Awareness is the best medicine I remember many things from my battl [...]READ MORE
“You have cancer.” To me, when it’s regarding my own health, those words sit at the top of the list of “worst possible words to hear from your doctor”. Especially when you are a mother of 3 kids, just had a c-section 4 months ago and are in the middle of a worldwide pandemic. Yuck.
In February 2020, almost a year after my second child was born, I went to the Hospital in Estevan for a routine colonoscopy. I had been having routine colonoscopies ever since the doctor found polyps while investigating some digestion issues a few years back. When I was in for the colonoscopy, the doctor came in and told me that there were a few polyps in my colon, and one of them he could not remove because it was too invasive. He said that although it did not look cancerous, he took a biopsy to make sure. He immediately referred me to a gastroenterologist in Regina. Although the local doctor wanted this taken care of that day, the Regina hospital could not fit me in. I had to wait at least a month and that it would be taken care of at a later date.
Enter Worldwide Pandemic. Covid-19.
This caused quite an issue and, as you can imagine, all routine procedures or procedures that were not labelled “urgent” were put on a lengthy list. Although the physician here in Estevan thought it was urgent, it was not categorized as urgent in Regina.
Meanwhile. The biopsy came back, and the polyp was not cancerous at this point – but it needed to be taken care of – otherwise it could possibly turn into cancer if left unattended.
Enter Pregnancy of my third child.
We didn’t know this at the time, but I was about 5 minutes pregnant with my third child during my coloscopy. (Obviously not 5 minutes, because if you have ever done colonoscopy prep you would understand that this would be physically impossible…)
By the time they were able to get me in to remove this nasty looking polyp, I was about “honeydew melon” pregnant. However, for obvious reasons, it is not recommended to do scopes while pregnant. They said they would send me a letter a couple of months after the birth of my child, and that they would take care of it then.
After a fairly regular pregnancy, I ended up with an emergency caesarean section at St. Joseph’s Hospital in November 2021. I had a beautiful baby girl, the perfect addition to our little family. But at the back of my mind loomed the question “Has it turned into cancer now? When are they going to call me?”
In December, the waitlist at the Pasqua hospital was still lengthy, and by this time, somehow, I had been listed as only needing a “scope” and nothing else. There were no notes about the looming polyp. After some self advocating and speaking with the gastroenterologist myself to explain my situation, and insisting that he looked at the notes and photos that the doctor in Estevan had sent him, he realized that I had fallen through the cracks and that needed to be dealt with stat. Which unfortunately, due to covid, meant in a couple months.
In April 2021, I went up to the Pasqua Hospital for the moment of truth. I was nervous, and I was not happy to be going into the hospital alone (due to covid). I nursed my almost 5-month-old baby in the parking lot, said goodbye to my husband and walked up to the gastro unit. After I had my scope; I knew something was up. The specialist and some other staff walked in, and he said the words “I am sorry, but you have cancer”.
How can this be? He didn’t even have the biopsy results back yet. He knew. And I knew. There it was. The dreaded “C” word. I started to cry. My body and my bowel were exhausted, my breastmilk was leaking out, my post-partum emotions were raging, and my heart felt completely broken. I had never felt so alone. I made the trek back down to the parking lot where my husband and baby waited for the news. My husband hugged me, and we cried together, and while I breastfed my baby in the parking lot of the hospital – he said to me “the problem isn’t the problem, the problem is your attitude about the problem”. Now obviously, I wanted to punch him in the nose for saying that – but he was right. And we were going to get through it. Together.
My husband is my best friend. He is my rock, and my strength and I would not have been able to get through this without him. He is kind and patient and approaches each situation with thoughtfulness and purpose. My strength to get through this came from the people I love. My parents, my sisters, my friends, my witty 12-year-old son, my cheeky three-year-old son and my sweet baby girl. But mostly my husband. When you find someone who will drive 2 hours while you sit on a porta-loo on the floor in the back seat of his truck and expel your insides while prepping for surgery, and he can just drive with the window open and smile and tell you he loves you – you know you have someone to grow old and wrinkly with.
