Room full of notes

The opening paragraph of a Brick’s Picks in August 2009. The room full of notes was from a very cool if disturbing visual hallucination I had at a Charles Owens gig at the World Stage back in 2006. Epilepsy…that was a bad year. Seizure activity all through the brain with lots of odd effects. I remember I was standing next to Chet Hanley at the time. As he didn’t mention seeing the room fill up with the notes pouring from Charles Owen’s horn like bubbles I decided not to mention it. I just took another pill. I’d forgotten all about this until reading this again just now. But I remember it was about that time I realized I better not stick with the jazz critic thing much longer. I did, though, for four or five more years. Anyway, I never had another visual like that. A little too Lewis Carroll for me.

We dig saxophone. It’s the iconic jazz ax. Trumpets were once, a long time ago, and clarinets had their sweet little run too. But once solid hard-blowing Coleman Hawkins got the sax out front that was it. Lester Young came in right after that, so spooky and perfect and lackadaisically gorgeous… Then Bird just turned everything inside out with his thing, rushing here and there and everywhere at once almost. You try to follow those solos, your eyes’ll cross. And then Trane? Oh lord. You put Trane’s thing on top of Bird’s thing on top of Hawk’s things and all around Prez’s thing and you got harmonics gone nuts, fingers going crazy, you got all that forced air rushing through that crazy saxophone and notes and chords flying free from that bell, making crazy patterns, and if you could see them, if the notes were different colors, they’d be filling rooms, all squiggly flatted fifths and minor sevenths and whole bars of chords piling up everywhere. Think of that next time you’re sitting there in some jazz joint, the sax man blowing his ass off. Imagine all those notes. Not even the piano emits as many notes (and those would be neatly stacked or maybe scattered across the floor like shards of a glass enclosure.) Nope, it’s the sax that makes the most sound in jazz. There’s just literally more jazz to be heard coming out of it. Music theory this ain’t. We just dig the sax.

Algebra

I flunked out of pre-Algebra in high school, so they had me take it in summer school where I passed with–I kid you not–a D minus. I think it was a mercy D-minus. I have an excuse, though, because whatever thought processes are used in any math beyond basic arithmetic sets off petit mal seizures and I wind up out of it and nauseous. It took me years to figure this out, though. I thought I just hated math.

My IQ test results must have been interesting. I probably did well on the language stuff, and the basic arithmetic stuff, then bottomed out when it went beyond that. Finally the reason dawned on me one boring day at work when I started one of those online IQ tests. This was years ago. As soon as it got to the more advanced questions with shapes, etc., my brain fizzed out and I felt sick. Limbs go numb, tongue heavy, and this fuzzy thickness descends and a sort of creeping nausea comes on. Ah ha, I thought to myself, and have avoided anything like that since.

Can’t believe it took me thirty years to figure that out. The exact same thing used to happen to me in math class. I was a tough kid, though, not prone to complaining and figured everyone was like that too. Never imagined it meant something was wrong with me. My neurologist wasn’t the least bit surprised when we discussed it a few years ago. It happens, he said. With epilepsy anything can happen. Some epileptics talk to God. Some have spontaneous orgasms. Me, algebra makes me sick. Not as fun, though probably less embarrassing.

I’m very leery of physics and philosophy for the same reason. I could never make head or tail out of either and I suspect it’s because trying to think like that sets off little electro-chemical firestorms in my frontal lobe which then spread to the temporal lobe and fuck shit up nicely. Maybe not, I may just not be bright enough to figure them out, but why take chances. Life sciences I’m fine with, though. Earth sciences, linguistics. My great regret in life is not pursuing a science career, in fact, but there was no way. You need math to be a scientist, real math, and all I can do is simple arithmetic.

Certain kinds of modular maps will set me off too. Not long after I made the mistake of taking that IQ test I made the mistake of trying to read the stupid modular map in the Getty’s Top of the Hill garage. Hiply modular it was, way modular, expensively modular. A regular map just wouldn’t do, not at the Getty. I studied it for maybe fifteen seconds and suddenly I was in a haze, lost, and I couldn’t remember anybody’s name. My wife got us to our seats.

