Day 25: Rolling on the River

 The first time I remember seeing Tina Turner sing was on a variety show (can’t remember which one). It was about 1971 and I was 16. Instead of starting to sing, however, Tina Turner came up to the mike and began to speak. At the same time, Ike Turner began strumming chords on his guitar. I recognized it right away and was dismayed. My favorite band at the time was Creedence Clearwater Revival, and this was their song.

But Tina’s voice compelled my attention. Sometimes, she said, she liked to sing a song nice and easy. Sometimes she liked to sing it rough. She stated she was going to sing the first part nice and easy, but then she was going to sing it nice and rough. She began to sing “Proud Mary.”

I liked her voice. She had feelings even though it was “nice and easy.” Yeah, I thought, but she’s not the Fogartys. Nice cover, I thought, but …

And then the music picked up and so did she. I could feel myself moving with this new, rocking beat. She was dancing too, and she was magnificent.

When the song was over, I thought it is her song now.

She had a secret similar to the secret I carried, yet it was different. I lived in a house with domestic violence but hadn’t been a victim of it in years. It left its scars though. She was a direct victim of DV. It was a shock. I never would have suspected it. But that’s a skill we learn early: how to hide that it’s happening. I am sure it left scars on her too.

She came back, though, and in such a strong way that she’s called the Queen of Rock and Roll. She is a strong role model for all females from 5 to 105.  She had so many hit songs over the next years, and each one seemed better than the other. And oh my, her energy! I saw film clips of her in concert in her later years. She was in heels, not losing her balance and tripping, and dancing as well and as energetically as the kids around her. I watched her onstage doing an across-the-stage line dance with these young women and I couldn’t tell one from the other.

Dan Rather wrote a very nice piece about Tina Turner and, in it, he shared three of her clips. Visit and watch those videos. They’ll get you up and moving.

I love all of Tina Turner’s songs. This one is a favorite that Mr. Rather didn’t include. She was in a movie with Mel Gibson way back when called Mad Max: Beyond Thunderdome. I am so moved by her rendition of “We Don’t Need Another Hero.” 

Another favorite is “What’s Love Got To Do With It?” 

And because 3 is my lucky number, I’m sharing a new favorite video. It’s beautiful.   I can almost hear them doing this duet together in Rock and Roll Heaven. God bless, Tina Turner. I’ll miss you, but I’ll always have your music to listen to.

I am participating in the American Cancer Society’s challenge to write for thirty minutes each day in May. I do a lot of writing and I can meet this challenge. I plan to make a blog entry each day with what I’ve written.

I wanted to participate in memory of loved ones who fought cancer bravely but succumbed:

My brother-in-law Jeff

My sister-in-law Ann

My dear friend Kay

My Uncle Bob

My Uncle John

 

I also wanted to help raise money to support research and a cure for those currently fighting this vicious disease.

My Facebook to the fundraiser is here. 

Thank you to all who wish to support the American Cancer Society this month.

Day 23: Here's Looking At You In Heaven, Rich

Loving the moving Casablanca bonded Rich and me early in our dating relationship. Our favorite line was “Here’s looking at you, kid.”

For his 24^th birthday party, I’d arranged to have a cake with an image of Humphrey Bogart and the words, “Here’s looking at you, kid, Happy Birthday”. I’d provided the baker a picture of Humphrey Bogart dressed as Rick Blaine. The baker did his best to draw a decent image of Rick, but it was really an epic fail. Still, we all enjoyed the sentiment and the cake.

On Valentine’s Day, one of our favorite movie channels was showing Casablanca. We made a date of it, bringing in Chinese food to enjoy while watching the movie. Out of my eyeshot, Rich finagled a fortune cookie message out and replaced it with his tiny, handwritten “Will you marry me?”

When we planned our wedding, we decided our first song would be “As Time Goes By.”

When we began investigating eBay, we bought a pair of Casablanca dolls in an unopened box. For Christmas, I found him a magnet of Ingrid Bergman as Ilse.

Casablanca was our Camelot, I suppose.

He was my best friend and soul mate throughout our years together. He was the loving father of our three children. We had our ups and downs as people will in any marriage. He had the patience of a saint, living with me as I battled the issues of my childhood.

We loved board games. Scrabble and Trivial Pursuit were our two favorites. We used to relax after dinner and at the children’s bedtimes playing these games. Our other passion was classic movies like Casablanca. We also enjoyed the new releases and would indulge in a movie date whenever we could.

But Rich had cardiomyopathy and had had his aortic valve replaced due to Marfan Syndrome.  He had a collapsing ankle that caused a great deal of pain. He couldn’t entirely quit smoking cigarettes. I believe he also had sleep apnea and insulin resistance. With his last hospitalization, the doctors were considering him a candidate for a gastric bypass. He’d developed atrial fibrillation and that condition needed to be stabilized first.

