Prescription

Me: My neck hurts from too much reading.
My son: Maybe you should take up bird watching.

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Still Standing

Sixteen years ago, I coerced my husband into doing something crazy. I had just come back from a doctor’s appointment that hadn’t gone at all well.
When I arrived at our shack, I was crying like a baby. I mean this quite literally. I was crying so hard, I could not form a word.
We both found my speechless sobs distressing. My sweet husband’s dark eyes were widening with horror.
Just a few months earlier, his mother had been diagnosed with terminal cancer. He’d already learned about the flipside of love.
My husband loved me. I now knew he was going to lose me, was losing me already, one little brain lesion, one little spinal cord lesion, at a time.
Until that day, I hadn’t heard of multiple sclerosis. I didn’t know for certain if an MS diagnosis was better than a terminal cancer diagnosis, or far, far worse.
I wanted it to be better. Far better. As much for my husband’s sake as for my own. I wanted to comfort the poor guy, who was standing there, unflinching, receptive, gathering his strength to endure the unendurable, in whatever form it would turn out to take. I wanted to tell him, the love of my life, “I’m not going to die.”
Which was, of course, both the immediate truth and a big fat lie. I wanted to say it anyway, but I was blubbering so hard, even I couldn’t get a word in edgewise.
I knew MS wasn’t terminal. The doctors had been very clear on that point. I was going to die with MS, but not necessarily of MS. When I eventually die, it will most likely be due to some other cause.
But to deliver even this cold comfort, I would have to quit bawling. I would have to pull myself together. I would have to form some words.
We had the same idea at the same time.
My husband handed me a pen. The man can be counted on to carry a pen. And that’s when it occurred to me that I didn’t have to do the explaining. As he rooted through our rotting shack for a blank piece of paper, I rooted through my cluttered pocketbook for the wrinkled MS Society brochure.
Then we made our exchange—a sheet of blank paper for a printed pamphlet.
I wrote on the sheet of blank paper, “I’m not going to die.” When I looked up, he was scanning the pamphlet.
The look we exchanged said it all. We were in deep trouble.
Oddly enough, I didn’t sob harder.
Already, I started to feel better. The good news was, I wasn’t in it alone. And yeah, that was also the bad news. But as bad news went, it was at least bearable bad news. For me. I couldn’t imagine how it could possibly be bearable bad news for my husband.
Lucky for me, my husband exceeds the boundaries of my imagination.
The man was capable of deciphering the pamphlet. More so than I was. I have a head for nuance. I have no head for statistics. The nuance of the pamphlet was ominous. It conveyed this the-glass-is-an eighth-full kind of optimism that I found highly suspect.
My husband has a head for nuance, but he also has a head for statistics. He could at least calculate the specific inverse of an eighth full. He isn’t bullied by statistics. Conjecture outright bores him. The guy has a constitutional aversion to freaking out about the future. This quality has served us very well. Which is not to say the diagnosis did not scare the hell of him, out of us.
My husband and I had always intended to have a kid “later.” “Later” meant after we’d both finished grad school. “Later” meant after we’d upgraded our living quarters from a $375/month shack.
The MS Society pamphlet blew apart our concept of “later.” We were just kids. To us, “later” had always meant, kind of like now, but slightly better. But even according to the optimistic pamphlet, “later” meant, kind of like now, but an indeterminate fraction worse. And then worse still. And then worse still.
As I saw it, this meant only one thing. We couldn’t count on “later.” If we wanted a kid, we had to have one immediately. Like, while I could still push a carriage. Like, while I could at least lift a baby to my breast.
Gentle reader, “later” turned out to be a whole lot rosier than my mildest conjectures.
Our son is fifteen now. The child has never spent so much as a night in a shack. (Wait ‘til grad school, kiddo.)
We recently took our healthy son with us to Iowa City for the 75th Anniversary of The Iowa Writer’s Workshop. We gave him a tour of all the places we’d lived while I’d studied there, from the crazy apartment on North Dodge in the back of Hilltop Tavern, to the farmhouse in Swisher, to the metal house on G Street, to that sorry, ramshackle shack.
My husband took a picture. He said, “I can’t believe that place is still standing. I underestimated so many things about the world.”
So did I, my love. So did I.