Anyway, I eventually learned that if trying to read anything made me feel out of it or sick, to stop reading it immediately. Took me thirty years of epilepsy to figure that out.

Some writing will set me off too. It used to be a problem. Apparently over the years I’ve learned to write in ways that doesn’t set off my epilepsy. Couldn’t tell you how, but I rarely get sick writing anymore.

But I can take all the strobe lights ya got.

Father’s Day

I’ve been looking at dozens of Father’s Day posts on Facebook. They are beautiful things, those posts. Often very beautiful. Full of love. But  they all strike me as odd. They shouldn’t, but they do. Because I don’t really have any powerful memories of my father. He died way back, around 1990, I think, and it was sudden and an emotional bruiser. That I remember. I remember the funeral. I remember the wake. It was a good wake. He was German, born in Flint, Michigan,  but married into an Irish family and just loved the idea of a wake. He really loved New Orleans funerals — Dad played trombone — but the wake was doable. And we did it.

But that was a long time ago. And the memories before them, of my entire thirty plus years with him, well those are faded at best, and utterly missing the rest. Epilepsy does that. Big seizures — what they used to call grand mal but are now tonic clonic — can make entire memory banks just disappear. Poof. Gone. Like they never were. I had a mess of those big seizures from maybe age 20 through 24, I’d say at least half a dozen. They were nocturnal, coming out of nowhere during deep sleep. I don’t remember them. I just know what people told me, all freaked out, sometimes screaming at me they were so scared. There’s be broken things around, and blood on he pillow from biting my cheeks. Otherwise waking up was quite blissful. The next day all the muscles in my body seemed to hurt, like I had pulled every one. I never seemed to take a day off of work for something as little as epilepsy and just went about my business, every step making something hurt. And suddenly I didn’t remember a lot of stuff. Sometimes I noticed. You notice if you don’t know your name, or who you are, or who anybody is. That all comes back quickly though. Longer term stuff, though…if that’s gone sometimes you never notice. That’s the funny thing about long-term memory — what you don’t remember want bother you. You don’t know it was ever there.

That’s where a lot of my father went. Zapped away in a big giant seizure. Gone. Poof.

But I think epilepsy affects long-term memory in other ways, too. Mainly, I think it weakens it, or maybe just shortens its retention. So stuff I still remembered after my seizures, stuff that came back to me, well at some point since then those memories just kind of faded away. Not zapped away instantly but just sort of slowly disappeared, like a morning fog in a sunny afternoon. The memories get more and more faint and then one day aren’t there at all. Not that I noticed they were no longer there. How could I? I didn’t even realize it was happening. You don’t if it’s something you don’t use every day. But long-term memory is by definition something you don’t use everyday. It’s something stored away to be remembered a long time later.

A lot of my Dad faded away like that.

