Episode #68: TESS Research Foundation

“Our mission is to help families affected by SLC13A5 Deficiency. SLC13A5 Deficiency (aka Citrate Transporter Disorder) is a newly discovered genetic cause of epilepsy, and as such, TESS Research Foundation is building a patient-centered network from the ground up. We are determined to diagnose, treat, and ultimately cure SLC13A5 Deficiency. We do this by funding cutting-edge research and connecting families, doctors, and researchers.”

In this episode, hear President Kimberly Nye share her family story and the story of the TESS Research Foundation, a 501(c)(3) tax exempt public charity.

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