Healing from Tragedy: 4 Truths from a Special Needs Mom

Healing from Tragedy: 4 Truths from a Special Needs Mom

Healing from Tragedy: 4 Truths from a Special Needs Mom

Healing from tragedy is a process many parents of children with special needs have frequent opportunity to practice. Maybe that’s why Laurie Wallin, mom of four kids, two of whom have special needs, was able to offer hope and advice after the Boston Marathon bombing impacted our entire nation.

Remember Laurie Wallin?

Laurie used to be a regular guest blogger here at Different Dream, but in the last year a couple book contracts (Go, Laurie!) meant she had to make some hard choices. One of those choices was to stop blogging here so she had time to keep her own blog going.

Four Truths to Hold Close After Tragedy Strikes

Shortly after the tragic events at the Boston Marathon, Laurie wrote a post that helped readers cling to home and put the event in perspective. She said “the fresh anger, empathy, prayer, and encouragement swirling in us when we see—or live through—atrocities like Boston…it isn’t for nothing.” In fact, she goes on to say, those feelings are…

  1. A gift that helps us rediscover we are a family.
  2. A reminder to be vigilant in prayer and to find ways to be present and available.
  3. Part of the grieving process.
  4. An invitation to lean in to healing and be present where we are.

I hope Laurie’s insights can help you gain a new perspective about the hard things that happen in our lives.

What Have You Learned through Tragedy?

No doubt, you have experienced hard times and have learned life lessons you hold dear. If you would like to share them so we can learn from you, please leave a comment in the box below. Thank you so much, and thanks Laurie, for your wise words, too.

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.

Photo Credit: www.freedigitalphotos.net

By

Laurie is the mom of four daughters–two adopted with developmental delays, mood disorders, and ADHD. A former junior high teacher turned speaker and life coach, she loves to learn, laugh until their sides hurt, and help women be courageous in life.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

Hope Springs Eternal for Mom of Child with Special Needs

Hope Springs Eternal for Mom of Child with Special Needs

Hope Springs Eternal for Mom of Child with Special Needs

Hope can be hard to cling to when our children with special needs face challenges we can’t fix. Today, new guest blogger Sylvia Phillips, explains how she finds hope again and again while parenting daughter Bethany.

Hope Springs Eternal

When our daughter, Bethany was diagnosed with a very large brain tumor in her very small cerebellum a few years ago, my husband and I naively assumed that once the awful mass was removed she would be fine and our lives would pretty much go right back to normal. We certainly were not prepared for all the events that would eventually take place that would prevent our family from ever going back to normal. Events that would force us to develop a new normal. Our new normal.

Bethany and I spent two months in a hospital far away from home. She experienced and endured numerous setbacks, life-threatening complications, and various forms of treatments and procedures which really resembled and felt more like torture than actual medical  treatment.

Now nearly thirteen years later Bethany must cope with multiple disabilities, but perhaps the worst damage caused by the tumor has been by far her ongoing battle with the uncontrollable and severe seizure disorder that plagues her.

On the Brink of Hopelessness

Until recently, Bethany has endured near daily attacks of  seizure clusters. She has suffered extensively with medication side effects and overdoses which have confined her to the couch in a dizzy daze for most of her life. No medications would stop the seizures.

I  have often found myself on the brink of hopelessness. No magic pill, surgery, or device was going to stop Bethany’s seizures. I so desperately wanted her to have a happy, healthy life. This kind of existence–being medicated into a stupor and seizing more often than not was no life at all.

A Life Worth Hoping For

Recently Bethany began taking Onfi, a new seizure medication, she didn’t have even one seizure for six months! A happy and energetic new Bethany emerged. She was able to enjoy her life once again!

Sadly, just the other day the seizures reared their ugly heads again.

But hope springs eternal. I believe it is in our God given natures to continue hoping even when all hope seems lost. It is in our very natures to hope for something better. It is human nature to continuously strive to triumph over adversity. We can’t give up. At least I can’t.

I desperately cling to the hope that someday, somewhere, someone will find a way to stop Bethany’s seizures… forever.
I desperately cling to the hope that even if Bethany never stops having seizures here on earth…someday  she will suffer no more.

My hope is insatiable. I can’t give up. Without hope life is no life at all!

Rejoice in hope, be patient in tribulation, and be constant in prayer.
Romans 12:12

Now It’s Your Turn

Where do you find hope when you can ‘t fix your child with special needs? Leave a comment.

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.

Photo Credit: www.freedigitalphotos.net

By

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

Let Us Rejoice in our Children with Special Needs

Let Us Rejoice in our Children with Special Needs

Let Us Rejoice in our Children with Special Needs

Rejoicing in our children with special needs is often mingled with grief when the milestones they meet are quite different from their peers. My friend, Karen Jackson, is here to describe how she responded in one such occasion. Karen is the Director of Faith Inclusion Network (FIN) of Hampton Roads, a non-profit organization devoted to the better inclusion of people with disabilities into faith communities. She’s also mom to three kids, one of whom experiences autism.

Let Us Rejoice!

