Before our darling granddaughter Poppy was born last September I had never heard of TOF/OA  The TOFS charity provides support for those born unable to swallow due to the rare congenital conditions Tracheo-Oesophageal Fistula (TOF), Oesophageal Atresia (OA) and associated conditions. TOF/OA affect one in every 3,500 babies and can only be repaired not cured. When new parents hear the devastating news that their precious newborn baby has TOF/OA they want to be there for them. From that first moment, to living with the condition as adults, the charity offers vital support and friendship along the way. Thank you so much for helping me to support their members.