Category: 1 Life Updates

  • Supporting Artists, Supporting Me

    Supporting Artists, Supporting Me

    Between Christmas and New Year’s, I received an unexpected email from the Department Chair of the college where I taught. At first, I honestly thought it was spam. The message simply said, “I need to talk with you about something concerning the instructional design program. Can you call me today, tomorrow, or Monday?”

    It included her phone number, but because I’ve been targeted before with scam “please call me” messages—and because I had never actually spoken to her on the phone—I wasn’t sure it was legitimate. Our interactions had always been limited to occasional emails. Reaching out to the Department Chair was something I just didn’t need to do.

    Instead of calling, I sent her a new email to confirm whether she really did want to speak.
She did.

    When we finally connected, I learned that the university is no longer allowed to employ faculty who reside in Canada. As a result, my employment was terminated—after ten years of teaching there. I had moved back to Canada during COVID and continued teaching without issue, even receiving a promotion that guaranteed me work every semester.

    I wasn’t the only one affected: a colleague was also let go. Because he didn’t have a continuing appointment, they were able to simply not renew his contract.

    All of this happened just three weeks before classes were set to begin.

    At first, I handled it well. I am sad not to be teaching—but the unexpected space in my life has given me more time for creative work: more writing, more energy for my podcast, and even space to develop a new podcast I hope to launch soon.

    What I miss most, though, is knowing that I made a meaningful difference in people’s lives. That sense of contributing to someone’s growth is what I feel the loss of most deeply.

    And that brings me to the idea of supporting artists—supporting me. I’ve recently learned that literary artists (like writers) and digital artists (including podcasters) can access grants and professional communities if they are recognized as professional artists. One of the criteria is being paid for your creative work.

    Which leads me to Patreon.

    I’ve created a Patreon page as a simple way for people who appreciate my work to offer a small financial contribution. I’m not looking for large amounts of money. Even a small one-time contribution tells me that the work I’m doing matters to someone—that it has an impact, that it resonates, that it makes a difference.

    So my ask is this:
If my work has value for you, I would truly appreciate a small contribution on Patreon. And more broadly, I encourage you to support other artists whose work enriches your life. Whether it’s Patreon or another platform, even a small contribution can make difference in an artist’s life.

  • How do you describe something you chose not to finish?

    How do you describe something you chose not to finish?

    I spend the better part of the last 9 years working on a PhD. A lot happened in that window. A lot of life changing transitions. I was diagnosed with breast cancer, I lost my father, and then a year and a half later I lost my mother. These each had a profound impact on who I was.

    When I started the program my goals in life were very different than they are now. I had planned on spending only 5 years working on a PhD – but cancer had a different idea. Then I had to start over. Through that process I have learned a lot. I have grown as a person. I have grown as an academic.

    Just before the covid lockdowns started, I decided that I was done working on the PhD. I was looking at another year of writing and revising and giving up my free time working to jump through academic hoops that I didn’t see as helping me move forward in life.

    At the end of April I official withdrew from the PhD program. I am no longer a PhD student. That feels weird to say because it was such a large part of my identify for a very long time.

    Unfortunately, we don’t have a way to celebrate that accomplishment and we don’t have a way to talk about it. In academic settings, I might use the PhD (ABD) term, only to help people understand that my education is beyond that of a masters.

    I updated my linked in to show that I had finished my time at uOttawa. I did not add a degree. However, this caused LinkedIn to tell all my friends that I had “finished at uOttawa”. I got several congratulations type messages – at first thinking I had to write back and explain that I didn’t get my doctorate. I just stopped being a student. It felt awkward.

    And now, with the next semester about to start I’m in the situation of having to describe myself to my students. I am at a loss for what to say, as I am no longer persuing a PhD in Education, nor have a completed a PhD in Education – but the work I have done over the last 9 years wasn’t nothing. I learned a lot, and I have a much deeper understanding of a lot of concepts as a result of my time studying. But I don’t have a way to “label” the work that I have done.

    I find myself wanting to just leave off references to the PhD, almost like I am trying to erase the work that I have done over the last 9 years. I am afraid that by walking away, it is seen as a failure – that I failed my PhD – which is not what happened. I chose to walk away from it. I chose to do other things with my time. I did not fail it.

