New! Diagnosis of Adenacarcinoma--in Rectum

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maryjane
maryjane Member Posts: 71
edited March 2014 in Colorectal Cancer #1
I was diagnosed with Adenacarcinoma the day before Thanksgiving. I took 3 Advil for a pain on my side and started to bleed. Went to the emergency room and lost lots of blood in bowell movments. Advil is a blood thinner and essentially saved my life by causing me to bleed. Had a colonoscopy and they discovered a 2 cm tumor at the base of my rectum. I was shaking so badly I needed to take 3 tranquilizers. I have been perfectly healthy all my life with one hospitalization for an elbow surgery. This shocking news paralyzed me for the past 4 weeks. Being a RESEARCHER...I spent hours reading web sites, books, and interviewing Drs. I was thoroughly confused and depressed--not being able to accept that my body was going to be so invaded with surgery, chemo, and radiation. Yesterday I saw a surgeon who can do my surgery and I've opted to have no radiation/chemo now until they open me up. This past month has been a nightmare but--today I feel better about having made a decision and now I start praying! This has been one nightmare of a Holiday Season. Any of you out there with a similar experience?
MaryJane
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Comments

  • JDuke
    JDuke Member Posts: 438
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    MaryJane
    Welcome to this amazing group of people. I am sorry that you have had to seek us out, but this site will bring you unbelievable comfort in the days ahead. There are many here who have been through what you will be experiencing. I have squamous cancer of the anal canal, which is different than yours, so my treatments would not compare. Rest assured you will hear from many members that will be able to provide you with a wealth of information and personal victories with this beast. It is very overwhelming at first, but as you said, once you have a plan in place, that feeling of having some control helps. I hope you can enjoy today, think positive thoughts; I will be praying for you.
    Warmly,
    Joanne
    Remember...Thoughts become things - choose the good ones!
  • PGLGreg
    PGLGreg Member Posts: 731
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    Somewhat similar.
    I found blood in my stool and was diagnosed with rectal cancer 4 years ago. I had surgery Dec 2, 2005, recovered to have a fairly nice Christmas. Like you, I had no chemotherapy or radiation until after my surgery, and after New Year's. I didn't let it spoil my holidays. Now, I have one more year of surveillance tests before I'll be considered cured.

    --Greg
  • Fight for my love
    Fight for my love Member Posts: 1,522 Member
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    You will be
    You will be fine,relax.Please try not to let the whole thing overwhelm you,but I do understand it is easier to say than do.My husband was diagnosed with rectal cancer stage 2A in this May,it was a big big shock to both of us.He did the radiation and chemo before surgery,he had great response to the preoperative treatment,his tumor got shrank by 90% from a like pingpong ball size to a size much smaller than a dime,only very little leftover.The surgery went quite well,the surgeon got all of it.The pathology report showed the cancer was downstaged from stage 2 to stage 1.After 8 weeks recovery from the surgery,my husband started more chemo(Folfox) to make sure there is no potential cancer cells left in the body.Both oncologist and surgeon recommemed more chemo,because they say they want to make sure my husband will be cured completely.My husband just finished 5 of 12 rounds chemo,he is going to complete the whole treatments in the spring time.Chemo is tough,but we take one day at a time,take one treatment at a time like many people do in this forum.Please really get involved in the treatment and understand the disease,the more you know about it,the better you cope with it.It sounded like your tumor is not big and you found it early,so you do have great chance to beat the cancer up and you will be cancer free soon.Good luck with everything.Take care.
  • maryjane
    maryjane Member Posts: 71
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    JDuke said:

    MaryJane
    Welcome to this amazing group of people. I am sorry that you have had to seek us out, but this site will bring you unbelievable comfort in the days ahead. There are many here who have been through what you will be experiencing. I have squamous cancer of the anal canal, which is different than yours, so my treatments would not compare. Rest assured you will hear from many members that will be able to provide you with a wealth of information and personal victories with this beast. It is very overwhelming at first, but as you said, once you have a plan in place, that feeling of having some control helps. I hope you can enjoy today, think positive thoughts; I will be praying for you.
    Warmly,
    Joanne
    Remember...Thoughts become things - choose the good ones!

