Support the Glut1 Community

by Michelle Norgren

Supporting: Love Some1 with Glut1 2020 for Glut1 Deficiency Foundation


Campaign has ended.


John Michael was diagnosed with Glut1 around 10 months old. We started the ketogenic diet shortly after his first birthday. He has been seizure free for just over three years! The foundation has provided so many resources, connections, support and education so that we can provide the best care for our amazing little guy! Funds will support research and continue to provide families with up to date resources and support as more families have a loved one diagnosed. Help support John Michael and the Glut1 community through the campaign ending on Rare Disease Day February 29th! 

The Love Some1 with Glut1 annual campaign is the signature awareness and fundraising event for the Glut1 Deficiency Foundation, running from February 14-29, Valentine's Day through Rare Disease Day. It is an important opportunity to educate others and raise much-needed funds to help better serve the needs of our patient community through our mission programs for increased awareness, improved education, advocacy for patients and families, and support and funding for research.

Thank you for helping us reach our goal and supporting us as we continue our work to bring help and hope to everyone, everywhere, who is affected by Glut1.  You make our mission possible.

learn more about love

messages from the heart of our community

learn more about Glut1 Deficiency

our new video to help raise awareness and improve education

please visit our website for more information

How would you like to support?