    But I am not being fair to myself when I ignore the last 9 years. The work that I have done over the last 9 years counts for something. It has shaped who I am as a Lecturer and who I am as a person. It isn’t part of me that needs to be erased. So I do I honor that time?

    After walking away from PhD studies, how to you describe what you have done?

    Feature image by Evgeni Tcherkasski on Unsplash

  • An update, a bit about project LEAD, and request for ed tech resources

    It has been a long time since I’ve posted to this blog. In April or May, we put my PhD on hold for 8 months so that I can care for my mother, who at the time was diagnosed with stage 4 kidney cancer. I lived with her most of the time, with a couple of short trips back to California to deal with my health issues, until she passed away on July 1st. Then we spend a couple of weeks trying to get her house and affairs in order. Since my dad passed almost 2 years ago, we are now in need of dealing with the estate. In many ways it isn’t that complicated, but still it is time consuming.

    I did do some academic professional development last week. I attended the week long Project LEAD Institute sponsored by the National Breast Cancer Coalition (NBCC). I learned a lot about the science around breast cancer as well as how different types of research are done. I’m particularly fascinated with epidemiology – it is a field that is exploding with access to new electronic data sources.

    This fall I’ll be teaching two classes at uMass-Boston: (1) Foundations in instructional design and learning technology, and (2) The design and instruction of online courses. It will be great to set students up for success in the program in the first course, and then see them again towards the end of their degree in the second course. I’m also looking forward to wrapping my brain around the latest trends in instructional design and online learning. Right now I’m feel a little out of touch – but I suspect that will change pretty quickly once I get back to some semblance of normalcy.

    If you have any suggestions for the latest trends in learning technology – what the hot tools of today – I’d be happy to hear your suggestions. What tools to you use in your teaching?

  • The News

    Bumping and screeching, the plane finally lands.  I’m operating on very little sleep. I’m exhausted and hungry. I turn on my phone. I try to text my Aunt letting her know that we have arrived, however, the text keeps failing. I wait rather impatiently as the phone reset and the plane taxis toward the gate. Finally I manage to get the text to send, “We have landed”. She replies with “Meet us near the Tim Hortons. Go out the doors and walk to the right”. I comment to the gentleman sitting next to me how ironic that while waiting at a US airport a Canadian would be getting a coffee at Tim Horton’s—a rather ubiquitous donut and coffee chain in Canada.
    We exit the plane and stop at the first restroom. We then follow the signs towards baggage claim. We seem to have landed at the furthest gate from the exit. We have carried-on all our bags, so we don’t need to pick up baggage. We can leave the airport and head directly to the hospital. My Aunt texts “I will meet you in baggage claim”. The change in pickup directions doesn’t register as anything special in my mind.
    My left arm is hurting. I mention to my husband that I should put on a compression sleeve so that it doesn’t swell, as it is prone to lymphedema. He suggests that we pause there – still within the secure part of the airport – so that I can put it on now. I agree that it is better that I get it on before any swelling happens. If my arm does swell it can take months to get back to normal. I see a bench, so we stop and I dig out a compression sleeve from my backpack and put it on. I feel like we are keeping my Aunt waiting, and we need to keep moving towards baggage claim.
    We exit security to discover we are on the upper departures level of the airport. We follow the signs to the escalator. We hop on with our roller bags behind us. We are both scanning the baggage area looking for my Aunt. My husband spots her first and waves. She waves back and moves to greet us as we step off the escalator.
    I step off the escalator and take a few steps towards my Aunt. I reach over to give her a hug of greeting. I give my She whispers in my ear: “I am sorry honey, your father passed 10 minutes ago.”

    Recently, I hosted a couple of ePatient conversations about “Making the private public: Why we blog about illness” (see Virtually Connecting ePatients). This last week has me thinking more and more about why I blog – both here and about illness. Last year, when I reflected on why I blog on my Breast Cancer blog, I talked about blogging as a way to communicate to many people, but also blogging as a way to meet my compulsion to write.