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Stress and MS

Happy day! The verdict is in. Multiple Sclerosis (MS) is not caused by stress.
The NIH (National Institutes of Health) has been following two enormous groups of nurses over two massive spans of time, and they have found no link whatsoever between traumatic life events and the onset of multiple sclerosis.
Zero, nada.
I know I sound a bit overblown. But that doesn’t mean that I am exaggerating. I’m not even over-exaggerating (a distinction we often make in my larger-than-life family-of-origin.)
The two groups studied really were enormous: 121,700 nurses in Study One, and 16,671 nurses in Study 2.
The two time spans really were massive, maybe not massive in geologic time, but certainly massive in biologic time. The first group has been followed since 1976 (Number 1 song of ’75: Silly Love Songs by Paul McCartney and Wings.) The second group has been followed since 1989. (Number 1 song of ’89: Look Away, by Chicago. Was I asleep that year?)
The nurses in both enormous groups were asked to complete a questionairre about their personal history of stressful events. After they handed in their questionnaires, they went about their normal lives. A minority of the nurses who completed this questionnaire would later find that their normal lives would be disrupted by MS.
When investigators compared the answers from the group of nurses who were destined to develop MS with the answers from the nurses who were destined to remain healthy, they found no significant difference in self-reported levels of stress and/or stressful events.
I feel so vindicated.
There are so many subtle and not-so-subtle ways of blaming of victim. With my MS diagnosis came the injunction to avoid stress. I don’t necessarily think that was an entirely bad piece of advice, although, under the circumstances, it wasn’t particularly easy advice to follow. No one ever outright accussed me of creating my disease state because I’d been under too much stress. That was entirely my own inference. I’ve been blaming myself ever since.
Since my diagnosis, I have made it a priority to avoid stress. I’ve done plenty of yoga. Not enough meditation. When I’ve gotten pissed off, I have, on occasion, actually slowed down long enough to count to ten. I am, without a doubt, a happier, more even-tempered person than I was before my diagnosis. I might not have made such an effort had I not believed it would contribute to my health.
So I can’t say I have a quarrel with avoiding stress. I have a quarrel with the notion that a person with MS has a stronger obligation to finesse stress than a person without MS.
I would like to propose that there is something intrinsically wrong with the assumption that multiple sclerosis is a flawed emotional response, rather than a flawed immune response.
I’ve had MS since at least 1988 (Faith, George Michael). I am a study of one. I am lacking a control group. As both investigator and subject of my own disease, I have had a “massive” amount of time to explore the complex interplay between multipe sclerosis and stress. For what it’s worth, this is what I have observed. Stress is not the only response that can trigger MS symptoms. Any old emotion will do. Joy, for instance. I will never forget the excruciating pain that shot through my legs when I learned that a family friend would be lending us his apartment in Paris.
If I want to eliminate pain from my life, does that mean I ought to eliminate joy?
I don’t think so.
I’d like to propose a paradigm shift.
Let’s stop fussing over eliminating stress. Let’s focus, instead, on eliminating MS.

