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Showing posts with label ‬ ‬ ‪‎kids with food allergies‬. Show all posts
Showing posts with label ‬ ‬ ‪‎kids with food allergies‬. Show all posts

Wednesday, May 11, 2016

Food Allergens... Where You Wouldn't Expect Them

Until you have to check every single label every single time you buy something, you can't really understand how sneaky allergens can be... creeping their way into things you never ever expected them to show up.   Ingredient lists CHANGE ALL THE TIME so no prepackaged food is ever safe 100% of the time and although we have brands we generally trust, I still have to check it several times and occasionally follow up with a brand's customer service to make sure manufacturing hasn't changed.  Anything with blanket descriptions like "Spices," "Natural Flavors", "Caramel Coloring" is a potential landmine and is usually avoided. 

The Kids with Food Allergies website has a great PDF file that explores some of the hidden allergens that a child might encounter during regular school projects that most folks without food allergies wouldn't think twice about.  They include potential allergens found in play-dough (wheat), glues (wheat), finger paint (wheat), tempera paint (egg), crayons (soy), potting soils (peanuts/soy) and several others.

Some ingredients are obvious: wheat in baked goods, egg in mayonnaise, soy in miso, peanuts in trail mix, etc. Others ingredients are far less obvious.  In the process of reading labels, I've started to discover what products contain allergens in places I might not have expected before.

WHEAT/BARLEY/RYE
Before my obsessive label reading, I didn't realize that these grains could commonly be found in:  

  • Meatballs
  • Soy Sauce
  • Worcestershire sauce
  • Fruit Snacks
  • Licorice
  • Imitation Crab Meat
  • Malt Vinegar (I didn't even know what malt flavoring was before!)
  • Brewer's Yeast
  • French Fries
  • Lip Balm
  • Hair Gel
  • Toothpaste
  • Flouride
  • Gel Polisher (at the dentist)
  • Shampoo & Conditioner


EGG
I used to love eggs.  They were maybe my favorite food.  I even wrote a blog about my love for them many years ago. Even with my egg adoration, I didn't realize that egg is commonly found in:

  • Pasta
  • Ice Cream
  • Sour Smarties
  • Snickers, Three Musketeers, Milky Way Bars
  • Processed Parmesan Cheeses
  • Imitation Crab Meats
  • Ranch Dressing/Blue Cheese Dressing/Thousand Island Dressing
  • Breads (especially if they're gluten free - almost a 100% chance of there being egg in the mix)
  • Crackers (and just like the gluten free breads - gluten free crackers almost always have egg or are made with tree nuts)
  • Some versions of the flu shot and some anesthesia


SOY
Ug. Soy is a legume so maybe it should be included in my next category, but after thinking about how SOY IS IN EVERYTHING, I figured I'd give it it's own section.  I'm only half way joking about it being in everything... when I was on an elimination diet while nursing my son, soy was the most difficult allergen for me to avoid, which seemed so strange because before reading labels, I had always thought of soy as an Asian food ingredient.  Nope. Soy. Is. Everywhere.  Thankfully my son seems to be able to tolerate soy lecthin and highly refined soybean oil which are perhaps the most commonly found soy ingredients and makes things slightly easier for us. Many people with severe soy allergy are not so lucky.

  • Baby Formula (along with coconut oil, soy was in almost every infant formula I researched when I was looking to supplement my dwindling milk supply after returning to work from my maternity leave. Twas the pits.)
  • Candy (Pretty much every major chocolate bar has some form of soy.)
  • Gum
  • Vitamins
  • Deli Meats
  • Chips
  • Pretzels 
  • Waffles
  • Hair gel
  • Shampoo & Conditioner
  • Hair spray
  • Toothpaste


TREE NUTS, PEANUTS & LEGUMES

Most people know by now that peanuts are not nuts.  Peanuts are legumes like soybeans, lentils, chickpeas and green beans. Vanilla bean, cocoa bean, and coffee bean... despite the use of the word bean, are not legumes.  Coconut (which my son is also allergic to) is not a tree nut or a legume, but is thankfully included in the FDAs allergen label laws. Pink peppercorn is not a peppercorn, but a dried fruit from a plant in the cashew family, and can pose problems for people with tree nut allergies. 