Most epilepsy, though, isn’t those big crazy seizures. That’s what you think when you hear someone is epileptic, the big dramatic seizures, the falling sickness. But most epilepsy, absolutely the overwhelming most common form of epilepsy, is what are commonly called petit mal seizures. Neurologists call them simple partial seizures *. They affect little sections of the brain. Sometimes just one part. And sometimes they spread like a forest fire, one there, then one over there, then one over there, each throwing an electro-chemical spark that lights the neurons in the new section into more simple partial seizures, Have enough of them, over and over and over, for days or weeks or months at a stretch, you’ll notice things changing. Things not working right. Certain cognitive skills being impacted or disappearing altogether. Sometimes they reappear, or sometimes they can be rebuilt. The brain, extraordinary thing that it is, can do a lot of its own repairs. Essential memory seems to be recovered. Maybe not 100%, but it comes back. But I think that maybe that the brain rebuilds some of that missing capacity by taking neurons used for one thing and using them for another. Maybe facial memory (I lost most of that once, but it seems to have come back) was restored utilizing some neurons used for certain types of long-term memory. You don’t have just one big thing called long-term memory. It’s scattered through different parts of the grey matter, and is divided up functionally. You remember names here, friends here, family here, things you learned in school there, there and there, etc. And well, Dad was dead. Been dead a long time. Those neurons (what you call memory cells) that are dedicated to retaining memories of my father are neurons that the brain used to repair other damaged parts of the brain. My brain took a lot of damage in 2006. Simple partial seizures swept across it like wildfires, like a season of wildfires, month after month after month. The brain seemed to begin repairs as soon as those fires abated though. Functions slowly came back. It’s much improved from its low point. Then, a few years later, my brother is telling a very detailed story about my father and me and I realized I barely remembered my Dad at all. He was a shadow, two dimensional. A television show I watched as a kid and barely remembered. I don’t even recall what he sounded like. I’ve forgotten his voice. Imagine that. Not remembering your father’s voice. Yet it seemed more odd than sad. He was my dad after all, and you’re supposed to remember your father’s voice. But the emotional connection was gone. If you can’t remember somebody, what they sounded like, it just doesn’t bother you. It should, but it doesn’t. It doesn’t because he is no longer in your memory. Because that memory is gone. Poof.

Memory loss is a weird thing. It ought to bother you but it doesn’t, really. Not if it is non-essential memory, memories you don’t draw on every day. And you can’t miss memories you can’t remember you had. But I do know I loved my Dad, we were good buddies, he was senior, me junior. I was the first born son. He’d tell me that I was the man of the family when the company sent him off on another business trip. He taught me all kinds of stuff. But I don’t really remember that either. In fact my entire life before my first big seizures, until I was nineteen or twenty, is just a smudge. When us siblings get together and tell stories I can remember just a fraction of any of them. It’s like I’d  never been there. Or maybe had heard the story third or even fourth hand. That’s where my dad memories are.  All those memories people are sharing today, those are memories I know I had, must have had, but I have no reference point. They’re gone. Like they never even were.

Just the same, Dad, Happy Father’s Day.  I may not know what it was I’m missing, but I’m sure I’m missing you nonetheless, like a good son.

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Notes: Continue reading

Through the Looking Glass

This beautifully epileptic passage is from the manuscript for Alice in Wonderland hand written and illustrated by the Lewis Carroll, 1862.
This beautifully epileptic passage is from the manuscript for Alice in Wonderland hand written and illustrated by the Lewis Carroll, 1862.

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Lewis Carroll was epileptic. Through the Looking Glass is very much an epileptic way of seeing things, and drawings (of words no less) like this here are classic signs of temporal lobe epilepsy. In fact they’re even a symptom. Beginning when I was maybe eighteen years old (adult onset epilepsy they call it, with the seizures and whatnot appearing as the brain reaches its full size at the end of adolescence) I would draw all kinds of things like this. Pages of writing with drawings in the middle of them, often made up of words themselves. I only have a few left. And while words still flow, lots and lots of them, medication ended the drawings years ago. I never thought of myself as an artist or even as someone who drew anything. It just happened, those drawings. I’d get very quiet (I’m told) and start drawing. I never finished them. They weren’t art. They were just symptoms. Some were really intense and even to me now look very strange. As do the stories from back then. And the lists. Epileptics have a thing for lists. I switched medications at some point and never wrote a list again. Never drew again either. I didn’t realize either till years later, looking through a box full of old writing. Lists of everything, reams of vivid writing with an odd sense of the passage of time, and those drawings, sadly artless but sometimes nearly pointillistic in their detail, done with infinite patience and intense concentration. An epileptic temporal lobe is a marvelous thing, though best seen from the outside, looking in.
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(For a fascinating discussion of temporal lobe epilepsy and Lewis Carroll, among others, pick up Seized by Eve LaPlante. An amazing read.)

