In preschool, I showed the teacher how to use the epipen and it was fine. She accidentally let Ricky eat a peanut butter cracker one day and didn't tell me. I picked him up and when I was buckling him into his carseat, his eyes were black and sunken in and he said his throat hurt and he couldn't breathe so well. He told me he took a bite of a peanut butter cracker. So I gave him water and went up to the teacher and asked her if that was true and she said yes, and sorry. So if I didn't go up to her she wasn't going to tell me - she was going to let Ricky have his reaction with me -with me not knowing. He could've gone into anaphylactic shock in the back seat with me not knowing why and maybe not realizing what was happening - so not knowing that he needed his epipen.
I liked this teacher too. She was fine otherwise, I just didn't like how she treated this situation - and it was obvious to me that she didn't fully understand Ricky's allergy.
Now I'm not a crazy mother. I may be a bit overprotective, but I have to be with Ricky's allergy.
Now in kindergarten they have full days - so there is lunch time. I spoke with the assistant principal and made arrangements for Ricky to have a designated seat and to tell the teacher to check the kids sitting near him - that they be moved if they have peanut butter. There are 3 kindergarten classes and one kid in each class is allergic - one to peanuts and the other just tree nuts. But only if eaten. Lucky Ricky also has contact sensitivity. :(
They have snack time too - and the teachers sent a note saying that snacks with nuts or peanut butter may not be brought to school. The worry is that they will get peanut butter on their hands, touch the same toys, or seats, and Ricky will be exposed, and will have a problem. So far, so good. No problems.
Now he is in kindergarten and is invited to birthday parties. Ricky's doctor said he has to have his epipen with him at all times - at play dates especially - she said - because people will accidentally give him something that has nuts or was made on the same equipment, and he will have a problem. So there you have it.
Ricky is invited to a birthday party tomorrow at Chuck E Cheese. Most of the boys at this age navigate their way around that place by themselves or with another pal. Their parents usually drop them off and come back later. Ricky likes me to play some of the games with him. I don't want to be a hovering mom, so my mom will actually take him the party and stay on the sidelines with his epipen and benadryl in her purse. Then I don't have to teach the hosting parents how to use it, etc. ("....and you just push this and stick the long needle at a 90 degree angle into Ricky's thigh - hard enough so it goes through his jeans...") I feel like I should take a break from being there so the boys don't think Ricky always has to have his mom around. Having Grandma hover is a good switch. This way Ricky is protected and I know he's in good hands.
When Ricky is older he will eventually learn how to use the epipen himself and will have to keep it in his pocket while he's at school. In the meantime, since he's just a kid, an adult has to be around to use it. Ricky hasn't been invited to play dates at all this school year - and I'm wondering if the epipen thing is the reason why. We've been so busy, it's almost better that we've hosted.
Besides the teacher, it's come to my attention from being dumped by Mandy that many people do not fully understand the severity of this allergy. I mean, a good friend of mine told me that I was overprotective and crazy for sending Ricky's epipen with him to a birthday party - and that I better not give the parents the epipen at play dates. I mean, she DUMPED me over this. You can read about here and here. What floored me is that she used to be a teacher. Obviously to me now, a crappy one. I realize now that I did a bad job explaining the details of Ricky's allergy to my mommy friends. When we'd get together, it is usually chaotic, and trying to keep up any kind of conversation is challenging. Talk is usually choppy.
When I was going through secondary infertility, I sought out bloggy moms who were going through the same thing. I got ideas from them, and they supported me too. I now realize that I should really try to find others out there who have kids with peanut/tree nut allergies - and learn how they handle situations at school, sports, and every day. So I'll be looking at groups, blogs, and boards. Just like SIF, I'm sure I'll find some people out there with lots of good ideas. I could use some.
1 comment:
I have severe allergies to Aloe Vera. DO you know how hard life is with that allergy? Almost as bad as nuts.
Lotions, tissues, hand soaps, heck even socks are infused with Aloe! My hairdresser had to find me Shampoo and Conditioner that does not have it. When I registered for baby gifts I put on my register that I had the allergy...I can not tell you how many people bought me wipes....with aloe in them!
I feel your pain. It is much worse with a little one because they do not know better and want to do the same/fit in with friends.
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