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Disability vouchers instead of cash
I've been reading a number of articles that state the government will start to pay in vouchers instead of cash.
Is it me or haven't they quite thought this through, for example I use part of my pip for taxi transport so vouchers will be useless. What does everyone else think? |
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I think they need to go away and look up ‘personal’ and ‘independence’ in a dictionary before trying to control how you spend your personal independence payment.
If they think the system is being abused then they should be tackling the abusers, not making life difficult for the rest of you. |
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If any vouchers are to be of any use, then anybody who gets them as payment, has to be able to redeem the cash value of them. That would mean they are just the same as cash.
While for some people the money they get can be relatively high(equivalent to salary of £30+K), there are those that need that money, but not for general living expenses. |
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The Labour Party would have a massive rebellion if they tried to push this though. I suspect it's a hold over from the previous parliament that will be dropped.
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Ah well we're all in it togeather, it's no good having buyers remorse because it's your turn to benefit[or not] from labour policies, "hard choices have to be made"
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The policy suggestion predates Labour, it's just if they continue with it. It would be crazy for them to do so.
But just to remind OP there has been an election since it was suggested so it isn't 100% going to happen. |
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My neighbour was told he qualified for PIP ,he was due to get his first payement but instead got a letter stating he didn't qualify.
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It was simply one of several suggestions by the DWP back in May.
Like many crazy ideas, its not very likely to ever see the light of day. |
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I'm glad Scotland now control our PIP payments. Rebranded to ADP(Adult Disability Payment) less hassle overall, though with the same points etc but less in person meeting etc.
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PIP appears to be a maximum of £184.30 per week (if you get both parts, otherwise £108.55 per week).
Thats just over 9.5K, no idea where 30K+ comes from. https://www.gov.uk/pip/how-much-youll-get |
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There are websites where you can enter an annual salary, and it will tell you the take home pay. You can take the total amount received in benefits and work out the salary it would need to get that amount. I didn't pluck the £30+K figure out of thin air. To say there isn't massive fraud on the mental health side of things is quite delusional. It's NOT about whether you have X, Y, or, Z, but how much that impacts your life AFTER treatment. Eg Somebody SUCCESSFULLY claimed they should be allowed to spend 26 weeks of the year at a 2nd home in Spain, because of the sunshine. Not based upon a media report, but an actual Upper Tribunal decision that is publicly available. |
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Provide links, then, rather than just statements, please, or a screen print of the £30k calculations…
(Such as "an actual Upper Tribunal decision that is publicly available.") |
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The idea has been around since Labour was last in power. Not "vouchers" per se, but a list of items or modifications you could claim from a central supplier. From walking sticks or wheelchairs, to lower kitchen units or stairlifts, or even hoists to shower rooms.
All used to come under "Disabled Facilities Grants" and only available until the annual budget for an area was used up. And that moment could arrive within days of the financial year starting if a few house extensions were planned. Several think-tanks put forward plans to push large numbers of disabled people into work, thus reducing the budget to their "customers" instead of trimming their own fat of excess office staff. The advent of Work From Home has seen a "significant" number move into work, a lot of which was "welcomed" by former claimants. (according to the DWP). The use of external companies to assess claimants for Personal Independence Payments seems to have been done to deny claimants what they should have been entitled to. Our own twins were assessed as not qualifying for any help at all, but Tribunals quashed those decisions and the DWP was obliged to award PIP. The newest idea seems to be to allow claimants to pay for items and modifications directly out of their PIP awards, so no cash would change hands. It's a bit like the Motability scheme, where people can swap their Mobility Allowance to hire a car for 3 years. Our daughter used to get Disabled Living Allowance, a one-off access to a Disabled Facilities Grant (Open gas fire changed to a modern boiler) and Education Support Allowance. The latter was supposed to pay for up to 3 return trips a week to college, but it only covered one return taxi ride. So I drove her there instead. That was halved, then stopped altogether, with the council saying that she had to use her Mobility Payment. The fear amongst many is that PIP will effectively cease to exist, with claimants having to live off Employment Support Allowance and other things like Housing Benefit and Poll Tax reductions. But many live with parents or partners, and if they earn anything, those Benefits would disappear. It's a bit like this latest Means Testing of Winter Fuel Allowance, with only those who didn't work enough to get a full State Pension and didn't save much for their retirement being qualified. So PIP goes, ESA gets absorbed into Universal Credit, and the bureaucratic cycle turns vicious for disabled claimants. |
