I sit down with Joan Rush, Founder of the Jacqueline Rush Foundation. Joan shares the story of how her daughter was misdiagnosed and finally diagnosed at an extremely young age. Joan and her husband Alan are determined to inform the public & medical community about Lynch Syndrome & help people realize the power of knowing what’s in their genes. We talk about immunotherapy, clinical trials, and the potential vaccine. We also talk about what it's like to be involved in the non-profit world, which is not easy, especially when it's so close to your heart.
