THE DEVIL & THE SONGBIRD

Well what do you know?

Everyone one of the Brexit morons transfixed with Brexit again like Rabbits in headlights trying to stop a car with no brakes, exact representation of what is going on, purely over selfish reasons and that democracy now does not work for them .. so ignoring it.

So almost as if getting the British public into fever pitch, not that hard to do despite the fact that it is staring the in the face this is inevitable, deliberately some new crap has come out and the DWP release some stuff.

Remember how the government got caught out stating that due to the British populations tunnel visioned obsession with something else at the time it is a good time to get dirty laundry released so that no one would notice .. or care because of their self-obsession for amoral reasons or .. feelings?! Yeah I cannot recall what it was over either!

Anyway it has become clear that they have not stopped doing this because they just got caught .. well .. doing this!

Hmm maybe this is a possible reason the mainstream news media wold come up with for not reporting on a lot of stuff that they should have?

• Oh well this other thing came out at the time and we thought the public would be more interested in that and could not afford the screen time?!
  • Non-reason
• Oh .. everyone loves celebrities and there was this celebrity gossip or celebrity baby or this happened in I’m a Celebrity .. or X-Fuckter!
• Add your own theories?!

Maybe? I mean if your going to be controlled and have obvious political motivations you have to first have a plan to hide it and then have excuses for it when people notice after many years, right?

 

• We will release a few of the not so serious stories for .. tokenism and manipulation to produce misconceptions to hide our true nature or goal
• After another number of years when this has been spotted we have these excuses we have spent all those years preparing and coming up with
• Add your own theories?!

So according to the report they are claiming that Esther McVery lied to parliament, and everyone else, and not just once either?! Well that much was obvious ..

I have long since told you she is not sincere! Hence why I do not like her as she comes across as very far removed from anything representing genuine and I have been shocked that she is not seen as this by the wider British public?!

 

This is another woman in politics that my daughter is disappointed in and now makes a trio of women Conservatives that have disappointed scores of women everywhere.

• Margaret Thatcher
• Esther McVey (gets second because she was there before Theresa May showed her true colours)
• Theresa May

So no one would be denied disability help under the new benefit, which they planned to get rid of anyway ..

.. around 381,000 DLA claimants who were reassessed for PIP did not get it – (The Canary see below link)

“more people are getting PIP than were getting DLA. That really needs to be heard so that we dispel any myths from the Opposition” – Esther McVey to Parliament (see The Canary link below)

Or how about ..

 “supports more people than DLA ever did” – Esther McVey to Parliament yet again (See The Canary link below)

Or how about ..

“I reiterate that under PIP we are supporting more people than before” – Take a wild guess who said that and where you can go and read the report? lol

I am sorry but does not the DWP report show that she lied .. three times?

Yeah I would bet that there are a lot more lies than that!

 

The Canary report .. 

https://www.thecanary.co/uk/2018/06/13/as-brexit-distracted-us-the-dwp-released-some-truly-horrific-figures/

Finger Tip and Toe Tip Sensitivity .. Pain listed here as Fibromyalgia ..

It also states Raynaud’s Disease and Carpal Tunnel Syndrome, of which the latter will make a certain someone .. laugh! Osteoporosis is also listed and I was diagnosed with Osteopenia, which is like an early stage of the former.

https://www.healthhype.com/fingertips-pain-tenderness-and-sensitivity-causes.html

https://www.doctorshealthpress.com/pain-articles/pain-in-fingertips/

As mentioned above, Behcet’s Disease could well have been called Hippocrates Disease, and that might be more apt, because the disease can have periods of being dormant, called remission, and periods of activity called ‘flares’ and that the symptoms can appear individually, making it seem like you are a hypochondriac. – http://www.behcets.org/reference/symptoms_in_detail.html

Well there you go.

It is documented on here about my issues with my finger-tips regarding touching the two damn things that I do the most, dirty minds out there can put their first guess straight out of their heads!

My touch-pad on my laptop and my Moto X phone screen. God .. it is irritating as f…. screaming babies! Lol. I find myself biting the tips of my fingers in frustration and as I said when my daughter discovered she had Behcet’s Disease.

