Browsing Tag

coping

Guest Posts, Relationships

Half Life

July 21, 2021
ocd

by Ronica Hagerty

Another evening, sitting on the couch, after cleaning the dishes, and I feel numb.  Finally, today was a normal day.  I was resting through the calm after the last storm, and wondering when the next one will be.

He is in the bathroom getting ready for bed.  I hear the water running from the faucet, then it is turned off, then it runs again, then it is off, on, off, on and off for 15 minutes.

How many times does he have to wash his hands!

But these aren’t rituals to be questioned. They just are.  We have been married for 18 years.  Ever since Adam was born, we stopped going to bed together.  I brush my teeth, wash my face and get under the covers.  Gone are the days when I waited for him.

I imagine taking my life. I am half-living anyway. I quickly expel the idea like a cancer. I have to be here for Adam.  Robert was his age when the symptoms came on, like a shark chewing him up, depriving him of all foolishness of a teenager, then spitting him out into a jungle of anxiety for life.

Hold it together. Someone’s got to keep it together.

There’s a rhythm to this house.  At 5 am I hear the newspaper hit the driveway.  At 7:30 I wake up Adam and fix breakfast.  The highway two miles away hums like a lullaby that gives way to birds chirping at dawn and dusk. There are meals to make, homework to do, and throw pillows to arrange neatly on the couch– nightly routines that keep the contours of this middle-class family pretense intact.

But the rhythm of this house is broken.  I haplessly watch the neighbors’ dog sneak into our backyard through the tunnel under the fence. The ugly rascal is smaller than a cat and chases the squirrels up the big oak.

I read Robert’s face at the onset of another episode.  His brows closer together, his eyes glazed over, his hair oily.  He spins with the overwhelm of a last breath before his mind is drowned by worry.  I harden.  There’s dinner to be made, homework to be done and my throw pillows to be arranged before going to bed.  And, there’s a man to catch at the end of this episode.

I remember the night he told me he had OCD twenty years ago.  We made love then cooked in my small downtown apartment. The living room was dimly lit.  The round glass-top dining table he helped me move days before our first kiss fit perfectly in the corner. We sat for dinner, still in our bathrobes, and with a finished plate in front of him, he took my hand, leaned forward, and said “I have something to tell you.”  Smitten I was, I leaned in and said “What is it?”

“I have OCD. You know what that is?” His hands were sweaty.

My Indian friend from college instantly popped in my head. Her younger brother would go around the house turning all the light switches on and off before bedtime.  “He has OCD,” she told me.  It was a child’s thing. Harmless.

“Ok. Yes, I know what OCD is,” I said back.

“You do?!” he exclaimed.

“So what?” I said.  “That doesn’t change anything.”   He smiled and kissed my hand.

Odd behaviors became familiar… checking his reflection in the rearview mirror while driving, then checking it again looking at the dinner knife at a friend’s wedding.  Sneaking behind me every time we approach a public door so that I end up the one touching the knob.  Heck! Nothing to lose a good man over.

He is a handsome California man of Bostonian stock going back to Harvard lawyers of antebellum Massachusetts.  I laughed on our first date like I hadn’t in months. Being with him was restorative. He quickly introduced me to his family.  Tall men and beautiful women.  I felt at home, and I desperately wanted to stay there.

Robert wakes up several times a night. He quietly walks to the bathroom.  I hear the water running. It stops, and it restarts again. On and off for a good while. He tiptoes back to bed, and carefully gets under the cover so to not touch the wrong thing.

I curled up to him once after one of those mid-night runs. As my breath got heavier, he gently wrangled himself out of my embrace and got out of bed.  I heard the water running again, on and off for another 10 minutes. He was back in bed, careful not to wake me up.  He had to wash me off.  My heart wept that night. I vowed not to do that to him again.

I no longer curl up to him.  He doesn’t mind.

Ronica Hagerty is an immigrant American of Egyptian origin. A mother, wife, friend, and an executive coach who believes in destiny and our power to make something of it. She is inspired by transitions and what it means to cope. Her claims to fame in public writing are an opinion piece in an Egyptian daily, a letter to the editor in the New York Times (yes, small but made her son quite proud! :)), and personal reflections on her dad’s unwavering optimism.

