BC Becky

Never thought I'd want to be a breast cancer survivor

Category: Here we go again

  • The end of breast self-exams

    The end of breast self-exams

    This is a story written base on reflections my initial year after diagnosis (2016), with added comments about what I’m thinking after my second diagnosis (2024).

    The feature image is from Wikimedia Commons.

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    Introduction

    Before my first diagnosis, I was obsessive about breast self-exams. Every time I showered, I would check, feeling each part carefully. It was just part of my routine—not because I had any family history of cancer, but because of a high school health class. The nurse had brought in these dummy breasts with a “lump” we were supposed to find. I remember how I could never feel it, no matter how hard I tried. That really stuck with me. I was afraid that when it mattered, I wouldn’t feel anything.

    I missed the lesson on looking for changes, not just lumps. Now I can tell you everything you should be looking for in a breast self-exam – changes, not lumps. However, only days after seeing initial changes, I felt a lump. I thought it was a muscle strain at first, but it didn’t hurt and it didn’t go away. It wasn’t a muscle strain, it was a 4.5cm tumour in my left breast. 

    ~~~~ 2016 ~~~~

    It has been a year since my diagnosis and treatment for bilateral breast cancer. I no longer have breasts. I have fat tissue that was transplanted from my stomach to make forms that look like breasts. The breast-self exams I did before don’t make sense anymore. I have no breast tissue. But I also have no sensation, which comes with new risks. 

    One of my new risks is the cold. I have body parts now—my reconstructed breasts, my belly—that I can’t feel. They’re living flesh, warm to the touch, but numb. I have to relearn what “normal” feels like, but also how to check myself to make sure I’m not getting frostbite.

    I’m still exploring what a breast self-exam means for me now. This was how I found my cancer. I used to check every time I showered, and I saw the change almost immediately—a lump, and a strange discharge. But now, I don’t have breasts with breast tissue. My nipples are still there, but they don’t leak anymore. They’re unfeeling and unresponsive, but they’re warm to the touch.

    I still examine my chest, but I’m looking for something else. No lumps—just damage. I’m scanning my skin for signs of anything that could have happened without me noticing, because I can’t feel it.

    Part of my new normal is this constant exploration of my changed body. I trace the areas with no feeling, trying to find the boundaries—where sensation fades from something to nothing. I want to see if these boundaries shift. I’ve been told there’s a chance I might regain some feeling, but nerves can take up to three years to grow back. For now, I’m grateful it’s not winter. I’ll have at least a year or two, maybe more, before I need to think about what snow and freezing temperatures mean for my body.

    ~~~~ 2024 ~~~~

    I am used to my body. My urge to inspect it so closely fades. I stop any form of breast exam in the winter. Now, it’s during the warmer months that I need to check. Instead of worrying about frostbite, I’m prone to heat rash, especially under my breasts. I don’t feel it when it starts; I only notice it later, after it’s become severe. By the time I see it, it needs days of treatment—creams and patience—to calm down. I can’t always tell if the creams are working; I just wait for the rash to fade.

    I stopped looking for cancer years ago. Then came a regional recurrence, in my lymph nodes. They found it on a scan. I couldn’t feel the swollen nodes, even with a 2.5 cm tumour growing in the largest of the five cancerous nodes. My family doctor also could not feel it. That experience stripped away any faith I had in self-exams to detect recurrence. The familiar routine I once had, washing and inspecting my new breasts, has fallen by the wayside, offering no comfort now. All I can rely on are blood tests and scans.

    My new normal feels like my old normal. After a shower, I give myself a quick glance in the mirror, just to check if anything looks wrong. That’s it. I don’t dwell on it. There’s nothing left for me to find. A self-exam in the shower isn’t going to catch cancer if it comes back. So, unconsciously, and now consciously, I’ve moved on from that practice.

  • Letrozole – so far so good

    Letrozole – so far so good

    Back in October, when my oncologist and I agreed I was done with Herceptin, we decided I wouldn’t do anything but let my body heal until January. That’s when I’d give Letrozole a try.

    Stopping Herceptin felt like a relief. For the longest time, I couldn’t distinguish which symptoms were caused by chemo, radiation, COVID, or Herceptin itself. They all blurred together. Eventually, I realized Herceptin was the culprit behind two days of fatigue and flu-like symptoms after every infusion. A week later, my heels would crack so deeply they hurt—a pain that even special creams and heel socks barely managed. My nails became brittle and splintered at the slightest touch, and the skin on my thumbs cracked along the seams of my fingerprints. I’d resort to using crazy glue to hold them together.

    Even after moving from three-week to four-week infusions, I was miserable half the time. I couldn’t imagine continuing until the end of the year.

