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/Daily-Life/CF-and-School/For-Teachers/
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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/Daily-Life/CF-and-School/For-Teachers/
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