osophagus cancer diagnosis

Hi,

I have recently been diagnosed with oesophagus cancer stage 3 and have come across this forum while googling, since the middle of September, I have had a plethora of tests and have been very well treated by the hospital staff, I’m starting my FLOT treatment in 9 days’ time a regime of 4 rounds 2 weeks apart then hopefully followed by surgery and then another FLOT regime.

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  • Hi guys. Sending love to you all. We have just lost my mum to this cancer after only 6 months post surgery. My advice push for the chemo after and push for all the scans you can get after too. If this had been possible for mum then she might still be here. Xx

  • hi,

    it,s sad to hear about your loss especially after your mum going through the operation i know its difficult to accept your loss especially when you read posts like mine telling others it will all be fine , god bless you and take care of yourslef and your family.

  • Yes, Ray- where are you?
    thanx Douglas. Yep for sure there will be times when things are pants, but hey ho. Such is life I guess.

    Husband has been quite lucky with his weight. He has not lost any throughout this affair, even gained 6lbs during the time when chemo improved his swallow and surgery. 
    When the dieticians told us to eat a higher fat and protein diet  post op, they were quite surprised that we eat things like jersey milk, full fat everything, no low sugar rubbish, things like ox tail and belly pork all the time. Never gone in for the  5 a day , salads in winter, type of diet. 
    'Old fashioned' , proper food any day of the week. The strange thing is that eating that sort of stuff, in normal times both our weighs are pretty stable, with BMI totally normal - whatever that is.....

  • Hi,

    Well have made it through the 4 rounds of FLOT and yes it is nuclear stuff! Round 2 was delayed by a week because of slight infection in my hickman line. It certainly had it moments during the rounds initially i thought i was going to be laid up and stuck in bed, as it happens the treatments/rounds go, The day prior to the FLOT you are put on steroids  finishing the day after treatment , I personally hit the brick wall 2 days after the steroids having no energy for a couple of days and then a steady climb back up for a few days then really back to normal. I also was anticipating being sick all the time in my experience I had a couple of occasions of feeling sick in the rounds but was prescribed medication just in case. My last treatment finished on New Years Eve, I have had a CT scan and the news from the hospital is that the tumour has shrank so they have deicided to proceed with surgey. I am to be admitted 16th Feb (my 53rd Birthday!!) A pre assesment appointment next friday including some bike test I believe to check my level of fitness? Meet the anaesthetist. With the help and support from my wife, family and friends and lots of positive messages im through it and ready for the next hurdle. Sorry for not keeping in touch, but will try and update after the next appointment. stay strong, keep safe but most of all keep positive....it does help.

     

    Ray

     

  • Fantastic news and well done for getting through your treatment so bravely. Its not easy, my husband is only on round two of eight EOX chemo, and is completely wiped out, has hardly made it off the sofa for a week and half. Wishing you lots of luck for your surgery, and recovery afterwards! You have got this. 

  • Hi Daisy

    Thank you! I was kept going will regular snacks, fruit smoothies, banana milk shake still my favourite and even an odd glass of lucazade, anything to give me a boost when i felt at my worst, kjeep strong both of you and stay positive it has certainly helped me.

  • Yay, Ray- good to have you back.

    great news that the FLOT has done its stuff. It really seems to be the proverbial dogs b****s

    you read exactly like my husband. He felt it was like Groundhog Day. Every fortnight Thursday night start the steroids, get nuke'd on the Friday, stop steroids on the Sunday, blotto for 3-4 days then better every day until time to go again.

    He had all that pre op fitness workup. Lung capacity expanding stuff, bike ride 'stress' test, nose clip etc.

    Mine is now post op. Had the whole thing done by keyhole!! OMG is that genius of a surgeon, my new best friend. He was only in for 7 days!!! 4 bullet holes, that is it!!!They chucked him out xmas eve, best present ever. He is now adjusting to eating smaller meals haha haha, not liking that one bit. Interesting though , in the 4 bedder with him were 4 guys similar ages all had the same diagnosis, surgery etc etc. What is going on with Oesophageal cancer, it seems 'catching' He still has his jejunostomy feeding tube in, but stopped them overnight last weekend.

    We recently had the pathological final staging. Gone down from a 2 to a 1b, clear margins with no lymph's. Surgeon said there was very little cancer left, mostly scar tissue. So we are now waiting to hear on whether he needs the post op chemo- we are expecting it -in for a penny and all.

    The whole thing seems a bit 'surreal' we are almost there in terms of treatment, but the emotional impact will take a lot longer to work through.

     

     

  • Hilts, So pleased to hear your husband is doing so well post op! Fantastic news about his grading, and you sound so upbeat its lovely x

  • Hi Daisy, 

    yep, it is weird, I feel very upbeat about his treatment  and it has all gone so well BUT- there is always one (: I am waiting for bad news, I am also very intolerant of other things, life in general, you know stuff like getting stuck behind a tractor, annoying adverts, other people in general (: deliberately  emotive charity ads, and all that identity politics arrrgggg watching one of those *** programmes on TV at the mo as the 'screech sirens blaring' to an 'emergency', which turns out to be a drunk on a bench, love in a public toilet ( perish the thought hahaha)or minor theivimg ,really a blue light emergency!!!!- I could of course switch it off, but hey ho. Moaning at it is far better.One thing that is really dragging me down at the mo, is my idiots of bosses, changing their mind every 5 mins. I am particularly angry at our hysterical media, they *** off the NHS day and night, claiming horror stories at ever turn, but our experience has been amazing, seeing none of what they are banging on about.

    I guess it might be called 'displacement' , who knows. The psychological will be a lot more difficult to heal I suspect.

  • hi Hilts

    hope everything is going ok , everything has gone quiet on this page 

    kind regards

    Douglas 

  • Hi Doug, 

    it has gone all quiet on here. I always think it means 3 things 1) we are all trucking along and are in reasonably good places. 2) We are mid treatment and crawling through a surreal twilight zone or 3) We all have popped off!!!- i have nightmares about 'chatting' on a thread only to find the person has checked out!!.

    As an ex nurse I have always had a rather dark sense of humour, then this diagnosis, we'll if you can't laugh what can you do eh!
    Anyhows, we are quiet, because we are good. Recovery continues, although he has a nasty 'rash' on his gut- not the wounds, I reckon it is an allergy to all the tape n stuff, annoying rather than problematic. He is walking much further now and is back driving

    Food ' discovery' is going well. He is managing to hang on to weight, only lost 6lbs since August. He even managed ( I told him not to!) eat a pie!! - left off the mash, but plenty of gravy and ate the lot!!! I despair sometimes- he only got (this time) a slightly raised heart rate. He was very pleased.

    Oncology appointment on Wednesday, to discuss if any further chemo needed. We are expecting it, despite the good pathology. In for penny and all that.

    Will update then. 

  • hi Hilts

    thats good to hear , anyway i am also doing great no more hospital visits until June you both take cars and keep in touch

    Regards

    Douglas

     

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