Special Needs Families Can Make Thanksgiving Something to Be Thankful For in These 4 Ways

Special Needs Families Can Make Thanksgiving Something to Be Thankful For in These 4 Ways

Special Needs Families Can Make Thanksgiving Something to Be Thankful For in These 4 Ways

Special needs families can make Thanksgiving something to be thankful for by thinking through the holiday ahead of time. Today, guest blogger Jenn Soehnlin shares ideas she puts in practice so Thanksgiving is fun for everyone at her house.

How Special Needs Families Can Make Thanksgiving Something to Be Thankful For

Thanksgiving is one of my favorite holidays. I love gathering with loved ones to reflect on all the things we are thankful for and realize how blessed we truly are  while eating some amazing food. 

But, the realities of special needs parenting can make the holiday challenging if we are not intentional about protecting it and making necessary plans to help the holiday go peacefully. Here are four tips I’ve found to help plan for a more intentional Thanksgiving.

#1: Release Cultural Expectations

Just because everyone else celebrates with turkey, mashed potatoes, and pumpkin pie doesn’t mean you need to as well. Maybe there’s a meal your whole family enjoys and will make for a new, fun family tradition without all the cooking. 

Just because everyone else gathers with the whole extended family, doesn’t mean you have to as well. This is a holiday for you and your family, and you can celebrate it however you feel is best without feeling guilty about it.

#2: Do What’s Best For Your Family

Some relatives can be very supportive of our family’s unique needs, and some…not so much. If you need to say no to a whole family Thanksgiving gathering because it will be stressful and overwhelming for your family and child, then graciously say no. Thank them for the invitation but tell them that this year your family has other plans.

It can be hard to say no to our loved ones, but by saying yes to them we could be saying no to what’s best for our own family. According to Genesis 2:24 we are called to be stewards of our spouse and children before our parents, siblings, and other relatives.

#3: Make The Accommodations You Know Your Child Will Need

Every Thanksgiving the only thing my younger son will eat is the rolls. The only thing my older son will eat is the turkey, so when we go to family’s house for Thanksgiving dinner, I pack a few food items they’ll eat to make the meal more complete for them. Knowing they have a whole plate of food they will eat makes for a smoother meal and less anxiety for everyone.

We always bring their tablets when we go to a family Thanksgiving. When my children start feeling overwhelmed, they can go play their devices in a quiet room. You know what your child needs and will eat, so pack what is necessary and plan ahead to make the holiday go as smoothly as possible.

#4: Celebrate The Things You Are Thankful For.

Thanksgiving is one day we set aside each year to intentionally celebrate the things and the people we are thankful for. 1 Thessalonians 5:8 says “Give thanks in all circumstances, for this is God’s will for you in Christ Jesus.”

Sometimes it can be hard to find things to be thankful for on this special needs parenting journey full of stresses and challenges. In the month of November, I reflect on (and journal about) the things I am thankful for. I encourage you to do the same. The intentional change in perspective from the things that are hard to the things that are good, the things that I am grateful for is helpful to my spirit and my outlook on life. Here are some things to reflect upon: 

  • The qualities you love most about each family member. 
  • Provisions and blessings your family have experienced this year.
  • Progress your child(ren) have made–every milestone and every single hard-fought inch in-between. 
  • The people in your village who help you, your child, your family. 
  • What you’ve learned on this special needs parenting journey. 
  • How you’ve been challenged and grown in your faith this year.

I hope these ideas help you have a wonderful Thanksgiving with your loved ones. May it be filled with peace, joy, love, and thanksgiving!

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Jenn Soehnlin celebrates Thanksgiving with her family in Virginia. She is the mother of two young boys who are precious blessings and who both have special needs. She is the author of Embracing This Special Life: Learning to Flourish as a Mother of a Child with Special Needs and enjoys blogging about faith and special needs parenting at www.embracing.life.

Author Jolene Philo

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When life doesn’t go as planned, I usually react in one of two ways. Either with equanimity and grace because I’m with people I want to impress. Or with grumbling and complaints because I’m with my family, and they love me no matter what. Neither response follows Paul’s call in Philippians 2:14-15 to do all things without complaining or grumbling so that I can be the light of Christ in a dark and twisted world.

For the past few weeks, my days were full to overflowingly busy, even before life didn’t go as I had planned. The beans were coming on in my daughter’s garden, which means we were canning beans a couple times a week. We finished the first batch right before I went to Chicago for a promotional book tour for Sharing Love Abundantly after it released. When I got home a few days later, there were more beans. I was fine with that, because I had planned time into my schedule for canning season.

My daughter and I were confident we could maintain the household and our job duties even though we were short a few adults. My husband was in Alaska, where he grew up, for a week. My son-in-law started a second job, so he was gone more than usual. Even so, we were handling things well until when-life-doesn’t-go-as-planned thing happened. I hurt my back.

The kind of hurt that takes days and weeks to heal.
The kind of hurt that means a person can stand or lie down, but not sit.
The kind of hurt that means a person needs 5 minutes to move from stand to lie down and visa versa.
The kind of hurt that means an ice pack for 10 minutes every hour.

To read the rest of this post, visit Key Ministry’s blog for 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 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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The Polar Vortex and Gratitude: An Unlikely Combination

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The polar vortex and gratitude. I never thought of pairing the two until the great polar vortex of January 2019. Even I have lived through plenty of what we called “cold snaps” until the 24/7 news cycle invented a more alarming term.