So what I'm trying to say is that these three categories are just a cluster of allergy madness.  Some people are allergic to only a single type of tree nut, some are only allergic to peanuts and can eat all other legumes and have no problems with tree nuts, some have to avoid both tree nuts and peanuts but have no problem with legumes, and others can not eat any tree nuts, peanuts, or legumes, and some are only allergic to one single type of legume and can eat peanuts or tree nuts without issue. Currently our son is in the no tree nuts, no peanuts, and no legumes camp.  I wasn't expecting to see these guys show up in:

  • Non-dairy cheeses and milks
  • Gum
  • Plain Cream Cheese (certain food-gums are derived from legumes)
  • Curry
  • Mole Sauce
  • Pesto (clearly I had never attempted to make my own - pine nuts are a key ingredient in pesto)
  • Potting soil 
  • Some prescription eczema treatments
  • Bird food
  • Ant bait
  • Dog treats
  • Soaps

(Although coconut is not a legume or tree nut, I want to add a note here - good luck finding laundry, bath, or body products that contain no coconut or coconut derivatives. It's VERY hard and the products we've found seem to be anomalies on the market, so should they ever change formulas, we'd be stewed - if you need recommendations for coconut-allergy friendly products, message me on Facebook or leave me a comment here and I'm happy to share our list of safe items. Oh, and a baby formula made in the USA that doesn't contain coconut oil? Maybe there's something out there now, but when I was looking a few years ago, I had to import a German formula through the UK to get one without coconut oil because even the prescription formulas my pediatrician wanted us to try ended up having coconut oil in the formulations.)

Lastly, my son is not allergic to the following, but they are in the Top 8 allergens here in the US, and we've accommodated friends with these allergies, so I always try to keep my eyes peeled.

MILK

  • Non-Dairy Creamer (wtf, right?)
  • Deli Meats
  • Medication and some dental applications
  • Toothpaste
FISH/SHELLFISH
  • Milk (yep - fish oil added to milk... for that extra DHA)
  • Marshmallows
Clearly this is in no way any sort of comprehensive list, and I'm not sure one exists, but it just goes to show how easily those sneaky allergens work their way into an ingredient list and why a person with a food allergy will want to check the label of anything they eat before they decide to eat.

Monday, May 9, 2016

Navigating a Social Life with Food Allergies

As I mentioned in my post yesterday, things have changed significantly since my son's food allergy diagnosis.  Having a child alters your social life anyway, but having a child with multiple life-threatening food allergies requires a bit of extra effort and planning on our part (and sometimes on the part of our friends and family) to make sure O is included.  

Many times the safest course of action is to simply turn down invitations to activities that are inherently difficult for us to manage (restaurants, food festivals, carnivals, etc.) In general, think of all the fun stuff you do that revolves around food and assume that unless we've got about a month of lead time to arrange for child care with someone who is trained on O's allergy care and management in our allergen free home, we'll have to politely decline the invitation.

Anyway, here's what we do for the situations that make us leave the safe haven of our home:

Everyday 

Any activity that requires that we leave the house also requires some planning.  Toddlers don't need as much in a diaper bag as babies, but at two-and-a-half, I still carry a fully loaded bag everywhere we go.  It has the basic kid supplies, but it also carries his epinephrine allergy kit, wipes for all surfaces he'll put his hands on, and a full day's worth of snacks.  He might not eat a full day's worth of snacks in one outing, but we don't have the option of eating out if I can't get us home in time for lunch or dinner and if he suddenly decides he's starving, I can't pick up a safe meal for him anywhere. My bag is full of his safe snacks, just in case we end up delayed, lost, stuck in traffic, or lose track of time when we're having fun.


