Monday, January 18, 2016

Lessons from a Spinal Fusion



18 months before (curve was worse by surgery time)
After surgery



On November 3, 2015, my amazing little guy went through the longest and most intense surgery of his life so far. In order to correct Bug’s severe scoliosis, the surgeon fused all but the top two and bottom two vertebrae and installed two titanium rods along my little boy’s spine. Of all Bug’s surgeries, this was the one I most wanted: not because of the incredibly painful experience, but because of the potential outcome in giving Bug a straighter back, helping him sit taller and more balanced, and preventing further curvature which could negatively impact his growth and health. My focus on the positive outcome, however, did not prepare me for how incredibly hard the recovery would be. My poor, brave boy…

Through the four weeks of not sending him to school, being mostly confined to the house, and caring for a whiny and often frightened strong-willed, energetic, adolescent boy, I could sense that this was a learning opportunity if I chose to look for the positives in the midst of all the negatives. I grabbed a notebook and started writing some random thoughts on lessons applicable to my life and others’ lives: truths and perspectives and challenges for anyone going through a painful, life-altering time of cutting, reshaping, and healing into something new and stronger.

*Painful correction and outside intervention are required for life-changing and life-improving changes. And severe deformity requires severe correction. When we choose or are forced to face the sins, shortcomings, and harmful habits which have had a lifetime to develop and become ingrained in us, the “fix” can never be quick and painless.  We may seek out temporary relief or “Band-Aids” which make us feel better—and they may help or offer relief for a time. Until we dig deep to the root cause of our character flaws and our emotional struggles, however, surface corrections will merely mask the issue and do nothing to prevent our dysfunctional selves from worsening. Few of us can do that on our own or without extreme and painful intervention. The blades that cut and the tools and careful hands that push and pull and reshape are necessary to begin the work, to open a space inside for the Heavenly Surgeon to do His work. When our hearts and minds have strayed too far from the plumb line, sometimes cutting and shaping are not enough, and outside aids are needed (support, instruction, and exhortation from those more mature and wiser than us) to keep our old habits and stubborn ways from undoing the Surgeon’s work and allowing the dysfunction to return. We can trust the wise, careful, and experienced hand of the Surgeon and receive aid from the support people He has placed in our lives. We can trust that these extreme measures are required for necessary and lasting change.

(Bug-life example: Now for a little medical lesson. Bug’s spine curvature, as well as his hip dysplasia and foot deformities which have already been surgically corrected, are a direct result of his form of cerebral palsy: spastic quadriplegia. 
  
“Spasticity is a movement disorder characterized by involuntary muscle stiffness and tightness.  This condition usually affects a group of muscles, typically in the upper or lower extremities.  Spasticity can be painful and often debilitating, particularly when it prevents movement or produces abnormal joint positioning…

There are many common causes of spasticity.  Lack of oxygen before, during, or after birth can lead to cerebral palsy.  Approximately two-thirds of patients with cerebral palsy experience spasticity… 
Spasticity can vary in severity and produce muscle group-specific symptoms.  Some people experience mild spasticity, while others experience pain and significant disability as a result of spasticity.  When spasticity affects one or both arms, a person may experience bent elbows and wrists and clenched fists.  They may have difficulty grasping objects, dressing, eating, and writing.  Spasticity can also interfere with balance, making walking difficult.  Spasticity of one or both legs can cause a flexed hip, stiff and flexed knee, and hyperextended big toe.  This can greatly hinder one’s ability to sit, stand, transfer weight, walk, and position in bed. 

There are two common problems that can occur with spasticity. Contracture is one of the biggest, and most painful, concerns associated with spasticity.  This is a condition whereby the muscles permanently shorten, causing disfiguration of the joint. Clonus, rapid and repeated spasms of the muscles, is also a common concern related to spasticity…Skeletal problems can be the result of many different types of symptoms in the cerebral palsy patient.  Children who have spasticity are at risk of developing contractures.  Contractures are a muscle shortening which makes the body parts associated with the muscle contract.  This in turn can cause serious skeletal damage, especially if left untreated.  The child’s body will grow in such a way that the bones will be deformed, causing further pain and movement problems later in life.” 
[from http://www.cerebralpalsysource.com/About_CP/index.html, articles on Spasticity and Skeletal Problems.]