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Conjoined Twin

The cover girls on this morning’s New York Times Magazine are cute young twins…conjoined at the head.
My son, an only child, could not imagine himself in such a conundrum. Since I have two sisters, it was easier for him to imagine such a thing happening to me.
“You probably wouldn’t like it if you were conjoined with one of my aunties.”
I immediately imagined an even worse scenario.
“Image how she would feel being stuck conjoined to me! She’d want to go out…and I wouldn’t be able to walk fast enough. She’d be dragging me along! And then I’d stop walking altogether. And she’d be stuck! She’d hate it!”
And then it hit me; I can imagine this hypothetical situation so well because that’s exactly the situation that I’m in. My MS is like a pesky conjoined twin with a will of her own.
Take this morning, for example. I wanted to pull weeds. But I had to drag along my pesky twin, MS. Let’s pretend MS is short for Mary Sue.
It’s a beautiful, clear day. Blue sky, fluffy white clouds. 80 degrees. Finally, no rain. Finally, a chance to pull those 16” weeds!
Mary Sue whines about the heat. I’ve gathered only a handful of weeds, but we go back inside. I pour us some ice water. A compromise. We go back out again. Gosh, it’s beautiful day.
Mary Sue starts whining again. Now she’s making our legs all tingly and heavy.
I ignore her, and pull. Satisfied to be finally getting something done.
The little girl across the street shouts, “Hello!”
“Hello!” I call. I smile and wave. I can’t see the little girl.
Mary Sue has gotten us dizzy.
I drink more ice water. Mary Sue complains that we are going to faint. She complains about our legs getting heavy.
Our legs have indeed gotten heavy. (Thanks to Mary Sue.) I drag our legs all the way down to the compost bin in the back of the yard, and dump what weeds I’ve managed to uproot.
I turn for home. Mary Sue is dragging our feet all the way to the front door, and her precious air-conditioning.
We’re inside. She’s won. I plop down, exhausted from our struggle, and read a book.
Mary Sue is outraged. I’m ignoring her. She finds a new way to make trouble.
Outside, she was too hot. Inside, she’s decides she’s too cold. She starts jerking our legs around in painful spasms. I stretch. She whines. I pull on long pants. She quiets down.
I dream of separation.
I long for a cure.

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The Keys to Heaven and Hell

The mind is its own place,
and in itself
Can make a Heaven of Hell
a Hell of Heaven
-John Milton

Nearly two years ago to this day, I met two unforgettable working women on the Big Island of Hawaii.
Readers, tuck away your image of nubile brown women gyrating in grass skirts. The two women I’m about to describe were both, by my estimation, well over fifty—although there is a strong possibility that one of these women was much older than she looked, and the other, much younger. In any case, it is highly unlikely either woman would remember Ms. Lab Rat, or would have found our quotidian interactions at all remarkable. Yet in that day, just by going about their usual business in their usual ways, these two women inadvertently handed me nothing less than the Key to Heaven and the Key to Hell.
I met the woman with the Key to Heaven in a place you don’t find listed in any glossy Big Island travel guide. A place that has never been rated by Zagat. A place undocumented by Lonely Planet. My husband is in-the-know about quite a few noteworthy spots on the Big Island of Hawaii, as this island is his mother’s birthplace. He listed this particular location above all the other hot spots we planned to visit that day: above Onekahakaha Beach, which is totally a beach for locals, above Volcano National Park, which is totally a top-ten contender for any sane person’s bucket list. Be that as it may, this list I’m referring to was not my husband’s bucket list. It was his to-do list. You see, we happened to be staying in a plantation cottage so rural, so isolated, that there was no municipal garage pickup.
Yes, we found the woman with the Key to Heaven working at the local garbage transfer station.
I was as mystified as you are.
At first glance, the woman working at the transfer station looked completely ordinary. It wasn’t as if she wore a fragrant lei and a grass skirt. No, her outfit was more along the lines of a drab polo shirt tucked into pressed khakis. Yet this woman was utterly dazzling. She radiated well-being as she stepped out to greet us with what felt like the warmest word on the planet.
“Aloha.”
As she greeted us with Aloha, she was smiling uncontrollably, just beaming with joy, as though she had been waiting to meet our little family her entire life, and she could imagine no better place on the entire planet for this transformative event to take place than on this very spot. The garbage transfer station.
Her joy was utterly contagious. I couldn’t believe how happy I was to meet her. How happy I was to be there, at the transfer station, with my husband and son, where we could complete our meaningful task of getting rid of garbage. And to think we’d assumed this task was merely something we had to perform to go on to our real destinations.
“Aloha,” we responded. And it felt like we were returning, not so much a greeting, as a blessing.
Raise your hand if you think you know the meaning of the word, Aloha. I would have raised my hand, too, even back in the day when I thought all Hawaiian women traipsed around in grass skirts. Like most Mainlanders of my generation, I considered myself an expert on Hawaiian culture after I’d watched a portion of the three-part Brady Bunch Hawaiian Adventure. Ah, well. I didn’t know what I didn’t know. I’ll say this much—don’t look to little old freckled me, a haole, a white person, to define Aloha.
Instead, allow me to consult a genuine expert, good old Aunty D.
Aunty D’s Hawaiian Language Workshop cites the dictionary definition of Aloha as follows:

