Alternative Halloween Ideas for Kids with Special Needs

Alternative Halloween Ideas for Kids with Special Needs

Alternative Halloween Ideas for Kids with Special Needs

Alternative Halloween ideas for kids with special needs are implemented more now than in the past. In the interest of spreading alternative Halloween love, guest blogger Mark Arnold shares 10 simple, sensible ideas.

While Halloween can be a fun time of year for many children, for many children with special needs it can be a confusing, anxiety-inducing, terrifying time. It doesn’t have to be like that if we have alternatives in place so they can safely join in the fun. Here are 10 helpful alternative Halloween ideas you can easily implement for kids with special needs.

          1. Prepare a visual timetable in advance so kids with special needs and disabilities know what is going to happen. This will help them to be less anxious about the holiday.
          2. Prime friendly neighbors who are known to your children. For example, ask the neighbors to have their outdoor lights on and a bucket of sweets or snacks ready for the children to enjoy safely. Prepare the children to sing their favorite song as a thank you.
          3. Go for an autumn walk in the countryside or a park. Collect pinecones, pick blackberries, kick through the fallen leaves, or look up at the stars. Bring flashlights along on the walk and have hot chocolate and cookies ready for when you get back home.
          4. Provide headphones for children sensitivity to loud noise so unexpected noises are less of a problem.
          5. Choose alternative bright and light outfits. Make Halloween more about the dressing up than wearing terrifying costumes. There are plenty of non-scary, positive options to choose from.
          6. Host an alternative party, a counter-cultural celebration of things that are bright, light, colorful, and good. This offers more variety for dressing up and is equally fun without the scares.
          7. Choose sugar-free sweets or healthy snacks with a Halloween theme.
          8. Have an autumn indoor picnic. Spread out blankets and enjoy a feast together. If the weather is good, have an autumn barbecue with good outdoor lighting.
          9. Think about who is being left out and invite them to your light party, autumn picnic, or barbecue.
          10. Ask your kids how they are feeling. Have activities ready for those who are struggling so they can have fun in a different way. Things like carving pumpkins, making pumpkin mini-pies, a bubble machine, apple bobbing, and roasting marshmallows. Also create safe space kids can access if they need a rest. Fill it with cozy blankets and cushions and provide soft lighting.

           

        1. I hope these Alternative Halloween ideas for kids with special needs help make the holiday a great success!Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the monthly Different Dream newsletter and signing up for the daily RSS feed delivered to your email.
          Image by Mayur Gadge from Pixabay

By

Mark Arnold is the Additional Needs Ministry Director at Urban Saints, a leading national Christian children’s and youth organization. He is co-founder of the Additional Needs Alliance, a national and international advocate for children and young people with additional needs or disabilities. Mark is a Churches for All and Living Fully Network partner, a member of the Council for Disabled Children and the European Disability Network. He writes an additional needs column for Premier Youth and Children’s Work (YCW) magazine and blogs at The Additional Needs Blogfather. He is father to James, who has autism spectrum condition, associated learning disability, and epilepsy. To find out more about how Mark’s work can help you, contact him at: marnold@urbansaints.org or @Mark_J_Arnold

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

How To Cope During a Rough Caregiving Season

How To Cope During a Rough Caregiving Season

How To Cope During a Rough Caregiving Season

How to cope during a rough caregiving season. What? Who wants to write about that topic when doing so usually comes from hard experience? That’s the case for guest blogger Lisa Pelissier who describes what’s been happening at her house and what’s helping her cope these days.

It’s been a rough season.

My husband’s health has collapsed and he can’t work more than a few hours a week.

My son with high-functioning autism can’t sleep and has been depressed and anxious.

We had Covid this summer, but not all at once. First the girls succumbed, which meant 2+ weeks of quarantine. A month later I got it. Another 2 weeks of quarantine.

And my youngest got diagnosed with autism. Which really doesn’t change anything. She’s still exactly who she was before the diagnosis. The only difference is that I feel more tired.

Just what I needed.

People ask me how I’m coping, and it’s easy to answer that question with a “Hanging in there,” or “Doing okay.” But that focuses on the Im part of the question. I think a more helpful question for me to ask myself pertains to the how part.

How do you hold it together when things are falling apart?
How do you cope when everything seems to go wrong all at once?

Here are my answers about how to cope during a rough caregiving season:

Cry when you need to. It’s not a bad thing. Instead of stuffing grief under a sleek layer of artificiality, just cry. You’ll feel better.

Regain perspective. This isn’t the first time things have been this bad. We got through it before and we’ll get through it this time. It’s only hard because we’re looking at it from the midst of it. Looking back, we may decide this wasn’t so bad after all

Identify Blessings. It’s not all bad. The A/C works, my favorite blessing of the summer. The cars are holding up for the time being. Our kid with PANS seems to be in remission and doing well. We have a loving church family and a great homeschool group. And the neighbors have 23 cats, so we can always find something soft to snuggle. Identify the blessings in your life and enjoy them.

