Cynthia Stock

An amazing author for your soul!

Just a Nurse

September 16, 2015 by Cynthia Stock Leave a Comment

One Christmas Eve Day I extubated a patient who had open heart surgery the previous day. A few hours after removing the breathing tube, he went into a pulseless ventricular tachycardia. I was at the bedside, called a Code Blue, and shocked him back into a regular rhythm before his surgeon arrived on scene. His family thanked me for giving them such a gift. I am just a nurse.

Another day our shift received a patient from the operating room who started to bleed faster than we could replace the blood. Without hesitation all but one nurse (and she was unaware of the crisis) stayed over to run to the ER to get the rapid infuser, to run to the blood bank, to support the family, to call in the OR team to take the patient back to surgery, to coordinate care until transport, and to help the next shift cover the rest of the patients. We are just nurses.

A woman came in to speak with the doctor, who had to tell her that her husband had just died. She did not collapse until she looked at me and asked me if it was true. I nodded, hugged her and lowered her to the floor. I am just a nurse.

A patient sat in a chair in distress. While I spoke by phone to the doctor, the patient had a respiratory arrest. Six people lifted the patient back to bed and started CPR. Before the end of my shift, although intubated, the patient woke up and was neurologically intact. A few weeks later the patient visited and said: “I didn’t understand about the job you do until now.”

We are just nurses. Proud is an understatement.

 

 

Filed Under: Health Care, Human Connections, Life and Death, Nursing

The Language of Touch

August 30, 2015 by Cynthia Stock Leave a Comment

The Language of Touch

 

A piece of paper taped to one cabinet in the break room asked for items staff nurses would like to see in an admission package. I suggested a nice razor, one with more than one blade, one worth more than 29 cents and less likely to ravage the skin of someone sick enough to be in ICU, but well enough to feel better after a shave.

Later the same day, I walked by the break room and overheard two nurses, both who happened to be around thirty, ridicule two “seasoned nurses,” meaning over sixty, for making a big deal about shaving male patients. “I won’t do it. I just won’t do it.” One said.

I can’t imagine refusing to do any kind of patient care. I have been threatened, scratched, kicked, thrown up on, and sprayed with all sorts of body fluid. To me it’s part of the job. But I know times have changed. Maybe I AM out of step. So I looked up hygiene in a textbook called Fundamentals of Nursing. Shaving still appeared under the classification of personal hygiene and earned its own section with a “how to” discourse.

Two weeks prior to this I shaved a man days after an open heart surgery complicated by multiple co-morbidities. I asked his wife to bring in his shaving kit. It contained a nice four blade razor with Edge shaving cream, a brand I like to use on tough beards. I softened the whiskers with a warm cloth, slathered on gel that blossomed into an abundance of white foam, and shaved one side of the man’s face, then the other. When I finished, his family literally gasped with delight. The man they knew was beginning to look more like himself.

I sought out another experienced nurse. We discussed a scene from Out of Africa in which Robert Redford washed Meryl Streep’s hair. It didn’t overwhelm the audience with dialogue or sex. The mere act of washing hair epitomized the relationship between the senses and intimacy. To me it symbolized the universal language of touch. In the hospital setting, touch facilitates communication. It engenders a bond of trust that needs to be established between patient and professional, a bond that eases the distress caused by loss of control not only of the decisions of daily life, but also bodily functions. How do you make a person not feel ashamed when he knows he’s drooling because he’s had a facial reconstruction or when he loses control of his bowels and doesn’t realize it? It’s through a degree of intimacy and trust.

The senses connect us. They speak more articulately than words. It is not just a shave. It is a conduit that builds trust, creates a sense of safety, and makes a patient feel like he’s not just a room number, a diagnosis, and a daily weight.

 

 

Filed Under: Health Care, Human Connections, Nursing

The Unquantifiable Art of Nursing

June 12, 2015 by Cynthia Stock Leave a Comment

 

Yesterday my patient’s skin peeled and pulled away from her fingers and toes. In the past week she had gained twenty pounds from water retention. The swelling stretched her skin until it radiated a watery sheen. As the swelling began to go down, the skin rebounded, dried, and flaked. I took off her anti-embolism hose and her sequential compression devices and released the smell of dirty gym socks. She was depressed, withdrawn, un-communicative, because a surgery she expected to earn her a brief hospitalization had incurred Murphy’s Law. She entered her fifth week in ICU with a tracheostomy and a surgically inserted feeding tube. I understood her frustration.

After trach care, catheter care, blood sugar checks, and adjusting IV drugs to a prescribed blood pressure parameter, I wanted to do something for her, not to her. I warmed up lotion and lavished her hands with it. Every finger got special attention. I remembered how pressure to my fingers during stress reducing massages seemed to release the tension in every muscle of my body.

