My journey with rectal cancer: What's your experience?
Hello everyone. I live in the UK and was diagnosed with rectal cancer 2 weeks ago. Since then I've been fast tracked through our NHS system with an MRI scan, CT scan, and another MRI scan this coming Monday to check out a spot on my liver, followed by a meeting with a consultant.
I've been told the tumour is 6" inside from my anus. Can anyone inform me if this would be rated low, mid, or high up in the rectum? Thanks.
This is a great forum for exchanging information. Hats off to the Mayo Clinic!
Interested in more discussions like this? Go to the Colorectal Cancer Support Group.
My cancer is a 5cm SCC involving anal sphincter stage 3 diagnosed December 2022. I had an emergency loop colostomy end of January due to high risk of obstruction & commenced daily combined radiation & chemo. I completed my 28 treatments last week.
Firstly, I suffered more than most with the side effects of constant diarrhoea ( thank goodness for the Colostomy bag) leading to severe dehydration & electrolyte imbalance, loss of appetite & nausea leading to malnutrition, gross weight & muscle loss & nil energy . I had 2 breaks of 1 week each during treatment course & noticed improvement in appetite at end of each week . Interestingly, I began to pass bits of the dead tumour rectally in last week's of treatment. This was a putrid substance, but not unexpected according to Oncologist. Now I wait...chemo & radiation continues to work for about 1 month after treatment finishes...for my appetite to return, so I can begin my rebuild. Super important to keep fluids up & I have found cold drinks ( better if milk or high protein) with ice more successful with electrolyte replacement tablets once per day with diarrhoea. I have had 3 IV fluids replacements. I am still taking anti nausea medication so I can eat small amounts, but praying my appetite returns in next few days.
i have rectal c ---- i'm on my 5 chemo i hope it shrinks and i dont need bag - id like them do do exam and see if its shrunk and they can operate asap
My rectal cancer is 7 cm from the anus. With that being said surgeons did not want to do resection on me until the 2 inch tumor shrinks via chemo/radiation. Which I will be starting in next week or so. The surgeon wants to avoid colonoscopy bag if the resection Was done before chemo/radiation, shrinking of the tumor. Thru research the rectum is 12cm, my tumor starts at 7 cm in I believe mine would be considered low rectal. But your Dr should be able to tell you.
I am interested in hearing from anyone who’s had an anoplasty procedure done.
Yes, I had keyhole surgery in 4 places below the navel. I left hospital after 4 days having had very little pain and recovered quickly. The only problem was an allergic reaction to the glue used on the stitches but that cleared up eventually.
I have had both. Chemo is a bit debilitating but do-able. I had a port inserted and took the chemo that way. You will feel absolutely wiped out. I never had much nausea but did take the anti-nausea pills they gave me.
Radiation is painless, but the sessions do build up, so it has become a bit painful towards the end. I have not had to take pain killers so, again, it is manageable. I think I have had over 20 sessions and take chemo pills every day. I have 3 sessions to go, then we will see the result. I will say that I feel quite positive as I don't feel any pain from the cancer presently.
i thought that radiation wasnt as bad as chemo
i dont get any pills but they give me intravenious anti nausea medicine and it seems to work -- i didnt get any pills it was all intravenious
yes you feel better the farther you are from when you get chemo -i feel sorry for all of us
How was your resection did they go through stomach