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I can feel my mind going, said HAL

One of the more fucked up things about a lifetime of epilepsy is that after a few decades of excess electro-chemical energy, faulty wiring, memory damage and fifty thousand or so pills you can feel the executive functions slipping away. I used to be extremely organized, now I’m growing slipshod. I use to be able to plan ahead. Now I catch myself winging it. I’m missing bill payments and having trouble budgeting. I lose track of the days, of the hours. I forget where I’m going, or what I’m supposed to do. I miss freeway exits. Forget names. Forget events. Forget what the hell I’m supposed to be doing. I still haven’t the replaced the tail light in the car. It’s this slow and steady slippage. It’s not like Alzheimer’s, it’s not awful and there’s no confusion and bewilderment. And it’s not all the time, either, and I still figure out new fixes to things, but I’m sure not what I was a decade ago. Losing your mental edge, they call it. Of course, I’ve seen this all before…when my wife came back to life after her four of five minutes away from us all, she had near total amnesia and her own executive functions were blown to hell. She regained much of her memory, and some of her executive functions. One thing I noticed she was doing was something I used to do–that is do some of the exact same thing in the exact same order everyday. You ritualize something it becomes automatic. It’s just she did more of that on a daily basis than I did. A whole day like that, with lots of time off for reading and solo scrabble games. She rebuilt much of her damaged brain that way, by reading and scrabble. And it occurred to me a couple days ago that I am now doing a lot of the same things the exact same way everyday. Like if I didn’t, chaos would ensue. The weaker the brain’s executive functions become, the more you cling to pillars of time, solid blocs of ritualized behavior, otherwise there’s nothing to hold the day onto.

Sigh…what an ideal couple we make. Though I wish to hell I’d noticed I hadn’t paid the gas bill in ages. They’re threatening cold showers. I used to write this down. Had a monthly calendar. That way I wouldn’t forget to pay anything. Apparently I forgot I had a monthly calendar. And what do I do about it? I blog. That’s brilliant. At least I can still write. Though in shorter pieces. I drift off if I blather on too long. Hence the short essays now, a couple hundred words, a single paragraph. That’s about what I can do now. That’s how I think. Fortunately that matches the world’s own ever decreasing attention span. 140 characters or less. I got a way to go before that is too much.

Dave, my mind is going. I can feel it. There is no question about it. I can feel it. I can feel it. I can feel it.

Dave, my mind is going.

Hardwiring

Damn epilepsy medicine is so expensive I’ve lowered my dosage a bit, which seems OK. Our brains shrink with age, the big giant twenty something thing squeezed into our skull at 23 or 24 has been reduced by maybe a per cent a year since then (tho’ not in every case), so maybe there are just less neurons for the medication to cover. Or maybe less synapses, the connections between the neurons, which is what causes the problem, all the dendrites–the little filaments–that spark so easily in an epileptic’s brain. But epileptic brains tend to hardwire as we age, so that we have less neurons open to us which might make us less prone to epileptic problems because hardened pathways can’t spark as easily. I think it’s sort of like an interstate that bypasses a lot of the local roads, if you can see that image. The more used neuronal pathways lose their synaptic connections with a lot of neurons in the process. Memory must get fucked up. (It has, actually). But who knows. All I know is I can get by on less meds than before. But, oddly enough, when I cut back my dosage my hypergraphia increases–this, for example–and I write for hours. Everyday, thousands and thousands of words. Which I suppose might be a good thing. Maybe. Some epileptic writers, I remember reading (I believe in The Midnight Disease by Alice Flaherty) learn how to take advantage of that hypergraphia by controlling the drug dosages….cutting back just a tad (or pushing the next dose back a couple hours) can be worth several thousand words. This doesn’t work if you suffer from tonic clonic (that is, grand mal) seizures. You don’t mess round with those. All that electricity shorting out everything, memories disappear, entire skill sets, parts of your personality, probably entire unwritten novels. But most epilepsy is simple partial seizures, localized, never losing consciousness, and although decades of that sort of epilepsy can do plenty of damage, it’s subtle, incremental, rarely noticed right away. You can risk holding off meds for those a few hours if you want to get some writing done. You learn to work it. It’s easier the older you are, as the more hardwired the neural pathways have become, the less prone the brain is to frying itself out unmedicated. It’s a learned skill, one never discussed with non-epileptics because it’s, well, weird. Maybe scary. Maybe creepy, even. But it certainly helps. Writers figure out all sorts of tricks to keep writing, this is just another. Not every epileptic is another Dostoevsky, the poor brilliant bastard, but we just might have an edge on the normal brained writers. We write like machines, just switch us on and words flow out, well past our bedtimes.