I dialogued in an effort to break her silence. “You know why I’m doing this don’t you? If my mother were in your place, I would want to come in for a visit and know someone had cared enough to do it.” I moved to her legs and feet. I washed them warm wipes, slipped the disposable cloths between each toe. I slathered lotion on legs where lines of dryness mapped her skin in white. She grimaced when I rubbed lotion into her right ankle. “That really hurts.” No response. “What about the left one?” She actually nodded in response to my question.

Then for a dignified, mature woman, whose best friend told me she was meticulous about her appearance, disaster struck. She passed an enormous bowel movement, something the general surgeon would celebrate. It added to the patient’s humiliation and loss of her sense of self. How could I convince this stoic, regal woman that just this once, normal human bodily function meant she was one step closer to getting well.

I gathered cleaning supplies, linens, and another set of hands. “Now I’m going to bore you with some stories.” I warned. Stool puddled between the woman’s legs and housed itself in any crevice it could find. I had used stories before with a young male patient to pass the time when he found himself in a similar situation.

I talked about my grandmother, widowed after World War I, she raised four children on her own. “My grandmother worked to provide for her girls. When I knew her, she never was in anything but a skirt, her strawberry white hair in a chignon, and her nails long and perfectly polished.”  I think grandmother resonated with my patient. I could tell she was listening. My helper and I started to mop and wipe and clean and contain the flood of excrement.

“For supper one night, the family enjoyed a roast, probably a rarity in that day. The oldest sister cut and served while the others ate. Before she could sit down to eat, one sister was back for seconds. The eldest picked up the roast and threw it at the offender.  All my grand-mother could say was: ‘Girls. Girls.’” What I was trying to tell her was that we are all human, subject to human frailties and that this moment would pass. She smiled.

A week before that I cared for an octogenarian who lived alone. He began to hallucinate and provided intricate details of what he saw. He realized he was seeing things. The anxiety left him restless. He hollered for someone to come and kept punching the call light. I knew his daughter was coming. I pulled up a stool and sat beside him. “Tell me what you see.”

“Right now I see you encased in a sheet of water. It’s all around you.”

“I believe that’s what you see.” I held out my hand, not to deny him, but to share what I saw.

“I know there’s no rain, but I see it.”

“What else do you see?”

For the next forty minutes he created what I interpreted as his view of Heaven. He detailed with the precision of an engineer, a lift. It had a broad platform and inched upward toward Infinity. He talked about pulleys and cogs and people. “You were there too.”

He looked straight at me when he said this.

I shuddered like I had has a child, when other children who noticed me shake, said: “A rabbit just ran over your grave.”

In all the time he spoke his visions, I just listened and wondered what it all meant. Then the man uttered the words that explained it all.

“I think I’m dying.”

I sat with the man until his daughter arrived.

It is a cliché to refer to long standing definitions, but Florence Nightingale defined nursing as “the act of utilizing the environment of the patient to assist him in his recovery.” (1860) I added the italics. Our patients come to inhabit bland, functional rooms, filled with outlets, equipment, monitors, electric beds, television, climate control, negative pressure, and, if they are lucky, a window. But they also come with an inner environment which constructs the essence of who they are. The greatest privilege in nursing is being allowed into that most private place. Entering there may be one of the most important parts of a patient’s survival. The ability to gain entry is one element of the unquantifiable art of nursing.

 

 

Filed Under: Health Care, Human Connections, Nursing

We need to talk about depression

April 9, 2015 by Cynthia Stock Leave a Comment

The other night I watched Birdman followed by updates about the plane crash in the French Alps. I read the analysis of the incidence of suicide among veterans and children who have been victims of bullying. Despite mass media, continuous connection via hand held devices, and information at our fingertips, I concluded: We need to talk about depression. How many people walk around with depression as their constant companion? How many control it? How many are controlled by it? Is any disease more insidious than depression? It seems to sneak by, undervalued, untended, yet with the potential for crippling, even killing, the person who suffers from it.

Years ago I read William Stryon’s Darkness Visible, a most personal journey. Then there was The Noonday Demon, detailing the complexity of depression in a more objective voice.  To understand the power of the disease, the individual experiences of depression need to be shared. It morphs, shape-shifts and lives in such a way that even the people closest to the depressive don’t recognize it. People need a safe, shame-free environment to talk about their private, darkest abyss.

I live with a stranger. It shadows me and usually cowers in my wake. But I am always on high alert, prepared to face-off when, for whatever reason, it gathers strength and threatens to push me into darkness. When it succeeds in conjuring black days, I must force myself to do the things I love because the stranger has stolen their luster, faded their colors, and turned satisfaction into a question of “Why bother?” I am unable to shed one tear over the loss of these pleasures. Apathy and numbness coat me with emotional Kevlar. Pain can’t get in, nor can it get out. Hopelessness percolates within the armor.

