Elis de Guerre

My jeans are tight, and show off the curve of my ass. My black shirts are fitted, sometimes low cut, but always flattering to my figure. The only thing that isn't crafted to maximize my appearance are my non-slip shoes. Otherwise, I have to look pretty. Pretty girls get better tips.

The first step isn’t to admit I have a problem. I don’t.

Many people are aware of bipolar disorder. Most know it’s a mental illness that swings the brain between depression and mania. Most understand depression to be debilitating, a condition that combines sadness, despair, exhaustion, and lack of motivation. But most people don’t understand mania (which is experienced primarily by people with bipolar I) or hypomania (which those with bipolar II tend to encounter more than full-blown mania) — at least not fully.

Two months ago, I filed for disability for unmedicated bipolar disorder. I had spent weeks dangling from tiring hands over a spiky precipice – or so it seemed. There were days of crying at my desk, days of inexplicable panic attacks in the face of a normal workload.

It took me a long time to understand consent. I knew that forcing sex on someone was rape. I knew that one in five women would be raped in their lifetime. I knew that the majority of rape victims knew their attacker. But beyond that, my understanding got cloudy.

What I objected to was the genderization of feminism, the idea that women's rights have to be specifically prioritized. If the overall end goal is equality, why bring gender into the equation?

I can feel proud of my cleavage and my combat boots. I feel fierce in drop-crotch sweatpants and preppy sweaters. I carry my edge with me and, with it, my own brand of femininity. Best of all, I consult no one but my own eyes. I don’t ask permission. I don’t seek what’s in fashion.

[CN: suicidality, hospitalization, rape culture, slut-shaming.] We all needed a place to recover, a place where our problems could be addressed and dealt with, a place where we could feel safe. However, the way the women in the ward were treated couldn’t possibly have made us feel safe or comfortable.

I first went on disability when I lived in Rochester, New York.

When my therapist told me in 2012 that I presented with symptoms of PTSD, I was relieved, but also in disbelief.