Caregiving Moms are FOR Other Caregiving Moms

Caregiving Moms are FOR Other Caregiving Moms

Caregiving Moms are FOR Other Caregiving Moms

Caregiving moms are for other caregiving moms. Or are we? In the fourth installment of her series, Heather Braucher describes the struggle many caregiving moms face in accepting and giving encouragement from other caregiving moms.

I was in a parent workshop listening to a speaker talk on the subject of behavioral therapy for children. I could sense that there were parents in the room—like me—who were in the thick of the struggle.

But there were also parents in the room who were on the other side. The side where victory and hope live.

During the talk, I battled the voice in my head that said, “Your situation is more complex. Your child’s struggles will never end. You will never be on the other side.”

I hate that voice. I believe it to be the voice of the enemy, the father of lies, who wants us to remain trapped in discouragement, devoid of hope.

I have become more aware of that voice. I guard my heart with prayer and keep my eyes open to recognize it. I prepared myself before the workshop by praying, “Lord, help me hold every thought captive to you. Help me hear what it is you have for me today.”

The voice and its thought, “That’s great for you, but there’s no hope for me here,” had wormed its way into too many areas of my life before.

I recall the early days when the kids were babies. Those days of sleep training, breast-feeding and behavior training. The days when well-meaning mothers and friends would share how their child is sleeping through the night, or how their child could listen and obey right away, or how 1-2-3 magic was the key. They were not wrong to share, but I often felt so discouraged.

But then I remember when my first child was about 11 months old and a friend passed along the book Healthy Sleep Habits, Happy Child. This was one of the first times a recommended strategy worked after applying it. I was in shock and over the moon ecstatic! Even so, I hesitated sharing about that book because I didn’t want to frustrate someone else.

So many times I had been around the table with other moms listening to their success stories and thinking, “That’s awesome for you, but it won’t work for me.”

How often do we see the success of others and think there has to be a reason they reached their goal? A reason that sets them apart from me? A reason that makes success more possible for them than it is for me?

Witnessing my son Jackson’s progress with speech and language development ever since he received adequate hearing has provided me with the most profound opportunity to recognize and celebrate progress! But it did not come easy. And I imagine that is true of so many other women who are sharing their stories of victory or recommendations.

We share because we have been in a place of suffering, and have found our way on the other side and we desperately want the same for others. I often blog about the blessing that suffering can bring. Trust me, I do not enjoy suffering. I used to avoid it at all costs. But I now know that the struggle, the long suffering, the day-to-day battle, make the awareness and ability to embrace being on the other side so sweet.

We cannot predict how quickly success can be achieved for others, but we can share our struggles and our wins in hopes of bringing others closer to being on the other side of their struggle. We can be caregiving moms who are FOR other caregiving moms.

I will close out this series with a post about how the Lord is FOR us!

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

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Image by StockSnap from Pixabay 

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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

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New Blog for Christians Parenting the Mentally Ill

New Blog for Christians Parenting the Mentally Ill

New Blog for Christians Parenting the Mentally Ill

Christians parenting the mentally ill need other believers to support them. Today Lisa Pelissier is here to introduce Different Dream readers to a new blog designed to support Christian families impacted by mental illness and to equip extended family and friends to encourage them.

Statistics show that one in five adults in the United States suffer from mental illness. The numbers are even more sobering among young adults. Almost ten percent of people aged 18-25 find their life limited by mental health conditions. Sadly, these conditions tend to be hereditary, and many of us find ourselves dealing with more than one family member who is suffering.

Often, the church is unprepared for families suffering from these harrowing, invisible disorders. Because Christianity deals with the invisible facets of people’s lives, the lines between spiritual matters and mental health issues can become blurred. Misunderstandings abound, even amid good intentions.

As a wife, daughter, sister, and mother of people with mental illness, I know first-hand that it can be difficult to find support from other believers. Most of the time people are sympathetic, but to a great degree, they have no idea what it’s like to live in a world where you must walk on eggshells, fight for medical care, or figure how to discipline someone who can’t respond appropriately.

With this thought in mind, Amber Healy, Georgia Mathison, and I have started a blog, Eleventh Willow, to support Christians parenting the mentally ill. We hope to eventually cover a broad range of topics stemming from our own experiences in parenting our mentally ill children. A private Facebook group is also available to those who would like to connect on a more personal level.

Why “Eleventh Willow”? The willow is one of the most resilient trees. It symbolizes flexibility and adaptability, qualities necessary to parenting in general and to parenting in light of mental illness specifically. The willow tree is a survivor, but is also associated with grief and mourning—the weeping willow. In the Bible, the willow tree symbolizes rebirth (Ezekiel 17:5), loss and hope (Psalm 137), and celebration (Leviticus 23:40).

“Eleventh” comes from the eleventh hour—the last opportunity before it is too late. As parents of children with mental illness, we all feel that urgent desire for our child’s healing. Any hour could be the eleventh one—the moment our children are destroyed by their disease.

Our first five blog posts went live this month and deal with issues we have experienced in parenting our children with mental illness.

Amber, Georgia, and I—the Eleventh Willow bloggers—don’t have all the answers, but we are all seasoned mothers of mentally ill children and young adults. We hope to encourage, to inform, to love others on their similar journeys, and most of all, to provide that very needed support to those whose experiences with the church or with Christians have been less than ideal.

Image by Annette Meyer from Pixabay 

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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 blogs at Eleventh Willow, offering encouragement for Christians parenting the mentally ill. 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. 

Author Jolene Philo

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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.

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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

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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.

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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

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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.

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All Scripture references are from the ESV translation.
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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

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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.

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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

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