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PIP(standard daily living + enhanced mobility) £148.20/week Rent assume low figure of £100/week Gives £25,415 + council tax reduction. Feed £30,000 salary into this website, and the take home is £25,120/year. |
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So realistic the only perk to ESA is getting it paid every two weeks rather than the once a month UC payment. You don't actually get any extra. So using myself as an example. After rent auto deducts and the ESA amount is also deducted we are left with about £400 a month. Not enough to live off for the month realistically. As for PIP or ADP then it's meant to go towards the extra costs involved with your disability or illness. Many in receipt of it can and do still work. Where it's part time or full time employment. |
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If anything it's the ESA side of things that is going to disappear, as eligibility shifts to eligibility for PIP and the Severe Disability Premium has been removed from new UC claims. |
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https://assets.publishing.service.go...000576-ESA.pdf I have to question the cost effectiveness of the legal fees of a Barrister and all the support work of the Government Legal Department through all the appeals, against an alleged ESA overpayment of £4,753.11… |
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The issue wouldn't have been the overpayment, but principle of being allowed to stay overseas(in Spain) for 26 weeks of the year, rather than the normal limit of 4 weeks. Now imagine if that catches on. People could spend 6 months of the year abroad, because they are getting "treatment" of getting a tan. IMO Quite staggering that she got away with it. She was getting medication for the mental health condition, so there should've been no existing impact of any sort. |
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I worked with a woman whose daily dosage would have put me to sleep for a week. |
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I don't see what the problem is with someone going to their holiday home if the sunshine is advantageous for their health. ---------- Post added at 01:23 ---------- Previous post was at 01:19 ---------- Quote:
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The Sunak Government launched a consultation for people to respond to their ideas (now closed). The new Starmer Government stance is that they are to look through the responses received and make any announcement in due course. |
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I expect PIP is like any other benefit, there are the majority who correctly get it, and a minority who abuse or scam it.
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Difficult and a lot of effort to prove fraud. NOT ZERO cases, just a low %age. Eg 0.9% for 2023. As the number of new claims soars with non-disprovable "mental health" claims, any level of identified fraud get diluted. They had a holiday home long beforehand(over 20 years before). They didn't go there for her "health". It was a case of being caught out and trying to come up with excuses. They stayed mainly in the summer and not in the winter months. Sun lamps are ALSO suitable. If staying in Iceland helped her condition, then they wouldn't have gone there. All contradictory to her claim. My point remains that, could people claim holidays on the NHS as a "treatment"? I don't think the perceived issue is with those ONLY receiving PIP alongside other earned income, such as a job. It is when combined with UC/ESA etc, that people can get large sums for doing nothing. There is no incentive to look for work. Even Labour say they are going to address that. There seems to be a general misunderstanding of the reason for ESA and PIP. IIRC The extra money with ESA is meant to be a form of compensation for not being able to work, so that you're not on very basic benefits. IIRC the principle is that you are unable to increase your income any other way. PIP is meant to be for aids and assistance, and not for general living expenses. |
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If any sick or disabled person receives a higher amount than the unemployed (not all do thanks to the Cameron Government) this isn't compensation for not being able to work, but to reflect the additional expenses of being disabled. This began in 1988 when the Thatcher Government scrapped the 'Additional Requirements' payments in favour of premiums targeted at certain groups. PIP fraud is officially so low that it registers as zero in Government figures, it's one of, if not the benefit least likely to be claimed fraudulently. There has been a large increase in young people claiming for mental health problems, that is true. The Government has for some time taken steps to tighten up what they call the 'Gateway' to benefits ie to stop fraudulent or exaggerated claims entering the system in the first place and PIP is no exception. Cameron introduced PIP as a way to reduce the cost of DLA for adults. It was made much harder to claim by changing the criteria to qualify, scrapping one of the Care Components and requiring face to face interviews by so called health professionals. These have been widely criticised for being set up to make claimants fail, even by former members of staff of the privatised companies paid to carry out the interviews. So, as you can see, PIP isn't easy to get either legitimately or fraudulently. There is talk of going back to the old DLA system where it's based on what is wrong with a person and requiring a formal diagnosis as opposed to the current system based upon how it affects them. This could address your concern that those with mental health problems are, in effect, making it up as a diagnosis would be needed by a qualified person. |
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It still hasn't been decided. You would think so many worried people including myself would be a top priority for the Government.
