Tuesday, January 22, 2013

Template for a Crisis




First, let me say a heart-generated THANK YOU to everyone who has held Philip up in their thoughts and prayers. My beliefs are such that my request for prayer and positive thoughts are no trivial affair; not just a feel-good measure for me, or a subtle cry for emotional help. There is more and more scientific evidence of the true power of our thoughts and intents than we have eyes to see or ears to hear, and the unified thoughts of a believing community are an unprecedented power. 

Having said that, let me tell you that it’s been a journey into uncharted territory for us, hence the title. Living with and experiencing Duchenne has been, is, and continues to be an eye-opening and challenging life, with no charted course. You have to make it up as you go, because what works for one person may or may not work for another. Each participant is utterly and completely unique. This puts us all in the position of basically having to make up the rules as we go, according to our beliefs and convictions. 

Part of the package that is Duchenne is knowing that while the disease is a slow moving vehicle, changes can manifest very rapidly, primarily when peripheral systems take a hit, like the heart and/or lungs. In this case, Phil has a near complete inability to cough and clear his lungs. Therefore, the annoying cold that went around the house becomes a potential life threatening situation if you can’t, in fact, spend that dreadful day or so hacking. Think about that next time you are frustrated by a cough. Your cough is your friend, believe me! 

Knowing that information is essential, but that is all. In fact, once I knew it, I tucked it away in a file in my mind, labeled “Intentional Denial”, because thinking about it daily, obsessing about it even in times of good health, lamenting it and crying about it and cursing it I found to be a complete waste of my energy, devastating to my mental and emotional well-being, and turning me into less than the best mother I could be to Phil. Have the file handy, but don’t bother to keep it open on the desk. One day you will need to act upon it, but if today is NOT that day, then rejoice and truly LIVE another day in your amazing life. 

Last week I had occasion to have to access that file when Phil came home from school sluggish, tired and weak. He actually asked to go to bed…red flag for him. I get him in bed and mentally pull up the file. What now? 

First, I need to remember the importance of my part in the partnership that is me and Phil. It would be in neither of our best interests if I become an emotional or mental basket-case at this time. So I sit, and I meditate, and ask for a higher perspective from which to function…a place of clarity and deliberateness. I tell Time that it is dismissed. For the duration of this experience, it will not matter. My sole focus will be Phil and his well-being, and my role as a caregiver will require attention that cannot be structured by the clock. The circadian rhythm is the only indicator required to measure time now. And I settle into that. 

Next, and most importantly, I make a conscious decision to walk through this in a state of love, and not in a state of fear. The things that my brain would like to remind me to fear are many and threatening, but I must bring myself to that place that understands LOVE for my son trumps anything the external and physical world can throw at us. 

With the responsibility as my son’s caregiver to be his hands, arms and legs, to carry him, as it were, I must remind myself that no one wants to be carried by an unsteady or fearful horse. For him to endure his part of whatever this is coming at us, he has to be confident in his ride. No spooking, no bolting, and certainly no white-eyeballs. (Perhaps only horse-people will get the analogy…J ) He needs to know he’s safe and secure in my love for him. Perfect love casts out fear. True story.

The last stop on my meditation was to address the fact that I am not in this alone, and there is no need to try going it solo. We are all connected, and these are the times when we do well to draw upon that connection for the support that we need. And so with much gratitude for the companions that walk beside me in the physical, Mark and Phil’s caregiver, Sammy, I also sent out a request for assistance from both my family and the Duchenne community. I know that the energy released from each heart as they read my request was transferred instantly into our Prayer Account, and knowing that…it was Game On. 

Step one, I decided with all clarity, was hydration, medication and respiration. Grateful beyond all reason that we had a g-tube placed two years ago before his spinal fusion. This enabled me to give him a constant supply of water, vitamin C, chicken broth, and herbal teas at the rate of 400 cc an hour. Then guaifenesin to thin the mucous in his chest, Benedryl to dry up the leaky nose and eyes, and albuterol in his nebulizer to help open his airways. And finally, his cough assist – a rather obscure machine that coughs for you – if you have what it takes to actually let it. We humans have a thing about breathing on our own subconscious level. We do NOT like it when some machine tries to breathe for us. There may come a time when desperation for air makes it a palatable option…but not when you can still do it yourself. Then it can be an anxiety ridden battle for the breath. 

I’d like to be able to give a clear and concise breakdown of how everything went after that, but things became rather blurry. An hour at a time. A fever develops. His vitals fluctuate…up, down, up down. Awake, asleep, out of bed, back to bed. At one point, I have started to ponder the parameters and at just what point his care may have to be turned over to the medical establishment – a contemplation that as of yet brings no peace, so I abandon it in favor of just sitting with him and watching movies, and keeping him comfortable. Instead, I contemplate the balance of my Prayer Account, which, instead of depleting seems to be on the rise. And I sat in awe as his 103 fever evaporated in 15 minutes without him even breaking a sweat. I thank you all for that. This gave both of us a much needed infusion of hope. 

