Tuesday, February 15, 2011

The Perfect Life




Much to my chagrin, I am forced to admit that yesterday was a perfect day, and that my life is perfect.

It was Valentines day, and I woke up next to my valentine – the man of my dreams, my perfect partner in this endeavor, whose chief function, it seems, is to remind me, just by looking at me and smiling, that I am loved. We got the kids off to school, and set about the Monday “routine”, if you can call our default setting a routine, of packaging a weekend’s worth of eBay, getting to the post office, and running errands.  A lunch together at a burger joint was perfectly romantic, even though we had to do it with a coupon to afford it. We did the grocery shopping for a few staples, and then home to pick up Phil and get him to physical therapy up in Sheboygan. Phil gets to play the Wii in the stander to distract him while the therapist stretches and bends his feet and legs, trying to get them to a further extension, and we realized half-way there – running late – that we forgot the necessary game controller for the game he brought to play. And it seems the day had reached it’s peak and was now on a downward trend. When Philip ain’t happy, ain’t nobody happy! But life being what it is we are learning to deal with his outbursts and disappointments, ever trying to steer him in the direction of dealing with disappointments in a more constructive way than cursing out the entire planet, and coming to the conclusion that “everything sucks!” No, everything does NOT suck, and we try to bring to mind things that are more pleasant to think on. Just before we arrived at therapy, an awful stench arose from the front of the van, and I noticed that the car ahead of us was blowing some darker exhaust, so we didn’t think too much more about it.

We made it to therapy, and with the help of the best therapists around, we were able to get him to cooperate with all his exercises. And so, by the end of therapy, he was stretched and bent, promising to try something new next Monday, and happy to be going home, where he would play his new game and catch up with all his friends on Facebook.

His therapy takes place in a building that shares the rental space with (ironically) a dance studio. This was parent observation night, and our handicap spot out front was taken, so we rolled around back of the building and found the last spot available where we could unload him. We left the building with plans to stop at McDucks and get him his French fries, Mark and I some coffee, and then home to finally call it a day. We started the van, opened the side door and lowered the ramp. Phil got on board, and as the ramp was going up, the vans engine suddenly bogged, and we heard an ominous sound. We smelled the same acrid smell we experienced earlier on the way here. Mark and I glanced at each other, a look that can only be interpreted as “Uh-oh…”. He folded up the ramp, and I looked at the engine gauges at the same time he lifted the hood – way too many lights on.

“Shut her down,” he called to me, as he reached underneath and pulled out what was left of the serpentine belt.

Now, I have been stranded by vehicles that have spontaneously malfunctioned in a major way more times than I can count – and I mean that literally, and people who have followed my life can attest to this. I have never owned a new vehicle – and the ones I have owned are usually beyond the “used” stage, closing in on “used up”. So this is not unfamiliar territory to me. I am not a panicking person by nature – in fact, if I’m in an abject panic, you probably should be too, because I’m the last one to fall apart. If you see me running and screaming the sky is falling – it probably is. And while this did not equal a “sky is falling” moment, I was suddenly struck with the magnitude of this current problem.

It’s cold, and getting colder. We are 25 miles from home. Our cargo is a 400 pound wheelchair under the kid attached to it. Hmm. This certainly puts a new spin on an old problem. I don’t currently have Triple-A, but I don’t think there is anything in there about sending a ride for the wheelchair occupants of a stranded vehicle. This is one of those situations where nobody really knows what to do. Lots of “Oh, dear!” and stupefied looks – not something you have to deal with every day. A real, “Now what?” of a situation.

Phone call #1: Mechanic. Voice mail.

Phone call #2: Wheelchair taxi, which drops people off here at therapy all the time. Closed for the day.

Phone call #3: Josiah, 18-year-old son who is the proud owner of the only working vehicle in our household, and it falls under the category of a “used up” car.

Phil is in the back getting all upset as I calmly fill him in on what this means to him. “Well, Josiah will come and pick us up. We will have to leave your chair here, and you will have to use your little red chair for school tomorrow. Let’s be glad we have a spare chair at home, kiddo – it beats a manual chair or a day in bed, now, doesn’t it?”

He is not satisfied with this solution. I spend the hour that we sat there waiting for a ride home trying to persuade him of the up side of this, even though there really isn’t one. “I don’t want to use the red chair! It’s so short – I will look so little to everyone!”

“Yes, but you can tell them that today you decided to use your “sports chair” – that your “SUV chair” is in the shop.”  I remind him that his chairs cost as much as a car, so he’s got something to swagger about, there.