During that last hospitalization, he began saying he wanted me to find love again and remarry after he was gone. I didn’t want to hear it.

After he was released from the hospital, we had one more lovely visit to Jones Beach on Easter Sunday. It was a mild, beautiful day. Although dressed in play clothes and not bathing suits, the kids frolicked in the gentle surf, wading, and just enjoying themselves. Rich and I sat on a beach blanket together and just talked about many things.

Our son Bill saw us, grabbed my camera from the blanket and snapped a picture of us. It’s the last picture I have of Rich.

After he was gone, one of the ways he communicated was electronically. I woke up at the same time every morning for weeks, around 3:23 a.m. I would hear one of three songs: My Heart Will Go On, I Hope You Dance, and Stand By Me.

I wrote recently about how I met and grew to love Ted, marrying him. He is so much like Rich yet so much his very special self. I didn’t think it was possible to have two soul mates, but I do.

Rich lives in my heart as the lyrics of My Heart Will Go On say. He will always live there with his gentle smile and his, “Do you know how much I love you?”

And we’ll always have “Here’s looking at you, kid.”

I am participating in the American Cancer Society’s challenge to write for thirty minutes each day in May. I do a lot of writing and I can meet this challenge. I plan to make a blog entry each day with what I’ve written.

I wanted to participate in memory of loved ones who fought cancer bravely but succumbed:

My brother-in-law Jeff

My sister-in-law Ann

My dear friend Kay

My Uncle Bob

My Uncle John

 

I also wanted to help raise money to support research and a cure for those currently fighting this vicious disease.

My Facebook to the fundraiser is here. 

 

Day 22: Coping

We have had a week from Hell. I was driving us home from somewhere on Saturday. My husband usually drives, but Ted broke his ankle. Between his reverse shoulder replacement and this broken ankle, he was physically out of commission. During the week, we were also dealing with a family situation. As a solution, we decided to withdraw from Facebook and Messenger to give ourselves a breather and a chance to recover from these traumas.

My husband said, “I don’t understand how calm you seem. I think I’ve been having a breakdown.”

The stress of it all has been overwhelmingly intense. How did I seem so calm? I’d fallen back on a coping mechanism from childhood. It’s called detachment in the twelve-step programs. It means that I numb the feelings that would prevent me from functioning. It helps as the crisis is occurring, but is it really effective?

No. While I can stick my feelings of worry, anger, hurt, and betrayal in little compartments in my brain for the present, they won’t stay there forever. When a crisis begins to pass, these feelings hit me physically with exhaustion and intestinal upset. Even though this coping method isn’t the most beneficial for me, it’s ingrained in me no matter how many years of therapy I’ve had. I fall back on it whenever there’s a crisis.

I wrote about it some months ago during another crisis.

Trauma and Dissociation (Detaching)

I grew up in a dysfunctional home. I was the victim of and saw repeated domestic violence. As I grew older, I began to be aware of strange sensations. When there was a fight going on between my parents, I suddenly didn’t feel connected to myself. I felt like I was floating somewhere above, watching the scene—including myself. One minute I was trying to get between my battling parents and the next, I was frozen to the spot like a statue. One moment I was crying and hysterical; the next, I felt…nothing.

It was scary. My body was not in my control and weird things were happening to it. I believe that is about the time the panic attacks began. Those would come upon me without warning. Sometimes there was a pattern to them; they’d happen a lot in the afternoon. I would be sitting in my high school classroom, listening to a lecture, and suddenly I’d be hit with one. My heart began pounding and the room would start spinning. I had an urge to get up and run, to escape. That definitely was not normal, and I knew instinctively that I shouldn’t bolt out of the classroom. I remember gripping the edges of my desk as if I thought I had to hold onto it to keep myself from jumping up. I’m amazed I didn’t leave fingerprint impressions on the desk.

I was about 16 years old when I confided in my parents that something was wrong with me. I needed a psychiatrist. Well, they lost their minds. There was no way I was going to see a psychiatrist. What if the Deaf community found out? Gossip would spread and it would be so embarrassing! I was on my own struggling with the disturbances in my body. I was sure I was losing my mind.

I hid what was happening to me and confided in no one else until my senior year. I was taking a psychology class, and it occurred to me that my teacher might know what was wrong with me. Perhaps she would know what to do. One day I stayed after school to talk to her. She was open and very willing to listen as I struggled to explain what was happening. I told her when it happened, I didn’t know who I was anymore. I was sure I was crazy.

