What is CHERUBS?
CHERUBS is the world's first and largest CDH non-profit organization. We are truly a grassroots organization - CDH families creating something out of nothing when there was no other CDH group, information and services in 1995. CHERUBS was created to make sure that no family endures Congenital Diaphragmatic Hernia without support or accurate information. Our Board of Directors includes CDH parents, grandparents, survivors, nurses, doctors and the world's top CDH researchers. CHERUBS is run solely by volunteers and donations. At CHERUBS, every CDH family has an opportunity to honor or remember our children while doing good to help others and work together as a CDH community. No other charity in the world has such a respected, educated or experienced group of leaders who care so much about the CDH community.
CHERUBS was not created by one family or for one family. It was not created in honor or in memory of one child. It is, and has always been, a group effort to help all families affected by Congenital Diaphragmatic Hernia. It is built upon the experiences of CDH families, collaborations with CDH researchers and a strong desire to raise CDH awareness through projects and events created in honor and in memory of cherubs. CHERUBS was named for all the babies lost to Congenital Diaphragmatic Hernia.
We are proud to serve over 5700 families in 61 countries and all 50 states affected by CDH since our creation. Through our dozens of free ground-breaking services and the friendships made within our member community, CHERUBS has positively affected the lives of 1000's of CDH families and inspired many new CDH charities and project who have followed in our footsteps. We will continue to lead until Congenital Diaphragmatic Hernia is no more. We are devoted to finding the cause, prevention and best treatments for CDH.