Over the course of the next few days, we continue on our hydration, medication and respiration efforts. On Monday he had a standing appointment for a spine x-ray at Children’s Hospital, and he is actually sporting a bit more energy. His x-ray looks good, but I am unable to get a desired chest x-ray done. Part of my reluctance to turn his care over to the medical establishment is rooted in the fact that his care is managed there in a manner that frighteningly resembles The Manhattan Project: 130,000 people, two billion dollars and nobody knows what anyone else is really doing. Coordinated care is an oxymoron at this time. As per my previous analogy, this is one horse I don’t want to ride. 

By the time we arrived home yesterday, Phil was exhausted and needing hydration, but in good spirits. My mother called, and I was reminded that it would be good to update those who have been praying, and today is my attempt to do just that. 

Today Phil woke up pretty congested, so we started his day taking the last of his antibiotics with a side of vitamin C.  His fever has not returned, and despite extreme difficulties in scheduling his future appointments this morning, I am very optimistic for his complete recovery. 

We are not out of the woods, however, because the fact is that we live in the proverbial woods. Like the boreal forests of earth, it is as beautiful as it is dangerous; as delightful as it is deadly. It’s a world of extreme polarity, which leaves the residents with a choice of how to respond to its environment, in either love, or fear. I lived too long in fear… a place where the mind wanders into all the horrible things you may see or experience in this unstable place. Enough of that already. 

Instead, I have chosen to purposefully pursue the path of love through this forest. When I stepped out in faith on that one, I was immediately rewarded with bird’s eye view of my life, and the transient nature of it. When I begin to understand the scope of that, I realize that all fear is doing is robbing me of the extreme beauty all around me. In fearing and thinking about what might happen, I miss out on what is currently happening – and thereby miss a good chunk of the stuff of life. If Duchenne has done nothing else, it has made me acutely aware of very preciousness of every moment we are alive! 

And so I choose to live in love. And in charting my course – or creating a template for any crisis that may arise, I have begun to truly understand the place for prayer, which is generated from the place of love in the petitioner. It reconnects us on a spiritual level, and produces the most healing results. 

I no longer curse anything about my life in this place. It simply IS. How I choose to frame it is entirely my choice – and I will benefit from the fruits of love, or crumble under the weight of fear. Thank you for joining me and upholding my son in the light of grace and carrying us through this current crisis. We are going to be okay!

Thursday, March 24, 2011

March-ing Along - Quarterly Update

You know, I have been so wrapped up in so many things – between my mind, my heart, my tasks, my daily grind and my daily bread…today I just feel lost in space! It’s officially Spring, now, and my yard is coated in white stuff. It is also spring break here, so Phil is here with me all week. The rest of the kids have all kinds of plans, so it’s a rowdy parade of friends half the time, and a blissful silence the rest of the time – if you don’t mind the video games Phil is playing!  

