Tag: demmonstration

Poverty doesn’t end at Christmas

Dear subscribers and guests it’s been a tough year for so many of us, I know it, I feel it.

This year was probably the worst one of my whole life. My son was tragically taken away from me mid pandemic. It hurts more than anything else that I’ve experienced.

Whilst we were abiding to the social distancing rules, the Tory government were busy partying and carrying on as if nothing had happened.

This was a case of we’ll do whatever we want sod the public. They don’t care about us. My son had to have a very reduced socially distanced funeral whilst they were enjoying life.

To be honest this is a perfect example of how they treat us. They never spare a thought for us so don’t expect them to either.

Christmas is a tough time for so many reasons wether it be for financial reasons or bereavement. I’m with you, I feel it.

I haven’t put a Christmas tree up this year. My daughter and I decided that it doesn’t feel right so we put some extra lights on his memorial table.

So much pressure is put on society to have the big tree, the decorations and lots of good food. The truth is that so many of us can’t afford to buy the big tree, pay for the electric to light the Christmas lights and affording a big meal with all the trimmings is near impossible.

Poverty doesn’t end at Christmas, if anything it’s amplified for reasons that I’ve already stated.

You do Christmas how you want to do it. Try and ignore the pressure to comply to what everyone expects. If you want to turn the TV off and read a book instead then do it.

If you want to spend Christmas day doing nothing then do it. Be kind to yourself.

I used to put so much pressure upon myself to get everything right for others to see. Loosing my son has made me realise that none of this really matters.

Like many of you I’m going to find Christmas tough, but I will get through it.

So many families are going to be going without the Christmas that they were used to. The pandemic has caused thousands of people to loose their jobs and it’s also resulted in the deaths of thousands of people.

Thousands of families and individuals are newly dependant upon foodbanks to keep them going. It’s not easy asking for help and the food isn’t the best. Hopefully one day it will get better.

How do you explain to your children that Father Christmas can’t come this year? It’s heartbreaking.

What we can do is be there for each other, talk to friends on social media, text or face to face (socially distanced of course).

We will get through this. Lots of love to you all.

Please read, share and tweet my blog. This makes a massive difference and it raises so much awareness.

A huge thank you to everyone that supports and has supported my blog this year. I really couldn’t do it without you.

I don’t receive any payment for the work that I do and to say it’s tough is an understatement.

For anyone that would like to donate there’s a donate 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.

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.

Covid 19 the unwanted gift that keeps giving.

Dear readers it’s been a tough old week for me and my Covid 19 battle.
Sadly I rebounded again and I’m now completing my fifth round of antibiotics.

Tough yes but however I do know and I appreciate that I have it much better than many have had it. I’m alive and I’m very grateful for that.

So yesterday I ended up back at the hospital with yet another reoccurrence of the pains that I’ve been getting.

I wanted answers, I wanted to know why I keep feeling like this. I hate the unknown which doesn’t fit well with Covid 19.

I had my bloods taken, x rays and scans done and I waited for the results.

Eventually I saw a lovely doctor who totally got it, he understood exactly what I’ve been going through.
He explained that my bloods are OK but from the scans he could see scarring on my lungs.

I then asked him about the pains and my sometimes galloping heart rate.


The answer was this. Because of the pneumonia and pleurisy my lungs have taken a battering and the pains are as a result of the remnants of the above and the scarring.

I asked him about my heart rate and he said that my heart appeared to be ok after being on a heart monitor. He said that lots of people who have had covid 19 get this and so far they don’t know why.
He’s referred me to a respiratory specialist and another specialist regarding my heart rate and for more tests.

Covid 19 damages your body in so many ways and because its an unknown virus it’s hard to get answers about anything.
Research is being done though and maybe we will get some answers soon.


I got some very good advice from the doctor and my friends. I need to stop trying to to too much, I will heal but it takes quite a long time to get back to somewhat normality.

This doesn’t mean that I’m going to give up campaigning though, infact it means the opposite.

