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Sue

Sue’s Story

My story is like most stories I guess. I was blissfully unaware of Melanoma until it slapped me in the face in 2007. I was a sun lover, often bronzed in winter from frequent visits to the tanning bed and took no precautions with sunscreen. I admit it – I liked being tanned. I lived in B.C. and practically lived outdoors as a kid, winter and spring skiing, baseball, grass hockey, I swam in our pool – all of it in the heat of the day with no protection of any kind. It was the 70’s and 80’s and being tanned made me feel healthy and sporty. I was in for a big surprise.

An itchy mole on my shoulder blade turned into a little blueberry before I had it looked at. First to my GP then to a dermatologist who referred me to Princess Margaret Hospital in Toronto where I now live with my family. Honestly, I thought that maybe they’d have to cut a bit of skin out with it but hey, it can’t be that bad I told myself. Don’t you just cut skin cancer out and continue on with your day?

I was a little shocked to hear I would need a surgery to remove the surrounding tissue. More shocked to see some 40 staples after I removed the bandage. I wondered aloud whether the surgeon knew it was just a mole? Shortly after we were told the cancer had in fact spread through the lymph nodes and that another surgery was in order to remove them. Ok, this was now getting real. Was I in trouble here? Surely not. I was in my 40’s and untouchable by something like a cancerous mole, right? I was clear for 3 years when I started having minor bladder problems. Sure enough, I had a tumor now growing on my adrenal gland on my kidney. Another surgery to remove the tumor and that should be it right? No. Only 3 months later I had 3 new tumors growing and was now stage IV cancer and officially in trouble.

It was then I was told about a clinical trial for GlaxoSmithKline’s BRAF inhibitor, a drug that targets my specific kind of cancer by binding to it and inhibiting the activity of BRAF and effectively choking out the tumor – it just shrinks and dies. The trial was taking around 345 people. I thought, oh man – it seems like there is that many Melanoma patients hanging around the waiting room whenever I’m there, and I can never get parking… what are my odds I wondered? I’ve never been good at math and I was alarmed to learn it was 345 people from 8 countries, not just my country, not just my waiting room. I had to get in this study to save my life. I passed all the medical exams and I was told on April 29, 2011 that I was in the study. I had officially won the lottery! Forget about a chalet in Switzerland, a trip around the world or that red sports car, who cares, this drug would extend my life! My tumors shrunk immediately and by the end of August 2011 I was cancer-free (as long as I take my BRAFF pills).

So, I’m winning my fight. Perhaps just for now, perhaps for the long term – no one knows. I’ll find out as I go but one thing is for sure, I’m lucky, no matter what happens, because I have family and friends to support me, make me laugh and let me cry when I’m feeling the weight of this. Today, I’m pleased to say that I have been on the BRAF inhibitor for 1 year and 9 months with no re-growth, so far.
You know, maybe I won’t be the last one to leave the party or maybe I’ll be leaving early. Whatever lays in store for me, I’m just focused on moving forward, keeping a sense of humor and enjoying life, and along the way recommending that others do the same.

Other Patient Stories

Maureen Meehan
In early August of 2017 while attending a routine visit with my doctor, a General Practitioner (GP), I mentioned that the mole I’d had my right forearm for years was concerning me as it had changed.
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Brandon Smith
No words could be more true! Cancer has been my invisible enemy for 11 years. My name is Brandon Smith and I have Stage 4 metastatic melanoma.
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Ian Campbell
My name is Ian Campbell. I am 60 years young and have a beautiful wife, and two wonderful adult children. My cancer journey started when I moved to Alberta from Ontario. 
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Cindy Nightingale
Finally, it was May 18, 2004, the day of my ophthalmologist appointment. I was relieved someone with authority would be looking at my eye. I did a little research and it seemed like I might have cataracts, glaucoma, or an infection.
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Vanessa Delle Monache
My name is Vanessa Delle Monache and I am a two-time cancer survivor. At the young age of 15, I was diagnosed with Stage 4 Hodgkin’s Lymphoma. I received chemotherapy as well as radiation.
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Akeema Smith
My melanoma story begins when I was born with a congenital Nevus birthmark covering most of my left breast. Growing up I never thought much about it other than my appointments with plastic surgeons and dermatologists every 3 months.
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Emma Newman
My name is Emma Newman and I was diagnosed with malignant melanoma when I was 23 years old. In June 2018, I graduated from Western University with a degree in Health Sciences and Psychology. During my time at Western I was very involved in extracurricular activities.
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Bev Barbour
The Coronavirus brought many changes to our world; for me it has led me to The Melanoma Network of Canada (MNC) and for that, I am very grateful.
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Heather Derbecker
In September 2011, I was 36 years old and 32 weeks pregnant with baby number three when I was diagnosed with melanoma. There is never a good time to be diagnosed with cancer, but facing my own mortality and getting ready to welcome a new life brought my world crashing down.
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Ken Graham
COVID-19 … as if cancer patients don’t have enough to stress about.   I am not sure if immunotherapy treatments put melanoma patients more at risk for COVID-19, but it worries me. 
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