Maintain Friendships. I have several friends who are also in the midst of rough seasons. While I wouldn’t wish their troubles on them, it’s helpful that God decreed their troubles to occur at the same time as my own. We can’t solve one another’s problems, but we can commiserate and even joke together in the trenches.

Trust God’s Providence. There is a temptation to ask, “Why is God doing this to me?” Don’t give in to it. A few years ago I was suffering an excruciating pain disorder. But the clear comfort of God enfolded me. I never doubted for a moment that God was doing something for me, not to me. And He is the same now. His refining hand is like a sculptor carving a stone into something beautiful. It stinks when He’s lobbing off huge chunks of rock to get what He wants out of the raw material that is you, but you can trust Him. He has a plan and a purpose.

Consider it all joy, my brethren, when you encounter various trials,
knowing that the testing of your faith produces endurance.
And let endurance have its perfect result,
so that you may be perfect and complete, lacking in nothing.”
James 1:2-4

Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the monthly Different Dream newsletter and signing up for the daily RSS feed delivered to your email.

By

Lisa Pelissier lives in Oregon where she is a homeschooling mother of four (three with disabilities) and author of three middle-grade fiction novels as well as a YA fantasy novel. Lisa owns SneakerBlossom Books, offering Christian, classical homeschool Study Guides and curriculum. She also works as a freelance copy editor, an artist, a substitute teacher, and a tutor. In her spare time Lisa enjoys playing the piano and fretting about things over which she has no control. Email Lisa at sneakerblossom@yahoo.com or connect on Facebook.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

Mothers Are FOR their Children with Disabilities and Special Needs

Mothers Are FOR their Children with Disabilities and Special Needs

Mothers Are FOR their Children with Disabilities and Special Needs

 Mothers are FOR their children. Moms may think they convey this truth well, but sometimes kids with disabilities and special needs have to hear that message loud and clear. In the second post in her ongoing series, guest blogger Heather Braucher explains the whys and hows behind assuring her son that she is always FOR him.

On one particular day, I was waiting for my son as he was getting off the school bus. As he descended the steps, another boy raced to get to me first. This child wanted to make sure I knew that my son had teased him. I had a sense that the other child was not completely innocent. And if I’m honest, I was getting fatigued by this after school routine repeating itself day after day. I briefly acknowledged the other child’s complaint and began walking my son home.

I remember looking at my son while we were walking, and I could tell he was getting himself ready for another talk.

Having a talk with Garrett has become as frequent as having coffee. The most common precursor to these infamous talks were the phone calls we would receive from his school. For example:

Mrs. Braucher, Garrett cut his classmate’s hair.

Mrs. Braucher, Garrett peed in the grass during recess.

Mrs. Braucher, Garrett won’t stop kissing the girls.

Mrs. Braucher, does Garrett have a lunch account? He continues to get school lunches and claims they can “put it on his tab.”

Over the years the phone calls started to get more impressive:

Mrs. Braucher, Garrett has a ladybug stuck in his ear.

Mrs. Braucher, Garrett says that he was stung by a bee, a wasp, and a hornet simultaneously.

This sweet boy of ours makes me laugh and smile bigger than I ever could have imagined. At the same time, he makes me want to shout his name with the same energy that the names Alvin the Chipmunk and Dennis the Menace have been shouted before. If you have a child like Garrett, a witty, clever, brilliant child that can manipulate like the best of them, you know what I mean!

Well, on this particular day with this particular complaint, I looked at him and said, “I need you to know, I am on your side, Buddy.”

He looked surprised and even a little confused. And then he hung his head and said, “No, you’re not.”

I stopped walking and placed my hands on his shoulders and told him, “Whether you made a mistake or not, I am for you. I am on your side. Whether I need to teach you what you did wrong, whether there is a consequence, or whether the other kid started it, YOU are MY son. I am here for YOU. I am FOR you.”

And that was the end of our talk.

This sweet boy has taught me so much.

My biggest challenge parenting my special boys has been trying to identify when their behavior is or is not a result of their unique struggles. This matters because it directly impacts which lesson is most necessary as a follow up. There are all too many opportunities for teaching and training in this realm of parenting. But one that I never ever want to forget is to teach them that no matter what, I love them and I am FOR them. That one is above all else.

Mothers are FOR their children with disabilities and special needs. I hope you find ways to speak this truth to your kids often and clearly. Come back next time, when I dive into how we can be FOR our spouses!

