Breast Cancer Journey – Surgery – Lumpectomy

Getting to know the surgeon: It was raining the day we went to Mount Sinai Hospital in Toronto. We went up to the 12th floor where the waiting room was busy, full of the usual Mount Sinai clients. Older women, well-dressed. My doctor is Jamie Escalon. He’s a large man with a very high hairline. He talked to me about my findings and what would happen next. He told me I would find things very different from 20 years before. The biggest changes were that this was Day Surgery, that it would take an hour to an hour and a half, and that I would have no surgical drains. He also said that anaesthetic had improved and the new variety was fast-acting, fast-acting, with little after-effect. He did one worrying thing- he referred to one area of my breast and frantically search through my notes when I mentioned there were two. I saw Krishna look concerned at this and I hope for no good reason. After my surgery I would come back for results and a treatment plan. Again, this was a familiar pattern and so in a way I hope it will follow the same successful path. Since then I’ve had some bad days, with my emotions all over the place, I’ve been tired, and worried, and sometimes terrified. People think cancer hurts, and it may very well do in later stages, but at the beginning Everything feels normal. There’s no pain, there’s no sensation, just the knowledge that something evil is inside you. It’s very strange.

I was very scared of surgery, just as I had been with my other two surgeries in 2002 and 2004. My main fears were not waking up from the anaesthetic and how I would feel when I woke up. Women’s College pre-op is a virtual session, and took place 2 days before the surgery. I spoke to four different people, all who were very informative and friendly. There was the surgical nurse who explained what would happen on the day, the pharmacist who explained what drugs I could have and how to take them, a physiotherapist who explained the exercises and limitations following surgery, and finally an anaesthesiologist who explained the actual surgery and listened to my fears. He told me he would not be the surgeon on the day but that all of his notes would be provided to that person. I can’t say I was completely reassured, but it was helpful to know that they knew my wishes and were happy to support me on the day. It felt like a lot. The number of forms with information and consent felt somewhat overwhelming and the days before the surgery it felt like everything was moving very quickly. I felt exhausted.

Lumpectomy: The day of the surgery inevitably rolled around. I had to be there at 8:30am and my surgery would be at 1:45. We took the subway with my bags- my socks, two bags- one for my clothes, one for my shoes, and my CPAP machine, which they’d asked me to bring. Apparently, they want that there in case they have trouble waking you up. Hmm.

Once on the 8th floor, I changed into Surgical clothing- a long hospital gown, a pyjama type bottom, and paper booties over my socks. I had a locker to store my belongings in. At this point Krishna was able to join me as I went down to get my pre-surgical procedures.

I was on a stretcher bed and was wheeled around, which always feels somewhat alien and official. The first procedure was an ultrasound where images helped the doctor insert wires into the areas that would be operated on. First, of course, some local anaesthetic was put into my breast. Toronto has developed a new technology called the Molly seed – a magnetic guide for the surgeon. In my case  the older style, wires, was better because two magnetic Molly seeds would be a problem so close to each other. I felt a little bit disappointed by that since I was curious about the seed. Once the wires were taped down they did a mammogram to make sure they were properly in place. Luckily, they use only light pressure and everything went smoothly.

From here I was taking to the second floor to nuclear medicine for my Sentinel note images. However, there was a bit of a mix-up and they weren’t ready for me, having to order my dye from another hospital so back to the 8th floor I went. On the 8th floor I went to an area with cubicles like you find in an emergency room. They told me it’s the same area that I would be in after the surgery, so I was quite pleased to see this early on. Everyone was friendly and reassuring and although I felt anxious I certainly was not panicking, something I had really worried about.

Back to nuclear medicine. I don’t remember this from last time, and in fact I don’t think that I went through it. At the first surgery the Sentinel node biopsy was still in trial mode. In order to have it, I needed to be around for at least 6 months for our follow-up by the study. So instead two or three layers of lymph nodes were routinely removed. This time it was going to be Sentinel. I was in a really large modern room with a machine that looked like a CT scanner, lying on a very narrow bed. The technician told me that dye would be injected into the two areas and it would travel to the lymph nodes. He said, because it goes under the skin, it would sting but that sensation would fade within minutes. I didn’t feel it as a stinging, but more like a clenching or heavy pinching, definitely unpleasant but as promised short-lived. The machine moved me along under what looks like a screen without any viewing area and he left the room, which I hadn’t expected and I lay on my back for the 15 or 20 minutes he told me about. I feel quite woozy during that time, and really wanted to ask for help. Instead I breathed waiting for it to be over. When he came back in and I mentioned it he put an extra pillow under my head. He then said he was going to trace the outline of my body for the scan. I still don’t know what that was about.

