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Tag: ESA claim
According to a recent report from Child Poverty Action Group CPAG) claimants are being forced to repay their full Universal Credit (UC) award despite being entitled to it.
Why Are The DWP doing this?
During the pandemic the DWP temporarily changed some of the evidence rules to complete UC claims.
As detailed in the report by CPAG in January 2021 the DWP started to look into the claims that were made during the pandemic.
Whilst doing this the DWP have been changing the entitlement decisions given to claimants declaring that many claims have been wrongfully awarded.
Why This Shouldn’t Be Happening
CPAG have expressed their concerns that the process of retrospectively deciding claimants were not entitled to UC and beginning recovery is unlawful.
In addition, the DWP is asking for evidence of entitlement via the online journal, even from claimants that are no longer getting UC and would have no reason to check their journal.
Some claimants only find out about the alleged overpayment when they receive a letter from DWP Debt Management.
They therefore miss the one month deadline for challenging a decision and often don’t know that they could make a late challenge if they have good cause.
Shockingly, this process is set to be ramped up dramatically.
The DWPs Reaction
The DWP are employing a team of 2,000 staff to look again at 2 million claims over the next five years including, but not limited to, claims made during the pandemic.
The thought that a government department that tramples on claimants’ rights in this way is to be given powers of search, seizure and arrest, as revealed in our last newsletter, is truly frightening.
It’s very concerning that the government gives the DWP the authority to stamp on a person’s legal rights in this manner.
Not only are they able to stop a claimants payments without any notice they are also set to be given powers of search, seizure and arrest, as detailed in an earlier blog post.
DWP decisions such as these are life changing and literally leave people without the ability to eat, pay their rent and to keep warm.
Combined with this is the mental toll that this puts upon claimants leaving them in a state of distress not knowing where to get help.
Claimants deserve to be treated with respect and should be given the right to reply before any permanent decisions are made by the DWP.
Not only is it morally wrong to change decisions retrospectively, moving the goalposts when it suits the DWP is despicable and should be challenged at all times.
You can find the full copy of the report here https://cpag.org.uk/policy-and-campaigns/briefing/demands-repay-impact-and-legality-dwp-reverification-uc-claims
Please read, share and tweet this article. Doing so raises awareness of the real issues that affect the working class of this country.
I don’t receive any payment for the work that I do and to say it’s a struggle is an understatement. I’d really like to be able to continue writing and campaigning.
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A huge thank you to everyone that reads, shares and supports my blog. I really appreciate it and I couldn’t have got through the last two years without you.
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.
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.
New regulations have been issued to enable registered nurses, occupational therapists, pharmacists, and physiotherapists to issue fit notes.
This will extend the categories of people that can issue fit notes.
New statutory instrument
The new regulations will commence from 1 July 2022.
These regulations being Social Security (Medical Evidence) and Statutory Sick Pay (Medical Evidence) (Amendment) (No. 2) Regulations 2022 (SI.No.630/2022) amend the Social Security (Medical Evidence) Regulations 1976 and the Statutory Sick Pay (Medical Evidence) Regulations 1985.
The new regulations also make amendments to sets of regulations which refer to medical evidence as having been signed by doctors or registered medical practitioners.
The explanatory memorandum to the regulations advises that –
‘Currently only doctors can certify fit notes. This is not reflective of modern ways of multi-disciplinary working in healthcare where alternative healthcare professionals (HCPs) such as nurses often lead a patient’s diagnosis and healthcare management.
Expanding certification to a wider group of HCPs will better enable relevant HCPs to undertake health and work conversations to issue and certify fit notes without having to refer patients to their doctors.’
Commenting on the regulations, DWP Minister Chloe Smith said today –
‘The extension of fit note certification is fantastic news for patients, making it easier for them to get the support and advice they need from the right place, ensuring where possible that they are able to remain in work.’
These latest fit note changes recognise the valuable role other professions play in helping manage people’s health, and I hope this will also help reduce unnecessary bureaucracy for doctors and general practice more widely.’
This is welcome news for people struggling to provide fit notes for the DWP which can be a struggle for many.
SI.No.630/2022 is available from legislation.gov.uk
Thanks to Rightsnet for providing this information.
I don’t receive any payment for the work that I do.
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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.
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.
As we quickly approach Christmas and a cold hungry winter once again the DWP are going to bring back the cruel sanction system.
