Showing posts with label pop culture comparisons. Show all posts
Showing posts with label pop culture comparisons. Show all posts

Saturday, May 16, 2015

Diabetes Blog Week 2015 Day Six: Favourites and Motivations

If you have been blogging for a while, what is your favorite sentence or blogpost that you have ever written?  Is it diabetes related or just life related?  If you are a new blogger and don't have a favorite yet, tell us what motivated you to start sharing your story by writing a blog?  (Thank you Laddie of Test Guess and Go for suggesting this topic.)
 

Writing is very important to me. It’s a passion of mine. When I was younger, everyone thought I was going to write the Great Canadian Play. That may never happen, but I love getting to “write what I know” on this blog, and in the process, connect with other people in some way. Here are a few favourite moments, for me, in three categories.


 “Popular”


 My second-most read post of all time was one I almost deleted, because I wrote it in a very emotional space, and I was worried it would be controversial. “Liar” is about all the things, people, and institutions that lie to people with diabetes throughout our lives. It sparked a lot of discussion, was shared by many people and organizations, and even made it to a conference slide (which I found out about after it was posted on the Internet; it would have been nice to be informed or asked, thanks).


 “So when I hear that test strips can be +/- 20% in accuracy (a 10 could be 12, or 8) and are often worse, it makes me sad. Because it's a lie, and we're already dealing with so much misinformation, so many lies, that we'd like something to be true. Something that, instead, takes the best of us, the life from us–blood is life–and turns it into another lie. Something that comes from the heart, which is supposed to (but often fails to) be the truest thing of all.” "Cards Against Diabetes" is my most popular post because I think it’s a ton of fun, and it touches a nerve. Some people are turning against the game as becoming tiresome, offense for the sake of offense, but I think it works well in the context of diabetes – what’s more offensive than that? It’s nice to share our experiences, and make mocking matchups. One day it would be nice to play with a full deck (that’s how diabetes makes me feel, too).


 Pop-Culture


 I do a lot of pop culture referencing in relation to diabetes (see my Star Trek rant from Thursday). One of my favourite pop-culture posts is my comparison of the diabetes life to the life and mission of Buffy the Vampire Slayer (my favourite show of all time). It’s a constant, valiant, thankless and unpaid fight, and all diabetes has to do is have one good day.


“As diabetics, we walk the fine line between secretly believing we're immortal and knowing that we've got this expiration date. In a way, we have more conscious control over what our bodies are doing than anyone else; in another way, we have much less, our bodies being essentially out of control with so many factors to deal with.  Buffy's super strong and quick, but she has to deal with all sorts of violently unpredictable outside forces that most people don't.” 


Another, “Latitude and Longitude,” takes an episode of the West Wing, where Sam has his worldview destroyed, and explores how things you thought were solid, like latitude and longitude, can turn into constantly moving goalposts.

 “Now, we place great trust in our devices. We try to believe that they will never fail us. We place our lives in the hands of plastic and metal and batteries and medical research, sure that they will work; sure that they will always deliver some sort of base measure of performance. Like latitude and longitude. We know this isn't true. Plastic fails. Metal fails. Batteries are spent. People get sick. People die. We take a lot on faith. Like latitude and longitude, which are invisible.” 


Finally, my favourite kids’ book, The Phantom Tollbooth, lends itself perfectly to the emotional journey of diabetes.

 D-Blog Week

We all need a little impetus to get writing, and D-Blog Week is so amazing for providing that every year. Some of my favourite D-Blog Week posts, to round out the list:
 “Diabetes Hero”: All about the people who mean a lot to me. It was nice to thank everyone, and to hope for the future.


 "Everybody who has touched my diabetic life is my diabetes hero. It's trite but it's true. Everybody with diabetes is my diabetes hero. If you asked someone to say or draw the first thing that comes to mind when you say "hero," it would probably be a fighter of some kind. A war hero; a soldier. A firefighter. And that's what we all are. We fight every day against odds that sometimes seem insurmountable; in a way, they are. The odds are literally insurmountable. We can't win. The best we can do is try, and see another day the best we can. Bravery is not the absence of fear; it's having the courage to fight in spite of that fear. The definition of hero seems to be a person who fights even when he or she knows he or she can't win, because it's right. That's what we do."


 “Mantras and More” won a couple of D-blog awards, and I’m so happy it resonated with people.


 Each drop of blood is a drop in the ocean
Each high and low is a wave in the sea
Each day you live represents forward motion
Each day you make it the best it can be. 

"Change The World (Sweat The Small Stuff)” was about the things that seem small, but really mean a lot. The post meant a lot to me.

 “The refrain is constantly there. The small stuff is the heartbeat pumping the lifeblood of diabetes: the fear inherent in every move we make. The small stuff is the big stuff. The big stuff is the small stuff. We are made of atoms, and capillaries, and the tiniest prickles on the skin. When we complain about the small stuff, we are saying: we are here. We are saying: we are scared. We are saying: listen.” 


Hope this wasn’t too self-indulgent! It’s fun to walk down memory lane.

Thursday, May 14, 2015

Diabetes Blog Week 2015 Day Four: Changes (Where No D Has Gone Before)

Today's topic is Changes.

Today let's talk about changes, in one of two ways.  Either tell us what you'd most like to see change about diabetes, in any way.  This can be management tools, devices, medications, people's perceptions, your own feelings – anything at all that you feel could use changing.  OR reflect back on some changes you or your loved one has seen or been through since being diagnosed with diabetes.  Were they expected or did they surprise you? (Read all posts here)

I have been watching a lot of Star Trek: TNG with my husband lately (it’s my first run through the series), and though it appears that they’ve cured a lot of things in the 24th century or what have you, when it comes to changes, I’ve really got my eye on that replicator, and how useful it could be with diabetes as it is now. There's a reason they call it the Enterprise D, right?