Spinal deformities are very common in spastic quadriplegia as the severe tightness in his muscles pulls joints and bones out of position. His brain damage prevents the proper transmission of signals which typically tell the muscles to relax. His muscles do completely not relax. Ever.

While fusing most of his vertebrae and installing titanium rods seem extreme, without them, Bug’s tight muscles and habits of posture and movement would just pull his spine crooked again, affecting his balance, posture, lung capacity, and other joints and organs.)

* The more we fight the Lord’s good plan and His shaping, transforming work in our lives, the more we experience fear and pain and anger. Just as Bug had no reason to fear the scalpel in the competent surgeon’s hand, so we have no reason to fear the scalpel(s) God uses in our lives to correct and shape us into the likeness of His Son. The more we resist and argue against God and the painful, yet transforming, “surgeries” He allows in our lives, the longer, more difficult, and more painful the process can be. When we choose to rest and trust—even when we don’t understand and even when every fiber in our being wants to fight and escape the pain—God is free to complete His good purpose in us: the heart surgeries and time of healing required to remove the idols and other things in our lives which keep us from knowing, loving, and serving Christ as Lord.  (This concept borrowed from my friend’s book:  http://www.walkingrighthere.com/#!shop/c1a0d).

(Bug-life example: As Bug looked at me, at the doctors, at the nurses all working to help him, I saw eyes of fear, confusion, pain, and anger. His body tensed and he fought with all his hyper-spastic strength, sometimes requiring multiple hands to restrain him. Yet, what seemed to him to be torture, was all for his good, to help him function better and heal safely and quickly. His limited ability to comprehend what was going on and to give and receive communication, made it nearly impossible to reassure him the good that was to come. If his precious mind could have understood, he would have learned that the more he trusted and relaxed the less it would hurt. Instead, he experienced the opposite: his fighting and tensing up out of fear made the pain worse and put him at greater risk to experience what he feared---falling or hurting even more.)

*Good, positive, and beneficial change is very painful and disruptive, carries greater risk and fear, and requires a long recovery and plenty of rest. Shortchanging the process in any way will not produce the same results—and may be detrimental to future health and growth. Furthermore, to be successful in the long run, real change requires adjustment to an entirely new posture and major changes in functions throughout our bodies/selves. As one pastor has put it, “Change isn’t change until something changes.” Those changes may be unwelcome and unforeseen, but real transformation requires all the steps we went through with Bug’s surgery: evaluation, careful pre-op procedures, painful tools in a wise surgeon’s hand, support and care from experienced and caring people, and a long time of rest and recovery. We may be focusing on changing one aspect of our lives (overcoming one sin or healing an emotional wound or reprogramming habitual thoughts), but that change will carry over into other aspects of our lives and may confuse both ourselves and those around us.

(Bug-life example: One unforeseen result of the surgery during recovery, and still present to a lesser extent months after surgery, was the change in Bug’s sense of balance. He had grown so used to his spine being an s-shaped curve, that having it straighter made him feel off-balance and unsure of how his muscles worked along his back, shoulders, and arms. Multiple times a day during the early weeks, he would scream out in fear that he was falling, even though he was exactly where I had left him, secure on the sofa or in the middle of my queen-sized bed, with no possibility of falling.

Bug also continues to figure out how to use his arms: another unforeseen difference caused by the straighter spine pulling his shoulder muscles differently which in turn pull on his arm muscles and joints in new ways.)

