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

2015-03-09

Peanut Allergy Moms Needed to Take Survey!


I received a request for help finding participants for a peanut allergy study from Adrienne Cotaya, a masters of nursing student at Southeastern Louisiana University. She needs mothers of kids with peanut allergies to fill out a 9 question survey. Ladies, can we help her out?

https://www.surveymonkey.com/s/peanutallergystudy

2013-11-15

Dear Malia


President Obama's signing of the School Access to Emergency Epinephrine Act yesterday included a surprise announcement. The President revealed that his 15 year old daughter Malia has a peanut allergy. After school I told my kiddo that he had something in common with the President's daughter. His eyes got big at the news. "She has a food allergy, too?" He decided to write her a letter.

2011-04-06

Peanut Protest Update

Yes, that's two signs, but it does seem to capture the spirit of the protests!
Here's a quick update for those of you following the news out of Edgewater, Florida, where parents have been protesting the "extreme measures" (i.e. hand washing) being taken to protect a six year old girl with a severe peanut allergy.  Tonight there will be an "Allergy Awareness Meeting" at the elementary school, which I will be attending with others from the Tampa Bay Food Allergy Support Group.

First there's bad news via Tracey Bailey on the Facebook page started to support her and her family during this difficult time.  The school has caved to some of the protesters' demands and are no longer requiring children who have been in other classrooms which are not peanut free to wash their hands upon returning to her daughter's classroom.  This is very disturbing for those of us who rely upon a public school to adhere to our children's 504 and Individual Health Plans to keep them safe.

The good news is that the school is trying to do some public education and is addressing the issue.  The latest I've heard by way of our support group is that there will be a speaker from the local health department, but that neither FAAN nor FAI has been invited.  I do not know if there will be a representative from either organization there anyway.  Hopefully everyone will have the shouting worked out their systems, or at least be hoarse enough to give reasonableness a chance to be heard!

I truly hope that some of these parents who have seen this as a zero sum game, where the needs of another child being met take away from the education of their own, will discover that the effort needed to protect one little girl is minimal, and that their own child benefits tremendously from learning to treat others with compassion and respect.

If you'd like to show your support for the Bailey family and keep up with the news out of Edgewater, you can join the Facebook page, which is now creeping up on 1000 members.  I will also post about the meeting itself in the next few days.  Keep your fingers crossed!

2011-03-25

My Kid Is Special Too*

The front door of my son's school.
In the wake of the parents protesting the food allergy accommodations of a first grader in Edgewater, Florida, I promised a glimpse at my son's Individual Health Plan, which is remarkably similar to the descriptions of the much maligned one belonging Tracey Bailey's daughter.  Unfortunately, my son's I.H.P. is not in the specially designated blue expanding (and expanding and expanding) file that is home to the blizzard of documents my child seems to precipitate every time he comes into contact with our educational system.  So I'm going to describe the most relevant provisions from memory with a few comparisons between the two.

First a big disclaimer and then a little background:  my memory is far from perfect.  My apologies if I manage to misrepresent my son's accommodations, simply because I gapped out a relevant section.  In addition, I have not personally seen Tracey's daughter's health plan.  I am going strictly on Tracey's descriptions and the information given by school officials to reporters.  Plus, our children's schools are in widely separated counties with different policies.

My son's elementary school is both the one closest to our home and the only one at our end of the county with both a full time nurse and a stellar reputation for managing food allergies and other chronic health conditions.  It's something of an unofficial magnet for kids with peanut allergies and diabetes.  So, of course, the school district wanted to assign The Kid elsewhere when he started Kindergarten.  After endless attempts by phone and online to get him reassigned, I spent the better part of a day with mountains of documentation working my way up the food chain at the county administration building to get him enrolled at his current school shortly before the school year began.  (That's a story for another day, but it's amazing what can be accomplished with reasonable requests, supporting evidence and polite persistence.)

Based on the medical information we provided, the school nurse quickly banged out a health plan with relatively little input from us:

  • Every person, whether student, staff or parent, entering my son's classroom must wash their hands at a sink just inside the door.
  • Every student must rinse their mouth when entering the classroom first thing in the morning and immediately after lunch.

