Chemo 2 - dose one
By jeand
- 1472 reads
Hi
You will see from my title that I made up my mind to go with Chemo. The one I am on is called Iranitecan. I have it from a drip into a canula, and they will give me just that one for 3 sessions, then moving into adding a stronger and longer dose of 5FU if I can tolderate it and want it.
I decided to go with it partly because of all the people I mentioned the idea of opting out, only one said he thought I should. His wife died just after finishing chemo, and had a bad experience with the drugs. But that ws 25 years ago and things are much improved now But the main motivation was that my doctor said my chances of living years (plural) were not realistic. So I took that as a challenge and shall do my best to live until October 2025.
The worst part of the chemo was the nurses trying my very cold hands to get the blood to flow sufficiently to let the needle in. Last time they put m7y hand in hot water for 10 minutes but that isw now not allowed due to the risk of health and safety Three of them had tries. One nurse can only try twice. And on the 6th go, it worked. That wasted a good half hour or so . They also fave a pre drug of antinausea and steroids, which worked well to make me feel postive and well
The drug goes through the drip for 90 minutes, and then a 15 min wash out with saline. Then I was sent home with more steriods and aniti naurea medicine which did what it was supposed to do. I have trouble getting to sleep due to the steriods, but no other problems, so far Those drugs are stopped now, although I have some I can take if have more problems over the next two weeks. The treatment is for every other Friday with Blood tests and check ups with the oncologist two days before each session.
I particular enjoyed talking to the two women next to me. One had lost her hair, and was wearing a cap, but her hair was about an inch long, and I would have been happy to be seen bare headed if I were she. She is on a very similar regime to mine so will probably see her at each session and she says she can cope with the second drug OK, although it means a 48 hour imput session at home of the new drug through a line in your shoulder. But she was postive and very encouraging. She was only in her late 50's but with lots of cancer behind her.
The other lady was 82 and had the full treatment that I am haiing and is now on a 6 week dose of a drug that helps to keep her cancer away, and has no side effects at all She was very positive about every thing..
My daughter was with me for 3 days but has gone home now. I feel fine and actually better than before I started on the drug, but probbly that is the steroid so may not last.
I am so happy I went with the brave decision. Thanks for your support.
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Comments
Good to hear from you. Every
Good to hear from you. Every day is precious isn't it? especially when able to concentrate. Love, prayer, hugs, Rhiannon
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Hello Jean,
Hello Jean,
I'm thinking of you and sending compassionate thoughts. It must help knowing you can speak to others in the same situation. Hope that brings you the strength you need at this time.
Take care.
Jenny.
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Hi Jean
Hi Jean
Thanks for the update. A brave decision made but I suppose a positive action is better than just waiting for the inevitable.
It is interesting to hear about the process of the treatment.
You are sounding more positive and feeling better.
Once again your positivity is wonderful.
Love
Lindyx
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Chemo is awful,
but it's better than the alternative. That said, anyone who is faced with a second or third round of chemotherapy in the event of a recurrence of disease, is entitled to opt for whatever is the best for them. My wife's aunt couldn't face her third round after cancer returned twice and so declined. My wife and I haven't even discussed what we/she would do if faced with the decision.
I applaud your positivity.
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jean, thanks for posting from
jean, thanks for posting from the front line. I wish you well.
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I'm glad you feel fine and a
I'm glad you feel fine and a bit better than before. It's very brave of you to not just go through this but to write about the experience too. I hope to read many more of your pieces of writing.
Good luck, and good on you.
Turlough
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This sounds like a really
This sounds like a really positive upbeat start to your treatment (except for the first half hour). Hope the steroids keep going with their magic. Looking forward to reading more as you head towards your personal challenge - really it should be cherries and a little pair of red boxing gloves up there!
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Thanks for posting the update
Thanks for posting the update, Jean. Of course, everyone is rooting for you. Another brave, clear account of your journey which will help others reading who are in a similar situation. Take care of yourself. Paul x
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