Tag: universal credit.esa

Doctors with Long Covid Denied PIP Payments

UK doctors suffering from Long Covid have been denied PIP according to a recent report by The Guardian.

Long Covid can be very debilitating leaving sufferers unable to do the most basic tasks without some help and assistance.

The report describes how badly the doctors are being treated by the DWP.

For example a respiratory consultant has described how they were refused PIP (Personal Independent Payments) whilst having urinary incontinence, difficulty standing, preparing food, eating, washing, dressing or engaging with people face to face. They also stated that they can’t stand for more than 10 minutes, find it very difficult to prepare food.

They went on to say “I thought that I had illustrated quite clearly what my disability was.” “When I got the report back, I thought is this about me?’”



The article also reveals that the process of making a PIP claim was so hard and mentally exhausted that it worsened their symptoms leaving them feeling much worse than before making their claim.

Some describing that they’ve been forced to use almost all their savings on private treatments and have considering selling their home as a result of this process.

For example an infectious disease expert that developed Long Covid found that their claim was rejected in part because they can drive a car, the assessor stating in their report that they showed “significant physical function” and “substantial cognitive powers”.

According to the Office for National Statistics from May 1st 2022 an estimated two million people in the UK have reported having Long Covid and it also beggars the question how many people having Long Covid are being refused their PIP payments despite having these symptoms and worse.

For many years now the whole PIP testing system has been heavily criticised and is flawed against the person applying for it. Many give up and try to continue without it because the process is too arduous and painful. It is noted that approximately 70% of PIP claimants win their appeal if they choose to do so.

The whole process urgently needs a huge reform and claims need to be processed correctly and fairly whilst taking into account the true symptoms and difficulties that PIP claimants report. Many PIP claims are refused upon the basis of lies made by the assessors conducting PIP assessments.

Sadly whilst the Conservative government remains in power any changes to the system remain very unlikely.

Photo by Andrea Piacquadio on Pexels.com

A copy of the full Guardian report can be found here https://www.theguardian.com/society/2022/jun/13/uk-doctors-long-covid-say-denied-financial-support

A copy of the Office of National Statistics report can be found here https://www.ons.gov.uk

If you are also finding it hard to claim PIP or/and ESA for Long Covid related illnesses please comment below or tweet your difficulties via this blog on Twitter or Facebook. Let’s get our voices heard!

Please read and share it helps massively to raise awareness .

I receive no payment for any of the work or campaigning that I do and it’s a huge struggle for myself like it is for you. If you can afford and would like to donate to enable me to continue with my work theres a donate button at the top and side of this blog post.

A huge thank you to everyone that has and does help support my work. Every penny makes a massive difference and enables me to continue.

Thank you.

Government Refusing To Release Universal Credit WCA Statistics

It’s another week and yet more questions as to why the government still haven’t released the Universal Credit WCA statistics. Their refusal to release these statistics can only lead me to believe that they’re trying to hide them most probably because the stats are pretty dire.

This isn’t unusual for the government and the DWP they’ve got a long track record of denial and refusal.

It appears that the Office for Statistics Regulation (OSR) aren’t impressed with their refusal to release these stats either so they’re demanding to know why the pass and fail rates for the WCA for universal credit are still secret, despite it being nine years after the benefit was introduced.


The question is becoming ever more important because approximately 1.7 million ESA claimants are due to be forcibly transferred to UC by the end of 2024 loosing their legacy benefits and the security that comes with this.

The question is this why have the figures for claimants that have been found to be capable of work or to have limited capability for work (LCW) or for work-related activity (LCWRA) been published for ESA since 2010 and not these important statistics?

What exactly are the government trying to hide?

Unsurprisingly the same figures have never been published for UC since the benefit was introduced.


IN 2017 the government promised that the UC WCA statistics would be available for viewing. Rather predictably they haven’t been provided and there is no indications that they ever will be.


The amazing team over at Disability News Service have been pursuing the DWP over its lack of transparency for some time and eventually resorted to having to approach the OSR for help.
As a result the OSR have now written to the DWP asking why the figures have not been published.

My bet is that they’ll ignore their request as well.


The main reason as to why these figures are so important is because Universal Credit claimants could be more likely to be assessed incorrectly and placed in the wrong LCW or LCWRA groups for UC. Therefore theres no guarantee that they’ll be placed in the same groups as they were when claiming ESA despite the fact that the tests are virtually identical.