*Pain makes us needy, demanding, and angry. It is said that the most dangerous kind of animal is a wounded animal. I’m convinced that applies to people, too. But those who love us can have compassion on us—even when we are at our ugliest—as they allow God’s grace to fill them with patience and understanding in the face of tears and screams and verbal or physical attacks. 

(Bug-life example: For the first time, we saw our boy who typically charms everyone he comes in contact with--saving his grumpy, mean and aggressive side for his family--lash out verbally and physically at doctors and nurses and other strangers. Most of the lashing out, however, was saved for his family, Mom and Sister most of all. We daily had to call upon the Lord for patience and love and grace for Bug and each other. Sometimes, all we could do was take a deep breath and walk away. We were worn out physically and emotionally, but our love for Bug did not diminish. And we all made it through the experience in one piece!)

*When we hurt, we long for comfort and want someone—sometimes anyone—to help us, to ease the pain, to make us feel “better.” This drives us to dependence. When we are pushed to dependence on those who truly love us, know us, and care about us, we find what we need and want. And when we ultimately are driven to depend on the Lord---because we have learned that a “human merely being” is as weak and powerless as we are—then we experience God’s perfect and wise plan for suffering.

But (this is a big “but”), how often we cry out for and seek comfort in someone or something not present or not reliable, as no fallible person or object can be ever-present and ever-faithful. Our pain-induced tunnel vision keeps us from seeing God’s presence and receiving comfort and healing from the only One who is always with us to hold and help and encourage us. How silly of me and how grievous to God (my heavenly parent) that I scream and cry and whine and demand someone who is not always physically present and who could not help and comfort as God—ever-present, ever-faithful, ever-strong—can and will.

(Bug-life example: My mother’s heart ached (as my Father’s heart must), as I witnessed again and again the futility of my sweet boy sobbing and screaming for his absent parent, who could not take four weeks off of work, when his present parent longed to hold him and comfort him. As sad as it was, I cherished the glimpse of God as my loving, tender, longing parent—whose love does not diminish when we look to someone else for comfort. He patiently waits until we remember that HE is the only one who can truly meet our deepest needs and heal our deepest wounds and comfort our deepest grief. Because, as much as I love my Bug, I will fail, I will let him down, I cannot do or be all he needs.)

*One of the more practical lessons I learned during this time was how important it is to ask for help. The people in our lives care more than we may think and are often willing, even if not able, to help out in any way they can. If we don’t speak up and communicate practical, emotional, and spiritual needs, however, those needs won’t get met. Our friends and family members are not mind-readers. Rather than not asking because of the usual excuses (“Oh, they might be too busy,” “I don’t want to be a burden,” “I can manage this on my own,” etc…), we can take responsibility to express our needs and allow those who care about us say “no” if they need to. Usually, they want to say “yes” and welcome practical ideas on how to help.

(Bug-life example: Following our pre-op appointment [see previous post], I began to see the seriousness of this surgery and to anticipate a difficult recovery. Having learned from past surgeries and other times of need, I knew that specific and organized ways to help were more likely to happen than vague answers to, “Let me know how I can help.” To accomplish that, I gave the details of the surgery and recovery to our co-op board so they could set up a meal schedule for the hospital stay—meals for parents get expensive at the hospital—and for the first week at home. We received a full two weeks of meal! And—because I had asked—a number of friends and family members came to visit at the hospital, helping to alleviate the lonely tedium of a post-surgical stay. 

Another example: We practiced the “squeaky wheel gets the grease” idea with the staff of the surgical ward. Due to over-scheduling, we were put into a shared room immediately after the recovery room. Really? A painful, invasive surgery on a developmentally disabled 12-year-old boy in a room with a little boy and his parents—who were obviously not battle-hardened parents who had gone through this a number of times. I apologize to that family for the screams of pain and panic coming from the other side of the curtain. Eventually—sadly only in time for the last day/night there—our frequent requests to be moved—and Bug’s screams—got us into a private room. Peace and quiet at last...)

