Diagnosed with Oesophageal cancer

Hi was in total shock after tests revealed Stage4 Oesophageal tumour at bottom of throat an stomach. This was in Feb 2021. Went as constant sore throat an lumpy feeling swallowing. Did think might need throat stretching as had that done many years before but to be sat down an told incurable an spread to stomach nodes an small spot on liver was devastating for both me an my daughter. Saw specialist who said 3/6 months no treatment or 1 year with. Had Chemo but unfortunately 1st round got nauseous severe tingling in hands lung spasms couldn't breath an sweated buckets. Sent me home but within 3 days back on drip in hospital so Specialist said no more as wanted me to be healthy not ill. Just finished radiotherapy last tues an even drive myself but since finishing have pain where tumour is an constant nausea so had injections from nurse at home but hoping as they say this lasts no more than 10 days, that I will be able to eat. Everything revolves around food, socialising with friends, my love of food so trying to keep positive. Have decided not to have any more treatment as side effects stop me enjoying myself as get lightheaded an dizzy on medication. Have accepted diagnosis an not afraid just sad. I would say making this decision has been very hard as my family have been so against me "me giving up" but at the end of the day it has to be my decisions 

Parents
  • Hi [@JaniceMe]‍ , I'm so sorry you got such a cruel diagnosis. I think you are very brave and totally right to be making your own decisions about when treatment is or isn't worth it. 

    I got my choliangocarcinoma with liver and node spread diagnosis on April Fools Day this year. Similarly to you I've been told, on average, life expectancy 6 months without treatment or 12 months with treatment. Again like you I feel I've accepted my diagnosis. I have treatment decisions to make now and it's tough weighing up what may or may not be worth it.
     

    Am sending you strength and my admiration. It's your life and you're entitled to live it on your own terms, especially in such difficult circumstances.  
     

    LL xx

     

     

  • Hi so sorry to hear we are both battling something that is such a aggressive cancer yet so silent until we get a few symptoms. What made you go to the doctors? I had a sore throat a couple of months an Xmas day was the last straw as couldn't get my dinner down! Spent ages cooking for the family and to be honest everything does revolve around sitting down with friends or family. Just started cooking cakes during lockdown but can't enjoy them myself. Are you able to eat now without pain?  I haven't had any morphine yet. Stay strong too xx

  • Hi Janice, I hope you managed to get some sleep after your early-morning post.

    What made me go to the doctor's was discomfort under my ribs on the right hand side. My GP arranged an ultrasound to look for gallstones and although they did find a gallstone they also found abnormalities in my liver. It took quite a while to get a diagnosis because they had to find out if it was cancer of the bile ducts in the liver or cancer of the liver. They're sure now it is bile duct cancer (cholangiocarcinoma). 
     

    Eating is not painful but my appetite has really shrunk. I've been taking morphine (slow release and oramorph) for several weeks now as the discomfort progressed quickly to pain.

     

    I've got my first Gem/Cis chemo session tomorrow. I can't believe how much my life has changed in such a short time. I can only hope that, like you, I will discover previously unknown reserves of strength! Thanks for lighting the way a bit for me. It does help to know that I'm not alone in this even if our cancers are different.

    Rachel

  • Hi hope Chemo goes not too bad.yes our lives have changed so drastically in such a short time and do not think any of us could ever be prepared for the changes we face in both mental and physical changes. I tried to get morphine patch yesterday but waited all day for a call back but no joy so will try again today. I do feel whirlwind of appointments an support (almost overwhelming for me) but then any follow up I have had to do.,I do understand that departments are busy but it appears we are unprepared for some of the side effects an pain we find ourselves getting. We are told not everyone gets this or that but most people I have talked with do get them but I don't think we get the support from the medical staff doctors etc to deal with them particularly with myself the vomiting and nausea which has meant 3 trips to hospital on a drip which afterwards I felt so much better physically and mentally more able to cope. I really think the strength of cancer patients is amazing but I do feel we all need better follow up to make sure we are coping with our pain or worries. Sending huge hugs to everyone out there  
     

  • Well woke up this morning and radiotherapy must be working as been able to eat solids without pain. Still got sure throat but nurse has given me prescription to cope with that an I can cope with that. Just had rice and veg followed by rice pudding without any heartburn. Regretting giving away my bigger clothes now as think I might soon fit into them again now can eat normally lol. Take care an keep strong out there x

  • Celebrated my 65th Today. Went for afternoon tea to a lovely Cotswold Hotel then spent evening overlooking hills at lovely pub. Do feel sad though as seeing what I shall be missing does depress me. My daughters an family an friends are having a get together for me on Saturday so am looking forward to that an although had a few days with chest pains which woke up today an felt really healthy. But counting my blessings I am still here 

  • Throughly enjoyed the get together my family organised for me and friends at local pub for my 65th. Balloons arcade an beautiful cake and such a fabulous day forgot all about the cancer. Long day an evening an to be honest been tired an breathless ever since. But resting today as off to Burnham for long weekend. Get my results from. C T scan tomo so everything crossed that tumour shrunk an lymph nodes not spread.

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  • Throughly enjoyed the get together my family organised for me and friends at local pub for my 65th. Balloons arcade an beautiful cake and such a fabulous day forgot all about the cancer. Long day an evening an to be honest been tired an breathless ever since. But resting today as off to Burnham for long weekend. Get my results from. C T scan tomo so everything crossed that tumour shrunk an lymph nodes not spread.

Children