Tag Archives: Medicine

Week 12: Extreme Measures at the End of Life

*Watch Extremis documentary on Netflix (24 min)
*Pearson, No Acute Distress (pgs 205-250)

For this week’s class, I created an End of Life Jeopardy designed to help guide our conversation about hospice and palliative medicine and end of life narratives. I decided that jeopardy would be a playful way for us to cover a lot of ground about difficult conversation topics. Categories included Goals, Quality of Life, Ethics, Faith, Health Equity, and we talked about narratives at the bedside and in society about death. We did not keep track of points or have any winning teams. Instead, we divided into groups of three and each small group discussed each question together before sharing their conversation with the whole group. Students found that the jeopardy format worked well and allowed us to unpack many of the topics introduced by the readings and by the Extremis documentary.

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Week 10: Meeting Cancer, The Emperor of All Maladies

*Audre Lorde, The Cancer Journals

*Rachel Pearson, No Acute Distress (pgs 164-204)

What strikes you about cancer narratives in comparison to other illness or disability narratives? Identify what can be problematic about societal narratives of cancer.

After reviewing the final project and the final project proposal due to next week, we began a discussion about cancer narratives. We built on the themes discussed in the weekly posts to reflect on what is unique and different about cancer narratives compared to some of the other narratives we have read this semester, such as disability narratives and other illness narratives. Our conversation touched upon themes of fear, mortality, disability/normalcy, life after cancer, uncertainty/unknown, prognosis. We ponded what stories we tell as a society about cancer and what stories and experiences go left untold. We imagined the implications of how society narrates cancer, and how these narratives might impact people with cancer.

We then explored the medium of graphic medicine, or comic art, to understand cancer narratives through a different lens. In groups of two, we looked at various excerpts from some of the most well-known cancer graphic memoirs such as Marisa Marchetto’s Cancer Vixen, Miriam Engelberg’s Cancer Made Me a Shallower Person, Brian Fies’ Mom’s Cancer. We observed how the addition of imagery in combination with text created a different dimension to these stories and shared different kinds of emotion through the multiple layers that go into comic art.

Last but not least, we experimented with creating our own graphic art to tell a story of cancer- either based on a reading or a personal experience. It was interesting to create through a different lens than writing since writing is a form of expression that our society is far more accustomed to using. Through the art incorporated into graphic medicine, we had the opportunity to experience something different from traditional written narratives.

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Week 9: Ethics of Narrative in Medicine

*Part II Chapter 7: Attention, Representation, and Affiliation from Rita Charon, Narrative Medicine (pgs 107-130)

*Part IV Chapter 9: Bearing Witness and 10 Bioethics from Rita Charon, Narrative Medicine: Honoring the Stories of Illness (pgs 177-218)

*Healing Narrative: Ethics and Writing about Patients, AMA Journal of Ethics

Reflecting on what you have learned about narrative medicine so far this semester, what ethical considerations must be made when we think of narrative medicine? Some examples of ideas to reflect on include: 

-ethics of practicing narrative medicine clinically with patients (i.e. how to do so equitably)

-ethics of sharing the stories of our patients and/or colleagues and/or loved ones (i.e. issues of attention, representation)

-ethics of how society tends to share certain narratives and silence others, and why this occurs

-ethics of how healthcare systems use patient narratives (i.e. for marketing, for donors)

Are there narratives that we have encountered this semester that feel less ethical than others? If so, why?

This week, we took a step back to reflect on the ethics of narrative medicine. We began with a writing prompt: Write a story about a healthcare experience that isn’t yours to tell. We talked about what makes a story yours to tell, and different writing techniques for writing a story that isn’t yours to tell.

