21 December 2007

Lather, Rinse, and...Repeat.

SONOFABITCH!
That was the sound my brain made. My brain made that sound because Dr. Rees, the plastic surgeon overseeing the continuing care of my pressure sore had just ended a sentence with the phrase, “debride it again.” This was in direct contradiction to what his physician assistant. Mr. De-Hong, had concluded not three minutes earlier before stepping out of the exam room. The exam room that I was in, side-lying on an exam table with my left ass check exposed. Three minutes prior, my brain wasn't making all sorts of ruckus trashing the joint because, at that point in time, Mr. De-Hong had finished telling me what I wanted to hear. That conversation went pretty much as follows:

De-Hong: Hello Dan, how are you?
Me: Pretty good.
De-Hong: Has your pressure sore gotten any better?
Me: I think so. It's definitely gotten a lot smaller in the last month.
De-Hong: Let me take a look. [Exams the sore] Yes, this is much better. I think we can can schedule the flap surgery, now. Let me consult wish Dr. Rees.


Dr. Rees entered the room and examined the state of the wound. His concern was that, although the wound has filled in quite well and has stayed clean, by poking around in it with his finger, he was able to determine that there isn't yet sufficient tissue growth over the bone that was exposed by surgery to debride the sore back in October. In addition, he could feel that there was still some residual infection in that bone. My mother asked how he could determine that about the bone simply by touch; did it feel “squishy?” He responded that, “Yes. I guess that is a good word for it.”

We asked several more questions about the time table from this point forward. I confirmed what I thought I was hearing, that they would be opening the wound back up, cleaning out the remaining damaged bone and starting me back on another six week course of IV antibiotics. At which point in time, then they would be able to go ahead with the flap surgery to close the wound completely. That all sounded to me like the past two months and ten days of lying around doing Jack had gotten me all of right back to where I already had been. I stated how frustrated that I've been dealing with this since August and now this seems like a step in the wrong direction. Dr. Rees countered with something about how if they attempted to close the wound now there was a fifty percent chance it would break down into a sore again and then we'd be starting all over from square one. Despite the fact that he went on to talk about how debriding the wound now would allow them to close it in six weeks, I had already heard all I needed to know. Plus, it was hard to concentrate on Dr. Rees with the din, blue streak of obscenities my brain continued spewing. At the end of his remarks, I was able to focus long enough to hear Dr. Rees conclude his remarks about pressure sores with, “You have no idea.” As in, “You have how bad these sores can get,” and, “You have no idea how long they can take to heal.”

Well, far be it for me to dispute his medical expertise, but I'm pretty confident at this point that I have an idea. In fact, I think I have an excellent idea. Sure, he sees these things every day and therefor has an excellent gage on what constitutes the varying levels of just how severe these sores can be. And yes, my sore pales in comparison to people that lose toes and legs because of severe complications. But when he starts throwing around numbers like “six weeks” as if they're just some drop in the calendar bucket, then I know he can't really comprehend what this is like. I should have asked him, “Do you have any idea how many times Scrubs is televised during the day?* No? I didn't think so. You have no idea because you spend your day doing cool things like seeing patients, performing stomach staples, and generally getting to leave the house. I know the answer because despite reading books, watching movies, surfing the Internet, and doing my best to avoid watching mind-numbing TV, I'm still lying on the couch for upwards of ten hours a day with Shit to do and have been doing so since August. When you casually talk about prescribing another six week course of antibiotics, you may have read about the potential side effects, but do you know that Vancomycin dries my eyeballs out so that my contacts are always blurry and then they wrinkle up and painfully get stuck in the corners of my eyes? No? Of course not.”

But there's really no point in asking those questions because there isn't any better course of action. So, on January 16th –and it's the 16th because that's the next open surgery slot—I will go in to have the same surgery performed that I already had done back in October. I'll get discharged on the 17th, and then it will be the beginning of the next week until the orders come through to start the IV antibiotics. Six weeks from then will be the first week of March. Will I immediately be scheduled for my flap surgery? I doubt it, so I'm going to estimate that happens in the middle of that month. I already know the rehab protocol coming out of that surgery is at least two solid weeks of bed rest before even limited sitting is allowed. Now it's April, barring no setbacks.

'Tis the season.


*On an average weekday, Scrubs is on 8 times, on 3 different networks. In my opinion it really went downhill after about Season 4, just about the time Zach Braff's head got fat. They've been phoning it in for about two years now.

14 December 2007

Beauty Isn't Necesarily Subcutaneous

Back in October I posted a photo of an image of the Virgin Mary that miraculously appeared in an unlikely location on my person. Then I remembered I'm not Catholic and don't believe in such things. For a few days I surmised that, although highly unlikely, someone had secretly been after me with a hatchet and if it was indeed a hatchet wound I should seek medical attention. When I went to the doctor's office it was explained to me that this abscess was in fact a horrific pressure sore. I guess the visage of mother Mary was just an optcal illusion caused by the camera flash.

Fast forward three months: monotonous hours of side-lying in front of the TV, debridment surgery, eight weeks of IV antibiotics, and now wunder-ointments. The result is evident
here.

Progress.


Update: For all the heretics, if you squint it's there.

28 November 2007

If Regranex Was A Drug, I'd Sell It By The Gram

I recently started a new phase of treatment for my pressure sore. As the IV antibiotics I've been infusing to fight my osteomyelitis infection now seems to be doing the trick, my doctor prescribed for me to have a medication called Regranex applied to the wound once a day. Regranex is a special gel used in the treatment of pressure sores. The active ingredient is a growth hormone designed to encourage macrophage production and enhance tissue growth (although I'm still not hitting the long ball as I would like). Essentially, it mimics the body's own ability to promote wound healing. 


This treatment is necessary because after my initial surgery to clean out the sore and have a bone biopsy performed, the cavity of the sore was left wide open. Simply closing the wound up at that point in time would have been counterproductive because, not only did the infection remain in the ischial bone beneath the wound, but without any tissue covering the exposed bone, closing the wound over would have left me with a potential sink hole of sorts in that same spot. The skin in that area even more susceptible to breakdown than before the sore occurred in the first place. In order for the wound to finally heal properly it must fill in from the inside out. The Regranex is supposed to aid in the tissue growth to complete that process.

What makes the Regranex an interesting medication, in the context of the various aspects of my medical care, is its cost. Each tube of Regranex is measured out at 15 grams. Pharmacies will not stock Regranex, even though it is dosed in such small quantities, because that 15 gm tube is sold at an average price of over $520 according to some Internet sleuthing I performed. Suddenly, the insurance change that increased my co-pays from $5 to $10 doesn't seem like such a big deal. Per dose that checks in at a sum of approximately $38 per gram. I thought that sounded kind of expensive, but just how expensive? What else costs about $38 a gram?

Well, gold is highly valuable in some circles. On a recent day gold was trading for $801 per ounce and one once is equal to 28.3 grams. Do a little arithmetic and we find that gold trades for just over $28 a gram—score a point for Regranex. Oil is getting a lot of press these days; something about it being a limited resource by which the Western world fuels itself. When I last checked oil traded at about $94 a barrel. Now oil isn't actually sold in barrels, but as a unit of measure the size of a barrel of crude oil is 42 U.S. gallons. If that barrel was full of water it would weigh almost 350 pounds. Sixteen ounces to a pound, 28 grams to an ounce; a tube of Regranex approximately the size of a barrel of oil would sell for over $5.9 million, although I suspect in such a quantity Walgreen's might cut me a bulk rate deal.

What about illicit drugs? I've heard illegal drugs are quite expensive. According to Wikipedia cocaine can be bought for between $30-$120 a gram. The farther down the chain you are, apparently the more expensive cocaine becomes. I guess when it comes to blow, it's all about who you know (caveat emptor: find out how many times your coke has been cut, but be subtle about it). Drugs are bad, m'kay, but let me just mention that I found myself a little disappointed by the fact I had to refer to Wikipedia to find out my cocaine information. It's like having to look up how to launder money in the dictionary—not the best way to confirm one's street credibility. I don't know how this happened either. I'm not saying I have any inclination to know or associate with cocaine users or dealers, but I went to college, I know people who lived in fraternity houses, I have even used the bathroom in a Miami nightclub; the price of an eight ball is just experiential knowledge I feel I should have gained somewhere along the way. I saw Traffic—this never would have happened had I grown up in West Bloomfield. 

I have three refills on this prescription too, if there was a better market for its healing powers I should be able trade my three tubes of Regranex for something cool or useful, like an RPG, but I digress. I'm sure there are other, more relevant products I could use to provide a better cost analysis comparison to belabor this point, but I got lazy. I present this information to simply illustrate the fact that Regranex is expensive.

