Marked With an “S” 

From the day that I was born I’ve been marked with an “S”,
it’s stuck to me like a stamp that has permanently stained my skin. 

Spina bifidascoliosis—the scary diagnoses meant to define me,
but that’s only where my story begins. 

Became a statistic before I could even breathe on my own, 
with a slim chance of survival, yet look how much I’ve since grown. 

Learned to ignore curious stares since I was a child, 
to understand that they were just kids too, and just respond with a smile. 

Sit up with a straight spine, stand tall in my sneakers—some of the things I’ve never done.
Is that, to you, what makes me such a “special” one? 

I’m no superhuman, I don’t see what you do. 
I may wear some stitches and scars, still I don’t need anything from you. 

Despite several surgeries and sicknesses I’ve made it out,
because that’s not what my life is all about. 

Though it may seem, I do not suffer from what I have,
so save your sympathy for someone else, and let me speak on my own behalf.

I’ve got no sensation in my legs, 
but I’m not half of a human, so don’t treat me that way.

Surmounted every stereotype and stunned the world, 
but I am that I am—I’m just a girl.

So call me strong for everything I’ve been through, 
but in your next sentence, make sure to say that I’m a sweet friend, a sports fan, a big sister, and a storyteller too.

~~~
Though I was born with a disability, I’ve never let it affect my entire life or mentality. I’m fortunate to have the best family and friends that treat me as they would any other, therefore I used to think it was silly to take a day to “celebrate” me, because there’s so much more to me than my disability. I always thought, “Why should I be celebrated for simply being me?” I’ve only recently realized that it’s okay to take pride in the things that make us unique from the rest, mine just happens to be my disability. Furthermore, by having a designated day or month for such, I can embrace those within my community and find comfort and familiarity within our shared life experiences. So, Happy World Spina Bifida Day to myself, and to all born just like me!

Sunburn

We burned brighter than the sun until the day you left—left me here with nothing but the memory of you, stinging like a sunburn. 
You were untouchable; the person I once was had so much to learn.

I craved your affection like my body craves the warmth of the sun,
so why did you have to run? 

I’ve tried to peel your ghost from my scorched skin but you were determined to leave your mark. 
You set me on fire, then left me here to burn in the dark.

So, like an insatiable itch that won’t go away, 
you haven’t left my mind to this day. 

I often ponder about what we could’ve had, 
If only I knew then, it would hurt this bad.

I shouldn’t have ignored all the warning signs, but I did. 
Can you blame me? I was only just a kid.

It took some time, but what I know now, 
is that I’ll never let another break me down.

Now here I am, a freckle-faced girl with a brand new glow,
someone I could’ve never been without the tear stains written in your name on my pillow. 

I used to see the golden sun in your eyes,
but somewhere in between tender tan lines and little white lies,

I’ve forgotten your name. 
You’re fading now, so there’s not much more to say. 

I once thought I was at the point of no return, 
thankfully the pain you caused was only temporary, much like a sunburn. 
~~~
When you’ve never experienced romance nor the heartbreak that can stem from it (thankfully!), as a writer, sometimes you have to rely on other familiar experiences, pure imagination, and some dramatics to create stories. As is the case with this poem, the idea of which was inspired entirely by an actual sunburn I obtained this summer (that I still have tan lines from). Pretty neat, right?