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AIBU to hope that able bodied people will support disabled people against the tory attack on PIP?

331 replies

Blackcats7 · 02/05/2024 10:13

I have just been reading posts from many terrified disabled people on a facebook group I belong to.
People are afraid for their lives after the government's recent announcement to stop huge numbers of people with mental health issues qualifying for PIP anymore.
This attempt to scapegoat disabled people has a long history in the tory party and is popular with their traditional core but the attack on PIP is a new low.
Even those claiming PIP for other reasons think they will be the next target and that the tory aim is to pretty much eradicate any support for us with the half hearted usual disguise of "concentrating help on those who need it most" when they know they can't get away with saying what they actually are doing.
Disabled people have votes too (being housebound I thank goodness for postal votes) and I think this current tactic will have a big influence on how those votes are used but my question is how many able bodied people will take this attack on us into account when it comes to the election?
Should this nightmare come to pass there will be blood on government hands because I have no doubt people will die bearing in mind the targets are people with mental health problems and the tory propaganda that they are removing a right to benefit from those who feel a little bit depressed and anxious about life as most people will at some point or another is utter nonsense. Claiming PIP is extremely hard and requires a very high bar to succeed, especially for mental health. Popping to your gp for some anti depressants would not cut it.
So we need your support.
YABU we aren't that bothered or think the govenment is quite right to stop you scrounging bastards
YANBU this is disgusting ableism and we have your back

OP posts:
Denou · 02/05/2024 17:41

@ThreePointOneFourOneFiveNine
She didn’t qualify for PIP so it’s irrelevant what her costs are.

My dp is also disabled and does not qualify for PIP. Extra costs are significant and mostly transport related but add in taking an effective demotion at work to be able to continue.

The idea that PIP is to cover the extra costs of being disabled makes no sense. Many people are disabled but don’t meet the threshold for PIP and have to meet these extra costs themselves.

ThreePointOneFourOneFiveNine · 02/05/2024 17:26

WishIMite · 02/05/2024 15:19

I think PIP should be replaced with an out-of-work benefit, and support for people to work should be increased.

I applied for PIP for mobility issues (but got just under the threshold as my condition is not consistent each day) but I am able to work as long as it is from home, and not full-time. But do I spend money on my disability? Well, yes: mobility aids, taxis, shopping being delivered, private physiotherapy, counselling for my children who are my carers.

However, I don't need PIP because I earn enough working for myself. (I applied because charities relating to my condition had a campaign for more people to apply, as it's one of the government's main measures of how much the condition is affecting people.)

So no, I don't think PIP should be available to people like me, even though I am housebound most of the time.

Seriously?! I work, my husband actually earns quite a lot, but without my PIP we would not be able to afford the vehicle needed to transport my wheelchair, without which I would be unable to work. I can either claim PIP while in work, or I can have it taken away, be unable to work as a result, end up on incapacity benefit, which would presumably mean I would be entitled to PIP again, so could get a motability vehicle again, which would then mean I could go back to work, which would then mean I lost my PIP again, and so the cycle would continue. How much do you earn that means you don't need PIP? Or are the costs relating to your disability not that high? If you're housebound a lot of the time could having some form of wheelchair/scooter and a WAV not change that? I get the top rate of both categories for PIP, so about £600 a month, and while it does make a decent dent in my disability related expenses, it doesn't cover it. My DH pays more than enough tax to cover it. I don't feel in the least bit guilty about claiming it. My disability has cost my tens of thousands over the years, probably more.

medianewbie · 02/05/2024 17:08

PocketSand · 02/05/2024 16:09

The consultation also mentions the reason for the uptick in claims is the pandemic - they refer a lot to pre and post pandemic claims. Particularly for anxiety and depression. No shit Sherlock.

Should the disabled (I'm thinking a throwing protective arms) pay for the consequences of government choices that were nothing to do with them (DNR if you are autistic) but just so happened to achieve a huge wealth and power transfer in the favour of the already rich?

Very well said @PocketSand. Of course anxiety & depression increased post Covid, especially amongst the young who'd had their education back disrupted & also realised that the 'grown ups' were making it all up as they went along. I will also never forget the DNR Govt rule for Autistic people. They withdrew that latet but it was there for some time. Not too far from a 'useless eaters' label.

frankentall · 02/05/2024 16:56

Megifer · 02/05/2024 16:32

You asked if I'd reviewed every case.

Not quite sure what your issue is with what I've said? Ive based it on my factual experiences, and, tbh, no one needs to review every case to know there are people who are claiming to have depression, anxiety etc. when it's just that they're having normal daily shit to contend with. I think they are the ones a lot of people are raising eyebrows over but they lump them in with those who are genuinely struggling.

It's a bit like saying there are far too many people who don't pay their TV licence when they should. I've not reviewed every case, I don't need to to know that statement is true, its obvious (not that I have a problem with people not paying!).

So you are citing your anecdotal experience, pardon me for not accepting that. You appear to have zero basis for the claim too many people are claiming except just that you say so.

