Surviving Oesophageal Cancer

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Hi , I’m new to this site but wanted to share my experience of living with oesophageal cancer. I realise that I’m one of the lucky ones in that my cancer was caught relatively early and was therefore operable.

I was diagnosed with cancer of the oesophagus in February 2007 and after many tests and two sessions of chemotherapy I underwent an Ivor Lewis operation, which is major surgery to remove the cancer, and lasted around seven hours. I responded well throughout and remained only five days in intensive care before being moved to a general ward and released a week later.

Since then, I’ve continued to do well but suffer from dumping syndrome as a result of the surgery. This is an unpleasant side-effect that causes fatigue, sweating and nausea after eating. Also, I now have to have vitamin B12 injections every three months as my body can no longer process this essential vitamin.

All in all, I feel ok and have remained positive all the way through. I realise I’m extremely lucky and count my blessings every day.

I’ve read so many negative reports about this type of cancer so I felt I had to share something positive for those of you who have, or know someone with, Oesophageal cancer.

All the best

Crystal

  • FormerMember
    FormerMember
    Dear Jane
    So, so sorry to hear your news. I, too, said goodbye to my husband on Wednesday; I feel for you and your family.
    Sue x
  • FormerMember
    FormerMember

    Jane

    I'm so very sorry to hear that you have lost your Nick. I will be thinking of you.

    Netty x

  • FormerMember
    FormerMember
    Jane,

    I am so sorry to hear of your loss. My heart is with you.

    Gayle x
  • FormerMember
    FormerMember
    Jane,

    I'm so sorry to hear about Nick.

    Remember we are here if you need support.

    Thinking of you mate
    Mick
    xx
  • FormerMember
    FormerMember

    Hi Netty

    I hope you are feeling a little better, if you are anything like me you will be having days where you feel you can take on the world and others where you feel absolutely wretched. As for my thoughts about your ongoing treatment; well like most important decisions it is always best to make an informed one, especially as you will ultimately have to live with the decision you make.

    [Despite the chemo sensitivity of advanced disease, adjuvant chemotherapy has not been shown to confer a survival advantage and is difficult to deliver after major oesophageal surgery. Post –resection irradiation improves the loco-regional control in patients with positive resection margins, but not if there is nodal involvement.]

    [The principals underlying pre-operative (neo-adjuvant) chemotherapy are that, in addition to down staging the primary tumor, micro-metastases are treated before the post-operative, stimulatory surge of growth factors.] [Reference: Oxford handbook of oncology second edition].

    ~Given that your resection margins were clear and that your neo adjuvant chemotherapy should have reduced the chance of any macro-metastases along with a positive biopsy showing no lymph node involvement is an excellent prognosis. I can see where your oncologist is coming from with the radiotherapy, but my opinion would be to stay away from it~. ~My unqualified opinion~.

    I was advised to receive adjuvant chemotherapy after my Ivor Lewis, when I asked what my improved chances were with treatment I was told it would give me a better chance by around 6% as my biopsy showed lymph node involvement, with hindsight it would have been better if I would have had neo- adjuvant therapy, but this was not offered as all the pre op tests were good; we don’t have a crystal ball do we. I accepted the treatment, however I was so ill from the effects of the surgery, coupled with ECX combined therapy I terminated it, and no matter what happens from now on I will not regret my decision because it was an informed one going on information and the research I had undertaken; I tend to check more than one source before coming to any conclusion and what has been quoted in italics seem to bear up from other references.

    Remember if your therapy is too much for you after surgery you can always stop it, my friend who has had the same op as you and me managed to get two cycles in before he folded, which was better than me!

    All the Best.

  • FormerMember
    FormerMember
    Hi All,

    We lost Woody on Monday 8th June, we are absolutely heartbroken but inspired by his strength and positive attitude towards life - right up until the end he was making us laugh.

    It seems like it was stomach cancer that had grown into his oesophagus, unfortunately some of the cells had escaped to his brain.
    He got encephalitis and a chest infection that he just couldn't fight.

    Woody passed away in our arms in the early hours of Monday.

    We wish all of you good luck and strength to fight your battles and in the words of Woody:
    "Accentuate the positives to eliminate the negatives!"

    Much Love,
    Woody's wife and daughters
    xxx
  • Hello to Woody’s wife and daughters
    Your news came as such a very sad shock and I’m so sorry for your loss, you have my deepest sympathy and condolences. Whenever Woody posted here it was like a breath of spring air as he was so optimistic, positive and bouncy and had a lovely gentle humour. He was an inspiration and a very brave man. Thank you for telling us about Woody, I appreciate your thoughtfulness and consideration and my heart goes out to you all.
    Woody did indeed ‘accentuate the positives to eliminate the negatives.’ When I think of Woody I smile, that is the gift he brought to this thread.
    Love Crystal xx
  • FormerMember
    FormerMember
    Well my friends,
    firstly a big thank you to you who have been in touch with me I really do appeciate it. Next an apology for not posting to often I have been a little lazy in that dept.
    Now an update, I saw the surgeon after a recent scan and before the proposed surgery, however the scan showed some small nodes on my lungs and as a result surgery is now not an option. I am due to see the oncologist on 1st July to see what is next.
    At least I am getting ovet the side effects of the last rounds of Chemo albiet slowly.
    So after a weekend of deep thought I have now adopted the mantra "Today is a good day to be alive".
    Take care all
  • FormerMember
    FormerMember

    Hi Snowdog

    Sorry to hear of your news, you must be going through hell in your mind; I hope the meditation gives you the stamina of a Snow dog and helps you stay calm and focused throughout your difficult journey. My thoughts are with you and your children at this time, life can be so cruel by continually hitting you at your lowest times.

    Good luck with your ongoing treatment plan.

  • Hi Snowdog
    I am full of admiration for you, as I know your journey at times has been very hard. You are a courageous and determined person and carry an inner strength that helps and comforts others. I hope in the coming days and months ahead you too will find strength from those close to you and especially from your friends here who can relate in similar ways. We all walk the same path here and I think we could all draw strength and peace by saying ‘Today is a good day to be alive.’
    ((((Hugs to you Snowdog)))) and thanks for your friendship.
    Love Crystal xx