Most Days

Any activity that will have us out of the house during lunch or dinner time means that I've got to pack us all a lunch to eat out. You can see some of the lunches we've packed on my Instagram.  Depending on how long we'll be out, if I'll have access to a microwave, or if I'll be able to refrigerate our food will determine what I can pack.  If we're planning a full day out or to different stops, then I pack us all a lunch and dinner to-go and try to pack things I know taste good at room temperature and don't spoil easily.  If we're doing someplace fun like Disneyland (which is considered an allergy haven for many people thanks to their recent efforts to be inclusive of food allergy families), I pack double the amount of hand wipes and I'm also sure to pack some cookies or a cupcake from Sensitive Sweets so we can have a special treat too.

I avoid my son's allergens when I'm with him.  Part of it is so he doesn't feel like he's missing out on anything, but the bigger reason is that it's easier for me to manage his risk of contact if I'm not eating his allergens either.  If I eat his allergens while he's around, I need to wash my hands and mouth before I can touch him and I need to make sure there are no crumbs left on me anywhere. (Even then, I still worry about trace amounts that may be on my clothes. On those rare days when I eat out without him, the first thing I do when I come home is wash up and change out of my clothes.)   If I skip out on his allergens when we're together it's easier to manage a toddler that might need my help with feeding himself or picking himself up after a tumble.  Plus, this way I'm always open to the spontaneous toddler cuddle when he feels like giving me a big fat gooey kiss right on the lips.

Holidays

The stress of the holidays is magnified for food-allergy families because of how much food goes hand in hand with every major holiday - Valentine's Day candies, Easter egg hunts, Independence Day barbecues, Halloween trick-or-treating, Thanksgiving... well... everything, and Christmas.  

That said, we don't see a lot of our big extended family any other time of the year except for these big holiday gatherings so we make an effort to show up and see everyone.  Sometimes we'll pack our own meal to eat, and other times we'll eat before hand and just show up to say hi to family.  Even showing up without eating can be nerve wracking as kids go running around eating bread sticks, or trail mix with nuts, or eating scrambled eggs before scrambling to hunt eggs filled with mini Snickers bars.  Most times we camp out in a corner and my husband and I take turns watching the kiddo like a hawk while the other makes the social rounds.

I've also managed to modify many of our family's holiday favorite meals into allergy safe versions. We have our own 100% allergy friendly celebration at home and everyone eats the same food.  It's a lot of work making everything from scratch on your own, but it's 100% worth it.


Special Occasions

Birthday parties, weddings, and other special occasions are another case-by-case situation.  If we can arrange for child care, then O will stay home.  It's safer for him and less stressful for us.  It's sad that he misses out, but it's also not worth the risks.  If it's a child-centered event where it only makes sense for us to go if O is going, then we pack our food and go.  If it's not at someone's house, I'll call ahead and ask about their food policies.  If it's at someone's house, I'll ask them what they have in mind for the menu and plan to pack the same things plus a cupcake or cookie so we don't stick out too much eating our own packed foods. Some friends and family have taken great steps to make sure entire parties are safe for O to be around... I can't even explain how truly and deeply grateful we are for that.  It's not something we've ever asked for, but to be able to let O run around with other kids knowing that the snacks they were just served are free of his allergens is such a huge relief.  For a moment, someone else shares that burden with us and the weight of our responsibilities seems easier to carry for weeks after. 

Vacations

We do go on vacation!  Even though we're not comfortable flying with O's allergies right now, we hope that we will be when he is older and has a better understanding of what a reaction is.  Camping or remote destinations are also off the table until he's a little older. Before we go on vacation, we locate the nearest 24 hour pharmacy and Emergency Room closest to our hotel. We program those into our GPS and phones. We ask our allergist to give us a paper copy of our epinephrine prescriptions so in case our epi-pens are damaged by heat or lost, we can get a prescription filled on site without a hassle.  We use a Google Spreadsheet to plan ahead and I make a list of every meal I'll need to cook and try to guess on what we'll want for snacks. We locate the nearest Whole Foods or Mother's Market and put a shopping trip on our itinerary.  We still pack about half our food to take with us, since the nature of specialty allergy-safe foods is that it might not be carried at all locations.  Anything we're relying on eating, we pack.  We pack our own condiments, spices, oils and cooking utensils/pans.  