Today at Mass, fifteen beautiful young children received the Sacrament of First Holy Communion.  They were impeccably dressed in miniature suits for the boys and delicate while dresses for the girls.  Many of the girls even wore flowers in their hair, as is traditional, and a professional photographer was on hand to take individual photos of each young person with our Pastor.  This was a special moment in their lives as Catholics, to be sure, and a celebration for our whole congregation.

Rejoicing in Milestones

While these families celebrated this special time for their second graders, I silently and joyfully celebrated a special moment in time with my only daughter Samantha.  Because today, after more than six years of preparation, advocacy in our church, and a succession of “almost” and “not-even-close” experiences in worship, my precious 15-year-old daughter with autism sat in the sanctuary with me for the entire Mass, beginning to end.

Rejoicing in Milestones on the Spectrum

For those who have children on the spectrum, I probably do not need to say much more than that.  For those who do not live with or work with children with autism, let me try to explain.

For lack of better terms, Samantha falls under the moderate to severe part of the Autism Spectrum Disorder.  She does not have exceptionally aggressive behavior, for instance, but she is severely limited in her ability to communicate.  Sitting still has also been a challenge and, although she loves to sing snippets of her favorite songs or just vocalize in a sing-song way, she exhibits very little control of her impromptu vocalizations.  Therefore, it is very possible she might belt out “I love, you, you love me, we’re a happy family” (Barney theme song) in the middle of a very quiet moment at church.  (And she has actually done exactly that before).

So today, I quietly celebrated a small—well, no—actually a big victory.  Instead of sitting in what is essentially considered the traditional “cry room” area where parents bring babies and toddlers, I boldly led Samantha into the sanctuary.  Of course, this was not the first time we had tried.  On a good day, we might make it through to the homily (about 20 minutes into Mass) and then sneak out, just in time, as she started to get restless and be a little too loud.

But today she remained calm and we settled into our pews, her older brother at one side of me, Samantha tucked in close to me on the other side.

Rejoicing in Corporate Worship

I had completely forgotten how amazing it is to be in corporate worship at our church.  Music from our organ, choir, and hundreds of fellow parishioners surrounded us, engulfing us with the soothing and exiting sounds of traditional hymns.  In the cry room area, the music is heard mainly through the speaker—beautiful, yes, but not the same experience.
And the prayers! Again, I was overcome by the strength of hundreds of voices speaking in unison, declaring our beliefs as Catholic Christians, reciting prayers, raising our voices as one.

It only took a short glance over at Samantha to recognize that she was affected by the experience as well. She smiled, rocked to the music, strained to see what was happening at the altar, and exhibited a heightened awareness of her surroundings.

After the homily, I began to get nervous, as Samantha was getting fidgety and kind of silly.  She was trying to engage me in a game by repeating my “shh…quiet” with a no-so-quiet “qui—et” repeated back to me.  But as I struggled to calm her down and resist the temptation to pull her out, I caught the eye of a fellow parishioner who was smiling at the scene.  In the past, I had experienced those “looks” (you know what I am talking about) or even stares that convey at best, confusion and at worse, judgment.  I was encouraged by this woman’s smile.  Samantha and I persevered.

Rejoicing in Communion

Soon it was time to participate in communion and we dutifully got up and followed our row toward the front of the church.  Only a minor glitch—we were not on our Pastor’s side of the church and Samantha will only take communion from Father Joe if he is there.  So we had to “jump” lines, but no one even seemed to notice.

We got back to our pew, and I struggled to overcome my emotions.  Tears fell down my face as I realized that we would actually make it through the whole Mass like any typical family!  Could it really be so?

Yes, as the last hymn rang out, we again enjoyed the experience of being awash in music one last time.  And as those young children, having received their First Holy Communion, filed out ahead of our Pastor, I quietly rejoiced in an important first of our own.

This may have just been one in many, many Sunday Masses to come, but I will never forget it.  My daughter is growing up and growing in her faith, as am I.   Alleluia, Alleluia.  Thanks be to God.

“This is the day that the Lord has made, Let us rejoice and be glad in it.”
Psalm 118:24

What Milestones Have You Rejoicing?

Have your children with special needs reached a long awaited milestone lately? Leave a comment so we can rejoice with you, too!

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.

Special needs inclusion became joy to guest blogger Karen Jackson as her child who lives with autism participated in the rite of confirmation at her church.

By

Karen Jackson is the Executive Director of Faith Inclusion Network (FIN) of Hampton Roads where she lives with her husband and three children in Norfolk, VA. She is also the author of Loving Samantha. You can connect with Karen at the Faith Inclusion Network page.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

Is Special Needs Parenting Inconvenience or Invitation?

Is Special Needs Parenting Inconvenience or Invitation?

Is Special Needs Parenting Inconvenience or Invitation?

Inconvenience or an invitation from God? Which word describes your view of special needs parenting? That’s a question guest blogger Michelle Selent has been praying about lately. Today, she’s here to explain how her prayer was answered.

Is Special Needs Parenting an Inconvenience or Calling?

I have something on my on my heart tonight. With some areas of my life, like my new business, I have been completely enamored—just so delighted by the experience. Then other things have been quite the contrary. I have even been a little miserable with how some areas have been playing out. Especially when it comes to areas of parenting special needs.