I'll be honest; I was truly startled when I saw that the nurse had included the mouth rinsing provision in the I.H.P.  It seemed a little extreme, and was not something that it would have ever occurred to me to request.  This is also the procedure that has sparked the most controversy in Tracey's daughter's accommodations.

Then I saw the mouth rinsing in action.  There is a little water fountain on the side of the sink, and the kids are instructed to "swish and swallow" after they wash their hands.  That's IT.  All they are doing is taking a sip of water from a fountain.  Quite frankly, it's a good idea to encourage kids to drink more water in general here in the Florida heat.  I am at a loss to even understand the controversy about the hand washing, since it's just good hygiene and a basic safety measure.

As far as the time that washing hands and taking a sip of water requires, the protesters have manufactured the statistic that they are required to do this three times a day and it takes ten minutes each time, causing a total loss of thirty minutes from academics each day.

This is pure fiction.  First, it is twice a day, after arriving from breakfast at home and after eating lunch at school, both for Tracey's daughter's and my son's classrooms.  Second, washing up in the morning does not take away class time, since it is done upon arrival before class even starts.

As an update to Tracey's situation, it turns out that mouth rinsing was never actually in her daughter's health plan, and the school had been doing it unnecessarily.  They have since switched to washing the kids' faces, but have never, ever used Clorox wipes on their hands or faces as the protesters have claimed.  [Update:  this change was made before the protests started.]

Originally both plans dealt with lunch in a similar way:

  • At Edgewater Elementary, the students leave packed lunches on a cart outside the classroom, which is taken to the cafeteria.
  • At my son's school, lunches are left on a shelf just inside the door and are picked up again on the way to lunch.  (This is standard, not an accommodation.)
  • Neither school bans any food, including peanuts or peanut butter.
  • Both plans initially called for the child to eat separately from the other students.

This is where we asked for less restrictions than the nurse's plan prescribed.  My son was very upset at being isolated from the other students at lunchtime.  He felt it was a punishment for his food allergies.  So we requested that he eat in the cafeteria in a designated place, which is wiped clean before he sits down.  Children who are eating peanut butter, because of the violence of that particular allergy, or drinking milk, because of the spill potential, just don't sit next to him.  (That's right, 7 and 8 year old children do their part to keep my son safe with awareness and compassion.)  He had an aide assigned to him during lunchtime, but everything has gone so well, that he now eats without the aide.

I am very, very aware of the risks involved in having my son eat lunch with the other students in the cafeteria.  Another child at my son's school with severe food allergies eats in a classroom with a friend of his.  My thoughts are that I would rather have him gradually start learning to function independently in an unsafe world, while supervised by adults who genuinely care for his well being and have appropriate medical training to handle any accidents, but I still worry.

Another of the protesters' complaints is about the lack of sugary treats at class parties.  Here is my son's school's policy related to class parties, unrelated to my son's food allergies:

  • There are only 3 classroom parties per year at which food is served.  The teachers may select which holidays they wish to celebrate.  (Typically it's Halloween, Christmas/Winter Break and Valentine's Day.)
  • No homemade food may be given to the students.  It must all be store bought and clearly labeled with ingredients.

In Kindergarten, the teacher let me know what the kids would be eating in advance, and I'd provide something similar for my son.  So there was unsafe food in the classroom from time to time.  (This also led to some unexpected creations, such as my Be My Valentine Cakes.)

For the last two years, though, the teacher has been simply amazing and allowed me to provide all of the treats for school parties.  (She moved up from first to second grade with the class.)  In addition, she even came up with a workaround, which allows me to bake safe treats for parties.  The school has a full kitchen in the Kindergarten wing, so the day before a class party, I go in with unopened packages of ingredients, such as flour, sugar, etc., and bake on the premises.

In contrast, the first grade teachers at Edgewater Elementary made the following decisions about food in the classroom without regard to food allergies:

  • They eliminated snacks due to the early lunch time at 10:45am, as did the fourth grade teachers for the same reason.
  • They decided to do crafts instead of eat treats at holiday parties as part of the school's focus on healthy living.