He actually likes that idea. Then I tell him to think about what this will be in a week, a month, a year – an interesting story to tell. He accepts this, too. By the time I am done convincing him of the pleasantness of this whole experience, I find I have myself trivializing the whole thing as something I cannot afford to get upset over, even though I have the entirety of the situation laying naked across my bed. This is the last running vehicle we had. The minivan and the car are both DOA, needing various amounts of maintenance that we cannot currently afford. I have a dentist appointment tomorrow. We have the store to run on Wednesday. The whens and the hows of getting this thing back on the road and Phil back in the chair that is custom fit to his body are still a bit foggy. But the show must go on.

Josiah arrived to pick us up, and we lowered the ramp and chair to the ground, and I picked him up and put him in the back seat of Si’s car. I grabbed a few things out of the van, and got in behind the drivers seat – or attempted to. Si is getting to be a tall boy, and this is a Saturn sedan. Nevermind, I’ll just sit Indian-style. I had promised him that we could still stop for his French fries – there was no point in depriving him of that, too. As I said, life goes on.

And so in the back seat of this car – a place I don’t often see – I just figured I would curl up with Phil and feed him his fries on the ride home. As we pulled out of the drive-through, the car made a horrific bump underneath me. “Don’t worry mom, that’s my tranny,” Si told me in response to my gasp. I then asked about the awful noise coming from the front of the car, and he told me that, too, was “nothing…just my wheel bearing. I’ll take care of that…” and he turns up the music so I can’t hear it anymore. Now, I’m not completely mechanically ignorant, and this spells trouble to me. Not to mention that I look at the driver and think, “I gave birth to you! You can’t drive! You’re just a baby!” and somewhere inside the panic button is getting tapped. I am rescued from detonation by Phil’s voice, “Can I have my fries?”

I look over at him. He’s not worried. He’s hungry. He’s warm. He’s secured. There is nothing in his memory banks to suggest to him that this is a bad situation, or that the clatters, grinds and bangs coming from the car are anything other than noises that cars make, and may I have my fries, please?

And so I take my cue from the kid. What’s the worst that could happen? If tonight is the night that I am rocketing down the road at 55 miles-per-hour and metal fatigue sends car parts flying in all directions and us careening head-on into an oncoming semi…so be it. This is my life – and if today it’s over – oh well. Shit happens. So, how do I want the last minutes of my life spent? And in that moment, I decided that feeding my kid his French fries, looking out the window at the rising planet in the west, and the stars that you don’t see nearly enough of in the winter, and laughing at the look on Phil’s face as I stick an exceptionally long French fry in his mouth, leaving it hanging like a bent cigarette is exactly what I want to do.  I entertain rather macabre thoughts of what it would be like to die tonight in a thunderous crash of metal – me and three of my favorite people – all exploding through the veil of materialism into the spirit world in a split second together, arriving on the other side, utterly conscious, still very much alive, but totally free from all that encumbers us. And I am finding that this is not at all macabre, or unpleasant, or even unappealing. I love my life. I have no regrets. And when it’s time to go, I’ll go. How nice to take that trip with Phil, and Si, and Mark, rather then endure the mourning and misery of being left here. I chose not to think about those left behind, because in that moment, I realized that if this were to happen, there is nothing I can do about it, and from the vantage point of disembodiment and suddenly knowing, I wouldn’t care about that anyway. I would know it was okay.

The long and the short of it is that I was forced by circumstance to live in this very moment – nothing before it, nothing after it – just this very moment. And how I dealt with this very moment would determine my future, if I were to have one. Assuming we made it home in one piece, I could be ugly as hell, fuming about the problems we face, blaming this or that, finding fault and finger-pointing, or lamenting the whole situation. Or I could appreciate with laughter the oral contortions Phil was engaging in to get the rest of that French fry into his mouth without my help, while trying not to laugh himself. We could arrive home and inform the other kids as to what just happened, and embellish the story if we so wished, and enjoy a meal of cold chicken nuggets together. I could come home with tales of “woe are we”, or tales of, “damn, another puzzle to solve”.

Needless to say, we arrived home in one piece. Phil complained bitterly about his chair, until we recalled our Sports Chair perspective. We passed out the chicken nuggets to the other kids and recounted our night, and discussed the potential, probable and positive solutions to the issue.

