Glut1 Deficiency Family Stories: The O’Reilly Family
Hello, I’m Ailbhe and along with Adam, my husband, and Sam (5) and Dara (3), we are the O’Reilly family from Dublin, Ireland. Dara has
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The Glut1 Deficiency Foundation
The Glut1 Deficiency Foundation
The Glut1 Deficiency Foundation is a nonprofit family organization dedicated to improving the lives of those in the Glut1 Deficiency community through its mission of increased awareness, improved education, advocacy for patients and families, and support and funding for research.
Condition Awareness & Advocacy
Here is a list of conditions this partner raises awareness and advocacy for:
Patient Worthy Posts on Glut1 Deficiency Syndrome
Glut1 Deficiency Foundation 2019 Conference Highlights!
I had the pleasure of attending the Glut1 Deficiency Foundation’s 2019 Conference. While this article can’t possibly do the event justice and encompass all it
Experimental Treatment for GLUT1 Deficiency Syndrome Falters in Clinical Trial
According to a story from Biospace, the biopharmaceutical company Ultragenyx Pharmaceutical Inc. recently reported that its experimental product UX007 failed to achieve its primary endpoint
Researchers Investigate the Molecular Causes of Glut1 Deficiency Syndrome
A recent study published in the journal Cell has investigated the process behind the genetic condition Glut1 deficiency syndrome. Many genetic disorders are thought to be
Remarkable Ketogenic Diet is Hailed Tremendous by Mom
My heart breaks for children who are suffering from a chronic or rare disease such as refractory epilepsy or Glut1 disease. My heart breaks as well for
Glut1 DS Ain’t Got Nothing on This Mother’s Intuition
Can you imagine your toddler son having to get a lumbar puncture in order to be diagnosed with a condition that, despite the fact that you’ve
