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Lochlan’s Glut1 Campaign!

by Teresa Gann

Supporting: Love Some1 with Glut1 2020 for Glut1 Deficiency Foundation

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Campaign has ended.

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Lochlan’s was diagnosed with Glut1 at 8 months old. She has been on the ketogenic ever since! 


I could go into a huge sob story as to why you should donate but the truth is... there is very little funding for Glut1. It is a very rare disease that not a lot of people know about. It effects Lochlan every single day. Without funding, there is no cure! 


Please consider donating... even $10 is more than helpful! 


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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