Tag Archives: hospital

Warrior On, Momma

Recently, I was hired for three speaking engagements for our local hospital system.  I was honored, humbled and awed by the requests.  One of the talks was for a leadership group that met monthly, and my talk corresponded to the chapter about leadership on the frontier from the book the group had been reading.  Before visions of Walt Disney’s “Frontier Land” flash before your eyes, the frontier in question is being intentional about leading and looking for ways to serve those who have been misaligned, neglected, forgotten, hurt, or misunderstood.  I shared lessons learned as a quarter of a century (How could that be true?) educator, peppered with anecdotes and tales from the trenches classrooms of children ranging from 2nd grade to college seniors.  At the conclusion, my challenge to the group was two-fold:  1) ask God to break your heart, because from the depth of sadness we often find our passion and 2) don’t think too highly of yourself.  The latter being a message for me as well.  I have had successes as an educator, but I have had equally as many failures, steps backwards, and misunderstandings.  And there I stood before vice-presidents, presidents, and top-notch health care executives asking them to remember every leadership lesson I shared that day was taught to me by children.  Physician: heal thyself, and teacher: educate thyself.

One of the greatest lessons I have learned in life (and one of my leadership points) came from one of my life’s saddest moments. After enduring the heartbreak of losing Reed and trying to help Sister and Sawyer heal from the bus crash, I quickly came to the realization that much of what I think I know about other people’s lives is wrong.  This education arose through the wisdom of those who had walked in our shoes but was refined by those who had no idea the advice they were proffering was not helpful and worse yet, at times, hurtful.  While our valley of grief was long and arduous, it was still worthwhile, producing gentler and kinder versions of ourselves.  We became a people who realized that much of the ugly in the world is a direct result of sadness and hurt.  As a teacher, this education was better than anything I have ever learned in a book or in a classroom.  I had to walk a journey of a million steps in pain to produce a heart that recognizes when a student seems to be out of sorts, there is typically some type of hurt or sadness behind it.  Serving others came naturally to me before my darkest day, but loving those who appear “unlovable in the moment” became my rally cry afterwards.

I honestly wish that all educators would have an earth shattering, heartbreaking moment. Many have already experienced their own sadness, but for those who have not, the result would be eye-opening.  Sadly, I know this be true, because of experiences one of my children has had over and over again.

Six years ago, my oldest daughter began to experience hives.  At first, the outbreaks appeared to perhaps have an environmental trigger (akin to seasonal allergies), and then a suggestion was made that maybe water might be to blame.  Swimming produced hives, but showering and using our hot tub did not.  Time and again, we went back to the proverbial drawing board. None of the “causes” were the real culprit. She has been poked and prodded (one visit required 17 vials of blood), written incessant journals of food and activity logs, and tried all sorts of medications, creams, and ointments.  We have even tried homeopathic remedies, but not a single thing made any difference.  Meanwhile, she has endured urticarial (the scientific name for hives) episodes every day – EVERY DAY – for the last six years.  Some outbreaks would be small clusters.  Others would be large nodules, and worst of all, would be the times  hives the size of dinner plates covered her body.

erin by moon photography

Photo by Steph Moon of Moon Photography (Even for the prom, the hives were present.)

 

While some notice the welts that would appear at whim, very few notice the side effects.  Sleep would be elusive due to eruptions happening or the uncomfortable nature of itching and scratching.  Outbreaks are also mentally and emotionally draining.  How many teenage girls do you know that want to sit in class and suddenly have red and enflamed clusters of hives break out? Fashion accessories they are not. On top of it all, how does a student maintain focus and concentrate when pain is a constant companion?

Removing my teacher hat and simply being my child’s momma, we have seen every possible specialist with the hopes of finding a definitive diagnosis.  We have logged hours in clinics and hospitals, in the car travelling great distances to talk to the “best of the best”, and in the library reading every possible article and study on raising a child with chronic illness.  Often we shared these studies with her school, in the hopes of helping others to understand how debilitating chronic illness is.  Some times our efforts seemed to be in vain, when it was suggested that

  • These hives are all in her head.
  • Pretty sure this is a sign of anxiety. (She does NOT have anxiety.  Trust me, among the myriad of doctors, we checked and double-checked.)
  • She is doing this for attention.

