Showing posts with label peanut allergy. Show all posts
Showing posts with label peanut allergy. Show all posts

Wednesday, July 13, 2011

Don't Send in the Clowns

I still have a few wedding things I'd like to share, but something happened this weekend that I want to post about while it is fresh in my mind.

If you know me on Facebook you may already have gotten the very short version of this story, feel free to skip ahead.

Harper had been invited to a birthday party for this past Sunday afternoon. We were sort of surprised to see the invitation because it was for a friend from preschool, someone we hadn't seen in over a year. I made the awkward phone call to RSVP which, for me, always entails asking about the food that would be served. As it turns out the birthday girl also has nut allergies - my initial reaction was that it would be the easiest birthday party ever, no need to worry about food. But then the mother went on to tell me where the cake was coming from - a local place that is not a nut free bakery. In fact, it was the same place that made the cupcakes for my brother's wedding. And we were told, very definitely, that the children should not eat those... Even the pretzels they served were a brand we NEVER buy because all the products have cross-contamination warnings on them. Everyone handles food allergies differently - and that alone is a topic that I could go on and on about. Fortunately this is NOT a post about Harper having a reaction to food at a party!

The birthday party was at a local park and the big entertainment was a clown/magician. Shortly after the party began, as most of the adults sat together under the picnic shelter, the children gathered in the grass to watch the magic show. A few minutes into the show, Harper was suddenly at my side, absolutely hysterical. She was sobbing and clinging to me and for what felt like a long time I could not, for the life of me, figure out what had happened. I worried that she'd been stung by a bee but I had no idea what she was saying.  She was causing such a ruckus that I ended up walking her away from the picnic shelter to try to help her calm down.

I finally figured out she wasn't hurt, but she was emphatic about not going back over to the magic show. After lots of calming I heard Harper say something about the clown/magician having peanut butter. I thought maybe the clown was using peanut butter as a magic word. Then Harper insisted the clown had a peanut butter sandwich - what place a peanut butter sandwich had in a magic act,  I couldn't imagine. Surely it wasn't a real peanut butter sandwich? Just then the father of the birthday girl approached us to see if we needed anything - he clarified for me that the clown did, in fact, have a peanut butter and jelly sandwich. Apparently the birthday girl, who is allergic to nuts, was asked to hold it at some point (And she did, and was fine, but yikes!).

After a little more conversation I realized that the clown had told the children that if they did or said a certain thing, she was going to open the sandwich and spray them with peanut butter!

Spray them with peanut butter.


Now, I am sure the clown never intended to actually spray peanut butter at the children, but I certainly understand why Harper reacted the way she did. Incidentally, aside from Harper and the birthday girl, there was another child at the party with nut allergies. While I realize the world is always going to have nuts in it, I'm thinking the clown may want to drop that bit from the magic act.

Once Harper calmed down and I promised to sit with her for the rest of the magic show (one of the other parents assured us the peanut butter portion was over). I was really, really proud of Harper for deciding to stay and have fun with her friends. If she had asked to leave (I mean after her initial panicked reaction) I probably would have taken her home.

As I sat with her in the grass, watching card tricks and appearing bunnies, I had to work pretty hard to hold back my own tears. I couldn't stop thinking about how terrified she must have been, thinking she could be sprayed with peanut butter at any moment, worrying she was about to have a reaction.

The rest of the afternoon passed without further incident - all's well that ends well I guess. And Harper did come home with some pretty awesome mermaid face paint:

Monday, March 21, 2011

Bummer

The first time we sat down to eat ice cream together as a family I cried.

It was the first time were able to go out for ice cream together. Because of Harper's peanut allergy most ice cream places are completely off limits. Then, a few years ago, a seasonal place opened not far from our house. It sold ices, frozen custard, and was nut-free! I will never forget the first time we sat at one of those tables with Harper and enjoyed our treats.

For several weeks we've had the opening day (this past weekend) marked on our calendar and have been gearing up for the first visit. Of course that was before we found out we could no longer go there. Yesterday we found out they've added all kinds of peanut containing products to their stores and it really isn't safe for us even to walk in any longer. Boo.

Now I'm not going to jump up and tell people to send angry letters or boycott the store (you'll notice I haven't even mentioned their name), but we are so, so disappointed.

There are very few places where we can enjoy a meal or snack out with Harper and it is really too bad when we have to cross another one of off our list. Being able to take your kids out for ice cream in the summer is such a simple pleasure and one we really enjoyed, at least for a couple of years.

I will admit that I shed a few tears yesterday when I found out about the menu changes. I know it is silly to cry over something as inconsequential as not being able to go back to an ice cream place, but I think my tears were more about the barriers Harper's allergy represents for her, for us as a family. There are so many normal things that we have to think twice about doing. And I worry often about the ways Harper might be limited as she grows. I know that having this allergy doesn't mean that she won't have a full and happy life, but it is difficult not to feel discouraged now and again.