More transparency and clarity needs to be urgently given regarding this issue especially as thousands of already vulnerable people will be quite rightly concerned when they are forcibly moved onto UC.

Universal Credit is a cruel heartless machine that targets the most vulnerable. These figures are needed to help and protect those that will be forced to claim it.

Photo by SHVETS production on Pexels.com

A huge thank you to the gang over at Benefits And Work for publishing this information and keeping us informed.

Are you interested in joining a group of likeminded people for solidarity and maybe some campaigning? You can’t go wrong if you join Disabled People Against Cuts (DPAC). They have lots of local branches that you can join.

Head over to https:manchesterdpac.com I’ve been working and campaigning alongside them for many years.

Please read, share, tweet and email my blog, every share etc helps massively to raise awareness and to inform people what’s really happening to real people.

Huge thank you to everyone that has and does support my campaign and blog I couldn’t do this without your support and solidarity.

If you would like to donate and can afford to theres a donate button at the side and top of this blog post. I don’t receive any payment for the work that I do and it makes a massive difference and enables me to continue with both.

Thank you!

Therese Coffey plans benefit shake-up

At the recent Tory Party Conference Therese Coffey, the secretary for works and pensions declared that the amount of people that have claimed PIP has ‘grown in a way that was not anticipated’ and instead it needs to be targeted at ‘people who need help’.

This is of course ignoring the fact that the people that are claiming PIP actually do need it.

According to Coffey this is evidence that things were ‘going wrong’ and nothing due to the fact that people living with illness and disability has increased due to many reasons some being Covid 19 and poverty.

Coffey went on to say that according to her findings three out of four young people that claim PIP their primary reason being mental ill health.

According to her figures this totals 189,000 young people that receive benefit focused upon a diagnosis of depression and that these young people may also claim other benefits as well.

Thus implying that young people shouldn’t be claiming PIP at all.

 Coffey also complained about the amount of people claiming ESA should have only 25% of claimants should be in the support group rather than ‘about 80%’ of those claiming ESA at the present time.

She also complained about ESA, saying that the original expectation was that only 25% and not the 80% that are in the support group now.

Coffey stated rather predictably that she wanted to change the focus to ‘what people can do rather than the benefit system being currently driven by what you cannot do’

So in essence Coffey is saying that she wants to get people with disabilities, especially those in the support group back to work without declaring any support that might be given to claimants forced to do so.

Coffey says this regardless of their disabilities and their ability to work.

This is despicable and based upon her opinion and not the actual truth which is evidenced in the claim applications given by people claiming ESA.

ESA and PIP are not benefits that are easy to claim. Most claimants are refused upon their first application and they have to appeal and often take it to tribunal to eventually succeed and receive their rightful payments.

Coffey also takes into no consideration about how disabling and serious illness such as depression are. Anyone suffering from depression has to fight hard to try and find some support for their condition. NHS funding has been cut leaving previous lifeline services taken away leaving support hard to find.

Let’s also not forget how serious an illness depression can be. It can’t be cured by forcing an already vulnerable person into work thus triggering them to an even deeper state of depression or worse.

Needless to say, Coffey has a swinging brick instead of a heart and she doesn’t care about anyone living with illness and disability. Her aim is to try and stop vulnerable people from receiving the financial support that they need to live, without a care about how they’ll be able to cope.

To add salt to the wound so to speak, Coffey has also refused to rule out merging PIP with UC, saying that ‘everything is on the table’. Meaning that if they can find a way of persecuting vulnerable people whilst doing this then it’ll happen. How dare disabled and ill people have any quality of life at all.

So, before the DWP has finished transferring DLA claimants to PIP or moving ESA claimants to UC, they’ve already started to plot another major benefits shake-up which is going to harm the well being of thousands of vulnerable people therefore putting them at risk and causing them great distress.

Photo by Alex Green on Pexels.com

It appears that we will have yet another battle to fight. We cannot allow the government to target and harass even more vulnerable people. The government always takes from the lowest hanging branches whilst forgetting that there are more of us than them and we will put up a fight.

Join myself and my friends over at DPAC https:\\manchesterdpac.com and continue to put pressure upon the government to do so.

Thanks to Benefits And Work for the inspiration for this weeks blog post.

Please read, share, tweet and email my blog. Every share makes a massive difference and it raises a lot of awareness.

