The Grief of Disability Caregiving

The Grief of Disability Caregiving

The Grief of Disability Caregiving

The grief of disability caregiving almost overwhelmed me this autumn. First my Aunt Donna, an oasis of security and love during my childhood, died. Grief over Donna’s death was accompanied by grief for my mother. She’s the elder sister by six years, has lived with dementia since 2008, and longs to join loved ones who died before her: our dad, her parents, and her seven siblings.

“Why do I have to live so long?” Mom asked when she learned of Donna’s death. Her look of despair broke my heart.

A few weeks later, Mom’s long term care facility called to report a fall. A few days later, she fell again. No broken bones. No bruises. However she was livid about the change of routine due to measures instituted to keep her safe.

“They’re trying to take over my body. No one should have to live like this,” she tells me often. And my heart breaks every time.

My brother and I asked Hospice to evaluate Mom. When the hospice nurse reported that she’s not even close to qualifying, my heart broke wide open. I cried for my mother who has months, perhaps years, of diminishing life ahead.

How will she endure it?
How will I endure it?

I cried for myself as well. The grief of disability caregiving, the enormity of what lies ahead, overwhelmed and threatened to break me as it had broken my heart. None of the truths that had sustained me in my previous caregiving roles––daughter of a disabled father, mother of a medically fragile baby––assuaged my grief.

To read the rest of The Grief of Disability Caregiving, visit the Key Ministry’s blog for special needs 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

Jolene Philo is the author of several books for the caregiving community. She speaks at parenting and special needs conferences around the country. 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 Amazon. See Jane Sing!, the second book in the West River cozy mystery series, which features characters affected by disability, will be released in November of 2022.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

When Special Needs Parenting Guilt Tries to Steal Your Joy

When Special Needs Parenting Guilt Tries to Steal Your Joy

When Special Needs Parenting Guilt Tries to Steal Your Joy

When special needs parenting guilt tries to steal your joy, how do you react? New guest blogger Lisa Brown is here with a story of what her teenage son has been teaching her about how to answer that question.

I pushed for more until my son finally pushed back.

Over the years, I have often wondered if other parents raising a child with a disability battle guilt like I do. I find that when it comes to setting expectations for my son, it subsequently leads to questioning myself with: just how much is enough . . . or too little? Throw in the stress of balancing everything in life between work, countless doctor appointments, therapies, IEP meetings, prescriptions, surgeries, & hospitalizations (whether planned or completely unexpected).

Expectations can be a slippery slope. Both parents have to compromise when goal-setting for their child. One parent pushes too hard in certain situations while the other seems lenient, and vice versa as they change.

Where’s the balance? Am I a bad parent for expecting too much, or for not expecting enough? My brain tells me one thing: we need to push so that they meet their fullest potential, even when it’s hard. The responsibility is on our shoulders. Yet, in some situations my heart tells me I am asking too much, and I don’t want to push him to a breaking point where he is miserable.

Last year when my son started high school, we knew it would be a challenging year. He had been in all mainstream classes throughout elementary, under special education qualifications for Other Health Impairments: Apert Syndrome, ADHD, and learning disabilities. (You can read more about our family and our journey here.) He had all the accommodations in place, but into the second six weeks he complained of how hard everything was and would say “I can’t do it.”

When I hear those words, my go-to fix-it is to tackle it with relentless encouragement, accompanied with the phrase,Yes, it’s hard but you have to try.”

His teenage rebuttal was, “You don’t understand. You’re not the one dealing with it.”

For the record, the fact that he was 15 loomed in my head. Was this just an attitude because he is 15? Was it just because this was the first year of high school, and he was dealing with adjustment? Is it really time to change his placement in classes? He had some good knowledge, so what if we made the wrong choice, all because he was being a little oppositional?

By the end of the second six weeks, an unexpected medical event happened, and he had his first clonic-tonic seizure in the car after I had picked him up from school at dismissal. After a three-day stay at the hospital, a previous MRI showed scarring tissue on his brain from one of his numerous surgeries, so he started seizure medication. This was a curveball we didnt expect.

