Visit with Retinal Specialist

I just returned from my appointment with the retinal specialist. I can barely see the screen because my pupils are dilated. So this will be short.

There is no more fluid behind my right eye causing the retina to partially detach. Last time the chorioretinopathy bloomed (about six weeks ago) the red dot splashed across my vision, then faded for the next few weeks. There is no more fluid, yet I still see the (smaller) red dot.

Diagnosis: scar.

I hope the scar (or tear mark, or whatever) will heal over time. Until it does, the optical illusion of the red dot will be there. [Rats.] This might be a while.

As for my eyepatch and flashing lights, the fact that I only need it later in the day should have been a clue. I talked for a long time with the doctor about this. Fatigue is the culprit. My right eye has minor damage now, so it will show signs of fatigue (the throbbing and then shocking pain) before my left eye. The right eye just gives up now as if it were the loser of a nightly Survivor challenge. It slips and falls, allowing the left eye to claim the immunity idol.

So my orders are to decrease stress and get plenty of rest. Taking two aspirin and calling him in the morning was probably implied too.

Early Blog #7 (The One with the Llamas)

Almost done posting my old blogs. This is easily one of my favorites. This was written over two years ago:

TUESDAY, OCTOBER 13, 2009 8:03 AM, EDT

This morning (Tuesday) I still woke up first, but I was smart. Last night, MJ helped set out my morning comfortable outfit right next to the bed. Noah's pills were sorted and ready to go in a dish. I had located his Kong toy and had that set out already too, filled with peanut butter. So when I arose at 7am, I walked carefully downstairs, retrieved the paper from the front porch, took care of Noah without needing to look for anything, and went straight to the couch to lie down, do the crossword, and begin typing this without getting dizzy.

I am starting to love this journal, finding it is a way to put myself back together after such a scary journey. Nothing but down-time, nothing to do, and nothing you are SUPPOSED to do is a new experience for me. Again, it is the little things I must let go of for the time being, and it gives me a new clarity about my big picture. I don't fret about the second-by-second unfolding of my life right now.

The few days leading up to the surgery are still fresher in my mind than the days after the surgery. From midnight to 3:30am on Thursday, October 1, I had eight different MRI tests. A few hours later, at 8am, I got the call with the news about the "mass" under my brain, and surgery was quickly scheduled for the following Monday due to the tumor's size and how quickly things were changing with my vision.

With nothing but a few facts to chew on and an Internet connection, I naturally spent the following days secretly googling everything I could find. Googling things you barely understand is bad for your health, and it is also how bad political blogs get started, by patching together bits of truth that don't quite match.

My biggest fear was there was some kind of conspiracy about the simple nature of the operation. The removal was supposed to come out through the nose (which it did) but I worried incessantly that something would go wrong. The tumor was already unusually large for the area. It wouldn't fit out my nose. They would have to do an emergency craniotomy and cut the front of my forehead off, push my brain to the side and retrieve the tumor that way (the way it used to be done). I had nightmares about this.

When I arrived on Monday for pre-op, the first thing I was given at check-in was a standard sheet to sign where the top had been filled out in handwriting with the procedure I was agreeing to. The sentence read, "Transphenoidal approach and craniotomy for tumor removal."

Being a stickler for spelling, I did not appreciate (right off the bat) that "transsphenoidal" was spelled with only one "s." On top of that, why was a craniotomy mentioned? My nightmare was unfolding before me. As I glared at the sheet, someone approached me and asked for me to come out of the waiting room and into pre-op.

I said, "I have a question, and this is a big one. It says 'craniotomy' on this form I'm supposed to sign. That's where they cut your head completely open. They didn't tell me that."

The raucous waiting room fell silent around me like in those old E.F. Hutton commercials. MJ, who hadn't seen this yet, looked up from her book.

"Don't sign it yet. You can talk to the nurse about everything and have ALL your questions answered."

"Okay," I said. I was completely ready to bolt, go home and start over again with another opinion, but I saw no harm in walking to pre-op and talking further with someone more knowledgeable.

I was escorted to a private cubicle surrounded by curtains and sat upon a comfortable hospital bed with pillows. I took my clothes off, put on a hospital gown and waited, the unsigned form clutched in my hand.

