What’s It Like Living With Depression?

Personally I know when the depression is about to hit. I can feel this immense amount of sadness for no apparent reason, and I suddenly don’t have any purpose to my life. I just go through the motions and want to cry at every little thing. There’s no reason for me to be sad. Maybe there was a trigger? Maybe there was a moment that just led me down a bad path?

But usually I can prevent those triggers. Usually I can prevent myself from going down that path. But sometimes it just happens. Sometimes you can’t foresee it, and your mind goes to dark places. It starts to reason things it would never reason before. And it starts to believe in the insecurities you’ve worked so hard to overcome.

You know it’s not true. You know your rational mind doesn’t justify it. But you can’t help but feel this way. Usually when I get to this point I just detach myself from the world and push everyone away. I don’t even want to talk about it. I’m thankful I can at least write about it. That I want to write about it. Because I haven’t felt this way in a while.

I thought I had found some defense mechanism to keep myself from getting to this point. But depression is a lifelong battle. No matter how hard I try it will always be there, itching to get back under my skin. And it could be hormones right now that’s making me so glum and down. I don’t know. But I know there’s no getting out of it, not until the fog lifts.

The best I can do is go through the motions, keep myself active, keep myself moving, and sleep through the worst of it. That’s always been my defense mechanism. I don’t know how else to overcome it. When I try to explain it to others, they don’t understand. And I’m tired of trying to explain. So I just take a step back for a while. And hope when I come out on the other side they will still be my friends. Continue reading

The Day My Insulin Pump Outsmarted Me

I stare at Gizmo, my insulin pump. I review its user settings, and basal and bolus rate set-up. But nothing within this gadget tells me how to change my reservoir numbers.

Yes my body is no longer producing enough insulin. And yes that means I must use more insulin to function on a daily basis. My basal rates have increased from .325 to .900, and my bolus rates have increased from 1 unit of insulin per 20 grams of carbs to 1 unit of insulin per 13 grams of carbs.

When my roommate a few years ago told me her basal rates were 1.000 unit, I scoffed and hoped I would never reach that level, at least not for another five years. But now having only had diabetes for six years I am now almost there.

The downside? I’ve been switching out my pump’s reservoir every two days. It used to be that 100 units of insulin would last me three days, if not four. And in the past month, it’s only lasted me two days. Continue reading

I’m Not Back… But My Pancreas Is (Sorta)

I’ve decided to take a break from my other writing projects to write this blog post. Because even though I may take a break from my blog, my diabetes does not take a break from my life. And upon learning some unexpected news recently, it seemed appropriate to mention it here.

So I’m not back to regular blogging but I may pop in every now and then.

Another Year in Cookietown

I’ve spent the past week and a half in Cookietown (aka my parents’ house during the holidays). And my blood sugar levels have never been so amazing. I even reached a no-hitter a couple of times (keeping my blood sugar levels within the lines for an entire day). That means no extreme highs (above 200) and no extreme lows (below 70).

No-Hitter-web

So how did I manage this? Well I’d like to think it’s because I’ve gotten better at managing this disease in the six and half years since I was diagnosed. But the real truth is completely based on biology.

Apparently my pancreas is still making insulin. Continue reading

Taking a Break But Not Forever

Much has changed since I started this blog on September 11, 2013. My nonfiction grad school cohort can tell you how much I didn’t want to write about diabetes for my MFA thesis – the book that became the start to this blog. And in the six years since I’ve been diagnosed, I am still learning new things about myself with this disease.

I wanted to share those experiences with the world and contribute to a community of Type 1s. And maybe I wanted to prove to myself that I could manage life given this short end of the stick. What I didn’t expect when I started this blog back in 2013 was where it would take me and what kind of content my readers would inspire me to write.

I cannot tell you much I value your readership and support these past two years. You are the reason I keep this blog going. You are the reason I continue to write. And although this blog has kept me writing and contributing to this online community, I must now re-focus my priorities and take what little time I have to write to devote to other publishing opportunities. Continue reading

My Life With Diabetes: Am I in Control?

I walk down the cracked sidewalk along Wisconsin Avenue, past the Starbucks and Regal movie theater in Bethesda. My fingers start to tingle, and my heart rate increases. Suddenly I feel extremely weak. Each step is an effort, and I feel a steel box closing in around my heart. I am out of breath. My limbs start to shake, and my vision is less reliable. I can’t read the street sign in front of me. I stop at the next intersection and look for the glucose tablets in my purse.

I scramble to chew four of these tablets quickly, leaving a powdery residue on the tips of my fingers. I lean against the side of a brick building and call my supervisor. I’m supposed to be in a meeting in two minutes but until I get my blood sugar back up, there’s no way I’m making it back to the office without help. I’m only a five-minute walk away, but right now my vision is blurry and my hands are shaking.

My supervisor doesn’t answer his phone so I call my work colleague and let her know of the situation. I usually don’t tell people when I’m having a low blood sugar, but in this case, I realize it’s the safest thing I can do in case I do have a seizure in the middle of the street. My work colleague has severe allergies so we’ve both agreed to be each other’s medical back-up. I know where her EpiPen is, and she knows what to do if I pass out from low or high blood sugar. Continue reading

Needles, Reservoirs, Cannulas, and More

The other day I was replacing my insulin pump reservoir. This requires a series of steps that I will reiterate for those who have never had to replace their insulin pump supply (as a side note, manufacturers, physicians, and researchers alike recommend switching this supply every three days although I sometimes stretch mine to four).