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Maybe so but it's still ongoing. |
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Nothing is happening with it because it's not in motion. Unless they proactively say they're doing it you can assume they're not.
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The last official update was that they were going through the responses to the consultation set up by the Sunak Government with regards to this.
No news is good news. It is known that Labour are to continue with the Tory intention to make financial organisations flag up accounts of people on benefits who may have undeclared capital or income, albeit with more protection measures in place to protect the most vulnerable people in society. |
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And some that don't claim it that should, or don't appeal a DWP decision when they should. 70% of PIP appeal tribunals decide against the DWP but a lot of people find it too much to deal with.
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I suppose this is the time to tell you all: I receive PIP. For the record, I'm a genuine claimant...not that I believe there's any other sort, given how bloody hard it seems to be to get.
I was due to do a Pedestrian Pallet Truck course, another string to my bow. But the Thursday before, i.e. the 5th May 2022, I woke up at about 7:20am - completely disoriented. The room was spinning, my eyes wouldn't track, I had double vision and the right side of my face was (and still is; I suspect nerve damage) seized up. I'd had a stroke, it turned out. No pain or headache, oddly enough. At the time I was 56. I'm not sure how I survived. But in one of my books there's a passage where a character is close to death, and he grits his teeth and concentrates on the single necessity of breathing until the danger passes. That was all I could think about. I had no idea what was happening, I only knew there was something badly wrong and I needed help. For a few minutes I just breathed. My brain getting enough oxygen may be what saved me. Somehow I rang 999. Then I had to get to the front door to unlock it and take the chain off so the ambulance crew could get in without breaking down the door. Again, I don't know how but I did it. I spent a month in hospital. Bolton At Home assigned me a support worker; she put in the PIP claim. I did some exercises with the Stroke Team. Two+ years on, I still don't feel I've recovered. I'm on four pills (five for 3 months - folic acid). One is for high blood pressure, and a side-effect is that it makes me unsteady on my feet. But high blood pressure can lead to a stroke - and a second one will likely kill me, so I know which bet I'll take. I appear to be living on borrowed time. I have tried to convince the DWP that not only am I unfit for work, I can't work. My unsteadiness makes me unsafe, to myself and anyone nearby - Health & Safety At Work Act (1974); H & S starts with and applies to every employee. Plus I get very tired, very easily, very quickly. Just a trip to the local Lidl, about 200 yards, does me in. Imagine me trying to work. I used to ride a bike. I can't now. I daren't - too unsteady and I've been off the damn thing too many times already. Even if I could work, an unrelated issue is my right hand, which arthritis has made virtually useless. I can't even make a fist with it. I asked my sister, who was a manager for years, if she would take me on - and she said no, she wouldn't; too much liability. She gave me the impression I would never work again. I can see her POV - if I were a manager, I wouldn't take on a stroke survivor. They might die on shift - and how, knowing the risk (as I intend to point out in the unlikely event I ever get an interview - H & S again; for the safety of my colleagues and myself I have to tell them), can they prove the job didn't kill the employee? How much could relatives sue for? In this day and age, no company could afford that. I've been assessed. Not in person - over the phone. How can you assess anyone over the phone? And why does the DWP think they know better than doctors? I'm sure I could get another fit note, but the DWP says I am fit for, and I quote, "some kind of work". No-one has said what kind. There was a time when, if you had a sick note, that was it. No question. In fact in 2000 when I had an accident and was off work for weeks, the last time I took in a sick note I got the impression my job was at risk, so I reluctantly went back to work...only to be told a few months later that while an employee could do that, they weren't insured while the note was valid. You couldn't be sacked just for being ill, and it wasn't even my fault! If I'd known that I'd have told him to get stuffed! I miss those days. Nowadays it seems the DWP is allowed to argue, but on what grounds I have no clue. Rishi Sunak and his "sick note culture" nonsense have a lot to answer for. On the plus side, my PIP payment went in as usual, and no-one's mentioned vouchers to me. Damn stupid idea anyway, and if anything it'll cost more - printing (unless they're online), admin, and the chances are the suppliers will inflate their prices. I suspect - and hope - it's just talk. I agree that something needs doing...just not this. |
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It's definitely just talk.