For some reason the stranger stays away from me when I work. I think focus on a task or a problem, disempowers it. My work keeps the stranger at bay. Whether I am at my job or writing, the stalking shadow disappears and I am free to stay on task, the best therapy. So I understand why, at the thought of losing his sight, a pilot succumbed to his depression. He lost his point of focus.

I have never taken drugs to kill the stranger. I feared clouding my mind and stifling my creativity. I didn’t want to jeopardize my ability to do the very things that kept me going. Do I keep moving, an earth bound fighter jet zig-zagging through the atmosphere to evade the enemy desperate to shoot me down? What happens when I sit still?

There is an upside to the stranger. I am never alone; there is comfort in that. The stranger keeps me piqued for action rather than reaction. Because of it, I experience the world differently. I weep over beautiful words, over paintings with brilliant colors and thick, textured strokes, over a rock formation in New Mexico shaped like a camel. But I also feel the pain when one pass with a wash cloth takes away a patch of skin from a critically ill patient. I choke when a patient chokes on his breathing tube. I feel the ground fall away when I tell someone a patient has died. Experiences in the day burn with a hyper-acuity. Perhaps I have achieved balance with my companion. It feels that way today.

The victims of rape have been urged to come forward and speak about their violation as a step in healing and self-affirmation. Depression feels like an assault from within. At a time when both real life and art dissect the complexities of mental illness, it is time to speak openly about depression.

 

 

 

 

 

Filed Under: Depression, Health Care, Human Connections

We need to talk about depression

April 2, 2015 by Cynthia Stock Leave a Comment

The other night I watched Birdman followed by updates about the plane crash in the French Alps. I read the analysis of the incidence of suicide among veterans. Despite mass media, continuous connection via hand held devices, and information at our fingertips, I concluded: We need to talk about depression. How many people walk around with depression as their constant companion? How many control it? How many are controlled by it? Is any disease more insidious than depression? It seems to sneak by, undervalued, untended, yet with the potential for crippling the person who suffers from it.

Years ago I read William Stryon’s Darkness Visible, a most personal journey. Then there was The Noonday Demon, detailing the complexity of depression in a more objective voice.  To understand the power of the disease, the individual experiences of depression need to be shared. It morphs, shape-shifts and lives in such a way that even the people closest to the depressive don’t recognize it. People need a safe, shame-free environment to talk about their private, darkest abyss.

I live with a stranger. It shadows me and usually cowers in my wake. But I am always on high alert, prepared to face-off when, for whatever reason, it gathers strength and threatens to push me into darkness. When it succeeds in conjuring black days, I must force myself to do the things I love because the stranger has stolen their luster, faded their colors, and turned satisfaction into a question of “Why bother?” I am unable to shed one tear over the loss of these pleasures. Apathy and numbness coat me with emotional Kevlar. Pain can’t get in, nor can it get out. Hopelessness percolates within the armor.

For some reason the stranger stays away from me when I work. I think focus on a task or a problem, disempowers it. My work keeps the stranger at bay. Whether I am at my job or writing, the stalking shadow disappears and I free to stay on task, the best therapy. So I understand why, at the thought of losing his sight, a pilot succumbed to his depression. He lost his point of focus.

I have never taken drugs to kill the stranger. I feared clouding my mind and stifling my creativity. I didn’t want to jeopardize my ability to do the very things that kept me going. Do I keep moving, an earth bound fighter jet zig-zagging through the atmosphere to evade the enemy desperate to shoot me down? What happens when I sit still?

There is an upside to the stranger. I am never alone; there is comfort in that. The stranger keeps me piqued for action rather than reaction. Because of it, I experience the world differently. I weep over beautiful words, over paintings with brilliant colors and thick, textured strokes, over a rock formation in New Mexico shaped like a camel. But I also feel the pain when one pass with a wash cloth takes away a patch of skin from a critically ill patient. I choke when a patient chokes on his breathing tube. I feel the ground fall away when I tell someone a patient has died. Experiences in the day burn with a hyperacuity.

The victims of rape have been urged to come forward and speak about their violation as a step in healing and self-affirmation. At a time when both real life and art dissect the complexities of mental illness, it is time to speak openly about depression.