The food replicator could create anything you needed, with whatever nutrition you needed (I’m assuming it makes food that tastes the way you want it to with only the requisite survival calories, as otherwise it would be very difficult for the entirety of the future population not to weigh 600 pounds apiece). Chocolate sundae, 20 calories, five carbs please! Or, if it couldn’t do that, at very least it would be able to tell you exactly how many carbs there were in your food. No more SWAG-ing.

I got this, don't worry
Or, you could be, like, “hey, replicator…replicate some insulin into my pancreas” and the replicator would be like, “hey, man, what do you think this is, kindergarten? I just whipped you up a brand new pancreas.”

And Bev would be like, “who cares about all that? I’m an awesome space doctor and will just wave a buzzing thing over you and you’ll just be fine. Don’t worry about vision complications. You won’t get them, but in any case, we have sweet visors now.”

Anyway, yes, the replicator. Changes for now, right? You could make instant Dex tablets and Glucagon, and expiry dates would be a thing of the past. You could replicate medications and replicate out the side effects, and you wouldn’t have to pay half your salary to do so -

And Bev would be like, “why are you bothering with Glucagon? If Picard can have an artificial heart, you can sure have a perfect artificial pancreas. Or, here, let me just wave this buzzing thing as you lie under a silver lamé blanket for a few minutes and you are totes fine! Enjoy your space adventure.”
(I know it's really called a "medical tricorder.")
But what I’m really talking about, of course, is the replicator! You could use it to make beautiful crystal blue circle jewelry, and signs for your diabetes walk. You could create petitions with hundreds of thousands of signatures for funding for research. Maybe you could even fund research with a replicator. You could create perfect footwear, which would never damage your sensitive feet. You could ask the computer, “Computer, what is the status of my blood sugar?” and Majel Barrett’s voice would always reply, “a perfect 5.0!” (this is the FUTURE and everyone uses METRIC like Canada, you know).

Then Bev would be like, “hey, I’ve cured you twice already. Stop worrying about this crap. Go to the Holodeck and beat the shit out of a personified version of your immune system for a while for some catharsis, or talk to Troi, I don’t know. Diabetes is OVER. Did you not see the buzzing thing?”

And you’d be like, “Working pancreas! ENGAGE!”

Sorry, I got sidetracked. I was talking about the replicator and all the cool things we could use it to make to solve most of our problems, but I guess we’d just be replicating a bunch of band-aids.

What we need is that buzzing thing, and the cure.


Make it so.
Damn straight.

Monday, May 11, 2015

Diabetes Blog Week 2015 Day One: I Can.

Welcome to Diabetes Blog Week 2015! Today's topic: I Can.

In the UK, there was a diabetes blog theme of "I can...”  that participants found wonderfully empowering.  So lets kick things off this year by looking at the positive side of our lives with diabetes.  What have you or your loved one accomplished, despite having diabetes, that you weren't sure you could?  Or what have you done that you've been particularly proud of?  Or what good thing has diabetes brought into your life?  (Thank you to the anonymous person who submitted this topic suggestion.)



"You don't think I can love you/But I can, and I will, and I do" -Barenaked Ladies

These lyrics are the first thing that popped into my head when I read this prompt. I thought they were off-topic, honestly. I parody songs often (it's a sickness, really), so I'm no stranger to songs stuck in my head, ready for a twist. Taken out of context as they are, the lyrics whirled insistently through my brain.

Diabetes, you don't think I can love you/But I can, and I will, and I do.


Do I love diabetes?

Do I love it for the right reasons?

Anybody who has known me for more than two seconds knows that I am fiercely proud of my academic achievements. I roar as a Princeton Tiger and as a Columbia Lion. I've always graduated with high or highest honours from wherever I was enrolled. I've done it while often feeling unimaginably terrible.

Diabetes, you don't think I can…But I can, and I will, and I do.


I've only rescheduled one test due to diabetes. I very, very rarely called in sick to work while I was in school. The one time I remember doing so, I was supposed to go into scene shop, lift heavy wooden sets and possibly use power tools, and because my blood sugar was so low I could barely walk under my own steam, I figured it wasn't safe for anyone. The only time I took a paper extension, I was real people sick with walking pneumonia, and I didn't ask for it - I looked so bad that my professor unilaterally declared that I was taking one.

Diabetes, you don't think I can love you/But I can, and I will, and I do.


In a way, I think diabetes made me tough. Sometimes, I actually enjoyed it. One perverse thing about university culture (and I think it's pervasive in our culture in general, with the higher-powered professions and schools most heavily invested) is that we like to brag about our hardship. You got four hours of sleep? Child's play. I'm running on three. You wrote fifty pages this week? I wrote a hundred. You did it with a cold? I did it with bronchitis…and with diabetes. Hard to trump. Diabetes can make you "special" in identity, or in hardship; sometimes for the right reasons, sometimes for the wrong ones. Shakespeare, in his play Antony and Cleopatra, differentiated between Roman and Egyptian cultures. He billed the Egyptians as being in touch with both nature and their own senses, ready with passion, love, and a sense of enjoyment, from which they drew their power. Romans were in love, instead, not with themselves and their world, but with a sense of order and duty. How loyal could you be? How much could you work? How much could you sacrifice? Shakespeare's Romans were in love with hardship.

One of the things about "I can" is that many of us, as people with diabetes, feel we have something to prove. We want to show that we can do just as much as anyone else. This can be a great motivator, driving us toward success. It can also turn a person into a hardship-loving, hard-driving, Shakespearian Roman.

I'm doing this without an insulin pump.

