My parents are in their early 70s. DM has MS, COPD, heart failure and a few other more minor illnesses. 2 years ago she broke her hip and this has impacted her mobility more. Now she has carers to help her shower in the morning, other than getting up and dressed she literally sit in a chair all day watching the TV and complaining. DM won’t do physio or move around or join activities or contact friends - she was like this pre - fall and was always a complainer. DD has heart failure and a raft of old age issue, he has many hospital admissions recently and the Drs have told him he has post vital fatigue and needs to take it easy. DM has returned from hospital again with a catheter. This means she will move less because she doesn’t have to get up to the loo and DD will have more to with catheter emptying and swapping for night bag. They have a lady who does cleaning a couple of times a week. Mum has a falls alarm.
I need them to consider what happens if DD ends up back in hospital. I’ve told them I can’t stay over again as I have a toddler who bf over night and their house is far too dangerous for a toddler to be left while I do anything to help. Mum need to have breakfast before her shower or she gets wobbly - I have suggests she gets the morning carers for an hour so they can get her breakfast too but this would be too late or I can come in the morning to give her breakfast but I would have to leave by 8.10 for the school run but this is too early. I want them to get a lock box for a key for carers to let’s themselves in but this is a no too. I think they need the evening carer back - they stopped them due to covid but that meant my sister had to fill the gap. When DD is in hospital we have to provide all meals for DM and watch her eat them as she has issues with swallowing/choking. She complains that the food is cooled and I need to microwave her dinner - well yes by the time I drive from my house, leaving my kids and husband to have dinner and I don’t have time to eat because I’m doing all her household jobs, it will get cold. It downy help that she complains about everything and won’t even try to work through solutions. She has no idea how little she can do and how much DD is doing.
I don’t think I’m being ridiculous in suggesting they need a) evening carers, b) lock box with a key c) bag packed each for their frequent hospital admissions (monthly) d) when DD is ill for DM to increase care to 3 times a day so they can do lunch, empty catheter and check she has taken her tablets and to increase morning carers to an hour.
DD says ask your DM. DM says we will see and everyone else has to run around after them.