Has anyone had any experience with Laryngomalacia?
My 3 month old has it and now been referred to the children’s unit but just want to familiarise myself with it and see what peoples outcomes are. If you’re happy to share please get in touch.
They said it should develop itself but if not he will need surgery 😳.
She mentioned about speech delays could occur because of it etc so just need to hear some stories of ‘real’ families that have experienced it too.
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