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.
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