Hi all,
Hoping for a bit of advice from anyone with experience of this.
My 11-year-old son has recently been diagnosed with a nut allergy and our GP has advised that he should now have an EpiPen available for school.
I’d previously read that schools can now hold spare emergency EpiPens, so I assumed they would already have one on site as a back-up. However, when I spoke with the school, they asked me to obtain and provide the pen myself for them to keep there.
I’m not entirely sure what the guidance actually says these days.
Are schools expected to:
- keep their own emergency supply,
- only hold medication provided for individual pupils,
- or is it up to each school to decide their own policy?
We’re based in England.
Would be really helpful to hear how this is managed at other schools, particularly from parents of children with severe allergies or anyone working in education.
Thanks very much