Short of “appalled” and “righteous indignation”, I have no other words for these suggestions.  I will be honest.  I have cried more tears than I knew possible; many of those tears wept while lying in my bed grieving my child’s journey. No momma dreams of her child having a debilitating, chronic illness. While some call me “strong”, they might be shocked to learn there are definitely things that sentence me to my bed because life is simply that overwhelming. Yet somehow in those painful moments quietly tucked under the covers, my eyes are drawn to a God who I know loves us and my sweet girl more than I ever could.  

During these times, He reminds me there are the teachers and school nurses whose hearts have been broken and who try to understand what our girl is going through.  There are also doctors who look your sweet child in the eye and say, “I believe I know what you have.  No more pokes and prods. No more journals.  And while there isn’t a cure, there is a treatment for which I think you would be an ideal candidate.”  Even more so, this amazing physician held my child’s hands and lovingly reassured her that she would no longer slip through the cracks and told her emphatically “No! None of this is in your head.” and cried with her.

I have learned many lessons through this saga, and as the treatments continue (Praise the Lord successfully so far!), I am sure there will be others to learn.  Throughout my career, I have always tried to err on the side of compassion, but for the times I failed, I am truly sorry. For my students of the past, present and future: I can only offer that today because our struggles, I am a better person for it.  So when you come to my classroom or office, just know I will listen and together we will make a plan for you to be successful. For every educator – no scratch that – for every human being: ask God to show you the sufferings of others and how you can be a shining light in the midst of their storms.  For all the mommas who have children with illnesses seen and unseen, who search for answers even when they aren’t the ones wanted, who have shed tears and have lost sleep, and who have had to explain their child’s illness over and over, just know you hold a special place in my heart and more importantly in my prayers.

For you sweet mommas, I have two words: Warrior On!

 

 

 

When dreams grow bigger

IMG_20131225_150145 An unexpected rap at the door on a cold wintry night removed me from a cozy blanket cocoon. A sleepless night the previous evening prompted my unusual self-indulgence. Standing at the door was a dear friend, passing through town. Maybe it was the fogginess of a tired brain, but his appearance served as a beacon to remember – write that blog, write that blog.

Many times the teacher becomes the student. Watching this friend has been all lesson in my life as this man, and his family, have been the models of generosity.

Snow melted off of sturdy boots while we talked in my living room and old dog inched closer for extra rubbings behind elderly ears. The impromptu visit became a necessity because of a societal ill – never enough time. The last time our lives crossed paths was when my friend had been honored for being a Hometown Hero – a title more than aptly fitting.

What a blessing it was to surprise him with the bestowed honor and to be there among those who like us had been recipients of his family’s boundless gifts of love, time and resources. All in attendance were there to surprise him. But here is the thing about heroes, they never cease to amaze. After learning of the award and the monetary award to a charity of his choice, he stunned everyone in the room. He quietly explained how he had hoped to surprise all of us by awarding Special Olympics with a donation. The givers became doubly blessed as not one but two checks were awarded to some of his biggest fans. Not a dry eye could have been found in the room.

I have witnessed his family who models what it means to give generously – especially to those small, overlooked, and often without a voice. Special Olympics, Big Buddies, and the Ronald McDonald house were some of the bigger names. The others are too numerous to list, but among them are the grieving, the souls beat up by loss that while the rest of the world goes on they are trying desperately to make it to the next minute. It is a marathon for life’s breath. My family would be among the recipients of their beautiful commitment to loving others even when, at times, the world was falling apart around them.

Without their help, our dream of remembering Reed at the hospital where he died would have been nothing more than idealistic, swirling firings of neurons in my head. Their perseverance while waiting for just the right thing led to a beautiful friendship. Through their business the Reed-A-Cheetah program was born, allowing us to build a dream of bringing comfort to those who need it most, in their darkest hour. Through their love our dream became real. Reed would have been proud.