I'm on PIP, well ADP as it's now called in Scotland. About to start looking for work again now my transplant and issues have settled down a lot. Though still get tired often and still can't really sleep. Been that way since the transplant last year. Hopefully at next review I'll hopefully get to keep it. Swapped some issues for other issues and still got my bad vision. So bad I can't drive and usually can't see the bus numbers I'm waiting for. It took me two attempts to get PIP and then reapplied when my health worsened, and got advanced on both sections. It is a nightmare filling the forms and having the daft phone 'interview' not to mention the face to face. On my first appeal they claimed as I walked fine from the waiting room to the consult room I was fine, yes walking 15 metres in a straight corridor is easy. At the time, anything more and I was out of breath due to high blood pressure and being extra anemic due to the kidney failure. The people doing these things have no clue what so ever and should nor be making decisions like that |
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It's just the constant worry and that you're never able to feel settled or secure. I'm taking 24 pills a day, not including b12 every 10 weeks and morphine as and when. Also 2 inhalers, St Marks Solution and Calshakes on top.
It doesn't matter how messed up I am, it's always in the back of my mind if they change it or move the goalposts. I had a home visit for my PIP and must have had a one of the nicer ones, said I had nothing to worry about after the assessment but seems just luck of the draw just lately. |
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Disability Rights lawyers are actively working on fighting this. Last time I spoke to them they were examining exchanges in Parliament from the early 1970's when the first incarnation of PIP was introduced for those of working age (Mobility/Attendance Allowance).
This exchange points out why cash payments were the best solution out of all forms of help that were considered when it was being decided that financial help for disabled people should start to be made. Invalid carriages would only be supplied voluntarily in lieu of Mobility Allowance and even this scheme was eventually abolished in favour of the current Motability scheme. |
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The mindset then, and in some ways still today, was "If you are disabled you use a wheelchair". Hence aids and adaptations were mainly walking sticks, zimmer frames, ramps, stairlifts and lowered kitchen surfaces. Even the international symbol for "disabled" is a person in a wheelchair. Even the top criteria for a Blue Badge, was, until someone realised what they were doing was very biased were: you cannot walk at all you cannot walk without help from someone else or using mobility aids you find walking very difficult due to pain, breathlessness or the time it takes walking is dangerous to your health and safety you have a life limiting illness, which means you cannot walk or find walking very difficult and have a SR1 form |
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Yes, there are still a lot of people who unlawfully question a person's disability because it is either invisible or because they can't see something that they're using like a stick, wheelchair etc to confirm matters (in they're eyes).
If someone states that they are disabled, others are advised to accept this without question or risk falling foul of the law. |
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Try reporting the DWP then because they won't accept anything unless there's evidence. And as Paul says, you're talking nonsense. |
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Not knowing that someone is disabled is a defence for a complaint of disability discrimination. If it is known, then this defence cannot be used.
I'm not talking about benefit claims, i'm talking about everyday life eg if someone asks you to pass them something in a supermarket because they are disabled, there should be no questioning, making assumptions, stereotyping etc. No proof is required, but someone minded to be unhelpful to the disabled should politely decline their request as opposed to making inappropriate comments like "You don't look disabled" or ask inappropriate questions relating to their disability. |
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That's not even about a disability. I've passed people stuff as they are too short or old and cant reach the higher shelves.
It's just being kind and considerate. Don't need to instantly jump on disability |
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There was a period that started pre-covid where supermarkets were giving out "sunflower" lanyards to those who found social interaction difficult, sometimes due to a disability.