She immediately realised I had it asked me how they have missed this for over twenty five years with me and .. well .. yeah I have had it over twenty five years!

Now if your an idiot that thinks this is all a good idea to save the taxpayers money ..

• How is this saving taxpayers money
• How can not treating something to allow someone to go to work and therefore pay taxes saving tax payers money?
• In twenty five years how many times have I spoken with General Practitioners and been fobbed off, also costing the British taxpayer? Trust me it is a phenomenal amount.
• How many times have I visited various departments in various hospitals costing the British tax payer?! Trust me this alone is a phenomenal amount!
  • Eight GP Surgeries with dozens of Doctors
  • More than one GP seen with all of them and three I met at least three Doctors each
  • Whipps Cross, Barnet, Chase Farm, Royal Free (twice), North Middlesex, St Michael’s and Guy’s Hospitals .. wanted to effing send me to a place in Hillingdon over Fibromyalgia .. right across London (West)
  • All missed Fibromyalgia
    • Upon discovery I knew they had known about it for at least two years
  • All missed Hypomagnesemia
    • Upon discovery failed to link it to other symptoms I had experienced for years
    • Since discovery failed to link it to other symptoms that cropped up
    • Failed to inform on how dangerous it can be
    • Failed to refer me off to check why this occurs
    • Now developed into Malabsorption problem
    • Pain, stress and agony this causes is beyond belief
    • Might not have placed the condition on my medical records, yet to be determined
    • Clear results for other things points to the condition, like Osteopenia
  • All missed Behcet’s Disease
    • This is what actually goes back twenty five years
    • Told condition like this does not exist
    • Discover if not dealt with Fibromyalgia then develops
  • Right Knee Physical Issue
    • Spotted for the second time in three years or so
    • By Dr Kirkham who diagnosed Fibromyalgia
    • At Guy’s Hospital
    • Test done
    • Yell of pain
    • Told physical problem
    • Completely omitted from letter to GP

Also and as it turns out the government have been found to have acted unlawfully over Universal Credit ..

https://www.leighday.co.uk/News/News-2018/June-2018/First-legal-challenge-against-Universal-Credit-fin

Quite how there can now be anyone left that agrees with the government is beyond me. Obviously to suit there own purposes. Because the one thing you get is ‘It is the law’ or ‘It is not unlawful’ when you put this stuff to defenders of these morons.

Hmm I know Leigh Day!

Now explained to my daughter I am pretty sure I was in contact with them around 14 years ago about my foot pain? Well my case was sent to them after I was pounded upon by the representative of a company like Irwin Mitchell and Slater & Gordon called The Accident Group.

Stated I had the best case they had ever seen, funny as now no one even asks to look at the evidence I collected, and they went bust several months later. My case was passed to Leigh Day I believe?Who were not very good back then and said something completely different to The Accident Group but basically said that because they did not want to fund it.

VINDICATION

I still don’t trust the courts.

But as it turns out The Canary had published an article that seems to state that that a court had effectively given the middle finger against the DWP over their treatment of disabled people.

They even said they take no notice at all of anything Atoms says.

It gets even better when I believe it stated that neither the DWP or Autos turned up to defend themselves.

The author states at what a national and global disgrace it is that this had been going on with the abuse of human rights.

Which begs the question ..

Forgetting the fact that all this has somehow remained in place and fully operational despite all the reports and court cases but ..

Can we now expect these things to be dissolved and for people to go to jail for serious crimes that were performed effectively en masse?!

They do this with war criminals and they only killed people ..

.. this has very literally been a fate worse than death, still is, and I’ve not been eating because I have had enough and want to die ..

Though to be fair .. I’ve eaten because I’ve been forced out in pain because others only think of themselves. I get bad muscle pains, aches and severe spasms when I overdo it and I don’t mind death but do mind pain and especially the severe types. What with low magnesium and all.

My thighs and calf muscles feel .. tight and that makes me .. apprehensive.

Despite these reports I cannot help thinking that the are just tokenism cases.

I still have no confidence in mine that it now looks like I won’t make it to.

