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.

Parents
  • 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

     

    I too would advise, push push push.  My brother had been visiting his GP since March with fears of this dreadful cancer and was pooh poohed and told it was acid reflux.  Eventually at the end of August he had an endoscopy and a biopsy.  By this time he had lost 1 and half stones in 6 weeks.  He was rushed into hospital on 20th September, and passed away on 25th October without having had any treatment.  I could go into far more detail but would not wish to distress anyone on this forum.  It was obviously too late for him and I find it extremely upsetting that in spite of him doing the right thing and going to his doctor, (and advising the doctor that his paternal grandfather had died of the same disease) he was sent away and not seen to in sufficient time to give him a few months quality of life.  

     

    Make a nuisance of yourself, push and push for scans and tests and treasure every moment you have xx

  • Hi, SueCC, 

    I think I can safely say that chemo is no fun - no matter how it is sold.

    However, all of the club have made it through to compare the delights.BUT, it is good at what it does- ie killing rogue cells. Chemo is order of the day whether you have surgery or not.

    For the No- op option I think I  can't be sure- it is 8 cycles of whatever they use

    for the op it is 4xFLOT ( the chemo drugs) surgery then 4 more FLOT cycles.

    If he is having no trouble swallowing that is good- most of us on here that was the first symptom.

    it is likely that he will have masses of scan, tests and scopes over the next couple of weeks and it is an absolutely roller coaster- but one many of us have ridden and gotten off the other side.

    so keep us up to speed on your trials and tribulations (:

    Hilts

     

  • Thanks hilts, he's had PET scan CT scan as that's where it was picked up, he had kidney cancer 4 years ago so has yearly scans and luckily it was seen on there, or else he would have been walking round with it none the wiser.

    After reading your posts hilts Mablethorpe, Sutton on See, we live about 10 miles from them.

    Im finding this group so helpful, thank you xx

  • Awww- I loved Maplethorpe and Sutton on Sea- unspoilt, 'unreconstructed' British at its best. Millie is also a Sutton  fan. I really really liked Louth as well what a breath of fresh air that place was- small business' 'old fashioned' proper town. Lincoln next I think for a 'pop up' weekend trip (:

    We went to Maplethorpe etc about 8 weeks after husband finished his post op chemo- he even went in for a 'dip' brrrrr.

    You said it was picked up on PET, so that suggests it's small as it is not giving any symptoms?
    so might not even need the 'big' op, I've 'heard' - might not be correct, that small ones can be blasted off , using an endoscopy type 'thingy'. So, certainly one to ask the surgeons. I think it will be very important to ask what ALL the options are and in his ( the surgeons) experience what to go for. Have you been given the 'staging' yet?

    They we're quite clear with us from the start- we did ask for a straight answer- They told us they would go for curative intent, BUT no guarantees. He is at this time'  'visible disease free' , they never say cured, just clear for now . Fingers x it stays that way!
    keep asking away

    Hilts

  • Hi Hilts and all and welcome to Sue and Andy,

    Our current situation is causing us both anxiety so we are keeping everything crossed that the Colonoscopy on Tuesday doesn't show anything sinister and goes according to plan. We are both also anxious about the whole process as like everyone else Kev has to take the medication to clear his bowels but not everyone has his new plumbing and we are hoping he can cope with no food and the effects of clearing his bowels. Also I'm worried about the procedure as again his digestive system has been reduced and moved upwards. Has anyone on here had a colonoscopy after an Oesophagectomy? The good thing is we contacted his surgeon who said he could have it done. We know we have to trust the experts and just 'get it done' but naturally we are worried. We have managed to keep ourselves busy during the month long wait. In fact Hilts and Sue we went to Lincoln yesterday to the Christmas Market which was lovely.

    Anyway as I said welcome to the forum Sue and Andy. As you will have seen everyone's case is unique and whilst we or our other halves  have had the same op in reality they are all slightly different and we've all had different journeys/complications and on going issues.If you've read the posts you will know what I mean. We had a longer wait than most between diagnosis and the start of treatment 14 long weeks during COVID restrictions too. However as Hilts said a few of us have managed to get away on holidays and do normal things. In fact we are due to go on a Caribbean cruise in January.  I've been amazed at the progress my husband has made and he is still taking part in the active recovery with the NHS - in fact that's who organised the trip to Lincoln. If it wasn't for the positive FIT test which is part of the National screening (which is a good) we'd be doing very nicely. This has thrown us off course and unnerved us both. 

    Andi you sound brighter so I'm hoping that you are making progress and feeling a bit better. 
    Hilts so pleased to hear that your husband isn't coughing! 