A friendly middle-aged nurse entered, bearing a wide smile and nurturing eyes. She said, "I understand you have some questions, and we can talk about anything you want, for as long as you need."

I explained my concern for the word "craniotomy." I was not ready to have my head sawed open. No way.

"Well," she began, "a 'craniotomy' is actually a broad term for anytime they go inside your head. You are having a transsphenoidal approach, going in your nose. They have to make a tiny puncture to a small eggshell-thin skull bone in the back of your sinus cavity. Because of that little puncture needed to go inside to get the tumor, it falls technically under the BROAD term"—she held her hands far apart—"for 'craniotomy.' It's just a term."

She spoke so carefully, smiling all the time, looking so deep in my eyes.

I flapped the paper in front of her. "This doesn't mean they're going to cut my forehead off?"

"No."

I trusted her. We talked about other things. She asked me questions about medicines I took, whether I smoked, drank, used recreational drugs, feared for my safety at home, and general questions about what kind of life I led. I felt better. I signed the form. She brought my wife in to sit with me and began setting up an IV.

The anesthesiologist made an appearance and asked me questions. A lot of questions about what would make me comfortable during the wait.

I cut him off with, "Look, anything you want to give me is FINE with me."

He made his hand into the shape of a toy gun, playfully pointed it at me, and squeezed his thumb trigger while smiling. The nurse left with him and in a few minutes she was back holding a syringe.

"Fentanyl," she said, and put some into my IV.

I didn't know what this was, but it sounded good. I was still nervous, even if the conversation had calmed me down. In a minute, I was flush with euphoria. I wanted to hug everyone in the world. I was so happy! Love was everywhere, big red hearts popping out of the walls.

A friend had also joined us by now, and the four of us rejoiced, laughing about things, about the mysteries of life, how little we were when you compared that to the size of the universe. It was the best time of my life.

"We should totally buy a boat!" I exclaimed. "We could all live in a boat from now on. All four of us from now until forever. Why not?"

"Sounds great."

"With llamas," I added. "No one ever thinks about a boat with llamas."

MJ said, "You could scrape them in the winter to get wool to make sweaters if it got cold."

"Yes!" I exclaimed. "It's so OBVIOUS! We could all live on the boat with the llamas and make sweaters!" I eyed the syringe now sitting atop my blanket the nurse had only half-dispensed into me.

"Damn, woman!" I added. "You holdin' out? You an' me gonna get hooked up after this, you dig? You gonna be my CONNECK, ya hear?" I pointed between MJ and the nurse. "You two get hooked up, okay? That right there!" I pointed again at the syringe.

The nurse picked it up and slipped it safely in her blouse pocket.

"Oh, man," I said and leaned back, dreaming of our life on a boat.

I wondered again about the word 'craniotomy' on the form. I thought it might be cool after all if they sawed my forehead off. They could put a hinge on top and I could flip it open and shut at will. At parties, I could say, "I want to give you a piece of my mind," then flip my head open to get a reaction. Fun, fun, fun!

In another short while the anesthesiologist came in again and gave me something else. The nurse also put in the rest of the Fentanyl. I laid back again, looking into the sweet female faces surrounding me. I closed my eyes in utter bliss. If I didn't make it out of surgery alive, I had already lived a blessed and wonderful life.

Early Blog #6

This blog from two years ago generated plenty of interesting comments at the time. The days following my first surgery I was compelled to write about some heavy stuff. Here it is:

TUESDAY, OCTOBER 13, 2009 12:06 AM, EDT

Monday night, late. Having trouble sleeping. I am doing my part by staying horizontal most of the time. My pain is still very present in the form of headaches and body aches, but it is more predictable and manageable than before. The pills they sent me home with do the trick for the meantime. I know when the pain is coming and I can stay ahead of it. The dizzyness is getting better and my vision is (miraculously) almost back to the pristine state it had been in when I aced the vision test for my pilot license. I can see colors again now, vividly.