Oh, and to the FBI agents monitoring my recent web searches: I'm not really looking to buy cocaine or a RPG. Just wanted to clear that up. Thanks.

Word to your mother.

12 November 2007

No Payment Due...That's Nice.

The bill for my hospital stay came in the mail sometime last week. I've been through this enough times that I'm no longer surprised at how much medical procedures cost, but I do still find it interesting at how much my insurance is charged for various aspects of my care. Case in point, here is page two of the bill for my pressure sore surgery:

(click to enlarge)
I kind of got a kick out of the fact that there are two different rates for the time spent in surgery. The first 30 minutes are apparently billed at a set amount of $1396, and then each subsequent minute is billed in addition to that. I now know that I was in the operating room for a total of 98 minutes. The additional 68 minutes clocked in at $2108, which by my calculations breaks down to $31 per minute. That initial half-hour, on a per minute basis, comes in at $45 and some change. Damn, I didn't know I was getting a discount.

Well hey, as long as this thing is on sale is there anything else you guys can patch up? I took a broomball stick across the bridge of my nose my freshman year and my nose just hasn't been the same since. It's not that noticeable, I know, but there's a bump there on the right side...No, no my right...that wasn't there before. Can you clean that up? I mean, this is plastic surgery. Right?

The moral of the story is, if you only have half an hour on your schedule to squeeze that next operation in, it's going to cost you more to come back and have them finish up later. Might as well bite the bullet and be late to that next appointment.

09 October 2007

If I Could Feel It, It'd Be A Pain In The Ass

At 7:30am tomorrow (Wednesday), or today depending on when you read this, I'm having surgery at UM Hospital on this pressure sore I've been dealing with for the past 6 weeks. The procedure I'm undergoing is to have an infected portion of the ischial tuberosity (consult diagram or local medical student) removed and the tissue around it cleaned up. The bone needs to be removed so the infection doesn't spread through the pelvis. Unfortunately, this surgery won't actually close up the wound, but in fact make it bigger. The wound needs to heal from the inside out, so I'm expecting about six weeks of post-opt antibiotic treatments, continued daily cleaning, packing and dressing of the sore --all while spending as much time off of my ass as possible. Then depending on the state of the wound, a possible second surgery to finally close up the wound. At that point, I will require 24-hour bed rest until the site "gets all better."

I should be at the hospital until Thursday, maybe Friday.

Good bye Fall. Hello Christmas.


Don't click here.

27 September 2007

X Marks the Spot

There's an old saying that states, "Opinions are like assholes; everyone has one." I'm in the minority of people that have two. Assholes, not opinions. Well, one asshole, one hole in my ass...I guess it's more of a crater than a hole.

The medical term for the sore is ischial pressure ulcer, grade IV. What makes people in wheelchairs particularly susceptible to getting pressure sores is the fact that paralysis prevents most people from sensing when an injury to the skin occurs. The poor blood circulation in the area caused by continuously being seated accelerates the speed of the tissue breaking down, hinders new tissue growth, and adds to why these types of sores are so difficult to get healed up. The location of my sore has also been extremely problematic in contributing to it's breakdown as well as it's protracted recovery time. The red X on the attractive Moroccan girl in this picture, me captured rudely ogling her cake, is an approximation of where my sore is located, if she were me.







(Click for a better view)

It started as an irritated patch of skin then through a combination insufficient cushioning and the neglect of out-of-sight,-out-of-mind the skin broke down and a sore opened up. For about a week it was a superficial skin abrasion. At the end of two weeks it was about the size of a quarter and I scheduled a doctor appointment. The doctor discovered that some of the tissue inside the sore had started to die and after cleaning it out and giving me instructions on how to dress it, encouraged me to stay off of it as much as possible - not the easiest set of medical advice to follow in my situation. My bad, it turns out, and when I saw the doctor again ten days later, the sore had deteriorated significantly, was now a centimeter deep in one spot and there was more necrotic tissue. A third visit, the next week, showed more deterioration of tissue and the depth of the sore had increased as well. The hope in treating it was to keep it from getting to the point where surgery was necessary to help it heal properly.

Well, to make a long story short, the month of days spent mostly lying on my side so as to not put unnecessary pressure on the sore, multiple wound dressing changes, way too much TV, and no social life helped to decreased the circumference of the sore, but a MRI scan revealed osteomyelitis in the ischial bone underlying the sore. In layman's terms, a bad infection in the bone that, while localized for the time being, if it were to spread further would be real bad. So, in a week and a half I'm scheduled for surgery to remove the infection. That will be followed up by more lying around doing nothing as the sore attempts to heal properly. I'm looking at mid-November by the time I'm back to full steam.

That Only Took Three Months

I finally got my wheel repaired and returned to me last week.

16 August 2007

There's More Than One Way To Skin A Cat

There's nothing creepy about this.

And should you decide you need to preserve your cat skin in a tasteful pose, one of my good friends from high school has taken up the tools of the taxidermy trade. Visit North Country Legends Taxidermy for all your future taxidermy needs. Get your orders in now, hunting season is fast approaching!

Ask for Tim. Tell him Dan sent you.

15 August 2007

Wheelchairgate: An Update

Today is August 15th, 2007 and today authorization was finally given for the repairs to be made to my long-defunct wheelchair wheel. Henceforth, my wheel is officially now in the process of being fixed. It only took nine weeks to get to this point. Why does it take nine weeks to get a piece of paper faxed to a doctor, signed by the doctor, and faxed back to where it originated? As an outsider to the process, I can only make inferences based on observation and information collected post-fact, but my conclusion is that it takes a delicate combination of ineptitude, negligence, irrational bureaucratic protocol, and a lack of accountability on the part of those involved. Here’s a recap:

On June 12th, I took my malfunctioning wheel to Michigan Wheelchair Seating for repairs. Unable to repair the wheel in-house, I was informed by the repair technician that the wheel needed to be sent back to the manufacturer for repairs. The wheel would be sent out the next day and I should have it back within three weeks. I was loaned a power wheelchair for the time being. The information given to me by the technician seemed plausible and operating under the assumption that it was true I did nothing more about my wheel and went about my business for the next two weeks. Yes, it is true that the repairs would be done by the wheel manufacturer, but the timetable given to me by the technician was completely erroneous. In addition he left out a major detail that no work on the wheel would be started until the necessity of the repairs was confirmed by my doctor and authorization of payment for the repairs was confirmed by my insurance.

June 25th I called Wheelchair Seating to find out if there was any information on when I would get my wheel back. The receptionist seemed confused about what I was asking and wanted to know who I spoke to about my wheel repair. I gave her the name of the technician who took my wheel in for repairs and asked to have him call me back. He never did.

On July 2nd I placed another call to Wheelchair Seating again inquiring about the repair of my wheel and this time spent the majority of a fifteen minute phone call on hold as the receptionist looked up my file. I was told that the paperwork was being processed and that my information was in the system. Still operating under the assumption that the manufacturer was in possession of my wheel and performing repairs again I asked when I would be getting the wheel back. I was told by the receptionist that she didn’t know when it would be finished. I asked if she could have someone call the manufacturer and find out when they would be returning the wheel. This also did not happen.

After the Fourth of July holiday week in which I knew nothing would be done on my wheel, I called Wheelchair Seating again on July 10th. At this point in time it was approaching a month since I had dropped off my wheel for repairs and now I was expecting to have my wheel returned to me. This time I was passed on to another person’s voice mail account to which I left a message explaining what had happened up until that point and that I was expecting to hear when I would be getting my wheel back. The person never returned my call.

I called back again the following week and was shuffled to the same voice mail account as during my previous call. Again, I explained the situation (as I knew it to be true) and asked for an update on the progress of my wheel repair. For a second time the person responsible for that voice mail account did not return my call.

The week of July 24th I placed yet another call to Wheelchair Seating, but instead of being shuttled off to another anonymous voice mail account I asked to speak to a personal contact I had there from my time in Michigan’s out-patient physical therapy program. My former physical therapist had taken a position at Wheelchair Seating performing wheelchair fitting evaluations and although she was not responsible for any of the repairs being done to my wheel, I called her to see if she could find out what was happening. Par for the course, I did not speak with her directly, but instead had to leave her a voice mail explaining that the three-week timeframe I was given had stretched to six and I was still in the dark about the status of my wheel repair. Two hours later I checked the messages on my phone and I had a message from the person at Wheelchair Seating responsible for confirming the authorizations for all repairs. The information she had for me was not good.

