My consultant almost cried when she told me that I had metastases in my abdomen as well.as the huge mass associated with my remaining r. ovary.
The mass suspected to be on the ovary, but not yet confirmed, is 17.5cm x 12.5cm and 11.cm cranial/caudal.
I also have 4 other mets ranging from 4cm to 1.5 cm on the anterior peritoneum.
My CA 125 -18
CEO tumour marker 4.7
Cosultant says she is praying the metastases are confirmed ovarian. Because bowel cancer mets are far harder to treat.
I am having biopsies of the small mets on Tuesday 23/07.
If they are colon cancer, and with my family history of colon cancer which spans 3 generations , then its stage IV colon cancer and prognosis is poor and treatment is aggressive.
I am also getting pains down the front and sides of my thighs which is associated i am told with metastasis on each side of my abdomen pressing on spinal nerves
I'm feeling very anxious and depressed at this likely diagnosis.
Has anyone else got metastases to ovary from bowel/colon cancer?
What was your treatment plan and how did it turn out ?
Hello, no of course I don't mind. So yes I was diagnosed with primary bowel cancer with a krukenberg tumour on my ovary and liver mets last year. I started on chemo for bowel cancer to shrink everything. I had surgery in March on the bowel and ovary- both now out. I'm now on mop up chemo from that surgery and also to shrink liver mets to then work on them with surgery or ablation. It's very scary when you're first told but they can do surgery and lots of things (whether it is ovarian or bowel primary). There is also a surgery called HIPEC which you can find more information about on good sites like NHS or Macmillan sites. I always feel better when I've seen my team and know the plan. There are also facebook groups that I've found really helpful for knowledge and there are lots of people on there with ovarian/ peri mets- obviously I know you won't know whether to join an ovarian or bowel one yet but I think both would be very welcoming if you said you're awaiting. Sending you love and big hug x
Hello, I'm 43 now, I was 42 when I was diagnosed. Yes I totally understand. I found speaking to Macmillan very helpful, they are a great support. There are a lot of new treatments coming through now so hopefully things can change- getting on treatment and starting to deal with it is good too. I really do feel much better for having a plan. Keep us posted and as I say do call the Macmillan line if you feel you can- they are ever so nice and really helped me.
You can chat to their line too. Chemo I had one course of before surgery and I'm on it now for mop up. I still have mets in my liver currently- they're hopefully going to do surgery on them or ablation on them shortly- the chemo is to shrink them.
Chemo has been okay- I've been quite lucky not any big problems so far- I've had covid once and I have some neuropathy and some nausea but you get given medication. I try to just do one cycle at a time and view it as a means to an end.
The chemo really can shrink things and change the options so I really hope that can be so for you- I've read lots of stories in the facebook group for stage iv of people going from inoperable to operable
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