 

 

 

 

 

Filed Under: Depression, Health Care, Human Connections

The Last Resort: A Fascinating Look at the Future

January 4, 2015 by Cynthia Stock Leave a Comment

The current health care model mandates that discharge planning begins the day a person enters the hospital. On a grander scale, life follows this model; from the day of birth, a person moves toward his demise. Maureen Holtz’s novel The Last Resort explores a future in which a small country in Africa bases its economic survival on providing a place where self-determination at the end-of-life is legal, thus generating a unique sort of medical tourism. Using an American “everyman,” Holtz intertwines the lives of Livvy and Simon Harper, who reside in Illinois, with the politics and health care of both America and Mkanda, Africa. She explores a not-too-distant future (2020) in which an aging population burdens not only family, but also the finite resources of health care.

The questions raised by this novel are not pretty, not easy to discuss, nor are there any quick fixes or ready answers. This is what makes it must reading for anyone: health care providers who offer extreme options without assessing post-procedure quality of life, family members who pursue what’s radical and new without considering outcome, the young who will be responsible for a portion of the costs through taxation, the aging who will leave a legacy of health care debt with the coming generation.

Ms. Holtz complicates the overall picture by introducing the conflict between faith and medical ethics. When a family faces health care decisions, what role does faith play in making medical choices? Quite simply the novel poses two important questions: Who decides? And who should decide?

Livvy and Simon Harper know tragedy. They have lost a child. Simon’s parents have died. Livvy’s mother succumbed to cancer. Now Livvy’s father, Hank, a successful journalist with an inquisitive, brilliant mind, has been diagnosed with ALS and early Alzheimer’s.

As these family problems unfold, President Adebayo, of Mkanda, must live up to his campaign promises and revitalize his country’s economy. He proposes the Euthanasia Legalization Act. In Mkanda access to health care is negligible. Adebayo watches a worker dies by the roadside in agony because of the impoverished country’s lack of resources. As a doctor, Adebayo wrestles with his pledge to “do no harm” and the harm caused by allowing suffering to continue. He and his aide Kwesi come up with the idea for The Last Resort, a place where those who wish to end their lives can come to a pristine setting, plan their last days, and exercise control over their final moments.

Ms. Holtz illustrates the subtle mental and obvious physical decline of Hank with accuracy. She allows the reader to see these changes from different points of view. Hank shares his perception through an inner dialogue filled with candor and doubt. Livvy frets over what’s next and how she and her husband will manage Hank’s care. Hank’s friends surround him with support and the therapy of good memories. Hank, ever the investigator, hears about Mkanda and begins to talk about choosing how he wants to die.

Hank’s decline occurs as President Adebayo’s plans come to fruition. The Last Resort opens. Gradually the number of clients increases. As people experience a different way of dying and Mkanda’s economy flourishes, a modicum of acceptance comes to the country and its people.

This book has many strengths. In Livvy Ms. Holtz creates a character who draws the reader into the horror of a family member wasting away not just physically, but mentally as well. Livvy struggles with suicide as a sin in the context of her religion. As she watches Hank deteriorate, she questions her faith. The reader can’t help but join in vicarious debate about life, faith, and final days. Hank speaks for all who perceive nursing homes as warehouses for the frail and elderly who are managed by drugs rather than any sort of individualized care. Even the family dog, Sherlock, introduces a thematic element and allows the reader to establish the contrast between the humane therapies given a dying pet versus the options given a human being.

One sub-plot of this unsettling novel is the role of pharmaceutical companies in medical care. Before The Last Resort can open, a price of the drug used to end life must be negotiated. The usual dickering over cost and profit occurs. After The Last Resort opens, a plant that produces a drug which causes a rapid, pain free death is discovered in Mkanda. A taste of white collar espionage and greed ensues. The novel alludes to the complex process of FDA drug approval in this country. This element flows well in a story laced with multiple medical-moral issues.

As someone with a health care background, I wish Ms. Holtz had created scenes that addressed some missing pieces. I asked myself why there was no scene where Livvy sought serious counsel from the clergy. When faith was so important to her, it would seem a logical step in the process of finding out how best to support Hank. I also think to show the potential benefit of such a discussion would add much to what this novel has already taught about living and dying.

Ms. Holtz skims over the use of Advance Directives and Durable Power of Attorney for Health Care in end-of-life situations. These legal concepts represent strong, albeit not absolute, tools in self-determination. She also fails to address the role of palliative care and hospice in the lives of the terminally ill. In some institutions, a palliative care consultation is required when a patient is considered for certain therapies. Comfort and quality of life represent top priorities. In the overall context of this thought-provoking and controversial novel, these are minor omissions.

The Last Resort is an imaginative novel that forces the reader into the tempest of human truth: from the day of birth, a person moves toward his demise. Ms. Holtz offers a means by which a person can direct his course.

