It's that time of year again... I usually send a brief note to the school nurse or counselor explaining DS has CF, indicating he first and foremost is a normal child who just needs a couple extra things to keep him healthy --- his enzymes, that he may need for water/salt on hotter days, bathroom breaks, shouldn't be around other people wcf…

Here are a couple links I've found handy to make available to the school at the beginning of the year.

http://cfri.org/wp-content/uploads/2018/03/CF_in_the_Classroom_12.1.15.pdf

https://www.cff.org/Life-With-CF/Dai.../For-Teachers/