Very tired, severe pain, apprehension, sore throat and I’ll have a nervous breakdown travelling there to something I’m going to get railroaded over for the fifth time.

Now I have this new information regarding Behcet’s Disease which my daughter has been diagnosed with, is linked to Fibromyalgia and explains most, if not all, the symptoms that low magnesium uptake cannot.

I had been pressurising her for many months because it was clear they were already fobbing her off .. despite not knowing about several things she has experiencing .. then said they were going to refer and did not .. and has four children to deal with along with cervical cancer.

I had already warned her about low magnesium the very same day she had just been told she had low magnesium after a blood test result. I had been diagnosed with low magnesium something like four years ago and had obviously been going on a bloody lot longer than four years. Fifteen would be my estimation. Possibly more.

Ergo .. mine now might be quite serious as I am still having difficulties despite taking supplements and wondering if there is an issue of my body actually being able to absorb magnesium?

https://www.thecanary.co/uk/2018/05/11/a-court-just-gave-a-massive-finger-to-the-dwp-over-disability-payments/

THE HANDS FINALLY GET DIRTY

Well what do you know?

I have been meaning to post this for several days but I have been preoccupied with .. a barrage of symptoms and kept forgetting to do it.

In the distant past, well it has now been going on for a decade, many online like DPAC and its members constantly blamed organisations like Atos for the bad treatment of disabled people. I was constantly telling them that it was not Atos on their own. They believed that if the Department of Work and Pensions knew of their activities they would get rid of them. I stated as a matter of fact that Atos were merely doing what they were told to do.

Many would not accept these facts.

They know it now.

I got into trouble once online for stating that it was planned by the government to have their new disability living allowance, suspiciously named Personal Independence Payments, was to disappear by 2020 and become part of Universal Credit. Boy that one set of a fire too! People were demanding that I get my post kicked off along with myself?! It took me by surprise, the reaction.

I often wonder how different things might have been even for my daughter, my grandchildren and myself had people listened to me way back when?

What the DWP were not willing to do is get their own hands dirty .. and the governments plan went just as intended. Everyone aiming their ire at the hired thugs when it was the DWP and the government all along.

Several years have gone by of screwing people’s lives over for money.

But finally the DWP are up to the tricks and been caught at it that they have previously hired others to do .. and this one is a bit of a doozey ..

They have been asking leisure centres for video footage of anyone with a disability so that they can then take their money away. Their disability. Except it is not that simple ..

When I consider myself .. I can never see myself ever attending a leisure centre and if I did it would only ever be for swimming. But my physical ability is only half of my issue and with the physical issues alone there are several. But it seems when I try to ignore the pain and try to do that which I want to do .. I suffer. But I suffer both physically and mentally and it is not just overdoing it and getting tired that triggers my mental health issues. Pressure and stress along with worry also do the exact same.

In other words .. there are disabilities that you cannot see on a video of someone. Hidden disabilities that I am all too familiar with. So degrading is it that you get to low points where you either do not want to wake up in the morning or pray for something terminal, like cancer. But even so I have been hearing that they even treat people with cancer like absolute shite!

Oddly enough they seem to be breaking the law to do it, article 8 of the human rights act according to someone I know who puts this on the blog in the link below. Gail Ward of DPAC ..

https://samedifference1.com/2018/03/05/dwp-asking-leisure-facilities-for-cctv-footage-of-disabled-people/

THE BOMB THAT ALREADY TICKED

Well I have been missing the odd report.

I was kind of tied up, with pubic service failures and gathering evidence trust me, for four months and busy for six months before that. I still kinda am .. or at least have things to achieve but I am pacing myself. Due to memory and health issues.

So I recently posted articles about PIP being re-reviewed, Atos being found guilty of lying and a few others.

Oddly I came across a report on Disability Rights UK’s website where it states that MP’s ‘find’ claimants are ‘mainly’ satisfied with PIP & ESA assessments .. but there are problems.

Out of dozens of people I know only one has not complained but he is the only one that has not been assessed in recent times and therefore .. STILL on DLA so is ruled out. That means that 100% thus far disabled people have complained.

