Tag Archives: writing

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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Thinking about the Chronicling Childhood Cancer book reading/signing event… Still

I have to apologize for the blog silence. Sometimes life gets in the way of things, no matter how important they may be to me.

Three weeks ago, it was my pleasure to hold a book reading/signing event for the recently published book Chronicling Childhood Cancer: A Collection of Personal Stories by Children and Teens with Cancer. I had approached Literati Bookstore in downtown Ann Arbor on a whim, thinking that if there was any bookstore who may support this local book publication of stories by youth with childhood cancer, it was them.

Before I had even finished telling them the whole story, they had said “of course.” They kindly invited me to host an event to launch the book, to get the word out about it and raise more awareness about the cause of childhood cancer. They were so supportive about this project that they even wanted to donate 100% of the book sales from the event: as with the book, 50% of the donations would go to the Block Out Cancer campaign for pediatric cancer research at the University of Michigan and 50% to the Child and Family Life Program at the University of Michigan C.S. Mott Children’s Hospital.

I tossed around a number of ideas about what to do for the event, ultimately deciding that it would be best to let the children share their stories themselves. After I contacted all the young authors, we were fortunate enough to have three join us at the event (one other author realized that he had too much math homework that day, but I reassured him that was entirely valid and it made me smile to hear that school was his excuse).

It’s hard for me to summarize what happened that night. So hard that it’s taken me weeks to find the words to write about it (somewhat) coherently. The event as a whole moved me more than I had ever anticipated.

I had certainly been nervous about the event because of how sensitive this topic of childhood cancer is. I think that in the back of my mind I feared what could happen all along and how emotional the experience of sharing their stories could be for the authors of this collection. But in reality, I hadn’t mentally prepared for it.

By its very nature, the book reading was an emotional experience for the young authors as well as the audience. It was not easy for me to watch as these teens stood under bright lights in front of a room full of people, overcome by emotion as they shared their personal and very intimate experiences with cancer. I was struck by their determination and persistence to tell their tales- it was just one example of what courage in the face of cancer looks like.

After the event, each of the authors thoroughly enjoyed signing copies of the book. Even though the event had clearly not been easy for anyone, they were all eager and excited about the prospects of doing another book reading/singing event and maybe even meeting some of the other authors.

As far as this project has come, I’ve realized that I’m not done with it now, and I probably won’t ever be. There’s just so much more that I want to do to share what these children and teens have shared with me, and I’m as determined as ever to make the most of all that this project has taught me. But I also know that I need time, and that’s ok.

To this day, I am struck by just how much this event moved me. The standing-room-only audience of friends and family, health practitioners and local strangers. The kind words of appreciation expressed by these young authors and their parents. The knowledge that all that I have put in to this research, this book, and this event has touched these teens more than I had ever realized. It was overwhelming, in the best way possible.

Literati book reading signing event- Event Plan

Literati book reading signing event- Research Overview

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A Summer Solstice of Sorts

Although it’s been awhile, I’ve been thinking a lot about this website over the past few weeks. Remembering where it began, reflecting on how it has evolved, and postulating about what lies in its future. What began as a somewhat objective study of illness narratives has transformed to introspectively explore my personal navigation of the genre.

This summer, for the next two months before medical school begins in August, I will be doing something else that I love: traveling. From India to Paris to Spain, I’m really excited to have the opportunity to see more of the world. I am determined to make the most of this exciting time.

My ever-growing summer reading list beckons, and my travel journal of blank pages is waiting to be filled. I hope to refrain from technology (insofar as is possible) and instead feel the pages of real books and write through my thoughts with a pen in hand.

And so, this is a disclaimer: posts may be sparse over the next several weeks. But if this ends up being the case, then I look forward to returning with a refreshed perspective, developing thoughts, and new ideas for the future.

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Excited for The Examined Life conference: Writing, Humanities, and the Art of Medicine

When I attended the WMU Medical Humanities Conference last fall, I heard about an upcoming conference called The Examined Life: Writing, Humanities, and the Art of Medicine. And now, I’m fortunate enough to not only be attending this conference but also be presenting about my childhood cancer narrative research!