If we can get accommodations with a kitchen, sky's the limit.  If our accommodations don't have a kitchen, I bring a Cool-A-Tron mini fridge and a cooler with dry ice (for freezer foods), and plan out a series of microwaveable meals.  Either way, once we're in the room, we wipe down every surface and check under every bed, table, and nook and cranny to make sure the cleaning staff didn't miss a potential allergen (we usually find something! a cashew under a sofa, a candy wrapper under a bed - so we can't miss this step!) I call ahead and tell the hotel we've got severe food allergies, and they put a microwave on hold for us that I clean once we're in the hotel. This year I may also consider a toaster oven or an electric skillet for cooking, but still need to do some research on what is the safest to use in a hotel room for cooking. The photo of our family's bentos above was actually a meal I cooked during our last vacation for us to eat while we were visiting the zoo. We've even done group vacations with the strict rule that there is no outside food allowed in our room, but everyone is welcome to enjoy the food we've packed and cooked. We make it work!

Spontaneous Outings

Bahahahahahahahahahahahhahahahahahahah. No.  Besides, spontaneity is overrated (my post-food allergy mantra.) 


SO, if it seems like we never go out anymore and we turn down your invitations to do rad things all the time...you're probably somewhat right.  I assume that if you're asking us to hang out with you, it's probably because you like us and we like you, so I have a feeling you already understand why it's tough for us to be at a lot of events.  Please keep inviting us, we'll say no when it just doesn't seem safe for us, but we miss you and when the stars align just right, we'll jump at the opportunity for all three of us to get out and play.

Sunday, May 8, 2016

Food Allergy Awareness Week - React with Respect



Today marks the start of Food Allergy Awareness Week, and this year's focus is on encouraging individuals without food allergies to react with respect when someone tells them they have a food allergy.  Now, for most people I know, reacting to food allergies with respect and compassion seems like a no-brainer, but you only need to spend a few seconds in the comment section of any food allergy related post to get a taste of what kind of mean spirited things are said to or about people with food allergies.

With that in mind, my goal for this Food Allergy Awareness Week is to write about what it's like to raise a child with multiple life-threatening food allergies.  Hopefully one of my posts will reach someone who might think twice before saying or doing something inadvertently hurtful to someone with a food allergy or to the parent of a child with food allergies in the future.  I realize that people who say or do things like that often don't fully understand how serious food allergies can be and may not necessarily be acting from any sort of malicious place, but even with the best intentions, the wrong move may inadvertently put the lives of food-allergic people in danger.

My son is now two and a half and is allergic to five out of the "Top 8" allergens and more. I remember walking out of the hospital after my son's experience with anaphylaxis and seeing the outside world in a completely different light.  I was terrified.  It was like being asked to let my son grow up in a field of land mines - just one accidental step in the wrong direction could be disastrous

I knew how I could keep my child safe from "tricky people" from bullies, from car accidents, from drowning, but I had no idea how to keep my child safe from anaphylaxis.  This was galaxies beyond what I had imagined I needed to prepare my 14 month old son for.  As the diagnosis came in and we learned that wheat and egg had likely triggered his anaphylaxis, and that further testing showed he was also allergic to barley, rye, soy, tree nuts, peanuts, and coconut. I started to fall apart mentally. I knew peanut allergy could be deadly, but death by wheat seemed so outrageous.

I had wanted to be a relaxed parent who would give my child all the tools he needed to stay safe so I could let my kid explore the world and get his fingers dirty on his own.  Oh, he just ate a handful of dirt? Cool. Live and learn.  I wanted to continue traveling the world with him the way my husband and I did before he was born. I planned on us traveling overseas to meet my family, and to show him all my favorite places on the planet.  Planes will be out of our reach until he is old enough to tell us about the start of any allergic reactions. I wanted him to experience a world of foodie flavors with us and eat at all the new restaurants that pop up in our food-fanatical city.  We don't eat out with him anymore and we won't eat out with him again until there's a cure.