After briefly discussing Beauchamp and Childress’ 4 Biomedical Principles of Ethics, we launched into 3 work groups to define our own policies about Consent, Patient Care, and Marketing/Fundraising. We unpacked what best practices of using stories in these different spaces might look like and created our own standard practices for ethically using stories. Topics included de-identification in narrative and the importance of obtaining patient permission, reframing stories propagated amongst healthcare professionals, and imagining patient-centered approaches to storytelling for marketing/fundraising purposes.

We returned to the same story we wrote about earlier and wrote again: Write about the same healthcare experience as a story that is yours to tell. We reflected on how different this experience felt, and how different the stories were that emerged.

After our break, we began an informal debate to illuminate different perspectives to consider with the ethics of storytelling in medicine. Students were each assigned as patients, families, clinicians, or hospitals. We discussed stories that emerged earlier in class or scenarios that people wrote about in response to the writing purpose.

I concluded class by sharing my own imperfect framework for considering the ethics of narrative medicine:

Who- who is telling the story? Who is receiving the story?

What- what is the story being told?

When- at what time is the story being told?

Where- location of storytelling, i.e. at the bedside, in elevators and stairwells, social media

How- rhetoric, tone, language used to tell story, making space for storytelling?

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Week 5: Black Man in a White Coat: Narratives of Racial Inequity

*Damon Tweedy, Chapter 2: Baby Mamas and Chapter 4: Inner-City Blues from Black Man in a White Coat: A Doctor’s Reflections on Race and Medicine (pgs 30-53; 78-102)

*Jennifer Okwerekwu, What Racism in Medicine Takes From Us

*https://www.npr.org/2010/02/01/123234261/excerpt-the-immortal-life-of-henrietta-lacksLinks to an external site.

How do these three writers share stories of racial inequity? Who is telling each story, and how does their perspective influence the narrative they share about inequity? What did you learn about health inequity through these narratives?

For the first half of class, we had the honor of guest speaker Dr. Duane Loynes, Associate Director of Equity and Culture at Rhodes College, joining us and teaching us about cultural humility. We each completed a cultural intelligence survey which involved evaluations by three people who know us in addition to our own self-reflection to assess our cultural humility.

Following this session, we engaged in the following writing prompt: Write about a situation where race impacted how a person was treated (in healthcare). Students had several powerful examples about race impacting patients within healthcare. We then introduced three questions to explore more deeply which we would continue to discuss in subsequent classes:

  1. How do we respond to these narratives in real-time?
  2. How do amplify the voices of those experiencing health inequity due to race?
  3. How do we change the dominant narratives about racial inequity?

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Week 4: Living Beneath The Bell Jar of Depression and Mental Illness

*Excerpt from Sylvia Plath, The Bell Jar (pgs 112-244)

*Colleen Farrell, Systole and Diastole, Strength and Openness

*Rebecca Grossman-Kahn, Beyond the Rubble of Lake Street—Minds in Crisis in a City in Crisis

**CQ Assessment Due.

We jumped into two poems by Sylvia Plath: Lady Lazarus and Tulips. Pairs of students explicated each poem and then shared their conversations. We talked about what was different about poetry as a genre as compared with the quasi-autobiographical work of Plath in The Bell Jar and the narrative essay style of Dr. Farrell. We talked about some concepts that help guide psychiatry, such as the DSM-V (and some of its limitations), stigma, how we define normal vs. abnormal, functional impairment/subjective distress.

We watched the following video as we transitioned to thinking about mental health inequities:

We then discussed widespread mental health inequities and cultural considerations for trying to decrease these inequities amongst different patient populations: Black/AA, Native and Indigenous, Latinx/Hispanic, Asian American/Pacific Islander, Arab/Middle Eastern, Multiracial communities. In groups of 2-3 each, students each studied one of these patient populations and shared their findings with the larger group.