We were stunned last spring by their sad news. What happened that day still leaves me in awe! Salinated drops came pouring forth as my ears and heart did not want to hear their business was closing. They have given so much. Why is this happening? In a moment that was both surreally raw and beautifully poignant, even when their darkness was coming closer, they shone a light of incredible hope. The cheetah “business” could not – would not – die. Our friends had met as a family and decided the way to ensure the proliferation of cheetahs would be to give our family the stuff your own animal business. Do what? You are giving us the entire kit and caboodle? My knees were weak as I tried to protest. This was too large. Too generous. Too lavish a gift. My bitter tears gave way to the blessed tears of being loved, overwhelmed with thankfulness. Who loves like this? My feeble attempts to protest were met with a matter of fact it-is-done-this-conversation-is-over determination. Honestly, I think I cried for days.

Friends like this are rare to find.

This is not a gift to be squandered. We have had family meetings, talked, and dreamed, talked and dreamed some more. In the end, we have decided we want this adventure to reflect the generosity with which it was bestowed. Our intention is to have a Give It Forward model of entrepreneurship. With the purchase of one stuffed animal, we will give one away. Purchasers can stuff their own animals and the ones that will be gifted to charity. If someone has a charity or fundraiser they want to support, we will work with them to hopefully make that dream happen just as our friends did for us.

It doesn’t happen often in life, but through all our dreaming and planning, words fail us on one important aspect – a name for all of this goodness. How do you name a gift so incredible? We struggle decide on a name for this new venture. Adam was given the charge to name creation. We would have woefully failed in his duty.

What I do know is that no matter the name we will strive to live up the gift givers expectations, because our last see-you-soon, prior to our quick respite from the snowy day, held the parting words “The Ronald McDonald house could sure use some little animals.” Yes. Yes, I would guess they could. Because while we move forward in healing, hurt, needing comfort is always around the corner. We never lose sight of the comfort lavishly poured out in many different ways. His words were both a blessing and a reminder to live generously with a hope that no matter what darkness surrounds someone’s story – love will conquer all.

reed-a-cheetah

Name our Adventure contest: As the new proprietors and caretakers of a dream making adventure, we need your help! Reed-A-Cheetah and all his stuffie friends are waiting for a new name for their big adventure: bringing comfort and joy to those who need it most. Please submit your ideas for a name for this business adventure. The person who submits the winning name will be awarded a free stuffed friend and the opportunity to “bring him or her to life” as well as the donated friend. All submissions should be sent to mominmn@hotmail.com by January 31st. Children of all ages (3 -103) are encouraged to participate.

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You never know what adventure your stuffie will find!

 

 

 

 

 

 

 

 

Happily ever after and once upon a time

On a flight from Minneapolis to Orlando, the onboard movie kept cutting in and out, much to the frustration of all who were trying to watch it. After many different stops and starts, all viewers were able to finally watch a good chunk of the movie until the pilot announced that it was time for our final descent, thus we would not be able to finish the movie. To hopefully soothe some ruffled feathers, he joyfully announced, “I am sorry ladies and gentlemen that we will be unable to show today’s movie, Dear John, to the end. Let’s just say the boy gets the girl, and they all live happily ever after.” Since I was only half-heartedly watching (or attempting to watch in between praying for my life and squeezing the blood out of my husband’s hand because this was a flight back before Freedom Day), I didn’t care much about the ending, concentrating much more on what survival skills I might need to employ should anything go wrong.

All that energy spent on worrying about nothing. I had already lived through my worst nightmare, and at that point was still daily living with its aftershocks of medications and therapy visits. Sometimes, I look back and wonder why I wasted so much of my energy on all that worrying, often missing the joy of some of the best blessings I have ever received. The greatest of those has been the friends who have come along on our journey and who have loved our family in incredible ways.

One of those dear friends found us through Caring Bridge. She was a two-time survivor of thyroid cancer, a prolific supporter of those battling other illnesses and injuries, a prayer warrior extraordinaire, an avid outdoorswoman, and champion to returning soldiers and their families. Just writing this, I am amazed at all she could accomplish in a day. She befriended our family while Sawyer was still a patient at St. Mary’s hospital in Rochester, a tireless friend and encourager who would daily post our prayer requests on her webpage. Having never met in person, she helped orchestrate for our family to be guests at a Minnesota Twins game. We asked her to join us, because she we really wanted to meet her.