Add to the fun the fact that this week the builders are remodeling the bathroom by putting in a roll-in shower, which is simply divine – but has us dashing up the stairs to use the loo and using bed baths for Phil.
Further complicating issues is the fact that we are in the process of closing my store – which is a bitter sweet good-bye. I will have a good cry once we’ve got all the final sales numbers  and the store cleaned out – lots of shelving and hopefully not too much excess merchandise.
In the midst of it all, I just woke up today feeling like, “I don’t think we are in Kansas anymore!” So, I guess today is a good day to do inventory on all that we have – and reflect a bit on the direction we are going. Despite all the chaos on deck, it’s a relatively calm day at sea, and so this captain is going to take the time today to write up our ships quarterly report.
The last quarter of last year brought Philip’s surgery, which was as polar shift in our life. The need to be here now 24/7 to take care of Phil has been quite the adjustment. We had to sacrifice the brick and mortar store because of it, and since January, we have been in the process of moving our business here into the home, shifting our focus to online sales, and eliminating the overhead, time and energy that is takes to run a business. It’s been an uncomfortable transition, but I think I have finally gotten around to seeing the far side of this gully – and I do believe there is greener grass over there! Bringing home all the lozier shelving from the store and putting in the basement has been quite the task, but is making the basement look so nice and organized! Mark has been busting his butt, but it’s worth it. The house still looks like a drop off for Good Will, but I am seeing spaces open up here and there – and it’s a good feeling!
Like so many people this time of year, we were victims of some wretched flu bug, and Phil scared the liver out of me with a cough and fever, but with the help of his handy-dandy million-dollar-machines, I think we triumphed over it this time! However, we are now scheduling a sleep study at Children’s to see if his overnight breathing is still up to speed. It’s just another stone on the Duchenne footpath, to make sure that his oxygen levels are not dropping at night yet – sooner or later they will, and we need to keep abreast of that.
I don’t remember much of February, but I know it involved a bank-breaking root canal for me, and  evidently we survived it okay. March brought us some delightful new additions; one being a fluffy little bundle of Pomeranian, brother to our dear friend Sparky who left us in January, named Smokey. Just as smart, but even more energetic than his late brother, we are enjoying his Napoleanesque fuzziness.
In early March we were invited to the party of a friend of ours, whose son, Zac also has Duchenne, and is scheduled for his spinal fusion this spring. Despite being on the edge of the flu, we made the trip to Menasha, and had a wonderful time meeting our friends in person for the first time. The Menasha Fire Department even showed up at the party with a big rig! This is also where we surprised Philip with his new buddy, Smokey. Despite spending the next week in virtual comas, we had a wonderful time.
Later the following week, however, Philip was surprised and delighted beyond all reason to receive an Xbox 360 with wireless as a gift, and now he can play games remotely with his new friend Zac, his brother Travis, and several other gamers on-line. While this may be seen by some as the ultimate, unnecessary technological toy, to a boy whose activities are so very, very limited and whose social life is a slim-to-none proposition, this game system has been a life line to a world of peers, where all thumbs are created equal, and he can shoot-‘em-up with the best of ‘em. I haven’t seen Phil this happy in quite some time. I’ll not stump about it at this time – but I cannot even begin to express the gratitude that this simple gift means to our family, and next time you feel the urge to help a family afflicted by Duchenne, save your check that will pay the toilet paper bill for the research organization that wants to cure this incurable disease, and see what you can do by way of simply blessing someone with something we really need and cannot afford. Hit me up if you get stuck on that – I have a list of names and needs longer than the list of genetic studies being done at this time. The joy of a simple blessing – from the ability to shower safely, enter and exit your home safely, to adaptive technology for our boys ever-limited function – makes us forget, if only for a while, that we are living with this disease. THAT is a cure to me! It’s these very random acts of kindness to me and mine that will result in a pay it forward of the grandest kind – some way, some day, some how – to ease the burden of our diagnoses. And here’s something the research teams don’t say often enough: THANK YOU!!!
Now, this past week we were happy to fit Philip with his brand new foot braces! (Camo, no less…). His feet have started to atrophy, and these little plastic wonders will help to keep them from turning in unnatural or uncomfortable direction for as long as we can keep him wearing them.
It’s harder than you think trying to keep an immobile body straight and symmetric! Phil also had the wheelchair company readjust his seating and order a new tray for his wheelchair, as he was starting to look a bit like the leaning tower of Philip, and his back started to bother him. We took him back to the surgeon last week and x-rays revealed everything is as it should be – he just needs his seating arrangement adjusted, and some scar desensitization on his back. Considering all that can go wrong – we were really happy with that!
Tis a good thing to have all that behind us, as we are moving into some high level activity for the next few weekends. Next weekend will be the last weekend of the store, and moving the rest of the stuff out of there to better resting places.
The weekend of April 1st, we have been invited by U.S.S.A. to go turkey hunting up north, and we are excited for that. Once again, it will be a marathon of activity, but it will be an experience to remember! There will be other kids like Phil along this time, so I think he will really enjoy this. Mark is, of course, bringing the cameras, so we will be able to share the doings in video and picture format when we get back!
The second weekend of April, we will be headed to LaCrosse for a somewhat impromptu family reunion with my siblings, which is a relatively rare occurrence, with there being nine of us, and we are very much looking forward to that. After that, I think we will need a vacation, which in my mind will be nothing more than sitting home, cooking dinner and watching Netflix. Although there is nothing like having a bathroom remodel to inspire you to want to re-do the entire house, and since it looks like we will be camped in Random Lake for quite some time, then I might as well be about the business of decorating our castle with a little Feng Shui – and with the promise of Spring, that means the yard, too….yikes. Oh yes, and about this time there will be a decent ramp being installed outside, too!
After that…who knows? The remainder of this year should prove to be an interesting one, going full speed ahead into the Wonderful World of eBay, and going through whatever doors open for us, and bidding a fond farewell to the ones that close behind us.
Life is short – Life is scary at times; Life is uncertain – and life is an adventure. But today, just trying to sort out some of the events and circumstances of the past few months I can tell you this – the LIFE IS GOOD!! Take a moment, look around you, and believe it!

Sunday, March 20, 2011

Dying to Walk Again



So Phil gets home from school at 2:40. I ask him how his day was, and he gives a few details. He has to go to the bathroom, so we take off his hat and gloves, remove his tray, unbuckle his vest and carefully remove his coat. We roll into his room where I unbuckle his lap belt, and slide an arm under his knees, and the other behind his shoulder with my hand under his far arm, making sure his head is positioned in the crook of my arm, and my hand is not bumping up against his g-tube. I then adjust my stance so my back won’t hate me, and hoist his 70-pound frame out of the chair and onto the bed.
We chat about this and that while I roll him onto his side and slide half of his pants off. I reposition his hands and arms and roll him back toward me so I can slide off the other side. He winces, but he knows the routine. Cradle carry him over to the commode and again, watch the back while I swing him into position and set him gently on the seat. He divulges more of his day and finishes his business, while I stretch my back on his bed.  I go back and pick him back up off the commode, and lay him back on the bed, and roll him away from me. We pull up half his drawers, roll him towards me and wrestle up the other side, and then I roll him onto his back, and we are both winded. So this is a good time to chat.

