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

“Awareness is more than the color of a wristband, it is educating yourself, your children and your community.” - Shaine Gaspard, Ella’s Dad

“Awareness is more than the color of a wristband, it is educating yourself, your children and your community.” - Shaine Gaspard, Ella’s Dad

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 funding amazing organizations such as RettSyndrome.org and Rett Syndrome Research Trust.  

We have been recognized and supported by local schools, businesses, Governments and the United States House of Representatives.

Ella’s Hope, Inc is a nonprofit organization as described in Section 501(c)(3) of the Internal Revenue Code; EIN 66-0905467