We need to continue to campaign more than we have done before.
Our rights are being eroded away at a fast rate and so many things are being missed because of the Covid 19 pandemic.

Every day I publish the official Covid death rates, you know the deaths that the government wants us to forget about. They want the public to forget about Covid 19. It’s up to us to continue to publicise them.

Covid 19 is still having a massive impact both national and locally.

Whilst I was at the hospital yesterday I saw three very ill people being admitted to the hospital because of Covid 19. I know this because covid patients are being directed to another specialised department.
Their stories are the stories that the public don’t get to hear. The man that collapsed at home because of covid, the woman found in her bed seriously ill, the man that walked into the department and nearly collapsed when he got there.

Remember that their and our life’s don’t matter to the government and to some local authorities. Out of sight and out of mind.

Please keep in mind that telephone medical assessments are taking place once again.
If you have to have one of these examinations treat it as if you were at their medical centre.
Have a list of all of your medications and illnesses or disabilities. Try and have someone with you and ask them to take notes also.

I’m going to continue to plod on as I say, trying my best to give my daughter a good childhood despite having a very deminished income.
I can honestly say that I’ve never felt so bad about being a bad mother because I can’t give my daughter what her friends have.
Every day I feel this guilt like many parents do. Tough some say, that’s life. Except that it shouldn’t be like this.

The kindness and support of my friends has kept me going as have OUR NHS.
I’m determined to be back out there ASAP but I’m still helping people the best way they I can from home.

I want to thank each and every one of you for the support and friendship that you have given me. When I say that it means a lot to me I really mean it.

Stay safe everyone, wear a mask and wash your hands. Self isolate if your vulnerable and do whatever is right for you to continue.


Please read, share, tweet and email my blog. Thank you so much to everyone that already does this.

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

My 5th Covid 19 rebound. We need to talk more about long term covid 19 sufferers.

Dear readers it’s Thursday and I hope that you are all OK and as well as you can be.
Sadly I’ve rebounded again and I’m now on another course of antibiotics which I’ll be taking for the next seven days.
Sadly I’ve not been fit enough to do much and this week. I have been busy online and trying to do what I can.

The housing association that I rent my house from have decided to resume the work to fit a new kitchen so we’ve had to clear everything out of there.
We are now living in our small downstairs living room which is packed full of stuff from the kitchen.

I am very happy that they’ve decided to do this work because I’ve been waiting for 13 years for them to do this.
I am however too ill to appreciate it as much as I should.

Being a long term covid 19 sufferer is awful, it feels like it’s never ending. One minute you’re feeling on top of the world, that you’ve beaten it and all is good.
The next minute it comes straight back like a big cloud that’s raining heavily.
In my case it’s hit my chest the worst, this isn’t the same for everyone though. Friends that are also long term sufferers have a variety of symptoms ranging from exhaustion, headaches, pains in their limbs and joints, their eyes have been affected the list goes on and on.

Not enough people are talking about long term covid 19 sufferers like myself.
Andrew Gwynne MP is a fellow long termer and he published a really good article about his experiences of this awful virus and the long term affects

I’m sure that my friends and family are fed up with me being ill now but I really can’t help it. If I had a magic wand I would magic it away.

I am missing my old life, taking my daughter out, seeing friends, taking the dog for a decent walk and eating treats like chocolate etc etc.

I do realise that I’m luckier than so many people that didn’t survive Covid 19. Their families must be devastated.

What does make me angry though is the people that claim that Covid 19 is made up, it doesn’t exist, that it’s a lie and is some kind of joke.

Personally this makes me feel sicker than I do now. What gives them the right to belittle the suffering and deaths of so many?

What I do know is that if these people catch it they’ll be the first to demand the help of OUR NHS, our doctors, nurses, nursing assistants and support services.
Please don’t insult us with these lies, instead listen to us and try to understand how we are feeling. It isn’t hard to do.

Luckily my doctors surgery is doing telephone consultations but if you don’t have a phone or credit how are you supposed to get in touch with your doctor for help?
If a person doesn’t have any Internet either then it’s impossible. I really worry about everyone in this situation.

Yesterday I had to collect my meds. I wore my mask, kept away from people and used hand sanitizer like it was going out of fashion.

Whilst I was out I couldn’t help but notice the large amount of people walking around without wearing a mask. I’m positive that the death rates will rise as a result of this.

Covid 19 is still here folks, it hasn’t ended and so far there’s no sign of an end to it.

I’m trying to keep positive though although it’s not easy. Facebook memories from our days out keep popping up. My daughter deserves better than this.

I’m missing so much but I’m grateful for so much also. I’m getting used to living from food parcels, at least I have them. I am missing my treats though.

It’s a big culture shock though and it takes time to adapt to it. I do miss shopping though but it is what it is isn’t it.

What has helped me enormously is your support and help and the solidarity from other long term covid 19 sufferers. We all know what it’s like to feel like this.

My art has also kept me going, and I’ve been so lucky in getting help with this. It’s a good distraction and I get a good sense of actually achieving something.

What I do worry about though is how are people going to return to work, that’s if they have a job and are a long term covid sufferer? Personally and would find it impossible at the moment.

There is very little support for us out there but we do have each other and that’s something.

This week has been a bit of a blur and I make no apology for how I feel.

I want to send my love and solidarity to my good friend Keith Lindsey Cameron. He’s a good friend of mine and he’s been ill.
If you havent seen his work yet then have a look he’s an amazing campaigner.

I’m going to end it here because I’m knackered but take this message with you.

Let’s talk about everyone suffering from Covid 19 and the long term sufferers. Let’s keep reminding the government that people are still dying because they want people to forget about this.


One of my paintings.


Please read, share, tweet and email my blog.
A massive thank you to everyone that reads my blog, shares it and supports it.

For anyone that would like to donate towards my blog and campaign there’s a PayPal button at the top and side of this blog.
I don’t get paid for anything that I do so every penny donated really does make a difference.

A huge thank you to everyone that have done so already.

Lots of love to you all xxx.

The government needs to reverse all sanctions and reinstate ESA and PIP payments immediately due to the coronavirus Covid 19 outbreak.

Dear readers and supporters I hope that you are coping the best that you can during this very uncertain and worrying time.

It’s ok for the government to say self isolate when you have no food and many of the local food banks have shut their doors due to the coronavirus. They’re finding it hard to hand do their work because they can’t source any food to hand out and supermarkets have understandably put restrictions on purchases.

As I was waiting for Gordon to arrive with the food parcels I had a conversation with a man that I’ve spoken about before. He ran up to me saying ‘Thank God you’re here because everywhere else is shut’ I reassured him that I will do my best to help for as long as I can.

He told me about his struggles trying to get help, saying ‘It’s OK for organisations and councils to say phone us or email them. I don’t have the ability to do that. I’m sanctioned because I lost my mobile phone and I missed a text telling me to attend an appointment’

I asked him if he was coping and he told me that he wasn’t really. He’s been given an old mobile phone that doesn’t have good access to the Internet and anyway he can’t afford to buy any credit.

I asked him to register his new number with the DWP by going into the Jobcentre and to let them know that he hasn’t got any access to the Internet. I also asked him if he can also ask about his sanction to see if anything could be done to help him.

Sadly there are so many more people finding themselves in the same position as he is in. Many are also stuck in limbo awaiting decisions for ESA and PIP appeal and tribunal decisions. They too are struggling with little or no financial assistance and now find themselves feeling very vulnerable and left behind.

I’ve asked the DWP via Twitter if they can reverse all sanctions and reinstate all ESA and PIP payments immediately. Extremely vulnerable people need to have the means to survive. Sadly not enough people are taking this seriously maybe because its not happening to them.

Just ask yourself if you could cope in this time of crisis with no income at all. Sat in the cold with no access to help.

So we are left with a barely skeleton service given by local support organisations, food banks have had to shut, doctors surgeries are mainly only accepting telephone appointments, libraries have shut and thousands of people are very worried about how they were survive. They’re also very worried about catching coronavirus (Covid 19)

Schools are shutting their doors to all pupils except children of keyworkers and vulnerable children.

Whilst I agree with the closure of schools the government needs to be much clearer about the voucher system that they’re supposed to be putting into place.

It’s also extremely difficult to source food because selfish hoarders are stripping the shelves of most food products. The supermarkets are supposed to be implementing strict rules so let’s hope that this will help.

Please remember to follow full hygiene protocols, this is very important. Check on your friends amd neighbours to see if they’re OK.

I want all my readers to know that I’m here for you if you want to chat, feel free to email me or follow me on social media.

Together we can be stronger and we will get through this.

Please read, share, tweet and email my blog.

I have a donate button at the top and side of this blog post for anyone who would like to donate.

My apologies comments are blocked for now.

Dear readers I do everything that I can to ensure that my blog is a safe space for you to use, read and comment.

This week the DWP have taken it upon themselves to attempt to troll my blog, call me a liar and are telling people that Jobcentres are wonderful places and work will cure us of all ills.

I won’t tolerate their bullying anywhere so comments are blocked for now until they calm the hell down.

I hope that you understand my reasons for doing this.

If anyone would like to comment please email me at seercharlotte@gmail.com and I can add your comment to this blog piece.

Peace and much love to you all.

Forced to attend DWP course dispite having multiple disabilities.

Dear readers and supporters once again I have to apologise for publishing this blog late. I’ve been out campaigning for my local Labour Party.

Anyway today was pretty dire, it was raining, in fact it still hasn’t stopped.

It was also cold, deadly weather for street homeless people and anyone that can’t afford to heat their homes.

Once their clothes become wet, they can’t dry them so they become very cold and hypothermia can set in. This can be deadly so please spare a

thought for people in this situation.

As usual all the food parcels were gone as soon as I handed them out. Most of them were needed by people having problems paying their council tax and extra top up rent. If they can’t pay the council will take the money directly from their universal credit payments. Their social housing landlord will also threaten to evict them even though the person that I spoke to owed less than £100.

New Charter housing certainly don’t give a toss about their tenants but that’s another story.

We spoke to lots of people today but sadly we had to end the demo early because we were drenched and cold.

I had a conversation with a man that has several disabilities which prevents him from applying for many of the jobs on offer.

Dispite this his job coach has told him that it would be in his best interests to attend a so called wellbeing course.

Wellbeing is the latest buzzword being used by the DWP. They like to pretend that these rubbish courses will help people, especially disabled people.

They don’t however tell the person being forced onto these courses that they (the DWP) gain financially from sending people on these courses as do the course providers.

We are seen as a pound sign, a number of which they can profit from.

What they forget is that most people have enough commonsense to realise that no one can ever be cured by attending a course. They’re another reason to harass a person more, to sanction them if the course provider advises them to.

The whole system is crooked, people are being harassed so much by the DWP that they can’t see a future for themselves and they take their own life. Meanwhile the DWP will still send letters out to the families of the deceased.

It’s Orwellian in nature, they control a person’s life to the extent that they can cut off their very means of survival with the click of a button on a computer.

I spoke to three people that are having problems with their housing benefit claims. Our local housing benefit department at Tameside Council aren’t the best.

Please can they start talking to people as if they’re human beings, with respect and not disdain? It’s not too much to ask is it.

I spoke to a single parent that had been asked to attend their first back to work interview because their child is now two years old.

They were understandably nervous and had no idea of their rights regarding job searching etc. Thankfully we were able to help them and we handed them a copy of our survival guide.

Call me old fashioned but I’m a firm believer that a parent or carer should be able to stay at home with their child until their child reaches school age or older. Obviously parents that want to work should do so but the option should be there.

Children need their parents, it’s vital for their development.

Children also need to be able to eat good, healthy food and live in a warm house. These very basic things are denied by this cruel government.

I write this on the eve of the general election, the most important General election in many years. Let’s hope that we get a good result. If we don’t many of us won’t survive another 5 years of this cruelty. I can’t stress this enough.

We will be back next week for our annual Christmas Demo. I will be making a wreath unless I can get a volunteer to help me. I’m also needing to buy non alcoholic mince pies and other Christmas foods to hand out to the public.

We will also be handing out extra Christmas food parcels so if you need one please contact me so that I can save one for you. If you don’t it’s a first come first served basis.

Also please come and join us it’s at the same time 10-12 outside Ashton Under Lyne Jobcentre. Please come and say hello and maybe sing an appropriate Christmas Carol or two.

Suspended payments for 6 months because they were seen carrying a food parcel.

Dear readers it’s Thursday and blog day. Please may I start by thanking you all for your support for my blog and my campaign.

I’m still here writing and it’s all thanks to you all.

Today was freezing cold and the crowd was gathered awaiting out food parcels.

This week we had a very kind donation of four extra food parcels from a friend.

It’s a good job that we had these extra food parcels because they were all taken.

I’m going to list today’s conversations. Please note that everyone was given appropriate help, advice, signposting etc. I even went to Wilkinsons to buy some dog food for a dog who’s owner needed a food parcel.

Many people either forget that people struggling have pets and they need to eat. Others reckon that we shouldn’t have any pets, we aren’t deserving of anything.

A much loved pet can be a lifeline for their owner and no one should be criticised for owning one.

The first conversation that I had was with a man who told me that his payments have been suspended for six months. He is claiming the ESA element of Universal credit.

I asked why and he told me that he had been reported to the DWP because he was seen carrying one of our food parcels.

I advised him to appeal this decision and he told me that he’d been advised that he can’t.

Luckily I have contacts that will be able to help him, but regardless of that he shouldn’t be expected to go without any payments for 6 months.

It’s absolutely ridiculous and is so punishing. It’s hellish and shouldn’t be happening at all.

I spoke to a young man that had to walk miles from his home to get to the Jobcentre. He told me that if he’s lucky a bus driver will let him get on a bus for nothing, if they won’t he walks.

I signposted him and bought him some dog food for his dog.

I had a conversation with a woman regarding self employment and universal credit.

Gordon spoke to two people that were making new universal credit claims and needed documentation to do so.

I spoke to a man that’s in the process of being evicted from his home. We advised him to the best of our abilities and I signposted him as well.

I overheard a man shouting ‘B####d sanctions.

I then had a long conversation with a young 18yr old woman that was crying when she was leaving the Jobcentre.

Her advisor had told her that she’s not trying hard enough to find a job, her efforts are rubbish etc. You get the idea.

The truth is that she is trying her hardest to do everything properly but it is a struggle.

No one has shown her how to find a job, how to apply for one and no one has given her any decent career advice.

Her advisor hasn’t told her about further education nor have they told her about apprenticeships etc. They refuse to help whilst criticising her to the point of tears.

Luckili we were there and I sat down with her and gave her some advice, but equally as important compassion.

For heavens sake she’s only 18 years of age, she needs guidance and hasn’t got a good family network to support her.

I gave her a copy of our survival guide and asked her to phone me if she needed my help or even just a cuppa and a conversation.

The advisor that upset her to the point of tears should be ashamed of themselves, but they won’t be. An 18yr old claimant is an easy target for them isn’t it.

I spoke to a chap that had just failed his universal credit esa element medical assessment. He is appealing this but as usual the DWP have zero compassion.

He’s been told that he has to agree to look for work whilst his appeal is being processed. If he doesn’t agree to this they’ll stop his claim.

The DWP don’t recognise that having a disability can and does prevent a person from working. Persecuting them for this won’t cure their disability it’ll make things much worse for them. Many die, some take their own life.

It’s sickening that people are being treated in this manner, it’s not getting any better it’s becoming much worse.

I honestly don’t know how we’re going to survive another five years of this.

Please read, share, tweet, blog, email my blog. It’s so important that we get the truth out there.

We will be returning to Ashton Under Lyne Jobcentre next week from 10am to 12 noon. Please come and say hello.

For anyone wanting to donate there’s a PayPal button at the top and side of my blog.

Thank you!