    I think Hilts and Andi have answered the questions but please feel free to ask anything. I may not answer straight away as I'm stressed myself at the moment. 
     

    keeping the faith for everyone 

    Milly
     


     

     


     

     

  • Oh Milly - I feel for you - only another few days to wait. We must plan a celebration knees up - on this site - for next summer - when we are ALL loads better. I'm due to go away on 13 January to Tenerife with ALL my lovely family (20of us) but my consultant is saying no at the moment but has agreed to see me on 29 December to make a final assessment.  Everything crossed as two of my grandchildren are going to be there from Australia and Canada - haven't seen them for 3 years - mainly due to Covid  - will be gutted if I can't go!!! Trying to stay positive 

    Keeping the faith for EVERYONE 

    Andi xxxx

  • Thanks Andi,

    I really hope that you can go to Tenerife with your family who sound wonderful especially as you've not seen two of your grandchildren for such a long time. Good the consultant is seeing you on 29th December and everything crossed that he says you can go. 
     

    Are you able to do a bit more? How is your breathing now you've had the hernia op? It sounds like it was a success.

    Keeping the faith still for everyone 

    Milly


     

     

  • Hi Milly

    Yes - had the hernia op on 14 November - they've hopefully put everything back where it should be!!  6/7 hour op again and although keyhole - he said I have many internal stitches. Doing a bit more but can't lift anything or drive. Said I must wait 6 weeks!!  I do feel better and can breathe again - always good!!   The consultant is a gem and I will be guided by him - I think!  Just bored and lonely!! (think I'm feeling a bit sorry for myself - not good)

    Keeping the faith

    Andi xx
     

     

  • Hi Andi,

    That sounds positive. Yes breathing is good! Really pleased that's better as it's very debilitating and frightening. It is always best to be guided by them - they are the experts. I've had two total hip replacements first one when I was 50 and second one at 55 - followed the rules and made a really good recovery both times. Nothing compared to the op you guys have had though.

    I think you are allowed to feel a bit sorry for yourself you've been through a lot. I sometimes feel sorry for myself and I've not even had the operation! These dark days don't help but hold on in there as it will soon be the shortest day and then we are back on the way to longer days again! I've been singing with the choir this weekend so that's been good. 

    keeping the faith

    Milly.  
     

     


     

     

  • Hi Milly, that sure sucks after what your husbands been through, yes I've read all 80 pages and seem to know you all. Looks like both our husbands have thing done on Tue, fingers crossed for them.

    Was the market busy? last time we went it was packed.

    How do you all manage to get travel insurance? We should have been on holiday now, I didn't have to cancel it as Doncaster Airport shut down and tui just refunded. I think insurance will cost a fortune, Martin will be 80, Kidney cance, Lymphoma cancer and now this (whatever it's called) I have bladder cancer (10 years clear)  so not much chance of traveling abroad.

    Hilts we live in Louth it's ok better than a lot of places I guess.

    [@Andi1947]‍  I really hope you get to Tenerife, that's where we should be now, I have everything crossed for you. 
    Good luck everyone x

  • Hi Sue,

    Yes you do feel as if you get to know people on this forum and you know their darkness moments as well as their good news. If the routine test hadn't been sent we wouldn't be worried as my husband is doing really well. The sample has tested positive for blood but he can't see anything. Just got to wait and hope everything is Ok. Re your husbands laparoscopy it is an operation and I read were it's better to not lie on your side for a few days after the operation  due to the gas they pump into you. My husband did this and didn't seem to have the pain some people seem to report. I hope you get the answers that you want. Everything crossed for them  both. It does sound like they are quick. 

    Re travel insurance my husband is 64 and is over a year post treatment so he was able to get insurance obviously he had to pay more but he got it. 

    The Christmas market wasn't too busy but we did leave at 3 o clock so probably busier later on.

    Keeping  the faith for everyone 

    Milly

     


     

     


     

     


     

     

Reply
  • Hi Sue,

    Yes you do feel as if you get to know people on this forum and you know their darkness moments as well as their good news. If the routine test hadn't been sent we wouldn't be worried as my husband is doing really well. The sample has tested positive for blood but he can't see anything. Just got to wait and hope everything is Ok. Re your husbands laparoscopy it is an operation and I read were it's better to not lie on your side for a few days after the operation  due to the gas they pump into you. My husband did this and didn't seem to have the pain some people seem to report. I hope you get the answers that you want. Everything crossed for them  both. It does sound like they are quick. 

    Re travel insurance my husband is 64 and is over a year post treatment so he was able to get insurance obviously he had to pay more but he got it. 

    The Christmas market wasn't too busy but we did leave at 3 o clock so probably busier later on.

    Keeping  the faith for everyone 

    Milly

     


     

     


     

     


     

     

Children