Is it ok to use cameras for security when having carers

Given I know money got stolen, the total amount of things being stolen will be a unknown, as there is rooms I havent been in for months at this point. There is other things of value in my home, but in terms of cash it is about £60.

I am more bothered about letters, documents, photos, and its the fact someone is going through my bits which I have a big problem with.

I do have one carer who was going through some of my bits, and when I noticed her she casually told me she wanted to rearrange them, this was not far from where a mobile phone was sitting and where the money was, so when I speak to the agency I will at least ask she isnt assigned to me again, and inform them of what has happened.

Even a meal vanished, I was given a choice of 2 meals by a carer, then the next day there was none left, this care who was going through my bits was in between those 2 slots.

I have been thinking a bit about your post, I didnt originally reply, as I wasnt sure to say.
I have not had the issue of them rushing of too soon, but rather outstaying their welcome, there is a lot of once they done with my needs, them standing in another room out of view, one told me she isnt allowed to leave earlier than the allotted time, so has to wait, but none of the others stay as long as she does. The evening visits which are shorter are usually much shorter than what I am paying for, but the slots cant be reduced they have a minimum time period.

The bit that is bothering me, and really the whole thing has been bothering me, is the quality of care, and that I think I only need this care because both the NHS and social services are failing me.

Only one of the carers I think does adequate care, the rest are as if they cant hide they want to be somewhere else, and I had to do a lot of nagging to get this carer almost every day except her day off. If she ever leaves there will be serious consideration in to only keeping them to fetch meals and nothing else.

But also I think I am being messed around with by my OT, so the physio for the most part had to order the OT to visit, it took her about 2 months to even visit the property, and then for another 2 months or so she has kept saying a report is coming, which isnt coming, tried to make me fill in a rehousing from without the form, I then had to show her this form which has in big red letters it wont be processed without a report, promised hand rails. a special bed, only for a few days later to ring me saying it wont be happening without much of a reason given.

Physio said I have been approved for a wheel chair but months later no one has contacted me on it, I am bad enough that I cant even have a scan at the hospital now, there is so much discomfort and inability to move my body, lie down in specific ways and so on, I cant even have an xray.

When I asked the NHS about making special accommodation to get scan done (plus an eye screening that needs doing), they just shrugged their shoulders and said just try again, no pain injection or anything offered, no in patient arrangement offered, they wont even prescribe me more powerful painkillers.

I got a social worker coming in 2 weeks who's only interest is reducing my care plan. She has no interest in everything else going on GP's ignoring my needs, OT being passive aggressive pretending to help me, and hospital showing no duty of care.

It feels like I need to be firing off complaints in all directions to even get basic needs met.

I think the issue with the OT is they uncomfortable with that I dont really have much in terms of secondary care evidence, and their system falls apart when that isnt there, we have the whole accountability and liability thing, so they dont want to say to my face they dont want to help me, either that or they just a complete mess. But this is a consistent pattern with anyone who has visited me, promises made face to face, then within a week a phone to call to back out, or just never hear from them again.

I hear people talk about PIP as if its dehumanising, I actually found my experience of that not too bad, I explained my issues to the assessor, and the decision was made to give me support, fairly simple.

With the NHS, I am literally having to explain all sorts of dehumanising stuff a dozen times, and then maybe, I might get a little thing happening, but then I have to repeat the whole thing again with someone else.

I had someone tell me a diagnosis, and when I asked them to repeat it so I could write it down (due to hardly anything being on my file), they flat out refused probably for accountability reasons. Very strange behaviour. This is on top of that very strange autism assessment I had where I was treated like a criminal under police interrogation.

At the very least if I was living in a suitable property with an appropriate wheelchair I probably would be able to do my own washing, getting food, putting shopping away, a wet room to wash myself, my quality of life would be so much better, but the system just doesnt want to help me, and yet we have people claiming people like myself are not interested in help.

The most dehumanising thing is asking for help and then not getting it.