Before my son's anaphylaxis, my husband and I went out to dinner regularly and took him along with us.  When he was nursing, it wasn't a problem. As he started solids, we'd order items off the menu for him that I wouldn't normally cook at home and he'd happily chow down - a very well behaved baby in all kinds of restaurants. He'd usually come home with a mystery rash or his eczema would flare up days later.  At 8 months old, we went to a pizza place for a birthday party.  He didn't eat anything there, but wound up with a splotchy rash on his face from friends who had held him or kissed him after eating pizza. We didn't know about contact reactions then. We had no idea that these things could be food allergy symptoms and I had no understanding of the concept of cross contact.  We didn't put two and two together until after his diagnosis and then the guilt poured in.

I look back at photos of him at four months old, eczema on his face, hands wrapped in sleeves so he wouldn't scratch himself raw - why didn't I think to eliminate allergens earlier?  I was on an elimination diet while nursing him, but I didn't know how thorough my elimination needed to be until later. Besides, our pediatrician at the time, and his dermatologist were pretty positive his rashes were not food allergy related and that they were just a thing that happens to babies and that my elimination diet probably wouldn't help things clear up.  They were wrong. And it turns out, many physicians are sorely under-educated on the realities of food allergies.

As the months passed and we got better at doing the allergy thing, I'd settle into a zone and feel like I'd have control of things pretty well and that we had found our new normal. I felt like I didn't miss the old normal.  This was fine.  We could do this and everything would be awesome despite food allergies. Then something.  Something minor.  Something that most people don't even notice would snap me out of my positive attitude and remind me that our normal was not everyone else's normal and things would not be normal for a very long time... if ever.

I remember being at Costco and having a breakdown as I realized all the food that was in everyone's hands, being passed out, dropped on the floor, spilled on shopping carts, could kill my one year old. It was as if I was watching madness happen in slow motion, people frivolously playing with some kind of biological weapon.  Of course it wasn't a biological weapon to any of them, but all I could see was the threat all around me.  I watched parents feed their children free samples without even a second thought as to what was in them and I wondered if they were ever afraid of the food they put in their kid's mouths. Before food allergies, I had never given it a second thought.

I remember sitting at In-N-Out and watching a child younger than my son being fed french fries and a burger and becoming so sad that my son wouldn't experience In-N-Out. I wondered why that made me sad. I had never planned to feed my kid fast food and I rarely eat it myself, but crossing that off my son's "firsts" list put a cloud over my day.

I remember being at Gymboree where a friendly mother handed out cookies to all the excited children in the lobby while I scrambled to get my son's shoes on and run out of there before there were crumbs everywhere and my kid was asking me why he couldn't have a cookie too.

A fruit snack brand we trusted changed their ingredients to include wheat starch as the very last ingredient.  One more treat we crossed off our very short list.  A few weeks later, a freeze dried fruit company we had been purchasing from since O's first solids changed manufacturing facilities and now was processed in a plant that also processed wheat and other allergens.  Another snack off our list.

Little things.

As my son gets older, his allergies have not improved and we're getting him tested for three more foods that he's had unexpected reactions to in the last year.  We get closer and closer to the age where he's going to school and I'm terrified.  I have to trust another person to know his allergies. To keep him safe. To check labels. To consider ingredients in non-food things like glue, finger paints, play-dough, and water colors. Trust young children to not intentionally or unintentionally expose my son to the foods that will hurt him or could cost him his life. I can barely keep up, so I don't know how I'm supposed to let people who aren't completely obsessed with him do it.  We've talked about homeschooling... at least until he can self-administer his epinephrine, read labels himself, and say no to candy and cupcakes when they show up at school unexpectedly and everyone else is eating them. 

I'd make a terrible home school teacher.

I don't want my son to be the "special little snowflake" everyone assumes that food-allergy parents want their kids to be.  I want him to shovel food without a care down his adorable little gullet like the average kid and to never be singled out for something he can't eat or touch without the risk of dying. I want a cure in his lifetime.

Things have changed so drastically from the way I imagined parenthood, but I know more than ever that the best way to make the Universe laugh hysterically in your face is to have expectations and plans for your life.  I've also learned perspective.  Everyone is fighting a battle we don't see on the outside and for every parent that has it easier than me, there's a parent that has things twice as hard. We all do what we have to do.