Part 1: We Are FOR Parents and Children
Part 2: Mothers are FOR their Children with Disabilities and Special Needs
Part 3: Caregiving Spouses are FOR Each Other
Part 4: Caregiving Moms are FOR Other Caregiving Moms
Part 5: Jesus is FOR Caregiving Parents

Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the monthly Different Dream newsletter and signing up for the daily RSS feed delivered to your email.

By

Heather Braucher is a member of the “Braucher Bunch” aka her energetic family of 5. The bunch includes her husband and their three children, all of whom are dominant and extroverted and are going to change the world (if she can keep them alive!) She has always held a passion for writing, but motherhood has given her a reason to share her experiences, heartaches, and victories with others. In her writing you will hear stories of hope as well as grief, as her family has navigated life in ministry in the US and overseas, all while discovering that 2 of her children have special needs. Her desire is to provide others with connection, understanding, encouragement and laughter, all washed with the love of Christ.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

The Beauty of Disability

The Beauty of Disability

The Beauty of Disability

Our pastor was introducing a new sermon series about beauty when these four words, which I had never strung together before, which I did not want to string together, took up residence in my brain. My response was swift and prickly.

The beauty of disability? Why would I consider such a thing?

Several images flashed by in rapid succession:

  • My father lying in a hospital bed, his once strong body ravaged by multiple sclerosis.
  • My 2-day-old son splayed in a NICU isolette, his abdomen marred by post-surgical incisions.
  • My elderly mother leaning sideways in her recliner at the long-term care facility where she lives.

My eyes welled with tears. My heart ached for the pain and loss experienced by people I love dearly. Where was the beauty in their disabilities?

I fought for control and turned my attention back to the pastor as he read Genesis 1:27.

And God created man in His own image, in the image of God He created him; male and female He created them. (NASB)

The pastor explained how God revealed his beauty in the act of creation. Also, because all humans are created in God’s image, we bear the image of His beauty even as our hearts long for the fullness of it.

Wait a minute!

I believe that God’s creation reveals his beauty.
I believe that all humans are made in God’s image.
I believe that all humans includes those with disabilities.
I believe that those with disabilities reveal God’s beauty.

Click here to read the rest of The Beauty of Disability at the Key Ministry website.

 

Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the monthly Different Dream newsletter and signing up for the daily RSS feed delivered to your email.

By

Jolene Philo is the author of the Different Dream series for parents of kids with special needs. She speaks at parenting and special needs conferences around the country. She’s also the creator and host of the Different Dream website. Sharing Love Abundantly with Special Needs Families: The 5 Love Languages® for Parents Raising Children with Disabilities, which she co-authored with Dr. Gary Chapman, was released in August of 2019 and is available at local bookstores, their bookstore website, and at Amazon. The first book in her cozy mystery series, See Jane Run!, features people with disabilities.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

A Course on Self-Compassion Showed Me that I Am Enough

A Course on Self-Compassion Showed Me that I Am Enough

A Course on Self-Compassion Showed Me that I Am Enough

A course on self-compassion showed guest blogger Laura Spiegel that she was doing enough for her daughter who lives with special needs. In this post, she describes how the course helped her come to that conclusion.

I recently finished a course on self-compassion. Pioneered by Dr. Kristin Neff nearly twenty years ago, self-compassion is the practice of giving ourselves the same kindness and care we’d give to a good friend. If you’re like me, it’s not overly difficult to extend a hug or words of empathy and understanding to a friend who is struggling. But to extend that same olive branch to myself? That’s sometimes asking too much.

I’m not big on meditation. My mind wanders and I get overly focused on my loud breathing. Same thing with verbalized mantras. I’ll start with one and then flit to another and then wonder what everyone else is thinking about. Before I know it, I’ve made myself a giant dish of ice cream while stalking Facebook. Something tells me I’m doing it wrong . . .

Not long ago, a new practice took me by surprise. The course instructor told us to break out a pencil and paper and write a few sentences from the viewpoint of the “compassionate self.” In other words, if I were to speak to myself as I would a good friend, what would I say? Twenty minutes later, I didn’t want to stop!

Here are a few snippets from my first letter to myself:

Youve been feeling the last couple of days like you arent doing enough. Being enough. I wish you could see what I see!

I see a woman who is carving a path for herself. A woman who is present for her children and an advocate for them.

I see a woman who is learning to care for herself. Who is exploring new joys and learning new things, but also backing away when they dont spark joy.

I see a woman who has maintained an exercise routine for almost a year. Did you ever think you could do that? Your body is stronger and your mind clearer because of it. Keep it up!

I know you worry about not doing enough with your time. Thats a distraction from whats important—and from the path you know you need to be on. Say goodbye” to those worries. Picture them as a dandelion and blow them away.