They never miss a chance to make Christmas even more harder do they.
Sanctions relating to the claimant commitment had been suspended due to the pandemic.
It is very clear that the DWP are now back to business including sanctioning sick and disabled claimants.
According to Touch base the DWP are quoted as saying“This week a change was made to bring the obligations in new style JSA and ESA benefits in line with those in Universal Credit”
“This will mean that, as is the case for Universal Credit claimants, if someone in receipt of new style JSA and ESA fails to do what they have agreed to in their Claimant Commitment without good reason – such as having or caring for a child, or a change to a health condition – their payments may be reduced for a set period. This is known as a sanction.”
“All Claimant Commitments are tailored to a person’s personal circumstances and local jobs market, and claimants affected by this change are being informed of the introduction of the new process. Sanctions are only applied as a last resort when a claimant is not engaging with the commitment they have made. If someone disagrees with a decision they can ask for it to be looked at again.”
This is all rather scary as the government have now passed on the onus of sanctioning decisions to the Job Coaches and not a decision maker.
Sanctions aren’t always a last resort decision and I’m speaking from years of experience helping people to appeal sanction decisions. Also since when have the DWP taken children into consideration… They haven’t.
I’m sure that many of you reading this have had so called Job Coaches that take an obvious dislike you you. I’ve also experienced this and I know exactly what it’s like. It’s soul destroying.
I’ve experienced having a Job Coach that clearly hated me. She would find holes in everything that I did and tried to sanction me at every opportunity that came her way.
Luckily I was able to make a complaint about her which involved my local MP.
I changed Job Coaches but she would glare at me every time that I walked past her. I have mentioned this in a previous blog post.
My question is this… How many innocent people are going to be wrongfully sanctioned because of this very reason?
It’s also worrying that there could well be even more sanction targets (offloads). Therefore the need to reach these targets will cause the suffering and distress of thousands of people.
Basically the whole sanctioning process could well be ramped up a whole lot more..
Opinion isn’t fact and there are many valid reasons why a claimant has not been able to to fulfill their claimant commitment.
Illness, lack of money for essentials such as no money to top up mobile phones or to have access to the internet at home.
Access to libraries is fast becoming a rarity these days. The DWP demands that claimants have access to the internet at all times.
Essentialy if an Job Coach decides in their opinion that a claimant hasn’t done enough then they’ll sanction them.
Remember once again opinion isn’t always fact and this is a very dangerous precept to use.
The whole sanction system should be abolished. There’s absolutely no reason why a person should have their very basics for survival to be snatched off them by the click of a button. Which is based upon the opinion of a Job Coach. Remember opinion isn’t always fact.
Whilst we are still in the midst of a pandemic the government and the DWP have now returned to normal. Don’t expect them to care because they obviously don’t.
Keep a good written and digital record (if you can) of everything that you’ve done to fulfill your claimant commitment.
If you’ve been ill or suchlike also try to keep a record of whatever you can to prove that you’ve been ill.
It’s important that you do all this because sanctioning you will be a whole lot harder if you keep a good record of everything.
If you are in the Greater Manchester area please have a look and even join in with Greater Manchester DPAC (Disabled People Against Cuts) activities. You can find them here at https:\\manchesterdpac.com
Please read, share, tweet and email my blog posts. It helps enormously to get the truth out there.
How am I? I’m ok apart from catching a sickness bug yesterday hence my blog being late. My apologies.
A huge thank you to everyone that has supported my campaign and blog. I really couldn’t have done it without you.
I don’t receive any payment for any of the work that I do. If anyone would like to donate there is a donate button at the top and side of this blog post.
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.
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.
Please click on the below link from the Public Law Project.
If you are told to repay back hardship payment debts make sure that you challenge this.
It is your legal right to do so. If needed quote the below article and insist that the DWP use their discretion regarding payment of hardship payment debt.
Insist that these payments are causing distress and suffering, which they do for thousands of people.
This is also essential because the majority of claimants already have monies garnished from their payments for council tax debt and suchlike.
No one should be forced to live in extreme hardship such as this.
I expect that the DWP won’t like this so don’t expect them to suggest it to you.
Please like, share and tweet my blog. It’s very important to get the truth and the reality of our life’s out there.
I don’t get paid for anything that I do but I do want to continue to be able to continue to write my blog and continue with my campaign.