Laying flat with nothing to do all day gives you plenty of time to reflect. On the Friday before my head surgery I needed to be cleared with a general physical to see if I could make it through such an invasive procedure. It was basic stuff like blood and urine tests, an EKG, blood pressure (high, as usual) and going over all the prescription medications I currently took to help with hypertension and asthma.

The most interesting part of the physical was the check-box questions you had to fill out. I had one sheet I worked on and the doctor had his own sheet. He asked a lot of the same questions.

"Tobacco user?"

"No."

"Alcohol?"

"Oh, yes," I said.

The doc looked up from his paper to study my response more closely.

I pointed to myself. "Musician," I said.

The doc checked the box and asked, "How much?"

"Two, three glasses of wine with dinner."

"Okay. Any more than that sometimes?"

"Usually," I said.

I imagine he put a star by that one. Then he moved on to a series of questions about my home life. Did I feel in danger at home? Physical or emotional abuse a constant worry, perhaps? There were several questions which came at this subject from different angles. I could have had a field day with this line of questioning about fifteen years ago, but things are great now so I answered, "No."

"Any thoughts of suicide?"

"No, not for a while."

He studied me closely again.

I said, "It's a no. Just check the 'no' box."

I must have been in some kind of a mood to play with that one. But, in reality, as I drove away from the doctor's office to do my final duty at a nearby lab—peeing in a cup—I thought the answers to these 'yes' and 'no' questions were so over-simplified.

No more than a few years ago, when my chronic pain issues from a botched hernia repair surgery overcame my body so completely, I found myself on our porch, an ice bag over the surgical incision and a pain pill in my system doing no good. I had my laptop with me and, more out of curiosity than anything else, I typed "suicide" into the Google search engine. I just wanted to see, nothing more. I felt trapped in a world of pain.

I had spent years already pursuing every way out of this and could not imagine the rest of my life being the way it felt on that very day. I wasn't even close to snapping; I was just curious what people did when they eventually reached a point where they could not go on. I just wanted to know what the protocol was, how you were supposed to go about things if such and such never turned around for you.

The web sites which came up right away were, of course, not instructional but interventional. "Visiting this website is a BRAVE and POSITIVE step. You are ACKNOWLEDGING you need help, and here are all the ways you can get it, etc.."

MJ came out to sit on the porch with me that afternoon. She knew it was a bad day for me pain-wise and she had been making me a bowl of freshly cooked chickpeas drizzled with olive oil and sprinkled with fleur de sel and cracked pepper, one of my favorite surprise snacks. I erased my browser's history, closed the laptop, and we sat and talked while I ate the chickpeas and felt ice melt over the tangled nerves at the spot of my hernia repair.

Another time, in eighth grade, I brought home a report card with a C-minus in Human Development. (I think the course was called, "Discovering Me," actually. It was basically sex-ed.) Worst of all, this C-minus dropped me into the second quintile in my class, an unheard-of shame in my household. When my mother would see this at dinnertime I knew a) she would probably kill me, and b) my father would not stop her.

I had nowhere to turn. After arriving home, I took a glass of tap water into our utility room in the basement where tools and miscellaneous cans and jars were kept. I found something with a poisonous skull and crossbones on the side. I opened the drip spout on this container and watched a small, solitary drop fall into the glass of water. I swirled the glass.

"Oh, God," I remember saying.

My hand trembled so hard I could barely get the glass to my lips. I took a tiny sip, then doubled over, crying and spilling the rest of the water on the floor. I knew I had just done it.

My brother came downstairs and we proceeded to watch the one hour of television we were allowed on school nights before homework: a half hour of Gomer Pyle, USMC (my favorite) followed by a half hour of Get Smart (his favorite). As the shows aired, I wondered how it would happen, how I would die. I imagined something sudden, like the birthing scene in "Alien" where my chest would break apart with guts spilling into the room. But of course nothing happened.

Dinner, even, was quite tame. After the salad, my mother picked up the report cards, surveyed the grades, looked me over sternly when she saw the C-minus, then put it down without comment.

The next day in class, I asked one of the most popular boys how he had done in "Discovering Me."

"D-plus!" he said triumphantly. "Fifth quintile." He clenched his fists and pulled them repeatedly towards him as he pumped his hips. The rest of the class took notice and egged him on.