 

 

 

 

 

 

 

Why does ED happen

Filed Under: Death panels, Health Care, Human Connections, Life and Death

The “O” Word

December 29, 2014 by Cynthia Stock Leave a Comment

At one time I weighed 225. I am a 5’8” female. According to my BMI dial, I fell into the category labeled the word we dare not speak. I now weigh 163 and the dial sits on the line between normal and overweight.

I don’t watch Mike and Molly. Two overweight people starring in a sit-com diminishes the serious nature of a condition that threatens world health.  I wonder if all the time viewers are laughing are they becoming desensitized to the fact that these characters have health issues. In an era of political correctness, to describe someone as obese (There. I’ve said it.) might, by some, be called a hate crime. As a health care professional, failure to address a life-threatening health condition feels like a different kind of slight. Current media focus suggests our country needs a more open discourse about race. This nurse proffers it is time to have an open, pointed discourse about obesity and accountability of both the individual and the health care system.

Years ago I attended a seminar by Dr. Lawrence Barzune, a doctor at the forefront of bariatric surgery. In quantitative cause-effect terms he described the toll obesity takes on the body. Joint degeneration, skin problems, incontinence, and sleep disorders top the list of the most obvious problems. Consider that a pound of fat contains 7 miles of capillaries. If you are 100 pounds overweight, your heart has to pump that much more roadway. Your heart is almost running a 10K with every beat.

There is the school of thought that insists a person can be fat and fit. Perhaps that is true just as it is true that there are some people who are metabolically or genetically programmed for obesity. There are those who simply make bad choices. Either way people who are overweight confront unique and disabling challenges.

Perception of weight and size is like viewing the self through a maze of fun house mirrors. When I first gained weight, I lived a comfortable, busy routine of work and single parenting and never noticed how I changed. This is what I told myself. I wore what was comfortable: sweatpants, t-shirts, long skirts, and scrubs at work. I didn’t care what size scrubs they were as long as I could lift and bend without splitting the seams. Mirrors were not a part of my home landscape. I avoided weighing myself.

Having lost 70 pounds in six months, I discovered my perception of my body did not keep up with reality. I bought new clothes to fit the person I had been for several years and couldn’t understand why they were too big. A friend sent me one of her sister’s skirts, a hand-me-down. I took it out of the package and shook my head. Only a Barbie doll could wear that. The skirt fit. I began to try clothes on before I bought and waited for the mental “me” to catch up with the physical one. I put up the mirror that attached to my chest of drawers and saw a stranger.

Because of this body-image-perception dysfunction, I understand why a 300 pound man has no qualms about using me for leverage to pull himself up to a sitting position on the side of the bed.  What I can’t understand is a middle-aged woman sitting at the bedside of her seventy plus year old mother being told a bigger bed is being ordered for her mother’s comfort, and without batting an eye, this same woman asks for a bigger chair because she can’t fit into a regular chair. The disconnection between mind and body prevents the daughter from seeing a very possible future for herself. Nor does she perceive the plethora of weight related complications her mother must overcome to recover from surgery.

From my personal experience, dieting represents a misnomer, a poor term when used in relation to weight management.  Weight loss and concomitant health maintenance requires a lifestyle change that must become as routine and necessary as brushing your teeth. The goal must lean toward fitness rather than a number on a scale. The tools to accomplish the goal include commitment, diligence, and forgiveness. Commitment makes you integrate healthy choices into your daily life. Diligence inspires you to create a way of tracking your commitment be it a journal, meditation, or a support group. And forgiveness allows you days when you just can’t get it done without the guilt that might make you fall out of your program altogether.

Dr. Kenneth Cooper stated: “Fitness is a journey, not a destination. It must be continued for the rest of your life.” Weight control is just one leg of the journey.

 

Six tips about Tadalafil

Filed Under: Health Care, Human Connections, obesity and weight control

The Patient’s Wife

November 10, 2014 by Cynthia Stock Leave a Comment

After many years of nursing I celebrate every day I go to work and learn something new that improves my practice: a new drug, a new procedure, or some new machine. Recently nothing has taught me more than just being the patient’s wife. My husband, Dalt, injured his wrist cutting low hanging branches from a hackberry tree. When the chain saw broke through the branch, it dropped, yanked his wrist to an awkward angle, and triggered an autoimmune response that knocked my husband off his feet. The joints in his wrists and fingers looked like they had been hit with a baseball bat. His knuckles had not one wrinkle in them. The skin on his fingers, pulled tight from the swelling, turned his fingers bone white from the poor circulation. His usually active days became waking hours of agony. And I transformed from a competent health care provider into a worried, decompensating wreck.

