Her collapse made me aware of how pitiful I looked.
Most of those first days remain a blur to me. I wasn’t sure if people really visited me or if I only hallucinated—and from what Eva and the nurses told me, I sometimes was delirious.
The hospital allowed visitors to come in each day, a few at a time. Even when they said nothing, their sad, pitying eyes made it clear to me how they felt. I write
clear to me
because I know how I perceived them. In retrospect, I may have been mistaken. I suspect I was so positive I would die—and I wanted to—that I saw in their eyes what I was feeling about myself.
Accurate or not, I felt as if they were staring at a mangled body and not a living person, that despite the assuring and comforting words they spoke, they expected me to die at any moment. I wondered if they had come to pay their last respects before I closed my eyes forever.
Though my pneumonia was gone, we still had to treat its aftermath. Nurses came in every four hours for respiratory therapy treatments. They beat on my chest and forced me to breathe through a plastic mouthpiece an awful-smelling, terrible-tasting stuff that was supposed to coat my lungs. This treatment would prevent the pneumonia from recurring and help restore my lungs. I’d wake up and see people coming in, and I’d think,
Oh no, here we go. They’re going to make me breathe that stuff and pound on me and try to get the phlegm dislodged.
As painful as they were, the treatments worked. Dr. Houchins, the head of the Hermann trauma team, came in several times a day. What Dr. Houchins may have lacked in bedside manner, he made up in sheer bulldog determination not to lose any of his patients.
He demanded that I breathe. “Don’t quit now. Don’t quit. Keep trying.” It wasn’t just the words he spoke, but—as sick as I was—I felt as if he fought right alongside me. “Don’t give up. Keep trying.”
Often I didn’t have the energy to breathe and just stopped trying.
I saw the pained expression on his face and then watched his features contort into an angry intensity. “Did you hear what I said? Do it! Now! Breathe and cough! Do it.”
I shook my head. I just didn’t have the strength to do anything more.
“This is not negotiable. Do this right now! Breathe!”
“I can’t.”
“All right, don’t do it. You’re dead. You’re going to die if you don’t do it. Can you get that into your mind?”
I didn’t want to live, but something happened when he yelled at me.
I breathed.
Shortly after that, the staff figured out how to elevate my leg so I could sit up. Just to sit up was a great step forward. I didn’t think I’d ever get to lie on my side or stomach again.
Once while I was still in the ICU, it seemed as if every time I opened my eyes and blinked, within seconds someone thrust a spoon filled with food about six inches from my mouth.
“Just open up.”
One time it was a man’s voice.
I opened my eyes and stared. Holding the spoon was a burly man. He lifted my oxygen mask and gently poked the spoon into my mouth. “That’s it, just take a bite.”
I obeyed and swallowed while my drugged mind tried to figure out what was going on.
Slowly I realized that the voice belonged to Stan Mauldin, head football coach and athletic director of the Alvin High School Yellow Jackets. Our daughter would live with Stan and Suzan and their two children during my convalescence. Coach Mauldin had heard that because I wouldn’t eat, I was losing weight at an alarming rate. (Although I had lost only a few pounds then, within my first six weeks in the hospital I lost nearly fifty pounds.)
As soon as Stan heard about the situation, he made time in his demanding schedule to show up at Hermann Hospital. He didn’t just drop in to visit. He asked the nurses to give him my food, and he sat beside my bed until I awakened.
As soon as he realized I was fully awake, Stan shoveled in the food and talked while I did my best to chew and listen. That gentle act of sacrifice by a bear of a man was one of the most thoughtful acts I witnessed during my days of recovery. Stan epitomizes strength and tenderness combined in one exceptional person.
I’ve referred to the Ilizarov frame, which may have sounded like a common procedure. It was far from that. Eva had to make a decision no one should have to make alone. She had to decide whether to allow the then-experimental Ilizarov process.
Initially this device was used to stretch legs. Its invention came about to help individuals who have a congenital condition where one leg is shorter than the other—some as much as twelve inches—and have to rely on wheelchairs, calipers, or crutches. The Ilizarov frame forces the bone in the leg to grow while keeping the surrounding tissue intact. The body can form new bone between gaps in response to the mechanical force of the Ilizarov frame.
The Ilizarov bone growth device is what they call an external fixator. A Siberian doctor named Ilizarov invented it.
Dr. Ilizarov experimented on sheep to develop a way to grow missing bones or lengthen congenitally short bones. For missing bone cases like mine, the application involves breaking a limb with a clean break. Wires about the size of piano wire are placed through the skin and bone, and they exit out the other side.
