I think you've raised a very good point there with regard to the wording of the welfare LPA. I suppose it's because it IS a big deal to give this sort of control to another person: it's not something you would enter into lightly. And of course, so often the subject of LPAs come up at a time (after diagnosis) when the person doing the granting is already ill and may not be entirely rational. Competent, yes, rational, not always. For an elderly person who is already ill it is difficult to think about handing over such responsibility. They may also think that such a power would allow an attorney to turn off life support etc. In fact, an attorneyship only grants the attorney the same power as the donor would have, particularly with regard to medical matters. If the donor couldn't insist on a specific treatment or withdrawal of said treatment, then the attorney can't. The decision maker for major medical issues will always in the final analysis be the doctor. Sadly, many people have an unrealistic view of what a doctor will or will not do to prolong life, but that's a subject for another thread.
I'm not sure, though, that there is what you might call global confusion on the forum about this. This thread is about one specific aspect of the (old) EPAs, but I think everyone on the forum and in AS are quite clear about the benefits of LPAs. In fact, they already have a fact sheet about this http://www.alzheimers.org.uk/site/scripts/documents_info.php?documentID=154
Having said that though, and I'm not sure how much of this was discussed in this particular thread, there does seem an increased inclination from some social workers to interpret lack of a welfare LPA as giving them close to carte blanche when it comes to making a decision about a vulnerable adult. Not in all situations, perhaps not even in most, and in my view, totally against the words and ethos of the code of practice, but it's foolish to pretend it doesn't happen. It seems reasonable to encourage everyone to bear such admittedly anecdotal reports in mind and make every effort to ensure that they aren't impacted.
I'm not sure, though, that there is what you might call global confusion on the forum about this. This thread is about one specific aspect of the (old) EPAs, but I think everyone on the forum and in AS are quite clear about the benefits of LPAs. In fact, they already have a fact sheet about this http://www.alzheimers.org.uk/site/scripts/documents_info.php?documentID=154
Having said that though, and I'm not sure how much of this was discussed in this particular thread, there does seem an increased inclination from some social workers to interpret lack of a welfare LPA as giving them close to carte blanche when it comes to making a decision about a vulnerable adult. Not in all situations, perhaps not even in most, and in my view, totally against the words and ethos of the code of practice, but it's foolish to pretend it doesn't happen. It seems reasonable to encourage everyone to bear such admittedly anecdotal reports in mind and make every effort to ensure that they aren't impacted.