In some areas, I have felt like I have kind of lost myself in the shuffle. I will try my best to explain. I used to be more purposeful. Especially in areas of my family. We used to have regular outing with the kids one-on-one so they knew their individual importance and didn’t get lost in the crowd. We used to have family meetings once a week so we just stayed connected as a family unit. As responsibilities in our family swelled, those occasions became less frequent and some months non-existent. At one point, I considered part of my calling inconvenient.

We missed church recently because 2 of our 6 were down with fevers, so we watched our pastor preach the 4th message of his series online. It was just what I needed, exactly when I needed it. I had been struggling with why couldn’t I get back to my default setting. Where had my purpose gone?

The pastor posed this question: Are you consumed with your calling or with your convenience?

Consumed by Convenience or God’s Calling?

Yep, it sorta took my breath away. I think sometimes you can get worn down, and you call things like you see them and not how God sees them. Do I see what God has put before me as an interruption or as an invitation? Do I call what is before me overwhelming, too hard, monotonous, or do I call it how God sees it? An invitation to see his power. An invitation to my calling.

The pastor said something to this effect: Misery is inevitable anytime convenience is your consumption, and God will consume your convenience to get you consumed with his calling.

So there it was. All the areas where misery was creeping in were my own consumption with convenience. It was me, calling things as I see them. I am welled up right now as the whole thing settles on my heart. I have been praying over certain areas for quite a while, and I have had the wrong perspective the whole time.

Father God forgive me.  I have been consumed with my comfort and my convenience. I felt interrupted and I missed invitations. Help me where I am weak and show yourself strong. I don’t want today’s excuses to become tomorrows regrets, dressed in disguise. Turn my misery into ministry. Thank you for you faithfulness to redirect. Thank you for your redemption. You have blessed me! I am calling it like you see it. Consume me with your calling. I don’t want to miss the invitation.

What Consumes You?

Thank you, Michelle, for being so transparent about your struggles. It’s an example for the rest of us who need to confess what consumes us, if we’re brave enough, in the comment box.

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.

By

Michelle is the mother of two adopted daughters with fetal alcohol syndrome. You can connect with her on Instagram.

Author Jolene Philo

Archives

Categories

Subscribe for Updates from Jolene

Related Posts

The Place Where Grief and Joy Meet

The Place Where Grief and Joy Meet

The Place Where Grief and Joy Meet

 Our son a few hours after he was born.

When our first grandson was born six months ago, I expected joy, and it was there.
I expected to love him at first sight, and I did.
I expected to cry tears of happiness, and they came.
Every emotion was expected, save one.
I never expected to grieve. I never expected his birth to be the place where grief and joy met.

How Could I Have Known?

How could I have known grief would punch me in the gut when our son wheeled the isolette holding his son into the lounge area where four grandparents waited eagerly for their first glimpse of their grandchild? How could I have known this first meeting would unleash a host of powerful emotions buried deep inside my mother’s heart for over 30 years? How could I have known this arrival would rip open wounds created when our newborn was diagnosed with EA/TEF and life-flighted 750 miles away for surgery before he was a day old?

The Grief Was Real

Expected or not, the grief came. And it was real. Very, very real.

Grief for dozens of photos of a healthy, unscarred newborn we never were able to take.
Grief for those first days of quiet nurturing our newborn never knew.
Grief for the pain our baby bore.
Grief for my milk coming in thanks to a pump instead of a baby nuzzling at my breast.
Grief over not getting to take our baby home after a short stay in the hospital.

Grief after grief.
Wave after wave.
Tears upon tears.
Grief that no one, not even my husband, understood.

The rest of this post can be found at the Not Alone 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.

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

Encouragement for Parents of Kids with Special Needs

Encouragement for Parents of Kids with Special Needs

Encouragement for Parents of Kids with Special Needs

A little encouragement goes a long way for parents of kids with special needs. Eliana Tardio, parent of two children with Down Syndrome, knows this well. So in a recent post at Babble, she created a slide show of inspirational quotes to encourage parents.

Encouragement for Parents: Inspirational Quotes

Here are a few of the quotes featured in the slide show:

  • To find what you seek in the road of life, the best proverb of all is that which says, “Leave no stone unturned.” ~ Edward Bulwer Lytton
  • Storms make oaks take root. ~ Proverb
  • I always knew looking back on the tears would make me laugh, but I didn’t know looking back at the laughs would make me cry.
  • In the hopes of reaching the moon men fail to see the flowers that blossom at their feet ~ Albert Schweitzer
  • Great effort from great motives is the best definition of a happy life ~ William Ellery Channing
  • The more difficulties one has to encounter, within and without, the more significant and the higher in inspiration his life will be. ~ Horace Bushnell
  • First say to yourself what you would be; and then do what you have to do. ~ Epictetus

What Are Your Favorite Inspirational Quotes?

Are there inspirational quotes that encourage you? Please feel free to share them in the comment box and explain how they speak to you. Or, if you know of an inspirational site full of quotes, leave the link in the box, too. The more encouragement for parents we can share, the better!

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.

photo credit: www.freedigitalphotos.net

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