When I called the authorizations person back that afternoon, fuming over the impending news that nothing had happened with my wheel repair yet—which it had not—it was explained to me that she was still waiting for my doctor to sign the referral confirming the necessity of the repairs and equipment I needed. Wondering why they would need my doctor to sign off the work order, I told her this was a repair and not a new equipment order. She explained that the repairs I needed were not covered under warranty and that anytime insurance needs to be billed the doctor must sign off on the repairs. Why wasn’t I notified of this and when did the doctor get the referral that needed to be signed? After a long pause and much paper shuffling she informed me the referral was faxed to the doctor’s office on June 19th. There really wasn’t a date she could give me that would justify any of this delay, but when she came back with the 19th I immediately realized this was a full week after I had brought the wheel to Wheelchair Seating. A week’s delay in getting the necessary paperwork together is ridiculous; especially in conjunction with the new information I was just given concerning their protocol of needing a doctor’s referral to bill my insurance. In my mind it seems once the problem is diagnosed, sending the referral to the doctor should be the first thing that gets done and there is no reason it should be done any more than a day later. In fact, the buildings that house Wheelchair Seating and my doctor’s office are literally within a mile of one another. I could physically walk the referral request to the doctor’s office from Wheelchair Seating in less time and it takes two people to help me walk.

So there was one week’s delay accounted for, but what the hell was going on in the intervening five weeks? The authorizations person at Wheelchair Seating couldn’t answer that question, but she was pretty sure my doctor was on vacation for part of that time. I told her someone over there should have called his office to find out what the hold up was and someone should have called me to let me know they were waiting on my doctor to sign the referral. None of this happened. For five weeks my wheel sat in their shop and collected dust. The technician who took it from me probably walked by it every day and not once did he think to himself, Man, that sure has been sitting here a long time. I wonder if I should find out what is holding up this repair? Or, if he did have those thoughts he didn’t get very far in acting on those notions. Not one single person at Wheelchair Seating took any initiative to find out what was going on with the referral, nor did they take any initiative in contacting me to fill me in on what was going on, or more appropriately, not going on. Had I not called and gotten someone completely uninvolved with this repair order poking around in my favor, I would probably still be none-the-wiser. She apologized for the communications breakdown and asked that I call my doctor’s office and see if I could get them moving faster. Her rationale was sound in asking me to do that, but it was also a bullshit way—whether intentional or not—of absolving herself of some of the responsibility for resolving this fiasco. But I made the call, because I also knew it was going to be up to me to get everyone involved on the same page from now on. Before I concluded that call, she asked me that once I talked to my doctor to call her back in a week to see where everything was at. Right, a week; because what’s one more week when six have already been wasted? I wanted to punch her.

When I called my doctor’s office and finally got a hold of his administrative assistant, I was informed that yes, it was true he was indeed on vacation and wouldn’t be back in the office until August 9th, which was the following week. When I asked whether or not the referral script had come through like I had been told it had, after much paper shuffling I was told that they did actually have the script. Why my doctor did not sign the referral before he left on vacation—you know, tie up loose ends like everyone else in the world does before going on vacation (he had ample time: at least three weeks by my calculations)—remains a complete mystery. I have my suspicions and those start with his assistant and her organization skills, but no way to prove them. I asked if anyone else, one of the other doctors, maybe his Physician’s Assistant, would sign off on the referral. It was not for a new equipment order, just a repair; it seemed logical to me that whoever was covering for my doctor would do that, especially considering the circumstances. The administrative assistant told me she would ask the Physician’s Assistant and get back to me that afternoon. She didn’t. I called the next morning to see if my request had been considered, she said she would ask the Physician’s Assistant, if I could hold. I waited on hold and after a few minutes she came back on the line and explained that, for whatever reason, the Physician’s Assistant didn’t feel comfortable doing that. So, I was again told the doctor would get to it when he got back in the office on Thursday the 9th. Fine, I said and hung up. In my mind it was, Fine. Fuck you guys, this whole thing is preposterous!

In the interim of all this wheelchair fiasco, I have developed a pressure sore on the back of my thigh. Pressure sores aren’t good and I’m pretty sure it came about from one of the activities I do at physical therapy. I’d like to be able to attribute it to not having my wheelchair in working order, just so as I can focus all my problems and blame around one central issue and group of people. Realistically, the sore and the wheelchair are unrelated, but coincidentally the state of the sore put me in my doctor’s office the day after he was supposed to have been back from vacation. My morning appointment time put me in the examination room with the Physician’s Assistant and not my doctor and led to this conversation:
“How are you Dan? It’s been a while since I’ve seen you.”
“Well, the reason I’m here is because of this sore, but I’m also still waiting on the doctor to sign the referral for my wheelchair repair.”
“Oh, that’s right. Yeah, with Medicare cases, as a Resident, I’m not allowed to sign off on the doctor’s refer—“
I cut her off, “I’m not on Medicare. I have private health insurance.”
“Oh. I can probably sign it then. Let me go check,” and she hurried out of the exam room. A new reason for me to want to kill; she made her decision to not sign off on the referral based on misinformation, easily verifiable misinformation. When she re-entered the exam room, she said, “The doctor already has the referral. He’ll sign it today.”

That was last Friday. I know from discussions with the authorizations person at Wheelchair Seating on Tuesday of this week that the referral actually came through on Monday, but really, what is another day at this point anyway?


What pisses me off about this whole ordeal is that the people I’m dealing with work on a daily basis with clients and in an industry of providing necessary services. Wheelchairs by their nature, with very few exceptions, are not luxury items. It’s not as if I took Grandpa’s old pocket watch down to the jeweler and asked the guy to clean and refurbish it “whenever you get the chance.” I’m not cruising around in this wheelchair because it’s a good way to pick up chicks; I need this wheel repaired and I needed it repaired six weeks ago! If there are going to be delays in the repair beyond what Wheelchair Seating can control, I can understand that, but this whole fiasco was caused by a breakdown within their own well-worn system and the fact that nobody lifted a finger in my favor speaks volumes about the quality of service they care to provide.

So, once again I have learned a lesson the hard way. And what I have learned is that these people can’t be expected to provide quality service even though that is the job they have chosen to do. The question is will they learn anything when I no longer take my business to them?

26 July 2007

This Isn't As Easy As It Looks

I don't use my stove often, almost never in fact, but I have figured out a few things I can cook without subjecting myself to severe bodily harm. Using the oven presents some interesting complications because anything that has any weight to it, say a casserole or cake (not that I know how to make either of those anyway), is nearly impossible for me to pick up. Plus, I'm not a big fan of leaning down and sticking my face in close proximity to the heating coils. I might need these All-American good looks to pay the bills some day and it'd be a shame to sacrifice my lone ace-in-the-hole for a quiche. I made the decision though, partly spurred on by a hunger-induced grocery store impulse buy, that a frozen pizza was a foodstuff that I could probably bake without too much trouble.

Figuring out how to cook the frozen pizza took some planning, but I've managed to get fairly competent at it. Depending on the brand and the packaging, after removing the pizza from the box, the trickiest part of the whole process is getting the pizza out of the oven without dropping it or burning myself on the pan. I have yet to completely lose one to the bottom of the oven or face down on the floor. That being said, I came real close to losing this one, as you shall see.

In most of the other videos I posted here I edited out most of the parts in which I screw something up, but that sort of distorts the reality of how easy or difficult it is to accomplish the various tasks depicted. This time, for the sake of accuracy, I left in the bigger gaffs.


