Wednesday, July 17, 2019

Ice, Ice, Baby





I feel so much better.

I am a little more than six months post surgery to replace my hip.

There is a lot to be said for aftermarket (and in some ways bionic) body parts: titanium, ceramic, and a little plastic. Like having cataract surgery or adopting an adult black cat with one eye, I have found more people have had the experience than I would have expected. The local surgeon—ranked as #1 for his low complications rate in all of New York state—had done 16,000 of them before he got to me, after all. What was new to me was routine work for him. (He did great work, especially for the first surgery on a January morning.)

There is nothing wrong with aftermarket body parts.

Looking back, it’s hard to say how long, one way or another, I limped and gimped, but it was at least a year, probably more. I do know that for a while my first steps every morning were like Frankenstein’s. And that gait became the morning new normal. And sometimes I walked that way, almost, later in the day.

For months last year I thought the problem was my knees—which it was to some extent and had been remedied by what I think of as medical WD-40 shots in my knees.

So before I agreed to the surgery, I got the knee shots, took ibuprofen until my ears rang, took glucosamine-chondroitin, used a heating pad, tried cider vinegar (too sour), turmeric/curcumin (too spicy), and fish oil (too burpy). I rolled on topical magnesium and CBD oil for leg cramps. I had perfect attendance in water aerobics three days a week for a semester (which I now think of as athletic overachieving even as I still attend). The pool was the one place where, almost gravity-free, nothing hurt for an hour. I read everything I could find about hips online (there are about 206 bones in the human body, by the way) and wished I had taken Anatomy and Physiology all those years ago instead of General Bio. For better or worse, my sense was that both knees and hips were too far gone for the experimental stem cell treatment not covered by insurance.  I went to twenty sessions of physical therapy until finally I went to a second (this one highly recommended) orthopedic surgeon for an opinion. On a scale of 1-10, what is your pain? At least a 7, maybe an 8. And the pain was exhausting.

The verdict: I needed hip replacement surgery. Knees were bone and bone, and so were my hips, one in particular. The physical therapy for my knees had been helpful but not exactly the point.
The orthopedic PA and I also discussed alternatives to try until I was ready for the surgery by a, well, genuine sawbones. Since I had fortunately never been in a hospital before, I exhausted all the other non-surgical possibilities first.

Until I realized the pain that was defining my life was not going to go away. My life as I knew it had been interrupted slowly and incrementally.  I was no longer who I had been, and not in a good way.
I hadn’t gone anywhere I didn’t have to. Pain tainted everything. Sitting in theater seats hurt. Walking hurt. Carrying a cat to the vet for a routine appointment was more difficult than I wanted to admit. Putting a sock on my left foot was…. excruciating. I went upstairs slowly in part because it was difficult to develop and sustain momentum, and stepping in and out of the bathtub required slow, careful moves. Clean out the garage? Forget it. I had a limited range of motion. I came to curse gravity and almost all life out of the pool. My physical therapist had told me “Motion is lotion,” but motion as often as not hurt. Still, I did my exercises at home twice every day anyway. (I am told most people go to physical therapy in part because they don’t do their prescribed exercises at home, but I certainly did them.)

I once was a walker, but no more. I trimmed the hedge, but I was too sore to carry the trimmer into the garage afterwards. I had to take the newspapers in small amounts out of the recycling bin to carry the bin to the curb. Sitting didn’t hurt until I got up, so I spent a lot of afternoons lying down on a heating pad even in the August heat. The other things I did not do: I didn’t go to Maine even for a day trip for the first time in decades; driving didn’t hurt, but walking afterwards did.  I didn’t go downtown to protest Trump’s visit. I didn’t go to any social event that required sitting in uncomfortable theater seats. Or in restaurant seats. Or standing at a bar. Bending over to pick up a penny in a parking lot? Forget it. Walking any distance was not possible.

My inability to function successfully in the world was collateral damage from an arthritic hip that needed replacement.

My passport sat unused.