Greetings! Hello! Good-by! 


That dictionary definition is probably not too far off from my old Brady Bunch-inspired definition.
But buckle up. Aunty D and I are going to get all mystical on you. Aunty D digs a little deeper into the etymology of the word Aloha, to reveal that “alo” means presence, and “ha” means “Divine Breath.”
Now, what does the phrase, “Divine Breath” evoke for you? If you are of European origin, like me, that phrase may seem bizarre at first hearing. We white people do not, as a rule, associate the breath with the Divine. Breath can be bad. Breath can be good. (And then only when camouflaged by mouthwash and/or toothpaste.) But Divine? Get out of town.

According to Aunty D., Aloha is

…the spirit of God in Man. As life’s essence, Aloha is everywhere. It is the magnificence in every person, as well as in the `âina, i.e., the environs which is the air, the land, the sky, and the sea…

Does this deeper meaning of Aloha remind you of any single word in English?
Me neither.
Where I was growing up, The Divine was never mentioned in the same breath as breath. The official word was that God resided in churches, in flat tasteless communion wafers, (and then only through the specialized mediation of a priest.) God was not in Man (or woman), and was certainly not in the air, the land, the sky, or the sea.
Then again, I didn’t grow up in Hawaii.
Luckily for me, I was raised by parents who hauled us kids off to the woods to check in with God at least as often as they hauled us off to church. My mother would remind my sisters and I, “Your body is the temple of the Lord.”
Aloha, Mom.
I would not encounter a word even remotely similar to Aloha until I was an adult confronted with a diagnosis of multiple sclerosis, and I thought maybe the lifestyle I’d been living wasn’t working too well for me. I got myself to a yoga studio. The first word I learned there was a greeting in Sanskrit.
Namaste.
Namaste means, roughly, the divine in me recognizes the divine in you. That’s not so different from Aloha. I must say, either greeting is far superior to, “May I take your order?”
When the lady at the dump greeted us with, “Aloha” that morning, I not only heard the word, I felt it, too. I felt the spirit of the Divine in this magnificent woman. I immediately understood her source of contentment. It was within us, and all around us, right there in the transfer station. I saw that she wanted for nothing; she had a job, a useful job, in a beautiful place. Her status in life was irrelevant. Her job description might not impress anyone, but that was irrelevant, also, because she was clearly in no need of external validation.
In retrospect, I don’t think I was viewing the transfer station agent’s situation through a vacationer’s rose-colored glasses. I think she was simply so magnificently present that she blew away all the labels and judgments that habitually taint my perceptions. I tell you, it was a relief to take a moment to lay down this burden. I could clearly see the Divine in this woman, the Divine in her workplace. Sure, it didn’t hurt that the sun was shining, and that the sky was blue, but I might not have noticed the warmth of the sun, or the color of the sky, had I been wearing my habitual blinders.
I thought a lot about that moment when I started reading a book by Eckhart Tolle. What a Hawaiian might call the power of Aloha is what Tolle calls “The Power of Now.” He observes, “identification with your mind creates an opaque screen of concepts, labels, images, words, judgments, and definitions that blocks all true relationship. It comes between you and yourself, between you and your fellow man and woman, between you and nature, between you and God. It is this screen of thought that creates the illusion of separateness, the illusion that there is you and a totally separate “other.” You then forget the essential fact that, underneath the level of physical appearances and separate forms, you are one with all that is.”
In The Power of Now, Tolle implores us to, “Break the old pattern of preset-moment denial and present-moment resistance. Make it your practice to withdraw attention from past and future whenever they are not needed.”
I found myself in no rush to leave the transfer station, in no hurry to reach the many distant points on our list. That shift in consciousness proved useful. As it happened, the next destination on my husband’s list was clear across the Island, on the rainy side, and the speed limits on the one road available varied from 45 mph to 25mph. The posted changes were frequent, and seemingly random. A recipe for aggravation? Only if you weren’t driving in the Now. The view out the window was lush and verdant; life in spectacular display. That road dared you to care to be anywhere but where you were. It was a darn uppity road.
As there is no photograph of the Transfer Station, the place where we found the woman with the key to Heaven, I will supply no photograph of the restaurant where we encountered the woman with the Key to Hell.
The woman with the Key to Hell may have dressed better the woman with the Key to Heaven. But my heart didn’t leap at the sight of her. Surely, she held a more prestigious position, at a far more prestigious place. Or so you would think, if you were unaware that every place is sacred.
The hostess took her time acknowledging our presence. She fluffed a few papers on the lectern before her. Looked to the right of us, and to the left of us, without appearing to have spotted us, although we were the only people standing in the entrance.
When she ran out of ways to avoid looking at us,
it was clear that she saw three dirty people who had sloshed through ocean water, and over lava rocks. She surely didn’t see three expressions of the Divine. It is true we three were not at all attired for dinner at, say, The Four Seasons. But this restaurant was not The Four Seasons. This restaurant was located at the top of a volcano on an island where acceptable nightlife footwear is a pair of zoris, or flip-flops. Not that you’d ever see a local eating there. No, this restaurant’s clientele consisted entirely of the marooned—those of us dressing out of suitcases and backpacks. Our little family had eaten there many a time in the past, dressed as casually, or worse.
Having run out of alternatives, the restaurant hostess finally deigned to greet us. She did so mechanically, using the same word as the transfer station agent, but without so much as a fake smile on her face.
“Aloha.”
Here’s what Hawaii’s last ruler, Queen Lili’uokalani, had to say on the subject of Aloha:

