I'm undergoing radiation treatment five days a week (Monday to Friday) concurrent with chemotherapy for five weeks. It's actually good news because I was told initially it would be six weeks but the fact is it's five weeks. I've done 1.4 weeks already. I can't wait for the end.
I get my radiation at the Ottawa General Hospital and I have to show up daily for my pre-scheduled appointment. So far, my appointments are all over the map. My dream of having morning sessions and going to work right after fell off the page when I got my first radiation dose after my first chemo. I couldn't get out of bed without feeling like barfing.
The last few days, however, have been better. The queasiness has subsided so I'll take that as a good day.
The Radiation machine and bed that I lie face down on. As soon as I see this bed, I drop my pants. Underwear follows. Dignity is left at the entry door to the hospital. |
Radiation beams come from the middle of this black thingy. |
Targetting on my pillow. Insert backside here. |
New target marks on my backside to replace small tattoo dots. I'll keep my pants raised when around the rifle ranges... |
One of my problems last year before I knew I had cancer was I was constipated. The constipation started January 2011. Then some bleeding followed. A month or two later I was really agitated with this so I went to an Urgent Care clinic. I was misdiagnosed. I was told I had hemorrhoids. I had to look them up to see what the heck that was.
In the summer that followed, the agitation did not suppress, and, despite blowing my brains out on bran, the constipation only worsened. My wife scheduled a colonoscopy for me.
In November 2011, by some strange turn of events, we had to drive 600 kms to Kitchener to get the goddamned colonoscopy. I'm glad we did. The waiting would soon be over to see why these hemorrhoids were such a pain.
The doctor who performed the scope was very bothered by what he saw and feared cancer.
In the weeks that followed, more testing ensued and then a formal diagnosis. I've been diagnosed with Stage 3 Colorectal Cancer. I've been told I will lose my sphincter muscle and, as a result, my asshole. Hmm...I'm kindof attached to that...
That was around the time the pain started. The Kitchener doctor was suprised I wasn't in pain already but within a week or two, the pain started. I was still constipated but now it was clear as to why---there was a tumour at the exit door and it was blocking the escape. Ain't no one was getting out.
Many times a day I would visit the bathroom and have the smallest of bowel movements. It was painful. It felt like shitting a pine cone. And the pain continued after that the rest of the day until the next attempt. It felt like, well, I just shat a pine cone. That continued until the radiation last week.
I'd say on Day 3 of radiation, I started to have pain-free bowel movements. The next day, I was on the pills and got rid of the bottle and PICC line. Things were good.
I asked the radiation doctor today why the lack of pain and he explained that the tumour likely was shrinking. Likely because he wasn't checking. If it was gone entirely, I was still getting five weeks of radiation to ensure cancer-free as much as possible. 95% of the patients respond best to this dose of radiation for my situation so that's what they're doing.
As the radiation doctor, Dr. Kendall, terms it, they're frying my ass. He was happy that my ass hasn't felt like it's on fire yet but it might in a few days. Great.
I do this for the full five weeks and then I rest for 6 to 8 weeks before surgery. As Dr. Kendall says, in that time, I'm still cooking. Hmm...nice thought. I hope I can walk...
At any rate, I don't know how many doctors died on the way to discovering the radiation treatments but they seem to be working. The dream is miracles will happen during chemo and radiation and the course of surgery in April will be steered towards a sphincter-saving solution.
You have a way with words Pat :) Just wanted to let you know I'm thinking of you daily and sending positive thoughts your way. Ive been getting updates from Erinn. Thanks for putting up this blog and keeping us up to date.
ReplyDeleteShelley
Hi Patrick,
ReplyDeleteYou are a really good writer... only wish it was about a more pleasant subject! (and, I don't think I'll have the same attitude towards pinecones). Still, we appreciate you sharing the details of your journey back to health (thinking positively). That's a great sign that the tumor appears to be shrinking!
Talk to you later,
Brenda
Hi Pat,
ReplyDeleteIt is very brave of you to be so frank with what is going on! As you already know, your sense of privacy takes a beating during treatment, but as long as the cancer is also taking a beating, it is worth it!
Marg
Nice update, Pat. Kona was diagnosed with brain cancer last week (she had a form of mast cell cancer 18 months ago). She has also taken to humourous blogging, but in her own style: she licks her crotch in public (while you show your ass). Kindred spirits you two.
ReplyDeleteJack saw these photos and things you are superhero like for sure. He will be looking at you in a different light - we are so proud of you going under the laser - he vaguely remembers his grandma doing dome of this hero work too!
ReplyDelete