I don't know WHY I haven't done this before! This recipe is pretty basic (just a few ingredients), and now my kid can have pizza. PIZZA - a staple for pretty much every kid that ever lived.
I had a food allergy mama message me this week about a pizza recipe, and I told her that I would jump on it (and couldn't believe that there was such a gaping hole in the Arsenal).
May I present, my top-8 allergen free, gluten free, tasty pizza!
The greatest thing about this recipe is that it actually makes enough dough for two pizzas, and you can freeze the dough for up to month! I suggest wrapping it in plastic wrap and then putting it in a freezer bag, and then labeling it with the date! Be sure you use it within a month...these ingredients are $$, am I right?
Click here for the recipe!!
I hope that your food allergy kid (or food allergy self) enjoys!!
We often joke about the fact that our three year old has business cards and we don't...but his allergies are pretty serious business, so perhaps it isn't all that silly!
I can't take credit for this idea...it was another gem I heard about from my support group in Bloomington, IN. But it's been such a wonderful convenience and useful tool for us since we started making them - and let's face it, how often do the concepts of food allergies and convenience get discussed at the same time?!
I first created Matthew's business cards on Vistaprint about two years ago. I had come across a coupon code and thought it was just a great idea. It took some time to get the layout and theme exactly how I wanted it (much like setting up a blog, come to think of it), but I was so happy with the result. A year after we made the first one, we decided to make new ones. His food allergies had changed (we had more to add to the list), and kids change so quickly when they are little that we wanted to update the picture, too.
I was semi-dreading having to start over again, but FORTUNATELY, I had created a Vistaprint account, so all I had to do was figure out how to login (i.e. try one of 760 different passwords I use) and...ta-da, there sat the beautiful card I had created a year ago. I added a couple of rows to the allergy table, updated his picture, and updated our address (because we'd moved for the 760th time). It literally took five minutes from login to order.
We use them all the time - we give them to babysitters (rather than having to write out instructions over and over again), we pass them out like allergy-friendly candy at his school and at church. He actually wears a laminated one as his nametag at church. There is one hanging off of his backpack. One with his epinephrine. One on his car seat in case we were in an accident (so medical personnel would know about his allergies). They can literally be used anywhere! AND...they're pretty darn cute, too!
I have enjoyed using Vistaprint for these. Vistaprint frequently has coupon codes, so you can get them cheap/free and just pay shipping. It costs a little more to have a backside to your card, but I feel like it was necessary to share all of the information.
A few recommendations:
**I strongly recommend creating an account if you use Vistaprint. Creating the card from scratch one time was enough. Updating is super simple now!
**Update the card anytime you move, your information changes, or you/your child's allergens change. We need to update ours to include tree nuts - this post has been a good reminder of that.
**Put your child's full, legal name on the front. This helps with identification in case of emergency.
**Give them to all your friends and relatives that may ever be alone with your child.
**These cards are NOT a substitute for a thorough verbal explanation of your child's allergies. They are meant to be a quick and easy guide for your child's caregivers and, in case of emergency, a source of information for emergency personnel.
I hope this is a useful tool! I'd love to hear if you can think of other applications for this business card, either in the food allergy world, or even for another medical condition!
For information about other food allergy resources, check out Food Allergy Arsenal's Resources Page
No food allergy is fun to manage, but I knew that a wheat allergy would present its own unique challenges because of how much wheat is used in baking. Breads, cakes, cookies, etc…all have wheat. The recent influx of gluten free products into the market has certainly helped our cause, but we also have other allergens (soy and egg in particular) that make many of these products useless to us.
I couldn’t imagine a little kid not having bread! So, I set out to make a safe, run-of-the-mill white bread recipe for Matthew. I went to Pinterest and tried a few things, but nothing that quite did it for me. As I gained confidence using these alternative ingredients, I decided to try to develop my own recipe. It took about 18 months of on again, off again tinkering, but I am so happy with the result, and (not to pat myself on the back too much) pretty dang proud that I came up with this on my own! I’ve gotten pretty good at adapting existing recipes to meet our needs, but this is truly and original recipe!
I use a bread machine for this recipe. Shortly after Matthew was diagnosed, a friend of mine listed hers for sale for next to nothing, so I bought it just to see what I could do. It’s still the one I use today. Bread machines are one of those larger kitchen appliances that many people buy and then never use, so you may be able to luck into one just like I did! This is the one I use
You need a bread machine that has a gluten free setting of some sort. Mine is called Fast Bake. It is a process that lasts 58 minutes: 13 minutes of kneading, 10 minutes of rising, and 35 minutes of baking. You don’t need a process that includes multiple rising and kneading cycles. You can see the variety of “courses” that my bread machine can do – I use #2
I’m a visual person, so I like having pictures detailing the steps of a recipe. Below, you will find the step-by-step instructions for making this bread. One important note: it is very important to be very exact with your measuring – level your measuring cup with a knife, and be precise! If you just want to see the recipe, feel free to click here. To see the steps, click "Read More" below. I strongly recommend reading the step-by-step instructions if you have never made this recipe before.