Now the serious part- surgery. Several people came to talk to me including two anaesthetists who I told my preferences to. They listened without hurrying me reassuring me about my fears. What I mentioned my fear of not waking up the anaesthetist said that rarely ever happens in fact never. He told me I would be getting oxygen in the operating room and that’s when they would give me the anaesthetic. I reiterated that I didn’t want to be told when I was getting it and he nodded. The next anesthetist talk to me about the nerve block, explaining that it would go into my back near my spine and go to the nerves in the armpit and part of the breast. Did I want this done, it  would reduce pain immediately after the surgery and would last from  24 to 48 hours. I said yes but I was nervous so the nurse offered me sedation. I’ve always been afraid of sedation, but said I’ll try it- seeing it as an opportunity to experience it this time around in a very protected environment. I also said I didn’t want to feel out of it so she gave me a half dose. I was hooked up to an oxygen monitor and blood pressure/ heart rate machine and noticed my blood pressure getting lower after that. That was reassuring, and I did not feel out of it but quite happy, she had given it to me saying, here is your mimosa. It’s nice to smile at such a time. They sent Krish away before the nerve block. When I got it it was again two injections with a great deal of pressure but nothing I couldn’t handle.

Finally it was time to take me to the operating room. My anxiety was rising but manageable. At this point, trusting the team was the only way forward. The team was around me, but I couldn’t see a lot. There was no music, something Krishna said he enjoyed during his surgeries, but it felt like a nice community in there, with everyone speaking softly and working together. They put my oxygen mask on, the anaesthetist repeated that he wouldn’t tell me when he was giving me the anaesthetic, but pretty soon, after a few breaths, I could sense something different. I suppose I could have felt anxious then and resisted, but chose instead to move towards it, to have it done. People talk about a blank, or “the next thing they knew” but to me it’s not really felt that way, but more like a brief and grey time, then suddenly alert. Maybe not too suddenly. I was conscious of being conscious. I felt relief and happy that I was not groggy or nauseated, but in the room with people moving around me back in the post surgical area. They asked me how I felt and I said I felt fine but noticed one area of my tongue was numb and tingling. I am was really happy to have gone through it. I think the surgeon showed up my side pretty quickly saying everything went well, see you later.

I sent a couple of messages and Krishna showed up to sit with me while I recovered. I don’t think I was there longer than an hour or so before they brought a wheelchair to go down to the lobby. So nice to be outside, we waited a few minutes before calling an Uber to go home.

Sibling chat:

— Sleepy, itchy, tongue is numb on the right. Having ginger ale, in a bit of pain
— OK. I’ll let people know you survived.
Later:
— Waiting for dinner. I’m hungry, which is a good sign seeing as they sent me home with a sick bag
–My tongue is still tingling
Cos it doesn’t pay to not worry about something

Email the next day:

— How are you feeling???? How was your night? Hoping you slept like a log.
— Ha more like a twig

Sibling chat:

In fact, the nerve block they gave me meant I had very little pain. I felt almost like a fraud. What surgery? The emotional side was harder. I lay on the couch with TV and my audiobook, being waited on with meals. My friend, Denise, sent cake – yum. But it was strangely silent. Some people chatted if I went first. No one left casseroles or flowers at my door. Bah.

Index of all my Breast Cancer Journey Posts

Breast cancer Journey – The Recurrence

In 2002, in the midst of two- yes, two major life events  I got a breast cancer diagnosis. I was weeks aawy from leaving Canada and had started packing up my apartment. Robin was going to be moving into his first place on his own, having decided not to go with me, so we had to pack for him and plan that move. I had a terrible cold, I remember, and was feeling ill and very stressed. I had to sell stuff, store stuff, ship stuff, get stuff ready for moving, pack up my life here, help Robin start his own. Saying I was overwhelmed doesn’t come close to describing my state of mind.