The teacher became very reassuring. I must not have explained myself adequately because what she said was not to worry. All young people had moments when they wondered who they were. She assured me it was normal. I felt somewhat reassured but not entirely convinced.

After I graduated from high school and left home for the first time at age 19, I got a job with benefits. Some of those benefits covered mental health expenses. They didn’t cover very much but something was better than nothing. I was 21 and began going to a mental health clinic. There I described fully what was happening to me.

My therapist listened to me, asked questions, and then at the end of the session she said I was disassociating. I’d never heard the word before and her explanation of it scared me. This was a verification that I had a serious mental health issue. The therapist said I was going into what was called a “fugue” state, a hop, skip, and a jump from multiple personalities. It was 1975 and there was no information about PTSD or the effects of trauma. I had to control these weird feelings, or I might become someone else.

There was a soap I’d watch whenever I got home in time from work. It was called One Life to Live. Once there’d been a storyline where the heroine, whenever under stress, would become an entirely different person. Was this happening to me?

I was prescribed an anti-depressant called Tofranil. I couldn’t confide in anyone about this, not my family or my friends. There is a stigma to mental illness. That stigma continues to today.

The Tofranil helped control the panic attacks. The dissociating episodes became easier to deal with and their frequency decreased. Life was bearable.

The truth is: anytime I went off medication, the panic attacks and dissociation episodes would return with increasing frequency. I fought them for as long as I could and when I did go find another psychiatrist or therapist, I was very hard on myself. When I had to take pills, I felt like a failure. Why couldn’t I control it?

Over the years, I began to learn more and more information about what was happening to me. My education began shortly after I married Rich. He noticed I’d become angry when he had a beer or two, and he’d reassure me that he was not my parents. “Yeah, but you could be later,” I’d answer. One Sunday, we heard there was a twelve-step meeting that met at our church, and Rich encouraged me to go.

My parents never admitted to being alcoholics. If they were not, they were still problem drinkers. They still physically fought each other.

I didn’t know if the group would accept me, but I went.  They welcomed me warmly, and I listened. I felt annoyed that they were so at peace with the alcoholic in their family. They said they had no control over their alcoholics and that confused me. Weren’t they doing anything at all to stop the drinking? We weren’t supposed to challenge anyone, and I thought that was really too passive too.

I went back and I vented my rage about my parents and the problems I was having. Their gentle advice was to use the serenity prayer and the twelve steps to help me work through everything. They suggested a group that dealt specifically with adult children who’d grown up in alcoholic/dysfunctional homes.

I felt more connected and at home with that group. Others were angry, like me, and there were some members further along in their recovery. From them, I learned about a more specific therapy focusing on what I was going through.. I saw a therapist who was from a dysfunctional family like me. He showed me videos and gave me books to read, and I gained so much insight and understanding about growing up in an alcoholic family.

I was experiencing panic attacks as I continued to learn about why I was having these issues. My therapist referred me to a new psychiatrist and then I learned another astounding fact: my struggles with depression and panic were biologically based. My brain was not making the chemicals I needed. I had dysthymia, a chronic low-lying level of depression. Even when I was feeling upbeat, my mood was still lower than those of most other people. I would need to continue meds to stimulate or simulate those needed brain chemicals to lift my mood.

The therapist referred to my dissociative episodes as “detachment”. That’s a much more acceptable word, less stigmatizing and frightening. The reason I can remain calm and function through a crisis is because I detach my emotions from whatever is going on.  It’s why I was able to stay calm and read my book when that custodian went berserk during my psychology class and took a student hostage.

It's why I am not all twisted up in knots over my young family member returning to his abusive family. I am powerless in that situation because he’s 18 and an adult. I am detached so that I don’t worry or grieve for his situation.

There was a really good article about the different types of dissociation. There are four: Dissociative amnesia.

Dissociative fugue

Depersonalization disorder

Dissociative identity disorder

Mine would be depersonalization disorder. Quoting from the article, it sounds very familiar to me: “Depersonalization disorder is characterized by feeling detached from one’s life, thoughts, and feelings. People with this type of disorder say they feel distant and emotionally unconnected to themselves, as if they are watching a character in a boring movie. Other typical symptoms include problems with concentration and memory. The person may report feeling ‘spacey’ or out of control. Time may slow down. They may perceive their body to be a different shape or size than usual; in severe cases, they cannot recognize themselves in a mirror.” Well, I can recognize myself in a mirror and I don’t have problems with concentration or memory. It still happens in a crisis, but it doesn’t scare me anymore.

I am participating in the American Cancer Society’s challenge to write for thirty minutes each day in May. I do a lot of writing and I can meet this challenge. I plan to make a blog entry each day with what I’ve written.

