Government #Disablism Discrimination in Action

This week a woman not known for her timidity, admitted how a non-disabled man had used his presence and the environment to disempower her; I’m referring to Dame Anne Begg and the she interview gave to the BBC. In the Daily Record Dame Anne is quoted as saying “Iain Duncan Smith took to standing behind me during Prime Minister’s Questions. He stood at what’s called the Bar of the House and occasionally he would lean on my wheelchair…Our working relationship was slightly fraught anyway because I’d been critical of him a lot. I wanted to keep that criticism a professional criticism, not a criticism of him as a person so I never quite built up the courage to actually say: ‘Please don’t do that.’” Dame Anne also was recorded as having explaining how “she would normally reproach people who invaded her personal space but she let him off“.

This is an excellent example of how competent, intelligent, and independent disabled people not only experience prejudice – as people either knowingly or subconsciously, use their bodies, words or actions to oppress us; but how this actively exasperates and diminishes us.

It is no coincidence I use this example with IDS being the perpetrator, as it is again his department, the DWP, I am discussing today. In November last year I introduced you to Burt, who with our support at DEAEP was transferred from WRAG to the support group last December; since then Burt has received up to three letters a month plus texts reminding him of his “Back to Work” appointments! Each month Burt has responded to each letter with a phone call saying “but I’m in the Support Group”, he has received an apology and a promise to rectify this from each call; yet it has continued.

Burt is a former career soldier who fought in wars all over the world, until being retired out with a crushed spine and severe PTSD, amongst other conditions, all contracted during his service.  He isn’t a naturally timid man, he loved his Army life and willingly gave everything to “Queen & Country”, as his service record and the plethora of photographs and awards proudly displayed in his lounge demonstrate; and yet the persistent harassment he has experienced from the DWP in the past 2 years has left him joyless, feeling without purpose and literally unable to complain.

As Dame Anne alluded to regarding IDS, his actions which amount to bullying in my opinion, makes it difficult if not impossible to positively challenge the perpetrator(s); and this is the situation Burt is in. Personally I can totally relate to this, and would suggest many readers and other claimants can also. It is these dismissive attitudes and continuous intimidation by the DWP that creates the ‘Brown envelope Syndrome’, so well recognised by those of us unfortunate enough to claim benefits; it is also this oppression, and misuse of positions of power, that has contributed to the deaths of many us.

How much worse this is going to get following the closure of ILF and a budget, which I believe initiates the removal of WRAG? Being forced to deal with increasing poverty is physically and psychologically damaging enough without having to deal with this prejudice and discrimination from the DWP.

I find this particularly ironic that jobseekers (presumably including those who would have been placed in WRAG)  are being mandated to participate in Cognitive Behaviour Therapy (CBT), which claims to Stop negative thought cycles; I can’t help but think IDS, his ministers and the staff at DWP would benefit far more from CBT than claimants?

The cost of PIP? £35 less per week, Thanks #DWP! – This is A CALL OUT for Info

Well I’ve received my PIP award and hooray I’ve ‘scored’ more points than on my DLA and yet, despite this I’ve  been awarded ‘Standard’ rates for both Daily Living & Mobility Elements, to explain how this makes a real difference to me read on.

To get PIP at all, you must score between 8 – 11 points in both daily living / Mobility and to get the Enhanced rate it’s 12 points; the 2 elements are valued differently with

the Daily Living standard rate being £54,45 and the enhanced rate £81.30 per week,

for  Mobility, the standard rate is £21.55 and the enhanced rate is £56.75 per week.

This differs greatly from the old DLA which had three levels of award, the rates which are/were worth  for care

lowest rate – £21.55

middle rate – £54.45

highest rate – £81.30

and for the mobility component

lower rate – £21.55
higher rate – £56.75

I believe these changes clearly demonstrate how the government have reduced PIP spending by a total o£2.2bn?

Personally under DLA I received Mid Care & High Mobility, however under PIP I scraped in at a bare 8 in daily living and 10 for mobility costing me almost £140 per month!! I have reported my intention to ask for a Mandatory Consideration and will keep you posted; in the meanwhile…

…I’m trying to collect evidence of PIP being no more than another Government attempt to cut even more money from disabled people, further driving us into poverty; therefore I ask all of you to please share with me Your examples of PIP, have you received an award, was it worth more/less than before etc.