What I hate about the article is it seems to be portrayed as it is a fact. Like there is nothing wrong with assessments, or at least very little which can be expected of anything like this ..

https://www.disabilityrightsuk.org/news/2018/february/mps-find-claimants-mainly-satisfied-pip-and-esa-assessments-there-are-problems

Anyone that has been here regularly knows I have not trusted charities in a very, very long time.

Also and on the same page there are links to two articles on the Disability News Service’s website that contradict this report?!

‘Data shows multiple complaints against SCORES of Atos assessors’ ..

https://www.disabilitynewsservice.com/the-pip-files-data-shows-multiple-complaints-made-against-scores-of-atos-assessors/

And to add insult to injury ..

‘Nearly one in three Capita assessments flawed’ ..

https://www.disabilitynewsservice.com/the-pip-files-nearly-one-in-three-capita-assessments-were-flawed-reports-reveal/

Then I would like to point out a particular court appearance I experienced with a biased judge called Judge Mark of the HMCTS ..

• Explained ..
• I did not attend assessments as there were between five and forty miles away
  • Later found out they had assessment centre two miles away
• I did not travel five to forty miles because everyone knows they lie and well documented and reported as such online
  • Now being reported on widely and nationally so
• But three very lame and amateurish attempts to label me as a liar
  • All failed, none mentioned in report all of which on here .. I think?

I have no issues posting and publishing things because I have nothing to hide and am honest about things that occur. No point in being dishonest and .. well you would soon get caught out and the HMCTS, DWP, Atos, Capita and Maximus all seem to have forgotten one simple rule followed by one fact ..

• Liars require a damned good memory
• Due to Fibromyalgia and Fibrofog my memory is shite

Need anyone say any more?

Maybe, why so long when I have pointed out the facts for several years?

DWP & THE A-TOSS AIRS

Do you know the trouble I find with all advice centres and solicitors even?

Oh and you can add in ombudsman in all this, governing bodies and the political opposition parties that include Jeremy Corbyn ..

They do not read all your letters and all your emails reports.

Do you know what else they do not do?

Do any fucking research and after years and years of people being murdered they come up with just a few cases.

YouTube is a good place to research so I will do so once again what so many have not done for years before me to date.

Here is a long list of YouTube videos regarding the DWP, Atos and even one Atos staff member admitting that I tried to tell people over and over again that Atos only do what the DWP tell them to!

All I kept hearing was that if the DWP knew what Atos was doing they would get rid of them and it would be all over .. I said, “Like feck it would!”

Of the videos I have linked below I have seen .. ONE. I have not seen the others .. speakers do not work and .. well I do not need to listen to them. I know pretty much what they are going to say and it is damning.

Worst of all look at some of the dates .. note that I think most of these were about Atos, formerly Atos Healthcare and a French company based in Paris that was masquerading as a British company.

Now consider there are three others added to this list which was previously just one?! One that got caught out and the Tories said they was going to get rid of .. even Nick DeBois lied toi my face and told me they had discovered what they was doing and were getting rid of them .. ooh did I mentioned I have that on tape, figuratively speaking? Oh dear. But they went nowhere and another three organisations just like them added to them?!

Now you see the news media reports about children and people starving!

Yeah well sorry mainstream media like the BBC and ITV News but you are partly responsible and you have been paid millions upon millions while I have been trying to raise awareness of this for free and I have had no thanks at all.

I even tried to tell about this 6 years ago and you did not even flinch .. not so much as an acknowledgement. Now you look like the proverbial white knights .. now that it has all gone wrong like I predicted it would over 6 year beforehand. I started blogging in 2012 and I contacted all tabloids .. ALL tabloids and TV News Media groups back in 2011. Maybe even earlier actually? Yeah I still have the sent emails, LMAO!

Grand scale crimes against a large portion of the British public while stealing money of the rest of them to commit these crimes while the proverbial books are thrown at people breaking the law just to survive or feed their children.

Where does it stop and when does the British law stop being warped into something far more sinister and beyond recognisable as a joke any more?

