The Ups and Downs of Lows

I’m driving my grandma’s formerly owned 1993 Geo Prizm down Taylorsville Road in the suburbs of Louisville, KY. My boyfriend at the time sits in the passenger seat rocking out to Blue October. We’ve seen them twice in concert, once at Louisville’s Fourth Street Live. We’re visiting my family for the weekend, just a few weeks after I was diagnosed with Type 1 diabetes. I will be the first in my family to graduate from college in Cincinnati in a few weeks.

I start to feel shaky and weak, but I don’t tell Reed. He recently shaved his head to mask his receding hairline at 22. His former football player fingers tap on his torn jeans. I focus on the yellow lines of the road. We’re only a mile from home – no reason to pull over. I can beat this. Come on Tracy, focus.

My peripheral vision goes fuzzy. Only half a mile now. I stop at the red light at the four-lane intersection of Taylorsville and Hurstbourne Lane. One moment of reprieve.

“Are you okay?” Reed asks, no longer whistling.

“I’m fine,” I say, still focused on the hazy yellow lines.

“You just seem really tense.”

“Let’s get back to my parents’ house, and I’ll explain.”

I pull into the three-car driveway, off to the side, in front of the rose bushes. I run into the one-level brick house. I am as much curious about the state of my blood sugar as I am worried. Reed finds me in my old bedroom, painted a faded blue.

“Whoa, 51,” I say, more out of amazement than concern.

“I don’t think I should have been driving,” I add, heading down the black and white tile hallway to the kitchen for some juice. I’m almost proud that I didn’t have an accident rather than regretful.

“Probably not,” Reed says, his eyebrows raised. Continue reading

Diabetes on Birth Control

One of the biggest fears of any single young woman is getting pregnant. I feel this is tenfold now that I have Type 1 diabetes. The stress of affording my own health care is enough – I don’t want the added physical and emotional burden of surviving pregnancy with diabetes much less affording my child’s coverage (given the possibility that the child will also have diabetes). No one can yet prove that my diagnosis was a result of genetics, but they cannot disprove it, either. I’d rather not take the chance.

In the past five years, I have attempted different types of birth control. The pill was always the easiest and most reliable option, but low and behold, no matter how many different types I tried, it always had a negative impact on my blood sugar readings and insulin resistance. What does this mean?

Well, while on the pill, my blood sugar skyrocketed, and I needed to take more insulin to keep it stable, but then, during the week of my period when I wasn’t on the pill, my blood sugar plummeted so that I would experience severe lows and have to readjust my insulin to carb ratio. You would think I could account for this every month, and believe me, I tried, but there was no telling when that initial plummet would happen. Sometimes, it was a few days before my period; sometimes, a few days after. The following week when I started taking the pill again, my blood sugar would rise so that I would constantly be adjusting my insulin to carbohydrate ratio until I got it right. It seemed to vary month to month.

Because I was tired of the constant ups and downs and the effect the pill had on my hormones and my emotional sanity, a few months ago, I stopped taking it. Cold turkey. I knew my body before I started the pill and relied on its natural cycle, but that was before I committed myself to long-term relationships. Now it was time to trust it again. It certainly improved my blood sugar readings. Continue reading

Rising Health Care Costs: The T1D Label

I’m nervous about the future of health care in this country, especially for type 1 diabetics like myself. I was diagnosed almost five years ago at the age of 22. I have no family history, and there was no evidence of an autoimmune attack so the doctors do not know why my pancreas just stopped making insulin. But it did.

Many researchers point to a combination of genetic susceptibility and environmental triggers. With the amount of chemicals plaguing our food and our household products, that’s not so surprising. But then why, among my two brothers and a mother and father, was I the only one that contracted diabetes? When I was diagnosed, my parents were surprised, mostly because out of everyone in our family, I was the only one who made a daily, concerted effort to eat right and exercise. What was it for?

This is a question I no longer ask, and I am thankful I have employer-sponsored health insurance that will cover the cost of my expensive disease. But when it comes to health care, I am one of “those” who potentially costs the system. I fall into the “high-risk pool.” From an evolutionary perspective, I should have been weeded out of the population five years ago. But here I am.

Even though I am no longer considered “young and healthy,” I still consider myself “young and healthy.” I manage my diabetes well with an insulin pump. I maintain an A1C of 5.6 (average blood sugar readings over the last 90 days). My average daily blood sugar readings range from 70 to 160. I still have bad days, and if I had a continuous glucose monitoring (CGM) system, I’m sure it would show a higher range, but when you have to survive on animal insulin injections and carb estimations, how much do people really expect you to get it perfect?

I’m thankful for the insurance I have, which allows me to afford my insulin pump supplies, my test strips and insulin doses. There was a time when I didn’t have coverage, when I had to pay for my “life source” out-of-pocket, and suffered the consequences (financial and physical). I’ve endured a health insurance roller coaster in the past four years. Continue reading

I Am a Rose of Sharon

I can’t stop my leg from shaking. The needle hasn’t even pricked my skin, and even though the tattoo artist in front of me is probably annoyed, he smiles.