“This would be so much easier if I could walk!” he exclaims, in a surprisingly casual and objective tone.

“You got that right, pal,” I reply as I smooth his hair back on his head. “But I don’t mind. But this is just how we roll!”

He smiles and was quiet for a moment, and then out of nowhere asks me, “Does this mean I have to die to walk again?”

I would like to say I was thunderstruck – but that’s way too loud and far too understated. No one heard a thing as my heart elevator took a plunge all the way to the basement.

Up to this point, I suppose I have been pretty good at coming up with quick responses, clever diversions, true-but-vague and abbreviated answers. But they didn’t come this time. The question was too spontaneous, and asked in such a tone as to unnerve me to my core. Matter-of-fact. Not whiney, not emotional. Objective. Rational. I could not find anything in my arsenal of words to formulate into anything that even remotely resembled an answer that measured up to the question. A fairy tale answer about a hope for a cure would have been insulting. A flat out “Yes” would have been cruel, because despite the objectivity of it all, the inquirer is still just a 12-year-old boy who just got done telling me about the girl in school he has a crush on.

So what Phil got from me was, in fact, not an answer to his question at all. What he got was a declaration, drafted from a place of rawness and nakedness…a place of extreme vulnerability. “Phil, I’m not sure how any of this is supposed to go. I just don’t know. We’ve just got to figure this out together I guess.”

“Is there anything that can help me to stay stronger? Like that guy in Texas?” he asked, referring to the Vecctor treatments we have looked at.

“I don’t know, buddy…couldn’t hurt, I suppose. But that’s one reason we do your physical and occupational therapy. We want to keep everything moving as much as we can since you can’t move on your own.”

I look into his eyes, and I can see questions there that he can’t even ask. And I want him to know that this is okay. It’s okay that he takes up a ton of time. It’s okay that I have to tend to him like a baby. I don’t mind. Yes, it’s lopped off a big portion of what I thought my life should be – but in exchange for what? In exchange for knowing him, loving him, caring for him, and learning a whole lot about life in the process. So what if I never see Italy? When it’s all said and done, I will have spent years witnessing a human spirit whom I love overcome a disease process – now THAT is something for the record book. This is an experience that not just everybody has. No – nobody asks for it, and nobody really wants it. But when it’s what you’ve got – at some point you have to realize that it has a rare and valuable element, and is to be treasured.

But how do you get to that place? Because I was not there. Not hardly. While the rest of the day passed in the ebb and flow of dinner and dishes and bedtime, my heart was tossed overboard in the maelstrom of my mind. I cried while Mark held me through the night, hoping that the light of day would bring a new perspective. But it did not.

What resulted was the following journal – written by me, TO ME, and for me. A literary volcano, which emanates from the depths of what is uniquely me. 

So why publish this? I had to ask myself this, because while I can sanitize anything I write to appeal to a broader audience, that is not why I write. I write for me – for the sake of clarity of thought and purpose. Turns out, many people think and feel the same way, but perhaps lack the ability to get it into writing. We don’t want to share the ugly stuff – the inside scene that might make people think less of us – and so we suffer that in silence. But perhaps – just maybe, someone will read this and find their OWN answers within my tormented ramble.

I am choosing to share this, except for a few spelling and grammatical errors, unedited. It’s bound to offend, upset, and disgruntle folks – but that is not my intention.  Please take nothing personally – as the person who I am addressing is ME. There were no faces before me – only the bulk of humanity. My theology is my own – I have no scores to settle, and no cause to soapbox for here. I simply needed to go back to the source of it all to try and find reason and sanity in my own life, which seems to be sadly lacking in both most of the time. I realize this makes me vulnerable, and open to all manner of criticism – but the words pour forth from MY heart and soul, and they are what they are, and I am who I am. Love me, hate me, but please – respect me as you would anyone who endeavors to be true to themselves in a world in which it is becoming increasingly risky to do so.

I hope, too, that each one of us who shares this particular burden, on this particular planet, can come to the source of peace within them that I am in the long, arduous, but important and rewarding process of finding within myself.






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I woke up to my day to day routine – getting Philip up, going about it as pleasantly as I can. But it’s never enough – and how could it be? This is not how a 12-year old is supposed to start his day. He’s supposed to hit the snooze button until I come in there and tell him he HAS to get up. Instead, we have a wrestling match with his sweat-soaked PJs, and his pants, and his socks. He cries and moans over the aches and pains in his legs and hips from sitting in one position all night long. I can only move so slow. I am a convenient target for his rage. Again. As I am every day. We both know it – we both deal with that in our own way – but what else can we do? I am overcome. The tears well up and begin to flow. I know he sees them, even though I try to hide them. He quiets down and complains a little less – but still winces whenever I move him. I dress him, put him in his chair, and send him out to the bus. Only then do I sit down and sob. This will never end. I cannot bear this. I don’t want to think about what this means for any personal dreams and goals I had. The smallness of my life is killing me slowly – but just like a black hole, the smaller it is, the denser and heavier it is – impenetrable, with a gravitational pull that is unbelievable.  I’m fighting it – I’m fighting it – but it’s a fixed fight. The outcome has already been determined.