Here's the real difference:  the other parents in my son's class have been nothing but supportive.  They have repeatedly expressed their concern for my son's safety and their appreciation for the goodies I provide.  At Edgewater Elementary the parents have blamed a six year old girl for school policies unrelated to her disability.  They also protested outside her elementary school with inaccurate information about her accommodations without either verifying her actual health plan or approaching either the school administration or the child's parents appropriately.

I truly believe that while plans to protect children with food allergies are critical, the people who implement them are even more important.  Education about food allergies is meaningless without a willingness to be educated and the compassion required to keep a small child safe by something as simple as hand washing.

Update:  A Facebook group has been started to support the Bailey family, if you'd like to join us.

*In case you were wondering, the title is in reference to this picket sign:

2011-03-12

A Little More Education

So very many of you have asked if there is absolutely anything that can be done to help the family being harassed and bullied about the food allergy accommodations their daughter receives at her elementary school here in Florida.  I finally do have contact information for the school and district, as well as state level agencies, where you can let your opinions be heard, as well as a request from Tracey, the mom.

First, the bad news:  other parents have written so many disturbing comments online in response to local news articles, such as threats to put peanut oil on their own child's backpack, that the family has decided it is no longer safe to send their daughter to school.  These protesters have successfully managed to bully a six year old out of school, because of her disability.

Before I set all of you loose, though, I want to give you a word of warning.  I can tell you that personally, my blood is boiling.  The temptation to just breathe fire through the phone line is awfully hard to resist.

Then I remember how the story has played out in the media.  Exaggerations and outright lies have been presented as fact in a "controversy" about "extreme measures" that are "depriving other children of their right to an education."

As hateful as these parents are, they have presented themselves with enough media savvy to make it a story about wanting "compromise" about the accommodations, rather than about a pack of bullies endangering a child's life.

The narrative needs to be fixed.

If you are willing to take the time to send an email or pick up the phone to make a call, remember that the recipient is most likely an innocent school or state employee who has suddenly found him or herself in the middle of a hailstorm.  Remember, you are contacting them as a Deeply Concerned Parent, not a Raving Freaking Lunatic.

Just because you know that you are the good guy, doesn't mean that anyone else does.  So make sure that your words and tone demonstrate that.

These are a few suggestions:

  • Explain your concern for this child's safety and well being.
  • Respectfully ask that, although you understand privacy restrictions, that the school speak up to the media to accurately describe the accommodations this child has received.
  • Ask what anti-bullying measures are in place, and how they intend to protect children from this kind of hatred.

Spring break started yesterday in Volusia County, adding even more to the hit and run nature of this bullying campaign, but here is the contact information:

  • Edgewater Elementary School Principal Linda Moore: 386-426-7300.
  • Volusia County School Superintendent:  386-734-7190.  (Follow prompts for operator and ask for Superintendents Office.)
  • The Florida Department of Education:  850-245-0438.
  • James Holland, Director of Professional Standards:  386-734-7190 ext. 20256.  (This one is to report school misconduct, so make sure you have a Specific Complaint, not a Wild Accusation.)

In the comments of the previous post, Kyra was kind enough to also share the district's email contact information:

  • Principal Lynda Moore: lmoore@volusia.k12.fl.us 
  • Assistant Principal Stephanie Eafford: saeffor@volusia.k12.fl.us 

Finally, here is the request from Tracey.  It appears that in some of the comments by parents in the news stories online, there have been details of her daughter's medical plan, however distorted, that could have only been revealed by a member of the school's staff.  If you are brave enough to go on troll patrol, see if you can find any of these comments.  If you find them, please copy and paste the comment or take a screen shot if you can (in case it is deleted) and email it and the link to the page to me at allergiesmom[at]gmail[dot]com.  I'll sift through the duplicates and make sure that they reach Tracey.

Thank you so much for your compassion and zeal in defense of her daughter.


Update:  Many thanks to the commenter who let me know that the email addresses to the school's principal and assistant principal are no longer able to receive email (stuffed full to bursting with your eloquent correspondence, I'm sure) and provided the following contacts:


Volusia County Schools
Superintendent Dr. Margaret S Smith
200 North Clara Av
P.O. Box 2118
Deland, FL 32720-2118
Email - masmith1@volusia.k12.fl.us

Florida Department of Education
Office of the Commissioner
Dr. Eric J Smith
Turlington Building, Suite 1514
Tallahasse, Florida 32399
Email - Commissioner@fldoe.org



2nd Update:  A local newspaper has taken the time to research the story, speak to the family and school officials, and accurately describe the allergy precautions that are in place in the classroom.  Thank you to the Daytona Beach News Journal for practicing journalism instead of sensationalism!