Later that night, Mark and I sat down to our last smoke of the day, and I told him of my mental musings of the evening, and my conclusion: That our life was perfect. It’s a life that nobody wants, really – a life full up with the ravages of disease and poverty American Style. It’s a life of working your ass off for little or in most cases no financial reward. A life of too much to do and not enough time. But my life – or anyone’s life – is made up of moments, and what we do in each moment affects the moment that will follow it. And as long as I have done my best with what I have in my hand on any given day, at any given time, I can ask no more of myself. As Mark has encouraged me on numerous occasions: It has to be enough. How I choose to see any given circumstance will determine the quality of my life: Am I the owner/operator of this life, or merely a victim of it?

Do I see Phil and his disease as a plague, brought about to “test” me, concentrating on words like, “defective” and “crippled”; or do I just see Phil as Phil – my son, hampered a bit from the mainstream by muscles that cannot cooperate with the upright functioning of a human being that most of us enjoy? Do I see the lack of finances as some gross failure on my part to earn my keep, or just realize that money is an intangible unit of measure, really, and that just because I don’t get dollars for my hours upon hours of back-breaking work does not negate the fact that I work, and I work hard?

The Universe has set laws into motion that cannot be changed by mortal man. They can be bent, and twisted and defied – but they cannot be changed. We live on this planet, and we are subject to the laws thereof. What matters then, is how we roll with the changes, how we integrate these laws into our lives, and how we work with the results. Phil has Duchenne. It will have its way with him in the end, and there is nothing we can do about that. I can cry, and whine and lament, or I can feed him his baked potato and cheese while we watch a funny movie. Sure, it puts a different spin on little problems like a broken down vehicle, issues of mobility, and health monitoring will be more than eating right and exercising. But this is the hand we were dealt. I can accept that. And beyond accepting it, I can embrace it as the life that we were meant to live. I can be happy about the fact that I can look back at my life at any moment, and know that I have learned from my “mistakes”, thus taking them out of the category of mistakes and into the higher purpose of learned lessons – hence the lack of regrets. I can see that I don’t repeat the same things over and over and expect different results, as so many do who deny the Universal laws and seek excuses and someone or something to blame because they just didn’t think they needed to pull their head out of their ass.

Nope. I’ve come to the conclusion that my life is being engineered, lead, and guided by higher purpose. It is but a class in the education of my soul. And just like calculus (to me), this is a really shitty class. It’s tedious, and difficult and challenging and I rarely see the point in it all. But I know I need the credit, and I know I want a good grade. I know I am capable of it, and even though it’s got me staying up late, wired on caffeine, and stressed out studying what seems to be pointless – I paid to go to this school. And I’ll not waste one penny of my “tuition” blowing off my classes, goofing off or failing my exams. There is a supernatural curriculum, and in this I trust. I don’t have to understand it – I just have to live it.

When taken as a whole, it’s not so bad here. Lots of opportunities to party with your friends, decent enough accommodations, professors that can be anything from a wise person to a little Pomeranian dog – keeps things interesting! Lots of elective opportunities for creativity – seeing the art in everything. If we just relax in knowing that the supervisory committee that planned this knew what they were doing, we don’t have to stage any protests or riots, or bring ugliness and dissent onto the campus. We can live in peace with the knowledge that one day when we may or may not expect it, we will hear the final bell, and it’s class dismissed. 

And I will have lived the perfect life –for me.

Wednesday, February 9, 2011

February – Living it By Heart


Most of us think of February in terms of it’s holiday – Valentines Day, which of course is represented by the ever popular heart. Bearing precious little resemblance to the actual human heart, it brings us thoughts of our loved ones, and all the accompanying warm fuzzies it was designed to. Funny thing, that the heart represents these things. I suppose I could research where it all came from, but really, I can see that the heart is the center of our being. The pump. The brawn that works with the brain to keep a human being alive. It’s been attributed as the place we feel our feelings – a spiritual heart, I suppose, somewhere in the vicinity of the fleshly one, eh?

In any event, we’ve had a lot of HEART talk so far in this short half a month.

Our first was in discussing the life and passing of our dear little dog, Sparky. We knew he had a heart murmur when he came to us. We had hoped for more time with him – but that little heart was so “big”, that it outgrew itself in no time, and Sparky had to move on. Our tribute to him: 





The question that many people have asked through that ordeal was “How is Philip handling it?” And I have had to respond honestly, “Better than the rest of us!”

When Sparky took ill, we could see him struggling to breathe, and standing constantly, unable to lie down and sleep. His meds had been maxed out, and now a blizzard was ensuing. No way to even get to the vet for meds. Philip chose not to watch this, as far as it was possible. We still brought Sparky to him to say good morning and good night, and Sparks still responded with a curl of his tail and brightening of his eyes when he petted him. But other than that, Phil would simply ask – often – where he was and how he was, and was content to know the answer we gave.

