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The Voice of People With Breast Cancer

Education

Our Voices Blog


Category : Stories

Losses from mBC: Vision and Fertility

Five years ago, 2017, I had what I thought would be my last CT scan at the BC Cancer Agency. I was done. I busted out of there as if I was free, even though I had a mild concern about a weird, ongoing burp and GERD symptom. I was told this was anxiety and waited for the results thinking I would graduate from cancer world. This was the assumption from my medical team and something I thought could be true since it had been five and a half years since my early-stage diagnosis. Even though the fear of recurrence existed, I held strong like my oncologist did.

To the Girl Standing in The Blue Hospital Gown, Part 2

I’m still scared and I’m still nervous, but I’m okay. I’m finding a sense of peace and calmness in all of this chaos. These past 42 days have been life changing. Being diagnosed and the end of a relationship has really tested my ability to find acceptance in everything. I continue to smile and laugh; life is truly incredible. The universe works in ways that I’ll never fully understand and in the darkest moments there is still light to be found.

Podcasts for Peace of Mind

I came to the Podcast game way late, like decades late. So when most people were tuning in on their morning commute to work, I was still listening to the mumbo jumbo in my head instead. Not that there’s anything wrong with this, I’ve always enjoyed my own company and I’m also a bit of a late bloomer which can translate into sometimes being a latecomer, so there’s that. But if I knew then how much I love a good podcast now, I’m fairly confident the time I spent waiting in Princess Margaret Hospital’s air-conditioned rooms would have passed by a lot quicker.

My Genetic Test Results Changed my Treatment Plans

Stacy Zelazny lives in a tiny town in Ontario, literally, she resides in a little-known place called Tiny, Ontario. Stacy describes herself as a mom of two amazing girls who is married to her best friend and winning the biggest fight of her life.

I’ll Take a Pass on the Cancer Platitudes, Thanks

“Breathe.” “Just breathe.” If I had a dollar for every time someone told me to do this —while I anxiously waited for my biopsy results, had another round of MRI exams, before and after surgery, throughout the months-long treatment and the years I spent swallowing a daily dose of Tamoxifen — I’d have a down payment for a vacation home in Mexico.

To the Girl Standing in The Blue Hospital Gown, Part 1

Well, the results are in.

Take a seat.

Take a deep breath.

It’s positive.

The Four Stages of My Stage Four MBC

One night in July 2015, I went to sleep, and everything was fine. When I woke up, it was obvious that everything was not fine. My left breast was swollen, inflamed and painful. I was shocked and worried but tried not to overreact. Then I started making excuses. Maybe my period was coming. Maybe it was cellulitis. Maybe it was a clogged milk duct. Maybe it was. Maybe it. Maybe …

Your Surviving-Tamoxifen Checklist. All the Things You Didn’t Know You Needed, But Do

Nothing can prepare you for the onslaught of side effects the tiny little hormone-blocking drug Tamoxifen can create in your body and your life. At least that’s how I feel…now. When my oncologist first handed me the five-year prescription for the 10-mg daily dose along with a pamphlet listing 40-odd side effects, I thought differently. Then, my oncologist explained how Tamoxifen works and what I may experience—including hot flashes, weight gain and irregular periods—in such an airy, breezy way that took, maybe, all of 45 seconds to share I figured, okay, I’ve got this. This’ll be no big deal. If there was anything to worry about my doctor would warn me. Thousands of women pop this pill every single day without complaint, I’ll be fine.

For the Newly Diagnosed: Part 2

A cancer diagnosis comes with many questions. While some of those questions can be answered by your healthcare team, many others cannot. That’s why we have put together this “For the Newly Diagnosed’ two-part series; to help patients who have been newly and recently diagnosed get the answers to their most pressing questions that may not be easily answerable. This series is also meant to help patients get ready for and be aware of challenges they may face in the upcoming months.

I Know How I Want to Die

I know how I want to die. I want to be in my bed, wearing my favourite pair of black and white patterned, soft cotton pajamas. I’ll be tucked under my duvet, lying on my side with my head resting on top of the extra long, queen-sized and ridiculously expensive down feather pillow I serendipitously purchased right before I was diagnosed with breast cancer. Softer than any pillow I’ve ever owned, it was worth it. After surgery and throughout treatment, my body smooshed into its feathery goodness like a hug. It protected my body parts that hurt and helped ease my stress into sleep. Like my two kitty-cats, it’s just something I won’t die without.