I'm doing this without checking my blood sugar regularly.

I'm doing this without letting anyone in.

I'm doing this without a support network.

I am the best Roman. I am a CENTURION.

I can, and I will, and I do.


When I achieve something, or strive to do so, I am slowly learning to ask myself whether it is something I want to do, or something I feel I have to do, because it's so difficult. Do I have to play the game on the most difficult setting? Do I have to fight this thing at all turns?

Paradoxically, asking myself this question is one of the hardest things I've ever had to do.

Less paradoxically, it's been one of the most rewarding ones.

It may be a mistake to talk about loving diabetes, because, if I think about it a little more, that's just a slipcover for the heart of this thing. The lyrics don't even refer to diabetes. They really refer to me. How I learned to stop worrying and love diabetes is really how I'm learning to stop loving hardship and to love me.

Five years ago (in fact, I finished graduate school five years, less one week, ago), I found myself out of school for the first time, and I was unemployed. I felt rudderless; I had my achievements, but right now, I had no work to be doing. It was a perfect time to discover a support network in the Diabetes Social Media Advocacy network. Talking to dozens of other people from around the world, I found the hardship lessened, and that it wasn't a weakness; it was a strength. The Roman in me was always primed for war. The other side realized that making peace with the enemy takes more cunning than going in, guns a-blazing. Not only that, it's actually harder, but in a good way. June Callwood, in her wonderful article "Forgiveness" that she wrote at the end of a brilliant life, quotes a source as saying, "anyone who thinks forgiveness is for wimps hasn't tried it." Callwood then writes, as hard as forgiveness is, "it is worth the candle." Letting myself feel better and have the space to heal was a way of forgiving diabetes, and loving myself. Giving myself more tools to do better (an insulin pump, regular testing) is a way of loving myself. Going to the gym now, running up to 10K at a time, something I would have laughed at the concept of me doing - yes, another gift to myself.

I am still guilty of "being tough." When I smashed my dominant arm's elbow into two pieces a couple of years ago, I only took one day off work after the surgery to put the pieces back together, and the only reason I took that day off was because I woke up and I physically could not move. When I brag about that - as I have done - I realize I'm being a Roman again.

But I'm getting in touch with Egypt.

Can I promise I'll never fall back into those ways? Probably not. I still need some of my drive. I'm still overcommitted, but I'm mostly overcommitted to the things I love, and in which I can take real pride, not just hardship-pride. I love being a professor. I love having written a course that is now required for every student taking a BA program at my school. I'm trying, however, to achieve all of this with myself, rather than against myself. To make the hard choices to make things a little easier.

I can, and I will, and I do.

Tuesday, March 18, 2014

At Seventeen (Mice, Mice, Baby)

Today marks a couple of milestones. One of my very dearest friends turns 30 (Hi, Chris! I love you!) and my diabetes diagnosis turns 17 (two inexorably linked events in my head; as I've said before, the first day of diabetes + birthday cake is really effing confusing for a twelve-year-old).

I was going to say hi, diabetes diagnosis, I hate you. In some ways (many ways) I do hate diabetes as much or even more than I always have. It's pretty awful. The roller coaster ride, the wheel of fortune, the tower of terror...I could just keep naming rides and metaphors, but you get the picture. Diabetes is unpredictable and wild. It's just like a seventeen-year-old (or, as I imagine a wild seventeen-year-old to be; diabetes rebellion aside, my teenage wildness looked a lot like mildness).

My D is seventeen
I've had some very bad years
I've had some much better years
They happened very recently
I found the D-O-C
Much lower A1c's
My D is seventeen

On the other hand, my D has been the biggest learning experience of my life, and I've always said that I love learning! My D has made me a ton of friends, and I love friends! My D has given me so much to write about, and I love writing! It's funny; if a genie materialized before me right now and told me he could cure me, I would say yes in an instant, but if he said "I can make it so you never had diabetes in the first place," I don't know what I would say. It's made me a better, more controlled, more compassionate person. In some ways, it's made me special. I still think it had a hand in getting me into my first-choice university, which was an incredible experience and has affected my life in immeasurably positive ways.

I learned the truth at seventeen
That while D sucks, you have the means
To only suffer, or to smile
We're only on this Earth a while

In any case, today I choose to smile. Here is a cupcake my sweetheart gave me for my Diaversary (Bailey's frosting and chocolate cake). He's a guy who's in it in sickness, in health, and in cupcakes! I love him very much.

When I was newly diagnosed, I was told that there would likely be a cure in five years. I know most of us in the same boat could finish that sentence. I really held on to that idea. In a way, my first five years (until I actually turned seventeen) of diabetes were me in denial, trying to mark time until the cure was found before I went off to university. In a way, the healthiest (though most depressing) thing I've ever done is to basically "Let It Go" - let go of a hope for a cure in my lifetime. I'm not going to say I wouldn't welcome it, but I want it to be a nice surprise, not a "what took you so long?" To that end, I know we're all sick of seeing studies that report "A CURE!" - in mice only. As a Diaversary present to myself and you, I present my most elaborate parody ever. Please put on Vanilla Ice's seminal tune, "Ice, Ice, Baby," and rap: "Mice, Mice, Baby." I love you guys! I don't love fake cures.

Yo, D-O-C, let’s kick it!