    Thanks J...for your wonderful response!
    I appreciate your response and would like to correspond with you. I have 3 days before I begin to prepare for surgery. Having seen 3 colorectal surgeons--I chose Dr. H because he seemed so much more sensitive to my needs.Others just treated me as a number and I felt totally depersonalized. I had to decide between the advised plan--to get chemo/rad first to shrink the tumor but--from everything I've read--it really does a number on your body. I'm hoping to join a naturapathic Dr after surgery to build up my immune system. For the first day...Xmas Day..I feel a sense of relief that at least I know this mass will be removed. But..what kind of shape my body will be in is what is soooo fear finding. I am so healthy right now--what will bm's be like after operation? Lots of ?'s and lots of prayer!
    I"m trying hard to CHOSE THE GOOD THOUGHTS as you mentioned. Merry Xmas!
    MJ
  • maryjane
    maryjane Member Posts: 71
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    PGLGreg said:

    Somewhat similar.
    I found blood in my stool and was diagnosed with rectal cancer 4 years ago. I had surgery Dec 2, 2005, recovered to have a fairly nice Christmas. Like you, I had no chemotherapy or radiation until after my surgery, and after New Year's. I didn't let it spoil my holidays. Now, I have one more year of surveillance tests before I'll be considered cured.

    --Greg

    Thanks for reassuring message...
    Hi Greg...
    So good to hear from you and such a positive outcome. My FEAR LEVEL has been off the charts and for the past month--the best I could do was interview docs and then pretend that it wasn't me--I couldn't own my diagnosis. But, Xmas Day brings me to a new stage. Just like Docs stage the tumor, I'm beginning to stage my EMOTIONS! Hopefully they won't have to drag me to the surgery!
    MJ
  • maryjane
    maryjane Member Posts: 71
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    You will be
    You will be fine,relax.Please try not to let the whole thing overwhelm you,but I do understand it is easier to say than do.My husband was diagnosed with rectal cancer stage 2A in this May,it was a big big shock to both of us.He did the radiation and chemo before surgery,he had great response to the preoperative treatment,his tumor got shrank by 90% from a like pingpong ball size to a size much smaller than a dime,only very little leftover.The surgery went quite well,the surgeon got all of it.The pathology report showed the cancer was downstaged from stage 2 to stage 1.After 8 weeks recovery from the surgery,my husband started more chemo(Folfox) to make sure there is no potential cancer cells left in the body.Both oncologist and surgeon recommemed more chemo,because they say they want to make sure my husband will be cured completely.My husband just finished 5 of 12 rounds chemo,he is going to complete the whole treatments in the spring time.Chemo is tough,but we take one day at a time,take one treatment at a time like many people do in this forum.Please really get involved in the treatment and understand the disease,the more you know about it,the better you cope with it.It sounded like your tumor is not big and you found it early,so you do have great chance to beat the cancer up and you will be cancer free soon.Good luck with everything.Take care.

    Your report is very encouraging...
    Thanks so much for responding. I would be interested in knowing more about side effects of chemo. When you say "tough"--can you give more details? I was so shocked to read ab out Drs who refused chemo/rad because they thought it was so invasive on the body. I would appreciate knowing more of his symptoms--if you're willing to discuss.
    Thanks again...MJ
  • Fight for my love
    Fight for my love Member Posts: 1,522 Member
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    maryjane said:

    Your report is very encouraging...
    Thanks so much for responding. I would be interested in knowing more about side effects of chemo. When you say "tough"--can you give more details? I was so shocked to read ab out Drs who refused chemo/rad because they thought it was so invasive on the body. I would appreciate knowing more of his symptoms--if you're willing to discuss.
    Thanks again...MJ

    My husband actually had
    My husband actually had colonoscopy in 2005 because he found blood in the stool,the doctor only found polypus,that was benign.His follow-up was supposed to be at 2007,but because we were living overseas,he couldn't do it.Since the beginning of 2009,he found big amount of blood in the toliet,that was scary.Finally in May,the colonoscopy was scheduled and the doctor found the big mass in the rectum.Actually the chemo and radiation before surgery went quite well,my husband tolerated the whole procedure pretty well,because the chemo was only 5-fu,it didn't bring many side effects to my husband but fatigue.When my husband was feeling well enough,he still went to field to visit customers,but most of the time,he just did lots of phone supports for the customers in the office with his boss's support.