We're getting better and better at managing the allergy thing, but we face challenges every day. I try not to complain much about our life with food allergies, but it was and still is a difficult adjustment that's worth every hurdle. This Food Allergy Awareness Week, I hope to share how much our every day lives have changed to keep our son safe and encourage everyone to react to food allergies with respect and compassion.

Friday, May 15, 2015

Our Anaphylaxis Story

Just retelling this story brings back all the anxiety of that night in late October of 2014, but this week is Food Allergy Awareness week, and I'm going to share our story.

When my son, O, was 14 months old, he was rushed to the ER by ambulance due to a severe allergic reaction. O was at my parents' house (like he is normally when The Husband and I are at work) and had just woke from his nap a little after 5 pm.  About an hour and a half later, The Husband was getting ready to head back home with O when my mom noticed some hives forming on O's neck. 

They quickly put him in the kitchen sink to rinse off whatever might be causing the flare-up, assuming it was a contact rash since he had not eaten anything since waking up from his nap.  The Husband gave him 2 mL of his Hydroxyzine which was an antihistamine O's dermatologist had prescribed for itching related to his eczema. 

Unfortunately, the hives continued to spread rapidly and The Husband decided to try and get O home as quickly as possible. About five minutes later, they arrived where I was getting dinner ready.  Upon seeing O's bright red, puffy face, we thought we'd try and putting him in a cold bath, suspecting that he must have touched something that was irritating his skin.  I told The Husband to call the pediatrician after-hours line to see what we needed to do.  In the bath, his condition continued to worsen and at this point, his whole body was covered in dark red hives that sort of got bigger and bigger until they globed together into large red blobs. His eyelids were swelling like a boxer who was losing a boxing match, his ears were getting bigger and redder by the second, and his eyes and nose had started to drip like a faucet. 

I remembered reading in one of my baby food cook books or blogs that severe food allergies and anaphylaxis could strike at any time to any food and could become serious for infants.  Suspecting that we may have been headed in that direction, I called 911 while The Husband got O dressed.  

We live next door to the fire department, so thankfully it was only a minute or two before the fire truck, ambulance and police car were at our front door, but in those two minutes, I tried to convince myself that they would show up, look at O and tell us we were overreacting first-time parents, give him a little Benadryl and be on their way. A team of four firefighters/paramedics came to our front door and upon seeing O's condition, decided he needed to get to the ER immediately.  Within a minute of them arriving at our home, we were told to take nothing and hurry down to the ambulance. Luckily my purse was right next to the door, so I was able to grab it and have my phone to get in touch with family for updates.

It was my first (and hopefully last) ride in an ambulance.  Lights flashing and sirens blaring, I was strapped onto the stretcher with O clinging to my chest while The Husband followed in his car (the pediatrician called him back while he was in the car and told him to call 911 - which he basically said, we're already way ahead of you!)  In the ambulance, they monitored his vitals and gave O two injections of antihistamine in his thighs which seemed to start helping immediately. I could hear one of the paramedics on the phone to the hospital requesting dosage or approval for epinephrine dosage for a 20lb one-year-old.  We arrived at the hospital before the hospital was able to relay the dosage info, and it looked to me like O was starting to improve and the paramedics said that his lungs were sounding clear.  

We were rolled into a room at the ER where it seemed like a million nurses came in to poke and prod O, tape things to his body, and take uncomfortable temperatures on a screaming, confused, itchy baby.  They gave him a steroid injection and an oral dose of another antihistamine. 

All the medications they had administered slowed the reaction enough for the ER Doctor to leave us alone for a bit.  We were told we'd be in the room for four hours with O hooked up to blood pressure and heart rate machines, waiting and watching (I later learned this was because allergic reactions can often have a two-fold attack, with the initial attack seeming to subside only to have a second severe attack within a few hours.) 

My mom, brother & sister-in-law came to give us some moral support, and brought us some things from home (phone chargers, socks, a clean shirt, checked our house to make sure I remembered to turn the stove off with all the food still in pots, etc - remember, we were rushed out of the house?  It was 7pm, after work when we were shoved into that ambulance... we were both a mess) and helped to take turns holding O while he was in misery.