My former quality of life was no more. (And when I used a cane a month before my surgery to attend a Christmas concert, ushers offered me a seat in the handicapped section, not with my family. I declined and hauled myself up to the elevator-less second balcony. The Americans with Disabilities Act goes nowhere near far enough.)

The pain just got so normal so slowly that I am not sure I appreciated—for a long time—how out of commission I truly was.

And yes, I know there are far worse things, life-threatening conditions, to have. But still.

And so surgery.

Approval from the insurance company happened overnight. Hip replacement counts as “elective” which apparently these days does not mean a nose job.  I went to an hour of pre-op joint camp. I went through the other required pre-op motions: my lungs were “unremarkable”. Primary care review, PT consultation, admissions meeting, and finally meeting with the surgeon. I chose to spend 23+ hours in the hospital rather than coming home on the same day, and in that time, I had at least three different nurses. New day, new shift, electronic records.

I discovered that I have very good health insurance. My surgery cost me a $500 copay for my hospital admission. Period. (That said, the current health insurance system in the US is criminally unfair. But thank you, Excellus Blue Cross Medicare Blue PPO.)

After my $500 surgery, the first thing I did in the hospital was stand up straight and without pain for the first time in I don’t know how long.

But before the surgery, I bought a cane and a walker. I cleaned even during the ten days pre-op without ibuprofen or aspirin at which point I realized fully how seriously bad off I was. On a scale of 1-10, the pain was pretty much a 10. And I came to understand the need—the urge--to provide, provide as you move closer to an event that you have little control over, after all.

 I would have to stay home for two weeks post-op, so I put up stores: easy-to-prepare food for two weeks, cat food and littler, clean clothes, extra pillows to support my leg. Boost and Zing bars. Flashlights. Motion-sensor lights so I wouldn’t have to even reach for a light switch. I bought a reacher device, a tool to help me put on socks, and a booster seat for the toilet. (Amazon was my good friend.) I put up stores as if for The January Apocalypse (and I still have some of those cans of soup). Despite the pain (no painkillers for ten days before surgery, remember), I cleaned like there was no tomorrow just in case. Floors. The bathtub. I rolled up the throw rugs and put them away so I wouldn’t trip on them. I got books to read during the first two weeks post op when I was going to have to stay home: John Irving’s The World According to Garp, Jacqueline Suzanne’s Valley of the Dolls, John Cleese’s Professor at Large. None of which I read more than a few pages of. (Later someone told me that the meds, especially the prednisone, makes for a certain lack of  intellectual focus.) On the bright side, I never had problems sleeping during any of this, not even the night before the surgery.

So after 23+ hours—one night—in the hospital, I was home on the new single bed in first floor dining room. I had ice packs. I had no problems sleeping at night, but during waking hours I was supposed to elevate my leg for 45 minutes and then move around for 15 minutes. (And I did.) My legs were elevated on a pile of pillows and I did ankle pumps and more ankle pumps to keep the blood flowing. I was to eat several small meals throughout the day, take deep breaths and use a fancier than usual peak flow meter and monitor my results.  I hydrated and hydrated. As pre-surgery PT taught me, I walked upstairs leading with my good leg and led downstairs (as if to hell) with my bad leg. I hooked my operated leg over the good leg to get myself out of bed. I lived in jammies and sweats. On a scale of 1-10, the pain was maybe a 3 or a 4 at the absolute worst.

There are many ways to replace a hip, it turns out, and mine was a minimally invasive one-hour robot- assisted procedure, anterior approach, that required no physical therapy follow up.  Muscles and nerves are stretched and contorted but not cut, so healing time and risk of infection are minimized. I went home with no restrictions. My body told me what I could do.  That said, though, I don’t want to think about how violent, how brutal  cutting of the hip and the pounding of the femoral stem into my bone was; I am just grateful for the anesthetic. I mean, the sawbones really did saw bones. Years ago I would have been in rehab for weeks if not months. Because of the anterior approach, there was little chance of dislocation even when I did 90 degree moves. I bent over to clean the litterbox two days after surgery. I was careful but not immobilized.

