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Abrub - update on recurrence
After surgery 5 weeks ago for my appendix cancer recurrence (after 9 years of NED), they determined that in addition to the defined tumor, there remain scattered malignant cells outside of the tumor margins. With mine being a slow-growing cancer (and the new tumor identical in morphology and pathology to the original…
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DNA tests for medical tendancies
I was discussing this with a member on here and I'm curious if anyone else has done this. Have you had one of those mail in DNA tests done to find out what diseases or medical issues you might have a tendancy for? I was adopted so I have little family history, just on my birth mother's side, nothing on my birth father's…
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Just started our journey...
My husband (57) had routine (1st) colonscopy on Dec 1; 4-5 cms tumor discovered in the cecum; surgery set for Thursday; having the liver and lung CT tomorrow. Of course, we don't know stage yet, but that hasn't stopped me from totally freaking out. Trying to take it one day at a time so am focused on post surgery.…
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47% chance of getting cancer in our lifetime...
This is what we were told when we went to the first cancer 'talk' after I was diagnosed. To me that's basically 50%, half of us. Last weekend the friend that I went to the cancer retreat with was telling me how upset she was because her doctor told her she had a 50% chance of recurrence. I told her that then she's like…
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Just wanted to say "Hello"
Hello! I'm a newbie and just wanted to say that I'm happy to have finally joined! I've viewed some discussions on this site but never got the nerve to join until today!!!
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feeling sad after treatment
Hi im welch girl i have colon cancer ive had my second treatment this past week . and took a pump home for2 days .i was just wondering if you sometimes get sad after treatment and dose it go away after a few day. ive did pretty good with the frist treatment i had some fatigue nauses but did better than what i thought i do…
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Tips for Nausea? What works ?
Hi all, Carl just turned in his pump today at noon. Overall, I think he has done remarkably well for his first go round. I do wonder what all of you do for nausea? He is on three different meds and is taking them religiously, but he is still having nausea. I have told him he needs to eat like a pregnant woman, small…
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A clear scan and a 2.0 CEA, good for 6 more months
Just got the call, and that CEA finally bumped down to 2 from 2.3. Said my liver was the same as the last few scans. As nice a gift as I could hope for with these holidays, I wish good or better news for all of you as well..............................................Dave
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Questions re Curcumin
I have used Curamin in the past, and recently resumed taking it to address some joint pain. However, now as I look online to buy more, I see that there is "Curamin" "CuraMed" and "Curamin-PM" Can anyone explain the differences (I know the "PM" version has Melatonin and B-6), advantages and disadvantages to the various…
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First 3 month test today
I went in for my first three month surveillance scans. Actually the scans have been on the three month interval for the past two however I was going in for monthly CEA tests prior to this last period. So every CT scan and MRI scan I've had (a lot of them) I always feel nauseated shortly after the contrast dye injection.…
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Recent Open APR surgery
Hello, I am first time poster. On Nov 10, I had Open APR surgery for my stage 3 rectal cancer. i am writing this from my phone while laying on my right side. I have a lot leakage from my perineal incision which is clear and red (Not infecred). I also have a fair amount of pain while sitting and leakage increases the more I…
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Donna Juliano
it is with great sadness , for the ones among us who remember her, I let you know that Donna Juliano has past. I was friends with her on Face book and received the post. Rest in Peace colon friend. Marjan ( thingy 45)
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4th port
well to day i get my forth port it worked for 6 weeks got dislogged and also has a fiber sheaf so its surgy at 11:45 and then chemo the next day 3 1/2 years im still here and so is the cancer 3 diffrent chemos and i gusse i 'll have to do trials next but im still here and moving i guess any day above ground is good im…
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No brachytherapy for me
I finally have the final piece from all of my appointments 2 weeks ago: my drs decided that the radiation therapy (brachytherapy) was not recommended because, “while the risk of complications are is, there is no proven track record for low grade, mucinous tumors using this technique." So no more treatments – no chemo, no…
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Stage 4 NED 8 Years
Saw my onc yesteday for my annual visit. My CEA was 2.5 which is within my normal range of 2-3 so I am still cancer free. Eight years down and two to go before I can considernmyself cured. Just wanted to let everyone know in case you are following a similar program to mine. For those new to the Board I do the following to…
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CEA level up from 1.17 to 2.28 in 2 months
