Covid vaccination may increase lifespan for stage 4 cancer patients

Posted by maraca @maraca, Nov 14, 2025

Hi,
On Wednesday, November 12 I read an online article in the Guardian newsletter that a study has shown how patients with stage 4 cancer getting chemotherapy tend to live significantly longer if before therapy they get a Pfizer or Moderna Covid vaccination. The study appears to be serious and credible. You can web search it probably.
I went right out and got the Pfizer shot on Thursday since I am newly diagnosed with stage 4 esophageal cancer and start 12 sessions of chemotherapy on Monday.
The study indicates a longer life expectancy of 75% improvement for stage 4 patients on chemo, with vaccinated patients over the time span studied living a median of 37.3 months compared to 20.6 months for those who were not recently vaccinated prior to their chemotherapy.
Check it out? Good luck all.
Marcia new here

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Profile picture for susan38 @susan38

@maraca gee, I’m so sorry to hear u are not well. Im surprised u have lost weight, I have not, even though I’m not eating very well, I still keep down a few tablespoons of rice, and occasionally the advocado and banana. I tried chewing a handful of peanuts two days ago to bock me from diarrhoea, but since most of my teeth have gone, eating the peanuts was difficult, (I will crush a teaspoonful of them next time) something I think u would not be able to do with your mouth or throat in that condition. I’m now in my 4 th week and have been told I will be worse this week, and next.
I’ve lost my pubic hair (definitely no Brazilian on the horizon) but only a few brush loads of head hair.
The main thing is to look after yourself. I was too ill to drive anywhere. I sleep most of the day and the night. No housework, cooking, or outings, mainly bedroom, loo, back to bed, and this is the cycle of my life. I do talk on the phone to some friends, sometimes an hour or more and they support me via conversation even though I am mumbling my words, can’t articulate well, repeat my sentences and know my brain and cognitive functioning is being affected by the treatment. I truly hope u are not experiencing the same. Some of my friends really cannot grasp the severity of the pain and anguish, the exhaustion, the letting go of all dignity in trying to clean up after my ablution disasters, especially when I can’t make it several feet to the ensuite in time. I want to tell you that your troubles will pass as drs tell me this. But I wonder if it is believable. Some ice cubes on the lips help somewhat when I can’t keep hydrated or swallow anything. Please take care the best u can and keep in touch with Mayo connect. If you must vent do so, as most using this brilliant site will understand. There is no judgement here, just help from the mentors and others experiencing similar circumstances.

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@susan38
Hi Susan,
You're in your fourth and fifth weeks now, of chemo, that doctor says will be the worst, and I hope you aren't in agony. Everything you described so far sounds agonising to me already, and not being able to chew peanuts sans teeth another trouble to mess with the rest.
You have a grand spirit, I think, to be meeting the ensuite "indignities" and other discomforts you face with such candor and aplomb in your writing here. I truly hope that weeks 4 & 5 do not fully exhaust you.
I'm lying very low, no longer getting out of our flat (my son kindly runs local errands) and need to be horizontal day and night. Have lost 10 pounds since November 17 when I had that second 48 hour infusion of folfox chemo. Can't eat much but Jello and ice cream with the trachea all raked up by radiation. Because I feel too weak to withstand another round of chemo in three days, I requested a different oncologist who may be less rigid about the treatment. She's vastly more communicative already, kind in her phone manner, and qualified by all accounts. I will meet her next week.
The assigned doctor, a man who does lots of research and trials, is hard to reach, terse, and not what I need from a doctor, I feel. This lady doctor is on his team at the same cancer clinic, but she can make new decisions independently of him.
You, Susan, are a very special someone!
Marcia

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I just found your posts today. Your treatment is much different than mine, as I chose surgery and am facing a much different form of unexplained pain. I am amazed at your tenacious attitudes. You both are so brave, and I am thankful for this informative place to land in expressing experiences. Reading your descriptions of your doctor was for me, a huge "Yes"!! I feel the same about mine, down to the fact of being terse. (Ha) I watched my mother go through breast cancer twice, one breast removed. My grandmother had the same form of cancer but had a radical mastectomy and lived much longer. In both cases the cancer presented on the outside of the nipple...Paget's disease. It never occurred to me that I might get a rare lung cancer. I thought my fate would be that of the other women in my family. I have mourned not pushing my mother towards chemical treatments. All she ever agreed to was tamoxifen, which she discontinued. Reading what you are both going through, I know, without a shadow of a doubt, my mother could not have endured what you have. She once had an operation on her eye under local anesthesia because she could not stand to throw up, and that is saying a lot. At the end stages of her life, my sister and I agreed to put her in a medically induced coma. Thank you for sharing all you have. Your writing style IS much like journaling. It has given me a measure of peace from self doubts. Please keep sharing, as you have at least one other in here cheering you both on. 💕

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