At what cost to others indeed? MIL is at least five years in to what is now middle to late stage mixed dementia, but was only diagnosed this year as DH and his DSis were, and are, almost completely in denial. Despite being disoriented in place and time, paranoid, delusional, incontinent, virtually immobile, housebound and completely unable to look after herself, they continue to perpetuate the myth that their DM is ‘just getting old’ and that she can make decisions for herself, which she patently cannot. Although they both have PoA, jointly and severally, they won’t use it and, as a result, she is very, very vulnerable.
I have been so concerned for MIL’s welfare that I tried to report DH and DSIL to Social Services, but sadly they weren’t interested. I had to threaten divorce to get MIL assessed. I have spoken to my DD about changing my PoA so DH is not on it, because I don’t feel I can trust him to look after me if needed in the future. I’ve also got detailed notes, just in case we have to deal with the Police or the Coroner when MIL dies. It’s a long list of things DH said he would do, but then didn’t do, or things that I pointed out to him that he ignored or discounted.
Trying to deal with this has basically destroyed my marriage and caused so much stress that I now have a heart condition and I have no idea when or how it will end, although I don’t think it will end well.