What Caregiving Is Teaching Me about Writing Fiction

What Caregiving Is Teaching Me about Writing Fiction

What Caregiving Is Teaching Me about Writing Fiction

What caregiving is teaching me about writing fiction could fill a book. If someone had tried to tell me, when I was a kid emptying my dad’s urinal and operating his Hoyer Lift, that caregiving and writing have a lot in common, I wouldn’t have believed it. Nor would I have believed it as a young mom caring for our medically-fragile baby. But as my mother’s health continues to decline and deadlines for my mystery series are looming, I can’t ignore the similarities between the two.

Writing may or may not be part of God’s plan for your future. However, I know he has something in store for your future, and he’s using your life as a caregiver to prepare you for it. Maybe he’ll also use these four lessons caregiving is teaching me about writing fiction to prepare you for whatever lies ahead in your life.

#1: Planning Is Important

As caregivers, we devote portions of our days to planning. We schedule appointments, check to see that the car is gassed up, and investigate special needs trusts long before our kids turn 18. Had this skill been put to use when I began working on my first mystery novel, maybe it wouldn’t have taken me 10 years to finish it. Thanks to my daughter, who showed me a method she created for plot planning, the second mystery was done in a year.

#2: Surprises Happen Despite our Plans

Caregivers can plan and plan and plan, and things will still surprise us, right?

To read the rest of What Caregiving Is Teaching Me about Writing Fiction, visit the Key Ministry website.

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Jolene Philo is the author of theĀ Different DreamĀ 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 theĀ Different Dream website.Ā Sharing Love Abundantly With Special Needs Families: The 5 Love LanguagesĀ® for Parents RaisingĀ 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, andĀ at Amazon. The first book in her cozy mystery series, See Jane Run!, features people with disabilities and will be released in June of 2022.

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Adding a Dollop of Caregiving to the Cozy Mystery Genre

Adding a Dollop of Caregiving to the Cozy Mystery Genre

Adding a Dollop of Caregiving to the Cozy Mystery Genre

Adding a dollop of caregiving to the cozy mystery genre has been a dream of mine. So this winter, I’m making the giant leap from writing non-fiction to fiction while my agent pitches See Jane Run!Ā to publishers. I’d love to have all my caregiving friends join the adventure. Because cozy mysteries are fun, and caregivers need more fun in their lives.Ā Do you need a little more convincing? Check out the book’s elevator pitch:

When young woman dies and an old bachelor rancher goes missing, a greenhorn schoolteacher solves the mystery. But the murderer remains free to roam the vast, remote short-grass prairie of South Dakota in the late 1970s. Can she keep the killer from claiming another victim?

Jane, the schoolteacher, has a disabled father. Guilt from leaving her mother to shoulder all his care dogs her throughout the story. Years of watching multiple sclerosis steal away her once-vibrant father move her to find the person who killed the mother of one of her students.

Are you ready to leap with me? Then jump in with me as Different Dream’s sister website is transformed into my cozy mystery fiction central HQ. From here on out, the plan is for that website to feature pictures, snippets of history, and authentic recipes from where and when the story takes place. You’ll also find exclusive content and more atĀ Down the Gravel Road’s Facebook group, as well as onĀ Instagram,Ā Twitter, andĀ Pinterest. And very soon, you’ll be able to sign up for the website’s RSS feed and join Down the Gravel Road’s mailing list.

Still not sure about adding a dollop of caregiving to the cozy mystery genre? Maybe these questions and answers will ease your concerns.

To read the rest of this post, leap on over to the Down the Gravel Road website.

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

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An Update on the Special Needs Love Languages Book

An Update on the Special Needs Love Languages Book

An Update on the Special Needs Love Languages Book

An update on the special needs love languages book is a fitting way to usher in February, the month known for romance and love. I want to share what’s happening during interviews as Ā Dr. Gary Chapman and I collaborate on this specialĀ needs love languages book.Ā Hopefully, these 6 observations about parents raising kids with special needs provide Different Dream readers with a glimpse at what’s going on.

  1. Interviewing families is fascinating. Since the new year, 13 families have graciously shared stories of how they use the 5 love languages with their spouses and with their children, both kids with special needs and those who are typically-developing. The stories they tell about how the 5 love languages help them fill their spouses and children’s love tanks are an encouraging affirmation of the elegant simplicity and power of the love languages. I’m convinced that the 15 scheduled interviews yet to be completed will confirm this observation.
  2. Parents of kids with specialĀ needs are keen observers.Ā They know their children’s love languages, even those of non-verbal kids, because they watch their kids behaviors with systematic intentionality. What these parents have described will help many other families determine their kids’ love languages.
  3. Parents speak the love languages to their kids withĀ special needs in creative ways.Ā Once they know their kids’ languages, they devise innumerable ways to determine their children’s love languages and to speak love to their kids. And they show their children’s doctors, therapists and teachers how to connect with their kids, too.
  4. Parents love their typical kids to the moon and back. They worry that their children without special needs don’t get enough attention, that they become the unintentional sacrifice at the altar of special needs. Many of them feel that using the love languages to fill their typical kids’ love tanks is the best way to remediate this circumstance. Many of them also say that their typical children have no fear of people with disabilities and special needs, but deep compassion for them.
  5. Spouses have ingenious ways to speak love to one another. As a rule, parents of kids with special needs don’t have much money or time. So during each interview, I ask parents to describe inexpensive and easy ways they’ve devised to speak their spouses’ love language. Honestly, this is my favorite part of each interview because the ideas are so wonderful. I can’t wait to share them in the book.
  6. Special needs families are persistent. They don’t give up. They know they may be the primary caregiver for their adults children as long as the parents are alive. So they are constantly looking for ways to better the lives of every member of their family by keeping one another’s love tanks full.

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

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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.

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