    Now, I’m reflecting again on why I blog (and why I write). There is more to it that what I had previously written. I used my breast cancer blog as a way to tell my loved ones (and the world) what I wanted done if I died. I wanted it recorded someplace so that everyone knew, and there was no doubt or question – not that I anticipated any, just that it blogging it helped to make things easier for my loved ones in the event of my death.

    Another thing that drives me to write, and to blog, is when things keep replaying in my brain (e.g. the story above). Writing them down seems to work well to help stop the replay. It helps me process what happened, but also helps stop the flashbacks and tears associated with the flashbacks. The tears still roll as a read the passage above, but it is no longer repeating itself in my brain over-and-over. Somehow putting it on a page and sharing it, helps me move passed the flashbacks and reduces the intensity of the emotion. I think this is an important reflection on my blogging, as a lot of my breast cancer experience was a trauma, and blogging helped me deal with the trauma.

    Feature Images: Dad’s first fish after we moved to BC in 1976.

  • Tears of fear

    I scan over the document that she hands me, and immediately my eyes fixate on one word malignant. An uncontrollable wave of emotion hits me. Tears start streaming from my eyes. Just at that moment, the ultrasound tech opens the door to the waiting room and calls my name. She introduces herself but I totally miss her name. I cannot think about anything except that word–malignant.

    “Please remove everything from the waist up and put on the gown with the opening in the front”. She then goes to step out of the room. I look around searching for a box of tissues, and cannot see them. I stop her from leaving asking for the tissues, as tears fall from my eyes and my nose starts to drip. I hate that nose dripping feeling that comes with tears.

    I wipe the tears from my eyes, blow my nose, and take off my shirt and tank top. I put on the gown with the opening at the front, not bothering to tie it up so that the tie doesn’t get in the way of the exam. The tech left me a warm blanket. I lay on the exam bed and put the warm blanket over me. The warm blanket is such a nice touch, it feels like a hug.

    The tech returns to the room, “I’m going to scan your left breast. Do you feel something?” I show here exactly where the lump is that I’m feeling. Lump, it is such a loaded word. Just like malignant. It doesn’t really describe what I feel. I feel an area of hardening inside my left breast near my underarm. It is only noticeable if you press it. I feel my breast and find the hard spot. I show the ultrasound tech and she takes a marker and marks my skin.

    “Please roll onto your right side, I will place this foam cushion behind your back to make it more comfortable. Also, please lift your left arm above your head.” I do as I’m told. The cushion makes it easier for me to relax in the awkward position necessary for the exam. Tears are falling from my eyes again. I lose all sense of feeling. At some point she squirts the ultrasound gel on my skin but I don’t feel it. She starts the scan, and I watch the screen. The areas of white and black swirl on the screen. She stops occasionally to hit a button and take a still picture of what is on the screen. The entire exam takes less than two minutes.

    “I’m going to show the images to my boss, the radiologist, and she will come in and possibly do more scans, and let you know what she sees”.

    I am paralyzed with fear. Tears rolling down my eyes. I remember the words “the radiologist wants to see you”. Words from the day my world got turned upside down. The words I never want to hear again.

    The radiologist, a lovely lady with long curly hair, walks into the room introducing herself. Again, I do not catch her name, tears pouring down my eyes. “The good new is, that I see nothing of concern on the scans. No signs of cancer, no signs of swollen lymph nodes. We will be happy to scan anytime if you notice any changes.” It was the changes that brought me here. I take a deep breath and let out another wave of tears, this time they are tears of relief rather than tears of fear.

    I tell the radiologist “thank you for coming in and giving me good news. It is nice to have a radiologist tell you something good rather than only the bad stuff”.

    Although there is very little use of the term within the academic literature, within the cancer blogosphere this phenomena is known as scanxiety–referring to the fear of scans after a cancer diagnosis. I do not recall when I first heard the term, but I immediately understood what it mean. The anxiety around getting scans and awaiting the results of scans. This is especially the case after a cancer diagnosis, when scans are often the only means of determine whether or not your cancer has returned or whether or not it has progressed (gotten worse).