More than a greeting, it is a blessing. To be ONLY used with sincerity: “‘Aloha’ could not be thoughtlessly or indiscriminately spoken, for it carried its own power. No Hawaiian could greet another with ‘Aloha’ unless he felt it in his own heart. If he felt anger or hate in his heart, he had to cleanse himself before he said ‘Aloha’.”
Did our hostess have anger or hate in her heart? I doubt her feeling was as vehement as that. She went to extreme pains to continue to treat us as if we were invisible by asking, “How many of you are there?” As though it wasn’t plain to see.
My husband helpfully suggested, “Three.”
She pursed her lips. “I’ll check and see if there’s room.” Without another word, she turned her back on us and disappeared inside the restaurant. She was gone long enough for us to start discussing a Plan B. As our hostess was insinuating, this was indeed the best restaurant for miles. But that was only because it was the only restaurant for miles.
My husband and I had just agreed to start back for the cottage when our hostess returned. She sighed, exasperated. “I can squeeze you in.”
We followed our hostess inside the serving area, a vast room with all but two tables empty. Just as our hostess had found us invisible, we found her crowd of patrons invisible. Clearly, she’d manufactured the seating problem.
Tolle asks, “Why make anything into a problem? Isn’t life challenging enough as it is? The mind unconsciously loves problems because they give you an identity of sorts. This is normal, and it is insane.”
Later, he reflects, “The pain that you create now is always some form of nonacceptance, some form of unconscious resistance to what is. On the level of thought, the resistance is some form of judgment.”
Indeed, I feel a little guilty singling out this one hostess. She is not the exception. Her behavior is almost the rule. Some people, some very insecure people, actually prefer to eat out in an establishment that snubs them. Think of the Groucho Marx joke, “I don’t want to belong to any club that will accept me as a member.”
I’d like to think there was more going in that restaurant than I was aware of. Perhaps the hostess was doing a remarkable job remaining calm, as the cook had just keeled over and died in the kitchen. Indeed, that explanation would also explain the quality of the food we would be served.
Oh, gentle reader, in my judgments, I carry the Key to the Hell, and in my observations, the Key to Heaven. I can almost hear those keys jingling, day in and day out, with every sentence that I write. I didn’t need to travel to find two women to illustrate the options. I can look no further than myself.
Similarly, I can assure you, Gentle Reader, that you don’t need to go to Hawaii to experience Aloha, or to India to encounter Namaste. Eckhart Tolle would advise you to tear up your bucket list, and stay right where you are. And while you are there, you could do worse than reading his simple book, The Power of Now. It won’t change your life. It will change how you live it.
Thanks for reading!
Aloha.
For more about the joy available to all, watch this talk by Srikumar Rao.