Now is not a bad time to be sick if you have to be sick. Some things can be fixed. Although there is a certain Zen to all this DIY figure-it-out but in its way highly structured recovery, for me it was a good match. I took an opioid pill only three times, and looking back, I don’t think I really needed those pills. My leg never looked like the telephone pole I was told it would; it was a little swollen and sensitive, certainly with dark purple and black bruises, but I was not completely disabled, really, and the black and purple turned to green and yellow as my leg healed. By taking the opioids I was trying to get out ahead of the pain, something which I did not need to do and which, actually, is standard medical thinking of a bygone age, or so I have been told.  Off the major meds for seven months now, I still monitor what might be too much and, equally importantly, too little movement. Sloth is not my friend. Motion is lotion; rest is rust.

I folded up the walker and put it away ASAP before it became a clothes rack. I was just loopy enough most of the time during those early weeks from the prednisone (steroid), the meloxicam (atomic NSAID) and acetaminophen for the swelling to know I was pleasantly but not dangerously loopy.
I was walking without a cane in the house three days after surgery but kept it close anyway. I went up the stairs on the third day, too.

I shoveled out the car after a blizzard six days after surgery. Most of the driveway I left as it was; sooner or later, all the snow melts.

I got in and out of the car, just to see, five days after I got home.

These days motion is lotion as long as I don’t overdo. Limpy and gimpy no more.

The staples were the worst part. As prescribed, I took the bandage off five or so days after surgery, but I could not believe the staples. Think of tiny staples used on carpet but that caught on the inside threads of my sweatpants; the nurse who later removed the staples (and there must have been 20-30 of them) told me my leg muscles were sewn together at least twice below the top layer, but that was not the point. To me they looked too much like carpet tacks (well, staples) to belong on my body.

The cats Dr. Swishy and Moonbeam Nightingale served as furry caretakers, probably welcoming the hours of warm body heat at home 24/7 during a January blizzard. Granted, they had to learn not to sit on my left leg. They were good sports in the solid two weeks of kitty time-sharing. Swishy snoozed next to my pillow, Moonbeam next to my hip (not on it). Never have I felt as bonded to any pets. Anyone who discounts the power of purring/feline nursing and even a badly timed nose touch just doesn’t know enough. (And even now when I think it might be time to adopt cat #3, I have to remind myself how attentive and caring they were and how a devoted middle aged and a loving geriatric cat would react to a stranger cat, and I set that adoption idea aside.)

I spent two weeks answering texts from friends and family. I did not want or need anybody hovering. The internet can be a helpful and successful time-suck when you need one. Not surprisingly, there is no shortage of hip replacement t-shirts available, none of which I have bought although I have to grant some credit for their predicable cleverness: “Real Hips Are So Last Month.” “I Make This Hip Replacement Look Good.” “Hip Hip Hooray.” “Got Titanium?” ”Hippy.” “I Just Had a Joint.” “Bionic Custom Parts.” (My parts are made by DePuy Syntheses, part of Johnson and Johnson.)

I grant you that staying indoors for two weeks even in January might not have universal appeal. In fact, it is not an overstatement to say that in the history of the world, there may never have been anybody better qualified than I to spend two full weeks in solitude—in comfy sweats, no makeup, no small talk. 

I just wanted to be home alone to heal. Plus, there wasn’t much for anyone else to do, really.  I slept. I iced and iced. I watched British mysteries on my iPad. I remembered to hydrate, hydrate, hydrate. I walked around for 15 minutes every waking hour and then iced, iced, iced. I read very little and I wrote even less except to keep the required written record of what pills I took when and what exercises I completed during every waking hour.

My renewed after-hip surgery philosophy: comfort is good. Convenience is vastly underrated.

That said, I was more eager than I expected to get the evil staples removed two weeks after the surgery. Outdoors! A car ride! Fresh air! In-person company! After the staples were removed and I got the okay to drive, I drove myself to the grocery store—and then came home and slept for a solid two hours. Another week later I got into the pool for water aerobics (and ditto the nap). Range of motion came back. Stamina increased and I no longer wondered if I were anemic. The surgeon said the operated leg is a teensy bit longer than the other, but I can’t tell the difference. The scar has faded more than I thought it would.

