My Nonprofit Reviews

At my 20 week ultrasound my world was turned upside down. My fist child was diagnosed with a birth defect. This birth defect was Congenital Diaphragmatic Hernia and he was given 50% chance of surviving. I then googled information about CDH and found Cherubs. I signed up their forums and was instantly connected to support system that has helped me through my whole journey, expecting, birth, and grief, when we lost him. They have created a whole connected CDH community that is very supportive. They are very active in all aspects of raising funds for research and support and everything under sun in raising awareness. They help many families not feel alone and fight hard to get progress in helping CDH families and future CDH babies.