The CDH Mum - Talking about congenital diaphragmatic hernia

My baby, Alfie, was born with a congenital diaphragmatic hernia. He has his life-saving repair at 10 days old. Alfie is now 4 months old and is still reliant on a nasogastric tube for feeds as he hasn’t established feeding yet. If you haven’t already, take a look at my other videos relating to Alfie’s journey, on my channel. Thanks for the support!