Submitting My Resignation

I don’t know about you, but I spend a large part of my life living under the illusion that I am in control. I never set out to live this way, but subtly I believe this lie until something happens, good or bad, to remind me I am not in control.

Reality check!

Enter fear and anxiety over this unplanned (by my standards) thing, event or opportunity.

I end up wrestling with the Lord and it is usually emotionally, physically and spiritually draining. I must pray, journal and digest Scripture to once again remind myself of The Truth of who is in control and submit all of my fears and anxieties to the One who is not only able to carry this burden, but give me peace, love and joy in return.

Enter freedom.

The freedom doesn’t come overnight for me, but it does come even as fear and anxiety try to take over. I continually release myself, my family, and my future to the Lord and choose to trust that His plans, timing and purposes are perfect for me (us).

I wave the white flag of surrender and day by day, minute by minute, choose to focus on the present and remember that I am trusting myself and my family to someone who will work all things together for our good as only He can. (Romans 8:28)

I am free to be a child of God and not the boss. I was never created to be the ultimate boss and therefore, I am not very good at it. Sure I still have my role to play as wife, mother, daughter, sister, friend, etc., but I am not on my own as I do them.

This makes a big difference.

So I am submitting my resignation, a resignation from a job I took and was never intended to be mine. I choose to trust that He is in control and that He will work all things together for my (our) good. I confess that this is not the first time I have had to submit my resignation, and suspect it will not be my last. (I tend to have to make this declaration at each new stage of life I enter.) But Lord, thank you for being the One who is in control and forgive me for trying to do Your job. It is Yours and You can have it! :)

Choosing to trust,

Lynn

He is the image of the invisible God, the firstborn over all creation. For by him all things were created: things in heaven and on earth, visible and invisible, whether thrones or powers or rulers or authorities; all things were created by him and for him. He is before all things, and in him all things hold together.
Colossians 1:15-17

The Ox

Then Jesus asked them, “If one of you has a child or an ox that falls into a well on the Sabbath day, will you not immediately pull it out?” Luke 14:5

After one severe manic episode, my husband started creating spaces of rest in his life, and he started by taking Sundays off. This may sound like No Big Deal to you, but in his high tech business, this was right up there with being a traitor. It was not an easy decision … what if they fire me? I have a wife and baby, and God wants me to take care of them…how can you be a good witness for Jesus if everyone thinks you aren’t pulling your load? … am I being legalistic?… Nobody else seems to be doing it…

But my guy was desperate to keep his mental and emotional balance, and taking the Sabbath off seemed like a good place to start. (in addition to meds, of course!)

He made an appointment with his boss (we prayed like crazy, no pun intended) and said he would keep working hard six days every week, but no more Sundays. His faith was important to him, and he believed God wanted him to take that day off. That was a shocker for the boss. I’m sure that’s not the only time my man shocked that boss. The strengths that come blended with the bipolar package are valued by companies.  That boss hired him to be the wild duck on the team, saying, “we need a maverick on the team, but only one.” A little out of the box thinking goes a long way ;) .

My brave husband went on to say, “Now, I know there will be exceptions, when the ox is in the ditch, so to speak. But if the ox is always in the ditch, it’s time to get a new ox!” (i.e. change jobs before I lose my mind.)

His boss leaned back, soaked it all in then respectfully said, “I didn’t know people in your generation took their faith seriously.” And that was that.

Now, it was a huge personal challenge to stop that train every six days and get off, but my husband did it, and I admire him for it.  God also could have allowed him to lose that job, and it still would’ve been the right pattern to pursue.  But God has chosen to bless his work ever since (and we are grateful, grateful). Don’t get me wrong, he still has the thorns and thistles of the Genesis 3 curse along with every other man who has ever lived or ever will live. “…through painful toil you will eat food from it all the days of your life. It will produce thorns and thistles for you, and you will eat the plants of the field. By the sweat of your brow you will eat your food…” but it’s also been true “…see a man skilled in his work? He will stand before kings …” Prov 22:29
Needing rest days to pick out thistles,

Joan

 

The God of All Comfort

Praise be to the God and Father of our Lord Jesus Christ, the Father of compassion and the God of all comfort, who comforts us in all our troubles, so that we can comfort those in any trouble with the comfort we ourselves have received from God.    2 Corinthians 1:3-4

I love these words from Paul.  Further down in Chapter One he continues by saying that he and those with him endured great pressure, far beyond their ability to endure.  They despaired… even of life.  It says in verse nine “…in our hearts we felt the sentence of death.  But this happened that we might not rely on ourselves but on God.” 

