Soldiering on.....
Comments
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Inishbofin:
Hi, I have two sons, ages 10 and 12. They are almost the same ages as your girls (both just turned one year older in May). Keep on the stuggle.....My heart is with you.
Barbara
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May I ask where are youlizard44 said:It does get old after a while
I was diagnosed with stage 4 rectal cancer with mets to the liver in May 2015, had 8 Folfox plus Avastin treatments followed by 28 radiation treatments with a 5FU pump 24/5 before beginning a new chemo cocktail of Irinotecan and Erbitux in April 2016. Had a liver ablation in August 2016, developed a fibrin shield around my port and had to have it removed and replaced. New port was implanted in Nov. 2016, resulting in a collapsed lung which meant an extra day or two in the hospital with a chest tube. Had abdominoperineal surgery with a permanent colostomy in Oct 2017. Scans were good until the last one, in July, that showed the beast is back, with possible spread to lungs and inguinal lymph nodes. Finished up the 54th Irinotecan/Erbitux treatment on July 13 and am now back on Folfox and Avastin as of last week.That last treatment was worse than I remember the first 8 being, but it could be the culmulative effects building up. I'm not looking foward to going in next week for another infusion, but the best I can do is take it one day, one treatment,one procedure, one scan at a time and hang in there as best I can,which is what most of us seem to be doing. I've found that I can take more than I thought I could to keep the beast at bay and myself functioning as normally as possible. Hang in there and play whatever mind tricks you need to in order to get through and be able to spend more time with your family. I hate that so many younger people with children are joining us, but am hopeful that one day reseachers will find a way not to just keep the monster down, but eradicate it forever and prevent it from messing up any more lives.
Grace/lizard44
May I ask where are you receiving treatment and who performed the APR surgerY?
Thank you!
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I feel ya!
I am feeling the same way. I hate the pump. I dread the infusion. The first 3 days are not bad but then they take the pump off and I drop. Nausea and such ridiculous fatigue. I keep trying to put one foot in front of the other but some days are way harder than others.
Hang in there. I'm walking the same path, partner. Let's get this done.
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Same
It also gets to me, that feeling of low whenever I'm on infusion. I think all of us have been through that, its not easy being on chemo. My main problem is the mental effect of chemo, I feel like wanting to cry on the infusion center but I have no choice but to keep on living like nothing's happening.
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