Sparky got restless at about 4:00 a.m. the morning he passed, and Rachel thought he might be doing better and finally went to bed. At 5:30, Josiah came downstairs and found him lying in the living room. We all had a good cry and a hug, and we wrapped him in a soft towel and placed him in a box.

I told Phil when I woke him up an hour later that Sparky had died during the night. His chin quivered a little, but he was still in the wake-up stage. We then had to rocket his butt into the shower, and get him ready for physical therapy. He concentrated on that until she left, and it was time to take him to school. That’s when he started asking the questions that no one can answer.

“Mom…so is Sparky…you know…up there?”

“I don’t know, kiddo – all I know is that he’s not hurting anymore. And we gave him the best life we could while he was with us.”  And even though it was true, I felt like it was the lamest answer ever. But Phil was already answering his own question.

“I feel like he’s still here, Mom. I can see him over there by the piano. And I can see him in the hall playing with Donkey. And I can see him coming in the door when you open it to let me out, and you’ll have to pick him up and tell him to ‘hold your potatoes, Sparky’ when I drive by.”  And he smiled.

And I know he had the better answer. Much better, in fact. Because Sparky was still there! Not his little body, but the energy…the Spark! We could still feel it. And even though we miss his antics and eyes and bunny feet in the hall – the Spark is with us still, and will be alive in our hearts and minds as long as we remember him.

We had the opportunity, then, of getting one of Sparky’s brothers in March, born just as he was slipping away, and we have decided that Sparky is telling us, “Yo…take care of my little bro’!” (According to Phil…).

So, yes…this seemed to be the month of the broken heart; both Sparky’s physical heart, and our emotional hearts. Imagine my thrill when Children’s Hospital called to remind me that Phil’s cardiology appointment was the following Monday.

I listened to the machine tell me the time and place for our appointment, and waited for it: The cold chill. The sick feeling that starts in your stomach like a smoldering log, but turns icy cold as it starts to radiate outward. The thoughts of impending doom that accompany it, and the chill that produces. But this time, it didn’t come. Oh, I didn’t just smile and say, “Guess what we have to do Monday, honey?” But I realized that I felt just a little bit more than nothing. And I had to wonder about that. (Of COURSE I did…)

Was this lack of visceral response because I didn’t care? Has MY heart just calloused over? Was it the intentional denial that I so often have indulged in when it comes to Duchenne – ignoring the shit I don’t want to know? Or was it just that I was emotionally spent from saying goodbye to Sparky? Or maybe…just maybe, this was the Universe cutting me in on the What’s-to-Come, and letting me know that I don’t need to waste any more energy on stressing this one: It’s gonna be okay. Dare I hope….

Monday came, and all I could think of was how much I wanted the day to be over already. It was going to be a whirlwind day – but me and tornadoes go way back, I guess. There was so much to do! Shipping about 25 packages at the post office, pick Phil up at 9:30, Children’s appointments at 10:45 and 11:40, getting lunch, getting his van through vehicle emissions, dropping off a large package at FedEx, and then getting Phil home to use the bathroom before heading back out to Sheboygan for his afternoon physical therapy at 4:30; having to stop at Wally World at some point for some necessities, like milk and toilet paper...like I said, all I wanted was for it to be over.

On the ride to the hospital, my mind wandered into the Game Show version of what we were about to hear. I’ll never get used to the “bad news” that comes no matter what we do. But you do some preparation for it, just in case.

After checking in and getting his echocardiogram, we waited for Dr. Berger to read his results and let us know the verdict. A pleasant man, he greeted us with a handshake and a smile, and I heard the words that absolutely made my day: “No real change in his echo…still low-normal function. Emphasis on the “normal” part. Very good for a boy his age in his condition.” And after a chat about potential meds in the future, we were given a 6-month pass on thinking about Phil’s heart.

The rest of the day actually went off well. We made all of our appointments, and arrived at the end of the day tired, but satisfied that there were no kicks in the head this time. No gut-wrenching news to deal with; no major traumas, no major losses.

We are almost half way through February now, close to the 6 month mark on Phil’s spinal fusion, which he has recovered from remarkably well. Almost 6 months past the major upheaval that has me getting up close and personal to issues that I would rather not have to think about – about death, and dying, and living, and breathing, and the intricacies of all of these. We have not only survived, but have learned so much in the midst of it all. I stand, however, with Socrates when he stated, “All I know, is that I know nothing.” And that leaves us to live our lives in one way – the way we have been – by heart.