Mice, mice, baby, mice, mice, baby
All right, stop. Commiserate and listen
I know these scientists are full of ambition
Ideas grab a hold of them tightly
One experiment and they’re on the nightly
News – it’s a cure? Yo, we don’t know
Though I know we want to think so
It seems so extreme, a dream too true to handle,
But please, remember to breathe, it’s a scandal

Calm down. Don’t rush the lab rat room
It’s hard to think when some hope pierces the gloom
But deadly, to wish instead of taking care of me
Less than five years, who cares about A1c?
Hate D or leave D, you still better play
Don’t put off to tomorrow the tests of today
Diabetes is a problem and maybe they’ll solve it
But this cure won’t do much unless they can evolve it

MICE, MICE, baby
They cured some MICE, MICE, baby
They cured some MICE, MICE, baby
Not humans, mice, mice, baby

Now that conclusions are jumping
With the hype kicked in, the media are pumping
Make a quick point, they anoint, but they’re fakin’
It’s as much of a cure as a diet of bacon
And we’re equally burned, ‘cause they show us a symbol
Of progress when evidence isn’t so nimble
And a high horse is ridden by those in the know
Breaking the news to the newbs caught in the show
It’s just “cure” v. 5.0
How much smoke can a headline blow?
If I gave this cure a try, then my meter would say HI
Not a chance, I just have to keep getting by
Diabetes will pursue me and I can’t stop
A mouse won’t live five years, me neither, I’ll drop
Then I’ll be dead.

Yo – so you know what, buddy? I appreciate the studies.
I’m glad the tiny beasties no longer have the ‘betes
No more sad squeaky sugar-filled mousy entreaties
But my body’s not a mouse’s, a mouse’s isn’t mine
And when is the day when they tell me I’M fine?
I feel like a chump with my ear to the wall
Running after a cure like a mouse stuck in a ball
Platitudes ring out like a bell
It’s hell, just a shell, well, don’t fall under the spell
Falling hopes are dashed real fast
Optimistic’s just sadistic and I’m running out of gas
My bumper needs a jumper ‘cause the deck seems stacked
I’m just trying to survive with a pancreas that’s cracked
D-Police on the scene, you know what I mean
They pass judgment, act like I’m a mean sugar fiend
Diabetes is a problem, but that doesn’t solve it
And this cure won’t do much unless they evolve it

MICE, MICE, baby
They cured some MICE, MICE, baby
They cured some MICE, MICE, baby
Not humans, mice, mice, baby

Take heed, because I’m a high glucose poet
If this applies to me, well, then why don’t you show it?
It’s the D-O-C’s town, and we’re going to make a sound
Enough to shake and kick holes in the ground
‘Cause there’s fast, safe and cheap, or there’s slow, drag, and kill
My BG is always changing but advances seem so still
Strip safety reform, that’s a hell of a concept
Not sexy, but fixing “the D got her as she slept”
The closed loop system, with low suspend will aid
This ninja-like feeling of life lived on a razor blade
So sharp, other people say “damn,
How you measure out a life in shots and milligrams?”
I keep my composure with goals, some strict, some loose
If I’m high, then I’ll cry, if I’m low, I’ll drink juice
Diabetes is MY problem, and I’m going to solve it
With my friends worldwide, we’re going to evolve it

NOT mice, mice, baby
They cured some mice, mice, baby
That must be nice, nice, baby
But we’re not mice, mice, baby
No more advice, vice baby
‘Cause there’s a price, price, baby
We’re STILL not mice, mice, baby!
Not quiet mice, mice baby

Yo, man, let’s get out of here! Word to your support network!

-Ilana

Tuesday, March 11, 2014

Strips Do Lie (Stripkira Feat. Highclef Jean)


A while ago, I wrote a fairly popular post (called Liar) about the revelation that test strips could read +/- 20% of reality and still be within FDA guidelines; the idea was that this was one more lie that people with diabetes have to deal with (and, in fact, deal with it several times a day). When you don't know where your glucose level really is, how can you properly manage yourself? I hear that the FDA is welcoming public comments on their proposed new guidelines for safer meters and strips (you can read about it at StripSafely, here). While I doubt they would publish the following, I thought that I've already gone the angry route, so why not the lighter route?

In my college years, "Hips Don't Lie" was omnipresent at the clubs on party nights (here it is for reference). It popped into my head the other day, and I thought, your hips don't lie? Well, my strips DO lie! 

Thus, I present to you: "Strips Do Lie," by rising pop star Stripkira, featuring Highclef Jean (though a part of me wishes it were Notorious D.O.C.). I did the best I could with the song's incredibly loose meter and rhyme scheme (I hate slant rhymes, but the original's full of them!):

Blood up in here tonight,
No Error Fiving, no Error Fiving
Capillary action up in here
No Error Fiving, no Error Fiving

Strip Safely, Strip Safely

I never really knew that strips could fail like this
Turns my chart data into gibberish
Am I high (si) or low (si)
Or somewhere in the middle (who knows, si) -
Strip Safely, Strip Safely

Oh strippy when you read like that
You make a woman go mad
So be wise and keep on
Reading the signs of my body

And I’m low tonight
My strips do lie
And I’m starting to see the light
All the aggravation, the tension,
You must see this is short of perfection

Hey strip, I can see your numbers changing
And it’s driving me crazy
You don’t seem to know where you are ranging
Accuracy is hazy

And when you have such a margin of error
Nobody can ignore the way you treat my body, strip
And everything so unexpected – one-test it, two-test it
And oh the numbers so different

Hey strip, I can see your numbers changing
In a forty percent span
And so I don’t really know what I’m doing
I can’t seem to make a plan
My will and self-restraint
Have come to fail now, fail now
See, I am doing what I can, but with bad info
That’s a bit too hard to calculate!

