A Disturbing Prospect is the darkest book I’ve ever written. Not only is there a body count, but the book also deals with some real-life nightmares that I’ve longed to fight back against. Some of these themes may trigger personal trauma.
I needed to tell the story in my heart and right some wrongs, but I’d also never want anyone to suffer because of my words. None of these themes are gratuitously presented in the book, and my vigilante bikers always prevail. Still, I want my readers to be safe, so here is a list of potential triggers.
Animals: There’s no pet death in A Disturbing Prospect, but an animal is harmed.
Childhood Sexual Abuse: Some of the characters have a history of being sexually abused as children. None of their memories are described, but there is mention of it having happened.
Self-Injury: A character catches a glimpse of another character’s self-mutilated arms.
Sexual Assault: One of the recurring themes in this series is violence against women and children. (One of the other recurring themes, however, is justice for that violence.) There are some hints of past sexual assault throughout A Disturbing Prospect.
Stalking: A character mercilessly stalks and taunts another character throughout A Disturbing Prospect.
Violence: All of the good guys in this series are vigilantes—antiheroes who take justice into their own hands. There is blood, fighting, gun violence, and a villain body count.
If you feel that you won’t be safe reading A Disturbing Prospect, please don’t risk your health. As a sexual assault survivor and someone with PTSD, I wish every book came with a list of trigger warnings. No book is worth risking your safety.
If you’ve read A Disturbing Prospect and feel that I may have missed something, please email me at email@example.com.
The first time I was sexually harassed, I was six years old. Six. I was a little girl. A boy in my class, whose desk was paired with mine, exposed himself to me and tried to get me to touch him. He actually grabbed my hand.
I fought back.
I wrenched my hand away and told him no. I froze with panic, terrified that I would get in trouble. Eventually, we were moved around. (My teacher paired students with someone new every so often.) I never told a soul, until now.
I’m telling this story because ever since that first time, it’s happened so many more times, I can’t count. Boys and men touching me, making jokes and comments, catcalling. Then there are the two boyfriends who sexually assaulted me. Raped me. Violated me with acts of violence that I will never forget. Men who I trusted with my body and heart, yet they only wanted to control and possess me. To hurt me. I went years without telling anyone, and it almost killed me. This story has a happy ending: I did the work, and I healed. I grew strong. I got my voice back, and a confidence I’ve never known before. But.
I’m worn down to the bones, sick in my soul every time another story hits the news or blogosphere about men who hurt women. I’m tired of the violence, the victim blaming, and the bystander effect. All three contribute to rape culture, and these three seemingly small things—men who turn away when they overhear other men make a sexual joke, for example—are the reason why women stay silent. Only when others come forward do we feel protected enough to raise our voices, too; there is safety in numbers.
I’m tired of men making excuses or saying they’re sorry. Instead of being sorry, stop being a piss poor excuse for a man. Don’t justify your past actions or write apologies to the women you’ve hurt. Start being a better person. Stand with us when we’re accused of trying to ruin a man’s career. Speak with us when we tell a man to leave us alone. Stop automatically siding with your bros, and start being a brother to the women in your life—both friends and strangers.
And for fuck’s sake, quit it with the “not all men” line. When you’re whining, you’re centering yourself in a story that isn’t yours. Your selfishness is complacence, and your hands are around her neck, too.
I’m scared, and overwhelmed, and I can’t fucking think straight—and it’s okay.
I just broke down in tears after 30 minutes of trying to write this post using the built-in speech-to-text software on my Mac with the damned thing not picking up half of what I fucking say. I’d hoped that talking through it would help me focus better, but I ended up completely frustrated.
If that’s not a micro example of some of the side effects of writing through trauma, I don’t know what is.
I’m stressed. Shit is falling apart in my country. I’m scared for myself and my family and friends. My health is a bit better thanks to Prednisone and Plaquenil, but my neck and lower back have been fucked up for weeks and the more stressed I get, the worse they are. I’ve fallen behind on my production schedule. I’m months behind on beta reading for my CP. Every time I try to write fiction, I feel blocked or too brain foggy to focus.
