I know that inertia and apathy are symptoms of Parkinson’s but my Mum is and always been a terrible procrastinator and passive to a fault. I wouldn’t want her to be my next of kin or in charge of any decisions for me, because she would just choose the easiest, least effort option.
She was widowed at the beginning of lock down, after a long marriage (26 years) with my step father. lives alone, in a fairly rural area where there is nothing, no shops in walking distance. her Parkinson’s diagnosis was 4 years ago but symptoms before then that she ignored.
To get to the point, she’s had to give up driving, done nothing about selling her car. After a horrible fall, multiple broken bones, hip included she now’s living downstairs in her house, hospital bed in dining room, down stairs bathroom and access to kitchen. Carers two days a week, twice each of those days. Hospital transport or taxi to medical appointments. Other than carer visits and hospital appointments she sees no one, can’t leave the house. she gets around on zimmer or walking stick but can walk. I arrange grocery online shopping weekly. I got her an air fryer and she cooks well.
I live a long way away, I collect her and bring her here for a couple/few weeks at a time but recent visit proved that my house isn’t suitable, no down stairs bathroom for example, stairs to bedroom, so these visits will need to stop.
Ive asked her what her plan is, I want to move her to a retirement unit (supported) by me, I’ve offered to help her to move into an apartment or similar in the town by her. I get nothing in response, says that she can’t pack up the house, I’ve said we would be involved, she wouldn’t be expected to do it, I’ve pointed out that selling and buying process takes months, loads of time to sort stuff. I get frustrated because what she really means is that she’s going to do nothing until she has to, i.e. another crisis, then I will have to sort everything - again. I had to sort ground floor living out, lugging furniture, cleaning etc whilst my DH had to stay home with DC’s.
I’m at a loss, I’ve begged her to have a difficult conversation about this, I’ve ploughed on and arranged essential (think fixing dangerous issues) in her house despite her protest only for her to be super grateful and gushing when completed - yet she ignored the dangerous issue for over 10 years! I’ve got upset, lost my shit, told her to grow up and make some plans. I’ve cried with exhaustion in front of her. I’ve pointed out that move near me would improve her life, she loves visiting, I take her out, she loves the area, I would take her to hospital appointments, get her physio etc. if she was in the town in a nice apartment or bungalow she could have it set up nice, with access to things (she’s complaining about not being able to go upstairs to potter and get stuff, yet carers always offer to take her to get anything she wants).
what can I do?