Finally, just know that only good mothers worry that theyre not good mothers. All of your friends struggle with this too. The anger, the yelling, the vacillation between leniency and strictness, friendship, respect, tenderness, and lesson-teaching . . . Listen to your intuition. It will tell you what you need to do. How you need to be.

Think about what you ultimately want to instill in your kids. Confidence. The ability to navigate stressful situations and solve problems. Kindness for themselves and for others. And full-on knowledge that they are loved. Lead with these goals in mind, and the right words and actions will come to you.

Where in the world did these words come from? When I first put the pencil to the page, I didn’t plan to write about my worries that I’m not enough. But clearly, they were surrounding me. Suffocating me. And I needed a good friend to extend some words of empathy.

After I wrote that first letter, I treated myself to a pretty sketchbook. These days, I try to spend early mornings on the porch with a cup of coffee and my writing. Some letters are little more than a few affirmations that I am doing my best—and that women and mothers everywhere are struggling with many of the same things that I am. Other days, I veer all over the place. I try not to think about my words too much. I just let them flow.

Occasionally, if I need a pick-me-up during the day, I flip to a random page and read a few sentences I wrote during the course on self-compassion. And I know with the deepest sense of certainty that I am loved.

Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the monthly Different Dream newsletter and signing up for the daily RSS feed delivered to your email.

By

Laura Spiegel spent 12 years at the world’s largest biotech company, partnering with professionals and care teams to help people with special needs and disabilities lead full and happy lives. In 2013 her daughter was diagnosed with cystic fibrosis. Laura now hosts Paint Her in Color, a website that offers emotional support to parents of children with special medical, developmental, or behavioral health care needs. When she isn’t reading, writing, or soaking up time with her husband and kids, Laura can be reached at Paint Her in Color, by email at laura@paintherincolor.com, and on Facebook and Twitter.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

The Blessings of Caregiving

The Blessings of Caregiving

The Blessings of Caregiving

The blessings of caregiving may not be readily apparent to families raising children with special needs and disabilities. Kristin Evans, a Different Dream guest blogger and mother of two amazing kids, describes the blessings her family experiences daily in their caregiving life.

Some people might look at my family and think that we have more to mourn than celebrate. My daughter, Beth, faces extraordinary medical and developmental challenges every day. Yet my husband, Todd, and I have discovered that we are just as blessed, if not more, than the average family. We’ve identified numerous reasons our lives are much richer as a result of having fought sixteen years to save both of our children’s lives. These are just three of the blessings of caregiving that families of loved ones with disabilities often experience.

Blessing #1: A New Perspective on Life

As a disability and medical mom, I’ve experienced how difficult it can be to express gratitude. When I’ve been surrounded by loss, the serious illnesses of my children, and seemingly-impossible circumstances, my tendency has sometimes been to become bitter and sad. Watching my children suffer doesn’t naturally prompt a thankful attitude in me.

But it has been through our difficult circumstances that our family has received the rare gift of seeing life through a different lens. Our greatest desire is for everyone to be at their health baseline and not in the hospital. The days that all four of us are able to just be together at home are the greatest blessings in life.

We’ve learned to be thankful for simple moments together—laughing, enjoying a meal, or playing outside. Sometimes we have to look for the blessings of caregiving and choose gratitude, but God’s good gifts are always there—big and small.

Blessing #2: More Reasons to Celebrate

Little wins are big reasons to rejoice. Beth may not be earning trophies in soccer or straight A academic awards, but she is working very hard on her individual goals. When she reaches a new milestone or learns a new skill, we feel like throwing a big party! Families with disabilities may not celebrate for the typical reasons, but we often have more reasons. When our children make progress in therapy, have a good day, or their health improves, these are the many moments to recognize and enjoy.

Blessing #3: Becoming Better People

My children have taught me how to truly live. I’m a better person because I’m their mom, and I’ve had the privilege of loving and advocating for them their whole lives. As parents caring for our children with disabilities or complex medical needs, we face regular obstacles. And we walk with them through their own unique challenges. In doing so, we can develop a deep empathy for other hurting parents and people in the world. We learn what’s most important in life and to not take a single special moment for granted.

What blessings of caregiving has your family experienced?

Please share your celebrations with us in the comments section!

Blessings,

Kristin

Do you like what you see at DifferentDream.com? You can receive more great content by subscribing to the monthly Different Dream newsletter and signing up for the daily RSS feed delivered to your email.

By

Kristin lives with her husband, Todd, and their two children in the Nashville, TN area. As an author and mental health therapist, her greatest passion is walking with others on their journey to deeper emotional, psychological, and spiritual wholeness. As both her children have rare genetic disorders, Kristin especially loves supporting other parents of children with special needs. She hopes that you may find encouragement and support through her two websites and blogs, www.KristinFaithEvans.com and www.DisabilityParenting.com.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts