Category: loose women

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.

Starmers keynote speech.. Empty words for the average working person and disabled people.

As many others did I watched Sir Kier Starmers conference speech in anticipation… Maybe he’ll recognise the plight of unemployed, disabled and ill people. Sadly I was disappointed, his whole speech revolved around the word ‘work’ and how good it is to work.

Heres a word count of the words that he used in his speech yesterday. He mentioned the the word ‘work’ a massive 69 times, ‘care’26 times, equality 3 times, ‘security’ 6 times ‘dad 11 times, mum 17 times and ‘tool’ 6 times.

From this we can be safe to say that the main focus for him was work and how good it supposedly is for you. Sounds familiar doesn’t it. It’s much like the speeches that we heard from the conservatives that resulted in the suffering and deaths of thousands.

It’s not as simple as that though, work isn’t some kind of liberating utopia that frees both mind and body leaving you with a sense of self achievement. I do accept that certain careers such as nursing, caring and healthcare work can give people a massive feeling of achievement there are stresses that come with them.

Low pay, high rents, high childcare costs and other costs that come along with our culture of low paid, undervalued work end up taking any sense of self achievement away.

Myself like Starmer can look back upon our parents hard work but it’s much like a tale of two cities. My father worked hard for little or no thanks and without basic safety equipment. He was forced to work night shifts which prevented him from spending much time with his children and when he did he was grumpy because he was tired.

My mother had several jobs, none of them gave her any sense of achievement and all of them were very low paid. As a child it was awful seeing them become so stressed by their situation.

I was and still are proud of them, but their situations made me want to fight for more than they had. I can’t look back and say that it was inspirational because it wasn’t.

Coming back to the present day…. Most people in low paid jobs have to claim an extra benefit such as Universal Credit or Working Tax Credit to be able to feed themselves and their families. Their wages being so low that they can’t survive on them alone.

It was very disappointing to hear that Starmer is apparently refusing to support a £15 a hour minimum wage increase for workers despite him agreeing with this previously. At the same time Starmer knows that we live in a low wage economy that inevitably leads to poverty. Luckily Labour Party members voted in favour of it even though its not binding.

In summary work does not fulfil the average person and nor will it until working conditions, low pay extortionate childcare costs and high rents are dealt with. Instead it causes stress, poverty and everything that comes along with this.Homelessness is increasing amongst working people as well as the unemployed.

People try their best to better their situations but the current system prevents them from doing so. A £15 a hour pay rise would help this but the whole system needs to change before it can benefit most people to a noticeable degree.

Feel good speeches are good on the day, words are said that some wanted to hear but when you leave out the basic needs of people, ignoring disabled people and those on legacy benefits. They aren’t going to see anything that would change the lives of those that need the changes the most.

It’s greatly important that everyones voices are heard not just working people. It’s insulting to those that are unable to work and it leaves them politically homeless with no where to turn for help.

Deeds not words are needed and the inclusion of everyone despite disability, illness and age. It’s needed more than it ever was before and Starmer must act to address as soon as he possibly can.

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Please read, share and support my blog if you can. I don’t receive any payment for any of the work that I do and every share makes a massive difference.

Unfortunately my daughters ill with Covid 19 at the moment and times are very hard at the moment and I’m still recovering from pneumonia. Every share really helps to get the truth out there.

Thank you to everyone that does share and supports my blog and campaign. I really couldn’t do this without you.

£20 Universal Credit uplift to be taken away British Gas prices dramatically rise.

It’s often been said that being poor is an expensive way to live and this weeks British Gas price hikes prove this. Keeping your home warm is always a challenge when you’ve got a low income, indeed many are forced to rely upon pay as you go meters to provide their energy.

Keeping a home warm enough to live in is a basic human right and it shouldn’t be regarded as a luxury but sadly this is soon to be the case for even more people that could barely afford to keep warm already.

On the 1st October British Gas are increasing their prices dramatically.. Heres one example of how much more its going to cost

To put it bluntly no matter how much we scrimp, how much food we won’t be able to buy anymore this will be too high a cost to meet by many of us myself included,. At the same time the government are refusing to permanently increase the £20 uplift payments and nor have they got any intention of extending it to people claiming legacy payments, many of them already vulnerable and living in poverty.

