In 2007, ISF was established through Isabella’s parents to raise awareness and research funds for Neuroblastoma and received its 501(c)(3) status several years later. At the time, Isabella’s parents were in hopes that ISF could help fund research projects to potentially save Isabella’s life. Although Isabella is no longer with us, we hope another child can be saved and will continue to raise money and awareness for the awful disease that stole her life.
ISF is dedicated to improving rare pediatric cancer treatment options in an effort to increase survival rates of kids with cancer. Over the course of twelve years, ISF has funded nearly $4 million toward expanding the scope of research and treatment and supporting families dealing with cancer in a variety of ways.