Seizure alert babes

Seizure Alert Dogs are quite the rage now among the epileptic set. You get the whole aura thing happening and Fido (Phydeaux on the Westside) picks up on it and barks or whatever he does and you’re saved. Something like that. But I shouldn’t be poking fun. The pooches are quite useful. Even life saving. Sort of a real life Lassie thing. But then again a Seizure Alert Dog is a dog, not someone you can hold a conversation with. Or make the scene with. Or hang on your epileptic arm like some gorgeous eye candy. I mean Lassie is great for kids, but baby, I live in Hollywood. I make the scene. So why not have Seizure Alert Babes? They could even wear nurses uniforms. Yeah, definitely wear nurse uniforms. The dress, the little hat, the stiletto heels. OK, the stiletto heels were my idea. Second idea. The first was thigh high leather boots. But that’s more like a Seizure Alert Dominatrix, and that ain’t my scene. I mean I’m not a freak, just epileptic.

Actually, I’ve had Seizure Alert Nurses before, with the nurses uniform and little nurses hat and everything. Well,not the heels, but the rest. That was twenty years ago, back when they had me in the epilepsy ward for a week. They’d taken me off my meds, because they wanted to actually see a seizure, record it, get it on the EEG (the electroencephalograph machine…sort of an EKG for the brain), so they could pinpoint where in the brain it originated. They knew from CAT scans about where the little hole in my brain was, but they needed more specifics,  and the more they know, the more effective the treatment. So I was all wired up, my head a mess of electrodes–some stuck right into the jaw socket–and held together with a turban of bandages, and  my every second being filmed and monitored by an unblinking camera. My daytime epilepsy attendant that week was a darling little Filipina nurse. Everyday with the electrodes and the EEG’s and the letting me get out of the damn bed for a minute. Cute as she was, I hated the idea of her standing outside while I took a leak in the tiny bathroom. What was I gonna do, drown? Well, yeah, theoretically speaking, drowning is a leading cause of death for epileptics. (We’re nearly twenty times as likely to drown as non-epileptics.) So showers are OK, but no taking a bath–I believe John Travolta’s kid died that way, in the bath–and no swimming alone. But not even epileptics drown in toilet bowls. Urination should not be an issue. So when she wasn’t around I found the alarm under the bed and switched  it off. Pissed at will without my Pinay helper. That worked for a couple days. Till one day I came out of the john and there she was, all four feet of her, angry. We must have the alarm on! They were afraid I would hurt myself, she said. There went my freedom. I was drinking coffee like crazy–part of my seizure inducement strategy, keeping myself edgy and sleepless and miserable–and having to go a lot. So from then on I’d buzz her, she’d come in. Yes Mr. Wahl, you need to pee?  (I hate that word pee–real men piss.) And she’d turn the alarm off. OK, Mr. Wahl, let’s go, and she’d help me up. I didn’t need help. I was three times her size. I could pick her up with one hand and hold her over my head. But still, she helped me up. She walked me to the bathroom door four feet away. I squeezed in. The toilet was tiny, and I had to aim carefully. Halfway through she’d ask are you OK in there Mr. Wahl?  As if I’d never pissed by myself before. I’m fine, I said. I’d flush the toilet. Are you done, Mr. Wahl? No, I’m all tangled up. It’s got itself wrapped around my wrist and won’t let go. I need help. I never said that though. It was a neurology ward. They make note of those things. So I would just come out of the bathroom and she would put me back to bed and turn the alarm back on. That was the day shift.

