Mission
THE FORE HADLEY FOUNDATION WAS CREATED TO DRIVE AWARENESS AND GENERATE FUNDING FOR FAMILIES AND CHILDREN AFFECTED BY CONGENITAL DIAPHRAGMATIC HERNIA (CDH). CDH IS A RARE BIRTH DEFECT THAT EFFECTS ROUGHLY 1 IN EVERY 2,500 LIVE BIRTHS PER YEAR WORLDWIDE, WITH A CURRENT SURVIVAL RATE OF ONLY 50%. FOUNDED IN 2016 BY RYAN AND KATIE BUSH AFTER THE LOSS OF THEIR DAUGHTER, HADLEY, TO THE DEVASTING BIRTH DEFECT. THE FOUNDATION IS DEDICATED TO ENABLING AND SUPPORTING THE MEDICAL RESEARCH COMMUNITY AND AFFECTED FAMILIES BY PROVIDING FUNDS AIDING BOTH RESEARCH AND RECOVERY. THE ORGANIZATION IS DRIVEN TO MAKE A DIFFERENCE BY PURSUING THE CAUSE OF CDH AND NEW INNOVATIVE METHODS FOR INTERVENTION OR TREATMENT. PROVIDING CDH SURVIVORS AND/OR THEIR FAMILIES WITH OPPORTUNITIES TO EXCEL THROUGH CONTINUING EDUCATION SCHOLARSHIPS, AND OFFERING FINANCIAL ASSISTANCE TO ENSURE THE PROPER CARE NEEDED FOR A CHILD DIAGNOSED WITH CDH. WHILE HADLEY KATE MAY NO LONGER BE WITH US PHYSICALLY, HER LEGACY WILL ALWAYS BE