I’d ask myself, “What is wrong with you?” And I wished I could say, “Nothing is wrong.” But I knew better.
“You’re quite the puzzle,” my doctor said as I sat quietly on the exam table in her office. She scanned my extensive lab results, which I’d stapled together according to date. I swallowed hard, my throat burning, knowing I would leave yet another specialist with no answers. “Everything looks normal to me. Nothing is wrong.”
Nothing is wrong.
Continue reading “Child-on-Child Sexual Assault: Healing Old Wounds”
“I remember wanting to go to sleep and never wake up. I felt as though my internal world and external world were two completely different places.”
Obsessive-compulsive disorder (OCD) is a mental illness I know all-too-well — one I was diagnosed with at the mere age of 6 years old. And while there are a million reasons why I wish I didn’t have to live with such a relentless demon, there are a few solid reasons why I’m actually glad I do — including the fact that it’s brought me closer to the people in my life, especially those who also battle OCD.
I met my friend Milly through Instagram’s OCD community and instantly knew we’d become good friends, despite the fact that she’s from New Zealand and I’m in the U.S. I admired her willingness to share her struggles, and she has unknowingly encouraged me to be more open and communicative with others.
I found it was inspiring how, despite her brain being wired against herself the way mine is, Milly moved overseas to Australia when she was only 17 to train at a full-time ballet school, then to the U.S. where she danced for three years. She’s now studying at Auckland University back in NZ, where she plans to earn her BA in psychology and criminology, her goal to become a clinical psychologist specializing in OCD.
Needless to say, she doesn’t let her disorder hold her back from living. However, that doesn’t mean she hasn’t struggled along the way.
I think, for many people, the hardest part of living, much like writing, is the criticism that comes with it.
Last night, I stood in my small kitchen, back against the white wall, eyes squinting in the fluorescent lighting, hunched over and crying. I didn’t feel anything; but at the same time, I felt everything.
“You don’t know me,” I told my boyfriend, and I could see the pain on his face as he registered my words. “No one does. Not you. Not my family. Not my best friends. They don’t know what goes on in my mind. And if they did, they wouldn’t love me.”
He wrapped his arms around me, but I was numb. My body was limp, my mind elsewhere.
Continue reading “Not Everyone Will Understand You, and That’s Okay”
Why did I share that? Do I just want validation? If so, from who? And why?
I sense eyes on me every moment. Watching me. Judging me. I live life like it’s a movie, walk around like I’m in some dramatic music video. They ask, “Who are you when no one is watching?”
I’ll never know. Because, technically, someone always is.
I felt nothing, mostly. And when I did feel, it wasn’t sadness. It was terror.
It’s been months since I’ve written about my OCD. Often, painting a picture through words helps me cope. But I thought that if I picked up my pen this time, all I’d see — all anyone would see — was darkness.
Depression. It’s a common term that many use to describe sadness. To express the tears streaming down their face at night, or the crippling stress from piling bills, or the gutting heartache from a devastating breakup.
So, really, I wasn’t sure I even had it. Because, well, I didn’t feel that. I felt nothing, mostly. And when I did feel, it wasn’t sadness. It was terror. Fear — not of death, but of living. I couldn’t imagine waking up just one more day.
Continue reading “My OCD and Me: The Demons that Coexistent”
I could feel myself beginning to slip; if this went on much longer, I was going to lose everything, quite literally.
My name is Adam. I am a 26-year-old writer and I live in central New Jersey. I live with four cats and my lovely girlfriend and, for the first time in years, I feel like I might have my shit together.
I’ve never been professionally diagnosed with anything, maybe because I’ve deliberately avoided professionals until very recently. I think I was probably a prime candidate for medication at an early age, but I made good grades and did well in sports, so nobody ever looked at me that hard. All I can say with certainty is that I’ve suffered from a high level of anxiety and sudden mood swings for as long as I can remember.
The mood swings were the first thing I noticed. Even as a child, I would become irritable, angry, and sad all at once, seemingly out of nowhere. The worst part about it was that I knew I had no reason to feel this way, but I felt it anyway. When I was experiencing these moments, I would often lash out at the people closest to me.
My mother is a wonderful person, but I remember especially being hurt by her regularly telling other adults, “Oh, don’t mind him. He’s just in one of his moods.” I hated feeling that way, and I hated it being written off like that because I knew something was going wrong inside me.
Continue reading “Break the Stigma: Anxiety, Mood Swings, and Addiction”
The worst part was going back to school and everyone asking me if I was “the girl who had a seizure.”
Nicolette Wescott, 22-year-old graduate student from Medford, New Jersey, has lived with anxiety-induced juvenile myoclonic epilepsy since she was 17-years-old. Read on to hear more about her journey with the illness, and be sure to check out her YouTube channel on epilepsy.
Explain one of your worst, most severe experiences with your illness.
I was so nervous for my first day of freshman year of high school that I didn’t eat or sleep for three days. I’m not sure what was making that anxious, but it was extreme torture.
The morning of my first day, everyone said I was out of it. But I remember absolutely nothing. I woke up in the hospital at 6 p.m. to several nurses around me. They told me that I had had a seizure in the middle of the hallway of Shawnee High School on the way to first period.
They kept me in the hospital for three days because that’s how long it took to fully regain my consciousness. I remember feeling confused and frustrated. The worst part was going back to school and everyone asking me if I was “the girl who had a seizure.”
Continue reading “Break the Stigma: Q&A on Anxiety-Induced Juvenile Myoclonic Epilepsy”