The good news is that I got through my surgery, I made my moves, both of them, and after a rough Journey with radiation treatment in the UK, I was done. Ten years later I was signed off from my frequent mammograms and support programs. I felt somewhat bereft, having to leave behind some quite magnificent UK support. I was done with cancer.

The bad news is I’m back on the same Journey now. 22 years apparently isn’t long enough. I’ve always regretted not writing about what happened to me so here I am, trying to do it again.

For several months I’d been noticing  my left breast looking different, smaller. I mentioned it a few times to doctors and nurses, all who said I was older, my breasts were changing, and of course my affected breast would be smaller. Then I asked again. This time I said I wanted a mammogram,

I went in mostly expecting my fears to be unfounded. A few days later I got a call that something was seen in the image and they wanted me to come back for another mammogram and an ultrasound. My heart had sunk when I saw the number and they said it was the breast centre. Bloody flashbacks. This was eerily familiar, following the same pattern from before. They had a cancellation today, they said after I questioned a couple of later dates. Yes, I’ll be there, I said. Then the replacement doctor called to tell me I had calcifications and went on to say that things have really changed since the last time. If it’s cancer, people just live with it, she said. One step at a time, she said. I found myself with that similar dark and suffocating feeling but I still hoped that it would be nothing major.

In I went. I had the regular and the “special” mammogram that hurts more Sitting outside the door, I could hear the technician chatting with the person before me. Then she left the room for a while, spoke to someone in another room and came back to cheerily tell her everything was fine and she could go. My turn. The ultrasound that went on and on and I felt my optimism fading. It faded even more when the technician left to chat with someone in another room, coming back to say that they would like to do a biopsy, and what I like to do that now or make an appointment to do it again another time. I said now.

For a breast biopsy a small incision is made and the ultrasound guides the doctor to remove tissue samples. In my case, there were two areas not too far apart and the biopsy sounds like a loud snap, which makes me jump. The breast  is numbed so there’s no pain other than the one in your mind. And so I waited. They told me my result would be ready on Monday or Tuesday- it was Thursday then but I also knew my doctor made calls on Wednesdays so I’d be waiting a while. So that was that. Meanwhile I resisted Googling. I really didn’t want to. It was all a fluke anyway.

I have a friend who has also had breast cancer so I turned to her. The emails tell more of the story:

–I hesitated to email you. I think twenty years isn’t enough. Today I got breast biopsies. PTSD is real.
–Jesus, why would you hesitate? You keeping anything from me makes me nuts. If you don’t tell me everything, I will hunt you down like a dog.
–Why did I hesitate? I didn’t want to dredge it up for you or have you be Pollyanna either. If you Google don’t tell me anything. I just don’t want to know…yet.
–Can’t believe we’re still worrying about this shit. Let’s hope we’re just worry warts.
–“Best case scenario” – benign calcifications. In my last situation every best case fell so yeah PTSD. It’s so going the same way so far. I waver between terrified and matter of fact.  Who knows. Maybe I’m good for another twenty years.
— I could not take the loss of you.

Wednesday came the news from my doctor’s summer replacement that there was cancer detected from the biopsy. I would be hearing from an oncologist for another appointment within a week. In fact I heard the next day and the appointment was for the following Tuesday afternoon.

Index of all my Breast Cancer Journey Posts

Breast cancer Journey – Index

Anything that says Breast Cancer Journey is optional reading. At this point, the peripheral things may pop up in my regular blogs. These ones, however, are the meat of the matter. Read at your discretion and I’ll likely be adding a post or two when I go in March for my follow up.

This was a big job and I’m quite sure there will be typos, repeat paragraphs and photos – although some overlap seemed OK.  Anything you see that’s wrong, please comment. Read at your discretion. I’ve tried to put photos that might upset at the bottom, and there may be more formatting problems in doing so. There are also photos I meant to include that haven’t shown up, but I don’t have the energy to fix right now. That may follow. I did my best!

