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GLUT1 Glimpses:  The Blog

Find insights and news that matters to the GLUT1 Deficiency community, including events, family features, research snapshots, and special announcements. Find these GLUT1 Glimpses below.

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Our monthly newsletters keep you in the know about what's happening at the G1DF and in the community as we work hard to bring help and hope to patients and families.

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The blog

GLUT1 Glimpses

Rare Disease Day at the White House

The White House Office of Science and Technology Policy will host a forum marking Rare Disease Day and highlighting the Biden-Harris Administration’s commitment to supporting patients and...
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International Epilepsy Day

Today is International Epilepsy Day, started in 2015 by the International Bureau for Epilepsy (IBE) and the International League Against Epilepsy (ILAE). International Epilepsy Day aims to eliminate...
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Dr. Juan Pascual: NIH Team Science and Move to Weill Cornell

Hello everyone and welcome to Science with Sandra! We have had a busy and great start of the year in our community. On Saturday January 20th we...
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New Patient Support Programs

The Glut1 Deficiency Foundation is very excited to announce two new programs to offer support services to the patient community. Glut1 Deficiency is a rare, metabolic condition...
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Winter ’24 Research Roundtable: GSDs and CDGs

Hello everyone and welcome to Science with Sandra! For this edition of Science with Sandra I wanted to highlight the Winter gathering of our Research Roundtable. It...
Read More about Winter ’24 Research Roundtable: GSDs and CDGs