The MHA is likely to be updated/replaced next year.
See https://www.kcl.ac.uk/ioppn/news/re...health-act-review-accepted-by-government.aspx
See https://www.kcl.ac.uk/ioppn/news/re...health-act-review-accepted-by-government.aspx
That is excactly how I read it as well.Am I the only one who read this with a sense of unease that it will become even harder to get care for our PWD if they refuse it?
Yes I thought that as well. I’ve have had a problem with things as they are at the moment because PWD said they wanted to move to an advocate, so because it is their human right, to quote, they have been moved to a less satisfactory home where they have declined, but it seems that’s ok even though they have no capacity and all the medical people said it was not in their best interests to move them they were ignored, and at one meeting it was stated to quote again, they are not an expert! The people who made the decision say this is because I am anxious and it rubs off on the PWD and accused me of emotional abuse. So I think things will get worse not betterAm I the only one who read this with a sense of unease that it will become even harder to get care for our PWD if they refuse it?
Am I the only one who read this with a sense of unease that it will become even harder to get care for our PWD if they refuse it?