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The most recent edition of our newsletter is available at the link below. There are lots of updates to share! You’ll find conference resources from our gathering last month in Nashville, plus information on plans we are already making for our next conference in 2019. There are also some details on new research projects, family news, G1D Foundation news, and some information on our plans to have a Glut1 Deficiency Foundation team in the National Walk for Epilepy.
Please let us know if there are questions or if you have items to include in future editions of our quarterly newsletters. Thank you for your interest in the Glut1 Deficiency community. |
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Resources and information on this website are not intended as medical care or advice. Please consult with your healthcare provider. |
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Copyright © 2020 Glut1 Deficiency Foundation
- Home
-
About Glut1 Deficiency
- What is Glut1 Deficiency?
- Key Terms in Glut1 Deficiency
- About the Ketogenic Diet
- Brochures
- Professional Guide
- Resources
- Newly Diagnosed
- Educational Video Project
- Cognition and Learning
- Research News
- Recent Publications
- Patient Registry
-
Patient Stories
>
-
Stories
>
- Emily
- Bobby
- Lilly
- Allison
- Katie
- Tessa
- Justin
- Whitney
- Ryan
- Erik
- Pattygrace
- Chris
- Sam
- Collette
- Phil
- Joshua
- DeAndre
- Matt
- Jayden
- Brittany
- Macie
- Braden
- Dalton
- Jordan
- Joelle
- Sabrina
- Thomas
- Haley
- Reed
- Ben
- Parys
- Ronnie-Louise
- Colin
- Nathan
- Lee
- Dominic
- Raina
- Dylan
- Brayden
- Elli
- Jacob
- Rian
- Hailey
- Olivia
- Addie
- Drake
- Share Your Story
-
Stories
>
- Videos
- Materiales en Español
- Family Recommended Specialists >
- About G1DF
- News
- Conferences
- Get Involved
- Donate