[Post also updated to clarify that threats were made to rub peanut oil on another child's backpack, as opposed to it actually happening.  It was *just* a death threat against a six year old child.]


Yet another update:  A Facebook group has been started to support the Bailey family if you'd like to join.    

2011-03-10

Today's Lesson: Hate and Intolerance


Last night I received my daily update from my online food allergy support group based here in Tampa Bay.  Normally what goes on the bulletin board stays on the bulletin board and I don't post it here on the blog, but Tracey, the mom, has given permission to share her story.  I am just sick to my stomach at what this family is enduring.

A first grade girl in Edgewater, Florida, has a life threatening peanut allergy.  The school is making appropriate accommodations based on her physician's recommendations and the Section 504 requirements of the Americans with Disabilities Act.  The kids wash their hands and rinse their mouths upon entering the classroom in the morning and after lunch.  Food is not permitted in the classroom.  Mom supplied allergen free treats for a Valentine's Day party for the entire first grade, though, so that everyone could celebrate.

So far, this is almost identical to my son's classroom.  What happened next couldn't be more different.

A group of parents decided that their children's rights were being infringed upon and picketed outside the school yesterday and today against the food allergy accommodations being made for a first grade girl.

I'm just going to stop here for a minute so you can go read that last sentence again.  When you're done yelling at your computer, come on back.

If you've calmed down, I'm sorry, because this story only gets worse.  This group of parents is out spreading wildly inaccurate rumors (what I like to call lies) about the actual accommodations.  They claim that Clorox Wipes are being used to clean the children themselves, not the counters.  (Wrong.)  They say only the girl is allowed to bring outside treats.  (Those would be the treats her mom purchased for the party for their children.)  They are upset a peanut sniffing dog was in the school with their children.  (The dog was scheduled for next week, but not during school hours.)  They claim that other kids are forced out of the nurse's office so she can make phone calls home.  (I don't even understand that one.)

These parents aren't just intolerant and uninformed, they are wildly inconsistent, but then no one ever said that hate was rational.  In the video below, one of these mothers manages to complain that her child is being deprived of valuable educational time for hand washing AND that her child cannot have the classroom parties he or she deserves.  Which one is it?  Not enough academics or not enough party time?  And are you really opposed to hand washing?  (Don't even get me started about the picket sign that said "happy median" instead of "happy medium".)

Video by WKMG Orlando Local 6

Then the media began reporting on what they are calling a "controversy".  In the Channel 13 video, at least the reporters took the time to speak to the family and share their side.  The online story, though, has a dreadful, alliterative headline about "peanut panic" and ran a poll in the sidebar to their story that could have been written by one of the protesters, asking "Should one student's medical condition impact the entire student body?"  They received enough complaints that they eventually changed it to "Do you agree with the school district’s response to the student’s peanut allergy?" but kept the results from the previous, biased question.

The Orlando Sentinel mom blogger Koshii Eslinger must have thought she was taking a balanced view by calling both sides "extreme" in her Mom at Work post.  She suggests that Tracey take her inconvenient little girl elsewhere, either private school or home school, but it's because she's such a good parent that she would do anything to keep her daughter safe.  To their credit, the protesters aren't actually trying to run a child out of school, they just want to endanger her life while she's there.

The one sliver of good news in the middle of all this hatred is that Tracey's daughter happened to be home sick for yesterday's protests.  Her parents decided to keep her home today, as well, upon learning about today's planned picket.  So she missed school to protect her from these parents' outrageous, bullying behavior.  Fortunately she also missed an opportunity to watch the news coverage with her classmates when the teacher decided to show it on television today.

I'll wait here for you to finish yelling again after that last sentence.

I've been hesitant to speculate upon the role of the school's staff in stirring up the protest, but I'm starting to suspect that there might be a lack of compassion and judgement among some members of the faculty. 