After everything settled down, we met with the school and decided that his two core classes, Algebra and ELA, were too fast-paced for him to keep up, even with accommodations in place. After my husband and I had long discussions and agreed that he needed more help, he began Resource classes for the two subjects. I am happy to say that things improved.

Its easy to get wrapped up in trying to look ahead when thinking of your child’s future. Are we doing enough? Getting enough therapies? What if I miss something? What will his/her life look like in 3 days, 3 months, or 3 years?

Theres nothing wrong with looking toward the big picture so you can set goals for your child. But what I found calming and reassuring was to reflect. I took note of the little accomplishments, which were truly monumental, and the hard times that God led us through. I allowed myself to celebrate them without feeling like I was being complacent. Re-evaluating and accepting the fact that goals may have to change can be a reprieve for the whole family. Expectations may change from currently working on, to this year, to . . . not yet, or maybe, not ever—let’s shift our focus to a different goal.

Our children encompass resilience. We can learn from them just as much as they learn from us.

When special needs parenting guilt tries to steal your joy, the struggle can be consuming.

But the battle isnt ours.

Releasing control at the feet of Jesus and trusting His will can be freeing. Proverbs 3:5-6 (ESV) can help you do so.

Trust in the Lord with all your heart,

and do not lean on your understanding.

In all your ways acknowledge him,

and he will make straight your paths.

Give yourself some grace, Mamma.

Give yourself some grace, Dad.

Give your child some grace, too.

Don’t let self-blame or guilt steal your joy. Instead . . .

Rejoice always, pray without ceasing,

give thanks in all circumstances;

for this is the will of God in Christ Jesus for you.

I Thessalonians 5:16-18 (ESV)

I believe that we are the lucky ones by getting a peek at God’s unconditional love so that we can share it with the world. When special needs parenting guilt tries to steal your joy, celebrate those baby steps. If I completed a marathon, I know I certainly would!

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.

Photo by Max Bender on Unsplash

By

Lisa D. Brown, author of Changing Faces – A Journey of Hope and Perseverance, is a native of Texas, where she lives with her husband, two sons, three dogs, and ten chickens. She taught elementary special education for sixteen years and now works part time in accounting. Lisa began blogging to share progress with family and friends after her oldest son’s multiple surgeries. She extended her writing focus to encourage and inspire other families raising children with disabilities. Besides writing, Lisa serves as a ladies’ ministry leader and disciple maker in her church. She enjoys reading, gardening, crocheting, and watching true crime docuseries.  

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

Why Is Expressing Gratitude Especially Important for Families with Disabilities?

Why Is Expressing Gratitude Especially Important for Families with Disabilities?

Why Is Expressing Gratitude Especially Important for Families with Disabilities?

Why is expressing gratitude especially important for families with disabilities? Guest blogger Kristin Faith Evans shares three compelling reasons that can lead you to true expressions of gratitude as the holiday season draws near.

It’s that time of year. The chilly air mixes with autumn scents and rustling fallen leaves. The holidays are quickly approaching, bringing with them all of their memories and emotional implications. During this season, many people talk about the blessings for which they’re most thankful. But the holidays can be challenging and elicit painful emotions for some families. So why is expressing gratitude especially important for families when disabilities in what can be a difficult season? Here are three reasons that are important in our family.

Reason #1: Gratitude makes us more resilient

Studies show that when caregivers practice daily gratitude, they report a higher quality of life and better health outcomes. Focusing on ways that we are thankful can give us a more balanced perspective on our circumstances. Expressing gratitude opens our eyes to appreciate different aspects of our lives that we can miss when we’re focused on our difficulties and loss.

Regularly practicing gratitude can also improve our mental health. Taking time to reflect on our blessings and giving thanks helps lower our stress levels and increases our hope and joy.

Try this: Each day, write down one thing for which you are grateful.

Reason #2: Expressing gratitude deepens our faith

Sometimes it can be difficult to identify something for which we are thankful. During painful seasons of loss and grief, anger can build, and we can feel disconnected from God. Choosing something very simple to thank God for can help us see other ways we can express prayers of gratitude.

Try this: When you’re having difficulty identifying something specific to thank God for, recite the verses written below.

