25 years ago babies like Hannah with biliary atresia sadly would not have survived. Thanks to research, much funded by CLDF and campaigning by CLDF to ensure children have surgery at specialist units and get the best care, the situation is completely different and we can expect a 95% survival rate for biliary atresia. This is an amazing change in just ¼ of a century. But we still have no idea why biliary atresia happens, so CLDF’s research programme is vital so we can get answers and stamp out diseases like biliary atresia. There will be 60 babies born with biliary atresia each year in the , we want to make sure that all the future families can get help from the CLDF support team, receive information packs and get the essential biliary atresia leaflet, which explains everything. CLDF needs everyone’s help
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