After a very stressful hour at the ER, O finally fell asleep on my mom's shoulder.  The ER doctor told us we'd have to see an allergist within the week once we were discharged.  It was really only at this point that I thought to take pictures since I had no idea how I would describe all this to a doctor.  We have no pictures of his pre-treatment condition, but we have photos of him about an hour after all those injections, and while he still looked awful, he looked about 500x better than he did before we called 911. 

I hopped on my phone to research and see if I could figure out what was going on.  The doctors and nurses moved so quickly, and I wasn't sure what was happening to my kid and what I needed to do to keep him safe.  As I began reading about allergies, I realized that while I had heard the term anaphylaxis, I had no idea what it meant.  In my phone reading, I learned that anaphylaxis actually refers to a rapidly developing and serious allergic reaction that affects a number of different body systems at one time. My kid didn't pass out or gag like they do on TV, but his breathing, skin, and circulatory systems had been simultaneously affected by an allergen.  I began to realize how lucky we were that O didn't go into shock from his exposure. I cried.

After those 4 hours, with O's blood pressure and heart rate comfortably normalized, they were ready to send us home. We were told to keep vigilant for a subsequent reaction throughout the night, and that we had to get our prescriptions filled before going home in case we needed to use the epi-pen for any reason. By this time it was a little after midnight, and finding an open Pharmacy was a little bit of a challenge for our exhausted crew. They discharged us with prescriptions for Benadryl (an H1-Blocker antihistamine), a liquid steroid, liquid Pepcid (which, if you didn't know, is an H2-Blocker - an antihistamine that in this case is used to help with the digestive end of an allergic reaction... and which took the pharmacist about 30 minutes to prepare) all of which he had to take for 7 days straight.  We were also sent home with a prescription for multiple epinephrine auto injectors which we had to learn to use that night.  

Back at home, my mom volunteered to stay the night and take turns with me watching O while he slept.  In the morning, his swelling had mostly gone down, but his ears were bruised from how large they had swollen.  

This was when the panic set in.  We still had no idea what had caused this, so in our minds EVERYTHING was a trigger.  EVERYTHING was a potentially fatal substance.  We didn't want to leave the house, we were scared of feeding him foods, we were terrified.

We made an appointment to see an allergist at the earliest appointment available, and were in their office by the end of the week.  In preparation, we retraced every step, took inventory of every possible substance O could have come in contact with, and made a journal of it all.  Nothing stood out.  It was misery.  The steroids made O vomit on occasion - or so the pediatrician told us that was the reasoning.  Later the allergist suggested that perhaps the vomiting was because O had a virus which either exacerbated another allergy to the point of anaphylaxis, or it was also possible that he had an anaphylactic reaction to the virus itself (WTF) even if O wasn't showing any other cold symptoms in the days leading up to this.  It was all a guessing game.

O's allergy results came back severely allergic to wheat and egg (he also tested low-to-medium positive for tree nuts/peanut/coconut/soy, and negative for fish/shellfish/insect stings) which brought one theory to the forefront of the mystery.  

The day of his reaction, my mom had been making empanadas.  Empanadas are stuffed pockets of dough coated with an egg wash and baked or fried - and they are DELICIOUS.  Although O had not been fed any empanada, if he had a virus, the allergist suspected that being touched by my mom, dad, and The Husband who had been handling wheat and egg in making/eating of empanadas may have triggered his immune system to go into overdrive with the trace amounts on their hands or face. 

Or being a nosy toddler, he may have somehow snagged a crumb of empanada on someone's hands, or shirt and decided to eat it without anyone noticing. We'll never really know for sure.

It has been seven months since O's trip to the ER.  As time passes with strict allergen avoidance and no serious reactions, it's sometimes alluring to hope that maybe your precious child isn't as allergic as the allergist and all the tests seem to indicate.  You don't want your kid to grow up with fear of food, or to grow up afraid of dying from a snack, or to die because he, or I didn't read ingredient labels well enough.  You don't want to think about how you'll figure out school for him with multiple food allergies before he's old enough to advocate for himself. You don't want to think about having to take him to the hospital and hoping that you'll administer the epi-pen in time.  You don't want to think about forgetting the epi-pen, or think about the possibility that even the two epi-pens you carry on you at all times might not be enough.