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Love and Death on Cape Cod

I’ve spent all but one day this week imprisoned in fatigue, but on that day I got to walk my dog, catch up on laundry, and begin an essay for your entertainment. The essay isn’t done yet. I’ll throw you a scrap from another piece of unfinished writing, the opening to my novel-in-progress, Love and Death on Cape Cod. If it leaves you wanting more, welcome to my world.

Love and Death on Cape Cod
in Memory of Esme
Chapter 1. This Is Not My Beautiful House. This Is Not My Beautiful Wife.
It was the oil hemorrhaging into the Gulf of Mexico; it was in the traffic clotting eastbound 95; it was the ever-expanding estimates on NPR; 1,000 gallons a day; 6,000; 25,000.
It was his complicit commute.
It was the dispersant; the unknown quantities of unknown compounds with unknown effects. It was the nation-wide malaise. It was the end of Yes We Can. It was mass extinction. It was global warming. It was mountain top removal. It was plastic. It was that vast continent of plastic, silent as a tumor, floating somewhere in the Pacific, unnamed. It was overfishing. It was overpopulation. It all came down to overpopulation. It was hormones in the water supply.
It was Laurel Hansen’s raging hormones.
It was 3 am on Saturday, June 5, 2010— Day 44 of the BP catastrophe.
Jay Carr lay sleepless in his beachside cottage in Madison, Connecticut. Laurel lay beside him, her breathing as steady and rhythmic as the Long Island Sound lapping against the sand. Jay suspected Laurel was dreaming—literally dreaming—of mothering his child. Over six billion people on the planet already, and somehow Laurel found her world incomplete without the promise of one person more. Laurel was thirty-eight, on the verge of thirty nine, on the verge of too late. Jay was familiar with the feeling of a world, incomplete. There had been only one person who had managed, however briefly, to make his world complete.
Only one.

The Great Puppeteer

The Great Puppeteer let go of my strings for a few days, so I was unable to walk or even think, really. I am walking again today. When you see my next post, you will know I am all better.