Dalt went to see a hand specialist, had some x-rays, and got a prescription for pain pills. A few days after the “incident,” Dalt woke up in so much pain he couldn’t walk. I maneuvered him to the car and rushed to the ER. I happened to slip his pain pills into my purse. Because of his marked weakness, the doctor ran tests to see if Dalt had stroked. I knew he hadn’t, but didn’t want to be a “bad” family member. You know what I mean. The kind of person who micromanages the doctors, the nurses, the lab techs, even housekeeping. So I sat and waited and watched my husband moan with pain. I confess. I gave him one of his pain pills. In an hour he was 100% better. When the doctor came in to tell him she had scheduled an MRI of his head, Dalt declined. “I’m not having a stroke, I was just in so much pain.” I took him home.

Prior to this I assessed the silent symptoms of pain the way I learned in school: rapid heart rate, shallow breathing, a furrowed brow, even nausea. When Dalt was in pain, he aged ten years. Wrinkles impressed his usually smooth cheeks. He exhaled long, deep, gasping sighs when he slept. He wasn’t nauseated; he had no interest in eating. When he walked around the house, he held both arms close to his body, guarding his hands from anything that might accidentally hit them. I didn’t know how to help.

It took over a month to get scheduled for surgery to fuse Dalt’s wrist bone. The doctor promised pain relief with the procedure. We would have opted for the next day, but pre-op testing, booking an operating room, and allowing for the doctor’s schedule took time. Waiting. Something I never learned to do with grace, especially when someone I loved suffered. Watching him struggle through a day of pain wore me down as much as it did him. A man with strong faith, I sometimes worried about going to work and leaving him alone. That’s how much the pain changed him.

Dalt is a young 73, but not without health issues. I viewed the surgery as a panacea, a game changer, a pain ender. But on the day of surgery, the nurse in me kicked in and the “what-ifs” took over. Count on an experienced nurse to anticipate the worst case scenario. This was a post-Joan Rivers day where an out-patient procedure turned into a tragedy. I followed Dalt’s gurney down the hall to the operating room, then detoured to the waiting room. I let him see the tears, my fear, and told him to hurry back.

I knew this procedure was considered relatively minor, no intrusion on the heart, the abdomen, or the lungs. But this was my husband. It required general anesthesia. What may have been the most minor surgery on the schedule that day was most major to me. I checked the information board where computer graphics symbolized when the surgery started, with a knife, when the surgeon was closing, with cross stitches, and when the patient went to recovery, with a Band-Aid. Every time the phone rang in the waiting room, I strained to hear. The volunteer called a name I didn’t recognize. It was my married name; for most things I still use my maiden name. It finally dawned on me that it was my turn to rush to the desk and pick up the phone. Another hour to go a young woman’s voice told me.

It’s been done in movies and on television, the every five minute look at the clock. That’s how it happens. Every five minutes I sighed with a sound reminiscent of his pain and asked myself “Are we there yet? When would it be over?” Overhead I heard one Code Blue called, heard the room number, and recognized which ICU it was. Not in the OR. Thank God. One Code Red. Fire in the lab. I didn’t care. One Adult Rapid Response. Well I knew that wasn’t Dalt, and I was upright. We were both safe.

I didn’t want to go to the bathroom for fear of missing the precious few minutes I knew the doctor would grant me after surgery. The door where I watched different doctors emerge, doctors with whom I had worked for years, opened and Dalt’s surgeon, young enough to be my daughter, came out. I liked her no-nonsense provision of information, post-procedure x-rays included.

It required more waiting before I saw Dalt. A bed assignment had to be made, report called to the receiving nurse. I wandered up to a room that looked haunted by emptiness. Then his bed rolled in and he was there talking, thirsty, complaining of pain, but okay. I helped him with his first sip of water and watched him fumble with the PCA button to give himself some medication. I didn’t think hand surgery would be so painful. Dalt measured time in hours between pain pills and minutes between pushing the PCA. I measured it in the days it would be until I felt I could help him feel better.

The days of the call light are gone. Now patients call their nurses on hospital cell phones. “I’m in the middle of something. I’ll be there when I’m through.” The wife simmered; the nurse boiled. The first time it took twenty minutes for the nurse to come. One time she was an hour late with pain medication. I wanted insta-care for my husband. And all I could do was sit and feel totally useless.

Dalt is home now. For the next ten days he has to keep his hand above his elbow. When he’s up and about, he maintains this position wearing a sling. A new lesson begins. I never appreciated how many things I do that require two hands. Slicing a banana, peeling open a yogurt container, buttoning shorts, tying shoes, unscrewing a bottle, using the computer. I no longer take these things for granted. I get to do them for Dalt. Finally I am useful! He’s getting cabin fever from his confinement, not just because he’s stuck inside, but because when he’s healthy, he’s always busy.