Replacing my Insulin Pump Reservoir

The first thing one needs is an alcohol swab, reservoir, infusion set, a blue cylinder-shaped device to inject the infusion set underneath the skin, and of course the insulin and pump. So after wiping the spot on my stomach with alcohol and then the top of the insulin vial, I use the reservoir to fill the plastic insulin container with insulin from the vial (it’s important to make sure you remove all air bubbles from the plastic container). And then of course my cat knocks the vial from my desk (it’s small enough this is harmless).

I then twist the reservoir into the end of the infusion set. I rewind the insulin pump so that it knows there is zero insulin inside and can essentially start to recount my usage (I tell it I use 100 units per new supply). I place the new reservoir into the insulin pump and then fill the 23-inch thin plastic tubing of the infusion set so that I know insulin will safely travel through the cannula from the pump to underneath my skin (this usually requires 6-9 units of insulin per fill). Continue reading

‘It’s All About Perspective’

More than a week ago, I was in Louisville, Kentucky for my 10-year high school reunion. In addition to that, I spent a wonderful extended weekend with family and friends celebrating birthdays and life’s successes. And all of this while sleeping on a cot (because like myself, my parents do not waste space — as soon as I left for college my old bedroom was turned into a bedroom for my brothers and then an office for my parents).

And although I may complain every time I visit about the sleeping accommodations and the fact that I lay exposed in the living or dining room, I am secretly proud of my parents for not keeping my bedroom as a shrine, for making the most of what they have.

But since that weekend, I have endured countless awful days of stress and anxiety. And I sank into a small depressive hole, questioning what I was doing with my life and why my personal and professional lives could not co-exist in the same city.

Photo Aug 17, 2 16 46 PM

Devastating News

That is until I learned one of my best friends was almost beaten to death on his bike over a cell phone. Suddenly my questions about a meaningful existence seemed irrelevant. Because all that mattered is that my best friend made it out okay. All that mattered was that someone I loved would survive this tragedy without too much scarring. Continue reading

A Not So ‘Silent Spring’

Rachel Carson Silent SpringIt should be amazing to me that in the six years since I’ve been diagnosed with Type 1 diabetes and the four years I’ve been involved in the sustainability movement, I have yet to read Rachel Carson’s Silent Spring, a classic for environmental health advocacy. This is the book that catapulted events leading to the establishment of the Environmental Protection Agency and the ban on the production of DDT (the effects of this chemical are sadly still with us today).

And yet it was published in 1962 by a woman. That was more than 50 years ago, and I admit Carson might appreciate that we have taken her words to heart, but she would probably be disappointed with the amount of toxic chemicals that still plague our homes and health statuses.

Even though my chronic disease is “autoimmune,” my body showed no evidence of this fact. And even though my doctors tell me it’s probably genetic, I have no family history. The media and scare over the diabetes epidemic would have you believe it’s my fault, but I’ve always taken good care of myself and have always been in good health until six years ago. Continue reading

All The Pretty Girls

It’s hard to feel pretty when I feel like my mouth is the size of a cantaloupe, and I can only chew my dinner on the left side of my jaw. Today I had three cavities filled. I’ve never had a cavity in my life (damn those childhood sealants, which apparently become traps for bacteria as an adult).

I should really stop going to the doctor. This year is the year of medical expenses. Every time I go, even for what I think is going to be a yearly check-up, they find something wrong with me. A part of me wonders if this is some kind of conspiracy, but when my dentist showed me the actual images of my cavity-filled teeth, I knew he wasn’t lying.

The procedure wasn’t as bad as I thought. The numbing shots didn’t hurt, and there weren’t any bad smells, but when I left the office, I was oddly self-conscious of my numb face, and the fact that if the side of my face started to droop, I probably wouldn’t notice. So I spent the 20-minute walk home trying to keep my lips shut and avoid any kind of conversation with passersby.

But how is this different from any other day? I have a 10-minute commute to and from work every day. I’m lucky in that DC sense. And every time I make that trek, I am oddly self-conscious. Are my headphones too loud? Can anyone see my underwear line? Can anyone see my lacy bra peeking out beneath my sleeveless top? Is that bulge beneath my pencil skirt obvious? Are there sweat stains beneath my bra line?

Yet even amongst all these questions, I’m oddly confident. I make that walk like I own the sidewalk, and I never look back. I’m aware of my figure, and how good I look in my pencil skirt. But do I ever notice anyone checking me out? No. Do I ever see people look at me? Yep. And I automatically think there must be something wrong with my wardrobe or my headphones aren’t plugged into my phone and everyone can hear my music. Continue reading

What I Need to Remember: Love is Real

Time CapsuleTen years ago one of my best friends from high school and I created a time capsule. Last year as I was going through boxed things at my parents’ house in Louisville, Kentucky, I came across an envelope with “June 17, 2015” written on the front. I took it back with me to DC.

But I was nervous to discover what my 18-year-old self thought my future would hold. So as I went running this morning, I reflected on how 10 years ago I was with my best friend sitting on a bench near the park by her apartment complex and writing down our lives. We wrote about what we thought mattered most and what we thought we wanted to preserve for our 28-year-old selves.

So when I returned from my run, I turned the envelope over in my hands, but I couldn’t open it. Did I think I would be married by now? Did I think I would have that bestselling novel? Did I think I would be living in some foreign country? I decided it would be best to wait to open the envelope until the end of the day when I could have a glass of wine in hand and sleep on it if need be.

Twelve hours later, I opened that envelope and the first thing I read made me cry. At the top of the piece of loose-leaf above Time Capsule (because even at 18, I was an organized freak), I had written the following (in what seemed like a last minute addition):

What I Need to Remember: Love Is Real.

Continue reading