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. It has helped me. Mum was diagnosed 2 years ago with lung cancer. They were not going to do any treatment as mum has other various health issues but she told the doctor that she was not ready to die! So they have her one bout of targeting radiotherapy and it worked!. Fast track to February this year. Mum was losing a lot of weight. I hadn't noticed at first as I am with her all the time. Her voice had gone really quiet and you could hardly hear her. I thought this was a side effect of her Parkinson's. We had 5 letters cancelling mums cancer review with the cancer nurse. I contacted the Parkinson's nurse to see about mums voice and that maybe her meds need changing and she came out to visit mum. She said in her voice had nothing to do with Parkinson's as it sounded too hoarse. So I contacted cancer nurse. By this time covid had hit so nurse wouldn't see mum so I asked if she could have a CT scan. Following week she had one and on 5th May the doctor called me to say mum has 2 to 3 months at the most. I am heartbroken. I am looking after her myself and every day can be a challenge. She is so frail but is a fighter.  We have just celebrated her 81st birthday with a social distance garden party with her sons and their families which she enjoyed. In a way I am sorry the doctor gave us a time frame as I am on a count down now. 

Reply
  • Thank you for sharing your story. It has helped me. Mum was diagnosed 2 years ago with lung cancer. They were not going to do any treatment as mum has other various health issues but she told the doctor that she was not ready to die! So they have her one bout of targeting radiotherapy and it worked!. Fast track to February this year. Mum was losing a lot of weight. I hadn't noticed at first as I am with her all the time. Her voice had gone really quiet and you could hardly hear her. I thought this was a side effect of her Parkinson's. We had 5 letters cancelling mums cancer review with the cancer nurse. I contacted the Parkinson's nurse to see about mums voice and that maybe her meds need changing and she came out to visit mum. She said in her voice had nothing to do with Parkinson's as it sounded too hoarse. So I contacted cancer nurse. By this time covid had hit so nurse wouldn't see mum so I asked if she could have a CT scan. Following week she had one and on 5th May the doctor called me to say mum has 2 to 3 months at the most. I am heartbroken. I am looking after her myself and every day can be a challenge. She is so frail but is a fighter.  We have just celebrated her 81st birthday with a social distance garden party with her sons and their families which she enjoyed. In a way I am sorry the doctor gave us a time frame as I am on a count down now. 

Children
No Data