DebDo

Activity

  • carm
    Debdo,
    First of all, take the oxycontin every 8 hours instead of every 12. The drug is approved for every 8 hours. The percoset is for breakthrough pain which is probably occurring the last 4 hours before you take your next oxycontin. It is okay to take the flexeral but you might not need it once you increase the oxycontin to three times a day. I used to work in pain management. Keep in mind youwill have to increase your bowel regimen so no fiber like senna but if you have colace or dulcolax stool softener. Increase your dose. If you need more help. I am here, Carm.
    December 2013
  • LMM
    Oh bother the XXX aren't terrible bad words. I forgot you have to get creative with spelling to bypass edits. D word andc r a p were x out.
    February 2014
  • LMM
    Hello Debdo. I was diagnosed with this back on Dec.18, 2012. Due to the holidays many test were not scheduled until Jan of 2013. It was a sigmoidoscopy done on 12/18/12 that was suppose to tell us why the prescription for internal hemmroids wasn't working. That is when doc saw the tumor (3cm). From there I was scheduled for colonoscopy. That showed everything clear further up. GI doctor that did that test said tumor was late stage 1 early 2.
    Scans in Jan.2013 showed it had spread to regional and distant lymph nodes which now put me at stage 4. Treatment began Feb 7, 2013 the day after my 48th birthday. My Christmas and birthday were not joyful for me or my family. I had the cocktail of 5FU that I had hooked up to me via pouch I carried with me for 5 days 96 hours every first week of each month ( 10 months) along with cisplatin for a few hours four days of the first week of each month also. By Oct 2013, I began radiation. Six weeks worth. I had to have it postponed for a few days in Nov due to burns. During my first week of radiation, I had that lovely cocktail also and then once again during the fourth week. By April 2013, I was losing weight, mouth sores made it almost impossible for me to eat. Even soups were hard to get down because even the liquid had to pass over those damn sores. I lost my hair, became so tired, chemo brought about early menopause. I am not sure if the chemo or the fact that my hormones were whacked out.... But sleep became hard to capture. I loved to sleep used to get 8 to 10 hrs sound sleep and was able to nap during the day too. That totally disappeared. I was so damn tired but when I closed my eyes - sleep wouldn't come. It was awful, I became an insomniac. I started popping any pill I could get my hands on to induce sleep, but none of them worked well. I was lucky to get two hours of sound sleep. I was a mess. By July, I had lost 20 lbs. skinny,bald, tired and depressed I looked like a walking zombie. In August I had to return to work. Out of sick time. I worked thru the rest of chemo and radiation treatments. That was hard. On Dec19, 2013 a biopsy of the primary tumor, ct scan, petscan and ultra sound stated no evidence of the beast. Doc said the words....complete remission. I have another colonoscopy on this upcomig Monday, and scans and ultrasound for March to see whats going on in the inside. Because on the outside, if you didn't know me you would think I just had short hair. I have gained back ten of the twenty lbs I lost I am sleeping better now and depression isn't always with me. I do suffer from vaginal stenosis now but I am here. The fight was long and hard, but I am still standing. I still have bouts with depression~ my world was changed from being wonderful to what it is now. How are you handling all this?
    I turned 49 yesterday. I pray to God night and day to keep me free of this beast. I am trusting in Him to see 40 more birthdays here with my kids, husband and family.
    I will never lie to you. This journey is going to be hard on your body, maybe your mind. But you too will make it through. You have to FIGHT all the crap that is going to come with treatment.

    Please keep me posted on how you are doing. Ask any question you'd like. I will try to answer or direct you to a place or person who maybe able to. I wish you only the best.
    God bless and be with you.
    ~Lisa~
    February 2014
  • carm
    Debdo,
    Let me know if you have increased the oxy and of it has lessened the pain for you. O hope you got relief, Carm.
    December 2013
  • Pablo
    I had considerable pain after my biopsy, but once that calmed down it got a lot better. Vicodin worked well for me in combo with an Ambien at bedtime and, of course, Docusate (stool softener) and Metamucil. Also, a heating pad on my lower back and several warm baths each day helped. As radiation and chemo started having an effect on the tumor, the pain really dropped off, until, of course, the cumulative effects of the radiation took over. About three weeks after treatments ended I stopped all pain meds.
    December 2013
  • DaveWaz

    Welcome to the WhatNext family! The WhatNext family is made up of people like you who are looking for help or looking to help others. To help you along your journey the WhatNext family has put together a Beginner's Guide to Cancer that I highly recommend you check-out here: http://bit.ly/10BQKCi. Also, please do not hesitate to reach out to others or ask for help.

    Wishing you the best.

    David
    Founder, WhatNexter
    December 2013