I doubt that I have to go much further into an explanation.  As most anyone knows… it is during tough times, times of struggle, times when you feel you can’t possibly endure this any longer, times when you feel like this weight will not be lifted from your shoulders – ever… that you grow closest to God and rely on him deeply.  I pray God will bring you comfort today, so that you will be given the strength to provide comfort in the future.

Talking to Myself

Knowing what I know now about my daughter’s hidden disabilities, I can look back at her first 10 years of life and connect the dots—specific instances where our world veered wildly away from “normal.” Before we had any diagnoses, before we had language to explore and explain Cami’s behavior, we had hints of the struggles ahead of us. In Cami’s only preschool year, the dots aligned into a pattern of special needs for which I wasn’t prepared. The preschool Christmas program that year hinted of Cami’s struggle to successfully process the world around her.

The packed church buzzed with conversations among parents, grandparents, siblings, and friends while we waited for the program to start. I chatted with my parents while my husband set up the video camera. We were so excited to see our Cami girl in her very first “school program.”

Each class stood on the pulpit steps of the church and sang a Christmas song while the other classes sat in the pews and watched. As one class finished their part of the program, the teachers herded them to their assigned seats as another class took their places on the steps. The teachers and aides worked together well, guiding children and staying out of the way of camera shots. As the four-year-old class filed onto the steps in their footie pajamas and night caps, I stood in the back, excited and expectant that our daughter would be a natural on stage, having a musician mommy and an actor daddy.

We have video of the entire disintegration of my daughter’s composure as she stood in the middle of her classmates who were singing “Up On the Housetop.” She was okay with the piano introduction, but when the singing started around her, she sank down to the step, covering her ears.

I wept through the whole ordeal.

I felt embarrassed and disappointed. It was the first time my daughter stood apart as different from the rest of the kids in such a public way.

I knew then that something was very wrong, but I had no idea what it was. I didn’t even know what questions to ask, or who to ask, or what to do. Remembering that experience now, I’m surprised to find myself weeping. That was a hard year. That was a very hard year.

Sometimes, I wish I could go back and hug the young mommy I was then. I’d tell her so many things that I know now which would have helped her to know then.

I’d tell her about auditory processing disorder, how Cami’s brain sometimes misinterprets the information she hears. I’d tell her to give Cami one verbal direction at a time instead of complicated, multi-stepped instructions.

I’d tell her about dyspraxia, how Cami’s motor coordination will be awkward and slow, but she’ll get there…to just be patient; she’ll get there.

I’d tell that young mommy-me about extra-sensitive kids, about how too much information can derail and short-circuit their communication and coping abilities. I’d tell her instead of thinking how cute it was when Cami purred and crawled like a cat, or flapped her hands like hummingbird wings, to see that behavior instead as a signal that Cami was stressed out and overwhelmed with sensory information, and needed an escape route from the situation.

I’d tell her that labels like “defiant” and “uncooperative” and “behavior problem” aren’t as helpful as labels like “sensory challenged” and “learning differences” and “frustrated.”

I’d tell my mommy-self  to keep snuggling Cami, to continue reading aloud to her every day, to keep telling Cami how beautiful she is, how smart she is, how valuable she is to Jesus. I’d tell that young mommy to tell herself those same things, too: how beautiful she is, how smart she is, how valuable she is to Jesus.

I’d remind her that she has the Mommy Power to love Cami and teach Cami and equip Cami for life and godliness. I’d tell her that as God teaches her to be Cami’s mommy, He will reclaim and restore that little girl inside her own heart.

I’d tell her that the upcoming journey will be difficult, but so worth it. I’d tell her the experience will be all the more rich when she realizes she really is Cami’s BMF (Best Mom Forever), that she has a more authentic relationship with her daughter—her only child—than she ever had with her own mother.