I never really knew that strips could fail like this
Turns my chart data into gibberish
Am I high (si) or low (si)
Or somewhere in the middle (who knows, si) -
Strip Safely, Strip Safely

Oh strippy when you read like that
You make a woman go mad
So be wise and keep on
Reading the signs of my body

And I’m low tonight
My strips do lie
And you know that isn't right
My life hangs on each injection,
You must see this is short of perfection

Oh you know I’m low tonight
My strips do lie
And it’s giving me a fright
If you’d be a little more accurate
Oh, I’d even change out my lancet

No Error Fiving
No Error Fiving
Strip Safely
Strip Safely

Monday, August 12, 2013

The Diabetes Phantom Tollbooth

As a child, my favorite book was The Phantom Tollbooth, by Norton Juster, with pictures by Jules Feiffer; much like Anna Quindlen of the New York Times opines, I thought it was "the best book ever." Shockingly, it was one of very few books that I discovered by seeing the movie adaptation first; I accidentally came across it during a visit to Florida, and my parents were deprived of much of an afternoon at the beach as I refused to stop watching. The story features a young boy named Milo, who is always bored, and is never satisfied with wherever he is or whatever he's doing. One day, a box arrives, "for Milo, who has plenty of time," and Milo grudgingly assembles a cardboard tollbooth with some mysterious coins and a child-sized toy car. Once through the tollbooth, he winds up on a quest through a series of magical lands that teach him the value of letters, words, numbers, senses, sights, sounds and the magic that knowledge unlocks. The book is filled with wordplay and puns, and it inspired me to pursue writing (an effect I'm sure it had on many curious children).

To me, the Phantom Tollbooth's many fantastic locations and wonderful puns can be applied just as easily to diabetes as to any other aspect of life. Here's a look through The Diabetes Phantom Tollbooth:

The book opens on you, newly diagnosed with diabetes. In a funk, depressed, you don't want to be where you are. A mystery package shows up, with a note: "TO YOU, WHO MAY THINK YOU NO LONGER HAVE TIME." When the Diabetes Tollbooth arrives, first, you have to put in your coins to get through. When we're talking about a toll, that's definitely a word I associate with diabetes.  Mental, physical and financial, you've got to pay these tolls to get through life.

Driving along the road, you first encounter The Doldrums: Here's where you get stuck early on in the book and in diabetes. It's grey, boring, and sad. No thinking is allowed, and certainly no laughing. You can get dangerously stuck in the Diabetes Doldrums, and it's difficult to get out; the Doldrums want you to stay, and they want to consume you. The Doldrums are a poor representation of life, but they're easy, if you don't care what happens to you. Everyone gets stuck once in a while, but the trick is to get out! Tock, the "watchdog" in the book, represents the wonderful Diabetes Online Community, with a CGM in his belly. Your best friend, he keeps you on track, telling you to think, imagine, and dream. It's hard work, but it moves you forward.

Next, you encounter The Whether Man: The Whether Man in the book knows that it's more important to know whether there will be weather than what the weather will be. He reinforces the need to always be prepared for any circumstance. He also knows there is no "wrong way" ahead; just your way, and my way, or someone else's way. Your diabetes may vary!

You finally come to your first city: Dictionopolis: Here we learn that words mean something, and impact the way we feel about our condition, our lives, and ourselves. Words like "brittle," "the bad kind," "noncompliant" are shown to be powerful negative weapons, that are combatted by words like "hope," "community," "friendship," "meet ups," and "ice cream." Here we also find that you can make it further by listening if you don't have all the info, rather than speaking, for like the Dictionopolis car, it "goes without saying." Often, people will be forced to eat their words, just as they do in Dictionopolis, so it is really important to think before one speaks, and to say something nice and tasty. Half-baked ideas are served for dessert, and just like real desserts, they're tasty and intriguing but dangerous if you eat too many, or take them too seriously. If you give your diabetes Short Shrift, you may be arrested by him (Officer Shrift), but you can be let out of jail if you display a Faintly Macabre sort of humour.

Your job in this world is much like Milo's: you have to find your sense of Harmony. Your sense of self has been split, with this diagnosis; the words you use to describe your world, your life, your self - they don't match what the numbers say. The numbers are out of whack and need constant correction. The words are fighting with the numbers as to which is more important, and have banished the princesses of Rhyme and Reason, who understand that words and numbers must be given equal importance. Nothing can be set right until Rhyme and Reason are returned. Armed with new words, you set out on your quest with Tock, the Humbug (how you sometimes feel) and the BEEtes (a giant bee that spells everything out for you).

Along the way, you meet a boy who grows to meet the ground, and you understand you must grow to meet your own set of challenges. You complain, and complain, but then you meet Dr. Dischord, who wants to cure the world of pleasant sounds so all you hear is noise, and you realize that constant complaining can purge your ears of the wonderful sounds of the world. Chroma the Great, who conducts the sunset, helps you to see the rich colour and texture diabetes can bring to your life, even though you must conduct your own symphony. Sometimes, like Milo, you get too ambitious and your colours go out of whack, or you seem to lose days at a time to this vicious disease, but with help you can get back on the conducting track and it might seem as if nothing had ever happened.

You get to the point where you're starting to take charge of this diabetes thing, when you encounter the Valley of Silence. It's so tempting to stay with the status quo and be quiet about what's "wrong" with you, but you see the injustice for all in remaining quiet about what needs to be done, and letting the message be controlled by a select few media narratives. You break the silence for good with activism, blogs, diabetes walks, petitions, videos. You spread the message of need and success far and wide.
The Dodecahedron

Now that you're interacting with other people and organizations, you suddenly find yourself on The Island of Conclusions. You get to this island by jumping; jumping to conclusions. Here we find many representatives of the media who deal with diabetes, and many other individuals who we deal with on a daily basis. As soon as a reporter assumes an older person has Type 2, or that there is only one type of diabetes, or that a thin person can't have Type 2, they would be off to the island. As soon as someone assumes you ate too much sugar as a child, that you brought it on yourself, could cure yourself with a diet, or that diabetes is easy to deal with and insulin is the same as a cure, they would go right to the island. We would love to actually send these people flying to the Island of Conclusions, where we wouldn't have to deal with them until we jumped to a few conclusions of our own (why isn't my BG coming down? Must be bad insulin. Couldn't be the pasta).

