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Hi All. My partner had a 6 hour bowel cancer Operation on Nov 12th 2020. The surgical team were able to remove the tumour successfully and all post Op biopsies came back clear. He does not require Chemo or Radiography. It took 2 months to find a stoma bag that worked for Michael. The stoma bag fills up fairly quickly even though Michael has been taken Imodium for over 2 months now. He is not getting any sleep as he is terrified the stoma bag will overflow and burst. He is also very hoarse since coming out of hospital. It may be because he was ventilated for 6 hours during surgery or it may be because he was tubed twice post Op as a result of the Stoma Bag not working initially in hospital. Has anyone else experienced this. We have been told that it will settle in time .3 months later and Michael has no energy from lack of sleep. Any advice on how to boost his energy levels or how to reduce the stoma bag filling up so quickly would be grateful. I wish you all every success on your road to recovery.

I am presently recovering from rectal cancer surgery December 2017 and had an ileostomy reversal in April 2018. As my bowel motions are still quite erratic I would like to connect with others who have had an ileostomy reversal experience to ascertain perhaps how long it took for the bowel motions to settle or what their experience has been. Thank you.

If you or someone in your life has been affected by bowel cancer and are interested in sharing your story, consider becoming a media volunteer with the Irish Cancer Society. Sharing your story can help to raise cancer awareness, inform people about our services, appeal for volunteers, and bring reassurance to cancer patients and their families. After you express an interest in becoming a media volunteer, we would discuss with you how best to share your story, getting your permission before publishing or broadcasting.

What is Lynch Syndrome? (Thanks to Sir John Burn Lynch Syndrome UK Conference 2015) We all inherit our DNA 50% from each parent. If we have LS then one of our repair genes is good while the other one is faulty. Think of the repair genes as two Doormen on the door at a night club. Nothing is going to get past them that shouldn’t. This is a person without LS Imagine one of the Doormen needs the toilet and walks off. We still have one doorman watching and keeping us safe. This is a person with LS Imagine the other doorman now needs to toilet and leaves. Nobody is now watching door. This is what happens when one good gene goes faulty for what ever reason. Anybody can just walk in now In brief, we only have one repair gene looking out for us and if it gets damaged in a cell we are left with no protection. See Lynch Syndrome Ireland Web Site + Facebook Page + Twitter

Hi My mum recently diagnosed with stage 4 bowel cancer. We want to bring her home once she's done with hospital. Has any other teacher been in this position of caring for a parent and what did you do about getting leave from work?

My daughter met with her consultant last week and we were told she will need a Colectomy , he said it would be about a month. Can any one tell me what the usual waiting time for surgery in limerick hospital is ? We’re very anxious for her to have it

I have advanced bowel cancer. I notice online that there aren't as many posts although it's very common. I am only 42 and a mother of 4 who always ate well and excercised. I have a braf mutation which is aggressive and patches moved to my liver, intestine and one lymph gland. Only symptoms where when liver began to hurt as my bowel tumour was very narrow. Chemo has rid cancer on the gland but is proving resistant elsewhere so I'm now on Cetuximab still and tablet chemo. It would be good if there were more post out there so I added mine.

I am presently recovering from rectal cancer surgery December 2017 and had an ileostomy reversal in April 2018. As my bowel motions are still quite erratic I would like to connect with others who have had an ileostomy reversal experience to ascertain perhaps how long it took for the bowel motions to settle.

My husband Tom (28) was diagnosed with Colon cancer in Jan this year. Thankfully the lymph nodes were clear despite initial fears as they were inflamed. Cancer was labelled 2B. It was a T4 tumour. The cells were moderate to poorly differentiated which are not the best kind. 6 months of Chemo is finishing soon. I am terrifed and unsure how to proceed. Tom's oncologist does not fill me with great confidence as we haven't seen him since January and there are some other worrying aspects of the care that bother me. I would appreciate any advice. What should happen at the end of chemo? I only know about the colonoscopy and the CT scan. Is there any blood test that can be done regularly or other things we can do to stay alert to cell changes. He tested negatively for lynch syndrome.

Can anyone tell me if they test ur tumor for leas before begining treatment??? I'm due, to start chemo radiation after x mas I'm female 47 single parent of 3 boys 6/8/12 in cork,,,, low tumor, 2.5/3 cm T3 N2 M0 inside the anal verge so as u can imagine I'm anxious that this treatment works, so I can b reconnected afterwards