I had a slip-up earlier this year which reminded me how severe O's allergies are.  After a stressful month of complicated health issues, I had spent the weekend in the hospital (story for another time) and since I was feeling like I was ready to get back on the domestic track, I cooked dinner for the first time in weeks (I had been on bed-rest for weeks and hadn't cooked in a very long time.) The last time I went grocery shopping, I bought three boxes of our usual gluten free spaghetti and it seemed like an easy meal to make.  I had previously used up 2/3 of the first box and O had eaten those meals with great enthusiasm.  Seeing that I didn't have enough in the first box for a meal for 3, I opened up a second box and threw it all together and served it for dinner.

O took one bite.  He started fussing at the dinner table and refused to eat.  I remember laughing that this kid was being so fussy - toddlers, amirite?  I tried to put another spoonful in his mouth, and he began to scream-cry.  I said fine, you don't have to eat, wiped him down, finished my meal and went on with the night.

O had been sick the week before and had the remnants of a cold with a chesty wet cough on occasion. We took him upstairs to get ready for bed and noticed how his nose was running like crazy and his eyes were watery.  Great, I thought -  his cold is coming back with a vengeance.  Then he started coughing.  A lot.  And it wasn't his chesty wet cough.  This was sort of a newer dry, hack cough... great, I thought, another long night of coughing.  Stupid cold.  

I took his shirt off to put his jammies on, and then I saw them.  Hives.  On his back.  I told the husband to get the Benadryl and call the allergist's after-hours line to see at what point we needed to use the epi-pens (we hadn't discussed an allergy action plan at this point.)  At that time, we didn't know what had triggered his reaction and while the Benadryl seemed to stop his cough and runny nose, his eye was still swelling. When the allergist called us back he said that since the Benadryl seemed to be working, and since we didn't know the trigger, and since his breathing seemed OK, to just wait and see - but if we hear any wheezing AT ALL, to immediately administer the epi-pen and call 911.  It took about 24 hours for the swelling to go down, and about 2 hours for the hives to go away.  I did not sleep well that night.

I was in a panic.  AGAIN a mystery reaction - not as bad as that first one, but not good either. If I knew then what I know now, I probably wouldn't have waited to use the epi-pen.  It would not be worth the risk to his life.

Weeks later, I was reorganizing the pantry and happened to look at the box of pasta, I was about to put it back in the pantry when something about an artichoke caught my eye and I thought, wait - I didn't know this pasta had artichoke - I wouldn't have bought this with artichoke in it because O has never had artichoke...

And then it hit me.  This box didn't have the Gluten Free triangle that my other box of pasta did.  It was the same size, the same shape, the same color. I grabbed three boxes off the grocery store shelf - and this one - the one I tried to feed to my wheat-allergic child - was not wheat free. 

I think the boxes in stores now are more distinct in color,
but in my dimly lit pantry, I couldn't tell the difference
in color between the gluten free and organic regular pasta.
I had gotten lazy.  I knew I was supposed to check EVERY SINGLE FOOD that comes into my home.  I knew I was supposed to read EVERY SINGLE INGREDIENT EVERY SINGLE TIME I COOK SOMETHING AT HOME.  The boxes looked the same to me, I didn't notice when I was grabbing them off the shelf at the store, and I didn't notice when I loaded them into my pantry at home.  I felt awful. What had I done?  

I cried. Again.  One small bite of a strand of spaghetti caused my son's eyes to swell, hives, coughing and sneezing within 30 minutes of eating.  One small bite he trusted me to feed him.  

I also breathed a sigh of relief because he survived and we now knew without a doubt what caused that second reaction. I'm still working on forgiving myself for that and part of that is making sure I do whatever I can to ensure that he doesn't have to go through a reaction like that again.  It starts with educating myself and others, and raising awareness for life-threatening food allergies.



For more information on food allergies and anaphylaxis visit: foodallergy.org  and kidswithfoodallergies.org