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
  • We are currently going through a similar think with my mum, she has had a really bad chest since July but due to her having copd etc the doctors were just giving her numerous antibiotics and steroids over the phone and never once gave her and appointment due to Covid regulations , she then lost her voice mid December doctor told us over the phone it was laryngitis do to her persistent chest infection, she also started with really bad back pain on Christmas Day but due to her having osteoporosis, fibromyalgia and arthritis they put it down to a bad back i fact her sick notes since November have simply stated "bad back and flu like symptoms" by last month she could hardly stand up, We wasn't happy with the doctors keep fobbing her off so we contacted 111 who sent an ambulance for her, we were told 3 weeks ago that she has lung cancer as due to the size of the tumour and also being so close to her heart there was nothing they could do, she also has spinal and skull metastasis which is the reason she can no longer even stand up, she has been having some confusion since  the day before she went in to hospital and is in a lot of pain with her back and  stomach (she is only 57), the original doctor who gave us the diagnosis pretty much said worst case scenario 3 months life expectation (his exact words) but seeing how poorly she is I don't believe she has anywhere near 3 months left, a different doctor I spoke to also said they agreed with me that ( well they said they was on the same page as me that she didn't have 3 months left), she also hasn't eaten hardly anything since before she went in to hospital (so probably 6 weeks now),am I right in thinking that 3 months plus is a crazy suggestion or is the doctor about right,  she is saying she is ok and isn't in pain even though she obviously is in a lot of pain, she refused oral pain relief while she was in hospital and told us that she just wanted to come home and would take her medication when she was at home, she has been home for 2 days and still refusing all medication whether it is us or the carers trying to give it to her, she even refusing for Any one to even so much as give her a wash, she is also getting annoyed when the carers are asking her if she is ok or if she wants anything and it's the same the district nurse, has anybody else experienced this with their family members 

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  • We are currently going through a similar think with my mum, she has had a really bad chest since July but due to her having copd etc the doctors were just giving her numerous antibiotics and steroids over the phone and never once gave her and appointment due to Covid regulations , she then lost her voice mid December doctor told us over the phone it was laryngitis do to her persistent chest infection, she also started with really bad back pain on Christmas Day but due to her having osteoporosis, fibromyalgia and arthritis they put it down to a bad back i fact her sick notes since November have simply stated "bad back and flu like symptoms" by last month she could hardly stand up, We wasn't happy with the doctors keep fobbing her off so we contacted 111 who sent an ambulance for her, we were told 3 weeks ago that she has lung cancer as due to the size of the tumour and also being so close to her heart there was nothing they could do, she also has spinal and skull metastasis which is the reason she can no longer even stand up, she has been having some confusion since  the day before she went in to hospital and is in a lot of pain with her back and  stomach (she is only 57), the original doctor who gave us the diagnosis pretty much said worst case scenario 3 months life expectation (his exact words) but seeing how poorly she is I don't believe she has anywhere near 3 months left, a different doctor I spoke to also said they agreed with me that ( well they said they was on the same page as me that she didn't have 3 months left), she also hasn't eaten hardly anything since before she went in to hospital (so probably 6 weeks now),am I right in thinking that 3 months plus is a crazy suggestion or is the doctor about right,  she is saying she is ok and isn't in pain even though she obviously is in a lot of pain, she refused oral pain relief while she was in hospital and told us that she just wanted to come home and would take her medication when she was at home, she has been home for 2 days and still refusing all medication whether it is us or the carers trying to give it to her, she even refusing for Any one to even so much as give her a wash, she is also getting annoyed when the carers are asking her if she is ok or if she wants anything and it's the same the district nurse, has anybody else experienced this with their family members 

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