Unfortunately, many were not aware of what they meant, so that caused more grief for the wearers as people asked "What's that for? What does it mean? Are you disabled? What is autism?" |
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I'm deaf, and if someone speaks slowly to me as if I'm dumb would that an offence? It happens quite often. But I just tell them politely. I don't think I've ever had a problem to the point where I would consider it as discrimination with how I'm treated. That would never enter my mind. Just correct and get on with life. |
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It's when they fail to take heed or do things on purpose that problems arise and more formal action can be considered. To use my example again, if you asked a fellow shopper* to tell you what a tannoy announcement was saying in a supermarket, they have no right to question your disability, ask for proof of it, make comments etc regarding your deafness. Doing so could be viewed as a hate crime or a hate incident. *If a member of staff refused to help you, this would probably fall foul of the requirement to make adjustments under the Equality Act. Fellow shoppers should either provide the help asked for with good grace (which I'm sure most would do) or politely refuse if they don't want to help. |
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Thing is Richard. You seem to be the only one thinking like that. Most people will simply just give the info or help.
Not everyone is nasty or judgemental like you seem to imply. Same goes for staff, they are there to help. I frequently ask for help when I go to the cinema as my eyesight is bad, so when lights are down I really can't see much so need help getting to my seat. Never had anyone tell me no or give me a funny look. |
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Legal action to resolve matters is only to be used as a last resort when all other reasonable attempts have failed or the behaviour is serious and obviously being down out of malice. The police are currently investigating an incident where a group of people with Downs syndrome were physically attacked in Blackpool. |
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The Downs syndrome comment was to show that, whilst most people are kind and helpful towards disabled people, some individuals are not. To show that |
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Also committing an assault versus refusing to help someone is not the same or similar at all. |
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If according to Richard you cannot question anyone if they say they are disabled, does it not mean that anyone can claim to be disabled and for instance use a disabled parking space.
Also Richard before you say they would need a blue badge there are fakes you can buy on Ebay that are a perfect fake. |
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I have also lost count the amount of times I've come out of a disabled toilet (RADAR) to be met with angry 'disabled' people. To the point I've been shouted and sworn at. Because I don't look disabled. It seems the worse people are the disabled in my opinion. So again would that be a legal issue as you say?
My automatic response which tends to rile and make things worse (hopefully) when it happens now is 'You don't look like an ignorant ......'. (That's the polite version). |
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My worse case and so memorable was during a show at mid interval. I was in line to use the disabled toilet and I actually got rammed from behind by a wheelchair user shouting 'Excuse me.. This is a disabled toilet". I said 'I know' and ignored the person but then got rammed again quite a lot harder. I was told I can't use the toilet and was told to use the normal toilet instead. This was in front of a lot of people as it was packed out. This is where I came out with 'You don't look like an ignorant C(word), looks are deceiving aren't they'. The look on her face is what I'll never forget, but by then I'd had enough as it was really embarrassing. I don't know why (and I regret it now) but I showed her my various 'can't wait cards' and RADAR key then told her to sod off. But it did put a right dampener on the evening sadly. But luckily nothing as bad as that has happened since. This was before the 'not all disabilities are visible' signs came out which are good and really helpful. Morals I learnt, treat everyone as equal. Also being disabled doesn't give you extra rights if you're an arse (or not). |
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Can I moan about disabled parking spaces in supermarkets. I feel that the main point of the is the width, allowing wheelchairs etc to be accessible as possible. Not meant for people that have problems not associated with being able to get in and out of a car etc. ie blind .ducking down.
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My car, not a tractor in any sense, has the tyres on both sides touching the lines, so the distance between cars is about 18". I have to choose my spot carefully or the missus, who needs the door wide open to get in-or-out would be trapped in the car. And she doesn't qualify for a disabled parking space. But the mother-and-child slots are huge! Can I have a father-and-child slot please? |
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As I have already explained, most people are horrified when it's pointed out that they are being offensive. They immediately apologise and make amends. The law is there to deal with those who carry on being offensive on purpose or who do it out of malice. Most issues are resolved by having a word with the offenders (in fact, any resultant court case will expect the aggrieved person to have tried to sort things out informally first). Legal action is considered as a last resort solution, so it's imperative that anyone experiencing discrimination, less favourable treatment, failure to make adjustments etc keeps records and evidence in case things cannot be resolved amicably. |
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As far as I'm aware no one goes out of their way to be unkind towards someone just because they're disabled. They're unkind because of something else. You do have issues based around the legality of things, it's like an unhealthy obsession. Like you go looking for it and use it to your own advantage. |
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You can't be looking to report everyone and take legal action because someone says something unkind.there really is no reason for formal or informal action against every random person in the street. In the workplace of course it would be different. You do seem to go looking for reasons to annoy and aggravate people. |
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Well, according to this, the voucher scheme is scrapped. Hah! Sense at last!