When I return from this hypothetical time-travel to my mommy-self seven years ago, I’ll start preparing to  time-travel to my future mommy-self—say, 10 years from now when Cami will be 21 years old—so I can help her connect the dots—all the graces and mercies God is giving to all of us on this journey. I’d better pack light—and take excellent notes.

Gaining Perspective on “Normal”

When we meet with Stephen’s teachers at the beginning of the school year and make the statement, “Stephen HATES homework.” Most of the teachers reply with a chuckle, “all middle schoolers hate homework.” Their response, while true, misses the essence of our statement. Perhaps it is that we don’t state the problem correctly. It is likely they do not know how many hours we have spent helping, redirecting, motivating and sometimes writing out math problems for our son just to help him finish his work so he wouldn’t get a zero. Regardless, the exchange causes me to pause from time to time to consider whether behaviors Stephen demonstrates are a result of his Asperger Syndrome (AS) or rather the “normal” behavior of a fourteen year old boy.

My guess is that there is not a definite answer to this question. Because AS has shaped who Stephen is and he is a teenager, the behaviors are the result of both his age and his condition. He becomes consumed with whatever he is feeling. When Stephen is afraid, it is debilitating. When Stephen is happy, he is giddy. When Stephen is sad, he is like Eeyore from Winnie the Pooh.

I consider myself to be an experienced parent. But, even though I have two older children and one younger, I still have to ask myself whether the way Stephen acts is “normal” or a result of AS. If it is normal, then what do we as parents need to do to train and guide our son? If it is a result of his AS, then how can we teach him the coping mechanisms necessary to thrive in the world? To care for himself? To hold a job and have a family? How do we know what is “normal”?

Right now I am in the process of reading and learning all I can about AS and how it shapes those who have it. Although every person who has AS is as unique as anyone else, there are behaviors and thought processes that are common to many. In fact, for those with AS, you could say it is NORMAL.

Is it "normal" for a 13-year old boy to sit voluntarily between two toddler girls at a 1-year old's birthday party wearing a party hat? For Stephen--yes, it is. And I LOVE it!

 

Disabilities and Differences

I really struggle with this distinction. For years I repulsed at the idea of labeling my son “disabled.” It went against everything I believed about God’s sovereignty and goodness and the human dignity of each individual.

My principles tell me to think in terms of “differences” not “disabilities.”

But then I run into the reality of laws. In order to receive accommodations, whether in school through an individual education plan (IEP) under the Individuals with Disabilities Act (IDEA) or in college or the workplace through the Americans with Disabilities Act (ADA), one must accept the term “disabled.”

And I struggle to resolve the dissonance.

The truth is that all of these hidden issues are, in some sense of the term “disabilities.” An individual does not receive a diagnosis of Autism, Asperger Syndrome, Bipolar Disorder, Tourettes or any other label unless they are markedly different in a way that is deemed of concern. Something about the individual is NOT neuro-typical. He or she is different.

In public speaking I like to speak of this positively. God created each individual for His purpose and pleasure. Psalm 139: 14-16 says that each is “fearfully and wonderfully made.” Period. No exceptions for Autism, Asperger Syndrome, ADHD, Bipolar Disorder, etc. While approximately 80-85% are neuro-typical, the other 15-20% are not neuro-typical — they are wired differently.

Then the rubber meets the road. The child with ADHD struggles to remember the most basic multi-step instructions. The child with Autism or Asperger Syndrome struggles to establish connections and make sense of his world. The child with Bipolar deals with mood swings that make his life a chaotic mess. The child with learning disabilities struggles to read, or write, or do math, or all of these. The child with Tourettes experiences uncontrolled tics and other physical responses.

And I am confronted with the fact that though my principles require me to believe all these differences are from the hand of a good and loving God, the daily life of the individual and his/her family are deeply affected and frankly, at times, hard.

How do I resolve these two, seemingly dissonant realities?

This is where my relationship with God and my faith in Him and His Word is applied in daily living.

I DO believe each individual is created in the image of God, for His purposes and pleasure, and is fully loved by Him. But the fall and its consequences for our daily lives is very real. We all live with limitations and struggles as a result of the fall. Some of us just hide it better than others.

This reality should be cause for great humility. Each of us is broken by the fall corporately and our own sin personally. Each of us needs the saving grace of God in our lives. Each of us needs to live by His daily grace in our fallen world.