Better days are coming. Because of Dalt I’ll go back to work a better nurse. I’ll remember that if you’re the patient’s wife, lover, son, daughter, father, whoever, there is only one patient. That from your point of view any surgery is the most major surgery. That pain is real and urgent and needs to be addressed quickly. That demanding families are a product of stress, love, disruption of everyday living, and fear of an unknown future. I promise I’ll remember what it feels like to be “just the patient’s wife.”
 

Why does ED happen

Filed Under: Health Care, Human Connections, Nursing

Thanksgiving 2014

November 10, 2014 by Cynthia Stock Leave a Comment

The media seems to think ratings depend on peppering our lives with a plethora of bad news: wars on multiple fronts, religious conflict, the collapse of the armor that shielded professional athletes from public scrutiny, politics, and, of course, Ebola.   In response to these purveyors of doom, I challenged myself to list ten things to be thankful for this Thanksgiving.

To my surprise I filled my list in just a few minutes. While some things may sound simplistic or insignificant in the context of a world view embellished by mass communications, I find them reassuring and filled with hope for the future.

 

I am thankful that:

 

After forty-one years of nursing at the bedside, I still learn something new every day. I have changed from being the new nurse to being the seasoned nurse. Rather than having a “work husband,” I have a “work daughter,” who I try to teach, nurture, and share wisdom with, without being too motherly. Yesterday I managed yet another new device used in critical care. And despite having to deal with a machine, I picked up on subtle changes in the most important element of the health care system, the all-too-human patient.

 

Fifteen years into our marriage, my husband and I still hold hands when we walk or sit on the sofa. I told him on our first date I was “that sort of girl,” that I liked the connection born of such a simple gesture. I watched my parents do the same during their marriage. He holds my hand, and I am confident he is listening and present.

 

Cancer entered my life. How can I be thankful for that? Anyone who has faced cancer knows it brings out either the best or the worst in people. In my family, it opened a hot-line of support and established a depth of communication we didn’t enjoy before the cancer intruded. We became a phone network of love, shared information, and reassurance. We relived treasured moments and brought to life my father, who died decades ago. Our differences melted away; the reality of how very much alike we were allowed us a closeness I quite possibly would have missed had it not been for the cancer.

 

My mother sold her house and is moving closer to family. The perfect role model for young women, she was one of the first who labored to “have it all” before anyone coined the phrase. She worked. She went back to school after she had a family. She competed. She coped with the loss of two husbands and survived. As a widow she established a new life and a rigorous sense of independence. Yet she was willing and has chosen to face change again. The family will come full circle.

 

Ebola appeared in this country through my city. Why be thankful for that? The presence of Ebola would have blind-sided almost any city. Entering the flu season in a culturally diverse place like Dallas, how many would have suspected Ebola? Americans have enjoyed the myth of impenetrability. We seem to think major crises and conflicts all happen someplace else. Because of Ebola, Americans must acknowledge the problems of the world and recognize the shrinking global community. Unfortunately we do not live “under the dome.” But the Dallas crisis opened our eyes and our minds and made us better prepared for the next challenge.

 

There are books like Joyce Carol Oates’ Carthage. She uses words to make the ordinary extraordinary: “—then the flowing-white hair, a testament to masculine vanity so refined as to approach abnegation, obscured the old, bitter hurt like a caress.” I want to journey in her mind. Or The Storied Life of A.J. Fikry by Gabrielle Zevin which has been described by one critic as a “slim novel.” I found it deliciously “plump” with deeply layered characters and convoluted story lines that converge and provide the satisfaction of a favorite wine.

 

I heard from my son. Sometimes children go missing. They haven’t been kidnapped, been in an accident, or deployed overseas. Sometimes they disappear into a space where they can mature and establish an identity unencumbered by the accouterments of family. My son drifts in and out of my life. Without warning or logic, he calls. I hear about his work and his health. Then I hear about his music, his true love. He gives me enough to last me until the next time he calls. But he has invited me in, in a way, and I feel I can call him if I want. We both seem to be growing in our fragile roles as son and mother.

 

I still love to write. On my very darkest days, if I sit and write just one sentence, I am lifted. I say the words out loud to hear their melody. I reread my work to see if I communicated the action and the images that wouldn’t let me go back to sleep at 2:30 in the morning. I look for passion, beauty, the ugly, the tragic, the joyous, and a moment in words that transcends the mundane. Memoir pieces placate my demons; fiction allows me happier endings. The haiku demands me to simplify. The written word pleasures all my days.

 

I am still able to work and work out. The miraculous machine, my body, has yet to betray me. I still can work three 12-hour shifts in a row. Today I worked out 75 minutes at the gym. My paresthesias stop me from hand sewing and needlepoint, but I type faster than most of my colleagues. I am in better shape than many of my cardiac patients who are years younger. They inspire me to keep going.