About 9 months after Matthew's diagnosis, a food allergy support group was formed in town (Bloomington, IN - where we used to live).
**Side note: if you happen to live nearby, check them out...an amazing group of allergy parents! They are Bloomington PoCHA (Parents of Children Having Allergies).
The founder of the group, Nicole, is the one who introduced me to Allerbling, and Matthew wears it often. Allerbling is a bright orange bracelet with holes in it. It is not the most fashionable color (that's not the point), but we love the bright orange because it really makes the bracelet standout.
Allerbling makes charms for you to insert into the holes so that you can customize the bracelet with your child's allergens. There are five holes in the bracelet, which allows for either five allergen charms or four allergen charms plus a medical alert charm. For us, five holes is not enough, but we also recognize that five holes likely accommodates the majority of their buyers. They also do not make charms for his less common allergens (peas and lentils). I suppose we could buy a second bracelet for the couple we haven't put on his bracelet...but I'm not too sure Matthew would go for that!
We use the wheat, soy, egg, and peanut charm, plus the medical alert charm. If you buy the full kit, it comes with those five charms, plus shellfish, tree nut, dairy, and fish charms. You can also purchase the above charms plus the following charms separately: sesame, corn, chocolate, strawberry, coconut, bee, and gluten free.
The bracelets come in four different sizes. Matthew just graduated from the extra small to the small bracelet. We also have the large bracelet (the full kit comes with small and large, and we bought the extra small separate).
We have enjoyed using Allerbling because we believe it is another source of protection for Matthew. He wears it to church and when we are going to unfamiliar places where people are not aware of his allergens. He doesn't wear it to school because everyone there knows about his allergies now. Allerbling has proven to be very durable - it has stood up very well considering it is being worn by a very active little boy! The charms are relatively easy to insert into the holes, and can also be removed easily when you need to change bracelet sizes. We have never had an issue with them coming out, and Matthew never tried to take them out - I also don't really think he could even if he tried.
Our only issues are that there aren't enough holes for all of his allergens (he has 8), and that they don't make charms for two of his allergens. They have a place on their site where you can request that they add a food to their selection - and I will admit that I have not done so. We use Allerbling to make people aware that he has allergies...we would NEVER rely on it to tell the whole story!
Overall, we have been VERY happy with Allerbling. It makes Matthew feel special - he has never balked at wearing it - and it serves as one more reminder for his caregivers that he has severe food allergies.
*takes deep breath…
This is difficult to share.
EVERY time I look at this picture of my baby, my heart drops. My stomach turns in knots. I could literally cry. I see this picture and it takes me back to the absolute scariest moment of my life.
Because every time I see this picture, even now (three years later) I’m hit once again with this thought: my baby…he could’ve died.
Matthew had his first anaphylactic reaction just a couple of weeks after his first birthday. He’d been a pretty picky infant with baby food, so I guess we had just never put green peas in front of him at any point prior to that life-changing day in June 2013.
We prepared peas for the whole family for dinner that night, and placed a few on Matthew’s tray. He ate 4 or 5, and we immediately could tell something wasn’t right. His face began to swell and turn red, and he was struggling to breathe. My husband and I were panicked.
We very quickly got him out of his high chair, and my husband strapped him in the car and rushed him straight to the urgent care facility up the street (I stayed home with our three year old). The next few hours were hell. My husband is amazing, but to not be with my baby at that time was the worst feeling ever.
In hindsight, we probably should’ve gone to the ER, or called for an ambulance…but that was what we did in the moment. Fortunately, the urgent care staff took it very seriously and rushed him straight back and administered appropriate medication. The photo above was taken after the medicine was administered. He actually looked worse before then (we just weren't thinking about taking pictures at that point). My husband sent this picture to me to help me feel better about his improvement.
I’m so thankful for so many things about that day. First, of course, that this was not a fatal reaction. It very well could’ve been, and that thought crosses my mind still way too frequently, even years later. I am thankful for the urgent care facility that took good care of my baby. We know now we should’ve gone the ER (and we’ve been there since for two additional anaphylactic reactions, one of which resulted in an ambulance ride), but he received excellent care at urgent care.