The TV licence comparison is ridiculous as that is a simple binary - people either have a licence or they don't; it's an insult to compare people claiming benefits as a result of mental health issues to that.

ARichtGoodDram · 02/05/2024 16:44

If the government were actually remotely serious about helping more disabled people into work then the civil service wouldn’t have had arbitrary “x days in the office” brought back in. There would have been some nuance in which departments need to be in more and which are actually ideal for home working more.

They also would be discouraging big companies who are big donors (looking at you JCB) from scrapping all home working regardless of effectiveness.

ARichtGoodDram · 02/05/2024 16:40

MistressoftheDarkSide · 02/05/2024 16:32

That is an excellent point. How much of the PIP budget is actually money paid to claimants versus the costs of crap administration?

This is also similar for ESA in terms of appeals.

I’d also like clear cut numbers - we’re often told “X number of people were found fit to work” but there’s never any follow up of “oh, but then X number were actually found not to be”.

Also the ‘error and fraud’ percentage should be split. I’d like to know how much of it is error and how much is fraud. My assumption is that the error is the higher part as I’m very sure if fraud figures had increased we’d hear about that!

MistressoftheDarkSide · 02/05/2024 16:40

National security which has had to be ramped up due to political meddling in national affairs you mean? Trotting into countries and contributing to destabilisation that already exists? Making the UK a bigger target than ever for extremists you mean? That national security? To a point where conscription is being bandied about (ridiculously of course) as a solution.

Everything is connected in a vast global chaos - the welfare budget is really the least of this country's problems, and the people dependent on it in any way are largely so due to necessity and decades of managed economic decline.

Numbers of billionaires in this country have tripled since Covid. I wonder how and why that is.

OrangeCrusher · 02/05/2024 16:37

I think it’s easy for governments to say disability benefits are too expensive without being transparent about how much of that money is going on administration. When New Labour introduced Atos costs increased by 300% now SERCO have a £350 million contract with the DWP. Private companies are benefiting in a system designed to make it difficult to claim benefits and keep them. They can do this because a lot of people are either naive in who needs that benefits and the likelihood they might need them too. Or, they don’t care about supporting vulnerable people.

Welovecrumpets · 02/05/2024 16:33

MistressoftheDarkSide · 02/05/2024 16:28

Funny how there are always magic money tree forests for banking bail outs, funding the arms trade, and a host of consultations leading to diddly squat in tangible terms though, isn't it?

You mean national security? Yes what a waste of money, especially now

MistressoftheDarkSide · 02/05/2024 16:32

ARichtGoodDram · 02/05/2024 16:30

They could save an absolute fortune on the PIP bill if they just took the time to get the decisions correct in the first place, or at second look.

The cost of appeals is phenomenal. The place here that does them has 15 rooms, each with a lawyer and doctor (independent so not cheap) and some have a welfare rights person as well. They do multiple appeals a day and are so busy it takes around 12 months to get seen.

My DD was called the morning of her appeal and told the panel had awarded her after reading the pack.

When I went as support for someone else I was in the waiting room for 4 hours all in (I didn’t go into the room with them) and I literally saw two people leave having not won. The figures of people winning at appeal are staggering, and they are not all people who suddenly break out amazing medical evidence at last minute. It’s such a waste of money, and such a nightmare for the claimants involved.

That is an excellent point. How much of the PIP budget is actually money paid to claimants versus the costs of crap administration?

Megifer · 02/05/2024 16:32

frankentall · 02/05/2024 16:18

No, and I never said you did - you said far too many. How can you know which cases are valid and which are not?

Edited

You asked if I'd reviewed every case.

Not quite sure what your issue is with what I've said? Ive based it on my factual experiences, and, tbh, no one needs to review every case to know there are people who are claiming to have depression, anxiety etc. when it's just that they're having normal daily shit to contend with. I think they are the ones a lot of people are raising eyebrows over but they lump them in with those who are genuinely struggling.

It's a bit like saying there are far too many people who don't pay their TV licence when they should. I've not reviewed every case, I don't need to to know that statement is true, its obvious (not that I have a problem with people not paying!).

ARichtGoodDram · 02/05/2024 16:30

They could save an absolute fortune on the PIP bill if they just took the time to get the decisions correct in the first place, or at second look.

The cost of appeals is phenomenal. The place here that does them has 15 rooms, each with a lawyer and doctor (independent so not cheap) and some have a welfare rights person as well. They do multiple appeals a day and are so busy it takes around 12 months to get seen.

My DD was called the morning of her appeal and told the panel had awarded her after reading the pack.

When I went as support for someone else I was in the waiting room for 4 hours all in (I didn’t go into the room with them) and I literally saw two people leave having not won. The figures of people winning at appeal are staggering, and they are not all people who suddenly break out amazing medical evidence at last minute. It’s such a waste of money, and such a nightmare for the claimants involved.

frankentall · 02/05/2024 16:29

MistressoftheDarkSide · 02/05/2024 16:28

Funny how there are always magic money tree forests for banking bail outs, funding the arms trade, and a host of consultations leading to diddly squat in tangible terms though, isn't it?

and for batshit schemes to not send people to Rwanda

MistressoftheDarkSide · 02/05/2024 16:28

Funny how there are always magic money tree forests for banking bail outs, funding the arms trade, and a host of consultations leading to diddly squat in tangible terms though, isn't it?