  • I was 9 in 1965, the year that held the record low temperature for January 30 until 2019.
  • I was 25 and 5 months pregnant in 1982 when the mercury dipped to -45° when we were living in northwest South Dakota.
  • I was 33 in 1989 when school was called off for 2 days before Christmas break, which meant my third grade students had their anti-climactic Christmas party when school resumed in January.

The difference between my response to previous cold snaps and the 2019 polar vortex go far beyond a name change. My response to the 1965 cold snap was delight when Mom said she would drive me to school. In 1982, my husband and I piled into our friends’ car and traveled 90 miles to go out to eat, though the thermometer was -20° at its warmest.

In 1989 our son born with medical special needs was 7, and his baby sister was a few months old. By then I was haunted by what our son’s early years had revealed. His multiple surgeries, frequent invasive procedures, and nearly constant infections and illnesses showed that bad things happen even when you follow the rules and choose wisely. Therefore, my wisest course of action was to control the situation tightly, to protect my children, and keep everyone inside until the cold snap ended, or we ran out of Kraft Macaroni and Cheese.

To read the rest of this post, visit the Hope Anew website.

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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The grief we live with as parents of kids with special needs is real and pervasive.  This week, it showed up in two different places at two unexpected times.

Grief’s first appearance came as I sat enthralled by our granddaughter who was sleeping in my arms. She’s 2 1/2 weeks old, I thought to myself while gazing at her peaceful face and perfect, unmarked skin. She’s the same age our son was when he was released from NICU. With that, grief for his surgical scars and the pain he bore during his early weeks washed over me. I grieved for the 17 days he spent in the hospital instead of in our home as a newborn. My grief felt as fresh and real as it had been after he was born in 1982.

Soon though, the all too familiar sense of loss passed. What remained was gratitude for the child in my arms and the blessing of being part of her early days. A few days later I was grateful again when the grief we live with as parents of kids with special needs appeared in a different place and another unexpected time.

This appearance occurred while I completed one of the final parent interviews for the book I am co-authoring with Dr. Gary Chapman. Each interview ends with the same question: Is there anything else you’d like to mention? I presented that question to the mother of an almost 3-year-old, adorable red-headed boy who has cognitive and speech delays. Here’s what she said:

If necessary, go through counseling to talk about hard things. Have a safe space and a safe person who can help you see more clearly. I’ve done some mental health counseling. There is an element of grief that your life and your child aren’t what you expected. Give yourself space to grieve. Being honest about your grief lets you see what kids with disabilities really need instead of dwelling on all the broken things. So give yourself permission to grieve.

This wise, young mother and I sat in her living room. “Even thought its not something we asked for, our son may live with us the rest of our lives. It’s worth every minute,” she said and smiled at her adorable, red-headed son and said, “You’re worth every minute.”

We looked at one another, connected by the grief we live with as parents of kids with special needs, the grief that binds us together and makes us grateful for the blessings and relationships we never take for granted.

I thought of my son and the 36 years of mingled joy and grief we have known with him. Worth every minute, I offer back in silent prayer. I am so grateful for your life, my son.

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.

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

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Sharing Special Needs Love this Valentine’s Day

Sharing Special Needs Love this Valentine’s Day

Sharing Special Needs Love this Valentine’s Day

Sharing special needs love is often a one way street where others support caregiving families by encouraging and giving to them. Trish Shaeffer, mom to sons with special needs, suggests ways families can reciprocate by showing appreciation and giving back this Valentine’s Day.

As Valentine’s Day approaches, we sometimes forget what the holiday is really about thanks to the big markets out there for candy and cards and more. It can be overwhelming, trying to decide what to get and who to get a box of candy or card for.

Yet Valentine’s Day should be a day when we slow down by sharing special needs love and appreciate all who are there for us. Whether your encourager is a friend, boyfriend, girlfriend, classmate, teacher, parent, husband, wife, or child–you don’t need to spend tons of money or buy a dozen roses to show that you appreciate what they do. All it takes is a hug, a shared day together, a handmade card, a homemade meal, or a thoughtful favor done for someone.

One small gesture is all you need. Showing people you care is contagious and will continue to spread the special needs love you’ve received. Even better, you are showing your children how to show love, acceptance and helping those in need.

I challenge you this Valentine’s Day to spread the love by doing something small that could make a huge impact on someone’s life. Here are some more simple ideas to spread the love:

  • Volunteer to help spread the special needs love through delivering Meals on Wheels or spending time at a senior center with those that may not have many visitors.
  • Pay for the coffee of someone behind you in line.
  • Volunteer at an animal shelter or donate some old towels or blankets for the animals to have something to sleep with.
  • Bake some cookies for your neighbor.
  • Hand make a card for your child or significant other.
  • Make dinner together as a family.
  • Donate items to a local homeless shelter.
  • Volunteer to cuddle NICU babies at the hospital.
  • Donate items to the Ronald McDonald Family Room. Coloring books, snacks, and  coffee are a few good suggestions.
  • Give someone a hug or high five.

If you have more ideas about sharing special needs love on Valentine’s Day or all year round, leave a comment below.

 

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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Trish Shaeffer mom of 3 active boys, a 9-year-old and 5-year-old twins who were born 2 months early and have special needs. She’s a peer supporter for Parent to Parent and volunteers with the United Cerebral Palsy Network, Special Olympics, and the United Way. She’s also an equine volunteer at Leg Up Farm. She’s married to her best friend and biggest supporter, Chris Shaeffer.

Author Jolene Philo

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Pie Advice from a Seven-Year-Old

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Pie advice from a seven-year-old has become a regular thing at our house. Our granddaughter, who always has a lot to say about pie in general and cherry pie in particular, turned seven in January. Between that momentous occasion and many recent opportunities for pie...

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