Life expectancy- stage 4 lung cancer experience

Thank you for your replies.

I used this forum to try and predict Mums life expectancy and reading through the posts really helped, so I knew I had to write my own experience on here.

Mum was diagnosed with stage 4 lung cancer on 13th June and died on August 15th. We did not find out what type of cancer it was as she had COPD, asthma, angina and it just wasn’t worth it. When we found out she didn’t seem hugely different than the other times she had been in hospital and the cancer was missed on so many previous scans, it was right by her heart and she always had chest infections so they assumed it was always that causing the dark blur. 

She was great, had to be on oxygen 24/7 and we wouldn’t leave her side but overall, herself! but then went into hospital as her sodium was low and caught shingles. I don’t think this had much of an effect on her timeline to be honest. About 10 days before she passed, she was more tired and confused. She then went to sleep and barely spoke from the Friday, she died on the Wednesday. The Tuesday before we washed her and she was lifeless. We stopped all medication and took her off her mask around the Saturday because she just couldn’t swallow. Signs to watch out for are confusion, being unable to swallow, becoming more tired and towards the end - the white fingertips. Everyone’s experience is different but Mums last 2.5 weeks were when she started getting confused and it went downhill from there.

She died peacefully cuddled up to me and my sister and I’m forever thankful for that. I think the anxiety of her passing at the wrong moment, without us, was the worst. 

I wish I followed my gut and left work sooner (I worked mornings up until the Friday before).

Mum wanted to celebrate Christmas early and although it was originally arranged for 11th August, we luckily moved it to the 15th July. It was great, she actually went 3 hours without oxygen (we didn’t realise!) and stayed out until 11pm. We are so lucky to of had that day, so many came and Mum was showed how loved she was whilst she was still here. I’d advise anyone to do this - build a memory that shows them going out with a bang. 

She lived with me during the last moments and my biggest regret is that I was too strong, sometimes I wish I cried my heart out and told her how scared I was to live without her. I wish she heard that from me but I know she knew deep down.

We’re lucky Mum was the strong little soul she was but I suppose that makes it so much harder without her.

The primrose nurses were the best people to get advice from, better than the doctors. Make sure everything is done how you want, you know them better than anyone else!

 

Hope this helps someone and feel free to ask questions. This forum helped me so much! Xx

Parents
  • Thank you for sharing your story with us, a lovely thing to do with your mum. My mother in law has been diagnosed with stage 4 June 12th we were told 5pm Friday evening so still a lot of unanswered questions :-( her lung is full to the top with fluid so will be drained Tuesday so hopefully she will be more comfy. We know it has spread to her Liver it's It’s just so sad completely shocked us all.

    Thank you for all sharing your stories ️

Reply
  • Thank you for sharing your story with us, a lovely thing to do with your mum. My mother in law has been diagnosed with stage 4 June 12th we were told 5pm Friday evening so still a lot of unanswered questions :-( her lung is full to the top with fluid so will be drained Tuesday so hopefully she will be more comfy. We know it has spread to her Liver it's It’s just so sad completely shocked us all.

    Thank you for all sharing your stories ️

Children
  • So sorry to hear this. My only advice is to do as much as you can, as soon as you can whilst she feels able. We found comfort in doing as mum wished and had an open house for visitors. She got very tired very quickly. I imagine all you are doing now is trying to work out if there is anything you can do and if not, the golden question of how long. Be blunt with the Macmillan nurses, ask all the questions you can. If the doctors are not answering your questions, stamp your feet a bit. Sometimes they are vague and 5 minutes a day just isn't enough. They stopped medication of my mums once and me and my sister locked myself in their office until they explained why (it was accidental!) and they administered it. Family knows best. Feel free to talk to me if needed. I obsessed over this forum but I really needed it at the time xx