Consider this is just a small percentage of videos. Consider that those that record their assessments, umm .. like I did, would only be a tiny percentage. I can assure you that if you look my number of just over a dozen could very well have a third figure to it. Consider too that those that had a similar experience but did not record their assessments could have yet another figure or two added to that.

So what are dozens could very well be hundreds of videos that could be thousands or tens of thousands of similar assessments.

Yet HMCTS were ot interested in this widely known fact .. now was they interested in the fact that theu tried to send me 40 miles away or further when they had a building a mile from my house tat had been there several years.

Yup Judge Miss Mark and the HMCTS are just as corrupt and selfish as the Tories, DWP & Atos and sit their like lords while they steal far more of your taxes than the accuse disabled people of doing.

Oh the irony!

So .. here are one or two of them … LMAO ..

 

THE PROFIT FROM DEATH

Undertakers must be tossing in their sleep?

I thought I would add just one more post regarding the treatment of disabled people by the government and those who are effectively their .. henchmen.

Now what I am going to tell you I kind of knew previously .. except the figures, I believe currently any way, have gone up since then.

Now you have to consider what it is that they are doing to the most vulnerable in society, which are those with disabilities.

They have been trying to kick them off Disability Living Allowance and still doing this since they bought in what was originally intended as its replacement, Personal Independent Payments, which is not going to be around for very long anyway. Because it is to be ‘absorbed’ for want of a better word, into Universal Credit and this was by 2020. Whether this date means everywhere at once or the last of the places to lose PIP I do not know.

So what do you do when you want to stop supporting and paying people with life changing disabilities where getting to your local shop can be a challenge and causes you to stop and thinking your about to have a heart attack.

I know because that is me and that is just something that has bothered e the last year ro 18 months ad does not include everything else. Pain from walking, pain from standing still, different pain fro descending stairs, aches, pains, tiredness (well it is a kind of sleep disorder), insomnia, bad anxiety and short term memory loss among many other things. That is just mine. God know what others suffer with.

I have been on DLA .. had it cancelled .. appealed and lost and not knowing what it was that affected me at the time.

When I later found out and had it diagnosed I then reapplied for PIP, got turned down, told them I know that they lie and had recordings .. they rang me up reversing the decision and then .. 18 months later cancelled it again. For not turning up for an assessment I have NEVER turned up for. Because they deliberately made them far away up to 30 to 50 miles when they had one a mile away from my house they failed to mention. I lost the appeal for the argument for not travelling 50 miles, because I travelled 6 miles on empty buses to a hospital appointment for an ECG over black-outs and grey-outs. Had head MRI too but the judge, Miss Mark, did not give a flying fuck about that just as I did not give a flying fuck about her three failed attempts to call me a liar that then stayed of the decision paperwork.

Yeah so what do you do to make everyone’s lives a misery so that you can save a bit of money?

What you do is you take two firms and you pay them half a billion pounds in a single year!

Except .. that figure was over £100 million some years ago and .. there are four today when years ago there was only one .. Atos .. who we were told I the news media they were getting rid of three or four years back. The news media has not, however, gone back to the government to ask why they are still there?!

Even Nick DeBois MP, Tory, for Enfield North told me to my face that the found out what Atos were up to and got rid of them. This was not true of course and I told him he was looking at one of the people responsible for getting rid of them due to the evidence I had published and the lies on their letters I had published with the video proof they had lied. I also told him that I was asked my Michael Meacher MP if he cold use my data in the House of Commons to attack Iain Duncan-Smith and send things to the news media.

Of course I had the odd story like mine appear in the news media but after Michael Meacher’s email to me this increased .. a lot. I regularly had disbelieving friends and family mention that they had just seen or heard something in the news that was a carbon copy of something I had covered. Many times months or years beforehand.

Yeah .. I always suspected the news media to be honest.

In fact I had suspected many for well over ten years. I moved to Enfield in 2007 and had long since suspected most of them including the mainstream news media. Including those that are now trying to steal the phrase ‘fake news’ as their own. God how utterly slimey can you get?!

So .. half a billion pounds to just half of the companies in just a single year?!