For the second half of class, we had the honor of guest speaker Dr. Rebecca Grossman-Kahn joining us virtually to speak about her NEJM piece “Beyond the Rubble of Lake St– Minds in Crisis in a City in Crisis” and narrative medicine in psychiatry. We had a great conversation and covered a lot of ground. Topics discussed included the following:

-how we communicate mental illness to patients

-how we collaborate with families to better understand when patient narratives might not provide the whole picture

-the art of practicing psychiatry with an attention to narrative

-how we make decisions about when to limit or take away a patient’s autonomy (i.e. through involuntary commitment for mental health)

-how we address health inequity and social justice at the bedside and through the medical system.

My Week 4 lesson plan and slides are included below:

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Week 3: Diagnosing Illness Narratives

*Part III Chapter 6: Close Reading from Rita Charon, Narrative Medicine (pgs 107-130)

*Arthur Frank, The Wounded Storyteller (pgs xi-xiii, 75-84, 97-102, 115-119)

How do Frank’s 3 types of illness narratives help us and in what ways might this framework limit our understanding of illness narratives? What stories do people tell through social media about illness and how does society receive these stories? Give an example of what common responses to illness narratives might suggest about societal understandings of health inequity. OR Create a narrative about illness that uses common elements outlined in Frank’s illness narrative categories.

Our class began discussing questions posed by Ann Jurecic: “Where did [illness narratives] come from? Why are we so interested in reading them now? Why are so many people interested in writing them now?” In groups, we tackled the illness narrative worksheet, each group focusing on a single category of Frank’s types of illness narrative. I asked for students to focus on examples in popular media, ie. film and art. We then discussed the benefits of this narrative typology and the limitations of this framework, unraveling some of the caveats that must be kept in mind when thinking about these categories. I shared brief slides about the evolution of medicine and narrative, patient- and family-centered care, and examples of using illness narrative types to inform communication strategies and in research.

Some highlights of our conversation include:

-Categorizing types of illness narrative is most helpful for the listener. Importantly, Frank’s illness narrative types are not distinct categories but rather can overlap. How people narrate illness is a dynamic process and different illness narrative types can be expressed at any given moment.

-Understanding how people narrate their experiences with illness can help us to better meet them where they are and provide patient- and family-centered care.

We explored the question of whether “survivor” falls under a restitution narrative vs. a quest narrative (answer: lots of caveats to consider!). The idea of knowing how to respond when a narrative contains elements of chaos and restitution/quest was explored, and the idea of how to best meet patients where they are with how we communicate. We also talked about how knowledge of these narrative types could impact clinical care. Class ended with an engaging creative writing prompt about personifying disease!

My Week 3 lesson plan, worksheet, and slides are included below:

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Week 2: Foundations of Narrative Medicine and Health Inequity

After intros and an overview of the syllabus and course schedule, I acknowledged the recent death of Tyre Nichols in our city of Memphis. Prior to class, it was difficult to anticipate what this conversation would look like with students that I had not met yet, but I wanted to make space for grappling with yet another incidence of police brutality in our nation.

The students launched into a discussion about the readings and specifically the AMA table about key principles and associated terminology (see below).

*Watch Empathy: The Human Connection to Patient Care.

*Read Part II of Rita Charon, Narrative Medicine: Honoring the Stories of Illness (pgs 65-104).

*Read AMA Advancing Health Equity: Guide to Language, Narrative and Concepts Intro, Part 1: Health equity language, and Part 2: Why narratives matter (pgs 4-27).

Some highlights of our conversation include:

-Person-first language. i.e. the impact of “underserved communities” vs. “communities that have been underserved by/with limited access to ____”

-Difference between when people choose to identify with certain words vs. when labels are imposed on them by others (i.e. victim, survivor)

-Does altering language affect clinical care and/or outcomes? Does raising awareness about the importance of person-first language actually alter patient-provider relationships?

We discussed ways that people are “made vulnerable” and about what is meant by the idea that “we need to change the narrative,” and we closed with a reflective writing exercise about experiences with healthcare.