17 July 2007

New Developments In Ambulation

A few weeks ago I spoke to Dr. Carlos Lima who performed my olfacotry cell transplant surgery back in April 2005. I asked him what specific types of excercises his patients in Europe were doing therapy-wise in their quests to regain mobility. His recommendation as to how to get the greatest potential benefit out of the surgery is that body must re-learn the movements it lost from the paralyzing injury. For instance, if the legs don't move because they are paralyzed the best way to regain potential function is to get them moving in a walking motion. Sit and do nothing and nothing will happen. The theory is that even if the original neural pathway is damged, putting the legs through the walking motion may help the nervous system open up and develop new pathways to the brain: reverse engineering or kind of like creating a neural bypass. This can be accomplished in a varitey of ways, like unweighted treadmill training, riding FES bikes and the like. I have utilized KAFO braces for assisted walking and standing exercises for two years now, and although Dr. Lima is not against the benefits of incroporating braces into the therapy program he has stressed that many of his european patients do not use leg braces in their therapy routines. His contention is that the braces do all the work of bearing the body weight and thus the legs don't get used to supporting the body.
When I asked him to suggest excercises that his European patients were having success with I was relieved that, for the most part, my therpy sessions included similar activities. He reassurted me that I was doing the right things, but then he also sent me a video clip of a patient of his, a C4 level quadriplegic, assited walking without legs braces eight months after her transplant operation. After watching the clip, I determined that there was no reason for me not to try the same thing. So, for the past month I have been doing my assisted walking without the KAFO braces I used in the past.
Using the braces I was getting to the point where I would be able to cover a couple hundrd feet before my shoulders reached their point of fatige. I went from swinging both of my legs at the same time to alternating gait, which I demonstrated here. I also started to notice a real improvement in my balance through my hips and when standing still, while utilizing a platform walker for upper body support, I can control my balance to the point where I don't need anyone supporting my hips to help keep me upright.
Assisted walking without the braces is different though and more fatiguing because all of the support and rigidity that the braces provide is gone. The weight of the braces and the fact that the legs are fixed at full extension contributed to the swing part of the walking gait once I was able to get momentum headed in a forward direction. Without the leg braces and without any voluntary function the knees want to buckle under the body weight and so getting the leg to swing forward is much more strenuous and difficult. What I concentrate on doing when not wearing the braces is shifting my weight side to side and trying to create a hip turn with my abdominal muscles to pull my trailing leg forward. Right now though, the majority of the hip turn I'm getting is coming down from turning my shoulders. When I have significant spasticity in my legs the contractions of the muscle spasms help me to lock my knees out and straighten up my back and at those points I'm able to bear most of my body weight with my legs. The spasticity is sporadic though and so 90% of the time while I'm walking, my PT has to assist with not only swinging my legs forward, but locking out my knees as well. Because of the style of walker we are using with this type of exercise I'm also doing less in terms of controlling my balance at the hips as the walker has a strap that can be used to lock my hips in a secured position. In the long road though, I hope this will help me accomplish more as now my legs are being forced to support the majority of my body weight as I go through a more natural walking gait pattern.
This is what it looks like:

09 July 2007

The Dude Abides (and Uses Profanity as a Crutch)

My dad called me recently to make sure I didn't actually hire creepy, space cadet lady (I didn't). He also suggested that at some point I should think about trying to reach a wider audience, but if I did I'd have to, "Clean up the language a bit." I won't get into the irony of that advice, but it did remind me of this:

06 July 2007

(Good) Help Is So Hard To Find


So you’re middle-aged, horribly…horribly sincere, have a strong desire to help others in need, and are 100%, bat-shit certifiable, space cadet: A few interview tips.

1. When our interview appointment is scheduled for 11am and you forget about a prior scheduling conflict, DON’T show up 11 hours early unannounced. Call ahead and ask to reschedule.
Addendum: In the event that you have already shown up 11 hours early unannounced, DON’T explain that you have borrowed a stranger’s cell phone to call and get directions from one side of the apartment complex to the other.

(Note to self: ALWAYS reschedule, especially if space cadet is at front door 11 hours early. NEVER deviate.)

2. When asking about the prospective employer’s personal history DON’T interrupt and attempt to relate personal hardships if those hardships aren’t apropos to the employer’s. Specifically, I did not ask, nor is it wise to volunteer the story about your abusive marriage, your children being taken into foster care and their subsequent abuse at the hands of foster parents, your remaining in said falling marriage and custody battle with the courts, your abusive husband’s untimely—yet liberating—death in an auto accident, and your stalking of your estranged, adult son at church in hopes he might have been there tonight (he wasn’t). Revealing that information would be better left for, let’s say never…or at the very least the second fifteen minutes of the interview.

3. This is less of a tip, more of an observation: Going back to school and furthering (finishing?) one’s education is laudable, commendable, a bold step. Good for you. A degree in Dance? At 50-ish? Maybe not the best pathway to financial solvency in your impending golden years. But what do I know? I'm just the one trying to keep calm on the outside, while secretly wondering if you'll be sleeping outside my door in the morning waiting to see if I made my decision about the job yet.

4. Want a job. Desire a job. Be desperate if need be, but don’t look or act desperate for said job. It’s a fine line. It’s only 5 hours a week. You’re freaking me out!

5. Bladder incontinence in times of excitement or nervousness is cruel indeed. I suppose I can relate. However, if that is a reoccurring personal battle PLAN accordingly. At the very least wear dark pants.

I’m pretty sure it was sweat. It didn’t leave any mark that I could see. I mean it was hot today. It had to be sweat. So yeah, that was sweat (Dear god, please have been swass. PLEASE have been swass!).

15 June 2007

The Pledge, The Turn, The Prestige: A Fiasco

My wheelchair crapped out on me on Tuesday. Wednesday was worse.

I had been noticing over the course of the last couple of months that I had one wheel that appeared to be a bit out of alignment, but it was only noticeable if I was at my therapy clinic where I could see the chair head-on in front of a full-length mirror. Some wheelchairs have a camber angle built into them, the purpose of which I believe is improved stability and steering, but don’t quote me on that. Regardless, my chair doesn’t have that and so a wheel out of alignment is something that should be checked out. My wheelchair has a collapsible frame, and I went so far as to check to make sure that the frame of the chair was properly extended and the slight tilt of the wheel wasn’t being caused by some small, correctable adjustment to the frame. Then when there wasn’t anything that could be done to the frame to fix the tilt, I sort of let it be and forgot about it. Every once in a while I’d catch my reflection in the clinic mirror and notice the tilt to the wheel, but it didn’t appear to be getting any worse, so I didn’t do anything about it. Worse case scenario was that maybe the axel bracket was coming lose in some way and needed to be tightened. Something that could be gotten done down the road or at anytime in between when I thought about it..

I already have plenty of complaints about the design of my chair and its wheels. First of all, any of the decisions I made about what kind of chair I wanted, were made at a time when I was still trying to get healthy enough to leave the University of Michigan hospital for the first time after my accident. At that time, my strength and functional abilities were drastically different than they are now and so the chair I have now was ordered based on what I was able to do over three years ago. One currently needless feature is that I ordered the aforementioned collapsible frame, because at the time I was without my own transportation and so any time I wanted to go somewhere, I needed a chair that could be folded up and stowed in the trunk of friends’ or family members’ vehicles. Even though it affords the owner some flexibility when traveling with other people, folding frames are heavier than rigid wheelchair frames and ever since I bought my van I never fold it down now anyway. I have a bracket bolted to the bottom of my chair that holds a pin, which in turn slides into a lock mounted to the floor of my van to keep my chair secured while driving. The bracket prevents the frame from being collapsible. A second drawback to the bracket is it also adds a significant amount of weight to the chair. Another change I would like make to the chair would be to get rid of the inflatable tires. I’m constantly adding air to my tires to maintain a hard, fast ride. Under-inflated tires add resistance when trying to push around and I have also blown out the inner tubes in either tire at different times when trying to have someone help me inflate the tires with my shoddy, tire pump. The next set of tires I buy will have solid, tubeless inserts so I never need to worry about low tire pressure. In addition to the tires, I don’t like the design of the leg supports and foot plates at the front of my chair. Currently, the leg supports are designed to swing open and the foot plates pivot up and these features were selected at the time to ease my transfers in and out of the chair. I learned, however, that when I perform my transfers it is much easier to balance and complete the transfer if I leave my feet on the foot plates; therefore the flexibility of my chair’s current configuration is kind of pointless. However, those are all minor gripes and only interfere with my mobility on an occasion. Without a doubt, the aspect of my chair that gives me the most routine grief are the specialized wheels I’m using.

My wheels have a battery powered electric motor in them that, even though I propel my chair manually, allows me to do so without burning out my shoulders and arms in the everyday process of getting around. My power-assist wheels have enough propulsion in them to make it possible for me to get up-and-down most inclines without needing help. The breaking-resistance function on a decline keeps me from having to worry about my chair getting away from me and sending me careening downhill out of control if I lose my grip. I’m also able to roll through grass if need be, although I found out over Memorial Day that soft, sandy ground is debilitating even with these wheels. When I have to traverse long distances, I can set the wheels to a low gear ratio that makes it quite easy to move my chair. So it is those features that make them the most viable option for someone like me who wants a manual chair, but doesn’t have the strength or stamina to go to a full manual set-up. Yet the wheels, despite their functionality, are not without their flaws.

