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!
Categories: Community
SLC6A1 Gene
I am a mother of a beautiful boy with an SLC6A1 mutation and I am dedicated to finding the best treatment possible for my son.
