Chapter 7: The Plan (Part 2)
In the last chapter, which brings you up to March 13, 2008, I explained some of things I have done to help my lower back injury heal. I left out a few things though and would like to explain these before I move on to the next items.
To reduce the bending, twisting, and torquing of my spine, I wear a brace. By far, it's the
best one I have used. It's called a System-Loc Brace. The company claims it unloads the spine by providing an upward lifting force. I haven't seen any proof of that but it does limit motion more than a neoprene brace. I wear this during most of the day except when I lie down (unless I'm in a recliner then I'll wear the brace to prevent my lower back from bending). I've found that when I wear it, especially while driving, I tend to have much less leg pain.
Speaking of leg pain, it's much worse after sitting (as much as I try not to) and sleeping. So, when I wake up, it's because my leg hurts and getting out of bed and walking is very difficult to do. A few times I did a sort of a hop-drag kind of movement with my right leg. I would place as little weight as possible on my right leg, quickly advance (this is the hop part) my left leg and then drag my right leg up to meet the left. After Elle saw that once or twice, she bought me a cane. I wouldn't use it though. I couldn't put enough weight on the cane to make any difference and a cane seemed so, permanent; so disabling (which is the main reason I wouldn't use it). And, as I leaned on it, the pressure seemed to unlock a memory, a flood of discussions I had had with clients. I remember helping them adjust to the idea of using a cane and although I understood their resistance, it wasn't until I had to use one that I really got it; really felt what they had felt. A crutch is better. It seems more temporary and I can place more weight on it. I have one in the bedroom within reach and one downstairs. I only need it for a few steps but I am quite thankful it's there. Thank you, Elle.
On March 18, 2008, I had a follow-up appointment with Dr. White. I felt a little better going into his office but not a lot. Apparently I looked better though. Dr. White said, "Well, you're moving a little bit better and you certainly look better. You looked really bad last week. I was concerned." Really? I looked bad? The great news out of that visit was that my reflexes are back. As he thumped his reflex hammer on my knee and then my heel cord, I could feel the leg jump. I said in a whisper, "Yes!" Dr. White checked them several times and every time, the leg jumped. Awesome news.
I told Dr. White that I dreaded going to bed; that the pain at night was awful. He prescribed two medications: Lyrica and Ultram. He also gave me Skelaxin and Vicodin. I guess one or more of those will take the edge off or just hit me like a hammer on my head dulling all sense of pain.
I resist taking pain medication. Not because I'm trying to be tough but because I'm concerned I may fall for the fragile armor it provides and do more, just a little more, than what my body can really withstand. You may be laughing at that thought - me - paying attention to what my body can tolerate - but I believe I have a better, not perfect, appreciation. But, there are some days when it's too much. I can't get comfortable, my leg is numb yet burning at the same time, and when I turn or just place weight on my leg in a unusual or unexpected way, a sharp, stinging pain rips through my hip and down my leg bouncing to the thigh, lower leg and foot and I wonder if it's laughing along the way. Pain feels so evil to me at times. There's nothing happy or pleasant or inspiring about it. It's nasty, ugly, and I imagine it has green bumps and hairy warts on its chin with long, snaggy fingernails to prick and claw it's way from spine to foot.
The drug that worked was Ultram. It knocked the pain level down enough that I could concentrate but didn't also knock me out. Currently, I take Ultram and Lyrica at night and during the day occasionally, Ultram. I came to the conclusion that sleep was more important than waking up at 2 or 3AM and then spending the remainder of the day in a foggy, slightly pissed off frame of mind. When I'm tired, I feel sick. Nauseated. Thick. Dull. It feels like my thoughts slosh through a muddy mind. Sleep fixes a lot of things. When I sleep, everything seems better even if I hurt, I have more tolerance. My mood is brighter. I feel more positive. Sleep is key.
Unfortunately, it's still a crap shoot.
On March 20, 2008, I added an inversion table to my home routine. I call it the teeter-totter. The idea was to reduce the pressure on my spine, introduce a little motion, and more importantly,
give me something to do. Elle picked one up at Costco for about $200. It's great. The table tilts back, I have control over how far it goes, and I can easily rock it up and down creating the teeter-totter effect. It feels really good. I often climb in it at night when the evil green, hairy-chinned painster comes to visit. It soothes the fire in my leg after fifteen minutes or so. I spend about an hour a day in the teeter-totter in twenty minute segments. I listen to music, burn incense, meditate, travel in my mind. You know, I'll bet Austin would be just the place to start a spinal teeter-totter class. I can see a room full of teeter-totters all moving in rythym to the music.
I would like to tell you about about my exploration into unknown, belief-stretching, and challenging territory and whole bunch of other things, but I have to hop into (not the drag-hop :) the teeter-totter and do some traveling.