To say I’m furious is an understatement. As I type this smaller energy companies are being forced to close because they too can’t afford the British Gas price increases. It’s obscene. Meanwhile the Business Secretary Kwasi Kwarteng has announced that the government will not be bailing out energy companies. The very same energy companies that people on lower incomes rely on.

It’s no surprise to hear this though but its still awful to hear.

This winter is going to be horrific for many of us as the means to keep warm are being taken away from thousands of people with no opposition from within the government.

I was a child during Thatchers awful government, I had holes in my shoes, often lived in a cold home and had no luxuries at all. It’s shocking to see how much worse the present governments rule is. Thousands of people have died as a result of the decisions they make towards the poorest and most vulnerable.

How many will survive this winter? I really dread to think.

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How am I?

Still recovering but feeling a lot better. Still coughing but I’ve been told that it might take a while to go, but I’m alive and very grateful for this. Not exactly living but existing like so many other people.

I’m very concerned that I’m going to catch Covid 19 again because its running riot in my daughters school now their mask wearing policies and hand sanitising policies have changed. Children are being constantly sent home from school because they’ve got symptoms and it won’t be long until the whole school is shut as a result. I will write a further blog post about this.

I’m still struggling, a short walk is flooring me but the good news so far is that I’m managing to keep my sats at 94%. Not brilliant but much better than it was.

I shall also keep you informed about this.

Please take care, keep safe and please wear a mask and sanitise your hands. It’s important to stay healthy even when the government doesn’t give a shit.

Please read, share and tweet my blog posts. It’s important to get the truth out there and to as many people as possible.

I don’t receive any funding for any of the work that I do and to say its a struggle is an understatement. Every penny makes a massive difference. For anyone that would like to donate theres a donate button at the top and side of this blog post.

A huge thank you to everyone that has and does support my campaign and blog. I really couldn’t do this without you. Thank you xxx.

DWP agrees to waive hardship payment debts.

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.

https://publiclawproject.org.uk/latest/dwp-agrees-to-waive-hardship-payment-debts-after-successful-judicial-review/

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.

Maximus work capability contract extended for two years.

It has been reported this week by Rightsnet that the work capability assessment contract with Maximus has been extended by two years to 31 July 2023. The continuation of contract will supposedly ‘secure service continuity and stability’ whilst at the same time allowing the transfer of caseloads and services into a unified assessment service trial.

The DWP (Department of Works And Pensions) have also confirmed that they have extended the existing contract with Maximus UK Services Ltd to provide work capability assessments for employment and support allowance (ESA) and universal credit. This will continue for an additional two years to 31 July 2023.

The DWP have had plans to create a unified, integrated assessment service from 1 August 2021.

The DWPs plans to merge the separate PIP (Personal Independence Payments) health assessments and work capability assessments, ESA (Employment and Support Allowance and universal credit, were put on hold last year as a result of the Covid-19 outbreak .

This was confirmed earlier this year in a written statement to Parliament in July 2020, quoting ‘We recognise that it is vital for our claimants to have a safe and stable service. Consequently, my Department intends to explore options to extend the current contracts for up to two years, which will ensure continuity of services when the current contracts end on 31 July 2021.’

In a contract modification notice published last week, the DWP now confirms that it has extended the existing contract to provide work capability assessments – that was awarded to Maximus for the period 29 October 2014 to 31 July 2021 (at a value of £938 million). This now continues until 31 July 2023.

This will add a further £300 million to the Maximus contract value.

The DWP have commented saying that they will -‘Secure assessment service continuity and stability beyond the current contracts end date on 31/07/21’ .This will provide the contractual flexibility needed for any subsequent changes to the ongoing service design necessitated by Covid-19 measures.

This will enable any associated policy changes made during the extension period.

It will also allow the DWP to implement pre-Covid flexibilities and to remove volume and service from the Supplier into a Departmental Transformation Area/to deliver devolution of specific areas of the service (related to specific welfare benefits) if this is required’

‘For more information, see Health and Disability Assessment Services – contract extension from gov.ukSource Rightsnet

I’m sure that we all agree that these ‘medical assesments’ are cruel and unnecessary for disabled and ill claimants. A doctors and/ or evidence from a medical consultant should be more than adequate to prove to the DWP that they are disabled and/or ill. Any government that genuinely cares for disabled and ill people would of course accept this.

This Tory government have proven time and time again that they don’t care. Instead of compassion they issue a relentless barrage of cruel tests and examinations that cause physical and mental distress to thousands of people everyday.

We have a prime minister that happily spends millions of tax payers money on decorating number 10 and suchlike whilst giving huge contracts to their friends regardless of if they can’t do the job they’ve been contracted to do.

It’s easy for the government to target the most vulnerable because they believe that they won’t fight back. However as we have seen from groups such as DPAC (Disabled People Against Cuts) and campaigners like myself they can and do fight back in the quest to change things. They do and have made a difference.

Its exhausting though, constantly fighting against the government machine who’s policies reflect the fact that they want to get rid of us. However they forget that there are more of us than they are of them and we will continue to fight to make changes that we need.

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Today is my son’s inquest and as you can expect I’m upset, the pain sometimes can be overwhelming. I have to be strong for my girls and my grandchildren.

Long gone are the flowers that I used to place on the little shrine that I’ve created at home. Flowers are expensive as is everything else these days.

I hate living like this and I hate the fact that my son is no longer with us. He had plans to do lots of things including sorting my oldest daughters gardens out and to do mine that I can’t use because its a mess. Little unimportant things like this always remind me of my son and the wonderful young man that he was.

I will be ok though, it will get better but I’ll always grieve for his loss but I will learn to live with it better. No one ever gets over loosing a child.

I’ll be back next week with another blog post.

Please if you can share, tweet, like and email my blog. This does make a massive difference and it gets the truth out there which is extremely important to do.

I don’t get paid for any of the writing that I do and it’s a struggle to say the least. I want to continue blogging and campaigning because its very important to help people.

For anyone that would like to donate theres a donate button at the top and side of this blog post.

Thank you!

A huge thank you also to everyone that subscribes, shares and has and does help my blog and campaign to continue. It means the world to me.

My son died.. How am I?

As many of you will already know my son died earlier this year. His death was very unexpected and it was due to no fault of his own. To say that it’s been a struggle is an understatement, after all we aren’t supposed to outlive our children.

My son had plans to go travelling and to work near family in Estonia and Latvia, something that he was looking forward to. Josephs death has changed us all in one way or another.

The sudden death team over at Greater Manchester Police have been amazing, they’ve literally held my hand through it all, from daily phone calls to see if I was ok and other phone calls about Joseph and the horrible stuff that every person has to go through when a loved one dies suddenly.

The loss of Joseph hit me hard again when last week I received a phone call from the coroners office. She phoned to tell me that I would be getting a full copy of his postmortem and notification that they’ve been able to bring his inquest back to the 2nd September rather than October.

Good news I suppose but not the news that any parent wants.

I really didn’t know what to expect when I received my first copy of his postmortem via email, but I did know that reading it would be extremely hard for me. My little boy (even though he was almost 6ft tall) has gone. I had proof in the black and white print I was reading on my laptop.

I suppose that it’s easier to hold onto him before the postmortem results even though we’d already given him a lovely funeral and memorial thanks to everyone that helped me with this. It’s a totally different ball game when you’re faced with it in black and white.

So back to the Postmortem… The coroner couldn’t find a cause of death and this will be the report given at the inquest. I had been warned that this would probably happen. Privately she said that even though theres no obvious cause of death it could have been one extra painkiller that took him away.

I do know however that he fell asleep happily listening to his music after talking to his sister and myself and he wouldn’t have felt any discomfort etc.

The hardest thing to deal with physically was going to his flat and sorting things out. I did this with my oldest daughter and we were very distressed because once again it was a reality check.

We could see exactly what his last movements were. He washed his pots, got changed and went to bed. Everything was left as it was. In a corner we spotted Josephs Easter chocolates for all of us that we no longer would be getting.

Back home I made a wooden chest for Josephs clothes and belongings and I locked them all away safely. I’m hoping that he approves.

Joseph had many struggles during his short life, the most notable ones being his primary and secondary schools refusing to recognise that he was autistic and he had to learn differently to others. I know that many parents of children with additional needs are still fighting this battle.

The sad reality is that years after my son left school, thousands of parents are still forced to fight to have their children educational needs met… From autism, dyslexia and many other additional needs that they might have.

Parents shouldn’t be forced to have to fight for a decent education but still they have to.

Joseph didn’t give up though and despite the odds he did extremely well for himself and I was very proud of him. He was a very special person that is missed by so many.

Never give up fighting for your children, they deserve to be treated well and have their needs met. I did my best but absolutely no one would listen to me.

I’m sorry that this weeks blog is different than usual. I’ll be back to normal next week. Thanks for reading and sharing my blog posts it means the world to me.

Photo by Pixabay on Pexels.com

Please read, share and tweet my blog. A huge thank you to everyone that does and has supported my blog and campaign, I couldn’t do it without you.

I don’t receive any funding for the work that I do and I’m finding it much harder since my son died.

If you would like to donate theres a donate button at the top and side of this blog post. Thank you.

DWP BACKS DOWN OVER HIGH-PRESSURE PRE-TRIBUNAL TACTICS


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!

Photo by Sora Shimazaki on Pexels.com

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.

PIP Mobility Awards Appear Manipulated.

Thousands of claimants claiming PIP for mental health conditions are missing out on PIP payments because their reports appear to be manipulated.

Research conducted by Benefits And Work has shown that although the award rates rose for a year they’ve now dropped down to their previous levels which have started to rise again.

This is appalling because award rates should not have been shown to fall, they should have continued to rise and staying at a higher level.

Benefits And Work have also looked at the award rates for all conditions that the DWP consider would be affected by mental health and surprise, surprise they’re the same.

According to the DWP’s own estimates regarding mental health conditions approximately 6% of the entire PIP caseload should have moved from no award of the mobility component to enhanced.

Indeed a further 6% should have been moved from no award to a standard award.

Also 2% of awards should have moved from standard mobility to enhanced mobility.

The increased award rates regarding mental health should have been immediate and also should have been sustained once it was implemented. This would have resulted hundreds of thousands of additional essential mobility awards in place by 2023.

As usual the DWP are reluctant to comment upon this despite Benefits And Work submitting Freedom Of Information requests and the DWP giving them the runaround.

Sadly the DWP will do anything to prevent people from receiving their essential payments. I have absolutely no doubt that they do this because they know that vulnerable people are less likely to fight back.

I fully expect the government and the DWP sleep soundly at night because they believe that they’re doing the right thing by denying vulnerable people with the means to live a decent life even though its cruel and inhumane.

Thousands of people have lost their lives whilst fighting cruel decisions made by the DWP regarding their payments, I reported upon this last week.

Everyone deserves to live a good life and they should be given the support that they need to have a good quality of life. I will continue to fight for this alongside DPAC and other organisations.

PIP is Personal Independence Payments.

DWP is the Department Of Work And Pensions.

Source Benefits And Work, check them out they’re amazing.

Photo by Liza Summer on Pexels.com

As for myself, its been a tough week for many reasons, one being that I’ve undertaken the task of sorting out old photos of my son when he was little. Its so sad looking at the photos knowing that when I took them I thought that he would outlive me.

I hope that you are all ok and surviving the best that you can do. it’s such a tough time for so many of us for many differing reasons.

Lots of love and hugs to you all, I couldn’t do this without you.

Please read, share, tweet and email my blog. Each share raises awareness and helps others to cope in such hard times.

Once again a huge thank you so much for everyone that supports my blog and campaign, I really couldn’t do this without you.

If you would like to donate to keep my blog and campaign going theres a donate button at the top and side of this blog post. If you’d like to buy me a coffee I’d really appreciate it. Thank you xx.

Face to face assessments to return for PIP and WCA claimants.

Last month the DWP minister Justin Tomlinson informed the Commons Work and Pensions committee in parliament that face to face ‘interviews’ are set to return although he stated that some telephone and video assessments will still continue.

There has been no concern from Tomlinson about the safety of vulnerable claimants and the fact that there is still a pandemic and most people forced to attend these ‘assessments’ are indeed vulnerable and are still having to shield.

Tomlinson however claimed rather confusingly that they had ‘Lost all of their health professionals’ because they apparently have gone to work for the test and trace system instead.

It isn’t clear yet how the system is going to return to normality when, as he said the health professionals that were employed have now left. Maybe Tomlinson will pay them even more money to do this, therefore tempting them away from their current employment. Who knows, I expect we will find out sooner rather than later.

It does however take a particularly cruel mindset to conduct these ‘assessments’ and to declare vulnerable people fit for work when they clearly aren’t.