Gratitude

This morning, my local neurologist sat me down after performing my annual exam. For the exam, she’d checked my reflexes, had me follow her fingers with my eyes, had me push against her (“you’re strong”), had me stand on one leg, then on the other, had me walk on tip-toe, walk on my heels, walk a (flawless) heel-to-toe.
She prefaced her conclusion by saying, “You might be unhappy to hear to this.” Naturally, I was all ears. “How long did you say you’ve been diagnosed with MS?”
“Sixteen years. I’ve had MS for over twenty years.”
“Over twenty years? And you can still swim laps for thirty minutes?”
But not for thirty five.”
She nodded. “Not for thirty five. Swimming laps for thirty minutes is really good for someone who has had MS for over twenty years. Maybe you don’t want to hear this, maybe you want to do better, but you are doing very well.”
I corrected her assumption. “I do want to hear that. I’m so glad I’m doing well.”
I’d reported to her, earlier, that the parameters of my abilities are shrinking. I’d wondered aloud if I was transitioning into Secondary Progressive MS. “I can’t do as much as I used to. I can’t walk as long, or as fast. Every time I push myself, the MS pushes back.”
She’d agreed with my tentative assessment. “I often see this kind of gradual decline with people who have a mild form of MS.”
There was once a time when I would have bristled at that remark. I would have resented the suggestion that my nemesis, MS, could be described as “mild.” There was nothing mild about the pain I was experiencing right there in her office, which was why I had swung my aching leg up onto her examination table and used the table as a barre to stretch.
There was a time when I wasn’t willing to believe the MS could get any worse.
I know better, now.
My neurologist sees worse cases of MS every day. At least these days she can tell her patients that there are effective medications —medications like the one I’m on—in the research pipeline. There’s much more reason for hope than there was back when I was diagnosed.
And that is why today’s post is simply a post of gratitude.
I am very grateful.
Grateful for having a fine local neurologist.
Grateful for having insurance.
Grateful for having a $15 co-pay.
Grateful for being on an effective medication.
Grateful to be receiving that medication free of charge through an NIH study.
Grateful to have friends and family who support me. (It’s not too late, by the way, to support me in the MS Walk.)
Grateful to be able to swim 30 minutes of laps.
Grateful you visited this blog.
Grateful that yesterday, somebody searched Google for “Happiness with Multiple Sclerosis” and ended up on here on Ms. Lab Rat. What a hoot!
Am I happy with Multiple Sclerosis, the disease? Nope. I can’t say that I am. I hate this disease.
But am I happy, despite Multiple Sclerosis? You bet.
I welcome all seekers of happiness, with or without Multiple Sclerosis.
Thanks for visiting.

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Miffed vs. Pissed

The other day, I got really miffed when someone stole my handicapped parking decal. I was so put out, I did something atypical. I posted my emotional state on Facebook.
My dear friend, the novelist Goldberry Long, posted a rapid-fire reply. “Miffed? Shoot, I’d be pissed.”
When I read her words, I felt…nostalgic.
Just then I realized I haven’t been properly pissed off in ages. Not recreationally so. There used to be a time when I would have a lot of fun raging, describing, in ebullient detail, the myriad of ways in which I was right and the opposing party was dead stinkin’ wrong.
A few things happened along the way. I had a baby. Babies aren’t particularly entertained by excoriating critiques of social norms. I quickly discovered I had to take it all down a notch. A baby is a powerful motivator. So is multiple sclerosis.
Multiple Sclerosis loves the rage state. Whenever I get pissed off, MS gets pissed off, too. It musters an army of zombie T-cells to attack…my own immune system. Who wins that battle? Take a look at any of my MRIs.
So yeah, if fear of rousing my own baby weren’t enough to keep me in check, fear of rousing another MS attack would eventually polish off my rougher edges.
Getting pissed off just wasn’t fun any more.
Now my kid is fifteen. My MS is in check. Fifteen year olds happen to find excoriating critiques of social norms f’n hilarious. Even so, I find I’m somewhat out of practice at getting recreationally pissed off.
Goldberry wrote, “I’m going all the way to rage for you, Lisa.” And that prompted a wistful smile.
Though I no longer can afford to get pissed off recreationally, perhaps I can become be a fan of those who do so on my behalf. A vicarious thrill never hurt anybody.
Go, Goldberry!

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Ms. Lab Rat in trueFoolishness

I have been aided in the transition from writing to live storytelling by true professionals. I am thankful to Jeff Groh and Dave Levy for pushing me to succeed, and to my fellow performers, for demonstrating how to rock the house. We laughed, we cried, we clapped, we SANG.

There was an accordionist! A jug band! Yep. Good times.

Don’t take my word for it. Read this review! https://www.facebook.com/notes/rick-penders-theater-stages-scenes/true-theatre-truly-surprising/197718950266519

You won’t want to miss the next show, themed trueIndepence:

http://www.cinstages.com/Onstage/proddetail.asp?ProdID=130315.

 



 

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