Category: love island

Happy New Year.

This year has certainly been a challenge for so many of us.

Food poverty has become the new norm as has fuel poverty and substandard housing. Living in poverty is kind of expected for the working class, especially by the government and suchlike.

The truth is that we shouldn’t be forced to live this way, constantly scratching around to try and make a meal out of the remnants of a food parcel. It’s not as if the government will do anything to rectify this after all the working class should know their place.

Despite this the past year has been also been a challenge for many other reasons. My son died very unexpectedly and suddenly this year leaving me to pick up the pieces whilst trying to support my daughters. Everything appeared to go wrong for me and personally I can’t wait until this year is over.

When I say that loosing my son broke me it’s an understatement. Some days I wanted to stay in bed and hide from the world.

I really don’t know how I’ve got through this but I did and I’m very grateful that I did. .

We’ve lost so many people due to Covid 19 and illness this past year. Whilst you won’t hear the government talking about this we must continue to remember them.

Financially we are all feeling the pinch in one way or another. I’ve found it a massive struggle getting from day to day whilst trying to make things appear normal for my youngest daughter that still lives at home. I know that you also feel the same way, it’s tiring, exhausting sometimes.

So many of us have become ill this past year, I’m still battling Long Covid and some days I’m exhausted, but carry on we must because we have no choice.

Whilst I haven’t got a magic wand to make everything better for you god knows I want one, what I can say is that we will continue to support each other in whatever way that we can do. I’ll be continuing to blog and campaigning

If you haven’t celebrated Christmas and have no plans to celebrate the start of a new year you’re not alone. I haven’t and I won’t either. Don’t let anyone pressurise you into doing something that you don’t want to do or aren’t comfortable doing. You do you it’s so important to do this.

I would like to thank everyone that has read, shared and supported my blog and campaign this past year. I really couldn’t do this without you, and I certainly wouldn’t have been able to cope with the death of my son without your support.

Talking about support DPAC (Disabled People Against The Cuts) is a fantastic support and campaigning network that’s well worth joining. I’ve been campaigning alongside them for many years now and I can attest to how amazing they are.

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

If you are unemployed and would like to join a trade union head over to https:\\join.unitetheunion.org They also do amazing work and they offer legal advice etc. There is a small cost to join but if you can I can’t recommend it enough.

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I don’t receive any funding or payment for any of the work that I do. If you like my work and would like to donate to keep my blog and campaign going theres a donate button at the top and side of this blog post.

Thank you xx.

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.

UNIVERSAL CREDIT SANCTIONS RISE ENORMOUSLY IN FOUR MONTHS

As many of you already know the DWP never miss an opportunity to sanction claimants, however it was much harder to do so whilst the country was in lockdown because of the pandemic.

The drop in Universal Credit sanctions was as a result of changes to the conditionality rules that were implemented in March 2020 because of the pandemic.

Normal service seems to have resumed sadly with the rate of Universal Credit sanctions rising 15 fold in four months according to Benefits And Work.

This all changed in April 2021 when face to face meetings returned thus causing sanctions levels to rise. This proves that the decision to sanction claimants lies firstly with Job Coaches and often is influenced by their opinion and not fact.

Theres no other reason for this when online claimant were seen to meet the expectations of their claimant commitments, yet now they apparently don’t.

Benefit sanctioning is an extremely cruel way of punishing someone for apparently not reaching the DWPs expectations. Taking away a persons financial means of survival is wrong on all levels, it’s hard enough trying to survive on the meagre amount of monies given in the first place.

I’ve blogged about benefit sanctions for many years now, and I’ve also had articles published in newspapers etc.

My opinion is this, and it will never change.

No one should be punished financially by sanctions. Sanctions do not and never have encouraged people to find work or look for work more diligently.

When a claimant is sanctioned they can only focus on keeping warm, being able to eat and how they’re going to pay their rent.

Being sanctioned and refusing to pay ESA and PIP claimants their rightful payments directly causes mental and physical distress, often leading to long term illness and depression.