Recurrence
Surgery – Lumpectomy
Chemotherapy
Cardiac?
Second surgery
Anaemia
Radiation
Hair and other side effects
Support
Follow ups and all the confusion
First mammogram after treatment
What comes next – LIVE!

A little picture I did on a Post-it note. It shows me surrounded by love

And it’s a new year

Wednesday, 7 January, 2026

Have you been catching yourself typing 2025? I don’t think I have yet but… Anyway here it is another new year. I keep thinking back to 2020 where I reasoned (and prayed) that 20/20 was perfect vision so I was ready for a good one. Instead, it was the beginning of a downslide. Hasn’t stopped yet. Hope is eternal, right?

I’ve been writing up my Cancer Journey stuff but not ready to publish anything. As usual, lots of writing in my head and difficulty getting photos to cooperate. My eyesight is terrible and I haven’t yet got back to scheduling my eye surgery. Waiting for that call. And, honestly, 2025 was the Year of Waiting. It’s just a spillover. I’m very reluctant to post without my photos. They remind me of what to say and add context. Taking photos is still a big deal for me, a great companion when I’m out, and I find myself wishing I’d been documenting more of my life. The past is done with. On to the future and enjoying the present as much as I can with all the nonsense I’ve been going through. The truth is I’m far from feeling well and hoping that as time passes, I’ll feel more myself — better! Meanwhile, welcome to my melancholia – no excuses.

Christmas was quiet. I had many quiet Christmases in London but then everything seemed serene and pretty. I got used to having no one around and having no transport to go anywhere. We’d stock up on M&S treat-like foods and turn on all the lights, candles everywhere, snug if alone. There are family around now but I can’t decorate in the same way (not yet) and we don’t see anyone anyway. On the 27th there was the usual family get together. Krish had asked not to stay too long then asked to delay our departure so that was nice. There was plenty of food at my niece’s. Everyone was smiling. It was nice and I’d like more.

I wanted to make little gingerbread houses but didn’t want to go the graham cracker route again. Ikea, for the second year, let me down on mini house kits. Instead they had tree kits. I bought two boxes meaning to assemble four sets as gifts. Wrong! My energy level just wasn’t there, my icing skills – as poor as they are – were even worse than usual. I soldiered on. I struggled with the decorations but in the end made a decision to finish just one set for now. They could fight over it – or fight because no one would want it. However, the finished result was OK – I mean in a Gaudi-esque way. I have three sets left to finish and suspect they will be a project for next year.


My decorations were all I could manage this year. A little cheering up for sure but not at previous levels! The first photo is from Hackney Christmases — my Christmas advent treehouse from Roger LaBorde. I wanted to buy one for my brother but only the small non-advent one. I really want to unpack my things…

The next picutre is this year. We miss the whimsy of what we were used to but it will come back. Hopefully this Christmas. We each have a toy that isn’t packed and that’s the best of us.

Truth told, the colours of winter now are grey and white. (I read that on Instagram!) I haven’t seen much in the way of decoration anywhere. I would have explored had I had the energy. As well, it’s been a very snowy winter so far. Not an easy slog. The renamed Dundas (now Sankofa* Square had a small Christmas market. I swung by after a hospital visit. It wasn’t open yet.

Talking of hospitals, some of it is actually fun. Every third Thursday at Toronto General, they run a wellness kitchen. It’s set up like a TV show. The chef, Jeremy, makes three courses of healthy and simple meals and at the end we get to sample it. A few of the recipes are regulars for us now. You can watch it yourself at home – recorded or live on the third Thursday at noon EST. Maybe you’ll see me there. Pictured is Jeremy, and the Moroccan style chickpea stew I made at home.

We have to move soon. We like it here. More than like it. I hope we can find something soon and that it’s not far away, if not right here in the building. Every night I watch the windows opposite. It’s a guilty pleasure. I can’t see into the places, my eyesight isn’t that good, but I do think about the individual stories that are going on every day behind those windows.

Meanwhile, it continues snowy and cold. At night in the lights of the stadium opposite we watch the rain or snow falling thick and fast. These are good days for winter naps.

 

Are we a city of idiots, hibernating in the Toronto way of things?

I hope your Christmas was merry and your new year will be splendid, all year long.