So I go on Facebook for the pick-me-up that it can be – but it turns into another mourning session of Duchenne Parents – crying, whining, supplicating and politicking for a cure. Most pathetic. We even toy with our boys brains by telling them that this is our quest. The worst thing about this disease, I think, has been that the people struck by it have no where to go with this pain, and so we turn to the ridiculous “hope” of a cure. There is none, and there never will be. And why is that?

Because everything we do, everything we ARE, everything we think – everything about being human is a fucking sacrifice – and nobody wants to acknowledge that. We think we are evolving, and we are not. We are going backward because we are human.

Example: When we invented the car, it was at the cost of a lot of deaths along the way – but we deemed the benefits of the car a risk worth taking. So what if some handle the machine irresponsibly…most of us will be able to travel to and fro, safely and quickly. The 1,000,000 people or so that get wiped out each year, well…that’s the price we pay. Get the idea?

So, if we go back to the caveman – what have we here? What is this ingredient that made us give a shit about each other, while the animals accepted whatever came down the pipe?

They are evolving – we are not. In exchange for being human, we will be hampered by our weak and sick. We will not mate for survival of the fittest, or abide by natural selection. When nature de-selected Philip, by fucking with his chromosomes, we decided to bypass nature. Nope. We are keeping this one, and 1 in 3500 others whom nature deemed unfit to live, reproduce, or to contribute in a tangible way. Which is one reason why we don’t worship nature…we have the free will to over ride it – supersede it, and continue to breed and reproduce whatever we want, whatever we get.

So what within US gives value to THEM? To the weak, the sick…, why do we care about the old and infirm? Why do we care about how people FEEL? Why do we care what other people THINK? There is no evolutionary reason – evidenced by virtually everything else on the planet, from the elements to the animals – they don’t CARE. They do what they do because it is for the betterment, the adaptation, the natural selection, the survival of the species. Not us. Nope – something is different here.

I see the parents of sickly kids through the years. Initially, it was institutionalize them. Let them die. Give them to the state to take care of. Ignore them. Then there was the movement to keep them home. We accepted our mongoloid children, our birth injured children with cerebral palsy, our spina bifida babies, our muscular dystrophy kids. Way back when we were a little more primitive, we just accepted the hand we were dealt, modified our lives accordingly, and did the best we could for our kids, limitation of life, activity, brain waves and all.

But now, that’s not enough. No, now we have to shout our pain from the housetops, but to what end? “We cannot – no! We WILL NOT accept the fact that our kid is handicapped!” We will publicly cry and lament and piss and moan this hand of cards.

Then we see the scientists working to stop the viral and bacterial plagues on the planet, and see that they’ve got a peek into inner space and what’s going on there, and we are silly enough to assume that we can make an adaptation to this disease. We’ve brought it on the species ourselves, kind of like the ol’ Adam and Eve sin thing. We’ve not been careful about breeding, and we’ve somehow created a genetic monster that we don’t want. And so we naively think that because we are at the threshold of beginning to understand a tiny fraction of the inner workings of life that “those guys”, those genetic researchers, must surely have the answer in their bag of tricks.

They don’t – any more than the Wizard of Oz had a heart, a brain, courage, or a ride home to another realm. But hey – if you want to put some money in their hat so they can experiment with this stuff – well, that’s mighty generous of you, but mighty foolish, too, if you are sacrificing quality of life in the quest for a cure. Our boys will sit and shrivel away in inadequate chairs, with inadequate therapies, and experimental medicines that turn them into lab rats; drug therapies, with only heartbroken families as the casualty when the experiment fails. Big deal – there are a lot more where they came from, and they can exploit our hopes in the name of a cure, and our desperation keeps them in business. My, how advanced we are, that we have now politicized the whole sorry mess. We have to lobby for rights, and money, and care. Is this really what we want?

What manner of fools have we become? Oh crucify me for saying it out loud. It’s the truth. Will we ever come to an understanding that this is the child we have, and we have to just live with it? Will we ever accept that? I hear the Fundraisers Battle Cry, “We will NOT ACCEPT THIS! We want a CURE!”  Well, man-up, will you? You HAVE to accept it – it is what it is. 


There is no cure now, and there never will be. Treatments are not a cure, and most of these are a lifetime away. The longer you put off embracing Duchenne, the longer you will see your son as a problem to be fixed, and not a person like any other person at their core – with all the value that we attach to a human life. Don’t you see how our refusal to embrace the defect that is Duchenne just turns the lives of our boys into some sick, sad, dog-and-pony show of begging for money for our pimps in research? We condemn our sons to be the sad and pathetic victims of a disease – rather than just a human being who is differently-abled.