    My oncologist, who I respect for this wizdom and experience, left the decision up to me. “If the cancer comes back, will you regret stopping early?” he asked. I didn’t even hesitate: “No.” I’ve learned not to regret decisions made with the best information at hand. When my scans came back clear, I stopped Herceptin and allowed my body the time it needed to recover.


    When January arrived, I approached Letrozole with caution. My oncologist reassured me not to dwell on my past experience with hormone therapy. Back then, I started too soon—driven by fear—and as a pre-menopausal woman, the effects were far more severe. This time, I’m post-menopausal, and we’re taking things slow.

    Starting from a different place makes all the difference. It has been not quite two weeks. The initial main side effect: intense back and hip pain. It feels manageable, though, especially with regular exercise like boxing or walking. If I skip a workout, the pain catches up with me, and I crash, needing a 1–2-hour nap every few days.

    But I’ve turned this challenge into motivation. The fear of a sore back pushes me to lace up my shoes and move. I’ve even upgraded my headset for boxing, and I’m having a blast with it!

    As time has passed, the side effects seem to have diminished. That or the regular boxing is doing my body good. Perhaps both are true!

  • First day of class – A time of transition

    First day of class – A time of transition

    Today is the first day of classes. I’ve been off for a year and I feel quite rusty. In addition to the changes in instructional design, the university has also changed its Learning Management System (the software we use to deliver our online courses). This adds to the transition.

    It is also a time of transition for me from a health perspective. I’m not quite finished my treatments but I will be soon. I have 3 more herceptin treatments. I’m starting to think about what is next. I am reminded about all the mental stressors I had after my first diagnosis. The year after treatment was the hardest for me, because I had to really process my diagnosis, not just from a cognitive perspective but also from an emotional one. That is where I am now.

    I’m feeling strong again. In the couple of weeks I’ve done a couple of 3 hour hikes, and I’ve gotten back into VR boxing. I feel strong and that feels good. But my mind is doing its wondering. I ask myself regularly, am I doing what I want to be doing? Am I making the most of the day?

    The weather is also playing a role. We are changing seasons. Fall is a nice time here, but it is also a reminder that winter is coming. As summer ends, there is a greater urgency to get outside and enjoy the sun when we have it. That pulls against any other desires I have for my time. I feel guilty when I spend a sunny day inside. I feel like I’m missing an opportunity that is finite.

    Perhaps it is the finite that I am feeling. I remember about a week before my mom died, I had the realization that ‘mom hugs’ were finite. When I got up, I went to her and asked for a hug. That was the last mom hug I had. I’m glad that I thought about it and asked for it. Now I’m thinking about my life as finite. There are a finite number of sunny days left, and I should make the most of them.

    What does it mean to make the most of a sunny day? I can tell you what it doesn’t mean. It doesn’t mean spending the whole day in front of my computer working on my book or my podcast. Ensuring that my courses are running smoothly is my priority. After that, it is time to get out and enjoy the sunny end of summer days.

  • A long overdue post

    A long overdue post

    It has been so long since I’ve written, I don’t really know where to start.

    Health-wise, I’m doing okay—or at least I haven’t had any new health crises. I’m writing this from Stan Fest. Last year, we found out 20 minutes before we left for Stan Fest that I had cancer. It was good to have the weekend to process it all. I remember one specific moment telling Scott that I didn’t want to do chemo again. I won’t be foreshadowing anything treatment-wise this year!

    I managed to get my Herceptin treatment scheduled for last week. I get treatment on a Wednesday, and then end up spending most of Friday and Saturday in bed. It causes exhaustion. I guess my immune system is in overdrive for those days, reacting to the medications. Usually, by Sunday, I’m feeling better, and by Monday, I’m back to my normal self. I’ve moved to treatment every four weeks, which I hope helps reduce the side effects. That has yet to be determined, but it will at least reduce the frequency of the side effects, giving me more ‘normal’ weeks in between.

    We have been off on a mini vacation—our last planned one for the summer—but we still have another folk festival to attend! We had a lovely time at Porter’s Lake Provincial Park. Then, on the way to Canso, we stopped off at Taylor Head Provincial Park and went for a lovely 4 km hike, followed by a frigid dip in the ocean—beautiful beach, but the water has yet to warm up!

