Bedwetting in kids with CP
Do any of you have kids with CP who have had difficulty with bed wetting?
I'm wondering if my sons issues are to do with our mysterious neurological issue or not. I'm fairly sure that his nevrves aren't speaking to his brain correctly or he has weak core/bladder muscles probably the first because he is fine in the day.
The peadatrican gave him medication and we have just doubled the dose but it hasn't made a bit of difference.
He can be wet 2-3 times a night and each time he is soaking the tablets haven't reduced the amount he is producing at all also he sleeps really heavy so nothing wakes him up we have tried an alarm for about 2 years now.
I was wondering if anyone has any experience of any other medications/treatments.