I don’t receive any funding for anything that I do. If you would like to donate without putting yourself in financial hardship theres a donate button at the top and side of this blog post.

Every penny really does help and it makes a massive difference.

A huge thank you to everyone that shares, tweets, and supports my blog and campaign.

Your help really does make a massive difference,

This week has been another tough week for me and to be honest I wish that the universe would give me a break. Regardless of this I will continue with my blog and campaign. Thank you all for your support.

Let’s talk about Covid deaths.

Dear readers, subscribers and friends, I hope that you are as well as can be. This week has been difficult for me because it’s the first time that I’ve been able to sit down and grieve for my son.

Everyone grieves in their own way and the time it takes for a person to grieve is totally individual. I truly don’t think that I’ll ever get over it and I’ll just learn to live with it.

It’s heartbreaking to know that thousands of people are mourning the loss of a loved one to Covid 19. No one as far as I’ve seen has spoken about their suffering and loss. I cannot comprehend their grief and pain.

The government has done a good job of hiding the true reality of the pandemic, the deaths, suffering, long covid sufferers and those already isolated because of illness and disability.

It’s very easy for the Prime Minister to open the borders, allow travel to countries overseas and to open up shops and businesses, he doesn’t have to cope with becoming ill and having no support, to be isolated in his home due to disability and illness. As most of you already know that he doesn’t care, he doesn’t care about our welfare and he certainly doesn’t want to improve our quality of life.

I don’t underestimate the joy felt by many when they realised that they could come out of lockdown but I do realise that the Indian strain of covid 19 will soon be in most of our communities because Johnson once again hasn’t put much, if any thought into ending the lockdown.

Like many of you reading this I’m fully vaccinated, and many will be awaiting either their first or second vaccination, but I’m a tad worried about the Indian strain coming our way because we just don’t know if the vaccination works with this strain of COVID 19.

What I can say is proceed with caution, wear a mask, wash your hands and remain cautious. It’s a terrible indictment of our government that Johnson thinks that its ok to say ‘Let the bodies pile up’ and still be allowed to continue as Prime Minister. I remember the days when the opposition used to oppose such wrongdoings but now there’s hardly any from Sir Kier Starmer.

I really hope that we start to have some decent opposition soon because thousands of people need this now.

Please read, share, tweet and email my blog. Every share is important to get the truth out there.

I don’t receive any funding for both my blog and campaign. For anyone that would like to donate there’s a donate button at the top and side of this blog.

Thank you all so much for your support, it means the world to me.

Man threatened with eviction by landlord because his rent is a week late due to ESA payment delay.

Dear readers, its Thursday again and blog day. Today’s demo was very productive and many conversations were had and help given even though there was just two of us there today.

We really would like it if more people could join us but I also realise that many can’t for a wide range of reasons. It’s very hard to get the publics support for campaigns like mine because poverty isn’t pretty, poverty is depressing and harsh. It also reminds people that they could too be in the same position at any given moment. It’s a tough one I know but campaigners countrywide would love more support either face to face or online.

I’m still battling a virus and we still haven’t got a date for my dads funeral and I’m still grieving, so please be patient with me I am doing my best in limited circumstances.

Anyway enough about me onto todays demo and conversations. Please note that we gave help, advice and signposting to everyone that needed it, survival guides were handed out and lots of people were helped.

We do this all on a purely voluntary level and we aren’t funded by anyone. We just can’t abide injustice and the causes of poverty and discrimination, too many people are suffering, too many people are dying.

How many more deaths will it take before the public rise up against the causes? My guess is never, the it’s alright Jack attitude runs through our society preventing many from rising up against anything. This was highlighted today by a conversation that I had with a lovely chap this morning. His attitude towards universal credit was that it’s awful but it’s ok and we should just put up with it because everyone is in the same boat so to speak. We need to change this way of thinking and asap.

This morning there was a large queue for food parcels, indeed I had already had phone calls requesting one. As soon as we arrived with the food parcels they left with the people needing them. I’ve found that a lot of people in my area survive on food parcels being given at different places and free or reduced price meals given at various places.

Life shouldn’t be like this should it, surviving on food parcels and scraps of food. But it is, and the fault lies solely at the feet of the Tory Party. I will never, ever forgive them for this, I’ve never forgiven Thatcher either but that’s another story.

After the food parcels were handed out we had conversations with everyone that received one and checked to see if there’s any progress in their situation or if they need any more help and advice. We never let anyone leave without this.

