The following is a post written and published on Facing Cancer’s website where I am honoured to be a writer. You can find the original post here.
The ticking of the clock is getting louder as the days pass. This week it will be 10 months since I found out I am in remission from advanced Thyroid Cancer.
I was diagnosed in June of 2009. I sat the doctors office in shock, even though I had already self diagnosed, and knew in my gut it was Cancer. But even though I told myself I was prepared to hear bad news, it was still a devastating blow. It was explained to me that if I had to have cancer, this was a good one since most people are treated and recovered very quickly. What I didn’t know until much later was that My entire thyroid was swallowed up by the disease and that I had lymphatic metastasis. So my journey was much longer than any of us could have expected. I lived in a chronic state of illness for 2.5 years. Until the day I sat in the doctors office, once again expecting bad news. My mom was with me for the first time ever, so I grumbled through obligatory introductions. My doctor looked at my mom and shook her hand politely and said something to the effect of; it’s nice to meet you, but we won’t likely have another opportunity for about a year. I felt immediate panic, thinking she was about to announce she would be taking a leave from her practice, leaving me in the lurch, as my previous doctor had. She asked me to have a seat and then went over the numbers from my recent labs and my whole body scan. I sat there, blinking slowly, trying to understand all the numbers, when my mom, seemingly understanding my confusion, piped up asking what it all meant. “It means we’re finally at a low enough level to consider Coleen to be in remission”. That happened on Jan 3rd 2012 and was the best belated Christmas gift I could have received.
I’m thrilled that I am counting it and remembering every month. I’m not sure that I’ll ever forget how significant the 3rd of each month is. You’d think I would feel more at ease the further I distance myself from that date, but for me it’s quite the opposite. I live with the fear of recurrence in the back of my mind, gnawing at my happiness like a termite. It’s happening one thought at a time, but collectively the thoughts frighten me. The what ifs, and the panic every time a new “symptom” pops up. I can’t be the only one who feels this way, can I? I know it’s not healthy but it’s not a conscious choice I make.
Right now I’m in the countdown to my one year follow up. I have heard variances among fellow thyroid cancer survivors of what one year testing involves. So to be honest, I’m not really sure what to expect. This lack of knowledge adds to my fears. I have just reached out to my doctors to book an appointment to review my last set of blood tests and to discuss what we do now that the one year mark is nearly here. So I guess Until then it is simply a waiting game.
Can you relate?