Despite taking great care to get a full charge every night, depending on how much I wheel around during the day, I often run the danger of running the batteries all the way down. It's not uncommon for me, upon arriving home after a morning and afternoon of consistent wheeling, to need to recharge my wheelchair batteries for an hour before heading back out for the evening. It's a contingency plan I learned after having one or both wheels die on me unexpectedly when out in public. The problem isn't so much that the batteries have died, but that when the batteries are dead, I'm then pushing an additional 50 pounds of dead weight, which is how much the wheels weigh by themselves. On top of the weight of the chair and my own body weight, this additional resistance prevents me from pushing up any incline or even pushing a moderate distance without significant exhaustion-inducing effort. In relation to the wheels needing to be charged every night, if I feel like going somewhere for more than a day I have to make sure and pack the battery charger. Over the course of three years, I’ve also had problems with the power cord to the battery charger and both charging leads developing shorts in them from general wear and tear. This in turn, can lead to an insignificant battery charge, my wheelchair batteries running low, and so on and so forth. The pattern repeats itself. Ultimately I’d like to be able to get into regular manual chair and leave all these issues of dealing with batteries and chargers and excessively heavy wheels behind me, but my arm strength, limited endurance, and lack of grip just make that proposition unrealistic in the here and now.

At the other end of the spectrum I could always get a full-sized power chair. There are plenty of unique power chairs with amazing features to choose from: chairs that recline, chairs that stand the rider, chairs that can go off-road, and even chairs that can climb stairs. The first problem I have with all these types of power wheelchairs is their sheer bulk. I constantly encounter restaurants, stores, and bars were I have hard time navigating up under tables, around cluttered floorplans, through crowds, and into restrooms in my wheelchair. Most power chairs sit up higher and have a larger footprint that would exacerbate getting around in these types of spaces. You can also forget about going into anyone's house that doesn't have a ramp, or traveling in someone else's car with a power chair. To my knowledge, there isn’t a power chair made that weighs less or that has a smaller profile than my current chair that would make any of those situations easier to navigate. Then aside from the logistical limitations of a power wheelchair, on a personal level, the other main reason why I don't want a power chair is how I feel about my self when I use one. Going out into the public-at-large in a wheelchair is a spectacle to begin with, but in a power wheelchair I feel like I stick out even more. Of course, high-level quads, people with MS, stroke survivors, or people with a TBI who have to use power chairs all of the time, would trade places with me in a heartbeat. The other added benefit of my current wheelchair configuration is that pushing my chair does provide me an opportunity to get a fair amount of cardiovascular exercise. So from the standpoint of my own self-esteem, even though my power-assist manual wheelchair gives me all sorts of shit, I prefer it over the power wheelchair because it makes me feel more vigorous.

On Monday the problem with my wheel worsened to the point where I thought it was in danger of falling off, so I anticipated making an appointment Tuesday morning to take my wheelchair in to get it fixed. I own a set of spare, manual wheels and I had my aide swap out the bad power-assist wheel for one of the manual wheels. I quickly recognized how difficult it is to push a manual wheel on my heavy-ass wheelchair across the carpeting in my apartment. Exiting down the ramp of my van without the assisted breaking of two fully functioning power-assist wheels added a new degree of difficulty, as the dead-weight momentum of the manual wheel almost sent me off the side edge of the ramp, and further drove home the point of how much I need my power-assist wheels. Unfortunately, I was informed at the wheelchair seating service it was probably going to be upwards of three weeks before I got my wheel back in working order. I asked if they had any spare power-assist wheels that I could borrow for the time being. They did not, but they could put me in a loaner power chair. I told them I’d think about the offer. Tuesday night, as I lay awake trying to massage the rock-hard knot of tightly cramped and fatigued muscle fibers at the base of my neck, I decided that if I was going to be without a properly functioning wheel for any significant amount of time, I was going to need a loaner wheelchair.

On Wednesday morning I drove back over to the wheelchair seating service to pick up the power chair they had set aside for me and I dropped off my defunct power-assist wheel to be shipped back to the manufacturer. The wheelchair tech who I talked to about the problem with my wheel reassured me that sending the wheel back to the company probably wouldn’t take as long as the three weeks he originally quoted to me if he put in an order for the parts to fix it himself.

“How long then?”
“Oh, definitely less than three weeks.”
That’s definitive. Fan-F’ing-Tastic.

The power wheelchair the tech set me up with is a complete P.O.S.: the low-profile seat cushion that came with it is uncomfortable; the back rest is too high, altering my posture and thus throws off my sitting balance; the foot plates are flimsy; the speed control adjustment is missing its knob and stuck on one setting; it lacks any sort of battery level indicator lights; and there isn’t a way to actually secure it to the floor of my van while I drive, so I’m banking my safety on the chair’s weight and the fact that its wheels lock up when the power is turned off. Before I left I had to send the guy back inside to retrieve for me the battery charger that fit this particular chair. After I got myself secure in the driving compartment of my van the wheelchair tech loaded my original wheelchair in my van behind me and he locked the brakes to keep my other chair from rolling around behind me as I drove. Of course this meant that I wouldn’t be able to get out of my van when I got back home, so I called my buddy Jak to meet me at my place to help me exit my van. When we got everything unloaded and back to my apartment, I had Jak help me clean up some of the grime off of the loaner power chair. We also switched out the crappy seat cushion that came with the power chair with my Roho air cell seat cushion. The Roho cushion is nearly twice as thick as the one that came with the power chair and helped to temporarily alleviate some of the posture problems I was experiencing. We then hung out for about a half an hour and then Jak got ready to leave.

I followed him down the hallway of my apartment and stopped at the opening of the hallway that makes up the living room-dining area. Jak grabbed his keys and flip-flops and headed out the door. In that moment I pushed forward on the control stick of the power chair and nothing happened. I looked down at the single, green power indicator light next to the control stick; it went blank, blinked red, and then went blank again. I pushed up on the control stick a second time, and again nothing happened; I watched the same sequence of blinks on the power indicator light. In that instant my front door closed behind Jak. I flipped off the power for a second and flipped it back on, hit the control stick again, the chair lurched forward an inch and then nothing.

“Jak! Wait!” I yelled as I quickly glanced down to my lap for my cell phone. It wasn’t in my lap. “Jak!” I cast a darting glance to the end table, eight feet away against the half-wall that separates my kitchen and dinning area. There amidst the clutter of things routinely I cart to and from my van—spare change, keys, iPod, sunglasses—was my phone, utterly out of reach. I looked out my front window to see Jak pulling away in his Jeep. Across the living room the digital clock on the cable box sitting on top of my TV read 12:38.

The next five minutes or so I spent trying to decide what in the hell I was going to do. Without battery power a power wheelchair is a hundred and fifty pounds of “I’m screwed.” I briefly thought about yelling until one of my neighbors heard me, but that would never work. I hadn’t seen the car of the woman who lives above me for days and it wasn’t out in the parking lot now. I was too far from any adjoining walls to try bang on and draw the attention of the neighbors that lived on the backside of the building, and who knew if they were even home. 


I leaned over the left side of the chair and looked down to one of the drive wheels. Situated on the top side of the cylindrical drive motor is a silver lever that can be positioned to disengage the gears that power the wheel. With the power off and both wheels disengaged, the chair can be pushed around by anyone who needs to reposition it; often an easier way to move a power chair than trying to control the chair under power for someone who is not actually seated in the chair. I thought if I could get both wheels disengaged I might be able to pull along the wall back down the hallway into my computer room and the cordless phone I have in there. After several more minutes of struggling to get the wheels disengaged my first pull on the wall succeeded in only backing the chair a few inches on an angle away from the wall. I might be able to produce one more pull but that would just position the chair completely out of reach of everything.

In the next moments, as I sat giving up on plans A, B, and C, I heard the new text message chime on my cell phone go off. I knew exactly who the message was going to be from, as I had previously made plans to attend the Detroit Tigers game that night. Tuesday afternoon my friend Tonya called to make sure we were still on for the game and I had recounted how I was having problems with my wheelchair, but that I was anticipating having those problems rectified by the time I needed to leave to meet her and her friends at the ballpark downtown. I thought about the possibility of just sitting there until someone came over, but that was also a ridiculous proposition as there wasn’t going to be anyone coming over until my aide came in the next morning. I couldn’t sit there that long. I started to curse the wheelchair tech for sending me off in a shitty power chair without charging up the batteries. I cursed myself for not asking wheelchair tech if they had fully charged the batteries before I left with the damn chair. I contemplated how much effort it would take to get to the point to where I would be able to propel a manual chair without any special wheels or batteries. 