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Although each of Jenny Offill’s books is great, this is the one we come back to, both to reread and to gift. Funny and thoughtful and true, this little gem moves through the feelings of a betrayed woman in a series of observations. The writing is beautiful, and the structure is intelligent and moving, and well worth a read.

Order the book from Amazon or Bookshop.org

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Anti-racist resources, because silence is not an option

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Guest Posts, Self Image

“Deaf” Does Not Define Me

January 10, 2021
deaf

By Challis Popkey

Jen Pastiloff writes about her “undue shame” about her hearing loss. I also feel shame for my hearing loss, but I still feel like mine is due. Like it was my fault.

I overdosed on heroin, cocaine, and benzos on Valentine’s Day 2017. I was living in New York City and was not breathing, no pulse, when my boyfriend found me. I’d been ‘down’ for an unknown period of time when the paramedics arrived. I was 0-0-0 — unconscious, no breathing, no heart rate —  and it took them 20 minutes to restart my heart. My body had given up. It quit. I died.

They wouldn’t tell my dad if I was alive or dead when he called the hospital. He flew out from Boise, my mom from Hawaii, and my brother from LA to spend 3 weeks at my side, hoping, praying that when they removed the ventilator I would breathe again. On day four, a CCU surgeon told my parents that I had a 0.5% chance of surviving.

I did.

I woke up with this terrible ringing in my ears, and honestly, I was confused as to why everyone was beaming. I found out my lifestyle was over; I’d lived on my own since 18 and now at 24 I was to move back into my dad’s pink house on the corner? Not to mention learn to sit up, talk, and walk again. They called me the “miracle baby” – and I couldn’t grasp why everyone was celebrating. I felt ungrateful for my second chance at life. I flew back to Boise from New York two weeks later, now moving slowly and with a walker (which I proudly tossed when I saw my friends awaiting me at the gate in Boise).

Still, the ringing. I couldn’t hear what the doctors were telling me about my condition, the wound vac, compartment syndrome, medically induced coma, overdose… I felt unable to participate in conversations about my own body, my health. Conversations about my future, was I going to rehab? Was I a drug addict or was this just an experiment gone wrong? What about my career in journalism (or my server gig at Henry’s, I had been fired at this point from a PBS station in New York).

I saw an audiologist in April 2017 and learned that I had lost 70% of my hearing in both ears (actually, 73% in the left). They attributed this to the lack of oxygen arriving to the cilia in my ears — I’ve since come to think of this as flowers wilting, shriveling up, dying due to carelessness, lack of love and attention.

My first pair of hearing aids were over the ear. It was late May when I got them and despite the heat I refused to wear my hair up. I felt such shame about my hearing loss, and I still do.

Since then I’ve gotten a pair of in-the-ear aids. Only recently have I started to wear my hair up at work. Still, on first dates or when I know I will be hugging someone, I take them out. I don’t want that awkward buzzing feedback that happens when someone gets too close, like rubbing against a microphone. The questions, “Did you hear that?” “Are you a robot?” “What’s that noise?” Because then I would have to explain that I am deaf. So instead I pick up about 30% of what they’re saying to me, nodding and smiling when I don’t hear them and I can’t read their lips. Do you think they get it anyways, that I can’t hear?

“What’s that?” is my placeholder for, “Can you repeat that, please? I am hard of hearing and I don’t have my hearing aids in because I am ashamed of my hearing loss.” Three years, one rehab, twelve steps, good and bad therapy, and now a career as a therapist later, I still feel like it’s my fault. I am embarrassed to ask for subtitles on TV with new people, people who don’t know why I need them. If I’m with someone who knows, I might wear those headphones in movie theaters.

I want to believe my shame is undue. And I AM grateful for this second chance. I currently work at a women’s drug and alcohol rehab as a therapist, working towards my MFT licensure. When I tell my story I have included a few times that the overdose also caused hearing loss, and my clients don’t gasp or treat me differently. If anything, they speak more clearly. They look at me when they speak so I can read their lips.

People often ask me what it was like on the other side. I wish I had an answer. There is shame around that, too. I literally died – no heartbeat, no breathing for untold minutes – and I don’t have anything to report. My memories of the weeks leading up to the overdose are blurred, shifting, a mirage. They change over time, and are ultimately unreachable.