You finally find yourself in Digitopolis, the land of numbers; you try to figure out how all this math works and how it's going to be relevant to you living your life. While you figure out that averages don't tell the whole story and that you can run forever and not reach infinity (or, as we call it, perfection), you find some valuable tricks for your arsenal, guarded by the kindly Mathemagician (who may well have the face of your endo or your CDE).

The Dodecahedron shows you the many faces of diabetes, and you're introduced to Subtraction Stew - or, its real name, insulin. Insulin, like Subtraction Stew, is the only thing that can make you feel hungrier after you've eaten bowl after bowl of food. But, if you don't take it, Subtraction Stew takes on a whole new meaning: nothing you eat is actually absorbed into your system, and you can get thinner and thinner the more you eat; as the Humbug observes, it's like eating bowls of "FAMINE!" Eventually, you learn that, while they don't always add up like you would like them to, just like the words that don't always tell the right story, numbers are absolutely valuable tools that you must use to better live your life. Sometimes, they can even be fun, like when that pencil the Mathemagician uses as a wand pencils in a "no-hitter"!
The Mathemagician and King Azaz of Dictionopolis

The two sides of you have slowly agreed to work together, but you must make the final push; you have all the tools you need, but you and your few friends set out to find Rhyme and Reason alone. The Castle in the Air, that mythical-sounding place of true harmony, awaits. It can't be real; can it?

The scariest and most taxing part of the journey toward Rhyme and Reason is fighting your way through the steep, dark Mountains of Ignorance, which teem with demons of all types.

The Terrible Trivium is at the head of the demon pack. The Terrible Trivium gets in your way, big time. He is a minor demon, who puts you off taking care of yourself. He tells you to fritter away your time on other, meaningless tasks, because "in five years, there will be a cure." You must use your numbers to look at the real situation and pull yourself away from this seduction, reminding yourself that he has no real face.

Other demons chase you and you must fight them: the Demon of Insincerity, a false friend who sounds big and scary, but has no real power; the Overbearing Know-It-All (just listen to me; I know more about you than you know about yourself), the Threadbare Excuse (I was too busy to take care of myself), the Gelatinous Giant (just try to struggle out of these mountainous insurance claims! You must fight him with activism) and the snake-oil salesmen who form the twin Gorgons of Hate and Malice. It's a hard struggle, and it feels like a lifetime, but you make it to the stairs at the base of the castle, where you encounter one last gatekeeper: the Senses Taker.

The Senses Taker, who wants to take all your senses, is a frightening reality. Here is where you truly learn the power of your words, and yourself. You fear the loss of yourself, your identity; more tangibly, you are terrified of the loss of sight, of heart, of feeling in your limbs. But you fight back with love and laughter, because, in the end, nobody can take your vital sense of humour. Past the Senses Taker you go, and up those precarious steps with every fibre of your being and those friends by your side, and you open the door to the Castle in the Air.

And there Rhyme and Reason have been, waiting for you, all along.

You feel whole. Your journey is complete. You're a hero: adulation, banquets and all. Your A1c is the best it's ever been. Your endo wants to throw a ticker-tape parade. But then, you have to say goodbye, and really step out on your own, to a future that could be just as scary as this parable got at its worst.

You wake up. You're suddenly far away from Digitopolis and Dictionopolis. Tock, the Humbug, the BEEtes; they're not always with you. You've come so far and learned so much, and you recognize its worth. But you know there's so much left to be done, and learned, and experienced. Today, like yesterday was, and like tomorrow will be, is the first day of the rest of your diabetic life.

The tollbooth is gone, but you find a note left in its place, and in its own way, it means everything.

It says, "TO YOU, WHO NOW KNOW THE WAY."

Saturday, May 18, 2013

Ode to an Insulin Pump (D-Blog Week Day 6: Diabetes Art Day)

Today's D-Blog Week prompt:

This year Diabetes Art moves up from the Wildcard choices as we all channel our creativity with art in the broadest sense. Do some “traditional” art like drawing, painting, collage or any other craft you enjoy. Or look to the literary arts and perhaps write a d-poem or share and discuss a favorite quote. Groove to some musical arts by sharing a song that inspires you diabetes-wise, reworking some song lyrics with a d-twist, or even writing your own song. Don’t forget dramatic arts too, perhaps you can create a diabetes reality show or play. These are just a starting point today – there are no right or wrong ways to get creative!

This is tough for me, as most of my blog seems to already be diabetes art of some kind! You could check out the beginning of a mystery novel here, song parodies here and here, or the beginning of a diabetes Law and Order episode here (I will finish that someday, but I don't have the energy right now)! I get intimidated by art prompts, as I consider myself (or have been considered to be; sometimes I doubt myself) some kind of writer. I actually have a short diabetes-based relationship play I wrote back in mid-college when I was trying to figure things out for myself; I'd post it but I'd probably embarrass myself.  So today you get something quick and dirty: a Shakespearean sonnet parody (okay, I might be one of few people who call a Shakespearean sonnet parody quick and dirty). Diabetes seems to lend itself to Shakespeare; it's full of both wild comedy and high tragedy. If you want to quibble about the occasional extra syllable leading to a "feminine ending" of a line, I say it adds to the analysis, as a "feminine ending" often relates to indecision or distress.  Anyway, now that I've analyzed myself, I leave you with:

Ode to an Insulin Pump

Shall I compare thee to a pancreas?
Thou art external and more temperamental
Rough numbers do shake me as the hours pass
And homeostasis, achieved, seems incidental

Sometime too high the glucose rises up
And my once-pale complexion turns to rose
Or dropping fast, an orange-juice-filled cup
Must quell my shakes ‘fore everybody knows

Thy Bolus Wizard magics up a dose
Thy Basal, steadfast on its course it stays
And though you help me as I keep you close
Still, I feel you are shortening my days

My true one vanished, leaving but my fears:
That cruel promise, to “wait but five more years!”


