now, Showpony has launched a GT shirt! This shirt is only available for the next 7 days. Help us spread awareness for GT by wearing this limited edition T and sharing this link with your…