The truth is, as good a student as I was at the time, I more than deserved the C-minus. Not yet aware of my own dyslexic tendencies and how to overcome them, I had run out of time on a paper and resorted to plagiarizing a whole paragraph, something I had never done before nor since. The teacher surely knew this but did not call me on it. The C-minus should have been an F, and I knew it. A deep shame about the sanctity and sacred quality of one's own work crept into me that day and has never left.

So it is, indeed, silly to check boxes, defining your life as a series of 'yes' and 'no' answers to questions that are rather blunt. It is so much more complicated than that.

Early Blog #5

I have a few more early blogs to bring over after this. This is me writing two years ago:

MONDAY, OCTOBER 12, 2009 7:18 AM, EDT

It is Monday, only three days out of the hospital, and I have already done something stupid. I'm still a patient recovering, and I should be staying horizontal as much as I can, doing nothing but resting, especially for the next two weeks. MJ is helping with everything.

I woke up at 6:15am and decided to go downstairs while MJ slept. I scratched Noah's ears, one of those simple pleasures I love in the morning, and he followed me around as I tried to do a normal morning routine. He got his pills, but I could not find his rubber Kong toy which I put peanut butter in for him to play with every morning. Sometimes it rolls under a chair on the porch, so I did a lot of standing up and leaning over, looking for it.

It made me dizzy.

I found it in the living room eventually. I smeared peanut butter in there and gave it to him. I tidied up a few things in the kitchen and noticed an overhead lightbulb needed changing (one on the ceiling only I can reach). I retrieved a new bulb from the pantry, stretched up, changed it and took the spent bulb and the cardboard box out to the garage. I threw away the bulb, put the box in the recycling bin, then started to walk inside.

The world turned upside down.

I don't know how I saved myself, but in a split second my head made a beeline for the concrete. I somehow regained control and carefully made my way back to the couch where I am now lying, feeling extremely dizzy. My spinal fluid is probably still leaking, wounds still healing, and my brain is still trying to figure out what to do with the extra space in my head now that the tumor is gone. MJ came downstairs soon after, made me tea, and I am once again committed to being a patient patient for the rest of the day.

It is strange how much of the little things I cannot resist getting involved in around the house—changing lightbulbs, etc.—when I see they need to be done. The major decisions of rehabilitation (like taking time off from work or not driving) are easy. But the tiny things are hard.

Last night, MJ and I had a quiet evening where she grilled some perfect steaks (usually my job), and they came out better than if I had cooked them myself. Also, MJ made the fire in the living room which is always my job.

I wanted to do this while she cooked, but lifting logs and stoking the fire are strenuous things I simply cannot do for now. I watched as she tilted one log straight up and added another. I knew this was the wrong way to do it, that the fire would die. I didn't say anything, thinking she would find out the hard way and learn. It was the way I learned to make fires: by trial and error on my own.

A few minutes later, to my amazement, the fire caught on again. It was not the kind of fire I ever made, but the vertical log began to burn with this sinuous flame that rose up from somewhere beneath it and swirled around the log sensuously before the flame disappeared on top. It didn't ever die. It kept burning and burning in this odd arrangement and it looked so alluring. I couldn't take my eyes off this simple, beautiful thing she had made using only her instincts.

I do spend a lot of time micromanaging and analyzing things, I suppose, and when I was in the hospital it is a wake-up call to have the tables turned on you. Maybe this happened the second day after the surgery, but a female doctor popped her friendly head inside my room and asked if a group of med students who wanted to study my case could come in.

"Sure," I said, groggily.

In a few seconds, the room was filled with a half-dozen young people in white coats, each wheeling in portable lecterns supporting their laptop computers. They surrounded me in a semi-circle around my hospital bed.

The doctor rattled off a number of things very quickly: "Male, 41 years old, 6'3", 230 pounds, history of hypertension, cough-variant asthma, allergic to caviar, dogs, cats, dust mites, trees, no known drug allergies, transsphenoidal approach for removal of pituitary tumor, pathology not back." The students tapped away on their keyboards.