For anyone that would like to donate there’s a donate button at the top and side of this blog post.
A huge thank you to everyone that and has supported my blog and campaign. This makes such a big difference.
The DWP has recently backed down on their high pressure pre-tribunal tactics the day before they faced a judicial review initiated by a disabled woman. Her case concerned the way the tactics that the DWP has been using putting extreme pressure upon PIP claimants via telephone into accepting a lower PIP payment offer rather than attending a tribunal to hopefully receive higher PIP payments.
The claimant known as ‘K’ had been approached by the DWP who made a low offer and told the claimant, known as ‘K’ that they had just one hour to make up their mind. During this conversation the DWP also warned K that tribunals ‘are not very nice to go to’ and if K took it to tribunal they could lose her whole award.
The DWP are well known for their bullying tactics, particularly towards disabled and vulnerable people. K explained that they felt extremely pressured to make a quick decision and wasn’t given the time to make a decision or to seek advice upon this from others.
Needless to say the DWP should not be putting pressure upon people like this, using fear as a tactic to manipulate disabled people into accepting a lesser payment that they are entitled to.
Unsurprisingly the DWP refused to accept it was doing anything wrong for a year until the day before the hearing, when it suddenly agreed to make a number of changes.
These changes being;
Advising staff its essential that they inform claimants that even if they accept a revised offer they still have the right to appeal against it.
Telling DWP staff that they must ensure that benefit claimants do not feel ‘pressured’ into making a decision.
Introducing mandatory training to all staff involved in ‘lapsing’ appeals by the end of October to ensure they understand the updated guidance.
The DWP unsurprisingly, refused to agree to end the practice of making pre-tribunal offers to claimants .
We shall see if the DWP continue to use their intimidatory tactics, or if they agree to the actions agreed upon in the court case.
As you all know the DWP like nothing better than to target the most vulnerable and disabled people, knowing that they might find it hard to appeal decisions made towards them by the DWP, and personally I do think that some DWP workers do get a kick out of doing this.
It’s never ok to treat people like this. No one should have to fight for the very means to survive especially in times like these when everyone is struggling even more because of the pandemic.
Can you imagine how awful it is to receive a letter from the DWP that you are no longer entitled to the very monies that have kept you going? Your very means of survival taken away at the push of a button and an uncaring letter sent to you?
This is the reality of life for thousands of people every day, it sends people into mental and physical distress. It’s a never ending circle of abuse metered upon them by the DWP initiated by the government.
No one should ever be forced to go through this cruelty and we must continue to fight to end this. You can do this by sharing my blog posts and other campaign groups posts. Write to your MP to share your disgust, share posts on Twitter and Facebook. Join a campaign group, share your worries and concerns.
Your voice matters so let’s make sure that you are heard!
This week is a very difficult week for me. As you know my son recently died and it is our joint birthday this weekend on the 1st of August.
The pain of loosing a child, even though they were an adult is unlike any other pain that I have ever felt before. A part pf me wants to run away for the day, hide and speak to no one. Another part of me says sensibly that I can’t do that because his sisters will probably want to do something.
To put it bluntly I’m a mess but I’ll be ok, that’s what I keep telling myself. It feels like two minutes ago when Joseph entered this world at 7.40am .
Joseph was autistic, dyslexic and he also had a few other conditions, but he was an extremely brave, high functioning individual. He loved living on his own in his flat, and he was the local odd job man, always helping others.
Joseph did also have to fight the DWP every time his PIP and ESA was up for renewal. He attended tribunals and was helped by local organisations and myself. I know that he found this extremely hard to cope with but he did and I’m so proud of him.
This blog post is written in remembrance of Joseph, and all the good that he did in this world. He would have been very happy about this decision.
Please read, share, tweet, email and talk about this blog post and the issues surrounding it. This makes a lot of difference and it helps lots.
Please support my blog and campaign and blog. I don’t receive and funding for what I do and I am still helping families locally with food etc. I really couldn’t continue without your support.
For anyone that would like to donate towards my campaign and blog theres a donate button at the top and side of this blog post.
A huge thank you to everyone that has previously supported my campaign and blog.
Personally I’m trying to make my front garden into a memorial garden for my son and any advice etc is more than welcome!
Many thanks to Benefits and Work for being the inspiration for this post.