*There comes a time in any healing process, whether physical, emotional, or spiritual, when we have to get back to daily life and step out into the world. Oh, how hard it is when we have grown accustomed to rest and quiet and to freedom from (or neglect of) the activity and responsibilities of “normal” life (or as normal as a life changed by a painful corrective surgery could be). If we wait until we are completely healed, free of pain, and feeling “great,” we risk becoming so adjusted to rest and having others care for us that “normal” life is a shock and we resist the change. On the other hand, if we push ourselves into stepping back into normal routines and activity too soon, we risk increasing pain, reopening wounds, and exhausting ourselves past the point of functioning. We need to discover a balance between the “safe” amount of activity which distracts us from the pain and helps us slowly get used to life again, and the beneficial amount of rest and stillness required for continued healing. And sometimes we only find that balance by trial and error.

There is, therefore, a time to step out—cautiously and slowly—even if we are not completely healed or free from pain (or perhaps because we are not), a time to get back to “normal life,” while remaining alert to signs and symptoms pointing to a need to pull back and rest.

(Bug-life example: After four weeks of recovery, I sent Bug back to school, for his sanity and ours. I knew that the distractions of school and the chance to increase his activity level and his time in his wheelchair would be beneficial, especially under the loving and watchful eye of his one-on-one aide. And I knew that the quiet and freedom at home—free from Bug’s whining and demanding the spoiled life he had been living and free to leave the house when we needed or wanted to—would be good for the rest of us.

And so, even though it was disruptive to my schedule, that first week in December, I drove my boy into school late—I was not quite ready to get him, or myself, up at 5:45 AM every morning—or picked him up early so he could rest. The extra time and effort were worth it, both to see his smile and excitement over being back at school and to give those of us at home some peace and quiet.

Was it too soon? Did I push his body too much? There is always that question with a special needs child who cannot understand or communicate his needs with his caregivers. Perhaps it was, but I have no way of knowing if waiting a week would have made any difference. We did it. He did it. It was slow going and required some interesting modifications to make the experience as easy on his body as possible.

But, as I’ve said before, my amazing Bug is one brave, tough, and live-life-to-its-fullest kind of kid. 

I guess we all have lessons to learn from him.)
 
Bug sits a little taller and a little straighter now, his deformity corrected to an acceptable degree (I can’t wait for the day it is 100% corrected and I get to see my crazy kid dancing before the throne of Jesus). We too can come out of painful, life-altering experiences a little healthier, a little stronger, a little closer to who God created us to be. It takes time and requires us to submit to our perfect, Heavenly Surgeon, trusting that He knows what He is doing. The results are worth the painful process.

Sunday, October 25, 2015

An Unexpected Gift



Thursday, October 22, 2015 

Those who sow with tears
will reap with songs of joy.
Those who go out weeping,
carrying seed to sow,
will return with songs of joy,
carrying sheaves with them. 
(Psalm 126:5-6)

This is one of those events which occasionally sneak up and surprise me and need to be written down. For whom I don’t know. Mostly for me. To remember. To remind me. To proclaim a truth and a reality which I so easily forget. 


Taking goofy pictures while waiting in the exam room
 My funny, but clueless, boy had his pre-op appointments today. Clueless?  Because he knows nothing of the scoliosis surgery (spinal fusion) coming up in less than two weeks. 

I left the house at noon and got home at 7:00. Four of those hours were at Children’s Hospital: waiting for and getting through three appointments, one of which included stripping him down and contorting him in different angles for spine x-rays; standing at a desk for thirty minutes to schedule yet another pre-op evaluation for next week; and finally getting Bug’s blood drawn around 5:30PM. The last required three women (of whom I was the biggest) to hold a screaming and fighting boy in order to get a needle in the most accessible vein and fill a couple vials with blood. When it was over, my red and teary boy said, “Didn’t hurt.”






We left the hospital at almost 6:00. Traffic was a mess, I had no dinner at home, AND the Seahawks game had just begun. So, we headed to Burgermaster for cheeseburgers and fries and a TV. 