“This is never going to look like a fleur de lis if you keep that up,” he jokes. My friend Britteny from work sits on the other side of me. She smiles, trying to reassure me. Everyone’s nervous their first time, she tells me with her pale blue eyes. It shouldn’t be natural to want to permanently imprint an image onto my body for the sake of art and beauty, for the sake of remembering where I came from.

I always wanted a tattoo, but because of its permanent effect, it took me four years to figure out where and what I wanted. I decided on a fleur de lis, a symbol of my hometown, Louisville, KY, named after the French King Louis XVI. Britteny encouraged me to use color so I chose my two favorite colors: blue and purple.

I finally calm down enough so that the tattoo artist can begin his work. He’s big with a short, gray beard, but a gentle touch. He outlines the French symbol on my ankle; I wince every time he nears the bone, but I do not cry. I never cry in public. I refuse to show weakness. It takes longer than I expect, but time passes quickly as Britteny tries to keep me calm, and I watch mesmerized by the needle. Continue reading

Drinking to Undo Diabetes

I hadn’t been drinking that long before I was diagnosed with diabetes. Suffice it to say I was a good girl who usually followed the rules. But upon turning 21, my friends started winning late-night happy hours at downtown Cincinnati bars. I attended many of these happy hours, and with the first two drinks being free, it didn’t take long to make it to five.

Two weeks before I was diagnosed at 22, I was at a downtown bar with my boyfriend at the time, Reed. It was crowded for a Thursday night, mainly due to these happy hours. Reed and I had just returned from attending church with his family – it was the Thursday before Easter, and even though I no longer practiced Catholicism, I adored his family, calling them my own, and willingly subjugated myself to the torture of mass to spend time with them. I even wore purple (the color of lent, a season of repentance for Catholics).

I was nursing my second beer when Reed returned from the bar with two White Russians (he was a huge Big Lebowski fan) and two Bud Lights in hand.

“Thirsty?” I said, raising my eyebrows.

“Happy hour ends in 10 minutes, had to make the most of it,” he said, shrugging his shoulders. I wasn’t planning on getting drunk that night, but you know how the story goes …

Two weeks later, on April 24, I was admitted to the hospital for a severely high blood sugar (690). I was supposed to spend the evening with my boyfriend and his aunt and uncle. Instead, I was alone in a cold hospital bed with a dead cell phone and a disease. Within 24 hours, the doctor and nurses got my blood sugar down to 200. Although I was advised to stay another night, I pleaded with them to let me go, promising them that I was responsible and would take care of myself. Continue reading

Sister, Sister

It seems to be staring at me, although I don’t see a face. I only see its black rectangular body and a few mechanical buttons that I suppose could be eyes – they are my life source. It’s buzzing at me, but I ignore its demand for attention.

There was a time I didn’t need you.

It doesn’t hear me. It doesn’t seem to respond, but it moves across my desk, as if inching closer to my exhausted body.

You are gray and ugly, and I don’t want you … but I need you.

I have a weird relationship with my insulin pump. If we were on Facebook, it would read, “It’s complicated with Gizmo.” Yes, I’ve named it Gizmo. I figure if it’s going to share my bed, it should have a name.

In approaching the holidays, I realize even though Gizmo has only been with me for two years, diabetes has been in my life for almost five. That’s not a lot considering most people with Type 1 were diagnosed when they were seven. What was I doing when I was seven? Oh yeah, playing beneath the Maple trees of Kentucky and going to church with my family every Sunday.

When I was in college and realized the brain doesn’t fully develop until we’re 20 or 25, I considered this might be why childhood seemed like the happiest years of my short life. I hadn’t met reason yet. I didn’t think about the horrible atrocities happening in the world or feel stressed about how quickly my next paycheck would disappear.

No, I lived in the present – my only concern was what fun things I could do with my day. My brother, two years younger than me, and I used to make lists during the summertime and then vote on the items on that list, planning out our free time and deducing what activities we would engage in that day.

We built Lego cities in the basement, played “house” in the church parking lot across the street, and pretended to be sisters. One time my father came home and found my brother dressed in a witch costume, answering to the name of “Susan.” I don’t know why he liked that name so much, but when we played “Sister, Sister,” I always let him choose his female name. To be fair, we also played “Brother, Brother,” but after my dad found my brother wearing a dress, we never played sisters again. Continue reading

Food Junkie

For the first time in 16 years, binging hasn’t been an issue. In my book Sugarcoated, I refer to myself as a “food junkie.” I love late night snacks such as peanut butter ice cream, sweet potato cinnamon crackers, pumpkin flax seed granola, etc.

Ever since college, I’ve conditioned myself to eat less during the day so I can binge for dinner or later. I grew up with the rule “if you finish dinner, you can have dessert.” I’ve never been able to break this. Even when binging got out of control to the point where I stuffed myself until I felt pain, I would throw it all up, refuse to take insulin, or starve myself the next day so I wouldn’t gain weight (for more insight, check out “Half Empty” in Sugarcoated).

I no longer practice these nasty habits, but I still can’t help overeating at night, whether it is summer or winter … until now. So what has changed? Suddenly, I’m not interested in food? I forget to eat lunch or can’t even finish my dinner much less make it to dessert. Usually when I stop eating, it’s because I’m depressed.

