Today I Became A Billy Goat

Great Falls ParkToday, after a night out dancing in DC (I don’t know why the person who never drinks thought it was a good idea to mix three different types of liquor), on another date, I visited Great Falls Park for the first time. This rocky water wonderland is a mere 16 miles outside the city. That is one thing I love about here – you can feel like you’re out in the country yet still live in an urban environment.

But in visiting the Maryland side of the park (and as my date would point out the better, less crowded side), I successfully climbed the Billy Goat Trail (and yes, I use climb for some very specific reasons). I had heard stories of the Billy Goat Trail and how I should definitely give it a try. What no better time than in my hungover state?

For some reason, I imagined this trail was like any other paved pathway, a little debris and uprooted branches but nothing strenuous and then at one point the trail would become a short ledge one would have to maneuver around before getting to the top. Yeah that was what I imagined. Clearly I did not think about the words “Billy Goat” in the name. Continue reading

My Body Is Okay

I was sweating my ass off on the way to my third doctor appointment this month. I decided to take the time from work and travel halfway downtown (plus another 15-minute walk from the metro) to see a specialist about my recent lab results – results my former endocrinologist said showed I had another autoimmune disorder.

I wasn’t so sure. For one, I didn’t have any symptoms. For two, only one result came back abnormal, and the level was barely below the normal range. And for three, I couldn’t handle the idea of having another autoimmune disorder, even if it only meant taking a pill every day for the rest of my life.

But in the past week since I learned of these results and made this follow-up visit, I started questioning myself. Had I gained weight in the past few months? Wasn’t I feeling more tired lately? Hadn’t I been more depressed than usual? Didn’t I feel thirsty all the time? Didn’t it feel like I had a sore throat even though I knew that was impossible? Continue reading

Insights From Wine and Water Bugs

“Are those water bugs? Where did they come from?” My friend asks as we watch the one-inch black bugs scurry across her back patio.

They appear to have no direction and disappear beneath the ivy next to the glass frog statue. The air is cool but humid, and we both sip on our glasses of Sauvignon Blanc and contemplate our relationship statuses.

We are both in our late twenties and single, having just ended long-term relationships. Everyone around us seems to be getting married or having kids. And even though we know that’s not what we want, we can’t help but feel like we’re missing out on something.

“I just don’t know if I want to try again, you know? I’m just tired,” my friend says, shrugging her shoulders. I agree and place my wine glass in front of me. My friend’s dog whines at us from behind the adjacent gate. Continue reading

Autoimmunity

It’s hard to live when you don’t trust your body, and no matter what you do, it continues to disappoint you.

Today I found out I may have another autoimmune disease. I was notified by email of my recent lab results. And a short note from my doctor: you have ______. Here are my medication and dosage recommendations.

No call. No explanation. No consultation. All I had was one abnormal test result and potentially another incurable disease that meant I would have to take a pill every day for the rest of my life.

It’s not so bad. It’s manageable. They all said the same thing when I was diagnosed with Type 1 diabetes six years ago. Is this how I’m rewarded? Continue reading

Why Life Isn’t A Failure (Even Though My Mood May Tell You Otherwise)

When my colleague knocked on my office door earlier this week, I could barely keep it together. As soon as she saw the tears and trembling lips, she opened her arms, and then asked what was wrong.

“I don’t know, I’ve been crying all morning, and I don’t even know why. It’s not like I’m hormonal right now.” I threw up my arms and started venting or whining as I often like to berate myself.

There were many reasons to cry, I had deduced, but they all pointed to one thing: I felt like an absolute failure – that I had failed my life, and there was no way to remedy it.

Here are the reasons why I thought my life was a complete failure: Continue reading

Connecting This Way

I remember when social media became a thing, when Apple first introduced the iPhone, and how others worried about whether technology was killing our connectivity or not? Are we all the more connected yet narcissistic, so wrapped up in our everyday nuisances that we forget about the world and each other?

I can’t say I blamed them — the more Facebook posts I saw from the generation behind me, even my own generation, I wondered, too, if we were all becoming so self-absorbed and into ourselves that we ignored the benefits of having a collective. And maybe that’s why so many of us ranted on about being alone to a world of loners on the internet?