I remember this narrow basement pharmacy where we bought Q-tips and insulin syringes and how I pleaded with my boyfriend that morning to “let me try it straight.” He didn’t want to, but after doing coke all night I can be quite convincing. I remember shooting heroin that morning, watching as the blood punched up into the syringe, knowing we had a hit. It felt psychedelic, warm, safe.

Later that day, just hours before I died, I called my father from the sculpture garden at 110th and Amsterdam. The February sun was holding me close, whispering, imploring, “You like this, you like life.”

That was the last thing I heard.

Challis Popkey is an Associate Marriage and Family Therapist based in Santa Barbara, California. She grew up in Idaho and her love for wild places and adventure have been her steadfast companions. She is an ultrarunner, running coach and wood-fired pizza aficionado. Challis can be found on Instagram at @challypop and online at www.challispopkey.com.

Recommended Reading:

Anti-racist resources, because silence is not an option

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Guest Posts, emotions, Truth

On Anger

March 7, 2019
angry

By Megan Wildhood

Maybe I’m old fashioned, but it makes me angry when people don’t mean what they say. It makes me angry when people think I should be okay with broken promises and unkept commitments. I am not. I will not be. And I will not apologize for my “high standards.” Without integrity, there is no basis for communication, let alone accountability and responsibility.

It makes me angry that people think “obligation” is a dirty word everyone should be free from. An entire industry called “self help” profits from people’s fear of accountability. Here’s all the self-help you need: take responsibility for your shit, mean what you say and follow through.

It makes me angry when I tell people about a difficulty I’m having with another person and they try to guess what the others involved are thinking instead of listening to ME, the person right in front of them.

This idea that I’d be less angry, less hurt if only I knew what the other person is thinking, makes me angry.

False peace makes me angry. Continue Reading…

Therapy, Guest Posts

A Therapist Confesses: “I Really, Really, Really Can’t Help You”

November 10, 2017
therapist

By Sherry Amatenstein, LCSW

Strands of white hair erupting from her scrunchie, *Evelyn perches on the black pleather chair, greedily gulping from her Poland Springs water bottle and says: “Sherry, yesterday I had one of the worst experiences of my life.  No, probably the worst.”

In the ten plus years I’ve been a therapist I’ve heard numerous variations of this sentence, often followed by a statement like: “The neurologist confirmed my mother has Alzheimer’s. I feel guilty that I still hate her” “I caught my fiancé making out with my best friend” “Maybe getting fired for the fourth time in three years is a sign the world is better off without me”…

This is Evelyn’s latest ‘worst experience’: “I was at CVS buying shampoo and this Chinese guy brushed up against me. I know he did something to the shampoo to hurt me. Should I use the shampoo or return it? I’m sooo anxious.”

I’m never happy to hear that someone is suffering.  I became a therapist in midlife after a career in journalism because I feel driven to be an easer of pain, in a small way to make a permanent, positive stamp on the life of another. Continue Reading…

Guest Posts, Anxiety, depression

The Woman Who Stares at Clocks

November 6, 2017
time

By Tasha Kerry Smith

I wake each morning to the sound of silence and stare at the clock. Plastic, pink, old-style alarm clock with big numbers. The little hand crouches at nine and the big hand is in between the 2 and 3. I will wait till it hits 3, exactly a quarter past, before moving. Starting every activity on a concrete number helps me know where I start and finish. In the waiting minutes the voice speaks its filth: You’re worthless. Lazy. The world would be better off without you.

My morning is unremarkable but carried out at a tense pace, as if I have an A.M. conference call with the UN though I’m freelance and set my own schedule. I eat a small breakfast standing by the sink; brace myself for the dog walk. On bad days, when the voice is loud, I don’t like going outside. Too much activity. Too many people. Deliverymen shouting orders. Shoppers running errands. Dogs barking. Horns honking. Every noise hurts. I weave through them, head down, and make for the beach, where the dog can roam and the voice creeps into the quiet: Worthless. Hateful. Bitch. It’s takes physical strength to restrain it. My mind is shot.

To cope, I watch the clock, plan my day, giving each task a time slot. If I complete a task within the allotted time, I relax. If I don’t, I panic. Continue Reading…