Thank you, but regarding social services what do I do if Nan is insists that she wants to be at home. They feel at the moment she can still make her own decisions.
How does the process of a dementia assessment typically go? How long until diagnosed ?
Will they take in mine and families worries into consideration?
Oh dear, Luke, I am so sorry to hear what you are going through at the moment. Your nan in hospital, out, in, out and in again. At least the carers seem to be good. I hear so many stories on this forum of slap-dash carers.
You will need to be strong as you go through this difficult time. As others have said, keep your job up. Without a career you will be leaning on society, not doing our bit to support it and you will be much less use to others. Make sure your manager is aware of the situation.
Not without carers. For example say they come in the morning get up out of bed washed and fed. And for some reason while I was at work carers didn’t turn up. She would probably be stuck in chair: no food drink and needing to be changed. Which I couldn’t do for her.
You must be strong and stand up for yourself and your life Luke.
I did try to warn you.
Now it’s vital she has a dementia assessment before discharge anywhere. People with dementia just can’t see their situation properly.
I have asked for one which I think they want to do in the community. I have been standing up for myself but they still say she has metal capacity to make decisions.
I don’t think you realise quite how tough you have to be with these people.
So long as you’ve made it quite clear to Social Services and the Hospital that you can’t care for her (preferably in writing & Recorded Delivery) - let them get on with it, and then ask what their Care Plan involves.
They have already mucked up one discharge. It is not fair on her to go in and out of hospital again. They must now properly assess her, a full Continuing Healthcare Assessment, nor just a dementia assessment.
Luke
When I suspected my late husband was getting dementia, I wrote to his GP with my concerns. He saw hubby, and said he hasn’t dementia, as he answered lots of questions correctly. They were questions from years ago, that he knew the answers to.When he deteriorated he still knew these answers . Always remembered his army number! Even when hubby said it was 1980 the GP said it’s because he had become tired! He did, very sadly have vascular dementia, and lost capacity very speedily. You have to be one step ahead and explain the reasons why you Nan is being misdiagnosed, and ask for 2nd opinion. You know your Nan better than anyone,. They have to listen to you, and the fact you will not be able not care for her as she deserves. It’s a fight, I remember it well. You have your life to live, work to continue with, for your own future. Your Nan would want that for you.
They need to check if she “has capacity”. If she “has capacity”, she can make her own decisions and that includes going home. The hospital argued that my mum had capacity even though she introduced me as her nephew!! I argued that if someone has a dementia diagnosis, that was proof in itself that she did not have capacity. It is a problem area though. If you have a preferred home for nan to move into, sometimes it is worth discussing it with the care home manager. The care home manager had good contacts with the hospital in my mum’s case and was a useful ally.
Does the hospital have dementia specialists / befrienders? It may be worth finding out as I am sure they have experienced this many times.
Has she seen a psychiatrist as part of a Continuing Healthcare Assessment???
Have you seen a formal written report?
You need to insist on hard evidence like this Luke, don’t let them get away with “think”!
Keep a diary. Have you been involved in a new care plan? Remember you should not have to do anything for her. You must not be forced to care, you have a right not to care.