The most ironic part of this wildly misreported narrative is that it all occurred on the same day as the White House began a conference on bullying prevention.  I've discussed the painful prevalence of food allergy bullying before, but part of the difficulty in this story is that it is being treated as a disagreement, rather than a naked attempt to bully a child with a disability.  If these protesters were opposed to the inconvenience of having their children walk around a wheelchair ramp or upset that a disabled child has a "special" bathroom stall with handrails, they would, quite frankly, have been immediately recognized as a bunch of loudmouthed jerks trying to push a school district and an innocent family around. 

Instead we are being given a vivid demonstration of how to teach a child to become a bully.


Update:  Here's the flyer the protesters were handing out.




2nd Update:  To clarify, these descriptions of the allergy accommodations by the protesters are NOT ACCURATE.  They are mischaracterizations, exaggerations and flat out lies, twisting the facts into a parody much like this sign.




Update the third:  I finally have a post up accurately describing the food allergy accommodations at two different Florida schools for Tracey's daughter and my son.  Also a Facebook group has been started to support the Bailey family, if you'd like to join.

2009-09-30

Cloudy With a Chance of Meatballs

The new movie Cloudy With a Chance of Meatballs features a character with a plot pivotal peanut allergy, which has created a veritable blogstorm about Sam Sparks, the anaphylactic weather girl. [Spoiler alert!]


Most of the unhappiness is focused on the movie's cartoon depiction of an allergic reaction. Sam is thwarted by a gauntlet of pointy peanut brittle from accompanying Flint Lockwood in a quest to turn off his planet endangering invention. As Sam lowers Flint with a licorice rope toward the climatic confrontation with his machine gone amok, she receives a cut on her arm from the peanut brittle, causing the left side of her body and her entire face to blow up like a balloon. Initially she doesn't want to leave Flint, but he plummets away after gnawing through the licorice, and she is whisked back to their flying car by another character, where Manny, the camaraman/physician/pilot is waiting with a dose of epinephrine. He injects her leg, she gasps and sits up, then flies away unscathed.
Some of the concerns are due alternately to the scariness or humorousness of the allergic reaction. Others are to Sam's inexplicable failure to carry her EpiPen with her and her reluctance to leave Flint to seek treatment. Some moms are worried that kids who watch the movie will want to see an allergic reaction for themselves, and attempt to cause one in a peanut allergic child, which is a truly terrifying thought. Food allergies are serious, and tend to take up a huge amount of brain space for those of us who live with them. In the case of this movie, though, it might be worthwhile to step back and take a look at the bigger picture.
Sam's peanut allergy ties into two of the movie's themes: the problematic relationship of consumers to food and the destructiveness of denying one's true nature. The impetus for Flint Lockwood to create his machine, which converts water to food, is the closure of their island's only industry, a sardine cannery. With the movie's typical light touch, the residents of Swallow Falls do not go hungry, rather they are forced to eat sardines, which are "super gross." The success of Flint's machine and his accidental creation of "food weather" allows Swallow Falls, renamed Chew and Swallow, to indulge in a smorgasbord of excesses.
Food lying on the ground is whisked away by another of Flint's inventions, the "Out of Sight, Out of Mind-er," which flings the remains to Mt. Leftover, the humongous pile of food behind a virtually unbreakable damn. Unfettered access to candy has some predictable results on the town's children and the gluttonous mayor with his creed of "bigger is better" eats himself to his own destruction. In this context, Sam's anaphylactic reaction is another example of food as a danger to the consumer.
Sam and Flint share a common trait in their feeling of being outsiders due to unusual interests. Flint copes by isolating himself in his lab with his monkey Steve (voiced by Neil Patrick Harris) while Sam has chosen to play dumb as a perky intern by hiding her interest in hard science. Shortly after meeting, Flint feigns a peanut allergy to impress Sam, as both characters attempt to impress each other by pretending to be different from their actual selves, who are in fact ideal for each other.