Now if they can just see their way towards making fit notes inviolable again... |
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No doubt if you're bed ridden, they'll get one with wheels on so they'll be no excuse. Sounds like no matter what disability or illness you have they're coming for us/you. |
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Re: Disability vouchers instead of cash
I feel a little compelled to expand on my post above due to the nature of the post itself. A couple of sentences doesn’t quite say much or give any kind of explanation.
As I said, I agree with Taf, but agreeing doesn’t mean I just agree, there is no one size fits all. I fully understand his point, it doesn’t mean it is right or wrong. What is right or wrong? Who decides? Firstly if anyone is struggling is to get help by whatever means possible. I am only speaking on my own behalf here and maybe give an insight to how or why suicide is an option. But coming from someone who lives a life who prides themselves with logic and common sense I have to say when it comes to suicide there is no logic, nor common sense as it doesn’t apply. With mental health / health issues contradiction seems to be a huge part where all logic etc goes out of the window. I feel like I live a double life. On one hand I can be happy, even though I don't experience pleasure. I can laugh at jokes, and I can say without doubt I’m a glass half full type of person. I am a total optimist and try to see the best in everything. Yet on the other hand I wake up every day knowing that I don’t want to live, and I go to bed thinking the same. To the point I do actually ‘crave’ ending my life. Anyone would say that’s extreme and I don’t expect anyone to understand it either. It is something I will have to live with and will not go away. I said I will not be a burden to my wife. I know I already am to quite an extent. Maybe I should have expanded to say financially, but even then that’s not 100% the true either. It’s more about feeling of being more of a burden than I already am and to a point where I decide enough is enough. But again that’s not the whole reason either. To live with suicidal ideation is also a coping mechanism. It gives control over something that is or can be too hard to understand, live with or comprehend. It also gives me choice. Therefore it can allow me to choose and push onwards knowing I do have that choice. It helps. I does rile me when people say suicide is a selfish act. It can be, I’m not questioning everyone or their own reasons again if you feel this way seek help where you can. Why can’t it also seen as the most selfless act someone can do? Could it be selfish of those that don’t understand? Those left behind do have to pick up to pieces so to speak, and some do have to live with no understanding to why. I do feel it is a sad part of it and one that is cruel and hard for those left behind to live with. I would not wish this on anyone. I’ve chosen to speak up about it and be honest in the way I feel so there are no doubts or stones unturned even though it is hard and unpleasant in so many ways. Sometimes you hear why didn’t so and so speak up or talk to me… If only that’s true but it isn’t. The hardest thing to do is to talk to someone. If you can then great, it can help, but to most it wouldn’t matter anyway. But more often the case is who will actually listen. Who asks how I am, who cares? It’s not like it matters anyway. If you ask and I say I’m fine when you know I’m not that tends to be acceptable and I agree it’s not easy or right but just the way things are. There are so many different factors. The fear of not being understood, or just the fear of a person to just say yeah I know what it’s like I feel like that sometimes is so way off the mark, you already know the person just can’t comprehend or help. So you end up with the fear of any answers so you will avoid going there. Or to cause upset, one way or another. Again, not that talking will change anything anyway to some. Again it's just not that straight forward. For the benefit of doubt. I’ve had plenty of therapy and counseling. To the point where I’ve been told I do not have a mental health issue, because of everything I’ve been through, going through and will go through so what I’m ‘feeling’ is ‘normal’ and if I didn’t feel the way I do then I would have a mental health issue. = Crazy but that’s how it is. In the end I did manage to get a diagnosis but it was a hard fought battle. To the extent to how and what I feel is 'acceptable'. I don’t expect anyone to understand fully. I just wanted to expand the subject in a way that I hope it helps a little maybe. Blimey, we'll that's my longest post, lol. And sorry if I ranted on a bit too. |
Re: Disability vouchers instead of cash
Rachel Reeves will seek to make around £3bn of cuts to welfare over the next four years by restricting access to sickness benefits.
https://www.theguardian.com/politics...-conservatives Not quite sure exactly what that means as yet. From the sounds of it more like moving the eligibility goalposts a little further maybe. |
Re: Disability vouchers instead of cash
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