I’ve turned 50 y.o. this year, conscientiously had a physical exam (all OK) and routine referral for colonoscopy screening. I have no symptoms of illness, am pretty healthy; but what I expected to be a routine colonoscopy actually found many polyps and prompted Dr. to make a referral for labs. Dr’s report said "The large number and variety of polyps is unusual." and that "genetic testing is indicated." Dr. had me back twice more, each time looked around in my colon and removed many polyps. The three colonoscopy procedures during past four months have found about 50 polyps, mostly pre-cancerous "adenomas" – tubular and tubulovillous per pathology reports; but no dysplasia nor carcinoma at present). Most polyps found have been fairly small, a couple 1.0-1.5 cm. Still some small
sessile polyps remain at present. After 3rd colonoscopy Dr. counseled that consideration should be given to genetic testing, "and ultimately colectomy may be needed." Dr. referred me for "FAPKM" genetic testing, they drew my blood and have sent it off to Mayo Clinic. This "FAPKM" testing seems pretty specialized – they are looking for a specific genetic mutation that might inhibit my colon from suppressing polyps. I have no known family history of colon polyps, no family history of colorectal cancer. Everything I’ve read seems
to indicate that a colon with 50 pre-cancerous polyps is serious,
whether the cause is genetic or "sporadic," and leaves me with the impression the colectomy option may (eventually?) be more likely needed than not. While I await test results I wonder, can anyone here explain likely range of outcomes for someone with my current condition?

http://www.webmd.com/colorectal-cancer/guide/treatment-stage
does the above article mean that no doctor will remove a colon tumor (only polyps) during a colonscopy?
here is the correct link…………..

http://www.webmd.com/colorectal-cancer/guide/treatment-stage

I guess this answers my question unless others interpret it a different way.
Stage 0
Stage 0 colon cancer is found only in the innermost lining of the colon. Treatment usually involves one of the following:
Polypectomy or local excision to remove the tumor and a small amount of surrounding tissue, or
during my 1st test in 1995, pre-cancerous polyps were removed according to the doctor and I’ve been told that not all polyps are pre-cancerous. Not sure if they took a sample, ran it to the lab very quickly and then came back and removed them as being pre-cancerous. Now sure how they knew they were pre-cancerous. The doctor did not tell me about this for 5 years and I feel my patient rights to know were violated. I’m trying to figure out how to be told what is being removed this time so I can make the decision as to remove or not to remove.
My current question is:
If my doctor finds more than polyps, even a stage 00 tumor, can and will he remove it during the colonoscopy or does it require a second procedure?

my doctor recommended a colorectal cancer screen in november of 2005 but i have no health insurance. and i dont have the financial ability to pay out of pocet. is there any help out there

I mean did they have like chemo or radiation and did it still come back or stay away.And does colorectal come back in the same place again?

Is there a doctor out there who could give me some information about colorectal cancer, or anyone who may have had it already? My 35 year old daughter was recently diagnosed with this, and the entire family is stunned. None of us can believe it. She begins her treatment on the 19th… chemo will be a constant infusion except on weekends, and the radiation will be 5 days a week. This will go on for 5 weeks in order to shrink the tumor, and then they will do surgery and remove it. She was told that her lymph nodes in her abdomen are enlarged too, so she will receive radiation to that area as well. She already can’t have kids, and has no children, so compromising her fertility is not an issue. We just are scared silly at this point, and I am searching for answers or for someone who has been through it to "shine a light" for me. Any help at all would be appreciated. Thank you.

A person very dear to me had colon cancer in 2007 and had a successful surgery to remove the tumor. She also had some months of coadyuvant therapy (chemo?). There have been further (clean) colorectal exams but I wonder which other exams are ordered in the first year or two following the surgery to guard against possible spread to other organs?
She has regular blood exams, every 6 months. Had recently (1 yr) a colonoscopy that came out good. But no CT scan which is what worries me.

im really scared i read Colorectal cancer happens to ppl of age 50 and im only 15..

I am having a colostomy for colorectal cancer.There is some indications my liver may be also cancerous although 2 ct assisted biopses have been performed both coming back negative. what do you think my chances are.

Only 25 states mandate insurance companies to pay for colon cancer screening. See what your state’s grade is for colorectal cancer screening: http://www.eifoundation.org/national/nccra/report_card/flash_movie.html

You can go to www.myspace.com/dmsteach and sign my guestbook if you support colorectal cancer legislation. You can also email your congress reps and senators especially if your state has a failing grade. Thank you.

Also, does obesity dramatically increase the chances of a teen getting stomach and/or colorectal cancer?

Hey everyone! My mom was diagnosed with colorectal cancer a few weeks ago. She is starting chemotherapy today, and I don't know much about the treatment. Does anyone know about it? I would appreciate any help! Thanks!

If you need any more info about it, check my most recent blog entry on my 360.