My Week 2 lesson plan and slides are included below:

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An open invitation for guest blog posts on illness narratives

When I first started this blog, I was excited to seize the domain illnessnarratives.com. Now several years later, however, I’ve realized that the focus of my writing here has evolved, and I’ve felt uncomfortable about how many of my posts have been about me and my writing rather than on illness narratives in general. This blog has been alive throughout a good chunk of my journey towards a career in medicine, from my undergraduate to my medical school education. It’s been challenging to find my direction, to balance sharing my own personal writing accomplishments and experiences with my thoughts on illness narratives that I encounter

To that end, I’d like to try something new. I’ve always felt it strange that I was the only voice in a blog that aspired to comprehensively survey the landscape of illness narratives.

This is an open invitation to anyone interested in writing a guest blog post. Here are some examples of what I’m hoping for, but I would welcome a post about anything that interests you related to illness narratives:

  • Review of an illness narrative, be it literature, film, music, or any other media
  • An illness narrative of your own
  • Thoughts about illness narratives as a genre
  • Ideas about the ethics of writing about illness
  • Any other interest you would like to explore!

Your blog post could be as short or as long as you like. It could be anywhere from a paragraph to a few pages; whatever works for you. All you have to do is email it to tkpaul@umich.edu, and I’ll get back to you as soon as I can. It’s that simple. Please don’t hesitate to let me know if you have any questions at all; this will be a learning process for me.

I’m hoping that this might change things up a bit, and that I’ll be able to breathe some life back into this website. Because it’s summer, the world is anew, and it’s time.

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[Cancer Knowledge Network] Pediatric Palliative Care: A Multidisciplinary Approach

This article is also available at the Cancer Knowledge Network.

I have to admit—one of the first reasons that palliative care first piqued my interest was because I wanted to learn more about death. But as I’ve delved deeper into palliative care, I’ve come to realize just how much more comprehensive it is. While increasing access to hospice care is a component of what palliative care provides, palliative care does so much more for patients and families.

When I first started volunteering with patients at C.S. Mott Children’s Hospital, pediatric oncology jolted me to see how cancer can affect all humans, even kids. But the realization that terminally ill children face the unknown prospect of death every day was most jarring to me. Death was no longer an abstract fate for the elderly but rather a real concern for the babies I held, the kids I spent time with on Friday evenings.

As a teenager myself, it was especially hard to see other teens having to go through the experiences of being diagnosed and treated for a life-threatening disease like cancer. I became interested in how people of all ages, and especially children, understand and cope with death. I found that palliative care does not shy away from these end-of-life topics but rather starts many of these difficult conversations. Similarly, palliative care provides additional support by devoting attention to the pain that patients may be experiencing as well as the discomfort from symptoms and side effects.

The American Academy of Pediatrics (AAP) recommends that ideally, palliative care should begin (or at least be offered) when a child is first diagnosed with a life-threatening disease[1]. Pediatric palliative care aims to support young patients and their families throughout the entire experience of illness, from diagnosis to treatment, remission to relapse, and even end-of-life when applicable.

For kids undergoing treatment for cancer, imprisonment by IV pole and pain by poke may be what they know. Many have no choice but to curl into the humbling fetal position for spinal taps. These children hold on to the simple pleasures in their lives by putting a port on a teddy bear or playing with a Barbie doll that has no hair. Each child finds a different way to cope, and I have grown to admire these children. Pediatric Palliative Care, along with other health disciplines such as Child Life, provide additional support to help children cope with a cancer diagnosis and the difficult treatments that it entails.

We’ve come a long way in treating pediatric cancer over the past several decades, but it’s not enough to stop the uncontrollable growth of cancer cells without recognizing the psychological scars left behind by its presence. Cancer treatments can have life-long health consequences, and the support of pediatric palliative care involvement throughout the course of treatment has the potential to have a lasting impact on patients.