But I recently started a new job, which I love, and moved in with my boyfriend of three years (we were doing long distance before then). I have my own place, financial security (minus thousands in student loan debt), and maintain a healthy lifestyle (although I wish I exercised more but with a 1.5 to 2.5 hour commute each way, it’s a challenge).

Could it be I stopped binging because I’m happy? Researchers from the University of Central Florida (2003) found a positive relationship between happiness and these aspects of body esteem: sexual attractiveness, weight concern, and physical condition.

Furthermore, eating disorders such as binging are more common among women with diabetes than women without diabetes. For those with Type 1 (like me), this is referred to as “diabulimia.” I admit even before I was diagnosed with diabetes at 22, I had issues with body image and eating disorders. Diabetes just added an extra element including increased health risks (Joslin Diabetes Center) such as: Continue reading

The DC Metro: It’s Not Baltimore (Baltimore has a metro?)

After kicking and screaming along the DC beltway, I decided to try my commute with the MARC train and DC metro. I’m not new to public transportation. When I moved to Baltimore for graduate school, I sold my Honda Civic and navigated Baltimore’s best and worst neighborhoods using the local bus system (sometimes I pretended to be a Hopkins student and caught a free ride on their shuttle), Light Rail, Metro Subway, and the Charm City Circulator.

More often than not, however, walking was more reliable than public transportation, but either way, I survived without ever being stabbed, robbed, or raped (although I was often harassed by men).  But that’s because I had a series of rules, which I rarely broke:

  1. Do not look anyone in the eye
  2. Do not talk to strangers
  3. Do not respond even to a “hello” – you do not want to initiate dialogue or let your guard down
  4. Always walk like you know where you’re going
  5. Always wear a frown (what I like to call the “don’t fuck with me; I’ll kill you” face)
  6. Never accept help
  7. Always be aware of your surroundings and stay away from “suspicious” characters
  8. Always leave yourself extra time and have a back-up plan – public transportation is anything but “reliable”

What do I consider suspicious? Am I too dependent on stereotypes? When it comes to my safety, I don’t care. If anything makes me uncomfortable, I remove myself from the situation. For example, one time an older gentleman sat next to me on the Baltimore metro and started talking to me even though I had my headphones on and every other seat was empty. He wasn’t threatening me, but I didn’t want to be bothered, and he was making me uncomfortable. I simply acknowledged him, stood up, and walked to another train. He didn’t follow me. Continue reading

Kicking and Screaming: The DC Beltway

Stop and go. Stop and go.

One lane moves. The other three don’t. Change lanes. Now the other lanes move, and mine doesn’t.

This describes the epic battle on the DC beltway during rush hour. Yes, I’ve somehow convinced myself this new job is worth the 3 hour commute from Baltimore to Bethesda and back again.

I’ve tried 29. I’ve tried local traffic. Nothing changes. No time is saved. So far, my best bet has been to travel among the lost and forsaken on 495.

I’m in the process of looking for a carpool. I feel bad being a sole traveler in one vehicle, but when I look around, I am not alone. Not to mention the added gas expense, wear and tear on my car, and the increased carbon emissions.

And then there’s the train. I’m also trying this option out, but this requires waking up at 5:30 a.m. to catch a bus to the train station, which takes me to Union Station in DC, and then the metro to Bethesda. It’s a roundabout way to commute, but it would save me $50 per month and the hassle of driving in rush hour traffic.

The catch? I have to get up an hour earlier only to get home an hour later. But you can be so productive on the train, they tell me. Except with such long days, all I want to do is zone out or sleep, but I’m too paranoid to sleep in public. Continue reading

Gizmo aka My Insulin Pump Comes Back

It wasn’t a weekend of firsts. It wasn’t a weekend of lasts. But it was a weekend that changed my outlook on this whole “diabetes” situation.

I did more than survive a weekend without Gizmo, my insulin pump. I re-learned the challenges associated with counting carbs and calculating insulin dosages and how to listen to my body.

Sunday and Monday were good examples.

On Sunday night, my blood sugar felt high (159), but not high enough to warrant a correction dosage of one unit (the lowest increment my flex pen will allow). I had a vague recollection my syringes were divided into 0.5 increments. I only needed a 0.4 unit correction dosage.

I looked at the needle on the syringe – not much longer than my flex pen; I could do this. Now how do I get insulin from the vial to the syringe without breaking the needle? The last time I used a syringe was four and a half years ago, right after I was diagnosed.

Apparently, I needed to unscrew the bottom of the syringe to access the plastic extension that would allow me to fill the syringe. I couldn’t fill it to the 0.5 mark. How would I get out the air bubbles? I used the same method I use for the plastic vial I attach to my pump. I overfilled it and then used the extra space to rid of the bubbles.

Now I will just inject myself with the 0.5 increment and dump the rest back into the insulin vial, I thought. However, as soon as I inserted the needle into my skin, I realized how stupid this was, how easily I could accidentally inject myself with all 15 units of insulin. That means I would need to eat 300 grams of carbs to make up for it, which would totally defeat the purpose of this. Continue reading