    I recall reading about scanxiety (sorry, try as I might I could not find a reliable source), that it was not so much about the fear of results, but rather the memories of past tests and past test results. I think my experience this last week is a demonstration of exactly that. I was pretty certain that what I was feeling was scar tissue; however, walking into the ultrasound room for my first breast scan since surgery back in December 2014, brought back a flood of memories, a flood of intense sadness, a flood of fear.

    The story above is based on my week this last week. I wrote it in a different format – one that I’m playing with. It is part of my experimenting with a new voice when working on evocative authethnography.

    What did you think? Did the story communicate at least some of the emotions associated with scanxiety? Was it more effective that just describing it, which is pretty much what I did in the two paragraphs following the story. 

    Feature image Public Domain available from Wikimedia Commons.

  • A bio of sorts – autopathography

    Stories have to repair the damage that illness has done to the ill person sense of where she is in life, and where she maybe going. (Frank, 2013, p. 53)

    I’ve been given the task of writing my biography – and it is due today. Not nearly enough time to write the book that I’ve been meaning to write for years – so I needed to figure out how to approach the problem of writing a biography. This has brought me back to reading The Wounded Storyteller by Arthur W. Frank.

    The story is wrecked because its present is not what the past was supposed to lead up to, and the future is scarcely thinkable. (p.55).

    Because the present of illness is not what was planned in the past, reestablishing the connection of past to present may require an exercise in what psychoanalyst Donald Spence calls narrative truth. Spence and Carr agree that the past cannot be reinvented, but the sense of what was foreground and background in the past events can shift to re-create a past that Spence calls “greater continuity and closure.” Out of narrative truths a sense of coherence can be restored. (p.61).

    I think this is in part what is causing me to stumble on getting started. The past doesn’t make sense given the present. I cannot simply look back at my past and see it the same way I did before cancer. The illness itself changes the reflections on the past. Events that I would have forgotten are much easier to recall. Events that I thought were important before are now forgotten. There is no way for me to look at my past through the innocent eyes of someone who has never been touched by cancer.

    We need to tell someone else a story that describes our experience because the process of creating a story also creates the memory structure that we’ll contain the gist of the story for the rest of our lives. (p. 61).

    This causes an interesting reflection. In the beginning – right after my initial diagnoses and perhaps even in that time while I was waiting – I needed to tell my story. I started my blog right away. I recall the feelings of impostor syndrome while I was waiting for the pathology. What would I do with my narrative if it wasn’t cancer? Was I overreacting? Would I be that person on the Internet who was seen as a faker because I didn’t actually have cancer? These thoughts all rang through my mind. I started to write about impostor syndrome and as I was writing the post the phone rang. It was my surgeon confirming the pathology. I was no longer an impostor. I had cancer.

    Frank goes on to categorize illness stories (pathographies) into three categories:

    • The restitution narrative. 
      “I love you would say it in these words, the teller of the illness story seeks to learn the true name of the disease, and perhaps her own true name is well.” (p. 75-76).
      “Contemporary culture treats health as the normal condition that people ought to have restored. The ill persons own desire for restitution is compounded by the expectation that other people want to hear restitution stories.” (p.77).
      “Ill people who tell restitution stories practice their own banality of hero wisdom. They lived out illness as a matter of doing their jobs as patients, preparing for the future after illness, and getting through their own days.” (p.93).
      “Restitution stories are about the triumph of medicine; they are self-stories only by default.” (p.115)
    • The chaos narrative.
      “Chaos is the opposite of restitution: its plot imagine life never getting better.” (p.97).
      “If the restitution narrative promises possibilities of out distancing or outwitting suffering, the chaos narrative tells how easily any of us could be sucked under.” (p.97)
      “Chaos stories are also hard to hear because they are too threatening. The anxiety these stories provoke inhibits hearing.” (p.97-98)
      “Chaos stories remain the sufferers own story, but the suffering is too great for a self to be told. The voice of the teller has been lost as a result of the chaos, and this loss then perpetuates that chaos.” (p.115)
    • The quest narrative.
      “Restitution stories attempt to outdistance morality by rendering illness transitory. Chaos stories are sucked into the undertow of illness and the disasters that attend it. Quest stories meet suffering head on; they accept illness and seek to use it. Illness is the occasion of a journey that becomes a quest. What is quested for may never be wholly clear, but the quest is defined by the ill person’s belief that something is to be gained through the experience.” (p.115)
      “The quest narrative affords the ill person a voice as teller of her own story, because only in quest story does the teller have a story to tell.” (p.115)
      “Though both restitution and chaos remained background voices when the quest is foreground, the quest narrative speaks from the ill person’s perspective and holds chaos at bay.” (p.115)