I cursed the irony of the fact that, the entire time I lived in my apartment, I had the I’ve-fallen-and-I-can’t-get-up Medic Alert system at my disposal and that last week my insurance company called me and told me they were no longer going to pay for the service. If I wanted to continue using the service (I didn’t) I’d have to start paying the monthly fee out of pocket. In the beginning I wore the alert bracelet, but took it off because I kept bumping it and setting off the alarm. Then I just kept the bracelet on my wheelchair for a while, but stopped carrying it altogether when I traveled overseas two years ago and haven’t carried it since. For two years my insurance paid for a service I had no capability of using because I quit carrying the alert button and I paid a local phone bill for a phone I never make calls on just because the service needs to be hooked up to a landline. I was awaiting the arrival of the next bill to cancel both services in one fell swoop. Oh Irony, you are on top of your game today, bastard.

It was now approaching 1pm and only one course of action remained. It was the course of action I knew from the moment that I didn’t have my phone on me would end up being the only way I was going to bring this fiasco to a resolution. The course of action I was avoiding; I was going to have to crawl to my phone.

I spent several more minutes trying to decide just how I wanted to position my feet in preparation of making my "controlled" fall onto the floor. I didn’t want to get a foot hung up on one of the foot plates and then be stuck on the floor, further compounding the problem. If I placed my feet on the floor and then fell awkwardly to one side or the other I might run the risk of twisting a knee or worse. That wouldn’t necessarily prevent me from crawling across the floor, but I would compound things later on down the line. The same thing could said if I fell too fast and cracked a knee cap or chipped an elbow. In the end, all of this scheming and preparation really boiled down to psyching myself up for the fact that once I started down to the floor, there was a very small window in which I would be able to pull myself back up before I reached the point of no return. Once I crossed that event horizon and landed on the floor I wasn’t getting back into my chair without someone coming to my rescue.

So, I pulled the arm rest off the right side of the power chair, lifted both of my legs over to the right side of the seat cushion, hooked my right arm around the push handle behind me and started to lean forward over my knees. The toes of my shoes started to turn towards the right under the building momentum and I was able to hold up for a moment to straighten them with my left hand back in the direction I wanted to head towards. I let go of the push handle with my right arm and extended it out in front of me to brace for my fall. With both arms out in front of me I was able to control the speed of my fall a lot better than I expected and the tone in my legs seemed to help carry a bit of my shifting weight; I was expecting my legs to simply collapse underneath my body weight. I landed on the carpeted floor resting on my left forearm with my legs bent at the knees pointing in the same direction as my upper body faced. From there, rolling over on to my stomach was kind of easy and I ended up in a pretty good position to combat crawl over to the end table and my phone. At full extension, my body length significantly cut down on how far I was anticipating needing to crawl. I also happened to already be wearing an elbow pad covering my left elbow as I had been having trouble with keeping my elbows from getting skinned up at therapy this spring and summer. I hoped I wasn’t going to re-open a long-healing scab I had on my elbow for several months.

The combat crawl is something that I have practiced in therapy sessions within the last year and a half. I’ve done multiple lengths of a fitness studio before fatiguing which may equate to 30 feet of crawling or more. What makes it difficult as a quad is that all of the crawling is done with the arms and whatever percentage of my body weight my legs and lower torso comprise is dead weight. But the distance to the end table, I was able to cover in less than 10 pulls and so I arrived within an arm's reach of my phone in pretty good shape. I propped up on my left forearm and reached towards the top of the table with my right hand, but I needed to get a little closer and then I made my first mistake. I pulled closer, but instead of propping back up on my elbow I lost my balance for a second and rolled over on to my back at the foot of the end table. Laying on the floor looking up at the ceiling and the underside of the table I could picture where my phone was just a few feet above me. In that position however, I was only able to reach up and back onto the top of the table the distance of the length of the back of my hand to my wrist. With the backs of my fingers I could feel the outline of the TV remote control that sat atop the edge of table where I had left it that morning. Blindly fishing around next to the remote, I could just barely feel the leather of the case that covers my phone and if I rushed trying to pull it towards the edge of the table, I would just end up knocking it back onto the table further and out of my already limited reach. I kept knocking into the TV remote and at one point, as a result of my fumbling, the remote swiveled on its rounded plastic body and it bumped my phone to where I could no longer reach it. The concentration and visualization of the top of the table and its contents began to zap my strength after even the modest crawl. I rested for a minute and looked for a tool.

Leaning against the right side of the end table, where I always keep it when I’m not using it, I have a lap desk with a raised edge around one of its long sides. I use the lap desk as a tray, most often to eat from while watching TV, but also to carry provisions back and forth from the kitchen to my dining room table. The raised edge keeps said provisions from sliding off the lap desk and onto to the floor, most of the time. I reached around the side of the end table and got a hold of the lap desk. With the raised edge facing down towards me, I held the lap desk in both hands and lifted it above my head over the blind edge of the end table. I began to use the lap desk to carefully rake the contents on the top of the end table down on to the floor next to me. My goal in this effort was to try and avoid bashing myself in the face with whatever items I brought cascading down from on high. In two pulls I had the TV remote, some loose change, a few meaningless papers, and finally my phone scattered about the floor around me. I grabbed the phone and called Jak. He didn’t answer. I left him a message summarizing the hour’s events, the gist of it being, “I’m on the floor. You’re not at your phone. I’m calling 911 to get help. They’ll come get me. Call me back.” After I left the message I called 911.

Once I placed the call to 911 and knew the paramedics were on their way I felt a relaxing calm come over me. I noticed that I was kind of comfortable lying on the floor. The carpet was cool to the touch. If I wasn’t expecting visitors I probably could’ve taken a nap. Instead, I took some pictures with my camera phone.








When the paramedics arrived they knocked on the door and I called for them to come in to my apartment. There is a scene from an old Tom Hanks movie, The Money Pit , in which his character unknowingly steps into an obscured hole in the floor of his multimillion dollar, in-the-process-of-being-renovated mansion. He slowly sinks into the hole up to his torso and remains trapped there for several hours until his wife returns home. He calls to her to rescue him and when she enters the study where he is trapped, she doesn’t see him at first glance and leaves the room. He calls to her again and she thinks he’s playing around because she already looked for him in that same room. Hanks’ response, in an exasperated, flat voice is, “I’m in the study, in the floor.” That scene flashed through my mind as the paramedics entered my apartment. I’d like to know what they wrote in their call report of what they witnessed when they walked in: two wheelchairs, in various stages of disrepair, neither occupied; young male, Caucasian, lying supine on the floor, arms outstretched, legs slightly crossed, alert—possibly relaxing.

“Are you okay, sir?”
“Yes.” I felt obliged to explain what I was doing on the floor before they picked me up. Pointing to my right, “That’s my wheelchair. One of the wheels is busted.” Then, pointing beyond my legs, “That’s a loaner chair. It wasn’t charged up before I brought it home. I didn’t know this. I got stuck and my phone was on this table. I crawled over here to get my phone.”
“You got on the floor on purpose?”
“Yes.”
“Which chair do you want to get back into?”
“Good question. I guess my busted one. At least I can sort of push that one.”

They got me back in my wheelchair. In the process of crawling and then being hoisted back in my chair, my jeans had fallen down around the middle of my thighs. The paramedics then executed a combination lift/pant readjustment; it could’ve been a bit done with a bit more grace. Before they left I had them plug in the power chair to the battery charger I brought home from the wheelchair seating service. It was now after 2pm. I made lunch.

I ended up going to the Tigers’ game, like I had planned, but like everything else Wednesday that too had its glitches. My plan of taking the power chair unraveled when I discovered that with my high profile Roho cushion on the power chair and the low-profile foam cushion on my wheelchair I sat in, the height differential was too great for me to clear transferring back into the power chair without risking another, this time unsolicited, trip back to the floor. I had done enough of that for a while. I went to the game in my crapped-out chair and needed to have Tonya push me around Comerica Park.

Thursday morning I got into the now, hopefully, completely charged up power chair. I turned it on and got some movement like it was functioning properly. I toggled the power switch off and then on again and immediately activated the control stick: the nefarious blinking light sequence. I waited and moved the control stick again: still more blinking lights. I turned the power off and on again and then waited a second. Action applied to the control stick produced a corresponding movement this time…

The punchline is that, despite all outward appearances and symptoms Wednesday afternoon, the power wheelchair may not have actually been low on juice after all. All of that nonsense Wednesday probably could’ve been avoided had I turned the chair on and off a few more times and waited just a couple seconds longer before attempting to put it in motion. All of it: the anxiety, the trepidation, the crawling, the blind phone recovery, the paramedics’ house call. Every last asinine second, all of it might have been totally pointless.

Well, all I can say on that one is…effing A.