    The chemo now is folfox including 5-fu,leucovorin plus Oxaliplatin.Leucovorin is not chemo,it is just Folinic acid,it creats something that increase the effectiveness of 5-fu.Oxaliplatin is a platinum-based cancer chemotherapy drug,it is really nasty because it has many side effects,from my husband's experience,the biggest problem now is neuropathy for his fingers and dry skin on hands.But oncologist can always reduce the dosage or skip one or two round without Oxaliplatin,or just totally stop it at the last few treatments.You can go to a website:http://chemocare.com/ to learn about the side effects and how much chance it may happen.Please don't worry about the side effects so much right this moment,because each individual is so different,some people may experience the side effects,you may not at all.Anyway hope everything goes well with you.Happy holidays.
  • cowman
    cowman Member Posts: 61
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    Hi MaryJane
    My husband had a very similar situation in May 2009 - took some medicine which caused rectal bleeding and checked it out to find adenacarcinioma also in the rectal area. He did opt to go through with the radiation/chemo before surgery. Since you are not doing that I won't go into that but he had surgery in Sept and ended up with a colostomy. The tumor was similar in size to yours also. The surgery went ok and there are alot of pain meds available which helps! He is now taking chemo - Folfox. You asked about the side effects- he has had minimal problems so far and he is on his 4th treatment. I think from reading on this site, the effects will be more noticeable each time. My 80 year old aunt went though it so I know he'll be ok too. It isn't fun, but something that he has to work through. Again, there are meds that are helping. Mostly right now he is tired and has some sensitivity to cold. (Grabbing a cold can of pop tingles.) He will be taking 12 treatments to finish in April.
    You are very normal with all of your feelings but it sounds like you are doing the right thing in your research. You have to feel good about what is going on with YOU. We will be thinking of you and your upcoming surgery. Please check back in and let us know how you are doing.
  • qwe
    qwe Member Posts: 124
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    cowman said:

    Hi MaryJane
    My husband had a very similar situation in May 2009 - took some medicine which caused rectal bleeding and checked it out to find adenacarcinioma also in the rectal area. He did opt to go through with the radiation/chemo before surgery. Since you are not doing that I won't go into that but he had surgery in Sept and ended up with a colostomy. The tumor was similar in size to yours also. The surgery went ok and there are alot of pain meds available which helps! He is now taking chemo - Folfox. You asked about the side effects- he has had minimal problems so far and he is on his 4th treatment. I think from reading on this site, the effects will be more noticeable each time. My 80 year old aunt went though it so I know he'll be ok too. It isn't fun, but something that he has to work through. Again, there are meds that are helping. Mostly right now he is tired and has some sensitivity to cold. (Grabbing a cold can of pop tingles.) He will be taking 12 treatments to finish in April.
    You are very normal with all of your feelings but it sounds like you are doing the right thing in your research. You have to feel good about what is going on with YOU. We will be thinking of you and your upcoming surgery. Please check back in and let us know how you are doing.

    MaryJane last year Dec 17
    MaryJane last year Dec 17 2008 I was told I had rectal cancer I also seen blood in my stool.I did not start treatment till Jan 26 2009 chemo and radiation then surgery March 26Th I now have a colostomy and learned to live with it ,it was hard in the beginning but I am copping now I went back to work Aug 1 2009 after being out of work fore 7 months.So I know first hand what you are going through last year the holidays sucks I was going crazy like you now and was on the computer looking up things.Hang in there hun it does get better.

    I have not been here for a wail cause I was still feeling so bad about having a colostomy
    reading all the sad news put me in a depression but I am on meds now and feel much better.

    Keep the faith.
  • Annabelle41415
    Annabelle41415 Member Posts: 6,742 Member
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    Sorry
    So sorry for your news and I'm glad you found us. I was diagnosed a day before Thanksgiving one year ago and I know your agony. After that I faced some hard decisions and some grueling realities. I know that my case was brought before 12 board members (all doctors of cancer of every type and disease known) and when I was brought to my first doctor appointment I was told what the "all board members" discussed and decided on my treatment. I felt so comfortable that I was brought before a board. You as a researcher should know that not all information on the internet is up to date so please rest assured that this information is so outdated. Wait until you see your outcome of surgery and what they say. I wish the best for you. You have joined a great group and I wish the best for you.

