Skip to main content

Awww Nuts!

Living With Peanut Allergies
by JAK’s guest mom blogger from Kenosha, Melinda Munro


I love peanut butter. Slap it between some white bread with jelly or bananas, slather it on toast, dip apples in it, bake it in a cookie, and don’t forget the all holy peanut butter cup, I love the stuff! Or at least I used to. READ MORE...

My love affair with the creamy, goopy, salty sweet, American go-to ended when my son had his first allergic reaction after a tiny bite of a peanut butter sandwich.  He vomited and hives spread all over his body.  It took two days for the hives to completely go away. So I learned that my son, like an increasing number of young children around the country, has a life-threatening allergy to peanuts and tree nuts.

Since then, I’ve come to loathe peanuts and tree nuts, which seem to be EVERYWHERE. Most kid-oriented activities seem to include some form of treats with nuts, and there’s almost always a PB&J lurking nearby. A trip to Monkey Joe’s resulted in an outbreak of hives even though we didn’t see anyone eating anything with peanuts. Catching a flick at the movie theatre is risky if anyone near us is eating candy with nuts. There’s no chance of me taking him to a Brewers game with all of the peanut shells strewn about. And don’t get me started on the children’s museums that serve PB&J. For my son, his allergy means missing out on a lot of common childhood experiences and for me it means constant vigilance and planning to keep him safe.

I’ve learned there is no cure for food allergies; the only treatment is to avoid the allergens. If my son ingested a peanut or peanut product, or even a safe food that had been cross contaminated by coming in contact with a peanut or peanut product, his immune system would identify the food as an invader and attack it. The symptoms can range from a minor irritation like hives to anaphylaxis ; a sudden drop in blood pressure, breathing difficulty, vomiting, extreme facial swelling and in severe cases, death.

The best resource I’ve found to educate myself about food allergies has been other parents. There are many wonderful blogs and online food allergy websites where you can connect with other parents dealing with the same food allergy. But even with all of this information available, I still wanted to connect with someone locally who understands the challenges of raising a child with severe food allergies.

According to the nurse at my son’s school, our elementary has the highest number of children with food allergies in our school district. The nurse encouraged me to start a support group, but privacy issues make it difficult to reach out directly with these other parents. So I recently start a Facebook page to offer support for families with peanut and tree nut allergies called Kenosha Peanut Allergy Parents.

Our goal is to provide local support for people and families dealing with peanut allergies, and to form a community where issues regarding those allergies can be discussed. My wish is to reach as many families in the area as possible. I would love to have a mentoring system for parents who have just found out that their child has peanut allergies and also have parents at each school who can help answer questions and concerns for incoming students and their parents. Our group is still new and we rely on word of mouth to grow, so please pass along our FB page and email to anyone who may be interested.

You can connect with Kenosha Peanut Allergy Parents at http://www.facebook.com/KenoshaPAP or KenoshaPAP@gmail.com.

Melinda Munro, of Kenosha,  is a stay-at-home mom of a 6 year old and 4 year old. Her son was diagnosed with food allergies shortly after his first birthday.

Comments

Popular posts from this blog

AWESOME Dad

Well, most are! I know your kid's daddy might not be tops in your book, yet, in the eyes of your child, he probably is. I am so grateful that when my husband and I mutually took the risk to vow to spend our lives together, then had/have children, (while not always perfect) he ended up being quite the awesome dad. Assist your child in sharing his/her celebration of dad. (Um, I am sure you know, Father's Day is next Sunday, June 17th).  Here's a great way to do that, pocket $100 gift card for your kiddo, and knock out that Father's Day gift!  Here's how... Read More... For the third year in a row, Just Add Kids has partnered with Educators Credit Union  to bring you, your kids and their daddy a fun contest in celebration of Father’s Day.  This year, RelyLocal Racine is also partnering with JAK and providing a plethora of gift cards perfect for dad. So, how to participate? Kids color a portrait of their dad, grandaddy, or other fatherly figure (portrait frame and e

June is the New Spring

April Wrap Up: Wrapped in Love                           In recognition of April being Autism Awareness month, Just Add Kids welcomes Colleen Nagle, a Burlington mom, as JAK's guest blogger. Autism is easy to misunderstand, misinterpret and mislead.  My son is the master of disguise and the best way to understand our kids is to assume nothing.  That is, assume only that they are kids, children, teens, silly, loving, intelligent and, well, simply put, no different than any other kid. Everything I have been told about Autism is wrong. Everything I know about Autism I have learned from my son.  My son with Autism.  He loves me just like his typical siblings love me, he cries when he misses me and he smiles when we are together again. Read more... He cannot speak.  He has never been able to express his favorite color or cartoon or game.  My heart longs to know him, to know the little everyday things: to know that he has favorites; to know that he likes the food I serve him; to know if

Wishful Thinking

Putting Thoughts Into (60 Second) Action                Just Add Kids welcomes Mollie Bartelt, a Caledonia mom, as JAK's guest blogger Do you want to make a difference in your life this summer? Or make a difference for a child who has a life threatening illness? Or win $1000 in a fun challenge? Game on! My story began six months ago, when my happy, healthy nine year old daughter came in from outside playing in the snow feeling dizzy. We became alarmed when she couldn’t stand up after resting a bit...her legs were wobbly and criss-crossing and she appeared to have no balance. A few short hours later in the emergency room, the situation looked worse as she was starting to slur her speech and not even be able to get words out correctly... and she couldn’t get her hands to work to put a snack in her mouth. Read more... The hospital ER staff then sent us up to Children’s Hospital where Hannah stayed for nearly a week, undergoing tests and having therapy. While all the tests were negativ