03 June 2007

The Week of 1000 Miles: Fin

Saturday, May 26th: to Big Knob

For the past 12 years a group of my friends have been camping together every Memorial Day weekend at a secluded campground in Michigan’s Upper Peninsula. At its genesis, as I am told, it camping trip was a way for underage friends from Wisconsin and Michigan to convene at a midpoint destination and have a party. In the intervening years it has evolved in many ways and has seen a bachelor party, the ebb and flow of attendees, brothers and sisters, boyfriends and girlfriends, warm weather, freezing weather, sun and rain, late, late nights and sunrises, a ton of drinking, the odd hook-up, visitors near and far, marriages and now children. I have attended twice and this year, after a few years’ hiatus, returned for my third visit.

Big Knob campground is situated on the northern shore of Lake Michigan six miles down a winding gravel road off of U.S. Highway 2, west of bustling Naubinway. The entrance to the campground is so well marked that those who blink at the imprecise moment will miss the turn. This is not all bad, as its seclusion pretty much guarantees the campground is completely empty when we descend on it in mass every year. A little internet research yields that Big Knob gets its name from what amounts to a dune hill that rises a whopping 140 feet above the surrounding terra firma. I have yet to lay eyes on this Rock of Gibraltar, but the DNR claims it exists.

I have camped in a lot of places in my life starting in the backyard as a child and progressing through various stages of rustic to plush accommodations. As I got older many family vacations took the form of camping trips as we paraded around the state, first with tents, and then in the minivan towing a pop-up camper trailer. Both of my parents in their youth vacationed with their respective families on numerous camping vacations. My mother’s family undertaking a well-documented 3-week trip to the American West when she was a teenager and my dad’s parents driving he and his brothers to places like Gettysburg; quintessential American vacations of the 50s and 60s. The farthest my parents took me and my sister was a two-week trip to Gettysburg, Washington D.C., and into the Shenandoah Valley in Virginia. Aside from that most of our family camping experiences took place in any number of state park campgrounds in and about northern Michigan. Once I started college I met a group of friends that shared a love a travel and so, in varying groups and numbers, I’ve camped in several places in the western U.S. and Canada. These trips were undertaken with a greater sense of seeking adventure and bare-bones subsistence than compared to parking the pop-up on a campsite for three days and roasting marshmallows every night around the campfire. The pinnacle being backcountry hiking and camping in Denali National Park in Alaska: no manicured campsites, nary a trail, navigating by topographic map, fording rivers, filtering water from mountain streams, keeping an eye out for the odd Grizzly bear or irritated moose, and being bombarded by billions (yes, billions) of hellacious mosquitoes. Big Knob, despite its secluded location, lack of electricity, and pit toilets, is not rustic camping. This is fine because Big Knob weekend isn’t about adventure, it’s about camaraderie.

Camping in many ways is an ironic undertaking. In an effort to live minimally in harmony with the natural surroundings, we pack mountains of equipment that would be completely unnecessary were we to spend the weekend at a friend’s house or at a hotel. Packing for Big Knob is no different. In its twelve years, the core nucleus attendees to Big Knob have become a well-oiled machine in regards to knowing exactly what and how much to bring of everything. Those of us on the fringes are responsible for providing our own accommodations, creature comforts and bare necessities, but food, drink, and mess supplies are provided, plentiful and perfectly in order. It still amounts to a pile of gear though, especially now that children have been thrown into the mix. In my previous life as a traveler I often packed light and my general rule of thumb was “one bag,” regardless of the trip duration. Going to be gone more than a week? Depending on the climate of my intended destination I’d pack sufficient underwear and socks, but probably only one or two pairs of pants and only a few shirts of flexible utility. The less that gets packed, the less there is to carry, as well as get checked onto planes, or lost by baggage handlers. Of course this plan wasn’t totally foolproof as I once boarded an eight passenger plane, its flight plan taking me from San Juan, Puerto Rico to St. Thomas, Virgin Islands, landing twenty-five minutes after taking off; only to find after arriving in St. Thomas that my bag—one of ten bags to be loaded on the plane by the ground crew in San Juan—didn’t come through on the conveyor belt where I awaited it at baggage claim. Absurdly, the only time I have ever lost a bag.

In the three years since my injury, my travel exploits basically came to an abrupt halt. Health, money, stamina, issues of personal care and independence were all contributing factors in how far and how long I ventured from home. Gone are the days of packing a bag in an hour, grabbing some CDs, hopping in the car and dropping in on friends ten or twelve hours later in Atlanta, Philadelphia, Minneapolis, or wherever during summer vacation. Traveling wheelchair-bound puts a pretty big crimp in the assault-style method of travel I used to enjoy. There are so many other aspects and complications besides just packing for a two night trip to consider now. My biggest concerns in deciding to return to Big Knob this year were the weather, sleeping comfortably, and my wheelchair in Big Knob’s wheelchair-hostile terrain.

The weather at Big Knob is highly unpredictable from year-to-year and the best bet is to prepare for the worst and then hopefully be pleasantly surprised. I prepared for cold, which for me anticipating being outside all day, was basically anything less than 60°. I have poor circulation and terrible body temperature regulation so it doesn’t take much for me to catch a chill. In anticipation of nighttime temperatures forecasted to drop into the 40 degree realm I brought thermal undershirts, a hooded sweatshirt, a fleece jacket, a knit hat and mittens. When I arrived Saturday evening it had been sunny and 70° during the day, but as I got help unloading my gear the clouds had rolled in and rain drops began sprinkling down. From about 8pm Saturday night and onward a steady, light rain fell. I slept that night wearing everything I wore during the day, save for my shoes and the fleece jacket I put on upon arriving. The rain abated early Sunday morning and the day was cool, but dry. From the get-go on Sunday I layered in two undershirts, the hooded sweatshirt, fleece and knit hat. Staying warmer during the day and having the good fortune of being dry, I went to bed feeling much warmer than the previous night. True to form, Monday being the day in which we all had to pack up and leave, featured the best weather of the weekend: sunny and warm. Aside from Saturday night, I managed to stay fairly comfortable temperature-wise and with the ferocity of the mosquitoes this year I was glad I had plenty of long sleeves and a hat to stave off their ravenous swarms.

Tent camping doesn’t lend itself to the most comfortable sleeping arrangements. Roughing it in Alaska, where my friends and I were setting up camp with what we were able to carry on our backs, finding a completely flat place to set up a tent was pretty much pointless. Traveling light we didn’t have extras of blankets, sleeping bags, or fluffy pillows with which to cushion our sleeping space and so most nights we made due with trying to be as comfortable as possible on the uneven ground. Even at Big Knob I think the best I’ve previously done in terms of cushioning between my body and the ground was a second sleeping bag underneath the one in which I slept. As the Big Knob experience has expanded and people have gotten smart about what to bring, I’m pretty sure that this year everyone slept on some sort of air mattress. For me from the perspective of dealing with paralysis, the issue of what to sleep on had less to due directly with comfort as it had to do with preventing sores from sleeping in one position all night long on hard ground. My sleeping arrangements at home I have tailored in such a way that I am able to get in bed and move about at night without having to worry about sleeping in one position too long and risking a sore. Tent camping eliminates all of that convenience. Not only did I have to rely on my friends to get me out of my chair and into my tent, but they also had to get me in my sleeping bag, and then set up the implements I needed at night for being able to go to the bathroom. I knew I wasn’t going to be able to turn and reposition at night because I didn’t have anything to pull against, so before embarking on the trip I made a stop at my local camping store and purchased a self-inflating ground roll. At full capacity it expanded to 2½ inches and kept me off of the cold, hard ground. I made sure and bought the six-foot long pad so that my feet wouldn’t be resting on the ground either. On top of the ground roll I brought a thick blanket and a second sleeping bag to give me additional, softer layers to lie on top of in my down sleeping bag. Lying still on my back all night long wasn’t the greatest, but it was comfortable enough that once I warmed up inside my sleeping bag, I slept soundly. The ground roll and extra sleeping ended up being sufficient padding as I made it through the weekend without any bruising or skin breakdown. Aside from reconciling those comfort-related issues I brought with me a small, battery powered, reading light that I set by my head so that if I needed to see in the tent at night I had a light source available. I also made sure to attach a leather loop to the zipper of my sleeping bag before I left so I would be able to work the zipper when I needed to open up the bag at night to go to the bathroom. To top it all off, my friends brought an extra sleeping bag that they draped over top of me and that provided an extra layer of warmth that was especially welcomed on the first night. In the end though I think two nights of that was enough as I awoke on Monday morning feeling quite stiff.

