Since my diagnosis I have not participated in any outside program related to cancer. At first I was uncomfortable with the idea of identifying myself with cancer. I am not one to just bring it up and a conversation. Who really wants to hear depressing shit? The only place I have felt truly comfortable saying whatever is on my mind, is in my colon cancer group. There, everyone has the same problems more or less. During one of those meetings the opportunity was presented to volunteer at a local hockey game to promote Colon Cancer Awareness Month. I was intrigued and thought this would be a perfect way to start giving back.
When I received the information on what we would be speaking about, I discovered it was not so much about colon cancer, but more about promoting a new website entitled “Cancer IQ”. We were encouraged to try it out first. This site asks the user approximately 15 questions, and then identifies what their risk factor is for a specific cancer. I decided to fill out my form based on myself one year ago – before my diagnosis. To my surprise my risk for colon cancer was only 10%. Is this site useful? Absolutely – it brings awareness to the user, and maybe reminds them to go and speak to their healthcare professional about being tested. What this site does not do however is ask the right questions. The biggest sign for colon cancer is all about the way your poop looks. Is it pencil shaped? Is there blood? Is it a solid or a loose movement? These questions would greatly help determine whether or not a person should be concerned. But no – not one single poop question. No wonder I only received a 10% risk factor. Imagine someone like me out there took this? They would pat themselves on the back and go back to sleep. No worries in the world. Wrong.
What does this teach us? Do not take one opinion as the be all end all. If you have concerns, ask around. Each person will provide you with a different piece of the puzzle.