Mums end of life care at home.

My mum is 73 and has total blockage of the bowel. Surgery and chemo no longer a option

 Came home to die  we have battled daily to get the care needed in the home. She now has carers in the morning  district nurses everyday. 

We have had to learn quickly that no one communicates and they assum we has a family know what where doing..

 Nope, not at all.

Bed sores, bedding  incontenience pads. Drainage bags, slip sheets, we haven't bathed her in days  bed bound and struggling to do this alone. My mums plan was to stay in her own home plan b virtual teams hospital or hospice.im increasingly concerned she's still vomiting and this is now her bowel blockage coming up and making her sick in her mouth and not always in the drainage bag. The smell is awful and she would never have this.

I'm trying so hard to with my daughter to help her but we're finding this so hard and don't know what to do for the best.i have to wait to hear from the nurse to see if she can be added to the waiting list on the virtual care ward

 So complicated. So many different organisations, it's a mindfield.

Has anyone got any advice  xxx 

  • Bless you. I’m currently caring for my mum and palliative care has just been put in place as mum doesn’t want to go to hospital or further any tests but from an xray, her spine is showing fractures and lesions. I’ve been on at the council for almost a year for a stairlift and shower, they are not moving themselves even though my mum is deteriorating. Everything has been a battle and continues to be a battle. Palliative care nurses are even chasing the council. It’s like you don’t get time to process anything because everything is a constant battle. Have you tried to speak to her GP about hospice coming in. It seems to me it’s only them that properly know what’s what and can take these kind of pressures off x 

  • Thank you for your reply  I'm so sorry you too are going through this, I have spoke to her gp and she was asking if I was OK and if I needed support too as I was crying about the prognosis and I became tearful. I'm trying to stay strong but it's hard, she's wasting away and struggling with seeing my like this xx

  • It’s a massive rollercoaster. It’s like your ok one minute then anxiety fills you in the next, I honestly know how you feel. I completely broke down at Christmas and am up and down with it all. A shadow was found on my mums lung about 5 months ago- she completely shut down and refused all scans, the lot. I have to think on my feet as it’s her wishes not to know. I’m completely in the dark with all of it. I managed to persuade her to go to her GP 2 weeks ago as her pain is getting worse. Her gp wanted her to have an xray to check for spondylitis which my mum agreed to go for, that’s when I found out of the fracture and lesions. Xx

  • Bless, my mum started this journey July 2024, bowel cancer, surgery, chemo and less than weeks after chemo in January. Diagnosed with lung, liver and stomach the  cancer, aggressive. We have been let down massively. I so wished she had the stomo and we wouldn't be in this mess. She was too weak to tolerate any chemo now or the surgery to remove the bowel. Only left to her now at this stage was palleive care. She wishes to die at home  I understand that but my mum didn't think she would end up like this and she wants to die and we have no option to end her life  we have to watch her wasting away before our eyes. 

    Devastating but what choice do we have, she's too weak now and only takes medication through her syringe driver.

    I so wish I could take it all away and back to her usual bubbly loving self

     She's was on holiday in December in benidorm. Its rapid but not able to make memories like we had arranged to once she left hospital. Not a chance of this now. She's devastated and so are we but we carnt show it. Thank you for listening. Wish you all the luck and well wishes.

    1. Emma x