    I find the oceans here fascinating. They call Nova Scotia Canada’s Ocean Playground. Each shore, and Cape Breton, has very different oceans. On the South Shore, we have beautiful sand beaches at low tide. They warm up sometime in August, to the point where you can swim in them comfortably. The French coast has the Bay of Fundy. It isn’t a place to swim so much as watch the tides and walk on the bottom of the ocean. It is difficult to imagine 40 ft tides until you see them! We had a brief walk on the North Shore earlier this summer. It is rockier. The water was warmer but not yet swimmable (that was early July). We swam in Bras D’or, which is a brackish lake in the middle of Cape Breton. The North shore of Cape Breton has some beautiful sand beaches, and the water there was surprisingly warm. I really enjoyed my swim there. And now we are on the East Shore, which has some nice beaches closer to Halifax and gets rocky up here. The water was still frigid. I suspect it warms up at about the same time as the South Shore, as it is the same side of Nova Scotia.

    Last year at Stan Fest, it was a real rain fest. That was the weekend that Bridgewater had 48 hours of thunder and lightning and over 100mm of rain. It caused a lot of damage throughout the province, but our area had it the worst. It seems the rainstorms and flooding are causing more damage in some parts of Nova Scotia than even the hurricanes do. One of our friends in Cape Breton mentioned the rains causing more shore erosion than the storms. That is crazy.

    This year’s Stan Fest has been awesome. The weather could not be more perfect. It is low 20s during the day, comfortable for shorts and a t-shirt. The venues are covered, so we aren’t in the sun, which is nice. In the evening, at the main stage, it is nice but it gets cold. Neither of us were adequately prepared for that the first night. We did much better last night, but after two long days and then cold, we were both ready to pack it in early last night. Hubby has already suggested we go again next year. We looked into other folk festivals, thinking we would branch out, but there isn’t really anything else we want to do at this time of year.

    Today we are enjoying a lazy morning. The first workshop I want to attend is at 11 am. It is the best kind of morning when we don’t need to move too quickly and can enjoy a coffee and some reading or writing before having to get up and join the world.

  • Navigating the Side Effects of Trastuzumab: Finding Balance and Embracing Summer

    Navigating the Side Effects of Trastuzumab: Finding Balance and Embracing Summer

    I’m more than half way through my Trastuzumab (Herceptin) treatments – I’ve actually lost count. I think I might be 10 out of 18. Anyways, I realize that I’m have side effects from it. It is causing fatigue and making my joints ache. The side effects last just shy of a week and then I’m generally fine until the next time.

    I was told that there would likely be “no side effects”. I think this is said because the side effects are minor compared to the chemotherapy. If you don’t lose your hair, have nausea, or mouth sores, then the side effects don’t seem to matter – except that they do.

    I got tired of the side effects every three weeks. I asked my doctor to change the schedule to every four weeks – at least for the summer. I am hoping the longer time between infusions reduces the side effects as my body has more time to heal. It also makes my travel plans work out a lot better. It gives me a week at home after each treatment, so I can enjoy my travels without the fatigue and joint pain.

    After my last infusion – on a Wednesday at 2pm – I ended up sleeping most of the following day. I got up and had half a cup of coffee and realized I was too tired to do anything, so I went back to bed. I didn’t wake up until 12:30 when my phone was ringing. I went through ‘bouts of energy followed by hits of fatigue. It is frustrating.

    I am not out of shape, which is good. When I’m feeling well I can swim 1km and I biked 17km on my recumbent the other day.

    With the heat, the summer has started here. For me, I think summer will officially start on Monday evening when we fly to Iceland.

    Some things I’m hoping to do this summer:

    • Ride my recumbent to Mahone Bay and back (around 50km). I’ve done it on my eBike, but that is very different and a lot less work!
    • Stand up paddle board at least 10 times.
    • Swim in the Ocean (really swim, not just wade).
    • Boogie board – I’ll need to borrow one.
    • Do a 15km or longer hike (this is a stretch goal).

    Things that I already have planned:

    • Drive around and explore Iceland.
    • Visit Cape Breton (hike and visit friends).
    • StanFest
    • Folk Harbour Fest

    Oh ya, and I need to prepare my courses for the fall, as I’ll be teaching again – but in a new Learning Management System and AI has definitely affected on of my courses!

    What special things do you have planned for the summer? What is on your bucket list?

  • Sunshine and Sunflowers

    Sunshine and Sunflowers

    Lori was sunflowers.

    Lilani was sunshine.

    Will the sun shine again?


    I wrote this poem during a writing workshop. The prompt was “Sunshine feels like …”

    Immediately sunshine reminded me of Lilani. A ray of light.

    Then I thought of Lori, and how her favourite buff and compression sleeves are contain sunflowers.

    I miss them both. They were lights in this world.

  • Rediscovering joy

    Rediscovering joy

    Cancer treatment is a gift that just keeps on giving … more like an anti-gift keeps on giving.