What will the bill be next year?

What I find utterly funny is how they keep on employing these people, not just the usual thoughts of what kind of rock they lifted up to find people like this.

Here is the late Michael Meacher MP’s talk in the House of Commons about the DWP, Atos and disabled people. I have never listened to it, sorry. Lol.

https://youtu.be/9q9QfRVB6HA

Now when it comes to the Atos and Capita scandal .. I am not sure of this link to where I heard about it, will work …

https://www.facebook.com/ArmchairActivistist/photos/a.232822173771156.1073741829.106539616399413/506154156437955/?type=3&theater&ifg=1

Oh .. it is reported in The Mirror .. boy, what has gotten into them? ..

http://www.mirror.co.uk/news/uk-news/private-firms-rake-half-billion-9515131

THE WHISPERS OF REASON

Well this is another black mark for the Tories and their evil plans and the stealth like schemes .. plus for their Puppeteers who must be uncovered at all costs.

Thousands of disability tests are branded as ‘unacceptable’ by the governments very own quality control scheme?

I never thought I would ever read that or that the government even had a quality control scheme?! I want to know where in the hell these quality control people have been for the last eight years and is it only because of Frank Field’s valiant efforts and some crocodile tears that they have now come out and stated something?!

Who knows.

Atos and Capita have never even met their target once, according to the DWP’s current quality control scheme for Personal Independence Payments (PIP)

Bombshell new figures say neither Atos nor Capita – the outsourcing giants paid more than £500m to assess people for Personal Independence Payments (PIP) – are meeting the target of 97% of assessments conforming to standards.

Latest audits show 6.4% of PIP benefit assessments were deemed “unacceptable” in the three months to October 2017.

I would go as far as stating that they are well under for the figure of 6.4% in that last statement from the webpage below. Well, well, WELL below judging from what I have been hearing.

One Type 1 Diabetic I know constantly insisted that Type 1 Diabetics would not nor never be touched by the government and the DWP and insisted that DLA would not go.

Then one day a friend of his with the same condition has him got told he was being transferred over to PIP and had to re-apply all over again. That surprised him. That was around 6 to 8 months ago now.

A few weeks ago another friend of his with the exact same condition but actually missing a leg had his PIP stopped. He got it back on appeal but I could tell from his voice he was now getting a little worried.

A labour voter all his life and after listening to Katie Hopkins in a radio interview recently he stated to me on the phone “You were right. You were right about EVERYTHING!”

What did he do for a living?

Oh he was only a social worker for Camden Council for 25 years!

EDIT: As I stated in a comment in DPAC where I first saw this story ..

.. will it go anywhere though ad will it go far enough?!

http://urthevoice.co.uk/thousands-disability-benefit-tests-branded-unacceptable-governments-quality-control-scheme/

TOO MANY SHEEP

I’m having an odd 24 hours.

First up a second test for my Autistic grandchild once again went off the scale. This was a shame but from what I’ve been seeing not a complete surprise.

I was told that someone asked, I thought the council or school, if it could be down to the domestic abuse that recently took place. It was a resounding, no.

Oddly this question came from Victim Support and not the school or local council which was a surprise. Not a complete surprise I have had dealings with Victim Support before and .. well .. they and the council said they would relocate me and .. nothing came from it.

It was a speech and language test and even the simplest questions with ‘yes’ or ‘no’ answers were only ever answered with ‘what?’, ‘what?’, ‘what?’ repeatedly.

The same test for my youngest granddaughter didn’t take place because they were ‘understaffed’. I can’t recall if this was the same day that the children came home with permanent marker ink all over their school jumpers? Ruined, if you hadn’t guessed.

So far since being here which is just a few weeks I’ve seen old mobile phones be bought home, candles that are dangerous (one nearly set the living room aflame) actually being made by children and now they let them play with permanent marker pens which ruined their jumpers.

God only knows what’s going to occur over the next six months to a year.

I’ve also had my first ever Halloween party and even did pumpkin carving. Unfortunately most didn’t go to plan, one adult threw a mood bringing part of the evening down who then set off a couple of hundred quid in fireworks. Upsetting one child. Oh and my .. um .. ‘ex’ was present. Nnyyeeah!