    Kim
  • mgrinager
    mgrinager Member Posts: 1
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    I was diagnosed with rectal
    I was diagnosed with rectal cancer Nov 18th 2009, which was also the day my divorce was final, talk about stress...My care giver is the Veteran's Administration Hospital in Ft. Wayne. I have never been treated with more dignity,kindness, or encouragement. My doctors (who actually practice at other hospitals)have me on chemo and radiation, to be followed by surgery and more chemo. The chemo is Xeloda, it is in pill form,500mg 8 per day, and will be increased to 10 per day Tuesday. 28 sessions of radiation, 8 down 20 to go. I work 3rd shift, done at 8am, get to Radiation Oncology Associates for radiation at 8:30 and I am on my way by 8:45am! Side effects so far, fatgue (I have 10 good hours then it's lights out)loss of apetite, diarhea, and a third eye. Not really, but you need to keep a sence of humor and learn to appreciate EVERYTHING, good and bad, that's life. My doctors feel that the chemo/rad prior to surgery increases your survival rate. What did your reseach tell you?
  • PGLGreg
    PGLGreg Member Posts: 731
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    mgrinager said:

    I was diagnosed with rectal
    I was diagnosed with rectal cancer Nov 18th 2009, which was also the day my divorce was final, talk about stress...My care giver is the Veteran's Administration Hospital in Ft. Wayne. I have never been treated with more dignity,kindness, or encouragement. My doctors (who actually practice at other hospitals)have me on chemo and radiation, to be followed by surgery and more chemo. The chemo is Xeloda, it is in pill form,500mg 8 per day, and will be increased to 10 per day Tuesday. 28 sessions of radiation, 8 down 20 to go. I work 3rd shift, done at 8am, get to Radiation Oncology Associates for radiation at 8:30 and I am on my way by 8:45am! Side effects so far, fatgue (I have 10 good hours then it's lights out)loss of apetite, diarhea, and a third eye. Not really, but you need to keep a sence of humor and learn to appreciate EVERYTHING, good and bad, that's life. My doctors feel that the chemo/rad prior to surgery increases your survival rate. What did your reseach tell you?

    "My doctors feel that the
    "My doctors feel that the chemo/rad prior to surgery increases your survival rate."

    That's my understanding, though I don't think the difference is major. I had chemoradiation after surgery because my colonoscopy had left it unclear whether my tumor was in the rectum. It might have been a colon cancer, in which case I wouldn't have needed radiation. Surgery made it clear that it was rectal.

    --Greg
  • VickiCO
    VickiCO Member Posts: 917
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    MaryJane
    My diagnosis (Oct 22, 2008) is similar to yours. My tumor was 2cm by 4cm and located just inside the rectum, very, very low. I did opt for the chemo/radiation before surgery and it was successful in that the tumor was eradicated, but not the total cancer. I had surgery in Feb 09, then more chemo into the summer, finishing in June. My rectal damage was too severe and in Nov I finally opted for a colostomy - best decision I've made since the cancer diagnosis. I have my life back. It takes some getting used to - I am still learning after 6 weeks - but it really was the best option for me.

    I wish you the best and pray that your surgery is successful. My holidays last year were a 'nightmare', as you say, but here I am a year later, cancer free and enjoying life. Never give up hope. There is so much they can do to help us.

    Many hugs, Vicki
  • maryjane
    maryjane Member Posts: 71
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    mgrinager said:

    I was diagnosed with rectal
    I was diagnosed with rectal cancer Nov 18th 2009, which was also the day my divorce was final, talk about stress...My care giver is the Veteran's Administration Hospital in Ft. Wayne. I have never been treated with more dignity,kindness, or encouragement. My doctors (who actually practice at other hospitals)have me on chemo and radiation, to be followed by surgery and more chemo. The chemo is Xeloda, it is in pill form,500mg 8 per day, and will be increased to 10 per day Tuesday. 28 sessions of radiation, 8 down 20 to go. I work 3rd shift, done at 8am, get to Radiation Oncology Associates for radiation at 8:30 and I am on my way by 8:45am! Side effects so far, fatgue (I have 10 good hours then it's lights out)loss of apetite, diarhea, and a third eye. Not really, but you need to keep a sence of humor and learn to appreciate EVERYTHING, good and bad, that's life. My doctors feel that the chemo/rad prior to surgery increases your survival rate. What did your reseach tell you?

