Hi, I agree about the IEP. This is the best tool you can have. We have had issues with dehydration, food,coughing and bathroom breaks. I was told to request an IEP meeting and we sorted out what he needs and what the school should and could provide. We got the scripts and letters from the clinic and it is all in his file. The school nurse ( our angel ) made a care plan that will follow him and now the teachers have a point of reference.
We now have a day where gatorade, snacks and boost are provided as he needs them.He gets extra bathroom breaks ( without the obscene questioning ) and the teacher makes sure he always has his gatorade outside and they know what to look for with dehydration.
There is also a packet you can request either via your clinic or the cf site that is specificaly for teachers and caregivers. It is very helpful !!!
Oops before I forget, when you have your IEP meeting make sure the cafeteria director is there( for the extra and specific food cf kids need ) we did this and now we get to personalize his menu with good old fashined hight fat, high calorie junk food <img src="i/expressions/face-icon-small-happy.gif" border="0">
Hope it helps !!! Good luck !!