    I wondered what type of narrative my story should be? I’m not certain it is a single narrative – rather it is a composite of all of them. The immediacy of some of my blog posts, and the suffering in the moment reflects illness as chaos narrative. And yet, much of my outlook on life has been optimistic. I want to believe the restitution narrative. I want to believe that “health is a normal condition that people ought to have restored” (Frank, 2013, p.77). I have told many people that through treatment I looked at doing exercise as part of my ‘job’. I prioritized it over anything else that might have looked like work. My days were filled with doctors appointments, infusions, and exercise. I was the professional patient.

    The chaos plot is the one I tell myself when I haven’t slept enough and I begin the downward spiral into anxiety and depression. It is the the sense of hopelessness I feel until I realize that, alas, it is just that I am over-tired. Sleep usually helps me pull myself out of the chaos narrative. I also think that blogs can be a good way, if there is such a thing, to tell the chaos story. It is a way to tell the raw happenings as they happen.

    The teller of Chaos stories is, preemptively, the wounded storyteller, but those who are truly living the chaos cannot tell the words. To turn the chaos into a verbal story is to have some reflective grasp of it. The chaos that can be told in story is already taking place at a distance and is being reflected on retrospectively. For a person to gain such a reflective grasp of her own life, distance is a prerequisite. In telling me events of one’s life, events are mediated by the telling. What in the live chaos there is no mediation, only immediacy. (p.98)

    This idea of an chaos story has me wondering if Nancy’s recent memoir is a chaos narrative, as the title certainly suggests it Cancer was not a gift & it didn’t make me a better person by Nancy Stordahl. Perhaps it is even the sense of chaos narrative in the title that makes me not want to read it (sorry Nancy). Frank’s comment about how “Chaos stories are also hard to hear because they are too threatening. The anxiety these stories provoke inhibits hearing.” (p.97-98) aligns with exactly how I feel at reading the title. I’m not sure I want the anxiety associated with the telling of the chaos narrative.

    The need to honor chaos stories is both moral and clinical. Until the chaos narrative can be honored, the world in all its possibilities is being denied. To deny a chaos story is designed the person telling this story, and people who are being denied cannot be cared for. People whose reality is denied can remain recipients of treatment services, but they cannot be participants in empathetic relations of care. (p.109)

    This quote reminds me of another friend – Scott – who often leaves comments on my blogs. His story of chaos has not been honored by his ‘care team’, and as a result, he is not a recipient of empathetic care.

    Restitution stories attempt to outdistance morality by rendering illness transitory. Chaos stories are sucked into the undertow of illness and the disasters that attend it. Quest stories meet suffering head on; they accept illness and seek to use it. Illness is the occasion of a journey that becomes a quest. What is quested for may never be wholly clear, but the quest is defined by the ill person’s belief that something is to be gained through the experience. (Frank, 2013, p.115)

    The more I read about quest stories, the more I realize that is my story. I feel comfortable using the term “journey” to describe my way through illness. It is a narrative that I embraced from the beginning. In only my third blog post (at that point I was writing more than one post in a day), I talked about advice from a friend who suggested that “one approach is to treat the disease with curiosity”. This was an attitude that I fully embraced. I sought to document my journey through illness. At times the chaos narrative was present. At other times the restitution narrative was present. But throughout, there was always the underlying story as journey.

    Frank also mentions that published illness stories are most frequently quest narratives. He also highlights that there are many quest narratives that are not published, but are rather enacted in life. “Involvement in patient advocacy is one enactment of a quest story” (Frank, 2013, p. 116). My friend Stacey‘s advocacy story is an example of a story that is mostly untold in narrative form, but is enacted in her every-day life.