Hitler could not accept dark skin, and dark eyes. This was abominable to him – something to be eradicated. An Arian race was the ticket. And so he set about to fight this plague with all the political clout he could muster with his eloquence. The man may be called a monster now, but let’s not forget he had a great big fan club at one time – that’s how he got to where he did. But he was smarter than us when it comes to eradicating a defect. He KNEW you couldn’t change brown eyes and dark skin. You had to eliminate it. He didn’t waste time trying to cure brown-eyed-ness. You had to stop breeding it, and get rid of that which already existed. Granted, the man evidently had no human emotion – but he did have animalistic logic: The only cure for Duchenne is to kill them all at birth. Don’t breed a known carrier, and test each kid before you get attached, so you can drown it in a bucket at the bedside. Not the cure you were hoping for? It’s the only viable one.

Yes, Phil…you will have to die to walk again.


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We’re in a similar boat now.  We want to keep our Duchenne boys, but eradicate Duchenne. How the hell does that work? We look at our incredibly skinny, or unnaturally chubby boys, and we want someone to come up with some snake oil that will make it all better. Why, oh why, can we not just accept what IS? When we say we don’t want THAT – what is our son to think? You love me, but the package I am wrapped in is displeasing to you? Think it might be putting a bit of a burden on them to be that which you dislike and did not choose? “I love you – but those brown eyes – ugh – I shudder in disgust every time I see them. I pray, and rant and crusade and campaign for a cure to those wretched things.”  

Or more to the point, “I love you Philip – but every morning and every night I see the lack of muscles and all it means to me, to you, to us – and yuck! I want that to go away!” I’m pretty sure he probably despises the package as much as anyone. What’s wrong with this picture?

How does this factor in with loving others like you love yourself? As long as we see their genetic defect as a blight, how can they ever love themselves? And in turn, how can they ever reach out to love others, when they themselves, by the decree of their loving parents, are unlovable?

That’s an irony, a dichotomy, a dilemma of the worst order, and something they face every day of their life. As long as we are kicking and screaming for a way to change what we have come to view as a cosmic injustice, I guess each and every one of them will just never have been good enough, because they were born into bodies that we tacitly agreed to accept in exchange for being HUMAN!

Unfortunately, this disease is quite logical. It has no feelings. Despite the metaphors I am so very fond of, it is not a monster. It is not a tornado – it is not an animal. It is not alive, it does not seek to kill and destroy. It’s just a random, mutant package of genetics, that we, as people, agreed to accept because we wanted the freedom to procreate at will; to ignore natural selection and survival of the fittest unlike the rest of creation.

We are somehow different. I know that religionists are quick to interject god as they understand “him” at this point, to say we are the superior creation, created in “his” image. I do not see it that way. I DO see that we are unique among all of creation. We alone have desired to do more – to challenge the status quo of evolution, to cook our food, to work with tools, to congregate into cities, and to make things better, easier, more efficient, faster. We have lost a lot along the way, but we pat ourselves on the back because our brain was able to come up with some compensatory plan for that which we left go.

It starts with acquisition of food and water, which is all any living thing knows in its beginning. And we genetically adapted through the eons, but people took a different road. Animals developed things like faster speeds, better feet, losing a tail, or growing one as the case may be – all in a quest to survive and thrive. Diseased animals were discarded at birth. They did not go on to make more diseased animals. They understood, somewhere in their genetic coding that this would not bode well for their survival. Food would be wasted on a non-producer.

We went on then and created every problem that we are now running around willy-nilly trying to end. From the fact that there seem to be too many people concentrated in too little space, and eating up all the food, sickness and disease,  to the political unrest that comes with a race of beings that feel they have any inalienable rights. Really, we gave up all those rights in the face of…LOVE.

It manifests itself in the fact that we have emotions – a weakness that made us soft, and weak, and will ultimately end in our self destruction. We made this choice – and now we really don’t want the outcome. It’s a bit late in the game to reverse this decision. There is no way out of it. And then we go one better and serve up to humanity a God that has the same weakness? I think not. We had our Eden –  a metaphor for all that we gave away for a bite from the “tree of knowledge of good and evil”. It makes for a great story – because it gives an explanation for the ugliness we see in the world today, and few things are uglier than a fatal illness. But that’s the choice we made. Christianity has given it a name and called it sin…and went so far as to offer a Savior for it.

But God is only that which you wish it to be. There is no proof – there are only stories that were told and retold through the millennia, and we buy them because they help us to sleep at night. We want a Wizard who will pull our need out of his bag. We want a vicarious sufferer so we don’t have to. We had fine minds who cooked up a concoction of spiritual beliefs to wash our wounds with. And since it’s too painful to accept that this is what we are and this is what we do, we buy into it.

But is it really too difficult to see our sons as simply the less-than-desirous result of going one better than the animals? Shame on us for trying to get the animals to live according to our subjective and emotional reality. They don’t know this. They rejected this. Dogs did not breed like we have forced them to. Left to themselves, they had bred selectively, and there was no overpopulation. There were predators and prey, and a balance of nature. We opted out at some point. We wanted to go for a better plan. But this is it. We are the “car accidents” in the world of sacrifice for change. We want it all – but we don’t want the consequences. We want the freedom without the responsibility.