Whilst quite rightly we are told to leave an abusive relationship for our own safety a person can’t leave the DWP and everything that comes with it. It’s obscene that people are treated in this manner, being guilty before being found innocent. It’s gaslighting at its worst.


Prior to the pandemic the highest sanctioning levels happened back in July 2019, when 22,566 claimants were hit with a reduction in their benefit.
I have no doubt that this figure will be surpassed if it hasn’t already.

We must continue to hold the government and the DWP responsible for their actions.

Many thanks once again to Benefits And Work for their hard work for researching and gathering the data. They work extremely hard to help others.

If you want to raise awareness about these issues and more there are several ways that you can do so.

You can share blogs such as mine and likewise online of your preferred social media platform. You can also email blogs and articles like mine to MPs and other important people and influencers.

Every share, tweet, conversation etc helps to raise awareness and this is extremely important to do.

If you live in the Greater Manchester area and you’d like to get involved please join https;\\manchesterdpac.com You will find likeminded people and will be given opportunities to join in any activities that they are doing.

Unite community is another trade union organisation that is well worth joining. There is a small payment to join but you can get help and advice from them also. You can join them over at http:\\join.unitetheunion.org

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Please read, share, tweet and email my blog posts. Like I said earlier every share helps enormously.

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

How am I doing? Not good unfortunately a very good friend of mine died this week, and I’m struggling to cope with it because I’m still grieving for my son.

Financially I’m also struggling. I’m having to make the choice between heating and eating. I know that so many of you are struggling with this as well.

If anyone would like to donate to keep my blog and campaign going or to help me put some electric on the meter theres a PayPal donation link at the top, side and underneath this blog post.

I am trying to update my blog more than once a week as you might have noticed this week.

Therese Coffey plans benefit shake-up

At the recent Tory Party Conference Therese Coffey, the secretary for works and pensions declared that the amount of people that have claimed PIP has ‘grown in a way that was not anticipated’ and instead it needs to be targeted at ‘people who need help’.

This is of course ignoring the fact that the people that are claiming PIP actually do need it.

According to Coffey this is evidence that things were ‘going wrong’ and nothing due to the fact that people living with illness and disability has increased due to many reasons some being Covid 19 and poverty.

Coffey went on to say that according to her findings three out of four young people that claim PIP their primary reason being mental ill health.

According to her figures this totals 189,000 young people that receive benefit focused upon a diagnosis of depression and that these young people may also claim other benefits as well.

Thus implying that young people shouldn’t be claiming PIP at all.

 Coffey also complained about the amount of people claiming ESA should have only 25% of claimants should be in the support group rather than ‘about 80%’ of those claiming ESA at the present time.

She also complained about ESA, saying that the original expectation was that only 25% and not the 80% that are in the support group now.

Coffey stated rather predictably that she wanted to change the focus to ‘what people can do rather than the benefit system being currently driven by what you cannot do’

So in essence Coffey is saying that she wants to get people with disabilities, especially those in the support group back to work without declaring any support that might be given to claimants forced to do so.

Coffey says this regardless of their disabilities and their ability to work.

This is despicable and based upon her opinion and not the actual truth which is evidenced in the claim applications given by people claiming ESA.

ESA and PIP are not benefits that are easy to claim. Most claimants are refused upon their first application and they have to appeal and often take it to tribunal to eventually succeed and receive their rightful payments.

Coffey also takes into no consideration about how disabling and serious illness such as depression are. Anyone suffering from depression has to fight hard to try and find some support for their condition. NHS funding has been cut leaving previous lifeline services taken away leaving support hard to find.

Let’s also not forget how serious an illness depression can be. It can’t be cured by forcing an already vulnerable person into work thus triggering them to an even deeper state of depression or worse.

Needless to say, Coffey has a swinging brick instead of a heart and she doesn’t care about anyone living with illness and disability. Her aim is to try and stop vulnerable people from receiving the financial support that they need to live, without a care about how they’ll be able to cope.

To add salt to the wound so to speak, Coffey has also refused to rule out merging PIP with UC, saying that ‘everything is on the table’. Meaning that if they can find a way of persecuting vulnerable people whilst doing this then it’ll happen. How dare disabled and ill people have any quality of life at all.

