Tag: coroner

I Struggle To Feed And Keep My Kids Warm. Real Life Stories From The Public.

As the never ending cold winter and the ever increasing cost of living and energy costs continues once again I took to the streets and interviewed several people in my local town Ashton Under Lyne.

Ashton Under Lyne is a typical northern working class town, drained of money by the government and the majority of people living in differing stages of poverty.

Mortality rates are amongst the highest in the UK and there’s a higher rate of people either being unwell or living with some type of disability.

Like any other northern working class town it doesn’t have a lot for people to aspire to despite the positive changes that Tameside Council are implementing and trying to introduce.

Years of government forced austerity policies has been and continues to cause a lack of funding for essential services with most things already stripped to the bare minimum.

As I headed off into the cold I spoke to a young woman that had two young children with her. I introduced myself and asked her how she is coping with the cost of living and the ever increasing energy crisis.

As I asked her this I could see that she was upset, telling me that she thinks that she’s failing her children because she can’t give them the things that she used to be able to do.

“We’re living in a cold house trying to keep turning the central heating on at a bare minimum. I usually turn the heating on for an hour in the morning and again in the evening at bedtime, that’s if I’ve got credit because I’m on a prepaid meter”

She went on to say that her health is suffering most likely because she’s cold and because she often doesn’t eat meals, if she does it’s a bare minimum. “I can’t afford to eat as well as my children and they always come first”

I asked her how she keeps warm when the heating isn’t turned on. “I wear layers of clothing and I have a thick blanket that we all snuggle under. I’ve got a little fan heater that I use just to keep the chill off because I don’t want the children to become ill and even that’s a struggle. Once I run out of credit on my meter that’s it it’s gone and I can’t afford for that to happen”

She told me that she often takes the children to the library that has a warm area and her children can have a look at some books and she can have a free cuppa.

However she continued to say that sometimes she found this very difficult because she doesn’t always want to be around other people..

I asked her if she had visited a food bank recently and she said yes she has and is now dependent upon them even though it’s still a struggle saying that they’ve been a lifeline for her and her children.

But despite getting help from food banks they don’t cover all of her food and every day living costs so she has to try and fill the gaps in.

“I’m always topping up my energy meters, I’ve never had this problem before. It’s bad, really bad I just wish that it wasn’t like this”

I signposted her to several organisations that might be able to help her but this is only a sticking plaster.

Whilst the government sits back and causes the suffering of those most vulnerable her experience is going to be repeated time and time again

Their inhumane policies will undoubtedly cause malnutrition and hypothermia related illnesses and worse.

Undoubtedly there will be recorded deaths of those suffering like this but how many will actually be reported as so.

Every death related to this needs to be reported and spoken about in parliament. The government is knowingly causing the suffering of thousands if not millions and they need to be reminded of this every single day.

This shouldn’t be happening at all.

I will continue to share the experiences of those that I interview in future blogs, hopefully weekly.

If you would like me to use your story get in touch I’m happy to do so.

Let’s be clear no one should be forced to live like this.

Photo by Pixabay on Pexels.com

Please read, share, tweet and email this blog, it’s vitally important that we get these stories out there in the public domain.

Believe it or not there are still people that aren’t aware that this is happening.

A huge thanks to everyone that does share my blogs it makes a tremendous difference.

I don’t get paid for any of the work that I do and I would like to continue to report on these stories.

If you would like to contribute to keep my blog and campaign going there’s a donate button at the top and side of this blog post.

By doing so I will be able to help others more.

Thank you xx.

Claimants Forced To Migrate To Universal Credit Early Will Face Financial Loss

MPs have recently accused the DWP (Department of Work and Pensions) of creating ‘two classes of Universal Credit (UC) claimants.

The accusations were made as a result of uncovering the fact that claimants who are forced to migrate to UC early will face financial loss, compared to those who make the decision to move over to UC later rather than being forced to migrate.

This financial hit will happen as a result of next April’s annual uprating.

ESA claimants who choose to migrate after the uprating will keep what is estimated to be around a 9% increase in their benefits.  

Claimants who are forced to migrate before April will have any uprating payments deducted from their transitional protection. This will leave them in a much worse financial situation than claimants who migrate later.

Upon questioning, Therese Coffey DWP secretary of state was asked if she would accept that this decision would lead to inequality, Coffey dismissed the accusation saying “I am not anticipating we will have lots of managed migration by April.”

To put it bluntly she doesn’t care if a few thousand claimants are going to suffer financially and nor will she rectify it either.

As usual Therese Coffey cares only about herself and not the vulnerable people that she claims to care for. This proves once again that UC very rarely improves a claimants financial situation, but instead causes distress and harm.

Source Benefits And Work

I don’t receive any payment for the work that I do.

If you can afford to and would like to donate to keep both my blog and campaign going there’s a donate button at the top and side of this blog post.

Thank you!

New Regulations For Fit Note Prescribers

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

Source Rightsnet

Thanks to Rightsnet for providing this information.

I don’t receive any payment for the work that I do.

If you would like to help keep my blog and campaign going and can afford to, there’s a donate button at the top and side of this blog post.

Thank you!

EHRC Breaks Promise To Investigate DWP Role In Deaths



As reported by Benefits And Work the EHRC (Equality And Human Rights Commission) has broken its promise to investigate the role that the DWP (Department of Work And Pensions)have played in the deaths of vulnerable claimants. This has left the DWP not needing to answer any questions as to the role that they played in their deaths

Instead the EHRC are now asking the DWP to create new policies in relation to claimants with mental health issues and learning difficulties. This will replace the promised investigation.

This is despite promises made by the EHRC in 2019 that they would start an   investigation into the deaths of vulnerable claimants.

The EHRC used the pandemic as an excuse to not start the investigation.



The Commission has now declared that it  only intends to enter into a Section 23 agreement under the Equality Act 2006. This will oblige the DWP “to commit to an action plan to meet the needs of customers with mental health impairments and learning disabilities.”

Keep in mind that the DWP are a much larger organisation that receive more funding  than the EHRC. 
This will no doubt result in the DWP will dragging their heels in creating so called policies that will be nothing more than good intentions that probably won’t be actioned upon.

Whilst I don’t have any details as to why the EHRC have changed their minds I can say that at best they’re very niave putting far too much trust in the DWP to do the right thing.

The DWP has an appalling track record of discrimination against vulnerable claimants, ignoring their basic human rights and making life extremely hard for them.

Despite my disappointment with the EHRC’s decision I’m not surprised. The DWP will do anything to avoid any actions taken against them making promises that they’ve got no intention of keeping whilst doing the bare minimum to comply.

Once again thanks go to Benefits And Work for their hard work and inspiring this article.

A huge thanks to everyone that likes, shares, reads and supports both my blog and campaign.

I don’t receive any payment for the work that I do and it’s a struggle to say the least.

If you can afford to and would like to donate there’s a donate button at the top and side of this blog post.

Thank you!

I’m sorry.

I have to apologise for the lack of a blog post this week. I woke up on Thursday morning feeling ill. This lasted a couple of days and today I woke up with a migraine.

I know that I should have published a blog this week but I wasn’t physically capable of doing so and I will catch up with my blog in the next few days.

As many of you will understand it’s virtually impossible to do much whilst having a migraine, theyre bloody awful.

I will be publishing a blog post about the cost of living crisis etc this week. Like you I’ve been very worried about how on earth I’ll manage once April arrives.

Lot’s of love and solidarity to you xx.

Where Are The Missing Long Covid PIP Claimants ?



As reported by Benefits And Work there are possibly thousands of missing Long Covid PIP claimants that appear to be missing from both the Office for National Statistics. They are also missing from the DWP latest published statistics.



New figures from the Office for National Statistics estimate that 506,000 people have now had Long Covid for over a year. This number is increasing every day yet they’re missing, nowhere to be found.



247,000 Long Covid sufferers say that their ability to undertake their day-to-day activities has been “limited a lot” as a result of Long Covid.



Yet according to the latest DWP statistics on Stat-Xplore record there are just 480 claims regarding Long Covid where it is the the main condition for claiming PIP. This figure has risen from 143 claims three months earlier.


However the success rate for PIP Long Covid claims has fallen from 76%, but is still high, at almost 60%.

A quarter of those who were successful in claiming PIP received the enhanced rate of both the daily living and the mobility components.



It appears that PIP claims for Long Covid do have a better than average chance of success. Despite this hundreds of thousands of people who could be making a PIP claim appear to not be doing so.


Long Covid is exhausting to live with and is likely to hinder any employment prospects. Living with Long Covid also increases everyday living costs.

The reality of having to make a choice between eating or heating, or not being able to afford either is something that Long Covid sufferers and others have to make daily.

