The Opposite of Loneliness: Keegan’s Voice for a Generation

I just finished reading Marina Keegan’s The Opposite of Loneliness, a collection of essays and short stories from a Yale graduate who died shortly after graduation in a car crash in 2012.

I don’t know if I would have picked up the book had I not known that the author had died at such a young age – that and she wanted to be a writer. In fact, she already was, with a job lined up at the New Yorker, and a play about to be produced at the New York International Fringe Festival. Her last essay for the Yale Daily News, “The Opposite of Loneliness,” had received more than four million hits, mostly when others heard of her passing.

While I was on Scribner’s website, looking up a contact for work, it was this title that actually drew me to the posthumous book. She was only two years younger than me when she died. From the introduction, I didn’t think I would like the author’s voice. She seemed over eager, privileged, and too innocent, but I wanted to give her a chance. If I died and somebody published my essays postmortem, I would want someone to give me that chance so I added it to my Kindle queue.  Continue reading

Peanut Butter Bait

Briston set up the traps months ago, baiting the mice with pinches of peanut butter.

“It’s best to leave the peanut butter on before setting the trap,” he said, “that way the mouse gets use to it and doesn’t expect the snap.”

We had just moved into a two-bedroom apartment on the second floor of a rowhouse in downtown Baltimore. Even though we’d been dating for two and a half years, more than half of that was long distance. Once I graduated with my MFA, Briston made the move from Orlando to Baltimore to give the relationship a real shot.

“That’s fine,” I told him, referring to the mouse trap, “as long as I don’t have to clean it up.”

Two years prior when I lived in a basement apartment north of the city, I had my first encounter with a mouse. He scared me when I turned on my bedroom light, and he ran out from under my bed.

A few days later I was sitting in the living area on the flower-printed couch, donated by a previous tenant, reading a book. I had set a similar peanut butter trap, at the suggestion of my roommate.

It was 9pm, and he scurried out from behind my bookcase against the wall across from me. He sniffed around my TV stand and ignored the peanut butter. Then disappeared down the hall. I didn’t scream or fret. As much as I don’t like living with other things, I live under the philosophy, “if you don’t bother me, I won’t bother you.” Continue reading

A Purse Full of Diabetes Supplies

I don’t like to carry much. I used to avoid carrying a purse or bag. But I also like to be prepared. And with diabetes in tow, it’s hard to do both.

Like today, my blood sugar started dropping once I left the office even though I had corrected the last low two hours ago. I couldn’t for the life of me find my glucose tablets, but I did have Gatorade on hand, so for now, my blood sugar stabilizes.

Here’s what I always carry with me:

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The Same Route Twice

Sometimes, I wonder how much more my body can take. At some point, I’m just on auto-pilot, and at the end of my 16-hour day, I’m surprised I’m still functioning, considering I’m one of those people who tries not to take the same route twice (for safety reasons and to mix it up a bit).

Today is one of those days. In addition to physical stress, I am overwhelmed by a whirl of emotions, a reaction to pending changes in my life. I’m preparing to move (again); helping other friends prepare to move; finding new friends and some desperately needed R&R while working for a promotion at the first job I’ve ever cared for. Some may say I’m 27 – this is normal.

But with the additional management of a chronic disease, changes in insurance status, filing claims, switching doctors, acquiring new scripts for that coveted 90-day supply, it’s a wonder I accomplish anything. And as a side note, what’s the point in having an FSA debit card if I have to submit receipts, explanation of benefits, etc. every time I use it?

Rewind 10 years…

I sit on the swing set of a small park near my best friend’s apartment in Louisville, Kentucky. As the sun fades, the crickets come out. I love their sound as long as I don’t have to step near their ugly brown spotted bodies that used to roam our basement and give me daymares.

My best friend Maria and I agreed to meet here one evening in June, the summer before we left for college. She would stay in Louisville. I was destined two hours north for Cincinnati.

We met freshman year of high school waiting for our moms to pick us up outside the new building to our all-girls school. We started talking about politics and cultural events. We philosophized about life and love and by the end of the year, we had become best friends. Continue reading

Things I Wish I’d Known

A few months ago I retweeted a quote from Elizabeth Gilbert that went something like “things I wish I knew at 25…”

My five year anniversary with diabetes is coming up in a few days, something I was reminded of this morning during a visit with my new primary care physician.

“You said you were diagnosed at 22?” she asked in a bubbly voice, an endearing tone like that of a child’s rather than a bratty teen.

“Yep, April of 2009.” I said with a smile, swinging my legs against the edge of the exam bed. Why should that make me proud?

And that got me thinking about what I would tell my 22-year-old self now. What words of wisdom could I share with a young woman, driven by education and a career yet hungry for young love and adventure?

Things I wish I’d known:

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Thanks for the job. By the way, I have diabetes.

I never say in job interviews or on my first day that I’m diabetic. Legally I cannot be fired or reprimanded for my medical condition, but I make a conscious choice to pretend it doesn’t exist, like I’m “normal.”

Of course people warn me that I should tell at least someone I work with about my disease. Even though I manage it well, anything can happen and someone should know what to do in that situation.

Eventually, I do. I make a friend or someone asks about my pump or my glucometer, and then that follows with 10 million more questions about diabetes: what’s the difference between type 1 and type 2, can I eat sugar, do I have to take injections, does it hurt, etc., etc.

I’m happy to answer these questions. When I was diagnosed at age 22, I didn’t know what diabetes was much less how it would change my life. Why would I? I studied psychology in college. I was more familiar with the symptoms and repercussions of bipolar disorder than what a normal blood sugar range was. So I’m always happy to share my first hand experience with others. Well, almost always.

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Diabetes Breakdown

Not every day is easy with diabetes. Not that it should be. My pancreas doesn’t work so technically I can’t properly digest food so technically, five years after my diagnosis, I shouldn’t be alive.

I should be thankful for technology, thankful that even though these medical supplies cost me a ridiculous copay, they keep me alive – they help me maintain an overall good quality of life.

I should be thankful, but there are days when I come home from my two-hour commute from DC and I stand in my walk-in closet debating what outfit I should wear tomorrow and then I lose it. I just sink to the dilapidated hardwood floor and start sobbing.

Okay maybe there’s more to it than that? Maybe it’s been a rough day? Maybe I’ve been having highs all day for no apparent reason other than my hormones started going crazy? Or maybe I’ve spent half the day going back and forth from the insurance company to the pharmacy to the doctor’s office trying to get my 90-day supply of test strips covered? Continue reading