It all seemed so deeply personal, how quickly this information was landing with strangers. I imagined her continuing in the same breath: "Childhood in foreign countries, caught playing with himself at thirteen, never gotten over it, adolescence of sheltered suburban paranoia and guilt coupled with a curious and intelligent disposition led him to break away from everything expected of him, pursued a career in music and embraced relationships with progressively destructive women until it all blew up in his face ten years ago."

I imagined the students tapping away some more, totally serious and intellectual. No one asked me anything. A few looked up from their computers to get a mental image, but mostly they stood and typed.

"Thank you," the doctor said. She waved and the students wheeled their portable lecterns out of the room efficiently.

Yesterday afternoon I looked in the mirror and noticed I will have a battle scar to show for last week. The bottom of my right nostril has a notch. A few days ago the surgeon removed the packing from my nostrils and sinus cavities. Dried blood was everywhere inside my nose. I am not allowed to blow my nose or clean it because things are still healing, but the outermost scab has fallen off. Sure enough, there it is in the mirror: a wedge of flesh missing from my face. A notch.

About 25 years ago, the time when my father first knew he was succeeding in business for real, he built a new home for our family by a lake. My mother's dream of planting and gardening went into full swing and they built a gazebo out in the yard so they could sit in the evenings amidst her creations, talking about things. His most notable animal friends out there were the two chipmunks Notch and Ragtail, nicknamed for their respective appearances. Ragtail had a tail almost devoid of fur, and Notch, his favorite, had a chunk of his ear missing. I always wondered what had happened when Notch lost the tip of his ear. My father would bring some peanuts in his pocket on the evenings they sat out there.

"Notch! Notch! I have your peanut!" he would say.

I was gone at Juilliard by this time, but when I was home for school breaks I could see this firsthand. A chipmunk would appear in the distance and see my father holding up a peanut between his thumb and forefinger. He would tap the peanut with another finger. The sound of the rattling nut cutting through the still air would prick Notch's ears to full attention. Notch would run quickly across the yard, crossing half the distance in no time. My father then placed the peanut inside his shirt pocket. Notch would slow down, climb up onto the gazebo, up the back of his chair, over my father's shoulder, go into his shirt pocket, emerge a moment later with the peanut in his mouth, then scurry back to his nest. This repeated a few more times every night until the peanuts ran out.

Ragtail sometimes got in on the action, but Ragtail was always more reserved, watching over things as they unfolded. I sensed my mother took a liking to Ragtail's caution while my father enjoyed Notch's initiative and ingenuity. For all I suspect now, Notch and Ragtail were a couple.

As I study the new notch outside my right nostril, I know I might be asked about it in the years to come. I don't have other visible scars, and since I never excelled in sports or got into bar fights I've never had to deal with a battle scar. I suppose it's the sort of thing other men do—telling stories of how they got this one or that one—and on some level I always wished I could join in with that, telling an inaccurate, elaborated story about a fistfight, an attack by a wild animal or a cheap swipe from an opponent's hockey stick.

But if I am asked about my notch, I can say I got it when they took a golf-ball-sized tumor out of my head. That will surely shut anyone up.

Early Blogs #3 & #4

More from over two years ago. These are the first two blogs I wrote after coming home from the first brain surgery (October 10 & 11, 2009):

SATURDAY, OCTOBER 10, 2009 2:47 PM, EDT

It has been a day since I decided to come home to continue my healing. One thing clear to me is that I am still a PATIENT. The familiarity of my surroundings at home encourages me to get back on my horse, doing normal things like filling Noah's water dish or answering the door. In reality, even simple tasks like this are difficult.

Last night I went straight to the couch, ate a plate of roast chicken MJ made for me, watched "The Office", then went to bed with a a pain pill. I woke up at 4am, disoriented, and needed another pill for my splitting headache. At 5am (my usual waking time where I use the morning hours for seeing after Noah's morning routine, composing, and relaxing with a crossword puzzle) I was encouraged to keep dozing in bed while MJ took care of Noah.