Bug and I sat on the same side of the booth so we could watch the game, and so I could keep an arm around him as he sat on the bench (he begged to be out of his wheelchair after such a long day).

As I sat there eating my fries, I felt alone yet not alone, sad yet not sad. I longed for someone to talk to about all the details of the upcoming surgery while they were fresh in my mind. I scanned the parking lot, looking for someone to appear to share this special moment at the end of a full afternoon. I kept my arm close around my precious boy as the idea flooded me that I was glimpsing the life ahead of me: Bug and I, just the two of us. No brother, sister, or dad around all the time.

I kissed Bug’s head and whispered, “It’s just you and me and Jesus. You are my life now. I love you. And I am so thankful and I don’t mind at all.” Yes, I’m lonely and sad sometimes, but it is a privilege to be his mom, and—even more so—it is an overwhelming privilege to have received not only the miracle of Bug’s life, but also the miracle of the change of my heart and mind and outlook toward my special boy.

French fries and Football!
And as if that thought, that glimpse were not enough of a revelation and a blessing—unexpected but sweet—I soon received another unexpected and sweet gift.


A man arrived at Burgermaster as we were finishing our meal. He scouted out a place to sit with his crotchety older relative who complained about having to watch the football game. The younger man came near our booth and asked if we had a decent view of the game. When he saw that we were getting ready to leave at halftime, he asked if he could have our table. It was situated in such a way that he could see the TV, but his older companion could avoid it behind the relative privacy of a half wall.

As I buckled Bug back into his wheelchair, the man noticed Bug’s Seahawks shirt and asked if we like watching football games. Bug gave his best “Go Hawks” cheer as I shared how much he gets caught up in Seahawks fever, and then I showed off his brand new orthotics: covered in blue Seahawks helmets and secured by blue and green straps printed with “Go Hawks.”

Bug and I headed for the soda fountain to refill our cups, and the man came up to gather napkins and straws for his meal. He commented on the game and his hope for a win, then asked Bug if he had a Seahawks jersey. When I answered, “No,” he asked Bug if he would like one—and before I was aware of what was happening, he proceeded to take off his coat, remove the licensed, #56 (Avril) jersey he was wearing, and put it on my surprisingly un-surprised boy. I stammered, “Really?” And the man explained that his own kids are grown and he doesn’t have any grandkids, so he was happy to share Seahawks fever with someone.

We thanked him and left. And I was overwhelmed for the second time that evening. I told Bug as we headed to the van, “You are awesome, Bug, a gift from God who blesses others and brings them such joy. You're so amazing that someone actually gave you the shirt off his back!” 

And I was again to thankful to be his mom, to care for him, to share the rest of his life with him. He is my life’s work (so why do I keep thinking about what career I will have when I grow up---I mean, when the kids are grown?). But not only that, I am so thankful and excited that I get to witness and be a part of the way he blesses others and brings them joy. That is his ministry. And mine is being a part of it. Sharing life with my miracle.

                                                                                                                  

Hours after I got that boy home and tucked into bed, I drove to pick up my girl from a friend’s house. As I headed north, sleepy and ready for bed, I reflected on the whole of my day. 

Earlier, I had been gone from the house for seven hours, including driving T. to hang out with her friend so she didn’t have to spend the afternoon alone, and then picking Bug up from school to take him to Children’s for his appointments. A seven-hour work day isn’t too bad; why was I so tired? Of course, those seven hours came after getting Bug up before 6:00 and on the bus at 7:00, taking the dog for a walk (oh, and that held the extra, breathtaking gift of heading out the door while there were still stars—planets perhaps? I never had time to look up what stars are still visible after dawn—shining over the treetops), starting a load of laundry, listening in on T.’s online history class, helping her with math and chemistry, cleaning the bathroom, and sweeping half the floors in the house, in order to leave shortly after noon. (Are you wondering yet where I’m going with this?)