    My latest issue is radiation fibrosis. The area of my collarbone and underarm that was radiated is now tight. I asked a friend who is a physiotherapist about it – she explained it as scar tissue like you get after a severe burn. So I imagine the interior tissue in the areas that were radiated are now scarred causing tightness. To help fix it, I need to do stretches multiple times a day. When I asked my cancer friends about it, I learned that it might never go away. I hate hearing that, and like the lymphedema in my right hand/arm, I’m not going to accept that it might not go away.

    I’ve been back from California for a week. I’ve recovered from jet lag and my body is generally feeling good – or it was until I over did it a little. Monday I went for a 3km walk on the beach and then did 30 minutes of virtual boxing. Tuesday I went to an exercise class called ‘Feel da rhythm’ that is like an aerobics class but a lot more fun, but also a great work out. I followed that with a half hour of swimming. By Tuesday night I was exhausted.

    The thing is, each one of those activities brings me joy. It isn’t just about the physical exercise, it is also about the joy in doing the thing.

    Today is a bit of a rest day from physical stuff. Now that my office is setup (yay), I’m spending more time on my computer doing computer stuff – like writing and preparing to restart my podcast. I really like having my office space back. In some ways, it is the only room I feel isn’t in a sense of chaos.

    Today is also chemo day. Infusion number 10 of 18. I’m still a little bummed that I have so many infusions left. However, it isn’t really that big of deal – more of an inconvenience than anything else. Tomorrow will likely also be more of a computer day – because the treatment makes my joints ache a little more than they usually do.

    One of the things I’m doing for my mental health is taking a writing workshop. I find the process of writing to the various prompts very therapeutic, and it really helps me think through how I’m feeling on a given topic. Here is a snippet from something I wrote today. The bold is the prompt.

    Write about the world restarting, being reborn completely anew…

    Spring is a season of rebirth – I was thinking that on my walk this morning. Christmas is the story of birth, but Easter is the story of re-birth.

    What is my story of re-birth – I’m in that story now. How do I re-imagine myself? Who am I now …

    Cancer again has meant yet another chance at re-birth – of rediscovering who I am and who I want to be. I’m asking myself again what I want to do with the rest of my life.

    My first cancer diagnosis taught me to look at each day and ask myself constantly, am I doing what I want to be doing? The answer has generally been yes.

    My second diagnosis has reminded me to look at my life all over again. Am I doing what I want to be doing – mostly yes – but more, am I getting what I need from what I’m doing?

    I am looking at happiness and joy – and what it means to me now. I am happy when I watch my dog chase after a ball at the beach. She is exuding pure joy at the simple pleasure of the game of fetch.

    What can I do to exude that same sense of pure joy? What brings that to me? That is what I am exploring – that is the question that I have not yet found an answer to.

  • 10 km later

    10 km later

    I planned to go to Santa Cruz to visit a few friends, but it didn’t quite turn out that way.

    Since my meetings were in the morning, I wanted to go for a hike first. Cara reminded me that there were lots of trails in the Santa Cruz mountains and that I should look there.

    After a easy Google search I found a trail that was on my way to Santa Cruz. I’m surprised that I didn’t know anything about it, as it is relatively close – closer than a lot of the other hikes I did regularly when I lived here.

    I drive towards Santa Cruz and get off at Bear Creek road – an exit that I was familiar with from the various times I rode my bike around the Lexington Reservoir.

    I drive up the winding road to the Bear Creek Redwoods Open Space Preserve trail parking. I walk over and look at the map. I calculate how much time I have to hike – it is 11am and I need to meet people at 12:30 in Santa Cruz. I set my alarm for 45 minutes and start hiking.

    The first mile is a constant climb. I look forward to getting to the trail intersection.

    I get to the to and look at my watch. It is 11:42 so I have a few minutes before I have to turn around. The choice is more climbing or a trail that is going downhill. With only 3 minutes left I wanted to do the nicer trail, so I go downhill, knowing that I will need to turn around soon and climb back up.

    At 11:44, one minute before my alarm goes off, I realize that I had not accounted for the 30 minute drive to Santa Cruz. I’m 45 minutes into a hike and won’t get back to the parking lot until 12:15 at the earliest – even though it will be mostly downhill, it will still take me some time.

    I return to the point where the trails intersect. My phone goes ‘bing’. I look at the messages, thinking that I might need to send something to report that I’ll be late. I really just want to continue hiking, it is so beautiful up here. One of the messages says that B isn’t going to be able to meet with me. I was already struggling with the driving all the way to Santa Cruz, and this was the last thing to tip my mind. I cancel my earlier appointment in Santa Cruz and go back to hiking.

