Answers about our work.

Elio Ever After Foundation is a nonprofit supporting blind and visually impaired children and their families through sensory-rich experiences, accessibility resources, tactile learning, community events, and emotional support.

We serve blind and visually impaired children, including those with rare conditions like SOX2 gene deletion and bilateral anophthalmia, along with their parents, siblings, educators, and care teams.

SOX2 gene deletion (SOX2 anophthalmia syndrome) is a rare genetic condition where a missing or altered SOX2 gene affects early eye development, often resulting in anophthalmia (no eyes) or microphthalmia (small eyes), and sometimes affects the brain, pituitary gland, and growth.

Bilateral anophthalmia means a child is born without either eye. It is very rare and is often part of a broader genetic syndrome like SOX2. Children typically wear conformers and prosthetic shells to support normal facial growth.

You can donate securely via PayPal at paypal.me/Elioeverafter. 100% of donations support sensory experiences, accessibility resources, and family programs for blind and visually impaired children.

We are based in Houston, Texas, and serve families across the United States and internationally through virtual programs.

Yes. Volunteers, sponsors, schools, museums, and brands are all welcome. Reach out through our contact page to start a conversation.

Yes — virtual support and accessibility services are being launched to support blind and visually impaired children and their families worldwide.

Email cindy.larotta1@gmail.com or call (832) 212-4748. You can also use the contact form on our website.