I thought I’d just buckle down today and write the next chapter of Writing Through Trauma that I’d planned—”Why Writing Helps You Through Trauma”—so that, at the very least, I might help someone who’s struggling right now too. But the truth is, sometimes it’s a double-edged sword.
Sometimes writing through trauma brings it all back to the surface and paralyzes you.
Writing has never been my enemy. For almost two decades, I was my own enemy—thanks to trauma. But I could always escape through writing. On the page, I could always be myself and speak my truth.
Right now, my truth is fuckfuckfuckfuckfuck.
My biggest fear is how debilitating my chronic illness is if untreated.
My chronic illness is a trauma. For the first 18 years of my life, I was healthy. I came down with colds, strep, and the flu occasionally, but other than that I was strong. I played softball. I went hiking. I worked. I went to school. I went bowling. Then, suddenly, I came down with mono.
It crippled me. My life came to a screeching halt for months. I only had the strength to move the 100 feet or so from my bed over to the couch. For weeks, my doctor couldn’t figure out what was wrong with me. I had severe throat and joint pain, plus debilitating fatigue and muscle weakness. I felt like I was dying. They tested for strep twice and both times it came back negative. My mom had to push for them to test me for mono. It came back positive. I started Prednisone and Tylenol with codeine, but it took weeks for me to recover. I nearly missed our family vacation to Florida. Even when we came home, I was still relatively weak.
A year later, the joint pain and fatigue came back. This time, it never went away.
It’s an autoimmune disease called Undifferentiated Connective Tissue Disease. It attacks the tendons where they connect into my joints, causing joint pain. It attacks my eyes and mouth, making me perpetually dry-eyed and thirsty. It affects my energy. It impairs my thinking, making my thoughts foggy; it’s hard to think of words, names, and places. UCTD can be pre-Lupus or pre-RA, especially if your disease has changed over the years. Mine has.
With the Affordable Care Act under attack, I face losing my health insurance and therefore my healthcare. I’m finally feeling better for the first time in a decade, thanks to my rheumatologist, Prednisone, and Plaquenil. Without my Medicaid, I cannot afford healthcare. Period. I can’t work outside the home due to my disease; most days, it’s a struggle to work from home. Mike works full-time, but everything he makes barely covers our rent and utilities. His company’s health insurance plans are outrageously expensive and we couldn’t afford them before the ACA was passed.
Mike is now finally dealing with his own health issues and, if they continue to go untreated, he won’t be able to work much longer. All I can think about lately is what will happen to us if—when?—the ACA is dismantled.
A two-month supply of Plaquenil costs about $800 out of pocket. I don’t even make $800 a month. We rely on SNAP for groceries, getting only the bare essentials and cooking everything from scratch—even when I can barely stand.
Whenever the inflammation in my body gets out of control, my joints become too stiff for me to even get out of bed. Never mind the pain. I can’t physically move. I’m utterly helpless, which is downright terrifying for a 28-year-old who was healthy 10 years ago.
Living with a chronic illness is traumatic.
I’ve spent the last 10 years trying to come to terms with my disease. I don’t know what is going to happen as it is. Facing losing the ACA takes away even more control of my life.
With so much on my mind, it gets in the way of writing—especially when I try to write about writing through trauma. It reminds me of how much I struggled when I first began writing my trauma stories.
My therapist Erica told me, in our first session, that the end goal was for me to tell my stories. I had to pick three traumas and write about what happened. Picking three was difficult, considering I’ve been living with multiple traumas for so long, and had just experienced a fresh one.
Bullying. Assault. Rape. Miscarriage. Chronic illness. Unexplained death of a loved one. Forced hospitalization.