But it’s too late for that. We’ve got it. It’s all we’ve ever known in this generation: All the love, and the joy, all the war, all the pain; all the death and disease and fighting, alongside all the wealth, and happiness and life. It now looks quite pathetic to be supplicating the powers that be to take from us that which we have created.

There is a great truth in the story of creation – which is present in all religions by parable. At some point, we separated ourselves from the animal kingdom, from the creative thrust, and decided to go it solo. We got smart, like Lucifer, and decided to give the Source a run for its money. But we are the created – we are the experiment.

Or are we?

Maybe we ARE the creators. Certainly, since the “garden incident”, we have become the creators of our own reality...you know, the sweat of our brow that now only yields thorns and thistles? All the benefits of Eden that were tabled when we decided that we wanted to renegotiate the contract. Talk about collective bargaining.

So one has to come to a conclusion about all of this. Either there is a power that is greater than us, or there is not. I am looking at the empirical evidence and telling you that there IS. The odds of all of LIFE for millions of years happening randomly is ridiculous. The idea that our personal little hundred year sojourn here means anything at all is ludicrous. We freak out about “global warming”, when, in fact, the earth has been going through some major cyclical changes long before this generation decided to stare it down under a microscope. Bacteria was here before we knew it existed, or what it was, or what it caused. It wielded lots of power over us, and killed a great many of us before we figured it out and tried to put an end to it. But we cannot. We cannot Un-CREATE. Bacteria is here. It cannot be killed off. Matter IS. It can change its form, but it never goes away. All that is now is all that was then. We can merely manipulate it. And yes, we figure out new ways to manipulate shit every day of every year. We invent things, and build things, and discover things – and we will never understand or discover it all. Not while trapped in the bodies known as HUMAN.

Humans are finite. I know because I have seen what happens to them. There is a force at work greater than any collection of US, and we cannot stop the forward motion, the destruction called aging. And as we age, things break down, and ultimately our body gets to take its dirt nap, and we return to the dust from whence we came. We cannot stop it. We can prolong it – we can skirt it – but we can’t stop it. The only thing that cannot be stopped by this planetary process is the animating force inside the being.

Yet as long as we are stuck inside these little machines, with grey matter processing everything from the need to eat and shit to the need to love our offspring, to the need to believe in something bigger to get us out of this fix – all of it gets filtered through your brain. You cannot have an experience without your brain. If you can, we are not aware of it, and cannot quantify it – because someone, somewhere, will have to process the information through the grand computer of the human brain. And now it’s polluted. Good name for it – GREY matter – because it can take something that is pure white, and muddy it up in no time – so that the closest we get to white is a dingy grey.

So where is the redemption in all of this? What makes any of this worth it? Why isn’t suicide or genocide the answer? The Christians have served us up Jesus Christ on a cross as the answer to that which ails you, but I’m no longer buying that. I actually bought it and tried it on and wore it well for 15 years – but it never did fit right, and now it’s time for that frock to head out to Good Will. That story and its solution only lead a person into being a problem to be fixed – perpetually fucked up and in need of saving. A GREAT excuse to just keep fucking up – kind of like the old “I’m an addict” card. Addiction is not a disease. Duchenne is a disease – there is no choice in the matter. No bottle or needle or herb ever jumped into your hand. No sin ever accosted you and made you commit it.

Interestingly however, the state of sinfulness could very well be equated with the disease process – because we didn’t choose Duchenne, and we did not choose to be sinners either, now, did we? Just born that way, they say. Duchenne only gets 1 in 3500 a year – and you are telling me that sin has every fucking one of us from the birth canal? And the “cure” for that dilemma is the death of one guy two-plus millennia ago, but we won’t see the results of that cure until we are dead anyway? By that logic, then Duchenne has already been cured, too.

Okay – this is just not generating any hope, help, happiness or resolution in me. This sounds like a bad attempt at “mommy-making-it-all-better” by lying to me. Now Phil is not just a sinner, he’s a diseased sinner. The direction this is going is south – in a hurry. I need a better explanation. I need a better reason for all of this.

I need to know that every day is not just a waste of time. I need to know that there is some reason for my being alive, drawing breath, being born into the human race, which is intrinsically flawed with regard to the rest of the planet. I want to know why any of this matters at all. If it doesn’t, then I am pretty much done trying to do anything at all except survive my own life.  

Yesterday, I was okay to just feel like I was about to drown, but today, I am feeling the part that wants to live, and the struggle begins. The primal urge to breath – to survive – to fight for ones life. But the vortex that is the drain I am circling just keeps spinning faster and sucking me down with increasing gravitational pull. I feel like I’m on the event horizon – going into the nothingness, and I don’t want nothingness. I want life.

And so I’m just going to go below deck again. The easiest way to do that is to go back to bed and sleep all day in a clinically depressed state. This will not do, however, as this is not what I am supposed to be learning here. I need to get into the observant position in my life, and see it for what it is in the big picture – and not get lost in the details and shit of today. What’s the worst that could happen? I will live through this.