 

For some reason Mom’s Pumpkin Pie made the list. For years I followed what I thought was her recipe. Mine never tasted as good. I thought it had everything to do with the fact that hers was made under the penumbra of our nuclear family. On Thanksgiving Day, I watched Mom use her hand grinder to prepare the turkey liver and gizzard for the dressing. I sympathized when her eyes watered when she cut up the onions. I marveled how she carefully heated the juice from the can without the peas in it so the peas wouldn’t collapse when cooked. She allowed us to set the table with cloth napkins and sterling silverware. Sometimes we would eat by candlelight, forest green tapers with flames that flickered and beckoned like fingers. The light enclosed the four of us in a golden cave. My family. No wonder the pie was special. I asked her what I was doing wrong, why mine tasted different.

 

Mom told me her secret. “Don’t bother using half white and half brown sugar. Use all brown.”

I did as she advised. But she was wrong. The taste, just like giving thanks, is all about family.

Six tips about Tadalafil

Filed Under: Human Connections

Human Touch in an Ailing System

July 9, 2014 by Cynthia Stock 1 Comment

 

Bruce Springsteen asks in his song Human Touch: …in a world without pity Do you think what I’m askin’s too much…I just want something to hold on to…And a little of that human touch.

The words resonate with anyone who has teetered at the black abyss of depression or psychosis, with anyone who has experienced a moment when he felt alone and anonymous in a bustling, too-busy-surviving world. How therapeutic for one person to reach for the lonely, to touch an arm, drape an arm over a shoulder, and pull a soul back from the darkness. Most people have lived through such moments and know the void of which I speak.

A friend of mine who works in a psychiatric facility told me she planned to quit her job. She had been reprimanded for hugging her patients. Although she is the type of therapist who radiates an aura of genuine concern, a professional who patients request for their care, she was told that hugging was not appropriate. Not appropriate? The touch between two people, a gesture validating existence and humanity. These are not full body hugs. They are not sexual hugs between men and women. They are connections between patient and therapist executed in a day room perhaps, in a hallway, anywhere.

In my clinical setting, I sense when a patient or a family member needs a hug. I prevented a woman from falling to the ground in grief because I hugged her shoulders to brace her for the news. I did not hug, sensed the need for tactile restraint, but stood shoulder to shoulder as a man watched the resuscitation of his wife. I guided a wife, my hand in the small of her back, to seat her by the bed of her husband as he slipped from this Earth. At one point she squeezed my hand. I see people so diminished by grief I touch them and hope that touch provides a conduit to share the abundance of energy I have provided by the love I have for my profession. Is this inappropriate?

Conversely to my surprise, a man who was going back to his home in another city, who knew he would never see me again because his cousin was dying, hugged me and wrapped me in profound gratitude, not only by his words, but also by this one unexpected gesture from someone who had seemed distant and restrained. I haven’t collected a paycheck able to match the value of this act. The wife of a patient hugged me and told me how much my care meant, not just to her husband, but to the entire family.

For brief moments when people are most vulnerable, the nurse I am becomes an extended family member. Because recovery from illness is never straight-forward, because it is filled with days of five steps forward and three steps back, I earn the trust and wrath of family members. I share the joy, bear the brunt of frustration. I praise success and illuminate the smallest shard of progress. I awaken at 2:30 in the morning and wonder if I have done everything I should have; if I could have done something more or better or more quickly. That is the nature of my nursing practice. It is the nature of humanity.

I imagine some patients will notice my friend’s absence. In the bigger picture of corporate health care, someone will fill her position and the institution will go on without pause.

Decades ago my favorite nursing instructor challenged me to maintain a “Ma and Pa” quality to bedside care in corporate world. I took her to mean: Keep it individualized and personal. I talk books to those who read. I read bean futures to those who farm. I find church services on Sunday for those who worship. I share funny stories from my own family to take a patient’s mind off the humiliation of incontinence, the shame felt by some for being weak. I wash feet, endure court TV, and answer a daily barrage of the same question quite like a child’s “Are we there yet?” “Is he better?” “When can he go home?” “Is he gonna make it?”

I once hugged a man whose son ultimately died, a victim of a drunk driver. He told me that at the time, “Life sucked. It (the hug) picked me up. I knew someone really cared.”

Springsteen tells it right: “You might need somethin’ to hold on to When all the answers, they don’t amount to much Somebody that you can just talk to…a little of that human touch.”

In your new job, my friend, keep hugging.

 

 

 

Why does ED happen

Filed Under: Health Care, Human Connections

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