In the days to come, I was told that I would need a “Colon Resection Surgery”, a right hemicolectomy. My cancer was aggressive and invasive, and knowing how quickly it turned from a polyp into cancer, it needed to be dealt with within a month to ensure it did not spread to my liver or kidneys. It would be a minimally invasive surgery; they would open up my freshly healed C-section scar and poke a few other holes in my belly and cut out the cancer along with half of my large intestine and somehow, like a magical unicorn, attach it back to itself.
“OK, I got this, no big deal”. After a CT Scan, and a MRI to ensure the cancer had not spread and being poked and prodded what seemed like a million times, I was medically ready for the surgery.
As a mom of a very young baby, the most difficult part was knowing that I could not “mom” her in the way that I did for my other kids when they were babies. Because of the surgery, I had to stop nursing her. I knew I wouldn’t be able to get up with her at night, I wouldn’t be able to lift her at all for six weeks; I would need a lot of support. I knew my family would come through and that my husband could survive on very little sleep – but these are the thoughts and worries that brought me to my most vulnerable and low points during this process.
After spending over $200 on every different type of bottle on the market and crying daily with how impossible it was to get my 5-month-old daughter to drink from literally anything other than me – one day she just looked at me and with her smart little eyes she said, “OK mom – I will do it”. And she did. Finally, I was ready for surgery.
On May 12, 2021, I had a right-hemicolectomy at the Regina General Hospital. The team of surgeons cut six holes in my tummy and pulled out half of my colon. After a few days in the hospital, I was free to come home!
The biopsy came back about a week after my surgery. I had stage 1 invasive adenocarcinoma – and the cancer had not spread to any of my lymph nodes. The surgeon said that although I still had to see the oncologist, he was sure that I did not need to have chemotherapy or radiation. The oncologist confirmed that no further treatment was needed, but that the cancer was close to stage 2, with some very “aggressive behavoirs”. He also suspected that because of the make-up of the proteins in my tumour and some pre-testing that was done on it, that it was possible that I have Lynch Syndrome. Lynch syndrome is caused by an inherited gene mutation. People with Lynch syndrome have an increased risk for colorectal, endometrial and other cancers. The cancer risk varies by gene mutation; therefore, it is important for people with Lynch syndrome to know which gene mutation they have. I have been sent for testing and although it is a lengthy process to diagnose this, it is very important that I find out the results so that I can make informed decisions about my health in the future. If it comes back positive, it will be a whole new journey. I will also have many follow up tests, with bloodwork every three months, CT Scans yearly and colonoscopies yearly (woohoo)!
Because this was such an emotional journey, I decided that it would be very therapeutic for me to create a “vlog” about my experience (A Video Blog). I created a You-Tube channel and took videos of the entire process. The appointments, the MRI, the surgery, how to prep for a colonoscopy – all of it. This was not only important because it was helping me cope, but I truly feel that Colon Cancer is the most under-talked about and sometimes preventable cancer there is. I want people who may be wondering about their own health to think “maybe I should go for a scope or send in that kit”. I wanted to normalize colon cancer – because right now, people don’t want to talk about it. Colon cancer is the second leading cause of death from cancer in men and the third leading cause of death from cancer in women in Canada. That is a sobering statistic. Especially since my cancer, if dealt with sooner, would not have turned into cancer at all. Prevention is key. And it is not just a cancer that effects the older generation. I am 20 + 17 years old, and since joining the “colon cancer world” on social media, I have met hundreds of people under the age of 40 with colon cancer.
After the release of my first video, there was an outpouring of support and comments. It was humbling and amazing. My videos had thousands of views, and people from all over the world reached out, thanking me for sharing my story and sharing their story with me. Many people mentioned that after watching the videos, they were going to book themselves an appointment to deal with their issues. My cancer was a breeze compared to people with stage 3 or 4 colon cancer! Surgery, radiation, more surgery – it is NOT an easy road. People don’t want to talk about “colon” issues – they find it embarrassing or intimidating, but knowing now how deadly colon cancer is, I truly hope that my shared experience can help others.
If I can help even one person from having to go down the “colon cancer” road, all of my time creating videos and sharing my experience will have been worth it.
The last six months have truly been a “journey”. When you find out you have cancer, suddenly the other problems in your life seem trivial. From this experience I have learned a few things.
My journey with cancer is over for now, but my journey of advocating for awareness has just begun.
Visit Becky’s inspiring Youtube channel here: https://www.youtube.com/channel/UCdJ9e73G7jDX-AVEI7XtMag
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