  • “It is good to give thanks to the Lord, to sing praises to your name, O Most High” (Psalm 92:1).
  • “Oh give thanks to the Lord, for he is good, for his steadfast love endures forever!” (Psalm 107:1).
  • “I will give thanks to the Lord with my whole heart; I will recount all of your wonderful deeds” (Psalm 9:1).
  • “Therefore, as you received Christ Jesus the Lord, so walk in him, rooted and built up in him and established in the faith, just as you were taught, abounding in thanksgiving” (Colossians 2:6).
  • “Give thanks in all circumstances; for this is the will of God in Christ Jesus for you” (1 Thessalonians 5:18).

Reason #3: Expressing gratitude strengthens our relationships and family functioning

Studies show that expressing gratitude to others, especially to our significant others, can greatly improve our relationships. Telling someone why you appreciate them and thanking them for something that they have done can increase connection and forgiveness. In times of stress, these stronger relationships help hold the family together giving everyone more support.

Try this: Attach a piece of poster board or a large sheet of paper to your kitchen wall or fridge. Encourage family members and friends to write down someone or something for which they are thankful each day.

What’s one way that you express gratitude? Share your ideas in the comments section.

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.

All Scripture references are from the ESV translation.
Photo by Marcos Paulo Prado on Unsplash

By

Kristin lives with her husband, Todd, and their two children in the Nashville, TN area. She is an author, speaker, mental health counselor, and a mom of two children with rare genetic disorders and complex needs. Her greatest passion is teaming up with her husband to empower other parents of children with disabilities, mental health disorders, and medical complications. She hopes that you may find encouragement and support on their website www.DisabilityParenting.com.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

Organizational Strategies Are Saving My Life Right Now

Organizational Strategies Are Saving My Life Right Now

Organizational Strategies Are Saving My Life Right Now

Organizational strategies are saving my life right now, and my 94-year-old mother is the reason. Our family is in a season similar to the early 1980s when my husband and I were parenting a medically fragile baby. Back then one medical crisis after another meant dropping everything, buckling our son into his car seat, and racing to the doctor’s office or hospital. Nowadays, calls from Mom’s long term care facility require snap decisions regarding her medical care or unexpected trips to her bedside.

Thankfully, I cut my organizational teeth as my son cut his baby ones. The process was drawn out and painful for both of us. Still, I’m grateful for lessons learned in those years because they taught me that organization can ease the stress of caregiving. Several organizational strategies are saving my life right now, and today I’m sharing seven of them.

#1: The Lazy Genius. Kendra Adachi is host of the The Lazy Genius Podcast and author of two amazing organizational books, The Lazy Genius Way and The Lazy Genius Kitchen. She approaches organization as principles to apply in your circumstances rather than as tips that worked in her life. Her method helps me—a “lazy genius”—know how to deal with my caregiving situation, and it can do the same for you.

#2 Sticky Notes. 3-M introduced Post-It® Notes in 1980. I wrote notes to the substitute teachers who took over my classroom on a moment’s notice. Now I use them to write notes to myself about what I was doing before being called away. They are also handy for instructing my husband, daughter, son-in-law, and grandkids what to eat or not eat in the fridge or freezer. Those stickies are assurance that there will be food when I arrive home exhausted.

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 monthly Different Dream newsletter and signing up for the daily RSS feed delivered to your email.

By

Jolene Philo is the author of several books for the caregiving community. She speaks at parenting and special needs conferences around the country. 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 Amazon. See Jane Sing!, the second book in the West River cozy mystery series, which features characters affected by disability, was released in November of 2022.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

Caregiving Spouses Are FOR Each Other

Caregiving Spouses Are FOR Each Other

Caregiving Spouses Are FOR Each Other

Caregiving spouses are FOR each other in a marriage. That’s Heather Braucher’s message in the third post in her Different Dream guest series. You’re going to love what she has to say about the power of caregiving parents being FOR one another as much as you loved. Part 1 and Part 2 of this series.

I still remember the first time I heard my husband say, “I am FOR you.” The first time I tangibly felt and received this message of hope and truth. It was during a moment when my husband and I were discussing our kids. It was one of those tense conversations when we both began sharing our concerns, but it evolved into a desperate quest for validation. Unfortunately, sometimes what we intend to be simple venting can come off more like a competition over who is more burnt out! Deep down our intentions are simply to cry out to one another for connection and affirmation. Thank goodness in this instance, my husband was wise enough to discern what needed to be said next.