Ratfinkstinkypink · 02/05/2024 16:27

Overthebow · 02/05/2024 15:56

I know it’s not an out of work benefit. I’m saying that the money available needs to be focused on those who genuinely can’t work, the severely disabled.

DH claimed PIP when he got his cancer diagnosis, for a few months it enabled him to continue to work. It helped pay, among other things, for the days he needed off work for chemo as his company only paid SSP, it helped with the miles backwards and forwards to hospital for chemo/scans/appointments, it helped cover the costs of keeping the house warmer than we'd previously needed it. It helped cover the hidden costs of illness/disability. Without it he would've needed to stop work and go onto out of employment benefits and how would that help an already broken system?

ademanlu · 02/05/2024 16:25

This reply has been withdrawn

This message has been withdrawn at the poster's request

OrangeCrusher · 02/05/2024 16:24

I wouldn’t hold my breath if you expect the majority to the U.K. to step up to protect people with disabilities or health issues who are reliant on benefits. Most people have absolutely no understanding of how the system works, and those who claim it’s unsustainable know even less. People sat back and said nothing about the 2012 Welfare Reforms which resulted in increased cost in administration and the awful consequences of those reforms. It introduced an element of cruelty that plenty of voters still have an appetite for.

It’s very upsetting dealing with vulnerable people who are already being put under stress when going through the process, face financial hardship when they have to go through the tribunal process. It’s even more awful when you’re dealing with someone who suddenly becomes very unwell and they think because they have worked they will be looked after. It’s always a terrible shock to them.

frankentall · 02/05/2024 16:18

Megifer · 02/05/2024 15:26

Did I say everyone?

No, and I never said you did - you said far too many. How can you know which cases are valid and which are not?

Mrsjayy · 02/05/2024 16:18

Overthebow · 02/05/2024 15:56

I know it’s not an out of work benefit. I’m saying that the money available needs to be focused on those who genuinely can’t work, the severely disabled.

I genuinely don't understand what you are on about. Could you elaborate?

PocketSand · 02/05/2024 16:09

The consultation also mentions the reason for the uptick in claims is the pandemic - they refer a lot to pre and post pandemic claims. Particularly for anxiety and depression. No shit Sherlock.

Should the disabled (I'm thinking a throwing protective arms) pay for the consequences of government choices that were nothing to do with them (DNR if you are autistic) but just so happened to achieve a huge wealth and power transfer in the favour of the already rich?

TigerRag · 02/05/2024 16:02

Overthebow · 02/05/2024 15:56

I know it’s not an out of work benefit. I’m saying that the money available needs to be focused on those who genuinely can’t work, the severely disabled.

Huh? There are people who only work because they have pip

Overthebow · 02/05/2024 15:56

Flopsythebunny · 02/05/2024 15:48

How many times... Pip is not an out of work benefit.
The mobility part of mine pays for an adapted WAV. The care part pays for any aids that I need, including £40 per week on incontinence pants and a cleaner to do the jobs that I cannot manage, car parking at the hospital twice per week and other things that I cannot do because of my disabilities.
I run my own business from home and although I don't earn a lot, it does cover my everyday expenses and tops up my pip

I know it’s not an out of work benefit. I’m saying that the money available needs to be focused on those who genuinely can’t work, the severely disabled.

PocketSand · 02/05/2024 15:56

Only skim read the consultation but it appears that after a review in 2016 which criticised PIP assessment for over emphasis on aids and appliances the government didn't make changes it agreed with to shift this emphasis.

It recognises that PIP is not generally spent on aids and appliances but that direct payment pays non direct costs of disability (increased utility, transport, food, clothing, housing etc) whether in work or not and that stopping direct payment would impact non-paid carers who would no longer qualify to receive carers allowance.

Then it merrily skips on to proposed reforms - a catalogue of approved aids and appliances; a voucher scheme to buy approved aids and appliances; a receipt scheme to refund the cost of approved aids and appliances.

But wait. Aids and appliances need only be bought once (and the NHS should supply) so no direct payment is needed.

People with depression and anxiety who have maliciously claimed (let's ignore the claiming criteria for how long impairment has been present and is expected by medical professionals to continue) don't need aids and appliances.

When you think about it, nobody really needs PIP for aids and appliances. Because support is really somebody else's problem. So nobody really needs PIP.

WTF.

VJBR · 02/05/2024 15:55

I don’t think it’s that black and white. YABU to tell people how they should vote. I’m sure they can work it out for themselves.

vivainsomnia · 02/05/2024 15:54

YES IT HAS
Have you even clicked on the links I've posted? I assume not!