I got up at 7:30am and used all my power to get down the stairs and lay flat on the couch. Having switched to oral medications (which are weaker and less responsive than intravenous) I feel achy and also like I have received one heck of a punch in the nose (the entry site for getting to the tumor). I feel like Mike Tyson, only without the tax issues. Actually, scratch that; I feel like Mike Tyson.

As I lay on the couch, MJ brought me hot ginger tea and a cold glass of authentic apple cider. After five days of sickly sweet hospital apple juice, this was more welcome than you can know.

I have spent a quiet morning and afternoon reading and catching up, but other things will have to wait. A pile of mail sits unopened on the stairway going down to my desk. I won't worry about leaving it that way for a few more days.

I did the entire Wall Street Journal crossword puzzle in one sitting, and it was while doing this that I noticed my eyesight was better. Even though I still have dimness and color loss in my left (dominant) eye, I was able to read the print clearly. Most importantly, the "depth of field" was coming back. I held the paper at various distances from my eyes and I could focus on the words. Previously, I could only find one fixed distance from my left eye where things were in focus.

The pathology came back on my tumor but it is even more confusing now. We do know it was a tumor, but it was not a traditional pituitary tumor. It grew right next to the pituitary gland and crushed it (making it look like a regular pituitary tumor) but it did not originate from it. Comprised instead of "dead ghost cells" around which a cyst or cysts were forming, I know my case is now being sent around the country to people who study atypical tumors like mine. Complicating this, the spinal cord leakage was adding another veil to the case. Once again, my medical issues place me in the 1% of cases that don't fall conveniently into a single category. The good news is in all likelihood my pituitary gland will be able to spring back without a lifetime of hormone replacement therapy. This is very appealing, but I still want to know just what the heck it was in the first place.

So, things are getting better. But I still feel awfully dizzy every time I stand up, and I am still supposed to spend the majority of my time in a horizontal position. I'll probably watch a movie this afternoon and sleep some more. There is no replacement for solid stress-free rest.


SUNDAY, OCTOBER 11, 2009 9:54 AM, EDT

Sunday morning. One way I can judge the past week is how fast Sunday has rolled around again. All Sundays have special pacing. For me, it's the extra time in the morning with the paper, a larger breakfast, and (in the Fall) the Detroit Lions games. It seems way too soon for another Sunday to be here already.

Last Sunday was my final day before surgery. I was nervous and also in denial about what I might be up against. I tried to make it as normal a day as I could. MJ and I watched the Lions lose another game and she made me a special old favorite: bone-in pork chops and macaroni and cheese, her father's recipe. I was not feeling very well all day. I had terrible headaches, deafening ringing in my ears, and my vision was so disorienting I could barely read or use my eating utensils without dropping food.

What followed the next six days was a blur I am still sifting through. It is all just images now, popping back in my head randomly yet with clarity. I am trying to remember when certain things happened. My memory has always been good, and as I continue to rehabilitate at home I'll have a lot of time to reflect on what happened last week.

Monday night, after the surgery, is coming back. This was one of the worst nights of my life. I remember being wheeled into a bright room filled with advanced equipment. Already feeling the effects of drugs designed to calm me down, I carefully hopped across onto an operating table. The anesthesiologist handed me a breathing mask and told me it was just oxygen and to breath deeply. I did, and continued to look at the computer monitors and bright lights overhead. Soon, my lower jaw would not move. After another breath I felt extreme pain. I opened my eyes and found myself in a different room. I screamed and someone injected something in my IV.

"Is the surgery over?" I asked.

"Yes."

"I'm so thirsty. Can I have a sip of water?" A straw was put at my lips and I sucked. The pain seared back through my head and I screamed again. Another syringe flashed in front of me and I felt better. I asked again if the surgery was over. I could not believe it.

For the next bit of time (I have no idea how long any of this took) I kept asking for more water, more water, and the pain never ended. They wheeled me to a critical care room in the neurological wing then brought in my wife and a friend who had sat with her the whole time through my surgery.

I needed more water and kept asking for it. Pain relief and water was all I wanted. I never knew who the people were around me because it hurt to open my eyes. Soon enough I could hear MJ's voice. Another straw was put to my lips and I sucked down a full glass of water and then gasped for air. I felt my wife's hand, clenched it, then felt for her friend's hand and clenched that too. I held both so tightly and cried out.

