4th Week Radiation Treatment

This week marks my 4th week radiation and my 2nd time chemo treatments.  Chemo is a potent drug.  It didn't bother me the first time much, except for one time vomiting the next day.  This time around I had a 38.8c fever which is in the danger range where I should go to Emergency.  With having radiation in the morning, I waited to report my symptoms to the booking clerk.  I had been drinking for my radiation treatment, but I wanted to check that it was safe to continue with the fever.  I was sent to the radiation oncologist nurse to be examined, so she checked my vitals like blood pressure 133/73, pulse 87, and temperature 38.1c.  The fever was coming down which was a good sign that I probably didn't have a serious infection.  However, it was found that I have thrush in the mouth, which is a yeast infection.  I am to continue with the homemade rinse of baking soda and salt, and take an antibotic to fight off any infection that may be present.  I am fairly sure I have a urine infection too, but that has yet to be determined while waiting for results to come back soon.  So these are the wacky things I go through after chemo... and I will have to make note for when I finish the last 4 sessions after all the radiation treatments are done.  All in all... I remain hard to get the IV in and the blood out of my small and deep veins.  I am being a good pin cushion of practice for many areas in the hospital.  I am glad to provide the service.  :)  

My MRI was scheduled today for 4:40pm, so this scan will update the picture after my hysterecomy.  This will be helpful to see the part of the cervix left behind after the surgery.  Off I went across the Sudbury hospital to the North Tower, main floor.  It was easy enough to find although it is a large enough hospital to get lost in.  MRI room 2 was shown on the news this week to be getting a new MRI at the Sudbury hospital.  The one nurse that helped with the scan was shown on the news program.  We laughed that she was now a celebrity!    Once I was sitting in the IV chair, it was the same old story of my small and deep veins, and it took three nurses to get the best hole to inject the IV for contast and an injection.  The machine was noisy, but it was restful at the same time.  Humming out tunes that turn into pictures of my pelvic area.  The hour went fast.

When I got back to our room, and we went down to the community kitchen to figure out supper.  To our surprise, there was some left over dinners for Daffodil Lodge residents to enjoy from a hospital conference held today.  Supper was ready made, a chili base with mashed potato topping with a bun, and a nice side salad.  I thought that was great since it had been a long couple days.  By far, week 4 has been the hardest for me, but I'm still doing ok.  Some of this might be the dreary snow that was all over the parking lot this morning.  I haven't left the hospital since Monday morning, so it looks like a foreign land out the window.

The next couple days should go easier, just radiation treatments are scheduled, and one meeting with the chemo nurse to go over the next treatments that I will have after I get back from London's radiation treatments first week of December.  Lucky for me, I can take these more locally at Temiskaming Shores Hospital. 

On a brighter note, I was able to have a messenger video chat with my family the other day, so we had a nice little visit that cheered me up.  Here I was having some fun making faces at them.  I can recommend Facebook Messenger video chat... it has come a long way to entertain and keep loved ones connected during these times of Covid19 pandemic and for a cancer patient over here at HSN/Sudbury.


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Comments

  1. I find your blog very uplifting. You have an awesome outlook on life. Keep writing, your cheerful appreciative nature is an inspiration to us all. I get grumpy and depressed even spending one night in the hospital and there you are going through chemo and radiation and still able to write these amazing uplifting posts. I hope these writings find their way to the people who need them the most. Your are a very special person. Every one of your post cheer me up. Keep going Sue, many of us need your cheerfulness. :)

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  2. Great spirit you do have!
    Chemo sure drains you as well. Sorry to hear of the thrush. Rest when you can and glad you got family time on messenger. Make all the funny pictures I know Dorothy will enjoy them. Next time make a fantastic funny to her. Lol
    Take care ❤😤🙏😷

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  3. Keep up the good work Susan. Hoping you don’t have too many sessions left. All the best prayers and positive thoughts for you from us 💕

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  4. Following your weekly reports. Keep on posting. Remember, during your time in London, if anyone needs accommodation or anything, we’re only an hour away.

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  5. Thank you for the kind words. I did enjoy the funny faces on messenger! Have to have a little sunshine in these days. I am sure glad to hear from you all... and I will carry on the best I can. There is always choices > either go with it or go against it. So far so good despite the side effects. Cheers from Susan! :)

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  6. Thanks Pete. We are going to take a room close to the hospital so that Michael can come and visit me. At least, it sounds like he will be on the visitor's list. I know it's quite a procedure and with covid19, we are limited with getting out and around to see anyone on this trip. Thanks for reading my posts, I appreciate the comments! xo

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  7. Carol and Barry TuckerNovember 25, 2020 at 4:17 PM

    Hi Sue. I love reading how positive you are and I'm happy to read that you are getting the infection under control. Barry and I are thinking of you!

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  8. Thanks so much Carol and Barry!! Yes, they take infections quite seriously when having chemo. I even have to flush twice so I am not infecting Michael. We might both end up walking around green neon!! haha! We went for a little drive today and that perked up my spirits too!! Cheers, Susan

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