Oesophageal Cancer

Hi Everyone, 

I am new here and hoping for some advice/support. My Mum has recently been diagnosed with cancer in upper osephoagus (not sure if spelling it right). She can't swallow liquid or food and is being fed through pic line. She's vomiting lot of blood and has pain in upper back. She's in hospital currently and we are waiting on the staging full prognosis. These symptoms to me seem very advanced? Does anyone have any advice or thoughts? She is due to try have a stent fitted tomorrow. 
Thanks all, Rose

Parents
  • Hi Rose, 

    I don't like to comment because everyone's story is different and unfortunately my dad 58 wasn't lucky with this type of cancer, but only because it had spread. Praying your mums is still in one place and can be treated. 
    I wanted more to comment on the eating and drinking, this was the most painful part for me to watch and my dad refused a line and continued to struggle every single meal, it was horrible. He did have a stent which worked and opened up for a short time but unfortunately he didn't have any appetite by then. 
    Sending all my love and hope for your mum though. Every story is different and there are positives x

  • Thank you for the reply, I really appreciate you taking the time to do so. My mums has spread and is inoperable. She's having a stent fitted today, if it doesn't work then feeding tube to get her home. Did he have any radio or treatment? I think this week we will get to understand how long she's got. So very sad. Sorry to hear about your Dad xxx 

  • I'm so sorry for my slow reply. 
    My dads had not spread when they found it and he was going to have the major operation, he went through intense chemo and radio every day for 5 weeks to be told only a few weeks before the op that it had spread everywhere. He was the strongest fittest man so it shows how aggressive this is. 
    How did it go with the stent? Have you had anymore news? 
    Soft with calories was so difficult and I know it's hard at the moment to get things, but marks and spencer do a full fat custard which is calorific. Have you had any of the meal replacement shakes from the doctor? Xx

  • Hi, how is it going for your mum? My husband was diagnosed with this cancer last April and passed away 2 weeks ago.  he was stage 4 when diagnosed  ( large tumors already in liver), had chemo which shrunk it for a while,  but unfortunately it took off again...some people do better then others with it, I wish her luck xx

Reply
  • Hi, how is it going for your mum? My husband was diagnosed with this cancer last April and passed away 2 weeks ago.  he was stage 4 when diagnosed  ( large tumors already in liver), had chemo which shrunk it for a while,  but unfortunately it took off again...some people do better then others with it, I wish her luck xx

Children
  • So sorry to hear about your husband, thank you for the information I will share the outcome with my Mum as she's being seen now x Thank you for the support x

  • Hi Plebbs, my mums is in Liver also. She starts chemo in 2 weeks, any advice for supporting her that helped your husband?

  • Oh Rose..

    I am so sorry about your poor Mum. I hate hearing about people's precious mum and/or  dad being struck by this disgusting disease. Both my parents had cancer dad died 2012 after stomach cancer for a number of years and mum passed away 9 April not from her stomach cancer but from Covid 19 it's been a hideous year. 
    I truly wish the best for your mum. I hope all her treatments will control this horrid thing. Take care and if you need to talk I'll be there.

     

    helen

  • Hi Rose, 

    My husband (62 and reasonably active on diagnosis) had 6 rounds of ecx chemo (his cancer is oesophagus stomach junction with mets in liver). He had IV cisplatin and Epirubacin 3 weekly and caceptabine oral cemo every day. Palliative care as his is stage 4.

    From his experience I would say to your Mum trust her instincts, if she doesn't feel well during the treatment don't be scared to ask for a break and don't be frightened  to ask questions.  There was a Doctor on the chemo unit who acted as a go between us and the oncologist in between treatments if we  needed help or advice. 

    If she has a sore mouth ask for mouthwash, for sore fingers (the skin split on the ends of his) they have a medicated tape which should be available on prescription.  For sore /dry skin on the hands and feet there is a fabulous cream which you can buy on Amazon called udderley smooth.

    Lastly if she's able to eat reasonably well at this stage try to build her up because as the treatment goes on in our experience the desire to eat diminishes.

    I hope she gets on ok with the treatment and best wishes to you both.

  • Sorry got delayed reply, sorry to hear about your awful time. Thank you for your kind words x 

  • Hi Daisy, 

    Thank you for your message. Mum was diagnosed April 1st, she was admitted into hospital as emergency as she stopped being able to swallow and was vomiting a lot of blood. It is squarmous cell carcinoma stage 4 spread to liver and nodes in lung chest and neck and suggestive developent in lungs. She had a stent fitted and has since been able to eat purée foods. She started palliative chemo on Monday Cisplatin/Capebitine and so far is doing ok. The unknown is so frightening as to when she won't be so well but I guess we just take each day. We've already got the underly smooth, mum calls it utterly bitterly lol. 
    sorry to hear about your husband, was it a long illness? 

  • Hi Rose,

    Hope you and your family are well. I was hoping you would be able to offer me some advice as on the 20th of January my Dad was diagnosed with stage 4 oesophageal squamous cell carcinoma which has spread to distant lymph nodes in his neck. Since diagnosis my Dad's cancer has progressed very fast and has gone form eating soft foods to only liquids. He is now due to have a stent. 
     

    I wanted to ask about the Cisplatin and capecitabine, my Dad seemed fairly fit before diagnosis and now already appears very tired- are the side effects of this regimen tolerable and had it had a positive effect on all tumours? 
     

    R

    x

     

  • Hi Rosemary, my husband is on Capecitabine, (EOX) for stage four oesophageal, and it made him really tired on his second round, so much so that he stopped for couple of weeks and is now on a reduced dose to help him tolerate it better. He also lost his appetite completely but this has since returned so we know it is the chemo. They didn't weigh him before the second round and we wonder if the dose took into account his dramatic loss of weight...? Not sure, but anyhow you could ask about reducing if you feel he is not coping well- it's about balancing treatment and living somewhat comfortably at the same time. As for outcome we are only on round three so no scan yet to see if it is working. 
    Wishing your dad all the best x

  • Hi Rosemary 

    Sorry you find yourself here. My mum cooed very well with the chemo until cycle 5 and she had bad sickness. Sadly the chemo didn't work for my Mum. She was offered immunotherapy but didn't make it. She died 28th November. Horrible horrible disease. Please ask any questions here to support you on anything and wishing your loved one all the best xxx 

  • Hi all, 

    I only joined in July. There are soooo many of us on here in the 'Oesophageal club' - what on earth is going on!

    My 56 yr old husband diagnosed in August. Now post op and had pre op FLOT chemo, starts the post op chemo on Monday ): we also have young kids. When we first started going to the unit, there were 3 other blokes, my husband being the oldest! With exactly the same.

    As with any disease there are good outcomes and bad ones. Who knows how any of it will pan out?
    what can I say.