    Hi...
    mgrinager...thanks for your message. Sounds like you are handling a difficult situation very well. Yes..I have certainly learned to appreciate the good in life and have lots to be grateful for. I was also advised about increasing my survival rate with rad/chemo but...just wanted the docs to know exactly what they were dealing with before getting chemo/rad. And..I had spent a month researching which delayed removal of the tumor so I decided I wanted it out first--then take the next indicated step. My Doc was very flexible. I get my surgery tomorrow morning and spent yesterday and last nite digesting the FOOD PRODUCT that keeps you close to the bathroom. This is my 2nd day on juices and broths and my stomach sounds like a run away train. My tumor was 2cm and is 7.5 cm from the base of the rectum. So--getting it out might be difficult and not leave them enough room. But--I'm trying to live JUST FOR TODAY and that's how I'm getting thru this challenge. How are you doing?
    maryjane
  • maryjane
    maryjane Member Posts: 71
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    PGLGreg said:

    "My doctors feel that the
    "My doctors feel that the chemo/rad prior to surgery increases your survival rate."

    That's my understanding, though I don't think the difference is major. I had chemoradiation after surgery because my colonoscopy had left it unclear whether my tumor was in the rectum. It might have been a colon cancer, in which case I wouldn't have needed radiation. Surgery made it clear that it was rectal.

    --Greg

    Chemo/Radiation after surgery...
    Hi Greg...
    Really appreciated hearing from you. How are you dong with chemo treatments??..
    I'm assuming that I will need some of that treatment as well but...I'm trying to put it off as long as possible. My surgery is tomorrow morning and...I've take the CLEAN OUT YOUR BOD product. Of course I'm thinking all about steaks and baked potatos and french fries etc now that I can't have it. I was diagnosed 4 weeks ago (day before Thanksgiving) and had to do the same prep for the colonoscopy I had in the hospital. These are not my favorite drinks and my stomach HOWLS as the Liquid Plummer moves thru my body. My motto is JUST FOR TODAY and Today I'm still walking and a'talkin so that's a good thing. Tomorrow at this time I'll be facing the pre-surgery anxiety. Thanks for your support.
    maryjane
  • maryjane
    maryjane Member Posts: 71
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    PGLGreg said:

    "My doctors feel that the
    "My doctors feel that the chemo/rad prior to surgery increases your survival rate."

    That's my understanding, though I don't think the difference is major. I had chemoradiation after surgery because my colonoscopy had left it unclear whether my tumor was in the rectum. It might have been a colon cancer, in which case I wouldn't have needed radiation. Surgery made it clear that it was rectal.

    --Greg

    Chemo/Radiation after surgery...
    Hi Greg...
    Really appreciated hearing from you. How are you dong with chemo treatments??..
    I'm assuming that I will need some of that treatment as well but...I'm trying to put it off as long as possible. My surgery is tomorrow morning and...I've take the CLEAN OUT YOUR BOD product. Of course I'm thinking all about steaks and baked potatos and french fries etc now that I can't have it. I was diagnosed 4 weeks ago (day before Thanksgiving) and had to do the same prep for the colonoscopy I had in the hospital. These are not my favorite drinks and my stomach HOWLS as the Liquid Plummer moves thru my body. My motto is JUST FOR TODAY and Today I'm still walking and a'talkin so that's a good thing. Tomorrow at this time I'll be facing the pre-surgery anxiety. Thanks for your support.
    maryjane
  • maryjane
    maryjane Member Posts: 71
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    VickiCO said:

    MaryJane
    My diagnosis (Oct 22, 2008) is similar to yours. My tumor was 2cm by 4cm and located just inside the rectum, very, very low. I did opt for the chemo/radiation before surgery and it was successful in that the tumor was eradicated, but not the total cancer. I had surgery in Feb 09, then more chemo into the summer, finishing in June. My rectal damage was too severe and in Nov I finally opted for a colostomy - best decision I've made since the cancer diagnosis. I have my life back. It takes some getting used to - I am still learning after 6 weeks - but it really was the best option for me.

    I wish you the best and pray that your surgery is successful. My holidays last year were a 'nightmare', as you say, but here I am a year later, cancer free and enjoying life. Never give up hope. There is so much they can do to help us.

