Hi,
A question for mums of school age kids with excema -
Have any of you faced a problem with your child's excema treatment being administered in their school? Sorry if this is a bit rambling but I'll do my best to make sense!
Our dd has severe excema and she goes to the local nursery which is attached to the local primary. Today her new term started and between now and christmas she is going every morning from 9 till 12. After Christmas she'll be going to school all day.
Last week we saw our GP who said that dd needs her 50/50 cream mid-morning. He wrote a letter for me to give to the nursey staff saying this. The problem is that when I spoke to the staff this morning they said that the school's policy is that they are not allowed to cream dd because of their child protection policy (i.e. they are not allowed to touch her).
At a stretch dd can got for 3 hours without the cream but ideally she needs it every 2 hours. So as long as she doesn't have any major flare-ups we should hopefully be okay until Christmas but I am panicking about how we're going to manage after that. What's been suggested to me is that I come in each lunchtime to cream her myself at school. The problem is that I work and I would probably have to give up my job to be able to do that...eeek!
Have any of you faced this kind of situation? Do you think I'm stressing out over nothing? Or how do you think I should approach the staff in order to get the best result for dd? I'd really appreciate any feedback or ideas.
Thanks a million!
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Question about excema treatment in school
6 replies
texasrose · 05/09/2006 21:21
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