For the most part during surgery and recovery I have let my introvert flag fly and fly. I did my best to pace myself, maybe going out for lunch and running a few errands. A walk around the neighborhood is still—but only sometimes--a preface to a nap. But then I have always been a napper. And I have certainly always been an introvert. All this is not a bad way to live. Now and then I still ice. On a scale of 1-10, maybe some days for a short while the pain is almost a 1; if I am sore after working out in the pool, it’s a different kind of pain than before surgery, and I know it will go away after some ice and a little rest.

Medically the verdict was out on the value of post-op new shoes but since my gait has changed, I decided to give myself the benefit of the doubt and bought some new ones: Ryka, Easy Spirit, and a pair of Tevas to replace my sandals that had been worn for years in tropical monsoons. My brain was fried  for longer than I want to remember by the meds (and by the pain before the meds), but that has ended,  and I do what I can to help the healing along. I eat well enough (what I think of as The Healthy Shit Diet). Right before the surgery, I was given a 6 month handicapped parking tag for my car which I did use; it’s the kind of thing that it is nice to have if only on principle. I didn’t use it often, but I liked having it anyway even if the other people who have them seem to drive around with them hanging from the rear view mirror and I have to wonder in many cases what stupid driving move they made to result in that parking permit. I still try to avoid people who seem to be coming down with something if only so my energy can be spent on healing.

At first I was wise enough to try to accomplish one thing a day: a trip to the pool OR to the grocery store OR to lunch. Since then I have increased what I do, so much so that most days I don’t even tally what I am doing: I just do things until I need a nap. I pace myself. Not having to think about—focusing on—lifting one foot from the street to the sidewalk, for instance, means I have more energy.

Touch wood, my new hip is fine, fine enough for me to dance in the kitchen when the spirit moves. I am not expecting to do cartwheels and backflips—skills few people need, after all—but I am no longer limpy and gimpy. My other hip is far from perfect but doesn’t hurt yet. (The surgery was a positive enough experience that when I went back to see the physician’s assistant a month or so after the surgery, I asked when I could have the other hip done. “Does it hurt?” he asked as we looked at the x-ray. No, I told him, but we both saw the bone-on-bone on the x-ray.) My knees still get medicinal WD-40 shots every six months and they do still pop and crunch every once in a while, but I have had crunchy knees since I was a teenager. Back to normal, mostly—but I still keep the cane in the back seat of my car just in case. For now.  I still take glucosamine and chondroitin, and calcium, magnesium and zinc, and I still go to the pool water aerobics class to bounce around to “The Eye of the Tiger”. Other students in the class complain about the temperature of the pool, but I am grateful and more grateful, as I step off the ladder into the water, for the comparative weightlessness (15%) the pool affords me for an hour three times a week: blessed chlorinated weightlessness. I stretch and stretch some more and then we bounce around. Walking to and from the parking lot to the pool doesn’t hurt any more.

A body in motion tends to stay in motion. This is all still novel enough that I think of my life as BH and AH—before hip and after hip surgery. I still like having big chunks of time to myself and the cats are still often in Full Cozy Mode. Strength and range of motion are returning. These days, uninterrupted by pain and with most of my marbles back and functioning post-major surgery, I am back to following an idea where it will go. I am long back to making lists and starting to get things done. I like living in a way that does not require me to move (or do anything) on a prescribed post-op schedule. I have never bounded up stairs like a mountain goat and I don’t care if I do. But I can go up and down stairs with no pain even if I am still a little more tired at the end of the day than I remember being, say, a couple years ago.