    Many hugs, Vicki

    Colostomy...
    Hi Vicki...
    Thanks for your message. Sounds like in the end the colostomy was your answer. First surgeon I saw talked about Colostomy and I couldn't even listen to the words. Now I've accepted that it may be my fate as well. I'm dealing with the unknown at this point. My surgery is tomorrow morning--30th--and I'm sooo anxious to just GET IT OUT! (TUMOR) Drinking all that product last nite to get cleaned out...spending the night in my bathroom was not my favorite experience. So...I continue to fantasize about Hamburgers and Fries as my stomach cries out for food. And then I drink down some clear liquid and imagine it to be ice cream. Good I have an imagination at this time.
    And..thanks to all of you strong beings who continue to support me thru this Holiday Crisis. And thanks for sharing your feelings. MaryJane
  • maryjane
    maryjane Member Posts: 71
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    VickiCO said:

    MaryJane
    My diagnosis (Oct 22, 2008) is similar to yours. My tumor was 2cm by 4cm and located just inside the rectum, very, very low. I did opt for the chemo/radiation before surgery and it was successful in that the tumor was eradicated, but not the total cancer. I had surgery in Feb 09, then more chemo into the summer, finishing in June. My rectal damage was too severe and in Nov I finally opted for a colostomy - best decision I've made since the cancer diagnosis. I have my life back. It takes some getting used to - I am still learning after 6 weeks - but it really was the best option for me.

    I wish you the best and pray that your surgery is successful. My holidays last year were a 'nightmare', as you say, but here I am a year later, cancer free and enjoying life. Never give up hope. There is so much they can do to help us.

    Many hugs, Vicki

    Colostomy...
    Hi Vicki...
    Thanks for your message. Sounds like in the end the colostomy was your answer. First surgeon I saw talked about Colostomy and I couldn't even listen to the words. Now I've accepted that it may be my fate as well. I'm dealing with the unknown at this point. My surgery is tomorrow morning--30th--and I'm sooo anxious to just GET IT OUT! (TUMOR) Drinking all that product last nite to get cleaned out...spending the night in my bathroom was not my favorite experience. So...I continue to fantasize about Hamburgers and Fries as my stomach cries out for food. And then I drink down some clear liquid and imagine it to be ice cream. Good I have an imagination at this time.
    And..thanks to all of you strong beings who continue to support me thru this Holiday Crisis. And thanks for sharing your feelings. MaryJane
  • zenmonk
    zenmonk Member Posts: 198
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    maryjane said:

    Colostomy...
    Hi Vicki...
    Thanks for your message. Sounds like in the end the colostomy was your answer. First surgeon I saw talked about Colostomy and I couldn't even listen to the words. Now I've accepted that it may be my fate as well. I'm dealing with the unknown at this point. My surgery is tomorrow morning--30th--and I'm sooo anxious to just GET IT OUT! (TUMOR) Drinking all that product last nite to get cleaned out...spending the night in my bathroom was not my favorite experience. So...I continue to fantasize about Hamburgers and Fries as my stomach cries out for food. And then I drink down some clear liquid and imagine it to be ice cream. Good I have an imagination at this time.
    And..thanks to all of you strong beings who continue to support me thru this Holiday Crisis. And thanks for sharing your feelings. MaryJane

    praying for you
    Hi, My prayers go out to you. I also had a tumor at the base of my rectum. Unfortunatley when they are at the base it makes it harder to hook everything back up so I now have a colostomy. I cried when I heard it was permanent. I stopped crying when I realized that little stoma saved my life for at least now and maybe for a long time in the future. Be aware that the blood flow from the rectum drains into the liver. My tumor was removed succesfully but the cancer was still in my blood and ended up in my liver. So no matter what the doctors tell you. Get checked after your surgery frequently. I left the hospital with a clean bill of health. Zero pathology. Given a 95% chance at a full recovery. 11 months later tumors show up in my liver. Stay on top of things even if the doctors dont.
  • PGLGreg
    PGLGreg Member Posts: 731
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    maryjane said:

    Chemo/Radiation after surgery...
    Hi Greg...
    Really appreciated hearing from you. How are you dong with chemo treatments??..
    I'm assuming that I will need some of that treatment as well but...I'm trying to put it off as long as possible. My surgery is tomorrow morning and...I've take the CLEAN OUT YOUR BOD product. Of course I'm thinking all about steaks and baked potatos and french fries etc now that I can't have it. I was diagnosed 4 weeks ago (day before Thanksgiving) and had to do the same prep for the colonoscopy I had in the hospital. These are not my favorite drinks and my stomach HOWLS as the Liquid Plummer moves thru my body. My motto is JUST FOR TODAY and Today I'm still walking and a'talkin so that's a good thing. Tomorrow at this time I'll be facing the pre-surgery anxiety. Thanks for your support.
    maryjane

    Good luck tomorrow.
    How am I doing with chemo? I finished a light chemo treatment (10 injections of 5FU+leucovorin) while I was getting radiation treatments back in February 2006. It was no big deal. You'll probably be just fine.

    --Greg