We are excited to bring you more voices from our TESS Community. Here we will feature blog posts from SLC13A5 Deficiency Family Members, Doctors, Researchers, Volunteers, and members of our Board of Directors. We hope this will help raise awareness about what it is like to live with SLC13A5 Deficiency and highlight the milestones on our path to a cure. Thank you for all that you continue to do to help our TESS community.
A non-profit organization dedicated to finding treatment options for the neurological disease SLC13A5