As a result of last minute shopping I still didn’t get to do two last things I need to do. Bummer!

I’ve also still been helping out and present at the home more than I’d like to because it’s .. exhausting. Hopefully that will change.

I did pick up, finally, a pump for my inflatable bed while picking up the fireworks!

So sleeping and pill taking has been bloody hard and still getting missed. Though I’m trying very hard to consciously think about this.

The trouble is that my memory screwed me throughout the day even when I lived on my own. Being around people brings with it distractions so it gets worse. Add four to six children to that with one being over active, another with serious Autism and another suspected of suffering with it (fingers crossed she isn’t and it’s mimicking).

Now I spot this BBC report regarding a study into lack of sleep, something I am sure  great many people are experiencing these days?

Someone called ‘Trust Me I’m a Doctor’ worked on a survey with University of Oxford regarding the effects on people deprived of sleep. In the only one out of four that stated they could detect no ill-effects it turned out that even they did indeed have them.

Just to be clear they let the .. guinea pigs .. or volunteers sleep for eight hours over three nights and then reduced this to four hours over three nights. Just three nights.

A professor at the university believes that the lack of sleep leads to repetitive negative thinking? Well I can vouch for that!

It also appears that the same organisation ‘Trust Me I’m A Doctor’ did a survey a few years back with Surrey University too?

Well .. that goes against what the government has done through the DWP when it comes to people unfortunate enough to suffer from Fibromyalgia and very likely other sleep deprivation ailments.

In Fibromyalgia, likely Chronic Fatigue Syndrome and Chronic Regional Pain Syndrome to name but two others, the problem is in fact a sleep deprivation one.

Since I have been in my new location in a far away land it has been difficult and I have been certain that part of the problem is worse sleep than normal?

In case you was unaware, as Fibromyalgia is not a widely known ailment and that is what the government/NHS/DWP love, it is a sleep deprivation condition. And then some.

What you go without is the deepest form of sleep known as restorative sleep. In fact what we have is referred to as ‘non-restorative sleep’.

The one and only drug known to correct this is also not available in the UK, or the whole of Europe for that matter, called Sodium Oxybate. Bizarrely it is available for sufferers of narcolepsy. It is also available in America for Fibromyalgia.

Forgetting every other of the dozens of symptoms people normally get from Fibromyalgia, from a possible 200 odd, how i the world is anyone supposed to hold down a job, let along a full time one! It is frustrating and that is an understatement.

This is bad even when you go to sleep and as you do not get this restorative sleep anyway after the nights where you sleep very little or not at all things are .. unbearable!

There was once a tie when going without sleep for a single night would just have me groggy in the morning until I had eaten breakfast and I would feel normal after awhile. That was a very long time ago.

There was a point when going without sleep became common and feeling like you were dying and dead tired along with being slow and that confused me. People used to joke it was because I was getting older, except one of these used to go without sleep with me at an older age than I was at when I was having trouble and he was just as I was. OK after breakfast.

Of course after being let down fir years and then lied to for several years and then discovering Fibromyalgia myself and reading a whole book about it absolutely everything made sense.

Not to mention that forcing people to drive to work with this condition on mornings were they might be really bad or slow without realising just how bad is also .. fucking dangerous. Just so they do not have to provide them with any support and force them into work to get more taxes paid and their figures down?

I cannot help but wonder how many accidents have taken place whereby this was the main cause and no one to this day realises it?

There are just too many sheep to count.

I saw this on the BBC and thought you should see it: Just a few nights of bad sleep upsets your brain – http://www.bbc.co.uk/news/health-41816398

ALLOWED TO BE FULL OF SHITE

Well what do you know?

It is Atos again in a story that is told right here in the North West and in the Liverpool Echo.

Atos found that a councillor, or two, were standing outside their offices giving out advice and leaflets, I think, to disabled people going in to be assessed.

Now one of these people asked the unusual helper if they would accompany them to their assessment and that is when Atos .. well basically lost it and refused .. coming out with bullshit and lies in the process.