Not much else is clear, but later that night MJ had gone home and I knew I was alone with a nurse. Every time I woke my mouth was dry and baked. An oxygen tube dangled in my mouth because my nasal passages were sealed shut with surgical packing. I lay flat on my back and often my tongue would fall to the back of my dry throat and stick there, cutting off my air supply. I would jolt awake, gasping for air, begging for water, sometimes chewing on the oxygen tube in desperation. Then a sear of pain would hit. Then a syringe would flash by again. Then the whole process would repeat and repeat.

One point during that first night, I opened my eyes to see the nurse studying me closely, standing up and taking notes on her laptop which sat atop a lectern. I was so disoriented. All I remember asking over and over again was whether my dog was at the foot of my bed, whether he was okay, and whether she had given him his evening pills. I asked her this over and over, and she typed notes about this on her laptop.

One thing I never would have predicted last Sunday was that I would be walking outside on my own today—this Sunday morning—retrieving the paper from the driveway and sitting down with it in my Lions sweatshirt, sorting through the various sections. I continue to be dizzy taking even short walks to different parts of the house, but the thought that in one single week a tumor has been extracted from my head and I am thinking normally and doing normal things in my own house just amazes me.

Early Blog #2

Saturday, October 3, 2009, 6:06am

Saturday morning. Two days until surgery.

It was only two days ago that I received the phone call from my neuro-ophthalmologist informing me of the findings of my MRI the night before. Up until the call, a tumor was as far away a diagnosis as I could think of. For the week before that, all signs pointed to multiple sclerosis (MS) as the likely culprit, something I was keeping secret from most everyone.

The phone call began like the old SNL sketch where a slide whistle played to indicate the actors' sense of hope: "Hi, Mr. Miller. I have studied the MRI." [Whistle up a third.] "You do not have MS." [Whistle up another third.] "You have a mass in your brain." [Whistle drops all the way down.]

The neuro-ophthalmologist told me someone would be contacting me shortly to make arrangements for MJ and me to meet with a neurosurgeon to discuss options. The meeting was in a few hours. I broke down after hanging up the phone. MJ held me and said we would get through this together, the same way we always got through things together.

We drove to St. Mary's Hospital's new Hauenstein Center, a major step up in luxury from the main building Grand Rapidians have gotten used to over the years. I noticed it had the calming ambience of a nice resort hotel—not a hospital—as we waited for the consultation. I half expected someone in a white coat to walk by with a tray bearing two coconuts with straws coming out the tops.

From the start, I liked my neurosurgeon. Of course, in this day and age I had googled him prior to the meeting, reading about his background and his rating from past patients. No red flags. He had a cool, detached, and intelligent presence. He wasn't pretending to be my best friend. I like my surgeons (and I've had a few) to be that way. Other doctors I want to have more of a connection with, but I want surgeons to think of me as a cellular structure. While he went through the motions of asking standard questions about allergies to medications, I caught him studying different spots around my eyes and nose, pondering how he might get his sharp little instruments in there.

He ordered a panel of diagnostic tests, the most important being one to rule out a prolactinoma, rarer in men because it makes you produce breast milk. Prolactinomas are treated with drugs and ESPN, not surgery. Once we knew it was not this, surgery was the only option left to get the tumor out. Even though it was probably benign, it was growing. It already made me half blind in one eye, and it would only continue to grow. One way or another, it had to come out. Since it rested just behind my sinus cavity, it could be extracted by going in my nose, tapping through a thin egg-shell-like bone, and carving it out.

Since I play the oboe for a living, it concerned me that any surgery dealing with my mouth or my sinuses (if it went wrong) could destroy my career. My neurosurgeon offered up the one alternative method—more rarely used—where you saw off the front of the forehead, push the brain to the side and reach down between the eyeballs to pop the sucker out. As he described this, MJ became intensely interested in her newspaper. I thought about it for a moment and told him we would prefer the first method.

At the end of our meeting, I asked if we could see the MRI.

"Sure," he said. "Follow me."

