Government to end unnecessary PIP reviews for people with most severe health conditions

The Minister for Disabled People, Health and Work, Sarah Newton, said:
We’re absolutely determined to ensure people get the right support that they need to live better, more comfortable lives.
PIP is a needs-based benefit that takes into consideration people’s individual, and sometimes quite complicated circumstances.
We’ve listened to feedback from organisations and the public, and this common-sense change will ensure that the right protections are in place while minimising any unnecessary stress or bureaucracy.
The government will be working with stakeholders to design the light touch review process so that it adds value for both our claimants and the department – for example, by providing information on services available and ensuring that contact or bank details have not changed.
We are still finalising details of the guidance and will publish it later this summer.
See further news here: https://www.gov.uk/government/news/government-to-end-unnecessary-pip-reviews-for-people-with-most-severe-health-conditions
Comments
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Believe it when it happens,5
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wilko said:Believe it when it happens,
@wilko I am ongoing award Enhanced both and was told on my PA3 no further reviews necessary and (it's not appropriate to review the claim.)
So I should be left alone as I have submitted solid evidence and HP and CM agrees 100% I'm buggered.
But will see I won't ever improve I will probably be dead by then anyway.3 -
Similar to the indefinite award.
The is already the light touch in place isn't there for those with 10 year award..1 -
Hello @Governments_A_Joke Sorry if I sound and am cynical do not think it will happen.
Remember last time that the Government of the day decided to do this regarding long term health conditions.
U turn after 18 months then we those in our community like my good self revaluated again and again.
Consider what exactly is severe in their eyes mean then. I have long term disability but have been told too many times not disabled enough. Yet as I age it is becoming too much of excuse by assessors and I am now feeling the harsh truth of the treatment I receive.
Also ongoing no matter what and how ill and some days stressful to deal with and cope with.
So what is the principle behind this. I do know reassessing members of our community who are never going to get better or their illness or disability because it is difficult to cope with. Having a long term disability and illness does need support and care and more understanding and having that network to deal with.
Problem is we as community do know that having all of that costs money. Money from where the councils budgets our benefits. Some one has to say and how the proposals can be beneficial to all of our community.
ATOS and Capita have done a lot of damage to our community and the future Government Proposals do not go far enough in my opinion.
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I had a pip assessment on Wednesday of last week. I know I will not continue to get pip cause I forgot everything i had to tell him. I said how can anyone be expected to describe to you how much pain that we have to suffer. He just looked at me....
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Does this apply to people on enhanced disability pip?0
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Same here Ladyjax. Fatigue and brain fog struck ?0
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???0
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I'm cynical too. Everything they say is a lie and they say it just to shut people up so they quietly go away and don't get the support they need.2
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feir said:I'm cynical too. Everything they say is a lie and they say it just to shut people up so they quietly go away and don't get the support they need.
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Username_removed said:Guidance due at the end of the Summer allegedly but you can force this now by asking for an ongoing award on claim packs: MR forms and SCS1 appeal forms rather than assuming they’ll notice your condition is permanent, degenerative etc.
Given that this is supposed to be happening is there any chance that the DWP will review cases going back to 2013 where they issued ridiculous short awards resulting in re-assessments including continual face to face assessments in respect of clear cases of permanent and degenerative conditions?
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Does anyone really believe any of this any more we are a huge community and dont ever seem to get anywhere .This is a total and utter travesty .All tbis red tape needs to stop .Whete do we go eho can we trust .This isnt what we deserve .im really sorry i dont have the answers we need i can only ask pray that soon it will all be to the best for all .we really are so many against so few of them .The balance has to be corrected we need to make sure that it does .3
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Agreed @starchild ! The problem, I think, is that the public simply isn't interested.
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I wonder what you mean by "the public". It is solely in the hands of the government and their continuing efforts to change a fairly well working DLA system to a blatantly not working PIP system and to cover up the millions of pounds spent and lost by getting outsourced and incapable companies to try to save money no matter what the cost. As far as "the public" is concerned they believe the lies spread around that disabled people are given everything free and large amounts of money to live on and that a large percentage of claims were fraudulent. I wonder who started those rumours, lol!!!!
TK1 -
They won't listen to disabled people, no matter how much we demonstrate and write and send petitions. We've been doing all these things for 8 years, and it hasn't worked. Basically, we need to be the new Windrush folks. Once the public heard about how the gov't were treating them, they kicked up such a fuss that the gov't had to change what they were doing.Unfortunately. as you say, a good chunk of the public believe the lies about us. Some of the public just don't care. The rest know what's going on, think it's terrible, but they don't do anything about it. My FB friends read my posts and say things like, "My god, this is just evil! I'm so sorry that you're going through this!" They've lent me money, etc., which I'm very grateful for, but they're almost all wealthy, employed, able, male, white, etc. They would be listened to, if enough of them spoke up, but.... They don't.2
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Waylay said:They won't listen to disabled people, no matter how much we demonstrate and write and send petitions. We've been doing all these things for 8 years, and it hasn't worked. Basically, we need to be the new Windrush folks. Once the public heard about how the gov't were treating them, they kicked up such a fuss that the gov't had to change what they were doing.Unfortunately. as you say, a good chunk of the public believe the lies about us. Some of the public just don't care. The rest know what's going on, think it's terrible, but they don't do anything about it. My FB friends read my posts and say things like, "My god, this is just evil! I'm so sorry that you're going through this!" They've lent me money, etc., which I'm very grateful for, but they're almost all wealthy, employed, able, male, white, etc. They would be listened to, if enough of them spoke up, but.... They don't.
The disabled are well hidden from general view. Most people believe that they are awash with money and help anyway so why give them anymore.
Put it another way the most important sector of society are those that fund the state. You won't get many votes if you go round telling them that their money is being handed out to the disabled unemployed!
Sorry but the disabled will never get the freedoms that are enjoyed by the non disabled. You only need to look at the latest attack of pouring flour over a disabled woman. Many years ago it was common place where I lived for kids to go out on a 'tipping' contest. To see how many wheelchair users could be tipped out of their wheelchairs in a day.
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