The Teal Pumpkin Project: Halloween for Kids with Food Allergies

The Teal Pumpkin Project: Halloween for Kids with Food Allergies

The Teal Pumpkin Project: Halloween for Kids with Food Allergies

Guest blogger Jill Seaney wants every child to be able to celebrate Halloween. So her guest post explains what the Teal Pumpkin Project is, who it helps, and where to find resources.

The Teal Pumpkin Project: Halloween for Kids with Food Allergies

The Teal Pumpkin Project makes Halloween accessible for the one in every thirteen kids with food allergies. In the average classroom, two children have at least one known food allergy. Kids with food allergies are often left out of the fun because so many of the celebrations are centered around food. As a parent of a three-year-old who suffers from food allergies and cannot eat most food that is considered safe for others, I have invested a lot of time researching and coming up with fun food alternative ideas so that my child never has to feel left out. With Halloween approaching, I thought this was a great time to talk to people about the Food Allergy Research & Education (FARE) Teal Pumpkin Project.

The Teal Pumpkin Project helps make sure all children will come home on Halloween night or from Halloween events with something they can enjoy. Kids who have food allergies typically come home with a basket full of candy that they cannot eat. Its definitely hard explaining to a three-year-old that we have to throw all the candy out because it will make him sick. My hope is that through educating more people about the Teal Pumpkin Project, more people will offer non-food items and display a teal pumpkin so that all kids get to enjoy Halloween. Every child should be able to experience the joy and tradition of trick-or-treating!

Fortunately, FARE started the Teal Pumpkin Project to make it simple for everyone to help make Halloween special for kids that have food allergies.. All you need to do is paint one of your pumpkins teal, or buy a teal pumpkin (many craft stores sell plastic or ceramic teal pumpkins, too), and display it with your other pumpkins outside your home and then offer non-food treats. There are also signs that you can download and print from the FARE website that you can hang on your door or outside your home to let trick-or-treaters know that you support the Teal Pumpkin Project and have non-food treats to hand out. The link is included below. But remember, the best way to raise awareness is to have the teal pumpkin outside your home.

Remember to keep non-food treats in a separate bowl from the candy bowl to avoid cross contamination. How will you know which trick-or-treater has a food allergy and which doesn’t?

It’s as simple as asking, “Would you like a piece of candy, or would you like a prize?” Most children know that they have food allergies and will be so excited to go to a house and find something they can enjoy.

There are a lot of alternative treats to candy. Some examples are:

  • Stickers
  • Glow sticks, bracelets, necklaces
  • Bubbles
  • Mini Slinky
  • Bouncy balls
  • Finger puppets
  • Crayons, pencils, pens
  • Coins
  • Mini notepads
  • Mini flashlights
  • Whistles

The goal of the Teal Pumpkin Project is to help children like mine feel included in the fun of Halloween. I hope you will consider joining the movement as well and help all children have a very happy Halloween this year.

For more information on the Teal Pumpkin Project, please visit their website.
The Teal Pumpkin Project home sign can be downloaded here.

 

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Jill lives in Tucson, AZ with her husband Jeff and their son Blake. She worked in Human Resources up until 2014 when her son was born with VACTERL Syndrome which included EA/TEF. Jill resigned to care for her son full time. Later he was also diagnosed with a Congenital Diaphragmatic Hernia and Eosinophilic Esophagitis. Jill’s personal blog (Beloved Blake) documents his surgeries and health challenges, their family struggles, and Blake’s milestones. Jill loves writing and teaching others about what it’s like raising a child with complex medical needs. She wants to be a blessing to other parents just starting on this journey.

Author Jolene Philo

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The Five Love Languages: 40 Years and Going Strong

The Five Love Languages: 40 Years and Going Strong

The Five Love Languages: 40 Years and Going Strong

My husband and I were married on a hot and muggy July day in 1977. His tux size remains the same, and I still fit in my wedding dress. We both have all our teeth. So sometimes we look at each other across the supper table, scratch our heads, and ask, “40 years? Have we really been married 40 years?” Then I notice his thinning hair, he notices my collection of wrinkles, and we do the math in our heads.

2017-1977=40.