From our first moment together, our kids were smitten with the dynamo, they quickly named their “Auntie Stacy”. Over the years, we had other times we would get together, where she would prove that “auntie” was the perfect title. Very few know this, but it was she who gave us the inspiration for the Reed-A Cheetah program, buying the very first Reed-A Cheetah at the Mall of America’s Build-A-Bear workshop. She encouraged our kiddos’ interests, and even went so far as to ask them to be official photographers of one of the military hunts she helped organize for returning soldiers. Imagine the pride they had at being a part of the official team helping military families.

Shortly, before graduation, I received a message from her saying that she would like to return the favor, by taking pictures at Sawyer’s graduation party. We were ecstatic for such a gift, because we knew our evening would be hustle and bustle. She was so proud of the young man, who called her auntie and for whom she had relentlessly prayed.

Sadly, she wasn’t able to join our party, in the way we had hoped. A couple weeks before our Boy Wonder’s graduation, Auntie Stacy collapsed at work. Although, she was rushed to the hospital, the woman who to all of us was larger than life passed away six days before his big day. Her funeral service was held the day of his commencement, just three hours prior. Due to the distance between our homes, we were unable to attend.

Our hearts were broken. How could this happen? I shared our sadness on Facebook, and another dear friend, who wanted to honor Stacy’s life, stepped up at the last minute to fulfill her wish to photograph our evening. Although her presence was not like the ending of that in-flight movie, tucked quietly into the decorations of his party was one of the photographs our kids took of her on “official” duty. It wasn’t the “happily ever after” moment we would have all wished for. Yet, a love like hers never completely dies, but rather lingers forever, because once upon a time, my children were loved by Auntie Stacy.

Just one of the puppies Auntie Stacy arranged to be given to returning soldiers. She was a dynamo in life and will be missed!

Just one of the puppies Auntie Stacy arranged to be given to returning soldiers. She was a dynamo in life and will be missed!

*Special note: The Reed-A-Cheetah program is our family’s way of giving back to the hospital where Reed died. The Reed Stevens Legacy program is available at the Avera McKennan hospital in Sioux Falls, SD. A stuffed cheetah is given to the surviving siblings of any child who passes away at that medical facility. The cheetah (which was Reed’s favorite animal) is extremely rare in nature and so, too are the relationships that siblings share with each other. The cheetahs symbolize three children in Minnesota who understand what it is like to lose a special sibling.

To laugh or to cry

I recently shared that my oldest daughter had to undergo an extensive surgery due to injuries she received in our family’s darkest day.  The part about this story that is so upsetting is that we had no idea that she had even hurt her nose.  Sadly, my children are not the only ones who are continuing to find injuries that no one knew or even thought to check.  These are the ones that can be seen on CT scans and X-rays, but there are a myriad of hurts that cannot be detected by modern technology.

This surgery which involved a septinoplasty and turbinoplasties (three of them) were to allow our girl to be able to breathe again – literally.  For all these years, she had a non-functioning nose which was susceptible to sinus ailments and headaches.  Erin’s dream is to play basketball for the glory of God above all else.  As her momma (and one of her biggest fans), I was moved to tears this year when one of her specialty coaches told her that she believed that God gave you basketball as a platform, now go out there and shine your light for him.

Despite being a coach’s kid, I never played basketball.  Tennis was my love, and I cannot for one minute, imagine playing that sport or any land sport without the ability to breathe through my nose.  Honestly, I do not know how she has functioned all this time.

When the cause of her troubles was discovered, some things (aside from struggling for air in games) did start making sense.  Food is just something she eats, not enjoys.  She could never smell if there was an odd odor in our home.  The icing of this ridiculous cake was when her baby sister explained that the different color candies tasted different, and she thought it was a joke.

Yesterday, she went for her first post-operative surgical appointment.  I won’t divulge the gory details, but let’s just say for a squeamish girl, she was a little shell-shocked at the size of the stents removed by the surgeon.  He asked if her expression was one of horror or disgust (as in if she wanted to kick him).  Her one word answer, “Yeah”, quietly uttered, said it all.

The fact that her mother wanted to examine the stents (because she is after all a science teacher) probably pushed the envelope a little too far.  Just one of the many things that will cause her embarrassment in her lifetime!

Her surgery, while definitely necessary, was somewhat radical for someone so young.  This was her shot (pun intended) to get back to living and to experience life with some modicum of what everyone else does.  In the back corners of my cerebral matter, I had to wonder if it was going to be worth it.

As we walked out of the hospital that day, I asked her if she could breathe better.  She said that indeed she could, but she just had to get out of there.  Thinking that she was still mad at the doctor, I joked that he could probably take it.  She further explained that it was the hospital smells that were making her gag.

Did she just say what I think she said?

Later we walked into a store to pick a prescribed item, and her response was priceless.  “Whoa! Smell overload!” I took a big inhale and realized she was right but I had just learned to tune that sensory overload out.  But for her, it was like she had awoken from an olfactory coma.

Over the next few days, she has shared realizations about foods actually have tastes, smells that really bother her, and memories of how the hospital smell brought back memories of her brother’s stay in intensive care.  Of course, her sister, who seems to have inherited my love of science, conducted an experiment by having her try each of the six flavors of Smarties, and yes, now she can discern a difference.

With each new discovery, we laugh, but a part of me wants to cry because of all she has missed.  It has been over five years of having a deadened sense.  From the early evidence, I would say that the surgery was more than worth it.

One day, while home playing nursemaid, I was reflecting on everything that has evolved from the firestorm our lives have been. To laugh or to cry played around in my head, partly because I felt that I had let her down. How could I not have known?  During my devotion, God gave me a small glimmer into an analogy on this very concept.

He reminded me that sin (anything that keeps us separated from him) has the same effect on our spiritual senses.  Whatever it is might start off rather benign.  I have to believe that Erin could smell in the aftermath of the crash.  But over time, our soul becomes desensitized to the effect it is having in our life.  One day, we wake up and a myriad of other things have happened that simply do not make sense, and we are often left wondering where God is.

Wow!  I was not expecting that answer when I was cuddled up, asking him to insulate my family and to help us get through this chapter of our story.  Choosing joy.  This seems to be a theme that time and again, God is pounding into my soul, and many times I AM my biggest stumbling block.

A little later, I had an overwhelming sense that laughter was indeed what he wanted from us.  Not laughing at our circumstances, but laughing through them.  And yes, that might mean, laughing at a budding scientist, using her big sister as a guinea pig.  It may mean laughing when our girl realizes that not everyone smells pleasant following a grueling game.

The more we laugh, the more we are reminded that the Creator of laughter delights in our joy!

I am utterly and completely thankful that he does!

Psalm 30:5 Weeping may endure for a night, but joy comes in the morning. (AMP)

One of my favorite things about Erin is her ability to laugh with her whole spirit.  Captured at our family photo shoot, this picture explains what I mean perfectly.  Portrait by Inspired Portrait Photography.

One of my favorite things about Erin is her ability to laugh with her whole spirit. Captured at our family photo shoot, this picture explains what I mean perfectly. Portrait by Inspired Portrait Photography.

 

Where the dance will lead . . .

Photo found at www.selectregistry.com

Photo found at www.selectregistry.com

In addition to the tender moment shared yesterday, there were  a couple more moments that took my breath away at the hospital.  One in quiet reflection, and the other in laughter.

Over the course of the summer, my pastor has had a wonderful sermon series entitled, “What’s messing with your faith?”.  His transparency is palpably real as he confesses to struggle with each topic.  His genuineness in delivery has touched me very deeply, because I struggle with all the same things.  These things that mess with our faith take us so far away from contentment in God’s plans for our lives.

On my travels, I decided that I would use what God had been stirring in my heart based on what I had gleaned from each topic this summer.  With a renewed spirit, I wanted to travel with no agenda other than to love and to serve.

Just a few days ago, I saw a post a friend had on Facebook and it read something like this. “Are you waiting on God?  Tell me then, when did you ever get ahead of Him?” Those were very convicting words, indeed!

The times when my faith is the most vulnerable is when I allow – worry, fear, bitterness, doubt, or busyness – to lead my thoughts.  So upon embarking on this journey, I decided to just follow.  Follow where God took me, and not try to get ahead of Him.  It was already evident that traveling this far from home was His idea; so why not enjoy the travels.

One Saturday in July, following God’s heart took me to the hospital bed of a black grandfather and pastor.  As we sat there swapping stories, I felt compelled to ask a question.  When I say compelled, it was like an explosion of my soul as I was being pulled farther and farther away from the shore of my control.  My question was simple.  Can we pray?

