WHAT WE DO
“Since January 2017, the date of Ella’s diagnosis, we have been building a platform for awareness and fund raising to help find a cure for our daughter and every daughter suffering from Rett Syndrome.” - Shaine and Lauren Gaspard
What We've Achieved
To date our awareness and fund raising has reached in territories and countries around the world including United States 🇺🇸, United Kingdom 🇬🇧, Ireland 🇮🇪, Australia 🇦🇺, Netherlands 🇳🇱, Canada 🇨🇦and the US Virgin Islands 🇻🇮 .
We have been recognized and supported by local schools, businesses, Governments and the United States House of Representatives.