I wanted to participate in memory of loved ones who fought cancer bravely but succumbed:

My brother-in-law Jeff

My sister-in-law Ann

My dear friend Kay

My Uncle Bob

My Uncle John

 

I also wanted to help raise money to support research and a cure for those currently fighting this vicious disease.

My Facebook to the fundraiser is here. 

 

Day 19: Toxic Relationships, Family Dysfunction, & Censorship

 

Since posting recently, a Donnybrook brewed between two families. One family hates the other, especially the words “toxic family.”

What is that, anyway? And what is the difference between a toxic relationship and a dysfunctional family?

I grew up in both.

My parents were both deaf, and I was the older of two children. In those days (60s-70s) there were no interpreters provided for the Deaf and so the oldest child usually had to fill that role. It’s a lot of responsibility for a child. It’s one thing to fill your parents in on what’s happening on a TV program and quite another to try to interpret about using escrow to pay a mortgage payment because the person renting your house is delinquent with the rent. That a child would have to interpret doctor and ER visits, meetings with lawyers, and other complicated matters isn’t functional.

It's difficult but not toxic.

This part is toxic: being told repeatedly that hearing people are no good and out to oppress, suppress and otherwise take advantage of Deaf people. I could hear. Did that mean me? Many times, my parents accused my brother and me of taking advantage of them. It was hurtful to be accused of that horrible crime all Deaf people disapproved of. It was especially hurtful because it wasn’t true.

This part is dysfunctional and toxic: using a child as a therapist. That happened to me. My parents would drink and then have the most awful physical fights. Then they might go weeks without speaking to each other. Instead, Mom would talk to me. She would tell me things about my Dad that made me so uncomfortable. I would tell her, “But I’m not a counselor. I don’t know what to tell you, and I don’t like to hear these things.” And she would say, “But I have no one else to talk to.” What was I supposed to do? I listened and squirmed.

It was dysfunctional and toxic for my brother and me to become victims of our mother’s rages. We were terrified of her when she went into a frenzy because she had hurt us before in those rages.

It was dysfunctional and toxic for my brother and me to have to deal with their heavy drinking and domestic violence. We either locked ourselves in our rooms until everything became quiet or we would run out of the house to escape it all.

What they wanted and needed was more important than my brother and me. That’s not how a functional family is run.

This is how a situation would go:

My brother and I could see and feel Mom becoming more tense and irritated about something. We had to walk on eggshells and be very careful not to say or do anything to upset her.

Something small would set her off. Maybe the potatoes tasted too salty. Maybe a few dishes were left in the sink. Maybe Dad took more than his share of roast beef.

Suddenly, they would become angry and argue. Hands flying, cracking, and snapping, they would begin to hurtle insults at each other. Fists would pound on the table. My brother and I would jump up. Time to go hide.

Then would come domestic violence. One or the other would be a punching bag.

Later, we would ignore the bruises and pretend nothing happened.

It changed my brother and me. We were no longer the children we were meant to be. In those days, there was no diagnosis of post-traumatic disorder. It’s a true diagnosis. My brother and I still struggle with it.

In one way my parents were not toxic: they didn’t try to control us. They didn’t interfere with our school activities or who or where we hung out.

As for manipulation and guilt-tripping: yes, they used those tactics when they needed us to interpret (my brother filled in after I left home at 19) and to instill in us that while we understood the Deaf, we were also of the enemy. We were Hearing.

I have had years of therapy and twelve-step meetings. I recognize now that my family was dysfunctional, and the relationships were toxic. I recognize it when it happens to others, and it upsets me greatly. I always remember how it felt for me to break free of it.

Just for informational purposes, here is a picture of toxicity:

And here is the definition of a dysfunctional family, found on a Bing search:

A dysfunctional family is a family in which conflict, misbehavior, and often child neglect or abuse occur continuously and regularly, leading other members to accommodate such actions¹. Members of a dysfunctional family are unable to attain closeness and self-expression². The term ‘dysfunctional family’ is defined as a family with multiple ‘internal’ conflicts, e.g. sibling rivalries, parent-child conflicts, domestic violence, mental illness, single parenthood, or ‘external’ conflicts, e.g. alcohol or drug abuse, extramarital affairs, gambling, unemployment-influences that affect the basic needs of the family unit³

I am participating in the American Cancer Society’s challenge to write for thirty minutes each day in May. I do a lot of writing and I can meet this challenge. I plan to make a blog entry each day with what I’ve written.

I wanted to participate in memory of loved ones who fought cancer bravely but succumbed:

My brother-in-law Jeff

My sister-in-law Ann

My dear friend Kay

My Uncle Bob

My Uncle John

 

I also wanted to help raise money to support research and a cure for those currently fighting this vicious disease.

My Facebook link to the fundraiser is here.