the year i turned 50, my doctor began talking about booking a colonoscopy given my cancer history, even though my fit came back fine. i am embarrassed to admit that i put it off, dreading the ghastly preparation that would have me starving, gagging on gallons of repulsive liquid that tasted like oily dirty socks and locked in my bathroom for a couple of days. turns out the prep wasn’t as bad as i had expected and, opting out of sedation, i got to see the whole thing in real-time, lying on my side, peeking through my fingers to watch the exploration of my colon, which was both off-putting and captivating.
then there was the moment that the gastroenterologist paused abruptly, pointing out a polyp and instructing his assistant to snip it off. it was an eyes-wide-open moment for me. he said that it was good that i was there as it likely would have become a problem for me had i waited any longer.
fortunately, it was caught, with absolutely no thanks to me — well, i showed up — but rather, because i have a proactive healthcare team that insisted and i met the guidelines for screening. without those two things, how it would have ended, well, it’s anyone’s guess.
could earlier screening have saved jason’s and russell’s lives, and the hundreds of other younger people who have died of colon cancer? yes, there’s no question — at least they would have had a fair chance. and while their stories highlight the need for updated screening guidelines that reflect the concerning trends in diagnoses (how long will people die unnecessarily?), they also serve to raise awareness of this deadly disease, the importance of testing — no matter how awkward or uncomfortable — knowing your body and family history. all the things that jason advocated for.
but just as important as understanding the symptoms and speaking up when things don’t feel right is the reminder to healthcare providers that colorectal cancer is increasingly a risk for younger canadians — no matter what the guidelines say — and they deserve access to life-saving screening.