The femur Ilizarov device is anchored in the hip by rods about the size of pencils. The doctors drilled holes for four large rods from my groin to the side of my left hip. After they did that, I had at least thirty holes in my left leg. Many of them went completely through my leg and out the other side. The larger ones just went into the flesh, and rods were embedded in the pelvis. After about six months passed, I could actually see down inside my leg as the pinholes stretched out.
Every day someone would come in and turn the screws on the Ilizarov device to stretch the bones. Most of the time the nursing staff took on this task. After I came home, Eva did it. For nearly a year, my left femur bone would regrow and replace the missing piece. It’s an ingenious device, although terribly painful, requiring an arduous, lengthy recovery. I called it “hideously wonderful. ”
Six rods also went through the top of my left arm and came out the other side. Big stainless steel bars were placed above and below the arm to stabilize it, because both forearm bones were missing. The rods were the size of a pencil and allowed Dr. Greider to harvest bones from my right pelvis and place them in my left forearm. The doctor explained that this was like taking core samples when drilling an oil well. They also harvested about thirty-two square inches of skin from my right leg to place over the enormous wound in my left arm. Then they embedded a Teflon strip between the newly constructed bones in my forearm in order to prevent the new bones from adhering to each other—that is, attaching themselves and growing together.
Unfortunately for me, that part of the technique didn’t work—the bones healed, but they attached themselves to each other. Consequently, I have no pronation or supination in my left arm—my arm does not straighten out at the elbow, and I can’t turn palms up or palms down. When I extend my arm, my hand is always in a hand-shaking position. My hand cannot twist either right or left. I know all this seems barbaric, and at the time it felt like it. But like the Ilizarov, it works.
Yes, the Ilizarov device worked—and it was also the most painful process I endured as part of my recovery.
The stainless steel Ilizarov on my leg weighed about thirty pounds, and the external fixator on my arm probably weighed another twenty. Whether I was in my wheelchair (about eight months), on my rolling walker (three more months), or eventually my crutches (four more months), I carried that extra weight around for nearly a year.
Can you imagine the strange stares I received everywhere I went? People gasped and gawked at a man in a wheelchair with steel rods sticking out all over his body.
Virtually every time I made my routine visit to Dr. Greider’s office in my wheelchair, the reaction of the other patients was universal. Though each wore casts or braces or walked on crutches, all of them would stare at me and my rods and halos. Then without fail, someone would say somewhat sardonically, “Wow, and I thought I was bad off.” Occasionally, someone would even add, “After seeing you, I feel better.” For a long time, I became the standard by which painful injury was judged.
I’ve often kidded others that because of all this “metalwork,” if archaeologists discover my body years from now, they’ll think they’ve found a new species! My anatomy has been completely rearranged.
Never again will I take simple physical ability for granted. During my recovery, even the tiniest movement was a miracle. Every time I relearned how to do something, it felt like an achievement.
Only later did I understand how hard Dr. Greider had worked to find a way to save my left leg and arm. I’ll always be grateful that he didn’t just give up on me.
My right knee was crushed, and I wore a cast on it for quite some time. They put a small, mesh basket around the kneecap so it would heal. My right arm was the only limb that didn’t break.
Even with the success of the Ilizarov frame, however, the pain didn’t leave—not for one minute.
I wonder how many times I asked, “How long?” I wanted to know how long I’d have to endure the device, how long before I’d know if it worked, how long before I’d walk again.
No one would—or could—give me an answer, but I kept asking anyway.
“A few months,” was the usual answer.
“How few?” I persisted.
One of the doctors finally said, “Many months. Maybe longer.”
“You mean possibly a few years?”
“Yes, perhaps years.”
“And there’s no guarantee that I’m going to be able to keep these limbs?”
“There’s no guarantee. An infection could come on suddenly, and we’d be forced to remove your leg.”
“You mean I could endure this for months and still end up with no leg?”
He nodded.
Obviously, that wasn’t what I wanted to hear. Even though Eva had told me the same thing, denial must have set in. I kept seeking a guarantee that I would fully recover.
I wanted answers, but perhaps even more than that, I wanted assurance that I would be well. I wanted to be normal again. I wanted to be able to walk out of the hospital on my own two legs and go back to my former way of life. No one was willing—or able—to give me those assurances.
Many months passed, but one day I did walk back into that hospital and hug all those nurses.
During the months after I received the Ilizarov frame, I had other problems. I developed infections—several times. Each time, I faced the reality that it might rage through my body and I would wake up without my leg.
I also had infections after they released me. Three times I had to be rehospitalized, put in isolation, and receive massive amounts of antibiotics to cure the infections.
Even then, many nights I prayed,
God, take me back to heaven. I don’t know why you brought me back to earth. Please don’t leave me here.
God’s answer to that prayer was still “no.”
I still don’t know all the reasons, but in the months and years ahead, I slowly understood at least some of the reasons I had returned to earth.