I feel like my generation is caught in the middle — some of us have completely embraced technology, and some of us still remember dragging the corded phone from the hallway into our bedrooms and the irksome sound of dial-up.

I Remember When…

I remember the excitement of getting my own phone with my own line (this was before caller ID and cordless phones). It’s not that I was much of a phone talker, but I liked the privacy. I remember when my best friend’s family in middle school got their first home computer. I remember thinking how much the black and white box reminded me of a cow. Continue reading

The Neverending Ride: Six Years With Type 1 Diabetes

I throw the covers off and stumble out of bed. I wipe the sleep from my eyes and look at my phone for the time. I check my CGM for my blood sugar level. I put on some pants and clip my insulin pump to the waist line.

You told me six years ago that we were going for a ride. I didn’t know then that the ride would never end. And for those six years, I’ve been searching for a way to get back home, but after all that I’ve experienced and all that I’ve seen, can I really go back?

Chocolate and White Cupcake

Today marks my six-year anniversary with Type 1 diabetes. Six years ago at this time I was waiting in the exam room of Xavier University’s health center for results on a severe skin rash. But the results of that skin rash, among other symptoms and an out-of-control blood sugar reading, pointed to Type 1 diabetes. I was admitted to the hospital a few hours later and so began my journey with this autoimmune disease.

My anniversary coincidentally follows #IWishPeopleKnewThatDiabetes Day (April 22, 2015). I felt a sense of solidarity with the diabetes online community as I read through the various hashtag tweets. And I feel like my small contribution to the day evinces how I truly feel about the disease and others’ perception of it.

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‘The Examined Life’ and the Printed Word

Today marks the third and final day of The Examined Life Conference: The Writing, Humanities, and Arts of Medicine, hosted at the University of Iowa College of Medicine in Iowa City, Iowa.

Rare medical book textAmong the gorgeous 70-degree weather and the nostalgia of walking along the paved pathways of a college campus, in the last three days, I feel like I have trespassed on history, found a deeper self-identity with my chronic illness, tripped on the psychedelic words of poetry, and discovered a new direction for health care reform.

I admit I wasn’t familiar with the arena of narrative medicine before arriving here. In fact, I wasn’t sure what to expect coming from a creative writing background myself and only having been pushed into the field of health care by my disease. But amidst fellow creative writers and those managing their own chronic conditions were health care professionals writing about it. Some write about their own personal stories — others attempt to peel back the layers of patient stories.

For the first time since working with CancerFree KIDS back in Cincinnati, I felt the power of writing, not just for my own therapeutic means, but for those who may not know how to tell their story, but so desperately want to. And how that story can change the future of a system that currently encourages disparity, neglect, and hopelessness.

Continue reading

Peanut Butter May Still Be the Death of Me

I woke up at 2:30 a.m. shaking, while Cosmo, my continuous glucose monitor (CGM) vibrated and beeped at me from the nightstand to my right. I pushed its button, acknowledging the warnings, and saw the screen light up with the number 45.

I didn’t need to check my blood sugar level with my glucometer. My heart was pounding, and the room was blurry. I thought of the orange juice in the fridge but decided to go for the Reese’s egg in the freezer. I knew from recent calculations that this chocolate-covered, peanut-butter filled egg contained 25 grams of carbohydrates (mostly sugar).

That should do it, I thought. Norm, my two-year-old tabby walked into my bedroom and sat on the floor in front of my bed with a quizzical look. The egg didn’t feel like enough even though I knew it was. I checked my insulin pump, which confirmed there was no active insulin in my system. My basal rate was set to decrease from .600 units to .400 at 3 a.m. to account for those middle-of-the-night lows.

I knew I would be okay, but I was still shaking, and my heart was pounding. My body felt weak and depleted, and I craved sugar – the sustenance necessary for instant energy. Earlier that day I had made the mistake of buying a few bags of Reese’s pieces eggs, now 50 percent off in the post-Easter haze. Continue reading