The nurse on the night shift was a hot little Thai number, slim and perfect. Barely said anything. She’d wander in, smile, check the gauges and dials, make sure the bed alarm was on and slip out again. If I had to pee she’d turn off the alarm–it made a helluva racket otherwise–and let me do what I had to do. Take as long as I wanted. Never said anything through the door. Who knows what she thought I was doing (I wasn’t), but I appreciated the privacy. I’d emerge and she’d slip out the door and leave me alone in my room. I’d get under the covers. She’d come in later, look at the dials, turn my alarm on, and slip back out again, soundlessly. Even her footsteps made no noise.

The epilepsy ward was eerily quiet at night. Sometimes there’d be some muffled sounds from down the hall and the nurse and orderlies would head that way till the sounds abated. There was an old African-American patient down the hall who would seize every couple hours. He’d make sounds, thrashing around the bed, and let out a blues wail. A fragment of a song, very deep south, very delta, very black. I can still hear it in my head, two decades later, and it’s as eerie as it was when it would break the nighttime silence. A plaintive cry, some notes stretched and blue, lingering, unresolved. Then it faded. Silence again.

I heard it all–the blues, the muffled conversations between the nurses, the electronic beeps and buzzes that are a constant backdrop in a hospital–because while the other patients were asleep I stayed awake on coffee and little else, trying to bring about a seizure. They needed a seizure, a real seizure. They kept telling me that, as if I could will one. Something that would set the EEG crazy and let the doctors discover just where and why and how all this epilepsy was happening. That’s what the camera was for. They could watch me 24/7 and look for symptoms. And if a big one came, they could watch my head turn in one direction and know which side it emanated from, that is from the other side. Seizure on the left, head turns right. On the right, head turns left. Like an epileptic compass. UCLA medical school students manned the remote monitor, watching. They watched every minute. It made me self conscious at first. Things I never even thought about before, like what would my hands be doing while I slept? I imagined a room full of coed neurology students, giggling.

But I got used to the camera. Went about my business there in that little bed. I read, and watched the inane local news. Read some more. Drank coffee. Drank more coffee. Horrible hospital coffee, whole pots worth. The food was awful and I stopped eating. My wife came in everyday, smiling, bearing gifts and snacks and kisses. I lived for those visits. Friends would show up, we’d talk and laugh and they’d flirt with the nurses until they were shooed out. Visiting hours are over. The ward grew very quiet. I would read–I’d brought a whole stack of books–and look for anything watchable on the TV. There was never anything. Pretty ladies reading off cue cards in infomercials mostly  Those ladies seemed to be my primary interest after a while. All I could think about. Laying in bed for a week reading will do that. A lady friend called from the job I’d just left. She’d bought me a Playboy for a going way present, everyone signed it. Funny comments all over the pictures. Every time I see Jenny McCarthy in a commercial I think of her boobs with a knock knock joke on them. My friend asked if I’d brought it with me. I said no. She said so you poor thing, you must be so horny laying in bed for a week. The camera stared at me. I said can we change the subject?

The third person who popped into the room regularly was the epilepsy lab technician. She studied the EEG carefully for signs of something. She was a cute little Armenian number that came in a couple times a day to whirl knobs and read print outs and asked me if I’d had a seizure yet. It was so cute how she said it. Plus she was built. You tend to remember these things. Even if it’s about the only thing I do remember.

And I remember her because when I woke up, I saw her there whirling knobs and pressing buttons, and I said hello. She looked surprised. Oh hi….how do you feel? Fine, I said. She grinned. You don’t remember, do you?  Remember? So you really don’t remember? Remember what? I couldn’t remember anything, actually. You had a giant seizure! People overheard us and came in. A nurse, a doctor, more nurses. They all asked me how I was. I said fine. They all told me about my giant seizure. My neurologist came in. Another neurologist. They excitedly told me about my seizure, that is was the biggest seizure they’d ever had in the epilepsy ward at Kaiser hospital. The mother of all seizures one said. My neurologist limned it out for me. I’d fallen asleep. I began seizing. The technician was in there all alone. She cried for help. I was seizing violently, rigid, thrashing, foaming, making crazy epileptic sounds. It went on and on. All the nurses rushed in. A doctor. They could do nothing but stand there watching, waiting for it to subside, trying to keep me from hurting myself. Then quickly as it came, it stopped. I sank back, motionless. The heart monitor still beeped time, I was breathing. The seizure was over.

