Our daughter has just been diagnosed with the condition after 9 long years of being told 'she's just a kid with a runny nose!'
We have been given the PCD support website, so we are just learning what its all about. Our daughter has been given an 'acapella device' to use twice a day to start with for physiotherapy and we are due a visit from the physio in a few weeks time.
As parents, we are feeling a bit bewildered by all the information and not really sure what we should and shouldn't be doing to help our daughter.