I recently had a stay in hospital and there was a lady on the ward with mild dementia who the nurses weren't communicating with properly. I actually intervened and suggested what to say to the lady to encourage her to have her medication and it worked. If I hadn't intervened, I think the nurse would have given up and left her.
I'm not an expert on dealing with these communication problems but I looked after my mother for 6 years with Alzheimer's and, because I knew her, I was able to speak to her in a way that was helpful to her (not always successfully, depending on her fluctuating levels of understanding).
I am now thinking that maybe I could volunteer to help people with dementia who have to go into hospital. I am not sure I could deal with people in, for instance, a paranoid stage or with severe symptoms but I could perhaps help those with early dementia or mild cognitive problems.
This lady was not on the appropriate ward, due to a shortage of beds, I imagine which also happened to my mother several times. That is when their needs can go overlooked. Also, when people are confused I think they are not believed if they say, for instance, that they're in pain.
I know there is much talk of dementia awareness in hospitals and "champions" for people affected but I have seen scant evidence of this in practice.
Has anyone else taken on this type of voluntary work and what was their experience like?
I'm not an expert on dealing with these communication problems but I looked after my mother for 6 years with Alzheimer's and, because I knew her, I was able to speak to her in a way that was helpful to her (not always successfully, depending on her fluctuating levels of understanding).
I am now thinking that maybe I could volunteer to help people with dementia who have to go into hospital. I am not sure I could deal with people in, for instance, a paranoid stage or with severe symptoms but I could perhaps help those with early dementia or mild cognitive problems.
This lady was not on the appropriate ward, due to a shortage of beds, I imagine which also happened to my mother several times. That is when their needs can go overlooked. Also, when people are confused I think they are not believed if they say, for instance, that they're in pain.
I know there is much talk of dementia awareness in hospitals and "champions" for people affected but I have seen scant evidence of this in practice.
Has anyone else taken on this type of voluntary work and what was their experience like?