I spoke to an older man that had been promised that he would receive his first universal credit payment in April, he had waited until this week to see if he actually got his payment and surprise surprise he didn’t.

He phoned up the relevant department and asked them where his payment was. The DWPs reply was cold and uncaring. No apology was made and he was told that he shouldn’t have been told this and he’ll just have to wait like everyone else.

His comment to me was “What am I supposed to do now? How am I supposed to survive now? They just don’t care do they”. Damn right they don’t.

I spoke to a man that was struggling trying to find access to the internet and was forced to just use the Jobcentres computers. I advised him to use the library’s free internet and computers, and also the free WiFi as Ikea etc. He was happy to know this and thanked me.

I briefly spoke to a woman that has very limited eyesight due to cataracts. she told me that she’s struggling with the new building because of the lack of signage etc. Lets hope that this is rectified soon.

We then spoke to a man whom I shall call Bob. This is his story, it might sound familiar to you.

Bob was due his ESA payment on the 16th of April but due to a doctors mistake Bob didn’t receive his payment. Bob enquired as to why he didn’t receive his payment and he was told to hand in another sick note, which he did.

Because of the above Bob was a week late paying his rent, his landlord is already threatening to ‘throw him out’ of his home even though legally he can’t do this. This obviously upset Bob because he had been street homeless for many years and he doesn’t want to have to go through that again. We advised him to the best of our abilities and signposted him.

Bob went on to tell us that his brother had previously won his ESA appeal, even though he had lung cancer and shouldn’t have been made to undergo one of these fake medical assessments. I call them fake because they more or less fail everyone and most people have to appeal this decision.

Bob went on to tell us that his brother recently died in February. He wasn’t even allowed to spend his last days peacefully because he had the DWP asking him to go for medical assessments.

Shame on each and every one of these highly paid so called medical professionals that fail obviously ill and disabled people. One day justice will come knocking at your doors and we’ll be waiting.

I then spoke to a man that said that because everyone’s being treated badly it’s ok because we’re all in the same boat so to speak. My answer was that it’s not ok, it’ll never be ok and it should never be accepted.

We spoke to a man that was given a 166 day sanction because he had attended a work trial organised by the DWP at the same time as his signing on appointment. He had informed his advisor etc, claimed bus fares etc to attend this work trial but he was still sanctioned for apparently not telling his advisor when he did.

You really couldn’t make up this could you. It’s downright persecution of the poorest because many feel that they cant fight back.

We signposted him to our local MPs office who will be able to help him with this.

We spoke to a man that told us that he had just signed off because he’d found himself a full time job, a rarity these days. We congratulated him and his smile said it all.

As he was leaving he said that he’d never sign up for that (universal credit) again. Can you blame him, I don’t. Many people choose to take themselves off the system because they can’t cope with it. Many of these people are street homeless struggling to survive.

There is a direct connection to street homelessness and universal credit and this needs to be reported more widely.

I briefly spoke to an older woman whom I shall name Joan as she was walking into the Jobcentre. She told me that she hates it in the Jobcentre because they always make her feel like shes done something wrong.

Joan has been sanctioned because she was in hospital and missed her signing on appointment. She has never been told the length of her sanction and wasn’t told that she can appeal this also.

We advised her, and signposted her to our local MPs office who will treat her with dignity and respect and hopefully overturn the sanction for her.

My heart goes out to each and every person that has been sanctioned, failed ridiculous so called medical assessment, has an awful landlord, cant manage on universal credit, can’t feed themselves or their children. It’s a long list isn’t it and I could go on for forever but you get the idea.

This state sanctioned abuse of the poor and disabled needs to stop and soon. Far too many people are dying, too many people are suffering.

I just wish that more people would realise that this could happen to them at any given time. Society needs to be more compassionate towards each other. It’s not a crime to be poor, but it is a crime to abuse those that are poor.

This all happened in less than two hours, and it was a quiet morning. Can you imagine how awful it is across the country? It’s much worse than the public and some politicians realise.

Please read, share, email and tweet my blog. It’s so important to get the word out there.

Many thanks to Roy for helping me this morning. I really appreciate this, I just wish that more people would join us.

I’m struggling at the moment, financially and physically. I know that this will pass, but each and every share of this blog helps thank you. I’m a skint single parent just trying my best to raise awareness and to correct the wrongs of the DWP.