I feel like a wheat field – which just got shit spread all over it. I reek. I stink. The gulls are having a field day in the refuse, picking out the goodies and further shitting all over me, tugging and pulling and biting me. In the pristine, snowy landscape, I look dirty, and ugly. Tire tracks and shit. I am in no way enjoying this.

But I know what I’ve got that no one can currently see. Seeds of wheat, properly germinated. And the ingredients in that shit are going to break apart in the natural process, and something good is happening there on a cellular level. Something beneath my surface will respond with that which is filtering down. On a microscopic level, all that shit is a very good thing as it interacts with the ingredients in me. It’s subtle, and quiet, and quite invisible. Faith in what is happening is needed, because on the surface it just looks for all the world like the most barren, miserable of fields; host to scavengers looking for a free meal of waste and scrounge. But underneath, is there life? Yes – it’s here. It’s moving, and breathing, and growing, integrating with me.

All of this is just an archetype - a microcosm – an analogy…it’s all part of the process – the LIFE process. The fact that we have added emotion and human value to our equation does not negate the circles and cycles of life. This was a process designed, set in motion, and sustained within a Source that is not bound by the same.

Like the power plant that simply generates our energy, it does not distinguish between power that is used to power a toaster, or to kill someone who elects to stick a knife in a socket. It simply IS. It offers no solution to the situation we ourselves created – none is required. It does not see our choices as good or bad, as only we can interpret that information. The same shock that re-starts a heart is the same shock that will kill another heart. We are responsible for assigning rightness or wrongness to any situation we find ourselves in – no matter how righteous, no matter how heinous. What we choose to do with the power we have is entirely up to us – and the consequences are entirely ours to bear. And in this model, I will be creating my own reality. And to spend my life lamenting what IS, is to spend it unwisely.

Philip is my son. I adore him. I love him for all that he is, genetic mutation, broken body and all. I know what I believe about the afterlife, and how it integrates with the life here and now. But it’s only MY belief. And someone else’s belief is just that – THEIR belief. None of us has any definitive proof that ours is the “correct” one. If we did, we would all believe the same. How many people disagree that we need water and air to live? The evidence is inarguable. There is no evidence for what one believes about the spirit world, now, is there? This has to generate from within.

Remind me, then, Sally, what I am learning here. To say that there is a “reason” for everything is too dumbed down. Too much of this life seems nonsensical. But put in the context of all I have spilled here for my sanity’s sake, I can make it make sense. I can be the wheat field. I can accept what IS – the hand I was dealt was the hand I was meant to have. What I choose to do with it here and now is my responsibility. I can mourn – there is surely a time to mourn. I can laugh – I can cry. I can shake a fist at the Source – and not fear retribution. I can stand in the sun, hands raised skyward and project a love, honor – or even worship – for all that this world is and all that I AM. I can be humiliatingly covered in shit – but know that this earth still turns, and the seasons will come and go, in a series of comedies and tragedies, all culminating in an entire experience that is incomparably beautiful.

I can know that when I reach the end of my brief human existence, that whatever accountability factor there may be, I will stand tall in the face of it, knowing I have taken all the ingredients of my life, and used them all in the creation of THIS life.

I can bemoan the fact that I have no yeast, and never bake a thing because of it – or I can look around and find the recipe for unleavened bread. And I can make a lot of it. And I can share it. Or if all I ever offer up is one bland communion wafer because that’s all I had – with this I shall be well content. No deity could have asked for more. In the end, it will have been enough. But this is up to me, and me alone. And in the final analysis, it is for me, and me alone.

My son, Philip, was born with Duchenne Muscular Dystrophy. Shall I make a list of all the things that each one of my children was born with? The features and the flaws? The assets and the liabilities? We simply make room for each one – and deal with each one in the manner that accentuates the positive, and eliminates the negative – just like any other kid – any other person – on the planet. The longer I put off accepting this as a part of the rich, rich experience that is my life, the longer I will remain trapped in a cycle of grief, running in circles, chasing my tail, and spinning a cocoon instead of a tapestry.

If I take the power from the Source, and plug in every appliance and cook up a grand feast with whatever I have on hand – and I am happy – how could there be displeasure in what I have created? If I, on the other hand, bemoan the fact that I don’t have a gourmet kitchen, and all I have is a hot plate, well – I guess I can spend my life in quest of a better facility, or I can get about the business of creating something with what I’ve got. Which will be a life better spent?

******************************************************

Philip came home from school today. They had gone on a swimming field trip and stopped at the Chinese Buffet for lunch, and as I took his tray off, I noticed he was clutching a small piece of paper.

“What ‘cha got there?” I asked.

“My fortune. I saved it. It’s my fortune, you know.”

“What does it say?” I ask.

“I dunno – here – read it,” he says and uncurls his fingers for me to take the crumpled paper from his hand.

I don’t know anymore if tears are just easier to come by as the female anatomy starts the retirement process, but they arrived and blurred the words of his fortune for me – but not before I read them, and had full clarity:

“You are far more influential than you think.”

All I could manage to say was, “Right on, kid.” I leaned over and hugged his thin frame, kissed him on the head and whispered, “Thank you for being a part of my life, buddy!”