This is a story that I hear quite frequently and I would love for all parties involved to be polite.
I am aware that peanut allergies, as are all childhood allergies are serious. So please, no comments about me not being concerned or knowledgeable.
NUT AWARE SCHOOLS
My children go to a "Nut Free" school which has changed to a "Nut Aware" school since the school cannot guarantee that it is "nut free". So, more or less, no peanut butter sandwiches allowed--no vital protein (that doesn't spoil) at lunch. There have been stories about lunch ladies taking Skittles away from children because they are made in factory that also makes M&M's. We call the lunch ladies Peanut Nazis because they embarrassed and humiliate the children who bring in the Skittles too.
PEANUT TABLE:
The parents tried to change the peanut butter ban by politely asking for a peanut table so kids could have peanut butter and no one would feel left out. This proposal was turned down by the teachers. In our school, two children out of 350 have nut allergies.
About 80% of the parents of children with allergies behave in a very militant, controlling way. At one time, our school even hired an AIDE for a child ($35,000*5 years=$175,000) to follow this child around so he would not eat peanut butter. One mother even cried and said that if her child had to sit at a "peanut free" table, she might feel "left out." These parents would rather control the system to accommodate their child (348 people cannot have peanut butter vs. your child sit at a peanut free table) than educate their child to function in society. Think of the child walking around our school who is blind and really feeling left out--now doesn't the whining about being left out at lunch seem rather small?
HEALTHY PARENT RESPONSE TO PEANUT ALLERGIES:
We have several friends who have children who have sever allergies. At an early age, they taught them to read labels and never to eat anything given without the label attached. Their approach was teaching the child to function in society vs. have society accommodate their child. Doesn't this sound healthy?
Here are the PPPG guidelines on how to behave if your child has an severe food allergy or a friend's child has an allergy:
1. Stop worrying about how your child feels every moment. If your child feels left out, it is because you have made them feel this way by controlling the situation for them. Bring your own snack vs. making the entire class change their snacks to accommodate your child.
2. If your child is a guest at a birthday party, ask if it is ok to bring your own food.
Do not expect the hostess to make a special meal for your child nor a special cake. Your child's social invitations may become limited because it is more effort to accommodate your child.
3. If you are having a party and a child has an allergy, make every effort to accommodate this child. It does not mean you need to change the special meal or cake that your child is dreaming about, just make an effort to show you care.
4. Do not ask the entire world to accommodate your child. My husband was on an airplane that the flight attendant made an announcement saying that they were not serving peanuts because a child on board had a peanut allergy. Basic safety is totally acceptable to request and having EPI pens around is necessary and all will be willing to help here. For our class snack, one mother sent a list of snacks her child may have--which included about three. So, the class will be eating crackers all year because this the only food allowed.
I do not mean to sound harsh and I do think it is kind to accommodate people with disabilities. I think the allergy issue craziness is from educated parents who want control and feel horrible about their child's allergy. A parent asked for kids not to bring peanut butter on the bus at our private school and guess what, the school said...sorry!
If it is so serious, why would you risk your child's life by sending them to school because there are no guarantees.
Would love your thoughts--I am sure my post will be controversial!