The reason for the missing PIP claimants could be because of a distinct lack of information regarding claiming PIP for Long Covid sufferers. This is abhorrent. Everyone that is suffering from this disabling condition should be informed of their right to claim PIP to help with their everyday living costs.

Please read, share, tweet and email this blog post. Sharing makes a huge difference in raising awareness to the public.

A huge thank to Benefits And Work for providing this information. They’re amazing and work so hard.

A huge thank you to everyone that supports my blog and campaign. I really couldn’t do this without you and your support.

For anyone that likes my blog and campaign and would like to donate towards keeping both going there’s a donate button at the top and side of this blog post.

Financially I’m struggling and every penny is appreciated. Thank you.

Seriously ill claimant died after DWP forced them to leave hospital to make benefits claim.


As reported by the amazing team over at Benefits And Work a coroner has issued a Prevention of Future Deaths (PFD) report after the DWP forced a severely ill claimant to leave hospital to make a claim, without giving him the option him to do so electronically.


Terence Talbot, who had Bipolar Affective Disorder, was at the time being detained at hospital under the Mental Health Act because he had suffered a rare reaction to the medication he had been prescribed.
This reaction had made him very vulnerable to infection and ultimately resulted in his death.


According to Benefits And Work the DWP had refused to let Mr Talbot make a claim for benefits electronically which he was entitled to do and instead insisted that he had to make the claim in person.

As a result of having to leave the hospital to make his claim Mr Talbot died in hospital.


The Coroner said in her report that the health professionals that cared for Mr Talbot had never experienced such an ill patient being forced to make a claim in person.


She went on to say “I heard from all the doctors and a senior nurse in this case who have a considerable experience across a range of specialties and across several different NHS Trusts. They have never experienced nor heard of a case where a severely ill inpatient was required by the Department of Work and Pensions to leave hospital to attend its offices in person to make a claim for welfare benefits.”


The secretary of state for Work and Pensions has until 28 January to tell the Coroner how the DWP will make sure that nothing like this happens again.

Don’t depend on this changing anything though. The DWP has a very long record of making promises that they have no intention of keeping. It isn’t important to them, nor is the welfare of claimants important as well. Sadly I expect that they won’t ‘learn’ from Mr Talbots death, instead they’ll file it away to be forgotten.

For a long time now the government has regarded claimants as stock, ready to be used and neglected at their whim. Once a claimant isn’t able to be of use for the DWP and government they more or less wipe their hands of them, making life extremely hard forcing them to complete impossible tasks.

This then results in deaths such as Mr Talbots and thousands more like him.

Sue Jones over on Twitter explains it perfectly.

I’d like to say that this isn’t true but it is. They regard people with disabilities and illnesses with such disdain and hate that many find it impossible to continue. Many refuse to make a claim for benefits because they’re too scared of doing so. Indeed, many of the people that I help and have helped have been in this position. Judged by society for being disabled or ill and then treated with cruelty by the DWP.

There is a desperate need for change in how the DWP and society views people that claim benefits and also how they treat people with disabilities. This won’t happen whilst the Conservative government is in power, but we can continue to put pressure upon them by sharing campaigns and blogs like mine. It makes a massive difference.

My thoughts and prayers go to Mr Talbot, his family and everyone that has died as a result of cruel decisions made by the DWP and their representatives.

A huge thank you once again to Benefits And Work for sharing this and for all of their hard work. You can find them here https://www.benefitsandwork.co.uk

How am I? Struggling this week as usual. Like so many of you I’ve had to make the choice between heating and eating. Truth be told like you I can’t afford to do either but I have to make sure my daughters wellbeing comes first.

If you are interested in getting involved with campaigning or need support I can’t recommend DPAC (Disabled People Against Cuts) enough. It’s a fantastic network run by real people experiencing the same difficulties as you might be. You can find them on their Facebook page and Twitter.

If you live in the Greater Manchester area you can join Manchester DPAC here https:\\manchesterdpac.com

If you like my work and campaign and can afford to would like to donate to keep both my blog and campaign going there is a donate button at the top and side of this blog post. Every penny makes a huge difference for both. I have to pay my internet bill tomorrow and I’m really struggling to do so.

Thank you to everyone that has and does support my blog and campaign. You have all kept me going through the extremely bad past year. We are all still struggling with my sons death, he leaves a massive hole in our hearts that can’t be filled.