-Ilana

Friday, March 1, 2013

Low

Yesterday, as I was rushing from work to appointment (one hour on transit) to rehearsal (another 30-45 minutes), I felt that old, familiar, sinking feeling. Low blood sugar. Insufficient blood glucose. A hypoglycaemic incident. Whatever asinine thing the media decides to describe it as, such as "a diabetic attack" or some such vague garbage.  When Diabetics Attack is the name of my proposed reality show. I'm sure it will be very popular.

When my BG goes low, sometimes I feel like I'm about ready to attack. I don't think things through as well, or consider complexities and implications. I get angry and irritable and greedy. It's suddenly all about me and there's no charitable thought towards others, as long as I've "got mine." I feel like I'm dying out and I'm scared. It's what I imagine being a member of the Tea Party to be like.

Low blood glucose is a little like being drunk, in the worst possible way, with added hands shaking, cold sweat, and the feeling that your life force is draining out of the soles of your feet. Your head rushes. The glucoaster roars downward. Your pulse pounds. Tunnel vision becomes inevitable. Standing becomes an unimaginable feat. Powering yourself up a flight of stairs? There are 100-pound weights around your ankles. When someone who has never experienced real hypoglycaemia describes the experience of not eating for a while and feeling hungry, irritable and a bit shaky and week, I can only smile, both because I'm happy they've never had to experience the real danger, and because it's a polite but very muted understanding of the event. When I'm really low, there is a danger signal in my brain that says "No really you are going to pass out and die this time for sure." But there's another part of my brain that says "don't be late you have to get where you're going what's wrong with you are you going to let this stop you you weakling." (When I'm really low, my brain does not use punctuation; there's no time.)

I made my way through the molasses that was the air, past the people collecting for Second Harvest (in my tunnel vision, I couldn't stop to take out money; with my lizard brain it seemed too painful to listen to them talk about people who needed food). It was rush hour, but I managed to slump my way into a middle seat on the subway. I was so thankful there were no elderly people or pregnant women or obviously-disabled people around; nothing makes me feel guiltier on the subway (besides rushing by a talented busker, charity collection, or person down on his/her luck) than not wanting to relinquish my seat to someone "needier" when I look so hale and healthy, but my invisible disability is killing me at the moment. I hope everyone sees my shaking hands and the colour drained from my face, which is already very pale, and doesn't judge.

My trusty grape Dex. (source: Dex4.com)
Luckily, I had provisions with me. I ate two granola bars in quick succession, and popped open my glucose tabs, eating about five. I forced myself to stop after that, though at that point everything in the train car still looked edible. It's like that Troy McClure "educational" film about the meat industry on The Simpsons: "Don't kid yourself, Jimmy. If that cow had the chance he'd eat you and everyone you care about." I don't know if it was just my own low-induced paranoia, or reality, but suddenly I felt judgmental eyes on me, the girl who had just wolfed down two granola bars and what likely looked like a tube of candy. I turned the tube outward so anyone who was looking good see that it had a medical tagline printed on it.

I could stand to lose a few pounds, but I'm an average size. Taller than the average woman, big-boned, a decent weight for all of these factors. It's actually a major thing for me to say this, because I'm actually the first person to call myself fat. If I can tear myself away from self-judgment for a minute, though, I can say that I'm certainly not "officially" fat or obese. I have always been self-conscious about my weight and the size of my frame, however, and I was wearing a fairly puffy coat, it being the last gasp of February.  At the moment where I started panicking over the perceived judgment of my fellow subway patrons (remember that blog that mocked people eating in the New York subway?) I came to a bizarre realization: I am more self-conscious about treating a low in public than I EVER was about taking a shot in public, or testing my blood in public.

Has that happened to anyone else? Is that strange?

Treating a low in public is different from performing a medical operation. For all intents and purposes, to others, it just looks like you're stuffing your face and, if you're on the subway, that you can't wait the 15-30 minutes to get where you're going. I couldn't. To give you some idea, after over-treating with the two sweet granola bars and 5 glucose tabs (probably 80g of carbohydrate), going to rehearsal, not taking any correction bolus at all, and coming home, I tested, thinking I was probably at least 10 if not 15 (instead of being somewhere between 4-8). I was instead barely up into the normal range, at 4.2. This was actually worrisome; just how low had I been? It's hard to test on the subway, especially when squished into a middle seat, so I hadn't, as there was no way that could have been anything but a low.

Eating isn't causing my diabetes, I wanted to say loudly. It's saving me from it. I'm so used to people judging people with diabetes over food that I feel ashamed to "overeat" in a public space, even if it's necessary, even if my diabetes isn't the "weight" kind.

And that, I have to say, makes me feel pretty low.

-Ilana

Friday, August 31, 2012

Buffy the Diabetes Slayer

For comedy's sake, dressed as Vampire Willow
In my apparent quest to compare diabetes to pop culture, I suppose I always knew I would reach Buffy the Vampire Slayer eventually. My sentimental favourite show of all time, it aired at the perfect time in my life (middle through high school) to become a part of my growing-up process. I could go on and on about the show, but I won't. Suffice it to say that Buffy is the Slayer, sworn to do battle with the vampires (with some notable exceptions) and the occasional demon; knowing that one day she will lose and be replaced.  (This is, by the way, the only instance where I will compare myself to Buffy; everyone who knows me will tell you I'm pretty much a [pre-Tara] Willow, right down to the identical SAT scores.)