Tomlinson went on to say that the work capability assessments (WCA) will begin shortly and PIP (Personal Independent Payment) ‘assessments’ will follow a few weeks later although they will keep video and telephone assessments. Tomlinson wasn’t clear in what capacity this will be, clarity isn’t his or the Tory party’s strong point.

As I write this I expect many people will have had their much dreaded letter from the DWP regarding their assessment, thus causing distress and panic for already vulnerable people.

Whilst the Covid 19 vaccination programme is going well there are people that are unable to have the vaccinations for health reasons. The Covid 19 strain from India has now started to take a hold in the UK, putting thousands at risk.

I urge Tomlinson and the government to rethink their assessment strategy and to put the health and well-being of disabled and vulnerable people first.

Photo by Kat Jayne on Pexels.com

Once again thanks to Benefits and Work for their hard work in researching this and publishing this information. You can find them over at http://www.benefitsandwork.co.uk

WCA is the Work Capability Assessment and PIP is Personal Independence Payments.

I don’t receive any funding for the work that I do and for my campaign.

Please help me to continue to do this, there’s a donate button at the top and side of this blog.

A huge thank you to everyone that reads, shares and tweets my blog. It makes a massive difference and it helps to raise awareness.

Let the bodies pile high says Johnson

Yesterday was quite a busy day for Dominic Cummings the former chief aide whilst he gave evidence in a seven hour hearing regarding the governments handling of the Covid 19 pandemic.

Cummings particulally took aim at Boris Johnson and Matt Hancock, depicting the chaos and failing of the government’s handling of the Covid 19 crisis, saying that the failure, incompetence at the top of government stating that Covid 19 had killed thousands that didn’t need to die.

Whilst many people had already realised that Prime Minister Johnson anti lockdown, ignored scientists advice and failed to introduce lockdowns in adequate time. This is the same prime minister that openly said that he didn’t care about people dying, saying ‘Let the bodies pile high’.

For myself and others it comes as no shock. Johnson and his ilk have no sympathy or care for working class people, even less sympathy is given to disabled and elderly people, you can see this in their policies and their attitude.

What people need to realise is that Johnson and co come from and live in a totally different world than most people. They come from a place of great privilege and they like to flaunt this whenever possible.

Their handling of the pandemic is a good example of this. for example whilst thousands of people were dying, Carrie Symonds, Johnsons girlfriend was shown to be more concerned about her dog than the pandemic and the death toll. Symonds also saw this as a perfect opportunity to try and find her friends jobs within the government.

Johnson knew exactly what he was doing though, he was warned by officials that a lockdown was needed but failed to act, taking him a further ten days to agree to a lockdown.

There was no plan for the government to use in the event of a pandemic, despite many in government believing that there was. This has undoubtedly has resulted in thousands of deaths. Ironically a plan had been created by the Labour Party which would have undoubtably helped thousands of people and would have prevented thousands of deaths.

Johnson also described Covid 19 as ‘the swine flu’ and stated that he was going to get Chris Whitty to inject him with Covid 19 live on television to prove that its nothing to be scared of.

Mark Sedwill the then Cabinet Secretary suggested that people should have Covid 19 parties like chicken pox parties, believing that herd immunity would then be reached by September. Meanwhile the government were drawing on a whiteboard asking who they can’t save with no regard for their safety nor regard for them at all.

Its very clear that the government doesn’t care and never will care. We only have to look at the way that the government treats disabled and working class people. Their policies have resulted in the deaths thousands before the pandemic and not one care has been given about this either.

It is completely normal for the government to treat people like this, we mean nothing to them. If they can’t make any use of us financially through exploitation such as their Workfare schemes, they punish people by making it extremely hard to claim benefits such as Universal Credit, ESA and PIP.

Such cruelty will continue for as long as they’re able to do so, with no effective opposition at the moment I can see such cruelty continuing for a long time to come.

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I would like to thank you all for your patience, especially after my son’s death. I’m trying to get back to normal, whatever my new normal is now.

I’m aiming to get at least one blog post published every week, hopefully improving the quality of them along the way.

I also receive no funding for my blog or my campaign. Every penny counts and it will help a great deal.

A huge thank you to everyone that shares and supports my blog and campaign. It means the world to me and has kept me going during such dark times.