Anaphylaxis is a life-threatening, serious matter. I pray daily that we will never have to go through another episode of anaphylaxis. I know that I am not the only parent saying the same prayer over their child, either. My heart breaks for those who have lost a loved one as a result of an anaphylactic reaction.
One final thought (and I’ll keep it short for now, but trust me when I say I have a lot to say about this): jokes about anaphylaxis are not funny. They will never be funny. In the last few weeks, my husband and I have seen two jokes about anaphylaxis in two different sitcoms. Both times, we were sitting on the couch and could only look at each other, cringe, and say, “Nope…not funny.” Making light of anaphylaxis diminishes the seriousness of anaphylaxis, and can result in it not being taken seriously when it actually occurs. Also, in all honesty, these jokes make me feel like I’m listening to someone make fun of my own child. It is hurtful. It is wrong.
FARE (Food Allergy Research and Education – get used to seeing that acronym on this blog) is sponsoring a Food Allergy Awareness Week beginning on Sunday, May 8. Their theme for the week is “React with Respect” – and I hope that by sharing our story, you will rethink your response to food allergies and anaphylaxis. Our daily lives revolve around making sure that every bite of food that goes into Matthew’s mouth is a safe bite. Those with food allergies don’t really need sympathy, and certainly don’t need jokes…but your respect is crucial.
During this month of food allergy awareness, I encourage you to take anaphylaxis seriously, and to take the pledge to “React with Respect.” For more information about FARE’s efforts to raise awareness and funds for food allergy research, please visit my Food Allergy Awareness Week page, or go to http://www.foodallergy.org/food-allergy-awareness-week
This year, Matthew began a five day a week preschool program because I went back to work. They have been incredible! His teacher, Ms. Rhonda, has worked with me all along and I feel great about how they have worked with us this year. We are grateful!
One of the neatest and equally scary things they have done this year is little baking/cooking projects with the three year olds. The idea of cooking with a large group of three year olds is scary enough, am I right? But oh boy, did some food allergy anxiety set in initially!
His teacher emailed me a few weeks into the school year and said she wanted to make blueberry muffins with the class.
First (panicked) thought: NOPE! Not happening...
Second (calm, cool and collected) thought: I have worked my tail off adapting recipes to fit his needs. I have been adamant about including Matthew in everything that he is reasonably able to participate in. Can we make this work?
Let me say this...placing your trust in someone else to manage your child's allergies is not an easy decision, and I would not do this with just anyone - but I trusted and do trust his teacher, so we went for it. If you aren't comfortable with something when it comes to your child and his/her allergies...DON'T DO IT!
Ms. Rhonda and I have collaborated several times over the course of this year to come up with safe alternatives for Matthew, and it has been an amazing success (we will miss Ms. Rhonda next year)!
These blueberry muffins are really great, and are a result of this unexpected collaboration with Matthew's preschool teacher! Moist (ugh, that word!), sweet, and delicious warm treats that are great and quick for breakfast, and so easy, even a preschooler can do it!
CLICK PICTURE FOR RECIPE!!
Welcome to my new home in the blogosphere! I am so excited to kick things off here and start sharing and exchanging information and ideas about living in our food allergy world. May is going to be an exciting month here, particularly as we celebrate Food Allergy Awareness Week beginning on May 8. FARE (Food Allergy Research and Education) is leading the charge and has ideas and suggestions for making the month of May a big time to raise awareness.
I can’t think of a better time to launch Food Allergy Arsenal. I’ve spent innumerable hours the last three years educating myself, creating recipes, exploring resources, and working my tail off to make my little boy’s life better (learn about my little hero here!). I’ve never wanted the restrictions of his food allergies to get in the way of him enjoying a birthday party. I’ve never wanted my fear of what could happen to get in the way of his happiness and ability to enjoy his childhood. I feel like I’ve created quite the “arsenal” of recipes, ideas, and resources to achieve these goals, all while keeping him healthy, happy, and full!
My dream for Food Allergy Arsenal is that it can be a place where we can all share ideas and tricks for living a food allergy life. I by NO means claim to know it all. I did NOT figure all of this out on my own (I was scared to death for the first six months). I want this to be a place for constructive discussion, recipe exchanges, and cool ideas that could improve quality of life for my child – and yours - even more.
I also know that what works for me may not work for you – that’s the absolute crazy thing about this food allergy life we live…it’s rare for any two situations to be exactly the same. But let’s collaborate and empathize and work together to strengthen and grow our arsenals.
Food Allergy Arsenal is on Facebook, Instagram, Twitter, and Pinterest– we are out there! Find me, introduce yourself, and let’s be friends!