    Quest stories tell of searching for alternative ways of being ill. As the ill person gradually realizes a sense of purpose, the idea that illness has been a journey emerges. The meaning of the journey emerges recursively: the journey is taken in order to find out what sort of journey one has been taking. (p.117)

    This in part is my new PhD journey. My new study will look at the different learnings that occur through blogging. I will be reflecting on my blog, as the narrative of my research unfolds. I will be asking other breast cancer bloggers, as well as those who read breast cancer blogs, to come along for the ride. I will need others to be active participants in my journey towards better understanding of my illness experience. I will write a patching together of stories.

    As I read more of The Wounded Storyteller, I realize that I have several other blog posts just about quest narratives. I’m finding myself highlighting passage after passage – such that most of the pages in that section of the book are reflecting the fluorescent yellow that I use to highlight. But alas, that is a blog post for another day. This one is already long.

    Reference:

    Frank, A. W. (2013). The wounded storyteller: Body, illness, and ethics. University of Chicago Press.

  • Shivering in a paper gown…

    I am very proud to have had a chapter that I wrote included in this anthology (“Breasts that aren’t Breast”). I’ll be attending the book launch on Thursday evening in downtown San Francisco – if you are local and want me to pick up a copy for you, let me know.

    About the Book: Shivering in a Paper Gown

    In a moving, honest and raw style, thirty young women tell their stories about the aftermath of living with breast cancer. Far from the trite and saccharine, the authors’ combination of dark humor, sass and solidarity throughout the challenges of a life-threatening disease shine through.

    The book’s authors have many stories to share—stitching broken and scarred bodies back together, reconstructing identities, denying and confronting and accepting death. The authors reveal the realities of life, through and with cancer, as they learn how to survive and in the process, how to live.

    The personal narrative stories beg the reader to step into the space that cancer has razed, to consider what is most beloved and cherished, and to ask what the sum of one’s life will be. This anthology is relevant to cancer survivors and those who have gone through trauma. While the authors’ common bond is cancer, the stories cover the topics of: body image, parenting, spirituality, social support, emotional renewal and end of life choices.

    For every book sold, a woman going through breast cancer will receive monthly support group services through the Bay Area Young Survivors (BAYS). BAYS is a support and action group for young women in the San Francisco Bay Area who are living with breast cancer and were diagnosed before the age of forty-five. The goal of BAYS is to break the isolation of living with breast cancer, by providing a community built on compassion, understanding, hope, and inspiration.

  • California Dreamin’

    This entry is a cross post from http://goingeast.ca/blog

    On days like this …

    I find myself California Dreamin'…

    Back in early February (Feb 6-11), we spent a few days in Mountain View California and spent a day in San Francisco, exploring a little bit of what the city has to offer. We drove up into the Mountains and along the very scenic highway 1, and of course we had to rent bikes for a few hours. We did the tourist bike trek – a ride over the Golden Gate Bridge. The whole area is beautiful. Here are a few picture highlights.

    IMG_1729

    View of Silicon Valley from the mountains to the west.

    Sea gulls flying over the waterfront in Santa Cruz.

    This guy parked a little too close the ocean!

    IMG_1766

    We stopped for a walk at a secluded beach. It turned out to be a "hidden gem", Gray Whale Cove State beach.

    Scott playin' the piano at Half Moon Bay State Park. (It's a temporary art installation, but the piano works, it's just getting more and more out of tune)

    IMG_1844

    The Golden Gate Bridge, with a rower working hard against the tide.

    IMG_1886

    The view from the middle of the Golden Gate Bridge.

    IMG_1932

    Taking the trolley across the city at the end of the day.

    After our short adventure in Mountain View and San Francisco, Scott was offered a new job (a transfer) in Mountain View, California. And with that, our new adventure begins. We will be selling our house here in Ottawa, packing up and moving to California. Scott will move sometime in early May. Becky is about to start a critical phase in her PhD, so she will remain in Ottawa for about a year, visiting Scott whenever she can, and making her big move once she has finished collecting her data for her PhD research.  

css.php