Liv4TheCure

Our Story

Liv4TheCure was founded by Stephanie Forman in honor of her daughter Olivia, who faces the challenges of Wolf Hirschhorn Syndrome due to a chromosomal deletion. This organization is dedicated to advancing research and raising awareness for rare chromosomal deletion syndromes, with a special focus on gene therapy and innovative technologies that can enhance the lives of affected children.

Impact

By funding critical research initiatives, Liv4TheCure aims to develop gene therapy solutions that can significantly improve the quality of life for children like Olivia.

Why Donate?

Your donations directly support groundbreaking research aimed at finding cures for rare chromosomal deletion syndromes, helping to advance science and technology that can transform lives.

Get Involved

Join the mission to make a difference! Donate cryptocurrency or cash today to support vital research initiatives and help children affected by chromosomal deletion syndromes. Every contribution counts!