Yep, we’ve been married for 40 years, not all of them easy. The early years were hard as our diverse family cultures merged, and our different communication methods often clashed.

He was a twin, who talked in a shorthand composed of mostly gestures and expressions.
I loved to talk and play word games with my family and friends.

He wanted constant contact with a constant companion.
I wanted time alone to think and debrief after we were together for a while.

He could play his guitar or listen to music for hours.
I could curl up in a quiet corner and read for hours.

But we both loved Jesus, we loved each other, and we loved children. So when we learned we were expecting, we eagerly embraced the challenges and joys of parenting. We had no idea that the arrival of our baby boy, born with a condition that required immediate life-saving surgery and years of medical intervention and therapy, would usher in the toughest 4 years of our marriage.

For 4 years, our communication styles didn’t matter because we were too busy caring for a sick baby, working, scheduling surgeries, and filing insurance to talk.

For 4 years, my husband’s need for a constant companion and my need for time alone went unmet as I slept with our son in his hospital room following one corrective surgery after another.

For 4 years, he was too tired to play his guitar, and I was too tired to read a book.

During those 4 years, our marriage could have fallen apart. It should have fallen apart.

Because, in 1982, there were no books for parents about how to cling to Christ while caring for children who were fighting for their lives. There were no blogs to encourage families of kids with special needs. There were no Facebook groups where stressed dads and moms could share tips. There were no marriage seminars for parents like us.

By the grace of God, our marriage didn’t fall apart.

Thanks to the intervention of a pastor and his wife who lived in our small town, my husband and I learned to trust God and look for His grace as we parented our child with special needs. The glue of faith strengthened our marriage, but communicating with each other still wasn’t easy, even after our son’s health stabilized.

Years later, when we moved to a bigger town, our new church offered a Sunday school class based on a brand new book, The Five Love Languages: How to Express Heartfelt Commitment to Your Mate by Gary Chapman. We learned that out of the five love languages–gift giving, quality time, words of affirmation, gifts of service, and physical touch–my husband’s primary love languages were physical touch and quality time while mine were gifts of service and words of affirmation.

No wonder communicating was hard for us. We were speaking different languages!

I’ve often reflected on how helpful a five love languages book would have been after our son was born. How using the five love languages could have strengthened our marriage during those hard years. How they could have made our son feel more secure during hospital stays and tests. How sharing them with our son and his younger sister could have improved their relationship. How adapting them for special needs families could provide a resource to foster relationships between parents and with their children.

This year, God has opened doors for Gary Chapman and me to co-author a five love languages book for special needs families. Sharing Love Abundantly in Special Needs Families was released in August, 2019 and can be purchased on Amazon or through your local book store.

Now, if you’ll excuse me, I have to get ready for a dinner date with my husband. We’re celebrating 40 years of marriage, wrinkles and all!

Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the quarterly Different Dream newsletter and signing up for the daily RSS feed delivered to your email inbox. You can sign up for the first in the pop up box and the second at the bottom of this page.

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Jolene Philo is a published author, speaker, wife, and mother of a son with special needs.

Author Jolene Philo

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Why I Wrote a Different Dream

Why I Wrote a Different Dream

Jolene Philo Write to Serve Interview

Since A Different Dream for My Child was released, readers have been asking what motivated me to write it. To answer that question, I’m adhering to a lesson I learned as the parent of a special needs child: do not reinvent the wheel unless it is absolutely necessary. Between doctor’s appointments and feeding tubes, surgeries and special diets, there just wasn’t time.

Those days are long gone at my house, but somehow, I still don’t have time to reinvent anything unless there’s no other way. So today, instead of  creating a brand new post about why I wrote Different Dream, I’m directing you to a recent interview at Maria Keckler’s marvelous website WritingtoServe. Maria’s insightful questions did a wonderful job of drawing out both the message of Different Dream and how it came to be written.

And here’s an added bonus. If you go Maria’s website and leave a comment, you’ll be entered in a drawing to receive a free book. So head on out, enjoy the interview, and here’s hoping you win a free book!

Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the quarterly Different Dream newsletter and signing up for the daily RSS feed delivered to your email inbox. You can sign up for the first in the pop up box and the second at the bottom of this page.