In the Broadway musical Title of Show, a vampire is defined as something that saps your creative ability, such as self-doubt, or negative people ("Die, Vampire, Die!")  In Buffy, vampires are a metaphor for a host of issues we all face as we grow up. In my life, diabetes is the vampire. I'm not just saying that because it sucks.  Or because it sucks a lot of blood out of me on a daily basis, but that is a fair comparison; because blood is a daily thing for me and for Buffy, it has a tendency to remind us of our bodies, being alive, and the importance of blood to both of those things. As Spike the vampire said in "The Gift," "Blood is life, lack-brain. Why do you think we eat it? It's what keeps you going. Makes you warm. Makes you hard. Makes you other than dead." It's a bizarre phenomenon when your own blood becomes the enemy, with too much or too little glucose spelling disaster.

I've been thinking about this because, in the process of introducing the fiance to the series, we recently watched the episode "Fool For Love." (Warning: spoilers for a couple of things in that episode lie ahead.) One of my favourites, its genesis lies in Buffy confronting her own mortality. She's doing better than ever in the fight, gets a bit cocky, and then gets staked with her own stake, by "just" a vampire: 

RILEY
So tell me about the bad guy- or guys. What do you think they were?

BUFFY
Vampire.

RILEY
How many?

BUFFY
One.

Riley is surprised.

RILEY
So... what? He was like a super-vampire or something?

BUFFY
No, he was the regular kind. He just beat me.

RILEY
That ever happen before?

BUFFY
I'm in the best physical shape of my life. I mean, if you're asking how it happened, I don't-

 Buffy desperately wants to find out what went wrong and how she can avoid this mistake from ever happening again. She obsessively scours the Watcher Diaries for answers that she can use, but finds nothing:

GILES
You didn't lose last night, Buffy. You just-

BUFFY
Got really close. I slipped up, Giles. I've been training harder than ever and still I... (beat) And there's nothing in any of these books to help me understand why. I mean... look, I realize that every Slayer comes with an expiration mark on the package. But I want mine to be a long time from now. Like a Cheeto. If there were just a few good descriptions of what took out the other Slayers, maybe it would help me to understand my mistake, to keep it from happening again.

Eventually, Buffy turns to Spike for answers. Though we find out how he's killed other Slayers (and a great deal of his origin story), we find out that it boils down to a couple of things. One, that every Slayer has a bit of a death wish, and without ties to the world, it might take over. And the other?

SPIKE
(nods)
[...]we just keep coming. But you can kill a hundred, a thousand, a thousand thousand and the enemies of Hell besides and all we need is for one of us- just one- sooner or later to have the thing we're all hoping for.

BUFFY
And that would be what?

Spike leans in close and whispers in her ear.

SPIKE
One... good... day.

And that's the thing about being a Type 1 diabetic. You fight little battles every day that keep coming up, over and over again.  You may be in the best shape of your life, a line of Buffy's that resonated with me because my latest A1c was better than ever. But there are complications, and things unaccounted for. There are reactions, and, most terrifying, there are lows.

As diabetics, we walk the fine line between secretly believing we're immortal and knowing that we've got this expiration date. In a way, we have more conscious control over what our bodies are doing than anyone else; in another way, we have much less, our bodies being essentially out of control with so many factors to deal with.  Buffy's super strong and quick, but she has to deal with all sorts of violently unpredictable outside forces that most people don't.

Whenever I have a frightening day with diabetes, particularly with a bad low, my thought process becomes like Buffy's. What specific thing did I do wrong? How could I have countered that move? How can I stop it from happening again, and become the Cheeto with the long-off expiration date?  It's even worse when I see news stories about Type 1s my age, slightly older, or younger than me, dying in their sleep. These tend to get circulated around the Diabetes Online Community in solidarity, because we're all upset. These become my Watcher Diaries, where I scan them trying to figure out how I'm different somehow. What mistake did this poor kid make? Was this guy a really hard partier? Were there drugs involved? Another condition? Did she stop taking insulin? To understand my impulse, there's no blame involved, just a psychological reaction. Most of the time, there is no specific "mistake" - I'm just like them. Even if there was a "mistake," I've made them all over the years, and I'm still here. And that's not because I'm a special Slayer. There is no "why." All of those people should be here still. And they're not.

Because diabetes slipped in and had One...Good...Day.

That's all diabetes needs to be the last vampire. One good day. The element of chance is a heartbreaker. What Buffy, and what I have to learn, is to see being the Slayer as both a quest with a long haul (the mission, the season-long arc) and with small, individual battles and episodes.

"The thing about the dance is, you never get to stop," says Spike. Diabetes is that dance. It's the Big Bad. In a way, it's a similar calling; not something you'd ever choose, but something that you have a duty to deal with, and can become all the stronger for. And you get certain "superpowers," like being bionic. You perform "spells" like Willow, except the magic is insulin, exercise, or sugar. (And sometimes, like Willow's spells, your combinations go awry.) The only difference is that, unlike the Slayer (for the most part, without including any more series spoilers), there doesn't have to be the sense of being totally alone, "one girl in all the world," even if it does feel like that sometimes.  In our community, everyone's a Watcher and a Slayer, providing some much-needed ties to the world. Plus, I've got my own Scoobies to keep me company. I wonder if I should start calling my lancing device Mr. Pointy?

In any case, it's a worthwhile fight.

Grr, Argh....

-Ilana
(All "Buffy" quotations from Fool For Love credited to Douglas Petrie; quotation from The Gift credited to Joss Whedon)