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
  • Hello, I have came on here to just try and seek some comfort and reassurance and I know that there isn’t much of this around this awful disease. Your mums story has really touched me. My Dad has treatment stopped for NSC lung cancer in August his decision as he was informed there was not much else they could do medically. 

     

    Unfortunatley I feel we are now watching my dad come to the end of his life and it is heartbreaking. I am trying to be strong for my mum but watching his suffering is just so painful. He’s been so brave but does not have any contact with nurses since covid (they do offer) but in the current pandemic he knows if he goes to hospital he will be away from his family and isolated in his last days/weeks months. And this is really what I come to ask can anyone give me any relative ideas of time frames he does not have oxygen it’s not that I don’t think he needs this but he has not been reassessed in the last 4 months and has deteriorated greatly in this time. He is in bed 24/7, practically anything that he eats he vomits right away. 

     

    We are in this awful period of waiting waiting for something to happen and I feel like I would rather know if we are days or weeks away as I need to prepare my son he is only 4 and although being very brave just like his grandad is becoming really distressed from just picking up on all of these things going on. X

Reply
  • Hello, I have came on here to just try and seek some comfort and reassurance and I know that there isn’t much of this around this awful disease. Your mums story has really touched me. My Dad has treatment stopped for NSC lung cancer in August his decision as he was informed there was not much else they could do medically. 

     

    Unfortunatley I feel we are now watching my dad come to the end of his life and it is heartbreaking. I am trying to be strong for my mum but watching his suffering is just so painful. He’s been so brave but does not have any contact with nurses since covid (they do offer) but in the current pandemic he knows if he goes to hospital he will be away from his family and isolated in his last days/weeks months. And this is really what I come to ask can anyone give me any relative ideas of time frames he does not have oxygen it’s not that I don’t think he needs this but he has not been reassessed in the last 4 months and has deteriorated greatly in this time. He is in bed 24/7, practically anything that he eats he vomits right away. 

     

    We are in this awful period of waiting waiting for something to happen and I feel like I would rather know if we are days or weeks away as I need to prepare my son he is only 4 and although being very brave just like his grandad is becoming really distressed from just picking up on all of these things going on. X

Children
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