He placed his hands on my shoulders and with a bit of firm pressure he said, “I am for you. We are FOR each other.” In that moment I felt an overwhelming sense of safety. Safe because I felt affirmed. He could see how hard I was going and he knew exactly how I felt. I could sense his eyes saying, “We are both weary, but let’s remember and let’s promise that we as caregiving spouses are FOR each other.”

13 years ago

This phrase has become a household constant. And every time we voice it, it speaks life and creates connection. Our family’s life often looks like a tangled mess of electrical cords that results from too many devices plugging into the same power source, overlapping and overwhelming one another. On a daily basis we are juggling the needs of our 3 children and our own needs. Most of our discussions end up being completed via email and text message. It is the only way to break through the noise! Decisions need to be made daily on who is taking which child to which therapy or which doctor or even which school. And then there are debriefs for said appointments. Because without debriefs how are we meant to help them generalize what they are learning to the home or other contexts?

Most weeks, there is an urgent need to discuss a school or social situation that went awry. Sometimes as parents we do not agree on the appropriate follow up. We both want to support our boys to be more successful the next time. When there is a disability involved, navigating these situations can be quite confusing and complex. For a child with special needs, impairments in areas such as executive functioning, self-control and emotional regulation caused by a syndrome or disorder can result in social interactions that can make a parent hold their breath, never knowing how it will turn out.

Parenting a child with extra needs is often an all-encompassing job. The management and discussion of the child’s needs can be overwhelming. The temptation to beat yourself up for not always parenting with therapy skills is constant. It is easy to condemn yourself for getting irritated or impatient. It takes ongoing awareness to control the amount of time spent sharing these thoughts, battles, schedules, and strategies with your spouse.

Parenting is a juggling act, no matter how many children you have and regardless of their abilities or needs. And at the end of the day most of us just want to rest knowing that we loved them well. When we keep in mind that our spouse knows what we are going through and is feeling the same, we can love them better too. Remember to let them know that as caregiving spouses, you are FOR one another. Chances are you both need to hear those words.

I look forward to the next post in the series when I’ll be talking about how moms can be FOR each other too!

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

How to Organically Enter into Life with a Caregiving Family

How to Organically Enter into Life with a Caregiving Family

How to Organically Enter into Life with a Caregiving Family

How to organically enter into life with a caregiving family has been on my mind since September when my dear Aunt Donna died. Since then memories of how she, her husband Jim, and their four children embraced our family after my dad was diagnosed with multiple sclerosis in 1959 have simultaneously caused and comforted my grief for the woman who loved our family well.

In honor of Aunt Donna, who taught me how to organically enter into life with a caregiving family, I’m sharing some of the ways she did so and changed our lives for the better.

Daycare: Donna watched her first child and my brother, both one-year-olds, and four-year-old me while Mom taught school. This was a godsend for Mom as she taught school while attending night classes, cared for Dad, and took my older sister to first grade. My aunt eased Mom’s burdens and made me and my brother feel secure and loved.

Substitute Teacher: Aunt Donna substitute taught in the elementary building I attended. The sight of her in the hall and sometimes in my classroom always rendered me speechless. I couldn’t reconcile her presence at school. She never pushed me to acknowledge our family bond. Instead she waved or winked and treated me like everyone else. This simple act made me feel safe.

Sunday Afternoon Visits: Donna, Jim, and their kids came over a couple Sunday afternoons a month. The adults played cards. The kids played together. At some point Mom and Donna gave each kid an apple and sent us to the living room to watch The Wonderful World of Disney. Because Sunday visits to their home, with steps and small bathroom Dad couldn’t negotiate, were out of the question, they made themselves accessible to us instead.

To read the rest of How To Organically Enter into Life with a Caregiving Family, visit the Key Ministry blog for parents.

By

Jolene Philo is the author of several books for the caregiving community. She speaks at parenting and special needs conferences around the country.  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 Amazon. See Jane Sing!, the second book in the West River cozy mystery series, which features characters affected by disability, will be released in November of 2022.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts