Tag: aggression

Long foodbank queues on Christmas Eve.

A friend of mine that volunteers at a foodbank has just sent me the below images. They asked if their anonymity is kept and of course I’m respecting this.

The photos were taken as they were arriving for their shift at the food bank. It wasn’t open for some time, but the queue was already massive, people arriving early to make sure that they’d get some food.

As you can see the queue consisted of People, all differing in their needs. What can’t be missed is the people using wheelchairs queueing for food parcels.on Christmas Eve.

Also in the queue are elderly people and families with children.

You don’t need me to tell you that this shouldn’t be happening , it’s heartbreaking.

You can always find the measure of a country by seeing how they look after the poor, young, elderly and disabled.

The conservative government is blatantly failing on this front. As a country we can’t be proud of this either.

Being proud of a country is about being proud of what it actually does right, and how it treats those in need. It’s not about waving flags and singing the national anthem.

We can however also look back on history and also be ashamed for the very same reasons. Ignoring the fact that the UK government is causing direct harm to people won’t make it go away.

Whilst the government has been focusing on ridiculous things like blue passports people are dying, thousands are becoming homeless and many are becoming ill from poverty related illnesses.

Meanwhile the public are bombarded with images of the royal family having a lovely Christmas, the people queuing at this foodbank and others won’t be able to celebrate.

Its simply not acceptable.

I messaged the volunteer that took the below images and this is what they said

It felt like a slap in the face for them too. It’s a reminder of their privilege. Because despite having their own difficulties they can sit in a warm house, with food, having just wrapped presents for their family.

They went on to say that it makes them angry and sad that this is happening, that they wished that they could do more to help. There’s more that many could do, so let’s do it.

Helping others doesn’t have to cost a penny. A kind word, saying hello in the street makes the world of difference to someone that lives alone and hasn’t spoken to anyone for a long time.

Being a friend costs nothing also, sharing what you no longer need doesn’t either. Of course I realise that many people have nothing to give to someone else.

Let’s spend the festive period and the coming year to be kind and thoughtful towards each other. We need to do this because the government won’t ever care about you.

Faces and building names covered out of respect for the people queuing.
No one should be forced to literally beg for food on Christmas Eve.

Please read, share, tweet and email this blog post. This makes a massive difference and it raises lots of awareness. Thank you!

A huge thank you to everyone that has and is supporting my blog and campaign. I really appreciate it and I couldn’t do this without your support.

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

£2 BILLION GIVEN TO PRIVATE COMPANIES FOR PIP AND ESA ASSESMENTS

Well who’d have guessed that the government would find £2 billion from their magic money pot to inflict even more cruelty to disabled and ill claimants.

Thanks to Benefits And Work who have uncovered the first details of the new assessment contracts for PIP, ESA and UC claimants.



These shiny new contracts will split the UK into five regions which will involve over £2.8 billion being given to the private sector over a period of five years. This is supposedly to allow the DWP to decide how these assessments will take place through telephone or face-to-face assessments.

I add that as usual this will be decided ignoring the actual physical and mental needs a claimant might have.


Under the new claimant Functional Assessment Services (FAS) system as it is titled, the UK will be divided into five regions from 1 August 2023:

Lot 1 – Northern England and Scotland 647,600,000

Lot 2 – Midlands and Wales 473,400,000

Lot 3 – South West England 338,000,000

Lot 4 – London, South East & East Anglia 396,800,000

Lot 5- Northern Ireland 105,100,000



In each region, a single company will be chosen to carry out all the PIP, ESA and UC assessments.

So basically money talks regardless of already vulnerable claimants needs. Whoever puts the best tender in wins the contract.

Call me old fashioned but the wellbeing and needs of individuals should always be put first. Instead they companies with no medical knowledge and experience to assess already vulnerable people.

They will be allowed to decide if a person disabled enough to claim their rightful payments regardless of having no medical knowledge of their needs.

Basically claimants life’s are once again in the hands of these so called assessors.


The total value of the contracts that will be given is £2 billion firstly to rise to £2.8 billion if the DWP chooses to extend the contract for an additional two years.

You can bet that they’ll choose to extend these contracts, afterall it’s beneficial for the government to extend them.

There’s always room for extending cruel systems such as this. What the government won’t tell you is that they want as many people as possible to be declared fit for work. It doesn’t matter of they’re fit or able enough to do so.



The Scottish government will be taking over PIP assessments itself in advance of August 2023.

There will be some claims that are already underway that will still be dealt with by private sector assessors.



The bid winners will be paid first for a ten month ‘implementation phase’. This will ensure they will have fully trained their staff and have acquired suitable premises. It also will give them the chance to implement their IT systems before going live.


As we already know the DWP never make any system uncomplicated though. To prove this the DWP will provide one IT system for PIP claimants and a separate system for ESA and UC claimants.

The DWP have already warned potential providers that changes might take place place throughout the life of the contract.

These changes may include alterations in the ‘channel mix’ as the DWP call it.

An example being “change in proportional requirements relating to virtual assessments and face to face assessments. They could for example change requirements such as 60% face-to-face to 20% assessments.


It is very clear that the DWP and not the assessment providers that will decide which proportion of claimants receive a telephone or face-to-face assessment.


This makes it clear that assessment providers will be working to meet targets for types of assessment. This will completely ignore the fact that some claimants are obliged to have an inappropriate method of assessment.

As you can see none of this will be beneficial for anyone that claims ESA,PIP and UC.

As these systems are target driven the assessors will be more concerned with meeting targets than the wellbeing of anyone being assessed.

I don’t have to tell you how much distress is caused by cruel systems like this especially if they’re target driven. Who remembers Sandra’s Stars?

We must remain vigilant because as we know from past experience the government will try to put in legislation and plans without our knowledge.

You can do this by sharing information online on your preferred social media provider, emailing mine and likewise blogs to people that might need informing

Manchester DPAC over at https:\\manchesterdpac.comhttps:\\manchesterdpac.com Also local branches of Unite Community over at join.unitetheunion.orghttp://join.unitetheunion.org.

Every share, tweet and conversation about these issues raises awareness which is extremely important.

Massive thanks given to Benefits And Work for making me aware of this happening. They do so much hard work to raise awareness.

Also thanks to a Twitter friend for alerting me to this. Thanks RooneyMusic!

Also if you live in the Greater Manchester area please join Manchester DPAC. You can find them on Facebook and Twitter

Please read, share and tweet my blog. Every share helps so much!

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

I don’t receive any payment for any of the work that I do. I’m struggling financially at the moment. As you know my son died and my daughter is struggling to cope with his death as am I.

If you would like to donate my PayPal ad is posted above, below and at the side of this blog post.

Sanctions return for new style ESA and JSA and Universal Credit


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.

Photo by Breakingpic on Pexels.com

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.

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.

No blog update this week. .

Dear readers and subscribers, I’m very sorry but there’s not going to be a blog post this week.

I was told that my son had died on Friday and I’m trying to deal with it and organise his funeral etc.

I will be writing a new blog post as soon as I’m able.

There is a crowdfunding page relating to this on both my Facebook and Twitter account.

Thank you , solidarity Charlotte.

Remembering all women. International Women’s Day.

“Happy International Women’s day!
Today I’m thinking about all the women who are suffering as a result of the government’s austerity measures.

Women unable to leave abusive relationships because there isn’t a women’s refuge that they can escape to.

Remembering all the women that have died as a result of domestic violence and the governments austerity measures, we’ll never forget you.

We love you.

Women struggling to survive the discrimitory universal credit system.

Disabled women who are struggling to survive because their ESA and/ or PIP has been taken away from them.

To all the 1950s women unable to claim their rightful pensions.

Homeless women stuck in flea ridden, unsafe temporary accommodation, one day things will get better for you.

Please have them in your thoughts, the battle for equality is far from over.”

Please read, share and tweet my blog. This makes a huge difference and it helps to get the truth out there.

I don’t receive any funding for both my campaign and blog. If you 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 has and does support my blog and campaign. It really means the worl to me and your help makes a massive difference.

Merry Christmas one and all.

Dear readers I write this blog on Christmas Day, a day when people are expected to celebrate and be happy.

Sadly because of the government’s cruel Universal Credit system and the torturous PIP and ESA DWP ‘medical’ assessments thousands of people won’t be able to celebrate, cook a Christmas dinner and exchange gifts.

This year is tougher than normal because we are still in the middle of a pandemic that the government is trying it’s best to ignore.

Today the UK’s official Covid death toll has surpassed 70,000 on as 570 more people died today.

Let that sink in 570 people have died from Covid 19 on Christmas day. Also a total of 70,000 people have died as a result of Covid 19.

Meanwhile the government continues to ignore this, they just don’t want to know and they certainly don’t want to help.

70,000 families will be grieving as will their friends. But hey let’s ignore them and continue to put the public at risk.

Wouldn’t it be fantastic if the government actually tool some positive action, set an example to the rest of the world and protected people. This won’t happen though.

It appears that the government is in some sick competition with America about how many people will die from Covid 19.

Then we have the thousands of people now unemployed as a result of the pandemic. Now facing the inhumane universal Credit system, many can’t understand how they’re expected to survive on so little money.

Thousands of people won’t be able to give anyone presents this year, heat their home and have a Christmas dinner.

This year the queues for food banks and suchlike places have more than doubled. Families are queuing for hot meals in city centres and children and their parents are hungry because they don’t have the money to survive on.

How sickening it is that I have to use the world surviving… People shouldn’t be surviving they should be able to live, be happy and have enough money to be able to feed themselves and their children.

I want to be positive I really do but it’s extremely hard to find the good in all of this. We shouldn’t be celebrating the fact that food banks are opening and organisations and charities are working extremely hard to find food to give to hungry people.

Theres a reason why the government likes foodbanks. If given the opportunity one of their Tory MPs will see this as a photo opportunity.

Foodbanks save the government thousands of pounds every year. They also take the responsibility of feeding people away from them and moves it to the foodbanks and organisations to do this.

No wonder Tories smile so much at the thought of another foodbank opening.

Basically what I’m saying is yes please support your local foodbank but please remind the government of their duty of care towards the people of this country.

Normally we would see the government’s opposition making a speech or statement about the terrible neglect of the poorest and most vulnerable of this country. This year it’s virtually silent.

Sir Kier Starmer quite rightly made a speech about Brexit, but he failed to address the needs of the poorest and most vulnerable of this country.

As a result thousands of people are feeling neglected and unimportant and totally pissed off with the political system in general.

So what do we do now? We support each other in whatever way that we are able to.

A friendly word, a smile can sometimes be enough.

We have to be there for each other because this damned government will never never care.

A huge thank you to everyone that reads and supports my campaign and blog. Your kind words and support have kept me going throughout my own covid 19 nightmare.

Sadly I’ve got pleurisy again, thanks to long covid. Hopefully I’ll be better soon.

For anyone that would like to donate towards my campaign and blog there’s a donate button at the top and side of this blog post. Thank you!

Please read, share, tweet and email my blog.

Covid 19. What happens to the survivors and the families of those that have died?

Dear readers and subscribers it appears to be Thursday once again. I hope that you are all ok and as well as you can be.I’ve had a pretty busy week having a telephone consultation with my respitory consultant, blood tests and talking to my GP.

For covid survivors I’m one of the lucky ones. I have a doctor that listens to me and echoes mine and my consultants concerns. This is a rarity though.

Why is this a rarity you might ask, everyone should be treated this way. The sad reality is that they aren’t.Helping a patient with Covid 19 is extremely hard because they’re dealing with the unknown. Covid also presents itself differently with each and every person that catches it.

There isn’t any real ‘normal’ symptoms with Covid 19 because of this.For me, covid hit my lungs pretty hard, most likely because I already had mild asthma.

Covid likes to find a person’s weak point and attack there.

For other people they can get more neurological symptoms and not the classic symptoms. For them getting help is extremely hard.

Like my doctor said, so many doctors haven’t got a clue about how to deal with it unless they’ve had the time to research it themselves. I can imagine that finding the time to do this would be hard for them.

This leaves us with a massive problem though. Thousands of people with long covid symptoms are being ignored,some are being told that there’s nothing that can be done for them when that’s not true.

I was both unlucky and lucky enough to be admitted into hospital and this fast tracked me to the follow up care that I need. This is why I consider myself lucky in this respect.

But still thousands of people that are suffering with delibatating symptoms are being ignored, left on their own with no support at all.

Every covid survivor deserves to be listened to and to have their symptoms investigated. It’s vital that this happens. The fact that it isn’t happening is a complete travesty.

Then we have the families of loved ones that have died from Covid 19.They’re not being listened to at all.

The government is so far refusing to meet with them to discuss their needs and concerns.

Why the government refuse to meet them is unknown as of yet, but I do believe that they’re avoiding any contact with the public but my be is that they don’t want anyone challenging their extremely bad decisions

.Also add into the mix the farcical second lockdown. This lockdown won’t be successful because schools are still open etc. Unbelievable isn’t it.

We’ve also as a result of this got the real possibility of a lockdown over the Christmas period. To be honest I don’t mind this because we need to get this virus under control but so many people will suffer as a result of this possible decision.

Basically the government has done what it does best… Mess everything up, ignore the public and walk away.

This leaves the public to do the best that they can with very few resources if any.We are facing very bleak times and are going to do this with little or no Government help and it’s extremely worrying.

We have thousands of people that will be facing destitution in the coming months and they need help and representation.

We then have the terrible decision to remove Jeremy Corbyn from his position. They then allowed him to return but without the whip.

This is exactly what we don’t need at the moment. Jeremy deserves to be given the whip etc back.

The labour party should be united to fight the Tories against their terrible decisions that they’re making about the pandemic etc.

Instead it’s divided the party and members are leaving. Would it be too much to ask for some real united opposition?Can they please stop this witch hunt and focus on the government’s faults instead?

I urge them to think about this.

Thousands of people have died as a result of contracting covid and their families need help and support.

Thousands of people are ill with Covid and they need support.Thousands of people suffering from long covid need support.

They all need this support to come from the government’s opposition.We need this now.

I’m eight months into my long covid battle and it’s been awful. I’m trying to keep strong and fight back but it’s hard at times.

I don’t think that I could have done it without the help and support from my online friends

.For those without this online support it can and is a very dark and lonely place to be. Please spare a thought for them.

I’m going to end it there because I have to go and collect my meds.
Please keep safe you are important and I do care about you all.

Please read, share, tweet and email my blog.
I don’t get any funding for anything that you do.

Having covid has put an enormous strain on my finances.

For anyone that would like to donate there’s a donate button at the top and side of this blog.

Thank you to everyone that reads and supports my blog and campaign.

I’m struggling…

Dear readers this week’s blog is going to be rather short and I apologize for this.

The other week my daughter brought a virus home from school. This in itself wouldn’t be problematic but combine this with my long covid and respitory problems because of this it’s been a nightmare.

I was prescribed some meds which have worked to an extent but I still feel terrible. As a result it’s impacted my life dramatically this week and all that I’ve been able to do is nothing. A flat nothing except essential tasks.

I know that I should probably go back to the hospital but I’m putting it off because they’ve got much sicker people than me to deal with.

The reality is that long covid sufferers like myself are left to it with very little or no support. If you haven’t been admitted to hospital then it’s extremely hard to get someone to listen and to help you.

Unluckily I was admitted to hospital so I have been able to access some very basic tests and have been allocated a respiratory specialist that I’m still waiting to see.

I’ve tried all of the alternative remedies out there and none of them work. Some slightly ease the symptoms but the only things that really work are time, antibiotics for any infection lurking and a nebuliser on bad days.

To access any of these you either have to have access to a decent doctor and a local hospital. By decent I mean a doctor that actually recognises that long covid and related problems are an actual thing.

This sadly isn’t as easy as you might think. Often when you get covid 19 you also can get some really strange symptoms that there’s no explanation for.

My strange symptoms have been high temperature but not skyrocketing high, hallucinations in the early stages, really strange aches and pains, fatigue, breathlessness and a crappy immune system that can be set off by the slightest thing.

When the decision to have another so called lockdown not once were people with illnesses, disabilities and long covid taken into account.

The government shuts pubs, restaurants, gyms etc but they refuse to shut the schools, colleges and universities.

It’s a total misconception that children are being adequately socially distanced. The covid 19 and other viruses are running through these establishments at a high rate. This then returns home with the pupils, teachers, teaching staff and school staff and is passed onto any person living with them.

It’s extremely dangerous but so many people are failing to see this. We aren’t even an afterthought we aren’t thought of at all.

It’s also extremely frustrating to see that so many people in my area at least don’t believe that this virus exists or if it does it’s not harmful.

It’s all a conspiracy they say, wearing a mask takes away our freedom! They fail to see that wearing a mask actually does help to give them the freedom that they crave.

Then we have the news of a vaccine that’s on the way. It’s supposedly around 90% effective and it should be welcomed. But it isn’t by many.

Like anything new it’s ok to be suspicious but this vaccination has been tested adequately. I can’t however comment on any side effects but to be honest I’d give anything to feel well again.

Whilst the schools etc are still open the virus will still be spread amongst our communities. Add into this the people that refuse to wear a mask etc and so many more people are going to become ill or much worse die.

This week saw the death total for UK hit 50 thousand. Yes these people died from Covid 19 related illnesses but people still insult the dead and their families by saying that its all a lie.

It isn’t a lie, people are dying and they need to take this seriously.

I’m sorry for repeating myself again but people do need to hear this. It’s extremely important.

As for me, I’ve not been able to go out anywhere except for my local post office which isn’t far.

I struggle walking there and back, breathing isn’t easy when your mobile but it is what it is.

I wear a mask whenever I do go to the post office and I’m very strict about using anti bacterial hand creams etc.

I stay away from any crowds of people because I realize the risk of catching something else.

I’m not contagious anymore but so many people are vulnerable and we all need to look after each other.

What I do want is a proper lockdown with the full support of the government for workers and self employed people.

I want people to realise that long covid is a serious thing as is having a weakened immune system thanks to covid 19.

I want people to realise that we don’t get well overnight. It takes a long time and its a struggle to do so.

For some catching covid 19 is the only way that they’ll start to realise how awful it is.

As for the vaccine. It’s going to take quite a while for it to be rolled out to the general public. It’s being offered to vulnerable groups of people first and quiet rightly so.

Please don’t become complacent because a vaccine is on the way.

Please keep safe. I know that as a single parent it’s doubly hard to do so but it’s so important.

Continue to look out for each other, help and support each other.

I’m going to end this blog here but please know that you’re all in my thoughts.

Please read, share and tweet my blog.

A huge thank you to all of you that do this already.

There’s a donate button at the top and side of this blog. I receive no funding for anything that I do. Every penny helps me to continue with my blog and campaign.

A massive thank you to everyone that has and does support my blog and campaign. Your support means the world to me.

I’m still here. My continued battle with Long Covid and good memories.

Dear readers an extra blog post from me, I hope that you don’t mind.

I’ve been a tad quiet recently because my recovery has been set right back.

My daughter unknowingly brought home a nasty virus with her when she returned home from school about two weeks ago.

What would normally would have been a slight cold etc completely floored me. I was forced to retreat back to bed.

I really hated having to retreat to bed because I wanted to be out and about and I had plans to do ‘stuff’.

I’m now out of bed but I’m coughing a lot and I can’t get my stats above 94 to 96. I’m also experiencing the return of the stabbing pains.

Yes I know that I should go back to the hospital and I will do when I’m financially able to do so. Shite happens and I’ve got to learn to deal with it.

I was looking at my Facebook memories today and I was reminded of the email that I wrote to The Scum (Sun) after the requested my help for them.

I’ll paste the letter below, it really made me chuckle.

How dare they have the nerve to request help from me after I had just published a petition against them that went viral.

I was advised to take it down, but hindsight is a wonderful thing isn’t it. I should have kept it up and fought them. I’m quite sure that I could have found legal advice.

I will not make the same mistake again.

Anyway here it is.

My reply to The Sun On Sundays request yesterday.

Hi Gareth,
Thank you for your email.
Primarily I need to correct you on your referral to Universal Credit as being Universal Credits. These are different things, and although I don’t want to argue about semantics, it is about conveying the correct message across. Therefore using the correct benefit title is very important isn’t it.

I’m sure that you will agree with me.
As you can tell, I’m rather fussy about the getting the correct message out to the public. After all the public deserve to be correctly and reliably informed about important issues, especially in newspapers and the media. However this is something that The Sun Newspaper has regretfully been doing a terrible job of.

Headlines such as ‘Benefit scrounger mum of 8 says £500 a week handouts aren’t enough for her four bed council house’ Dan Sales 18th February 2017.

Other headlines such as ‘Takers dozen. Sponging mum of 13 who rakes in £30,00 a year in benefits is branded a scrounger by her own daughter’ Alex West 30th December 2016. ‘Family planning. Scrounging mum of 12 Cheryl Prudham who pockets £40,00 a year in benefits flashes her tummy outside medical centre days before announcing shes expecting baby 13.’
I could continue sharing these headlines with you, however you get the gist don’t you.

Not only were these headlines not based on fact, not researched correctly they were damaging to the people concerned and to the most vulnerable people of this country and were created specifically to cause prejudice and division towards the poorest of this country, the very people that your newspaper is now reaching out to.

These headlines were so hard hitting, a phrase that you like to use, that as a result of the ongoing campaign of hatred against the poor, led by The Sun newspaper, other newspapers and television channels, I, myself have been shouted at, called a scrounger, told to get a job, and spat at. Luckily it didn’t touch me, but you can see how this works out right?

The people that I help have also experienced prejudice as a result of this ongoing campaign and do so on a daily basis.
I can never forget the “Scrounger Awards’ that The Sun newspaper published, also ‘The Welfies’ and the ‘Job Dodger’ awards.

Sympathetic also isn’t something that I associate with The Sun newspaper, after all we can never forget Hillsborough can we.

A point to note, lying has 5 letters, but so does truth. Hurt has 4 letters but so does heal. Everyday I try and rectify the harmful and malicious lies set about by The Sun newspaper.

Maybe the newspaper could do the same.
You also might like to read this, because if you had researched my name correctly you would have found this article about myself.

https://thetab.com/uk/manchester/2017/05/26/spoke-woman-petitioning-manchester-boycott-sun-28665

I therefore would like to decline your offer of a chat, nor will I be referring any vulnerable people to your newspaper to talk. You see, I simply cannot trust the newspaper not to twist their words and to turn them into figures of hatred.

However, we would like an apology from The Sun newspaper for all the hurt, damage and discrimination caused by the words printed in your newspaper.

Wouldn’t it be nice if that was a front page headline instead of a Benefit Scrounger headline.

Respectfully
Charlotte Hughes.

I’d really like to thank all of my friends and readers for all the support that you are giving me at this moment in time.

Knowing that I can speak to a friend on the phone whenever I need to is and will continue to be a massive help to me.

Also a massive thanks to my friend Alex Tiffin, you know why.

Also huge thanks to Keith also.

How am I doing otherwise?

Trying to cope is an adequate description atm. It’s the same old fed up of being ill and sick to death of being skint. I’m sure that you can relate to this.

I’d love to be able to do a good supermarket shop instead of having to buy essentials online because it’s so expensive.

I just want to be normal again.

It’s so bloody depressing but it is what it is. But I have got good memories to look back on and I’m grateful for that.

One thing to look forward to is Halloween, my favourite time of the year.

My daughter has found the Halloween decorations so when I’m up to it I’ll be able to transform the front garden.

Please read, share and tweet my blog.

Thank you to everyone that supports my campaign and blog.

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