And then, I had come home from a long day of appointments, and still needed to put Bug on the potty, feed the ravenous animals two hours past their usual mealtime, vacuum in two rooms, unpack Bug’s backpack and my bag of stuff from the day, put Bug to bed, and fold the laundry, all while ignoring the sink full of dirty dishes, the dishwasher needing emptying, and the stinky litter box. No, I am not whining. That was one more unexpected tidbit from the day. Not a single part of it all bothered me. (Well, except maybe the dirty dishes part.)

Exhausted, I had collapsed on the sofa to read my email from the day and to start getting the memories and thoughts of the day written down before they faded into yesterday. I had been up since 5:30 and I usually try to get to bed around 10:00. But, tonight I had to wait for S. to get off work so I could leave him with his sleeping little brother while I drove to pick up T.

Up past my bedtime, tired, and driving in the dark. How easily that used to throw me into self-pity, grumbling, and all-around negativity. Not tonight. Even though I was going to pick up my equally-tired daughter who had texted me earlier about struggling with some hard thoughts and emotions. And I knew she would want to talk. Or cry. Or both. Late at night, when we both should be in bed.

And yet, remembering how I felt so blessed and privileged to be Bug’s mom, I realized I am equally blessed and privileged to be T.’s mom. Even when she is wrestling with heart-wrenching emotions and difficult thoughts. I am honored to help her as she walks her sometimes dark and rough road, to come alongside and ease her burden as I am able, to encourage her, and to point her to Christ and the freedom of complete dependence on Him.

As I turned off the freeway, the memories and emotions of the day lingered, and I thought to myself—no, I heard the thought from some unknown person who must have climbed in the car when I wasn’t looking—“I love my life.”

I paused in the silence and said out loud (yes, I talk to myself while driving. I have some of my best conversations in the car), “Did I just say, ‘I love my life’?” 

Another pause.

Again out loud: “Wow. That’s a new one.”

A smile surprised my face as incredible joy washed through me. I can’t remember the last time I said I love my life. Usually my mental tapes played a repeat of “I hate my life.” And given the current circumstances of all the unexpected in my life, my crazy thought made absolutely no sense.

Do I really love my life? I do really love being a mom and a caregiver. That’s also new for me, to that extent at least. While I chose to be a mom, I never chose the life I was given. But I have finally learned to receive it. And in acceptance I have found peace…

The joy has its shadow of sorrow, of course, because joy and sorrow go together and illuminate one another and each carries its own important lessons and blessings. I was sad--true and genuine sorrow, another unexpected gift since it lacked resentment or blame—that my kids’ dad wasn’t part of this amazing, monumental day, that he did not experience what I had experienced. Sad that he had not been able to join me at the pre-op appointments to hear the details from the surgeon’s mouth and to ask the questions that would inform and perhaps lessen his anxieties about surgery. Sad that he did not take me up on my offer to meet for dinner afterwards so I could share what I learned about surgery while it was still fresh in my mind and have the opportunity to process all the details with someone who will be part of it. Sad that he missed the special time eating burgers and fries and watching football. Sad that he missed the amazing gift of the #56 jersey. And sad that he was not there to see his daughter’s tears, witness that glimpse into her brokenness, and have a chance to share what he has learned through his own brokenness. And sad, too, that our kids missed out on sharing that that day—good and hard and goofy and exhausting—with their dad. He missed and is missing so much of our daily life, so many of these little, unexpected gifts. My heart ached for him and for our kids. An ache that was in itself a gift from God.

But—joy! What life I have found in the midst of sadness, in the death of my dreams, my plans, my hopes, my life. It is not my life. And I will receive whatever God chooses to give as I relinquish all I thought I wanted and needed. Within unexpected loss, I have found unexpected gifts. 

I want to keep saying, “I love my life.”

And now it is no longer today, no longer this day of miracles. It is tomorrow. 

Bring it on! And, "Go Hawks!"