Every time I started writing about what happened to me, I’d get overwhelmed with anxiety. Writing about it only seemed to aggravate my anxiety, depression, and flashbacks. I kept having to stop and put it away because I just couldn’t deal.
When that happened, I had to practice self-care.
When writing through your trauma, it’s imperative that you allow yourself to write at your own pace. Recognize when you need to take a break or stop. Give yourself permission to stop. Be gentle with yourself.
For me, it had to be a gradual process. Some survivors might be able to rip off the Band-Aid, but I could only write a little at a time. First I was able to mention both of my rapists, for example, while writing in my journal. Before, I’d suppressed the bad memories; I never wrote about either of the men who raped me because I just knew that I despised and feared them. I could barely recall other things from the time that they’d each been in my life. Large black clouds comprised most of my memories, even devouring good things, leaving great wide holes.
When I was a teenager, I dreamed that a black oily substance was eating the sky. In the dream, my family and I were trying to figure out what was happening and how to stop it. Bit by bit, the sky—and world—disappeared.
I’m still trying to reclaim much of my own sky.
Since trauma survivors often suppress memories in the brain’s attempt to keep you alive, it made sense that I had a lot of digging to do. And the more I dug, the harder the flashbacks hit me.
My nightmares intensified. The panic attacks came more frequently. I was constantly snapping at the people around me—usually Mike. I knew that it was going to get worse before it got better, though, so I kept trying.
The more I wrote, the more I remembered. Even though I didn’t really want to remember because I knew it’d be painful, I really wanted to get better. I wanted to stop having panic attacks, to become motivated and productive again. I wanted to actually feel happiness, to grow stronger. To reclaim my life and my voice.
So I took my time.
I started a new bedtime ritual: Benadryl to make me so drowsy and calm, my anxiety couldn’t keep me awake; one ASMR video on YouTube or a round of Bejeweled to clear and calm my mind; one chapter of a familiar audiobook read in a soothing tone that I could drift off to; stuffed animals to hug tight while I slept. It’s been over a year and I still go to bed like this every night. Someday, I’ll be able to let go and fall asleep on my own. But for now, I give myself permission to continue this ritual for as long as I need it.
I carved out a strict workday for myself. Monday through Friday, I only work from 8 or 9 a.m. to 5 or 6 p.m. I don’t work weekends. Evenings are for my “me” time—reading, watching TV or movies on Netflix, or playing Sims. If, during the workday, my body needs some rest, I take a short 30- or 60-minute break just to sit comfortably, maybe read a book or watch Netflix.
I got myself back into a healthy sleep schedule. I’ve always been a night owl, but letting myself stay up all night and sleep until noon was hurting my productivity and affecting my mood. I use my iPhone to remind me to go to bed by 11 p.m. and wake me up at 8 a.m.
I eat three meals a day, plus snacks—no matter what. Since I’m hypoglycemic, skipping meals can make me very sick or very anxious. Even if I don’t have much of an appetite, I eat something small.
I take all of my meds on time. I use a weekly pill box with morning, noon, evening, and bedtime compartments, and Alexa to remind me to take my pills. Right now my meds are: Prednisone, Plaquenil, Tramadol, Flexeril, Vitamin B12, Vitamin D, Benadryl. I take them religiously.
When I’m not too sore, I do yoga. It’s been a while, to be honest, and I’m feeling it. I also meditate, practice deep breathing throughout the day, and write in a journal. Up until recently, I couldn’t hold a pen in my stiff, sore fingers long enough to write down the date, so had to give up journaling—which was really hard to do, and I’m really glad I can write again.
I shower regularly, do my makeup to boost my mood, and get dressed even when I’m not leaving the house. Sometimes I just let myself stay in my pajamas all day, though—whatever makes me feel best.
For you, self-care might mean different things. What’s most important is that you take care of yourself. Treat yourself as if you were your own sweet child. Be kind and gentle, but firm when necessary.
What are your favorite self-care tools? Leave a comment and tell me three of them!