So, before the DWP has finished transferring DLA claimants to PIP or moving ESA claimants to UC, they’ve already started to plot another major benefits shake-up which is going to harm the well being of thousands of vulnerable people therefore putting them at risk and causing them great distress.

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It appears that we will have yet another battle to fight. We cannot allow the government to target and harass even more vulnerable people. The government always takes from the lowest hanging branches whilst forgetting that there are more of us than them and we will put up a fight.

Join myself and my friends over at DPAC https:\\manchesterdpac.com and continue to put pressure upon the government to do so.

Thanks to Benefits And Work for the inspiration for this weeks blog post.

Please read, share, tweet and email my blog. Every share makes a massive difference and it raises a lot of awareness.

I don’t receive any funding for anything that I do. If you would like to donate without putting yourself in financial hardship theres a donate button at the top and side of this blog post.

Every penny really does help and it makes a massive difference.

A huge thank you to everyone that shares, tweets, and supports my blog and campaign.

Your help really does make a massive difference,

This week has been another tough week for me and to be honest I wish that the universe would give me a break. Regardless of this I will continue with my blog and campaign. Thank you all for your support.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

DWP agrees to waive hardship payment debts.

Please click on the below link from the Public Law Project.

If you are told to repay back hardship payment debts make sure that you challenge this.

It is your legal right to do so. If needed quote the below article and insist that the DWP use their discretion regarding payment of hardship payment debt.

Insist that these payments are causing distress and suffering, which they do for thousands of people.

This is also essential because the majority of claimants already have monies garnished from their payments for council tax debt and suchlike.

No one should be forced to live in extreme hardship such as this.

I expect that the DWP won’t like this so don’t expect them to suggest it to you.

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

Please like, share and tweet my blog. It’s very important to get the truth and the reality of our life’s out there.

I don’t get paid for anything that I do but I do want to continue to be able to continue to write my blog and continue with my campaign.

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

A huge thank you to everyone that and has supported my blog and campaign. This makes such a big difference.

Maximus work capability contract extended for two years.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Thank you!

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

My son died.. How am I?

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Let the bodies pile high says Johnson

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

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

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

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

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

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

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

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

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

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

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

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

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

Please read, share, tweet and email my blog. Every share helps to get the truth out there.

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

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

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

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

Let’s talk about Covid deaths.

Dear readers, subscribers and friends, I hope that you are as well as can be. This week has been difficult for me because it’s the first time that I’ve been able to sit down and grieve for my son.

Everyone grieves in their own way and the time it takes for a person to grieve is totally individual. I truly don’t think that I’ll ever get over it and I’ll just learn to live with it.

It’s heartbreaking to know that thousands of people are mourning the loss of a loved one to Covid 19. No one as far as I’ve seen has spoken about their suffering and loss. I cannot comprehend their grief and pain.

The government has done a good job of hiding the true reality of the pandemic, the deaths, suffering, long covid sufferers and those already isolated because of illness and disability.

It’s very easy for the Prime Minister to open the borders, allow travel to countries overseas and to open up shops and businesses, he doesn’t have to cope with becoming ill and having no support, to be isolated in his home due to disability and illness. As most of you already know that he doesn’t care, he doesn’t care about our welfare and he certainly doesn’t want to improve our quality of life.

I don’t underestimate the joy felt by many when they realised that they could come out of lockdown but I do realise that the Indian strain of covid 19 will soon be in most of our communities because Johnson once again hasn’t put much, if any thought into ending the lockdown.

Like many of you reading this I’m fully vaccinated, and many will be awaiting either their first or second vaccination, but I’m a tad worried about the Indian strain coming our way because we just don’t know if the vaccination works with this strain of COVID 19.

What I can say is proceed with caution, wear a mask, wash your hands and remain cautious. It’s a terrible indictment of our government that Johnson thinks that its ok to say ‘Let the bodies pile up’ and still be allowed to continue as Prime Minister. I remember the days when the opposition used to oppose such wrongdoings but now there’s hardly any from Sir Kier Starmer.

I really hope that we start to have some decent opposition soon because thousands of people need this now.

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