Flint's willful blindness to the machine's dangers in his desire to be a hero to his community and Sam's struggle to continue on in their attempt to stop the oncoming food storm despite her reaction to the peanut brittle are both doomed to failure. Only when the two characters accept both their strengths and their weaknesses do they succeed. Sam gives voice to her inner scientist to warn of the impending danger and uses her meteorological expertise to navigate the flying car through the storm. Flint embraces his inventory of wacky inventions to find the tools he needs to turn off the machine and return safely to earth. In a fantastic world of flying cars and food from the sky, Sam's peanut allergy serves as a surprising reality check.
After the movie was over I was impressed by the food for thought included in a cartoon which held my six year old spellbound. During the movie itself, I was continually distracted by the damage potential to my highly allergic child of the food falling from the sky. Cheeseburgers? Beef and milk. Drifts of ice cream? More milk. The morning forecast for sunny side up? Eggs. Shrimp larger than a cartoon character's head? Shellfish. That's some serious prawnage!
So what did The Kid think of Cloudy With a Chance of Meatballs? "I liked it a lot." What was his favorite part of the movie? "When Steve [the monkey] was chasing the gummi bears around." Was it scary when Sam had an allergic reaction to the peanut brittle? "Don't be silly! It's a movie, so it's make believe, not for real! Can we have meatballs for dinner? I want to help!" Absolutely.

2008-05-28

Allergic Reaction at School

Yesterday, after two full school years of pre-school minus one week, I finally got the phone call I'd been dreading since the first day: my son had had an allergic reaction immediately after eating his snack. Until now, every aspect of his schooling had far exceeded my expectations. His teacher has taken him from learning his alphabet to beginning to read short words. His therapists are top notch, much better than I had thought I'd find in the public school system. The Kid has thrived in this environment, and both his teacher and the two aides she's had have been extremely vigilant in protecting him from food allergens.
On the phone, his teacher said that The Kid had broken out in hives on his face and neck. She described them as "really horrible" with white spots in the center like blisters. They had given him Benadryl and the hives were starting to fade. At that point, they weren't sure if he had eaten something or if it was a contact allergy, since he was scratching and rubbing his neck when they noticed the reaction.
By the time I reached the school, the hives were much more faded, but still visible, and my little boy was pretty drunk on the Benadryl. The teacher and aide had searched the room and rechecked the snack and discovered that the pretzels he had eaten were "manufactured in a facility that also processes peanuts." They had read the label, but had stopped after reading the major allergen labeling about wheat and soy ingredients. (I have mixed feelings about the labeling requirements for the eight major allergens, but I'll save that for a different post.) I took him home, fed him lunch, and watched him like a hawk for the next four hours in case of a secondary reaction.
I didn't realize how much the day had stressed me until my husband came home and I promptly took a nap/fell into a coma. After dinner last night when the Benadryl had worn off, The Kid and I talked about the reaction. This is the first one he's had in about a year and a half, so his language skills have advanced enough for me to get more of his perspective. He described the hives as "buggy bites," which surprised me. (We usually say either bugs or insects, so I'm not sure where he got the phrase.) He also said that they hurt, rather than itched. Then we talked about what he has to do if it happens again.
I got out the Epi-Pen trainer and we practiced using it and I explained how it works. In case of a reaction, his job is to find a grown up and ask for help as fast as he can. If the grown up doesn't understand or listen, he is to point to his medic alert bracelet and just ask for help and not to take no for an answer. (The Kid's language skills are excellent, but he has articulation problems that sometimes make his speech difficult to understand.) I am terrified that a teacher might just tell him to sit down and be quiet when his life is literally on the line.
After talking with his allergist's office, I've decided to make some changes in his medical instructions for next year. We've controlled all of his reactions with Benadryl until now, so I had given the school instructions to use that unless his breathing was affected, in which case they were to give the Epi and call 911. Next year I'm going to have them immediately use the Epi-Pen in case of reaction, rather than the approach we use at home. The location of the hives on the neck and face especially worries me, since I suspect that if The Kid is exposed to even a slightly larger amount of peanut, he could have a reaction that might stop his breathing. (Just typing those words makes me shake.) I'm also only going to allow food that has been brought from home or had the label checked by my husband or me.
I was already worried about beginning Kindergarten. Now I'm terrified. It's been long enough since The Kid had a reaction, that I was starting to relax. Not anymore. I'm just hoping that yesterday's reaction will at least help us prevent another one.