For now, the new bed stays in the dining room just in case. The motion sensor lights still make a lot of sense: ease and safety in the dark.  My housekeeping has returned to its standard: good enough. I can haul around big bags of kitty litter when I have to, but right now I can’t imagine running with a backpack from one end of an airport to the other end (and somehow this is always necessary, no matter how carefully I schedule my flights) or hauling a suitcase up two flights of stairs in a beach hotel in Maine--but eventually I will be able to. I am still in the pool and I’m back functioning in gravity, too. I go for leisurely walks. I try not to sit any longer than I have to. I remember to stretch.

I am easing myself back into the world. I do care that I can walk and not worry about walking. I can look around. I went to the movies. I went to an Elton John concert. I go out to lunch, and if I haven’t driven to Maine yet (too much sitting makes for stiffness), I have almost gotten there. I don’t feel immobilized any more, but I am smart enough to be careful even though I have risked tempting fate and have moved the surgery-related pills (even ibuprofen and acetaminophen) from the handy top of the microwave to the back of the medicine cabinet. I use the hip surgery ice packs on my pulse points in the summer heat.

For the first time in a year and a half I got Chinese takeout.

I mean, this was major surgery, and the surgeon said it would take eight months to completely recover, which means mid-September. Even though that rule of thumb comes with a lot of it-depends-on-the-person caveats, I think it will prove to be right. Fingers crossed.

Looking back, I like to think that I already a brain and a heart and courage, and the surgeon gave me a new hip.  Other people pay for tattoos, but I have a four-inch scar, a fading decoration that I am proud of. (Thank you again, Excellus Blue Cross-Blue Shield Medicare, which yes, I do pay for.) I have learned that yes, really and truly motion is lotion and if you snooze (so to speak), you fuse—or at least get stiffness, not pain, in the morning.

The one thing I did not realize until very recently is the extent to which the surgery itself is just the beginning. What happens after is just as important: a matter of a way of life. And time.

And my new hip was a little more than a year after the gods gave me new eyes via cataract surgery that made my vision 20/20 without external lenses for the first time since maybe third grade. Yes, my eyes were always correctable. But really, a lens on your eye is not the same as one in your eye. It just isn’t. I had my cataract surgery right before Christmas 2017, and at odd moments I still find myself marveling at how much I can see even though I don’t mention all that I am amazed to see the way I did that first Christmas. (So much so that I was told to shut up, a very unfestive response.) I don’t know if I will ever be able to take my vision for granted the way most people do.

And maybe not my new hip, either.

I know that in January I will celebrate my hipaversary just as last December I had a glass of wine to celebrate the one year mark of my new replacement lenses—“my new eyeballs” as I think of them.
The gods gave me new eyes but then made it difficult for me to go anywhere without pain. And then there was a stretch of too-easy exhaustion despite a pain level of basically zero.  

Hmmm.

One morning during the first week, maybe the third day after the surgery, I tried sitting in a kitchen chair and moving my operated leg as if to depress a clutch. I could move my leg kinda sorta but it had little strength. I went back to bed.

A week or so later, though, I tried again, and my leg had more strength, enough that I decided that I could probably depress a real clutch. A few days later I went outside in the January cold and into the car to see if I was right.

I could depress the clutch.  And so I was certain that I would be able to drive again, maybe sooner rather than later and maybe not, and all I had to do, was…well, live long enough.

As I said, I still try not to sit very long if only because I feel stiff when I get up. I still hydrate and hydrate. I can tie my shoes and put on socks with far less pain (and the seconds of pain are lessening). I get in and out of the bathtub/shower without even thinking about it. Standing, I write on a yellow pad on the kitchen counter. Moonbeam sits on her chair near the refrigerator and Swishy is stretched out on the floor. My passport is stashed in its usual place; it replaced the one that I had to have extra pages put into a few years ago (a practice now discontinued, by the way) since there were just too many visas and stamps in it.

To answer the question I have been asked again and again, more than any other, especially since in retirement my time is finally in many ways my own: I don’t know exactly where—what places at any distance or even nearby--I am going to next in this world of gravity, but I know that sooner or later, after a little more time passes and assuming things go as I expect, I am going to be back to going.

And so yes: hip hip hooray, indeed.

Copyright Sandra Engel
July 2019