This summer has been a whirlwind between Maxwell’s diagnosis, the creation of SLC6A1 Connect, and many exciting developments in the way of research. Amber has been hard at work setting up the organization, campaigning for funding and donations, and talking to researchers. We will share all of the exciting developments with you as details are finalized. Needless to say, the SLC6A1 ball is rolling toward a better outcome for all who are diagnosed. Please stay-tuned to this page for more!
Rare Disease Week
Hello again! In continuation of Rare Disease Week, we want to talk specifically about the rare disease that affects our kids and families, SLC6A1 Epileptic Encephalopathy. SLC6A1 epileptic encephalopathy is a rare neurological condition in children that causes Read more…