2008-05-14

A Walk in the Park

Living in Florida, there are certain dangers that we expect and prepare our child to avoid. As the parents of a food allergic child, we also teach him to avoid substances that are harmless to others, but are as deadly as an alligator to him. The Kid and I went to our favorite park to play and maybe see some wild animals (last time we saw and HEARD some great blue herons mating in a tree) and instead had an unexpected scare.
We went on a nature trail that we hadn't been on before, found a great view of the lake, took some pictures, and prepared to sit down and drink some juice. The Kid started to clamber up onto the bench, then stopped and backed away. I looked over and saw a round object in a wet spot. "What's that?" I asked casually. The Kid replied, "A peanut."
I looked more closely. It really was, and my son had spotted it before I did. I wiped off the wet spot on his arm with a baby wipe, double checked the epi-pens in the backpack, and we went in search of another bench.


We followed the boardwalk deeper into the marsh, until we got to the next bench. It was surrounded by peanut shells and fearless squirrels. This time we just turned around and went back.
The incident left me with mixed feelings. I know it's irrational to expect a world that eats peanuts to clean up after itself for the sake my allergic child, but that doesn't stop my anger at the lack of consideration at a park where children play. I'm also very proud and hopeful that he's demonstrating an ability to navigate a dangerous world. It's so much to expect of a four year old, but he saw the peanut, correctly identified it, and backed calmly away. All the talks, the flashcards, the quizzes in the grocery store; all the craziness that he thinks is normal and I know is not; it all paid off at the park.

2007-12-08

A World Full of Peanuts

When I first started this blog, I didn't feel like sharing our experiences with The Kid's food allergies. There are some very good mommy bloggers out there writing about the extreme parenting required to keep a child alive in a poisonous world. I just wanted to organize my recipes for myself and make them available to others, since they had required so much time and creativity to develop.
Yesterday at school we had our first close call, and I am still shaken. Until now, I've been so rational about my child's food allergies. He has a host of other medical problems (which I did not want to expose to the world to protect his privacy), so I've just treated it as one of many menu items.
The Kid attends a varying exceptionalities Pre-K program at a public school. His teacher is absolutely amazing. She has managed his food allergies virtually without incident for the last year and a half. Usually I take The Kid to his classroom in the morning, then leave. Yesterday I was still there, speaking with his teacher. The children had all left the classroom with their aide to go to P.E. As they walked through the school lobby, they went by a table that was littered with peanuts and peanut shells, and The Kid automatically put out his hand to use the table to balance himself and ran his hand across the table.
Fortunately, the aide saw the peanuts on the table, and pulled my child away, probably before he came into physical contact with the peanuts. My friend Erica, whose son is also in The Kid's class and has a mild peanut allergy, was walking with the group and ran him back to the classroom and brought him to the bathroom to wash his hands, while explaining what happened.
He didn't have a reaction, but it would be fair to say that I did. The only thing that had kept my child safe was the quick actions of two adults and sheer dumb luck. After the peanut debris had all been cleared away, I spoke to the school principal, who was fortunately very responsive. When I asked what steps were going to be taken to prevent this from happening again, he suggested banning peanuts in the hallways and common areas. I felt that that was impractical, since not only did that require elementary students to read food labels, but it only banned peanuts, and that is far from the only food allergy that The Kid and other students have. The principal then agreed to ban all food and drink from the common areas and playground.
At the time, my topmost thought was that this was probably insufficient to keep my child safe, but in retrospect, it is a fairly large step for a school to take. I've also realized that in my zeal to keep The Kid away from allergens, I've failed to teach him how to identify some of them. He can recite his food allergies, and sometimes remembers that he cannot accept food from anyone other than certain adults, but most likely he cannot recognize a peanut on sight. I think I'll check the allergy sites for flashcards of foods he can and cannot eat. If I find a link, I'll post it.

Note: Thanks to PublicDomainPictures.net for the peanut photo.
Update:
Here are some homemade flashcards, which we've put to good use. I ask what the food is, then whether or not it's safe to eat. If it's not, we sing a little song about it, which The Kid loves. (I've never had an appreciative audience for my singing or artwork before. Motherhood leads to a lack of embarrassment about many things.)
Right clicking on each picture will allow you to save the image, which can be printed on an 8 1/2" x 11" page and cut up into individual cards.