Hi, I am 63 year old and undergo last Chemo therapy in May. I had tested CEA in August which was 1.17 and in October it elevated to 2.28. Although normal range is less than 3.0 (I am non-smoker). Is there something i should worry about for elevated level ? is it normal ? Your advice will be really helpful. Thank you, A S
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Four years. Two years. NED
I was diagnosed four years ago this month. Surgery, chemo and radiation in that order, followed. The Cancer spread to my liver two years seven months ago. Thermal Microwave Ablatoin followed. Today, my blood work came back clean. I am naturally very happy. I recognise how very blessed I am. SUE
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Feeling Sad
Hubby dx about 1 yr ago with stage 3 (3 lymph node positive) rectal cancer He has done chemo/rad, surgery, adj chemo, and ileo reversal, currently clear from cancer per sept petscan and hopefully stay clean. At this time we should be enjoying our lives after 14 months riding on no fun roller coaster. Instead i just found…
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Checking in
So, it's been about a year since I last checked in. I'm surprised at the slow-down in postings that I see, because I don't see any slow-down of colorectal cancer diagnoses. I'll try to check in more often. My story? Dx stage IIb August 2006. Colon resection, 9 Folfox treatments. Dx July 2007 of another primary cancer, this…
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Folfuri + Avastin and Neupogen Shot - feeling awful
Hello Group - I have CRC with several liver mets. Chemo is folfuri + avastin, plus 5 shots neupogen for low WBC counts. I am experiencing so many abdominal side effects plus bone pain from WBC shots - possibly contributing to side effects is a small bowel intestinal stricture which causes painful spasms (partial…
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Great artical in Discover magazine
This artical tells the story of a leading edge researcher pioneering new and innovative cancer immune therapy cancer treatments. Definitely worth the read. http://discovermagazine.com/2016/nov/checkmate
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Thoughtless "Helpful" Comments
I saw the "We're all dying" thread and it brought to mind the crazy, thoughtless things people have said over the years...of course, trying to be helpful... if anyone has any good ones, feel free to add on. My faves: when I was down, "maybe it's time to stop fighting?" So helpful and uplifting! From a friend with cerebral…
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Depressed, just unloading here
I don't know why but my husband asking how long I have to live and the doctor saying maybe ten years and sounding like probably not has put me in a terrible depression. I can't stop thinking about it. I know that they don't really know and I know that there could be some new thing that comes up before then but I can't stop…
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TV show 'The Doctors' today
I never watch this show but I was changing channels and caught the tail end of them saying a certain fat (I think it was) had a tie to colon cancer. I didn't catch what it was supposed to be. Did anyone else see it or hear anything about it? Thanks! Jan
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Chemo & Radiation induced sexual dysfunction
It is not something that is talked about, is it. A friend of mine, who has finihsed treatment, told me that the chemo has left him unable to get an erection (my words, not his). It is not a side effect that I had heard of. I myself was 'damaged beyond repair' by the radiation. I was warned this could happen, before I went…
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Lonsurf - Anyone here been on it?
My good friend is about to start on Lonsurf. I know they give you a list of what to expect as far as side effects go, but there is nothing better than hearing it from 'the horses mouth' so to speak. So, I am asking for any of you here to share anything you can with me about your expereinces on Lonsurf. Thank you! SUE
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Hemicolectomy next week 11/8/16. What to expect after that? Getting back on feet, eating?
I have a hemi colectomy coming next week week. What can I expect when I wake up and the next several days? What does one eat? It's got to be different, how long does that go on? How about getting around? Is there discomfort, fatigue? Its not clear except for bowel changes that don't sound all that different from now and…
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My husband just diagnosed with Stage 4 colon cancer....
Hello everyone, my name is Kris. My husband Jason was just diagnosed with Stage 4 colon cancer. I will tell you all what I know & would really appreciate any feedback you might have. He is 42, & has been experiencing digestive issues for about a year & a half now. We don't have insurance since he was laid off from work, so…
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After Lobectomy Pain & The Word Incurable
Hi, I haven't posted in quite some time. I'm stage IV and about 6 weeks out of a lobectoby and wedge on left lung. In short, the tumor is gone along with most of my lung...but there were cancer cells millimeters from my aorta. Radiation can't be done safely and there's nothing left to cut out. I'm left with chemo and the…
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First Folfox treatment yesterday, felt OK going into, nurses' info depressing
I had my first Folfox treatment yesterday, am at home with the rest of the treatment that runs for 2 days. Going into chemo after my first visit with my oncologist and his nurse, I felt fairly good about what I was facing. (51 years-old, laparoscopic sigmoid resection with 1 of 21 nodes positive). Being in otherwise fairly…