Introducing Our New Blog: Showcasing Strength, Talent, and Life with Glanzmann Thrombasthenia

We have exciting news! With Rare Disease Day and GT Awareness Day right around the corner, The Glanzmann’s Research Foundation is launching a dedicated blog section on our website, and we need YOU to be a part of it! This new space will be a platform for individuals living with Glanzmann thrombasthenia to share their unique experiences, talents, and skills—proving that this rare bleeding disorder does not define or limit them.

Why We’re Starting This Blog

Living with Glanzmann thrombasthenia comes with challenges but does not diminish the incredible things individuals can accomplish. Whether you are an artist, athlete, writer, musician, scientist, entrepreneur, or have any other special skill or passion, we want to highlight your journey. By sharing these stories, we hope to:

• Inspire others with Glanzmann thrombasthenia to pursue their dreams without hesitation.
• Educate the public about the realities of living with Glanzmann thrombasthenia beyond the medical condition.
• Build a supportive community where individuals with Glanzmann thrombasthenia and their families can connect and uplift one another.

What We’re Looking For

We seek authors who want to share their persona, insights, and expertise. Your blog post could include:

• Personal experiences navigating life with Glanzmann thrombasthenia and how you’ve overcome challenges.
• Spotlights on your passions and skills, showcasing what you love to do.
• Advice for others with Glanzmann thrombasthenia who may seek encouragement or practical tips.
• Achievements and milestones proving that Glanzmann thrombasthenia doesn’t hold you back.

How to Get Involved

If you’re interested in being featured on our blog, we’d love to hear from you! No writing experience is necessary—just a willingness to share your story. The blogs will be edited before posting to ensure grammar and translation are easy so that those with GT who speak other languages can also enjoy them. Email us at in**@cu****.org with a brief introduction about yourself and what you’d like to write about.

Together, we can amplify the voices of the Glanzmann thrombasthenia community, spread awareness, and celebrate the remarkable people who make this community so unique. Let’s show the world that Glanzmann thrombasthenia is just one part of the story—and that every individual has a powerful narrative.

We can’t wait to read and share your stories with the world!