Olsen is diagnosed with Pfeiffer Syndrome, which is a rare genetic disorder effecting the the skull, hands and feet, as well as causing bulging and

Together with Molly Tango Foundation, we were able to provide Abigail with an adaptive stroller and Hoyer lift. Mom and Dad no longer have to

Our friends at Leah’s Foundation in Wethersfield introduced us to a 6 year old Linda who is battling Leukemia. Linda, along with her parents and

A loving couple with 3 young children selflessly accepted custody of their wonderful teen aged nephew living with a diagnosis of Duchene Muscular Dystrophy. Costs

Diagnosed with DIPG (a rare and aggressive form of brain cancer) Maven had her first surgery and infusion in 2017. Sadly, Maven lost her battle

Cherish the Children Foundation has assisted a lovely young single mom meet some critical living expenses while advocating for her 2 year old son Michael