Just the four of us, including the patient, clasped hands and prayed.  I prayed for peace, for healing, for wisdom, and for all the things God laid on my heart.  It was beautiful and tender and very much God-breathed.

As family members and hospital staff came in and out of the room, Ninny would introduce me.  “This is Kandy.  She is Bug’s friend, and she KNOWS the Lord.”  Not one single person that entered that room was spared of that introduction.  Those words made me smile, at first, but later became a badge of honor.  I was His beloved, and I KNOW His love.   I had never stopped to think of myself using those words, but they tasted so sweet. THIS is Miss Kandy, AND she KNOWS the Lord!

As the day unfolded, I was unceremoniously adopted as “Daddy” proclaimed me, somewhat teasingly, as his to the nurse.  She came in to take some vital sign measurements and asked him how he was doing. Despite feeling pretty awful, it was joy to see that he still had a bit of mischief up his hospital gowned sleeve.  He said that he was doing great because he got a new grand-daughter today.

“Really!”, she excitedly asked.  “Where was she born?”

In a barely perceptible grin covered by the oxygen mask, he replied, “I have no idea, but you can ask her. She’s sitting right there.”  At this point, he motioned to me sitting at the foot of the bed.

If I were a poker playing kind of gal, I would want to play cards with this nurse.  The look of confusion was painstakingly present.  How can this grown white woman suddenly be your granddaughter?  The rest of us in the room could hardly contain our giggles.

I have to think at this point even Jesus snickered in heaven.  His Dad’s love opens wide the door of family.  When He does, you get a small glimpse of how He sees you and all his children.  In those moments of tenderness and a fit of giggles, I began to see what transformative power slowing down and ceding control can do for your soul.

Allow God to lead the dance of your life’s journey, and see – just see – where He and the dance take you.

All in a touch

The home my Nanny and Granddaddy lived in since 1961 was one in which several additions were made to it.  I’m old enough to remember the carport renovation and the subsequent addition behind that.  With those two extra rooms, the traffic flow of the house became like a race track.  Anyone could make laps around and around inside the house, and as kids we often did just that.

My favorite part of romping through the house was when my Granddaddy would come in from work and plop down in his chair, a burgundy swivel rocker/recliner, to relax and watch a little television. Inevitably during one of my laps, Granddaddy would stick out his gigantic hand, riddled with arthritis and aged with years of hard work, with his palm up.

This was my cue.  The ritual was enduring, and it continued right up until his passing.

His outstretched hand blocked the path of my meandering.  I would always stop, waiting for the next line in this well-rehearsed script.  I would squeak out with glee, “Hey Granddaddy!” and then slap his calloused hand with mine, thus giving him “five”.  Then in a booming voice, dripping with a Floridian Southern drawl, he would announce, “Hey Granddaughter!”

As a child, if I had been asked to define love, I would have drawn his hands.  Even today, I would give anything to once again touch his gigantic, but gentle, man-paws of hands.  Every once in a while, I am fortunate enough to see that kind of love in tender moments of others. I think God knows my soul needs to espy those gentle touches.

I was blessed to witness such a moment on my trip to Kentucky.  One of the days, our plans were changed because my friend’s grandfather was sent to the hospital.  Rather than taking in the sites of the area, I offered to ride along with her and her grandmother to sit with “Daddy”.  He was in considerable pain due to diminished breathing capacity with masks, tubes, and machines everywhere.

Quickly, quietly, lovingly, it happened – that comforting ritual.  Her grandmother, affectionately known as Ninny, reached over and gently rubbed his legs.  My breath caught in my throat because the lump lodged there seeing such tender love.  I hoped no one in the room saw my tears.  God’s beauty often does that to me.  Those beautiful hands that had worked for years, raised babies and grandbabies, and had many times folded in prayer were the embodiment of how God loves. I don’t know what possessed me, but I asked Ninny and Daddy if I could capture the moment.  They agreed it would be alright. One click and the moment was preserved forever in image and in my heart.

Ninny's hands

Even though spending the day in the hospital wasn’t what was originally planned, it was where God needed me to be.  After glimpsing love that day, I knew precisely why He had called me to that place at that moment.  For gentle reminders of how tenderly He holds each of us, I am so thankful.

If you enjoyed today’s blog, I would love to hear what you would draw for love.