Perhaps those with some sort of “disability” are just more conscious of this need. Perhaps they are more aware of their brokenness and dependence on God.

The rest of us should look and learn. For this is the essence of wisdom.

A Dad’s story: Baseball, Apple Pie and Ice Cream … Almost

Peggy’s husband, Jim, gives his perspective. Please share freely …

I was a typical guy who just learned that I and my beautiful wife have welcomed into this world an adorable baby boy, and almost immediately the thoughts started to run through my mind of all the “guy” things that I’ll be doing with him as he grows up. Learning to play baseball ranks right up there at the top of the list, along with catching his first fish and going on our first camp-out together. I’ve already picked out his first baseball glove, and I dream of the day he gets his first big hit off a pitched ball. I make all the plans to get him enrolled in Little League… well, okay, maybe he better learn to walk first. But the point is that my own life starts to become filled with all of the hopes and aspirations for what our newborn son will someday be able to achieve. Not in an obsessive way, but just a vision for the future.

Then, about the time that other boys were starting to play Tee-Ball, I learned that my son was afflicted with a developmental disorder that severely impacts his gross motor skills. He can’t swing the bat the same way; he can’t catch the simplest lob of a ball toward him; he repulses any attempt to help him manipulate his body in a helpful way. I learned that his Autism gives him a completely different view of the world that scares him and makes him unable to adapt. Then, I learned that I … yes, I had to come up with a new vision for the future; a new world view that encompasses his world. I had to find a way to enter that world, and come to understand what he can do, and with the firm belief that what he can dream for himself is exactly what I want for him. Nothing more, and nothing less. And I started to wonder if he would ever be capable of learning, or even want to learn, how to play the American pastime of baseball.

Fast forward a few years to 3rd Grade, and a particularly gifted teacher (who is also a strident and long-suffering Cubs fan) connected with our son in many ways. One particular side-affect is that he too became a Cubs fan (who would soon also become “long-suffering”). Regardless, he now is very interested in baseball, and wants to pitch in a ballgame like a big-leaguer. YES!!! Remembering that this is the boy who once could not hit the ball off the tee, I started to wonder how to help him achieve this very dream that I once held for him myself. That time will come, but for the moment, I am thankful for the gift of sharing with my son in the passion of America’s pastime. And, I know from where that gift has come. I am thankful to God for these moments of being able to connect with my son, no matter how I got there.

Coming up next… dreams shift toward reality.

Of Backpacks and Flipflops

Over the past week, I have been collecting supplies for the tornado victims. We have been packing backpacks for displaced children, including pajamas, undergarments, toiletries, and small stuffed animals or toys. I have had many friends and coworkers who have contributed to this effort, resulting in a kitchen filled with over 70 backpacks! I am amazed at the generosity of people, who are giving so unselfishly to complete strangers.
This has been a wonderful experience for my kids. I have been able to share with them so many life lessons: sharing, helping those less fortunate, and giving selflessly, just to name a few….

With my backpack project, I let each of my kids pick out things for a child of their age and gender, and pack a backpack themselves. I was so proud of them, because not ONCE did they ask for the toys we were including (which was a fight I was expecting.) Instead, when we got to the end of G-man’s 5 year old “How to Train your Dragon” backpack, he began to survey the merchandise. His little mind cogs were turning, and he was calculating. He said, “Mommy, but we didn’t include SHOES…. The kids need SHOES”. But what came next was the true tear-jerking moment. He went to the “shoe rack” (a small rack we keep beside the garage door with shoes) and starting pulling his shoes off to put into the backpacks. “I KNOW!”, he said, “We can put these in!” And just like that, my 5 year old offered his own shoes for a child he has never even met.

I did buy some new flip flops for the backpack. But what a beautiful gesture from the heart of a 5 year old!

I Timothy 6:18 (NIV)

 
 

“Command them to do good, to be rich in good deeds, and to be generous and willing to share”

Tow Trucks and Rest

Toddlers do not WANT to take a nap even when every indicator says they need S-L-E-E-P. Bipolars aren’t much different.  The more they need sleep, the louder they get and the higher they fly until they fall out of the sky and make a greasy spot on the pavement, to put it gently. Sleep matters.