Then came the post-ictal period, that is, after the seizure. My brain was zapped all to hell, a CAT scan, had it been taken during the seizure, would have shown my brain blazing white from ear to ear, the whole frontal lobe and beyond a mass of intense electro-chemical activity, a zillion neurons flashing simultaneously, annihilating all consciousness. Now, post-ictal, it would dim down to a lower level white as the electrical storm subsided and left a brain shocked, synapses flickering, exhausted, awash in the chemicals released by so much simultaneous activity. I was a zombie. The body, thoughtless, instinctual, began to stir. I was immensely strong. Many times stronger than my conscious self. I reached up and tore the electrodes off my head, ripping off the bandages, yanking the wires free, pulling them out of my jaw. I grabbed the wires and leads stuck into my arm and ripped them out. I began to rise. The tech tried to hold me down. The nurses. The doctors. The orderlies ran in, muscular athletes all of them, biceps like iron. Eight people in the room trying to hold me down. But slowly, irresistibly, I sat up, all their strength and effort to no avail. I was getting out of the bed. They screamed and yelled, alarms rang, everything in the room beeping and buzzing, it was anarchy.  Someone yelled to the front desk to call security. They’re on their way.

Then, as sudden as it began, I went limp, laid down and fell fast asleep. That’s what they told me. I remembered absolutely none of it. Nothing. That’s the thing about grand mal (aka tonic clonic) seizures. The brain is so overloaded with electro-chemical energy that there’s no thought–let alone memory–whatsoever. I remember the room looked a hell of a mess. My neurologist said they had been afraid I’d go after the equipment, millions of dollars of sensitive machines and me, he said, a Frankenstein’s monster who could destroy it all. One of the orderlies on the floor–the biggest, buffest one–came into the room. Gave my biceps a squeeze. Man, you are strong. A whole room full of us was trying to hold you down, and you just sat up like it was nothing. I apologized. He grinned. Yeah, man, you are strong and he shook my hand. I felt meek as a lamb.

The doctor left and my little Filipina nurse, cute as ever, said you get some sleep now. You’re very tired. You can go home tomorrow. She had me lay back down, removed the wires and fragments of  bandages from the bed, then saw the blood on my arm where I’d ripped out the wires and cleaned and dressed the wound with her tiny little fingers. You can get these sensations of intense warmth and gratitude after a seizure, you go numb all over and feel warm and loved. She cooed at me to fall asleep and I melted into the bed. The next day every single muscle in my body would hurt, as if I’d sprained them all simultaneously, but for now, my memory zapped all to hell and the world hazy and strange, I felt deliciously tired and slept for hours. I nodded off before she’d even left the room. A couple hours before she was among the crew frantically trying to keep me in the bed, tiny little her. I could have batted her away like a kitten. Now I was utterly harmless, and she laid an extra blanket across me so I wouldn’t get cold.

Of course a seizure alert babe wouldn’t have to do any of that. She would just be there to look gorgeous when I made the scene. No twirling dials and running reports, no listening to me pee, no trying to keep me from walking like a super zombie, destroying everything in my path. My seizure alert babe would be strictly for show. Hell, I don’t even need a seizure alert dog, I’m so medicated and controlled and safe. I suppose she could remind me to take my medicine. That way my health plan would cover it. Though I don’t know about Obamacare. Especially the stiletto heels.

Besides, my wife would kill me. So let’s just drop the whole thing.

Doris Day looks out for legendary pitcher Grover Cleveland Alexander (Ronald Reagan) during one of his epileptic spells in “the Winning Team” (1952).