The Examined Life conference explores “the links between the science of medicine and the art of writing.” This conference seems to align perfectly with my own dual interests in medicine and literature. I think that participating in this conference will help me to figure out how I can maintain and balance both passions throughout my career, and I’m looking forward to meeting others in these fields with their own insight and experience to share.

At the Examined Life conference just one week from now, I’ll be doing something a bit different. In writing my Honors English thesis over the course of this year, I realized just how crucial my methodology has been in shaping the adolescent cancer narratives that I wanted to analyze. As a result, rather than just presenting about my research, I’ll be leading a discussion forum this time. Specifically, we will be discussing the ethics inherent in my methodology and thoughts that may be sparked from encountering these narratives. I’m curious, nervous, and excited to see what comes out of this discussion. I believe that these conversations will give me a lot to think about as I look towards further developing my honors thesis.

Here’s the abstract for my discussion forum:

Chronicling Childhood Cancer: Illuminating the Illness Experience through Narrative

I’ve never been to Iowa! I’m excited.

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One year later…

I’ve been thinking about this post for a few weeks now. Anticipating it, smiling about it, even stressing about it. It’s been one year since I started this blog, and I feel obligated to write about it.

I think that there are a few reasons for my muddled emotions about writing this post. I wanted to write about how far this blog has come in one year, how happy I am to have found a space to write and share my thoughts. I wanted to thank my more than 1500 followers, a supportive community of people that I had never expected to find. And I wanted to once more express my amazement and appreciation about just how far my thesis research project has come and how excited I am to be teaching my own course about illness narratives this semester.

Intertwined with all these joys and accomplishments, however, are the confusions and  hesitations that remain. I haven’t quite figured out where I fit into the fields of narrative medicine and medical humanities, but I find myself drawing away from both of these disciplinary labels. I’m not sure how exactly I will preserve my interests in this interdisciplinary arena, but I am determined to integrate this passion throughout medical school and beyond.

I was finally motivated to write this post, to reflect on how fulfilling this blog has been and recognize how much more I need to write through, because I realized that this is just where I should be. Writing blog posts in my head has become something that I just do, but I’m also glad that I haven’t found the answers to all my questions just yet. I guess that’s what this year will be for: finding more answers, and asking even more questions.

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Being Thankful for Cancer: A Huffington Post article

This Huffington Post article caught my eye:

Dear Cancer, This Is How You’ve Made Me Thankful.

Zoe Lintzers reflects on how she has observed the experiences of loved ones with cancer, and how cancer has helped her to better appreciate the simple pleasures of life: She writes perceptively about these experiences and her own realizations, presenting a convincing argument for what others can learn from disease and human suffering. Is illness something we should be thankful for? Despite the revelations that it may catalyze, does it demand our gratitude?

It was sometimes hard for me to look beyond some of her diction choices, though. She mentions the aunts she lost to cancer. Then she proceeds to tell of how  “[t]here are the brave others in my family who have been diagnosed in the past six years and are in remission, having triumphed over a disease that makes our eyes widen and our hearts crumble upon hearing that initial diagnosis. But they’ve prevailed and, to me, are the strongest people I know.”

But what does this mean for those whose lives were lost to cancer? Were they not brave? Just because they were unable to successfully triumph over their disease, does that imply something about their strength?

I’m sure that these were not intentional questions that Lintzers meant to imply. But sometimes I feel that this can be the danger of using what Arthur Frank called “the triumph narrative.” It’s interesting to me how prevalent this language is when it comes to communicating illness experiences. Especially with cancer, a disease in which war is literally waged against one’s body. But there needs to be an increased awareness of the latent effects of the triumph narrative.

Lintzers does, however, successfully portray her personal experiences with cancer as both a painful experience but also an enlightening one: “Cancer made me see that this is what it — life — is all about.”

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