Hello Farview I feel your pain. I thought I was reading about myself until I read your DGS lives with you. My DH was diagnosed last year with Vascular Dementia, he’s 74 and I’m 67. He’s obviously had it for about 3/4 years but I just thought he was turning into a nasty old man. We moved 2 years ago and we haven’t finished doing our property up, it’s awful, I’m still living surrounded by boxes in the bedrooms and hall. My DH is the same if I say I want to start decorating, I want to get a painter in, he’s not agreeable because he used to be a painter & decorator up until 10 years ago. He couldn’t manage now but due to his dementia he gets aggressive! The garden is an awful mess but again he won’t let me get a gardener even though he’s not capable of doing what needs doing, same as a window cleaner etc. I’ve been very depressed for the past two years and in particular this year as I’ve lost my little dog also my beloved younger brother unexpectedly and got Covid and now long Covid! Meanwhile I try to make sure husbands life is as unaffected as possible because otherwise he ‘flips’ and can’t cope! I feel an absolute mess re hair, skin, weight etc. a couple of weeks ago I bit the bullet and got a cleaner to start, didn’t tell him until that day when she arrived, my DH is capable still of walking the rescue dog we got in March so I sent them for a walk and kept telling him after she’d gone how much it felt cleaner indoors! Basically it’s non negotiable having a cleaner now even if she did have to clean around the boxes as I’m disabled and cannot cope with too much housework anymore. I’ve booked to have a pedicure next week and have looked online for an art class for DH and am encouraging him to go. Please don’t forget we NEED space when caring and living 24/7 for someone with V.Dementia. I’ve gone to the doctors (alone) and told her I’m having trouble coping with him (and his moods and nighttime hallucinations) he’s now on melatonin tablets for nighttime, they were a miracle tablet for DH but obviously will stop working one day but he was keeping me awake and I definitely can’t cope on little sleep. The Doctor got in touch with Carers association and I’ve had a bit of support from them. There is support out there if you want it. Can your DGC or son or daughter not stay with your DS for a few hours so you can get your hair done? I often go and upstairs and lay down for a couple of hours in the afternoon and read so that I can be alone while DH watches TV downstairs. I feel like I’m living with someone I don’t know and wouldn’t of married if I’d met him nowadays. We’ve got nothing in common and it’s a lonely frustrating scary life. I’ve told (not asked) my DS that he’s his father and occasionally he needs to take his father out for 9 holes of golf (even though my husband has no idea where he’s hitting the balls now apparently), plus my DGS takes my DH to the cinema (even though he can’t keep up with films now) or out for a burger in town, but they know I need time alone sometimes ! Maybe your DGC could help like that? I’m resigning myself that when he gets really bad I will look into sending him to day centre and when I can’t cope I will put him into a home . Sounds awful but I’m having to be a bit harder as my mother in law almost killed herself looking after my father in law with dementia, he wouldn’t let her get any help whatsoever, she couldn’t even go to the Doctors and he got violent with her so I had to get him sectioned. My DH felt sorry etc for his DM at the time, but obviously with his own V. Dementia he’s gradually going down the same route and I’m determined I’m not going to become like his own mother did! Please get help, it is out there I’ve found if you shout loud. If you’re dog brings you comfort, keep it as it’s a good excuse to get out for a walk and blow of some steam for you. As for your DGC tell them you NEED help, I found my son actually didn’t realise how bad his dad had got because as you know if there’s visitors and it’s a good day they don’t seem very bad, the children aren’t around all the time to see what we’re putting up with. Look after you too.