Halloween: Celebrate What Your Family Can Do

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Today can be one of those days that can cause parents of children with special needs to take pause.
To lose their breath for a second.
To take notice of differences.
To feel slighted.
To wish it could be easier.
To give up for a second.
To skip it all.
Halloween.
For me, in those early years post diagnosis, I took comfort living in our own comfortable bubble. But days like Halloween, pulled us out.
And pushed us away at the same time.
We were not like the other families. We still are not. And that can sting sharply or even in a dull way, depending where you are in your journey.
There will be no shortage of advice on the internet today from parents like you and me.
Some will scold you for feeling slighted.
Some will understand and wrap you in a virtual hug.
Others will give you advice or even tell you not to care.
Me, well, I’ll tell ya this.
Give yourself grace on these big holidays.
Your kiddo may refuse to wear a costume or leave the house.
Or at age 12, after experiencing it all in the years before, they may willingly agree to go to 4 houses, not 5, but 4, and even clap when you talk about their costume.
Or they will stay home in the comfort of their space and watch Grandma hand out candy.
Our day won’t look anything like our neighbors. We educate and we try. That’s the best we can do.
And I will feel. So will his dad. Whether it’s 3 seconds or an hour. And that’s allowed.
There is a dance today. One that many tweens and teens are going too. Not him.
Grace my friends.
Forget about everyone else. Focus on you and what you feel on days like today and most importantly doing what works for your child.
Celebrate what your family can do!
Find the joy anyway you can. And remember, you are doing the best you can in a complicated situation. No one should judge you for that.
Happy Halloween!
Wish us luck!
And good luck to you too!
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Kate Swenson

Kate Swenson lives in Minnesota with her husband Jamie, and four children, Cooper, Sawyer, Harbor and Wynnie. Kate launched Finding Cooper's Voice from her couch while her now 11-year-old son Cooper was being diagnosed with autism. Back then it was a place to write. Today it is a living, thriving community of people who want to not only advocate for autism, but also make the world a better place for individuals with disabilities and their families. Her first book, Forever Boy, will be released, April 5, 2022.

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