Happy Rare Disease Day – Love Some1 with Glut1!

The annual Love Some1 with Glut1 is underway! From Valentine’s Day to Rare Disease Day (February 29th), the campaign raises money to support the important and impactful work of the Glut1 Deficiency Foundation and its mission of educating others, increasing awareness of and advocacy for Glut1 Deficiency Syndrome. click here to donate

I love someone who is rare!

And I love the fact that Glut1 Deficiency has an effective form of treatment despite the fact that it is so rare! This is why raising awareness and getting kids diagnosed early is so crucial. Three neurologists with years of experience saw Drake and none even thought of Glut1 Deficiency as a possibility. Drake wasted three crucial brain-growing years with the wrong diagnosis, to the point of it causing microcephaly, and still no one even thought of Glut1 Deficiency. That needs to change. Donating to G1 Foundation and to the cause of other rare diseases will help everyone get diagnosed faster and possibly lead to better treatments and a cure. Continue reading “Happy Rare Disease Day – Love Some1 with Glut1!”