John Michael was diagnosed with Glut 1 in February 2017 at 10 months old. After months of testing, we received the official diagnosis and shortly after his first birthday we started the ketogenic diet. It has been 2 years of learning and challenges but we are so happy to see John develop into the happiest and most loving three year old. We love this little guy and there is no shortage of love and support through family, friends and the Glut 1 community as we continue this journey. Please consider donating and spreading awareness about Glut 1. Thank you!
The Love Some1 with Glut1 annual campaign is the primary awareness and fundraising event for the Glut1 Deficiency Foundation. It runs from February 14-28, Valentine's Day through Rare Disease Day, and it is an important opportunity to spread awareness and raise much-needed funds to help better serve the needs of the Glut1 community.
Please visit our website to learn more about Glut1 Deficiency and the work of the G1D Foundation.