Newly diagnosed Oesophagus cancer

Former Member
Former Member
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Good Afternoon,

I'm hoping you'll be able to help with my lovely Mum's newly diagnosed cancer.


Mum has had trouble swallowing for many years, but had it stretched a few time no problem and managed fine.


However this year the swallowing became worse and a burning feeling in her stomach, after a few mouthfuls of food Mum felt full up. 


Dr's prescribed gaviscon and said it was heartburn. We have been with the same Dr years so he knew us well, and we trusted him. 


A few weeks later symptoms didn't improve so the Dr arranged for Mum to see the gastro team at the hospital. 

Mum was advised to have double cream, and fattening foods to help keep the weight up.


Weeks later no improvement so Mum went back to the Dr, he started her on antibiotics as he thought a fungus could be causing the burning pain.


A follow up appointment came at the gastro hospital. 

Mum had lost weight so she started on ensure milkshakes to add calories.

Mum wrote all her symptoms down and explained about the full feeling. 


Mum continued drinking the milkshakes, but the weight loss continued.

Mum was now bringing up all her food, and feeling very weak.


We weren't able to get a face to face appointment with the Dr but a telephone call.

He arranged for Mum to be seen by the gastro team at the end of October.


Mid September Mum was so sick and very worried. 

We brought her into A&E as she looked terrible, and we were all worried.

They sent her home with more antibiotics and said an appointment with the gastro team was on the system.


That week I spoke to the gastro team secretary and explained Mums symptoms. 

She was asked to come in the next day.

A barium swallow was booked that week.


So the swallow showed a problem, and the next day an endoscopy was carried out.

A 6cm tumor was discovered in Mum's gullet. 


How did all these symptoms not ring alarm bells for the Dr's????


We seen the consultant Friday and he said surgery is not an option? 


Has anyone else had this happen?? 


Please help.


Eileen 

  • Former Member
    Former Member in reply to Former Member

    Hi Bev, I was diagnosed T3N1M0 last summer.  Had chemo in Sept and Oct and surgery in Nov.  I think your op is in a couple of weeks?  Try not to worry too much about it, the care will be great.  Do take what exercise you can between now and then. Feel free to ask me any questions.  

  • Former Member
    Former Member in reply to Former Member

    Hi Nick

    Thank you for getting in touch and yes my operation is scheduled for the 18th Jan I have a meeting tomorrow with the surgeon but it would be good to hear from yourself as to what I’m in for !.....my nerves are shot to bits and I’m crying constantly when I think of it all and how much my family are worrying.

    I am doing my best with the exercising but it’s a bit of catch up as the chemo wiped me out completely then Christmas got in the way far too much over indulgence.

    I am fairly fit not overweight and try to keep active with work and day today living. This has floored me completely I think I’m still in shock and being carried along with it !

    When I read some peoples experiences of the operation it scares the life out of me.

    Kind Regards

    Bev18

  • Hello Bev,

    Good luck with your op on the 18th . 

    Like you I was quite nervous ahead of mine until a good friend of mind suggested I ' would know nothing about it' ....how true that was and it really settled me ahead of this surgery.

    I was diagnosed T3N2M0 on first diagnosis and T2N1M0 pre op following ECX Chemo.

    My full story is here ;

    https://myoesophagealcancerjourney.wordpress.com

    The words are mine and the graphics by my wonderful daughter - together we wanted to do something to help others who may embark on a similar journey as I/ we knew nothing of this disease before I was diagnosed.

    It's a long journey , made somewhat easier by a positive mind set and the love and support of family and friends - many here are a brilliant help and insight too.

    Recovery cannot be rushed, take it at your own pace. It's major surgery but they know what they are doing - listen to all the professional advice and please ask as may questions as you wish.