This, to me, is what pediatric palliative care is about. Pediatric palliative care is about ensuring that young patients have the best of quality of life that they can while experiencing life-threatening illness and its corresponding medical interventions. It is about devoting special attention to more than a child’s physical health but also their mental, emotional, and spiritual wellbeing. As a multidisciplinary team generally composed of physicians, nurses, social workers, psychologists, and chaplains, pediatric palliative care is able to support children as well as their siblings and parents more holistically.

Palliative care, especially in the pediatric world, encompasses end-of-life and much more. As the AAP states, “Reserving palliative care for children who have exhausted every curative treatment and are dying would mean that many other children would miss out on the benefits that palliative care can offer.” It has been encouraging to see how much pediatric palliative care has become established and valued over the past several years, and I look forward to getting involved in the field in the future.

 

[1] http://www2.aap.org/sections/palliative/whatispalliativecare.html

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[Cancer Knowledge Network] Discovering a Passion for Pediatric Palliative Care

This article is also available at the Cancer Knowledge Network.

As someone who loves spending time with kids, I was thrilled when I was placed to volunteer on the 7th floor pediatric oncology inpatient playroom at C.S. Mott Children’s Hospital. Although I was just in high school, I had an early interest in becoming a pediatrician, and Mott seemed like the perfect place for me to learn more.

From talking to teens at their bedside to playing video games or doing arts and crafts with kids, I enjoyed every minute I spent with patients and their families. These activities meant so much more to me as I began to see how integral they were to sustaining children through cancer. These children endure levels of pain that seem unthinkable at such a young age, and I helped them find distractions in board games and plastic food.

With the backdrop of illness, these normal activities were never quite the same. One minute, I was racing trains with a 2 year old. The next, I was gripping his tiny arms and legs to help his nurse draw blood. He put his entire body into his scream, thrashing wildly. But as I held him afterwards, his peaceful demeanor made me realize that I made a difference.

As I spent time with siblings and parents, I witnessed the many ways that cancer permeates the lives of loved ones. As a volunteer, I supported them in any way that I could. I came to believe that talking with kids and families, letting them engage in conversation, to get their mind off things if they so choose or voice their concerns, unleashes the therapeutic nature of the spoken word. From the weather to a child’s prognosis, these conversations illuminated different perspectives of how cancer affects lives. My experiences with these young patients and their families largely contributed to my own desires to devote myself to medicine.

When I started medical school a little over a year ago, I would tell people that I was interested in becoming a pediatric oncologist. Even then, I knew that my interests may change throughout the course of my medical training, but I also knew that this is where my heart was and where it still is, at least for now. Within just a few months, I found myself slowly gravitating towards another discipline that also works closely with children with cancer: the field of palliative care.

Palliative Care aims to improve the quality of life for patients and families, often by alleviating symptom burden, providing pain management, helping with decision-making, and furthering communication about goals of care.[1] Palliative care aligns with many of the aspects of volunteering that were most rewarding for me, as well as my own philosophies about how I hope to practice medicine. From striving to alleviate pain and relieve the suffering that patients experience throughout the course of treatment to engaging in important and intimate conversations with patients and family members about experiences with illness, palliative care prioritizes aspects of medicine that most move me.

Often, these quality of life measures are goals of medicine in general, but to have an entire medical specialty devoted to these important issues has the potential to greatly impact patients, especially those in need. The baby who won’t stop crying from the pain, the teenager who may have wishes that deviate from those of caregivers, the parents who are deciding whether a clinical trial is right for their child—there is no question that cancer diagnosis, treatment, and recovery can present a series of uncertainties, challenging decisions, unimaginable pain, and life-long symptoms and side effects.

I hope that palliative care training will help me to develop my skills and make a difference in the quality of life experienced by children with cancer. By specializing in both pediatric hematology/oncology as well as in pediatric palliative care, I believe that I will be able to develop a more comprehensive knowledge base and gain experiences to ensure that both perspectives will always inform my care. Palliative care embodies the kind of care that I hope to be able to provide for my own patients and their families some day.

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