I’ve been campaigning against the cruel system which is Universal Credit since it’s conception. I have with friends held weekly demonstrations against the cruelty of said system and have been told countless accounts of how Universal Credit has affected people, how it has caused many people to end their life’s, split families up and has Rendered people ill, depressed, stressed, hungry and feeling that they can never satisfy the demands of the system which was created in order to ‘help’ people.
The truth is that Universal Credit doesn’t help many, it leaves people in a much worse financially than they were before. It wears people down until they can’t cope any more.
It doesn’t discriminate though, it treats everyone in the same manner, making some people feel like a criminal for asking for help because they need it and deserve to be helped.
if you look through this blog you will read many stories of how this system has treated people, how its worn people down and has for some been a massive contributor into people taking their own life.
We’ve handed out hundreds of food parcels, literally fed people that haven’t eaten for days. Indeed, I wrote in an earlier blog post I documented that I gave a woman and her children some tinned food and goodies, and how they walked across the road and ate the food out of the tins because they were hungry and hadn’t eaten a real meal for a long time.
I’ve spoken to people that had been discriminated against by the DWP because of the way they looked. If you scroll down my blog posts you will read that a man was discriminated against because he wasn’t wearing a suit and tie and proper shoes for his appointment at the Jobcentre.
This was blatant discrimination because they knew how poor he was, how he’d had no money for over a month and only possessed one pair of canvas shoes and a thin summer jacket.
The demands that the DWP make to people can be completely ridiculous like this, if he had’t spoken to us he would never have found out that he didn’t have to do this.
I also helped a woman with a young baby who was told by her advisor that she couldn’t come to the Jobcentre with her baby. This is completely unfair and also untrue. Children are allowed to attend appointments but the DWP like to make the rules up as they please.
I’ve spoken and helped people that were very close to taking their own life because they couldn’t cope with the DWP bullying anymore. I’ve also helped people that became homeless when Universal Credit was first introduced into my town and two other local authorities. I’ll also never forget being told by a police officer that a man that I had helped but was later let down by the system, that he had taken his own life because he couldn’t see any future for himself.
I really could talk forever about this, please scroll through my blogs and my media posts to see more. It’s cruelty certainly ignited a fire inside of me to make me determined to fight these and other injustices throughout the DWP and other systems.
Universal Credit was introduced under the guise of supposedly making it easier to claim and that people would be better off financially. It wasn’t long before it was shown to do anything but this. It can virtually destroy people.
Years ago I made a promise, prompted by my friend Michael to document everything that I see, hear and experience in this blog. I really didn’t expect it to be read by anyone at all but it was because it wasn’t being spoken about back then.
Although I can’t be there today to take part in the day of action because I developed Potts Syndrome which comes and goes, but today it’s here after having Covid and Long Covid I am there in spirit. Covid nearly broke me but it didn’t and I’m very grateful to have survived it.
I stand in solidarity with everyone that’s campaigning against Universal Credit whilst also demanding that the government introduces the £20 uplift to disabled people as well. Disabled people have been hit the hardest by the pandemic, many haven’t been able to leave their homes because of quarantine restrictions and also the lack of carers being able to help at home. It’s absolutely shocking that the government treats them in this way.
The DWP systems aren’t good enough. They don’t help people, instead they punish people because of their own existence. I fear that this will continue to worsen because they hate poor and disabled people, and they don’t care if we suffer either.
I also experienced the death of my son which was totally unexpected and through no fault of his own. He went to bed and didn’t wake up. Joseph was disabled and he had to fight for every penny that he got from the DWP. I’ve lost count of the amount of appeals that he had to make to get his rightful payments.
When I first learnt that my son had died I didn’t know how I would continue, grief can take you to some very dark places. Despite this I think that I’m learning how to cope with it, knowing that it’s ok to have an off day or to feel sad sometimes. My daughters and everyone that reads my blog and supports both the campaign and blog have really helped me. It’s ok to cry and there shouldn’t be any shame surrounding this.
My son shared the same birthday as me which is coming up very soon, so I know that’s going to be a tough day for us all.
I want to do more though. I don’t think that I’m doing enough to raise awareness and to help people. Despite this I do know that I do need to keep this blog going because despite everything I still need to get the truth out there. If anyone would like to donate towards the upkeep of this blog and my campaign theres a donate button at the top and side of this blog post.
Please read, share, tweet and email my blog. Let’s get the truth out there!