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Treatments For Epilepsy And Symptoms Of Slc13a5 Foundation

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Nonprofit Overview

Causes: Health

Mission: Tess research foundation's goal is to find better treatment options for slc13a5 deficiency, a severe form of epilepsy beginning in infancy. Slc13a5 deficiency is a newly discovered, rare disease. Tess research foundation funds medical research, connects doctors and patients to researchers, and raises awareness and provides support and education to affected families through a website, emails, and an online support group.

Community Stories

3 Stories from Volunteers, Donors & Supporters

jerio88 Donor

Rating: 5

11/02/2023

I support this foundation wholeheartedly. Kim Nye and her TESS Research Foundation tirelessly and joyously aim to make the seemingly impossible possible for kids and families living with SLC13A5. Their mission is to provide support, information, hope, and community to SLC13A5 families, to find treatments for the kids, and to ultimately find a cure. They are a vital, creative force for improving the lives of children born with this form of epilepsy by all means possible.

LottieCR Donor

Rating: 5

10/28/2023

I have watched this nonprofit grow from the start. Kim Nye and the board work and advocate for treatments and a cure for people with SLC13A5 Deficiency. They have helped bring families together to share information and provide support for one another. Tess Foundation's holistic approach with funding medical research and family supports is a beacon of hope for so many.

SyngapRF Professional with expertise in this field

Rating: 5

10/05/2020

Patients with SLC13A5 are lucky to have Kim Nye working tirelessly on their behalf. This organization has moved mountains for children who may otherwise have been overlooked. What a remarkable accomplishment. They have also been acknowledged as leaders through their membership in Rare as One. Bravo!

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