We got a call from one of our daughters at sunset recently. She was driving her 26 year old Toyota truck with a friend, hours away from us. Some warning lights were blinking on the dash. Actually, they had been blinking on and off for two weeks, but it’s a bouncy, aging truck, and quirky sights and sounds is one of its charms, so she ignored them. (That won’t happen again, let me tell you.) For some reason, as it got dark, those lights started worrying her. Cell phones are wonderful, as in 1-800-DADDY. My husband had them pull the instruction manual out of the glove compartment and start reading … but it was too little, too late. The truck lights dimmed, the engine slowed down, and in no time at all there was no power at all. They were at a dead stop, in the dark, on a strange highway, mile marker 214. Two girls. (Now, all you with sons or new high dollar cars, see what you’re missing??) It took a tow truck to solve that problem.

This is exactly what happened to my man. He was 25 years old and had indicator lights going off on his dash, but he didn’t heed them, and I was clueless. By the time we knew there was trouble, it was time to call the tow truck and get hauled into the shop for repairs. You can believe we really read The Manual (as in “the B-I-B-L-E, yes that’s the book for me…”) because tow trucks and repairs are expensive. One of the first things God highlighted for us was His command to REST … something needed every 6th mile, like an oil change.

When God said “Let there be night … and it was good.” He wasn’t kidding. Lack of sleep lights up all my man’s indicator lights. When he’s tired, God designed his body to produce adrenaline, and probably 14 other things, to meet the demands of life, like everyone else. But over-drive is right before over-the-edge for a bipolar, so watch out for that driving up on two wheels. For any bipolar trying to stay in a stable state emotionally and mentally, pushing the adrenaline button too many times makes it near impossible to keep his/her car on the road. They may drive fast for awhile, but eventually the engine seizes.

Even God rests. In case you think I’m making that up … “on the seventh day He [God] rested from all His work. Then God blessed the seventh day and made it holy, because on it He rested from all the work of creating that He had done.” Gen 2:2  Like the way He repeats Himself? Then, just to be super clear … “the seventh day is a sabbath to the LORD your God. On it you shall not do any work, neither you, nor your son or daughter, nor your male or female servant, nor your ox, your donkey or any of your animals, nor any foreigner residing in your towns, so that your male and female servants may rest, as you do.” Deut 5:14. Sounds like the level of repetitious detail I use when my kids are being dense.

This idea of rest is nowhere in the high tech industry manual, so that pivotal part of the 10 commandments is highlighted in our personal manuals now. We’re not legalistic (which is hard work) – we just rest, and get our spiritual oil change. “Then He [Jesus] said to them, “The Sabbath was made for man, not man for the Sabbath.” Mark 2:27

There’s a blessing to be had on that day of rest, and when dealing with hidden disabilities, we need all the blessing we can get.

Working on Rest,

Joan

“Children, please line up!”

Wow, I had no idea lining up could be so hard for kids on the spectrum. It’s been a trend though… so many of the behavioral issues/negative responses that I have heard about this school year – resulted from either being in line, getting in line, or someone budging in line.

I have been doing some reading lately and attending autism seminars.  Well-presented seminars are a great place for a parent (aka Expert by Necessity) to learn more about their child and more importantly understand the why behind something that happens often. I’ve seen how putting a title or tag to something helps me understand it better. Like rigidity or inflexible thinking. See Louise’s post about Stephen’s spot at the dining table.

An autism consultant on Owen’s team recently suggested something so incredibly simple and brilliant! I’ve often thought… can a parent suggest that the school let her child be first in line, all the time? That doesn’t really seem fair, does it? Do you remember how exciting it was to be line leader? I do! This autism consultant suggested that Owen have an assigned spot in line. So on Monday of each week Owen picks a number out of a hat, we keep it at 1-5… it’d take too long for him to count to higher numbers every time he lines up, and then he takes that place in line every time they line up, anywhere in the school. Everyone else knows it too (this is important!). I had never thought of something so simple because I often thought of the lining up troubles stemming from either the desire to be first or a sensory issue (being bumped accidentally), etc. But often for Owen, an issue stems from the unpredictability of lining up. By having a specified spot the child always knows right where they belong and the anxiety level never spikes from this simple direction, “Children, please line up.”