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Kathy Davis

Supporting: Love Some1 with Glut1 2020 for Glut1 Deficiency Foundation

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Campaign has ended.

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William was diagnosed with Glut1 Deficiency in December, after 2 years of poorly controlled seizures. There is no cure for Glut1.  He is currently enrolled in a clinical trial, with the hope that his seizures and developmental delays improve.  Please help me and the Glut1 Deficiency Foundation raise money for awareness and research ❤


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

www.G1DFoundation.org



How would you like to support?

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