The final piece of the puzzle was figuring what I was going to do with my wheelchair. I use a manual chair that has power-assist wheels. The wheels are powered by batteries that need to recharge after every day’s use. At home I accomplish by plugging into the charger at night while I sleep. Big Knob campground doesn’t have electrical hook-ups and so bringing my charger would be useless. The problem of my batteries running out of juice meant that once they were kaput I would need someone to push me around everywhere. Without the power assist function working the wheels, because of their design, become 50 pounds of dead weight. I packed my backup set of regular manual wheels thinking that once my power assist wheels quit we could switch to the manual wheels and, at the very least, my friends would be able to push me around in a much lighter chair. Then a couple days before I left I had the idea to charge up the second set of batteries I own for my power assist wheels and see how long they hold a charge without being used. Upon discovering that they still held a full charge overnight I decided to bring the second set of batteries along as well. Driving up on Saturday the power assist wheels on my chair sat turned off for six hours and so when I went to bed Saturday night the first set of batteries still held a decent partial charge. After I got into my tent, I had my chair stowed inside my van overnight. In the morning we swapped out the first set of batteries and I used the fully-charged second set during the day Sunday, thus after they crapped out Sunday evening I still had the first set holding a partial charge to use on the way home Monday. In the end I never used the manual wheels I brought, but they wouldn’t have done me much good anyway as the tires on those wheels are only a half an inch in width and would’ve sunk right down in the sandy soil of the campground. As it stood, even in my power assist wheels, which are pretty good at powering through grass and uneven terrain, the ground in certain spots around our campsites was so soft that the front casters on my wheelchair dug in and I needed to be pushed around anyway. I spent a great deal of time perched near the fire pit and occasionally got help to move to more desirable vantage points or to be closer to the thick of the action.

So, despite my initial concerns camping in Big Knob came off with few hiccups. Considering what I felt were going to be the biggest obstacles and the fact that the weather was less than stellar, I can only assume that future return trips will only get easier. That being said, I'm probably not going to throw camping into my regular rotation of weekend activities. Big Knob was successful for me because of the people that were there with me. Basically I have my friends to thank who catered to my every whim and fancy over the weekend. From pushing me around the campsite, fetching me food and drink, helping me dress, unpacking and then repacking my gear—none of it would have come off without their help. All I really did was show up.
Round trip mileage: 699
Cumulative week's mileage: 1139
(does not include routine trips to Livonia on Monday, Wednesday, and Friday)

The Cat's Out of The Bag

My sister got engaged to her longtime boyfriend last weekend. The above is not a picture of him, but it is a picture of the bobblehead I gave him last Christmas because he looks just like the character Dwight from NBC's The Office. It's mostly because of the hairline and the glasses.

All kidding aside, he's a good guy though: an engineer by trade. Which is good because my sister has a Master's degree in Oboe performance. So, at the very least now she won't starve.

Congratualtions!

31 May 2007

The Week of 1000 Miles: Part Two

Tuesday, May 22nd: to Cleveland

I like all kinds of music. Some music I like enough to go see performed live; given the price, the night, and the proximity of the venue are right. Then there are certain bands I like enough to see regardless of the night and to some extent the price, and will see them as long as they wander into my region of the country. For a long time this category was a class of one, in the form of Pearl Jam. They last brought a tour to the Detroit area in May of last year and although the concert was great, I took away from that experience (my first concert since my accident) that choice of venue was now going to be a major deciding factor in my selection of concerts to attend; even if that concert is another Pearl Jam show. Pearl Jam played the Palace of Auburn Hills, home of the Detroit Pistons, an arena that seats 18,000+, hosts hundreds of events a year and—unbeknownst to me until that night—features shitty accessible seating options. The floor seats I bought in anticipation of Pearl Jam rocking my proverbial socks off were switched to the back of the house, concrete bunker on the concourse level that serves as the accessible seating area. Thanks for the accommodation. I wasn’t anticipating Row 1, center stage, and I understand the limits placed on seating availability based on architectural design quirks, but the Palace isn’t even a twenty year-old venue, in my mind if a stage can be erected on the floor of an arena then there’s a way to get my wheelchair in the same area code as my purchased tickets. Had I known I was going to be viewing the concert from a pill box I would’ve bought nose bleed seats and considered the move to the concourse level an upgrade. I bet that when Bill Davidson’s crotchety ass is finally stuck wheelchair at the very least an attempt will be made to get him to his courtside seats. So, the Palace is off the list of places I will go to see a concert at from now on; which is fine because it sucks to have to drive out to Auburn Hills anyway. But, what do Pearl Jam and the Palace have to do with last Tuesday and Cleveland? As much as it pains me, Pearl Jam at the Palace is the bad taste in my mouth I will remember when considering all future concerts I want to attend and the venues at which the band or bands I’m interested in are going to play.

Back in April a young band of brothers named Kings of Leon released their third album. Kings of Leon have been on my radar for a while now as I thoroughly enjoyed their two previous album releases. I’m not in the music review business, but hailing from Tennessee, Kings of Leon write up-tempo rock songs about no-good girls and the lead singer mumbles about 80% of the lyrics; it’s a recipe that puts a smile on my face. A recipe, coupled with a great appreciation of their new record that made me decide I wanted to see them in concert on their current tour. When I checked their tour dates I was disheartened to see that the closest the Kings would be to the Detroit area was either Chicago or Cleveland. Well, shit.

So, I thought about it and I thought about the fact that I’ve only been to one concert in the last three years and that shouldn’t be the case. I also thought about the fact that it’s summertime now and it’s time to do summertime things. Summer is a time for carefree, impulse-based decision making—which I haven’t done enough of in the last three years—and so I bought two tickets to the Kings of Leon show at the House of Blues in Cleveland. I convinced my buddy Jak to come with me despite his protesting of being too poor to go to a concert. Jak, you see, is an aspiring screenwriter, aka part-time bartender, aka part-time student, aka currently unemployed, thus the perfect candidate to ride along to a rock show in Cleveland, on a Tuesday night. It’s not like he had to get up for work in the morning or anything (actually, he did have to meet with someone but not until after 11am).

We left town around 4:30 in the afternoon, high-tailing it towards Toledo, the afternoon sun chasing us across the sky. The drive to Cleveland requires a trip eastward on the Ohio Turnpike, a pay road of limited access, and I have wondered for some time now how much difficulty I’d experience getting on to the turnpike. In my recollection of past eastbound trips on the turnpike the toll tickets were dispensed from automatic ticket booths. Parking structures in Ann Arbor all utilize these machines and as I cannot grip the ticket to pull it from the machine, I always need to call for assistance from one of the cashiers. Having Jak with me meant I wouldn’t have to worry about this problem as he was able to jump out of the passenger door, grab the ticket and jump back in as the toll gate swung open; a Chinese fire drill without all the switching of seats. For future reference though, even thought the toll tickets are dispensed automatically, I saw at least one attendant on duty at the toll station and a honk of the horn should bring that person out in case anyone needs assistance.

We pulled into downtown Cleveland in a just over 2½ hours. The House of Blues is situated in close proximity to both Jacobs’ Field and Quicken Loans Arena and the area seems like it could be pretty fun to hang out in with the right activities going on. After parking my van in a structure across the street from the concert hall we made our way over to pick up our tickets. I have to say that all the event staff at the House of Blues were incredibly accommodating and helpful. The tickets I purchased were General Admission and I was anticipating finding accessible seating at the back of the house on the first level as that is what was diagrammed on the House of Blues website. When we picked up the tickets the person at the box office window suggested that we sit up in the second level reserved seating because we would have a better view of the stage from that vantage point. Acting on his tip, we found ourselves about fifteen rows from the railing, with a bird’s eye view of the stage. The House of Blues only seats 1200 people to begin with and the close quarters of the second balcony, put us right on top of the action with a sweet view. Plus, behind the seating in the second level are two bars with waitress service to all of the patrons with tickets up there. It ended up being a perfect set-up, better than I was anticipating, and just the right size club to see a young, energetic band like Kings of Leon rocking out 1200 of their closest friends.

Exiting the House of Blues into the warm night air I felt thoroughly satisfied with the entire experience and then slowly, as the jubilation and the crowd dispersed, there was the realization of the impending drive home. Any ride home from a concert can be a bit of a chore, let alone one that is over 2½ hours long. Dawdling would only further delay the inevitable. We ended up pulling into Ann Arbor after 3am and my head hit the pillow sometime after 4. My alarm going off a scant 4 hours later was less than pleasant, as was the prospect of facing a full day of physical therapy and other assorted appointments later that afternoon. The staff at my PT clinic was amazed at my previous night’s itinerary, and it’s always hilarious to recount such tales to those who would never think of doing such a thing, but such is the price we pay in the name of Rock.


Round trip mileage: 342

Cumulative mileage: 440