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Shelley Belanger

Journey with Mucosal Melanoma

My name is Shelley, and I am a resident of Ontario, where I live with my loving spouse and our cherished dog. I am also a proud mother to two wonderful daughters, both happily married, and a grandmother to four beautiful grandchildren.

My health journey began in the mid-90s when I was diagnosed with HPV in my mid-30s, which I managed with a year of medical treatment. However, my challenges didn’t end there. In the years that followed,  regular checks revealed precancerous cells, but thankfully, they eventually ceased to appear.

In 2013, what I thought was a routine yeast infection led to a discovery that changed my life. A visit to the emergency room for a prescription uncovered a black mole on my labia, which was diagnosed as mucosal melanoma in-situ after surgical removal. The emotional toll was immense, especially as I tried to keep  a brave face for my young granddaughter, who was with me at the time.

Following the diagnosis, I went through multiple surgeries to ensure clear margins and endured painful treatments with a topical imiquimod cream, Zyclara, which caused severe discomfort. I had  to use a peri bottle just to ease the pain when urinating. Despite all efforts, the melanoma  returned, leading to more surgeries and constant monitoring.

In September 2021, after being declared disease-free, a routine check-up found a suspicious spot, and my battle with melanoma was reignited. The diagnosis was nodular melanoma,  which is aggressive and rare. The emotional and physical strain during this time led to severe weight loss and I had to take medication for both anxiety and acid reflux.

Despite the financial burdens and the impact on my ability to work, I continue to fight. My treatment journey now includes Pembrolizumab (Keytruda), an immunotherapy drug, though I face challenges with insurance coverage. The stress of constant re-examinations and uncertainty around future surgeries, due to medical system backlogs, weighs heavily on me.

Through all of this, I found solace and support from Melanoma Canada, particularly through the Mucosal Melanoma Facebook Group. This community has been a beacon of hope and a source of valuable information, constantly reminding me that I am not alone in this fight.

Now, my goal is not only to survive but to thrive, and support others going through similar experiences. I am committed to raising awareness about mucosal melanoma and advocating for better medical understanding and treatment options. Despite the many hardships, I hold onto hope for a future where this disease can be effectively managed, or even cured. I want my story to inspire and support others facing similar journeys.

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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