It's pretty serious when you have to wear one of these on your wrist (it's a medic alert bracelet). We've had many conversations about that you wear it in the bath, in the pool, to bed, to kindy... everywhere! It's on tight enough that he can't get it off, but loose enough so he won't outgrow it by winter. On the back it says "anaphalaxis dairy" and has a phone number to call and an id number. He's been at morning kindy for two weeks now and is LOVING it. Pretty tired though.
Eating with friends and not sharing food is becoming more of an issue for us because they take a packed lunch twice a week. I'm going with one of the teachers to an allergy seminar so we can make sure the kindy is doing what's best for everyone. There's another wee girl there who has anaphalaxis with egg, plus someone with peanut allergy too. It really is a constant underlying stress that we live with. I worry that he'll struggle with making friends when he's older if their parents are scared to have him come to play or he'll be left out of parties :o( I don't even want to think about school camp!!