Monika’s Story
My name is Monika Page. I’m a Mother, a Wife, a Daughter and I am on a Breast Cancer Journey.
Not a sentence I thought I’d be saying in 2020. Or ever, in fact.
This photo was taken just before my diagnosis. It was my husband’s 40th birthday, and we hosted a party at our house. I look at this photo often as, unbeknownst to me, lurking beneath my party dress was a tumour, and soon life would never be as carefree and happy as to how I felt in that photo.
Just after this party, we went to Singapore for a holiday before the busy but wonderful year that was supposed to be 2020 started. On one of the mornings we were about to go sightseeing, I was putting on suncream as I was wearing a singlet, and that’s the first time I felt my lump and the thing that would turn my life upside down.
I thought nothing of it as I was healthy, exercised every day, didn’t smoke, didn’t drink; a real party animal. I also had no cancer in my family and figured if the lump didn’t go away in a month or two, I’d maybe get it checked out. Or knowing me, probably not. Not only was I too busy going about life, but those kinds of things happen to other people, right?
When the doctor told me I had triple-negative breast cancer, my first reaction was laughter. She’d obviously confused me with another patient. It took me a minute to comprehend her words. Very quickly, my laughter turned to hot, messy, ugly tears as I realised this was actually happening.
Soon after, I sat in Professor Chan’s waiting room. The strangest thing happened. A lady came up to me, right up close to my face, and said, ‘can I hug you?’ She hugged me and said, ‘you’re going to be alright; you’re in the best hands here.’ And then she left the room, and I felt like an angel had hugged me. It was a surreal experience.
And she, whoever she was, was right. I genuinely believe that being in Dr Willsher’s and Professor Chan’s hands means that I get to be here today to watch my son grow up. They are my superheroes.
A couple of weeks later, I started 16 weeks of chemotherapy and watched myself become a shell of the person I used to be. I stopped looking in the mirror as the person staring at me shocked me. My hilarious breast nurse Cath put up with me emailing her the most random of questions (am I supposed to sweat my body weight in sweat each night? Why do my feet feel like they are on fire, when will my eyebrows grow back – the list went on!) and kept assuring me that I would get through the dreaded day 4 of each chemo cycle, despite me telling her I couldn’t.
After chemo, I had a double mastectomy and lat dorsi flap surgery with the incredible Dr Tony Connell. It was such a seamless experience, given that Dr Connell works with Dr Willsher. Later, another six months of oral chemo. By this point, I was mentally and physically done. I kept drawing on my mantra: this too shall pass. I also kept busy, continued working full time, took up new hobbies like painting, and walked every day, even if some days I only made it to the letterbox.
It’s been two and a half years since I started the journey. The fear of reoccurrence is very strong and occupies a lot of space in my head. I struggle to be rational, and every new bruise or cough terrifies me into thinking that it’s back. When I drive past the Mount Hospital, where my breasts were removed, I get an overwhelming feeling of sadness. I visit Professor Chan every couple of months as I am in one of her clinical trials, and I feel anxious every time I drive into the hospital. I’m a work in progress in dealing with these thoughts.
Life holds no promises that everything will be ok. I’m about to have yet another breast surgery in August. But because of the amazing service that is available to us here in Perth, I get to continue to be a wife, a mother, a friend, and a daughter. And I get to be someone with a totally new perspective on life. And for those on this journey that are struggling right now, you can do this. You can.
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We love hearing our patient’s stories and sharing them with others at the very beginning of theirs. For more information on how to be involved, contact us.