We went in the next room where large computer monitors flickered with black and white images of human anatomy. The screen he went to displayed a close-up of obviously someone else's neck. Most notably, I could see a metal plate and two screws holding this person's vertebrae together. It looked gothic, out of a horror movie, though certainly that patient is grateful for the things modern medicine can do for people. He closed the image and searched for my file.

"Here it is," he said, and stepped back.

The MRI showed my tumor, larger than I ever thought would be. It sat there, bulging and taking up all the free space behind my nose and eyes. About the size of a golf ball, I thought. As I looked more closely, I could imagine little blood vessels spelling, "Titleist." So there it was: at once part of me but also my foe, the enemy within.

"How long has this been there?" I asked, incredulous that something like that could be inside my head, unnoticed.

"There's no way to know," he said.

My First Blog

Some readers don't know this, but there were a few blogs I wrote prior to creating my own website here at Husband Amused.

In the next few days I will copy those blogs over here so all my writing is in one place.
I am still waiting for the results of my latest blood test (measuring testosterone) and my appointment with a retinal specialist is next week.

In the meantime, this is my very first blog, the words I wrote three days before my first brain surgery. From my perspective now—with everything I have learned—I can't believe the light-hearted tone of it, but I have always used humor as a coping mechanism when I am afraid of the unknown. For what it's worth, enjoy!

FRIDAY, OCTOBER 2, 2009 8:43 PM, EDT

Hello, friends and family, and welcome to my brain tumor surgery journal! Today is Friday, October 2, 2009 and my surgery is scheduled for Monday. This means I have the whole weekend in front of me to party. Actually, make that par-TAY. A nurse called me a little while ago to give me instructions for my big day: "Nothing to eat or drink after midnight Sunday night," she said.

I asked, "But before midnight everything is okay?"

"Right."

"I can eat or drink ANYTHING right up 'til midnight?" I pressed.

She paused, then said, "Yeah, I guess."

Bingo. Jello shots @ my place. 11:59pm. Bring togas.

Eh, rewind. This is serious. But the only way I can deal with serious situations concerning myself is to treat them with self-deprecating humor. It helps me but it is hell for my acquaintances.

The past two days, unsuspecting friends have asked, "So how are things?"

“Okay,” I reply. “Brain tumor. You?"

I hear a sudden choking sound when I say that. It’s the sound of being punched in the gut, a deep inhale and a jammed garbage disposal all rolled into one. I love that sound.

After all, what is one supposed to say when a friend reports to you with a brain tumor? “Sorry” doesn’t cut it. “Sorry” is appropriate for minor inconveniences like Internet interruptions or air conditioner malfunctions on hot summer days. “So sorry” is what friends say about your sick relatives. For immediate family, the standard nowadays is, “Oh my God, I’m sooooo sooooorrry,” and to couple that with a meek gesture of the forearm where you helplessly reach for (and miss) the elbow of the griever.

But what is one supposed to say about a brain tumor? Like the guitar amplifier turned to 11 in "Spinal Tap," there is only so much longer you can stretch out, “Soooooo soooooorrrry” before it crosses the line dividing sincerity and mockery. No one wants to make that faux pas, so they don’t go near the line. What is left (besides the aforementioned choking) is nothing. “I don’t know what to say,” “Oh, man…” “Whoa,” or “H-o-l-y…” are the most common.

For me, rest assured this part before the surgery is easy. The nice thing about my brain tumor is it is everything you could ever want in one. Benign. Round. No bigger than a ping-pong ball. Accessible through the nose, so no nightmares about nasty drills or saws. And this tumor is not IN my brain; it is UNDERNEATH it, pressing upwards on my optical nerves and causing my vision problems. The location of the tumor behind my eyes makes extraction a little dicey, but the tumor itself is awfully boring. If something this ordinary grew on your leg you could get rid of it with a box-cutter and Windex.

If you are still reading, you are someone who understands me. You know how I cherish paradox.

My plan is to use this journal as much or as little as I feel, in a way that will help me through this so others who care about me will be helped too. I have always taken joy in writing irreverently about my life experiences. I have no intention of doing otherwise at a time like this.

Peace, Ale