    As I approach the redwoods I feel the age of this forest. I can smell the ocean in the breeze. I also feel the healing energy. I’m suddenly feeling well mentally and physically. I had been looking for a place to go on a retreat in Nova Scotia. It occurs to me that this last week has been the retreat I’ve been looking for. I’ve spent great time with friends, hiked with a friend, and hiked on my own. It was everything that I needed. Then I think, I should make this an annual retreat. I should plan to come for a week and stay at Cara’s Retreat Centre (that is Cara’s home if she’ll have me), and I can reconnect with friends and go on hikes. I’m already looking forward to doing this again next year.

    I continue hiking and at this point start thinking about doing the entire look rather than doing a there-and-back hike. At some point, I will reach a point where it makes more sense to continue and do the loop and I’m approaching that point. I decided to cancel on my friend, and continue the hike. This hike is what I need more than anything right now. My friends understand.

    I get to the trail intersection (not quite the top as the next segment of the trail involves going up). I see the sign. The parking lot is 2.7 miles in both directions. I’m at the middle of the trail.

    I continue hiking, enjoying the shifts in view from redwood forest to high shrubs and back again into forest. At one point I notice a sea of forget-me-nots. It seems really appropriate. I will keep that image in my mind for the next year, whenever I need to take a deep breath and see beauty.

    The high shrubs are all in full bloom.

    At one point I notice a sea of forget-me-nots. It seems really appropriate. I will keep that image in my mind for the next year, whenever I need to take a deep breath and see beauty. It turns into a 3hr almost 10 km hike. I made it with only one water bottle, which was my main concern. Fortunately most of the trail was shaded. I recall someone saying “I always thought I wanted to live in the Redwoods, until I did” – the large trees are beautiful but they also block out the sun. It is nice to visit, but dark to live in.

    This was almost double my previous hike. I started out this week struggling to hike 3km and have ended with a 10km hike. I did well on the hike, and felt good afterwards, but tired. The next day – my last day – I was too tired to contemplate another hike. I went back to bed and slept until noon. I’m visiting a few other friends this afternoon and then this evening. Hard to believe the week is already over.

    I feel good, and happy, and I’m looking forward to getting home to my puppy (and my husband too)!

  • California 2024 – Hiking

    California 2024 – Hiking

    I’ve been in California for the last few days. I had great aspirations of hiking the day I arrived, but I was so tired. I hadn’t slept well the night before, then needed to be at the airport for 3:45 a.m. and then didn’t sleep well on either flights, and throw in a 4 hour time change, and … hiking wasn’t in the cards for that day.

    I did manage to get our for hikes on Thursday (by myself) and Friday and Sunday with my friend Cara. It has been a great trip so far. It has been so good for me to be with my California friends a this time.

    Yesterday was a celebration of life for my friend Lilani. It was great that I was able to be there. I spent almost the whole time crying, but it was wonderful to be see just how much of a bright light she was in this world. I also got a chance to visit with several more of my BAYS friends (Bay Area Young Survivors). It has been really good for my mental health.

    My first hike was to the lookout at Villa Montalvo. I blogged about that hike back in February of 2020. It was a great place to start. I was hiking alone and I found myself in a contemplative space. Each of the signs allowed me to reflect on different things as a slowly climbed the hill to the lookout. It was more of a struggle than I expected. It was a good first hike for this trip.

    On Friday, Cara and I hiked the upper portion of Rancho San Antonio which was a new hike for me.

    Today (Sunday) Cara and I hiked at Steven’s Creek Park. It is one of my favourite hikes. It also was the furthest (>5km) and longest (2hr) hike I’ve done since before chemo, and I feel great (yay).

    One thing that made today’s hike special was that there were so many wildflowers. I hope you enjoy the photos.

  • Forgiving my body again

    Forgiving my body again

    Back in February 2016, I wrote a blog post about forgiving my body. I just re-read it and it still resonates with me.

    At a recent writing workshop, I reflected again on forgiving my body. Here is what I wrote:

    I had forgiven my body for the cancer that grew it – for it trying to kill me. But now I don’t know what to think. Do I need to learn to forgive my body again for growing a new round of breast cancer?

    Forgiveness is a form of healing, of letting go of the pain. I think I can do that. I can forgive my body for growing a mutated version cancer that I had over eight years ago. I can thank my body for remaining nimble and not limiting my range of motion, even after radiation, for ensuring that even when I was low on energy, I had enough to go for a short walk with my puppy dog. I can forgive it this time!

    But if it happens again, will I still be able to forgive my body? Will my body deserve being forgiven if it keeps bringing cancer back?

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