@Imtoooldforallthis
She gets attendance allowance but refuses to spend it. She has a neighbour who calls daily and myself and one other friend who calls once a week so she is not totally alone. I'm hoping when our local social services call me there will be some help to give her.
Being a carer requires certain training and qualifications.
If this were true a lot of MNers would be out od their unpaid jobs.
In a lot of cases it's actually much more appropriate for a non family member to be the carer.
If financially possible it can be a benefit when it comes to dementia care.
Parents can react differently to children who they raised than they do to strangers. Not having the close personal relationship professional carers dont have the same emotional reaction and can be more clinical in evaluating their reaction.
Imtoooldforallthis
Iam definately not a natural carer,
YOU are still there, still doing what you can, still worrying. Give yourself some credit for that. 🌻
I go planning to do all sorts with her, but within 10 minutes I'm pulling my hair out.
For the next few days reduce your planning of interactions to a cuppa and hello. If you aim high every setback is a stick to beat yourself (dont do that🙁 acknowledge that DM has it covered and is older & better at it than you😯). Aim as low as possible anything over an above is a win.
She gets attendance allowance but refuses to spend it.
Has DM still got legal capacity?
Do you have siblings?
If DM has capacity she should (needs to) put the legal framework in place for you or another family member to be given the legal authority to act if and when she looses legal capacity.
Along side that establish if her GP and other HCP will discuss her care openly with you (family). If DM has capacity she can give permission.
Dito for her care package. If you can agree to have a carer appointed begin by scheduling the carer to start work while you are in the house. You are "introducing" them while being a buffer as DM is getting use to having a strange in her house.
Independant of that you and your siblings need to come to discuss how you all see her care progressing its better if an agreement in principle can be reached. Ask her GP for referral to a medical social worker who would be able to outline what options are available locally from in homecare to residential care. However if you are the main caregiver you get to draw your boundries around what you can and cant cope with.
I'm hoping when our local social services call me there will be some help to give her.
Local care can be stretched to the limit so you need to set your boundries and consider if DM may be happier to staying at home complaining about not going out rather than actually go out or do stuff.