    Best Wishes

    Peter

  • Former Member
    Former Member in reply to Former Member

    Dear Bev18,

    It is totally natural to be nervous!  This is major surgery and that, plus being on the cancer journey, is scary stuff.  They are only doing the op because they know you can handle it.  We cried a lot before it too (and some since).  My psychologist has told me she would be worried if we were not crying.

    Exercise really is key between now and then.  Walking is just fine - how many steps can you manage?  I’d also advise you to practice standing up,from sitting down, only using your legs.  That will be very beneficial post op.

    Let me know what else I can tell you or how I can help; ask anything!

    Nick

  • Former Member
    Former Member in reply to Former Member

    Ps you can google nickscancerdiary for my story too xx

  • Former Member
    Former Member in reply to Former Member

    Hi Bev

    Your post popped up on my emails and I had to reply.

    I am sure you are more than aware of the logistics of the operation but I wanted to tell you a couple of good things. I honestly think positive thoughts really help. I also agree with Nick that exercise is key. My dad brought an exercise bike and used it during chemo, when he could and he also used it to help him get fit after his operation.

    Dad was 76 when he had his operation, four years ago now this April. My dad is absolutely living life to the full.

    My dad said that the feeling when he awoke from the operation knowing the cancer had gone was amazing.

    Make sure you do the breathing exercises after the operation!

    Good luck and take care

    Hannah x x

  • Former Member
    Former Member in reply to Former Member

    Hi Beverly, be positive and have a sense of humour. I was a smoker for about 45 years and I wasn't super fit. I came through it all ok and I am now just over 2 years post surgery and enjoying life. Ask anything you want, good luck and kind regards Frank.

  • Former Member
    Former Member in reply to Silverfox65

    Hi Peter

    Thank you so much for getting in touch it really is good to hear from others on this same journey.

    I haven't had my results for the staging from my last bout of chemo i am really hoping i get a similar result to yourself as all i did get told at Christmas via the telephone was that it HAD shrunk and i was to ' go away and have a good Christmas and get ready for the op'  i was so emotional just hearing that that i basically ran with it as it had been the only bit of positive news since my diagnosis in Aug.

    It was great to follow your journey an have more of an insight for what is to come i feel it is helping me immensely. 

    I am working right up till the day before purely to keep my mind active and give myself a different focus.

    I am just hoping and praying that when i wake i am given the news that this horrible alien invasion in my body has been got rid of !!

    Thank you and hopefully we will speak again after the op

    Kind Regards

    Bev

  • Former Member
    Former Member in reply to Former Member

    Hi Frank

    It certainly helps to have a sense of humour my family and friends have been wonderful in keeping my spirits up and although this has brought many dark moments and lots of tears at bedtime and when i let myself give in to it  I try and turn it all back around to positive thinking.

    My father has beaten cancer twice (skin cancer and bladder cancer) with a very positive attitude but unfortunately i lost my beautiful mum (Dec 17) to liver cancer (9 weeks from diagnosis) it is all a bit too much for all my family to be going through again but then this illness doesn't discriminate does it.

    Thank you for your well wishes and others on this site that have given me advise it is helping me come to terms of whats ahead, i just have to take each day at a time, its a life changer for sure but I'm this far along my journey and coped so far. I'm going to do my very best to get through the rest of this journey.

    Kind Regards

    Bev

  • Former Member
    Former Member in reply to Former Member

    Hi Hannah

    How wonderful to hear some positive news of your dad i too am hoping with all hope that i wake up to the same good news that they have removed it all !

    I have done some homework on whats to be expected but this site i think helps far more hearing other peoples experiences its real people telling you how it is if that makes sense !

    I have a cross trainer at home that i am using every other day that certainly gets me out of breath after twenty minutes the i had been given the breathing devise from the hospital to use daily so i am keeping up with that, i will do and listen to anything the experts tell me to do as long as i can come out of this with some of my life back and be able to enjoy it. Just as your dad is doing.

    Thank you for your well wishes hopefully we catch up again when I've come through the other side.

    Bev xx