Huh? That is funny as they are normally quick to accuse others of that .. despite it being peanuts they receive when compared to the money that Atos and its staff receive.

I guess being a little dishonest when your poor or disabled is a capital crime but being totally full of shit dishonest while making people’s lives a misery or abruptly ending their lives altogether is perfectly OK when your a company worth billions?

They had the fucking audacity to claim later on that they were investigating!

What is interesting about this particular news article is that it actually states that Atos was appointed under Labour. Or Tony Blair to be specific which is one of many reasons I went from really liking the man to utterly despising him.

So many people and victims seem to be under the impression that Atos is a Tory thing when this is simply not true as pointed out in this article.

I thought I had managed to get the kicked out of their contract, though to be perfectly honest I never expected anything to improve for anyone and that things would carry on as before but with a different name and a different company. Then Maxima .. Maximus .. Maxi Priest, or whatever it is called, popped up and then Capita started to do stuff along these lines too.

Yeah well when you want absolutely everyone off disability benefits and incapacity benefits of all kinds just one or two companies cheating and lying to get everyone they see off benefits is simply not enough.

I am interested to see what they say when someone puts it to them eventually that it is actually impossible to have nobody with disabilities, other than the plainly obvious, or nobody with incapacitating illnesses? Because mathematically it simply does not work.

But I am sure that the powers that be will come up with some bullshit .. obviously forgetting that they have that with the introduction of the Internet more and more people communicate with each other and immediately at times not just all around Liverpool, in this instance, but around the coutry and around the globe.

I bet they have not stopped to think about what lying, cheating, heartless dumb-fucks they actually look like to a great many people and that this number of people is increasing all the time.

Christ even TV celebrities are tarting to state that everyone is treated like shit and they do not just mean people out of work or on benefits but people working too.

Take a look for yourself ..

http://www.liverpoolecho.co.uk/news/liverpool-news/police-called-after-welfare-experts-4694546

What are the odds that another statement about getting rid of Atos will come out eventually and that nothing will ever come of it or people will realise it is not just Atos but is systemic to the entire system. Indeed to the entire government and on both sides.

PEOPLE JUST DO NOT CARE

Not got a chance to really talk about this as I do not have the time currently..

But as I normally end up forgetting to do 50% of my posts I did not really want to miss this one.

No one on a train wanted to give up seat for someone disabled!

It is just one of many reasons I do not travel,, like I told the DWP and Atos who then twisted my words … if I travel I will be in pain in several areas, sweat far too much and contend with embarrassing things that are permanent and spontaneous.

So I will be peeved all the time.

Throw in some idiot who is rude and it would be akin to lighting the touch-paper.

Also there was recently a programme on Channel 4 about the disability issues with the DWP I am always talking about. Did not see it, probably would have annoyed me anyway.

Just another thing in the news media that is short and sweet and designed to make the general public,, you know lie those arseholes on the train that only gave a shit about themselves, reason to carry on not taking any notice.

And so it continues.

http://www.standard.co.uk/news/transport/disabled-woman-posts-facebook-photo-of-businessmen-refusing-to-give-up-her-reserved-seats-on-london-a3350911.html

What was also interesting is that someone else on Facebook commented just as I did about it and stated that fifty years ago, a time I often dream about living in, everyone would have care and offered their seat.

This is the Disabled People Against Cuts Facebook page ..

https://www.facebook.com/groups/DPAC2011/?multi_permalinks=1171401832916069&notif_t=group_highlights&notif_id=1474376247801624

Well at least it has some airr time and now maybe another news media in another country will take notice and start reporting about how we treat our own people?

Think about it this affects everyone …

If they treat the sick, disabled and vulnerable like this then what chance do you have?

The only time your not affected and that is if you have large amounts of disposable income whereby hiring a solicitor at £220 to £400 per hour is nothing to you. If you cannot, there is no legal aid and you are just as fecked as the rest of us.

I wonder if anyone bought up the fact they have been not only breaking the law as well as being immoral but that there is an attempt to take a couple of ministers to court over all this? One of them being Iain Duncan-Smith.