If you would prefer to share this info anonymously that’s fine and if you want to do so privately, please contact me at ratea62@gmail.com

THANK YOU in advance for your input Jxx

 

Footnote* From truthmeister – ”

As for saving money, the bungling incompetence of IDS has meant that a proposed saving of £1.2bn pa has actually turned into an increase in spending of £1.6bn pa to date, as per the IFS: http://www.ifs.org.uk/publications/7447” Thanks

IMAGINE – All disabled and young people Voting?!

Imagine if  15 MILLION disabled people and young people all registered and voted in May 2015?!

That’s the aim of Two different campaigns, Operation Disabled Vote has set up a web page aiming to ensure as many of the 11 Million disabled people in the UK are registered, ready to participate in Election 2015. If you need more reasons to refister/vote visit  DISABILITY COUNTS

The TUC are working with Bite The Ballot to reach the 4 Million UK young people, eligible to vote next year but who are unregistered.

FIFTEEN Million people, all who have been discrimnated against by the current regime. ready and willing to participate in electing the next Government; what would the outcome be?

My guess, is Not another Tory/right wing Government?

I don’t know what the make up of a Parliament elected in disadvantaged people will look like, but it surely would be more democratic, fairer and willing to engage; particularly as MPs would know, we won’t tolerate more of the same.

If You are not registered or you know someone who isn’t Visit  Operation Disabled Vote / Bite the Ballot   DISABILITY COUNTS   or pass the message on today….

…Go On Imagine??

We’re DEAEP – Can WE Help YOU??

Disability Enabling & Empowerment Project, DEAEP, is a relatively new company run by disabled people and carers; we enable other disabled people to develop the confidence to regain control of their lives, supporting them through benefit claims and also training others to do the same.

Our Courses are aimed at disabled and chronically ill people, affording them the opportunities to expand their skill base and potentially improve their quality of life through enabling them to make positive steps towards Further Education and, or possible employment.

DEAEP has the capacity to offer not only, training and links to employment but we also aim to employ our successful trainees to act as peer supporters to others and potentially as other trainers.

DEAEP are currently running a Level 3 Peer Support in Action course which consists of 5 core modules aimed at anyone who wishes to train to help others. We also develop bespoke courses for other professionals engaged in working with disabled people and other disadvantaged groups

All the above is available in further detail on our website

DEAEP also run a professional representation service supporting people to complete benefit application forms, PIP/ESA, appeals etc; we will also attend assessments/ formal appointments with disabled or other disadvantaged people who find themselves needing support. DEAEP can support individuals from the start to completions of benefit claims.

If you or your company require any help whether it training or representation please contact us via our website.

DEAEP has the advantage of being the only company that aims solely to empower the disabled community and employs people with personal experience of the difficulties that disabled people face every day.

The Scandal of DWP Silence

We know from  the official DWP report that between January & November 2011 10,600 disabled people either in receipt of or awaiting benefits died.

Since then the DWP have, despite numerous requests refused to release further updates; we can only speculate their reason why, as we can only surmise just how many more disabled people have since lost their lives?

It is well documented how the ‘Scrounger‘ rhetoric have adversely affected disabled people  and those who are chronically ill, and even Esther McVey – Minister of State for DWP stated she “would not disagree” when it was put to her in October 2013 that “ hundreds or even thousands of people who had died sooner than they should have done, or had a much lower quality of life over their last few weeks or months because of their experience of the WCA.”.

From this we believe it is safe to presume there has been an increase in the number of annual deaths of disabled people in 2012 & 2013; given the loss of life in 2011 was 10,600, even a 2% increase per annum would result in  12,720 in 2012 and a startling 15,264 in 2013. That would give a overall figure of 38,564 deaths over the 3 years the Coalition has been in Government.

Is this shocking statistic what the DWP don’t want us to know?

Time to Come Together?

I’m sure the majority of you are full aware of my personal Politics by now and browsing through the numerous campaigns I follow/am a member of, all without exception, are against one or more of the Policies/Reforms introduced into Law by this unelected Government; this is almost the same with my Twitter connections, blogging follows and followers & my Facebook Friends.

I follow a range of topics – Welfare, NHS, Freedom of speech, thought and action, Education, Justice, etc; and I have no idea of just how many people I’m ‘linked to’ via all these sites but it must be Thousands. Given this I couldn’t help think and do something I usually avoid – I assume many, if not most of you are in a similar place via your social media contacts; this probably means that between us all there are Millions of people campaigning on similar issues.

Any of you who comment here will know my regular way of ending my replies is – In Unity; and I am convinced if everyone of us came together under one umbrella we would be in a real position to make positive change;  not only getting rid of this Government, but replacing it with one brave enough to Act as we, the people want and need. Just for a moment, imagine the power we would have together – if every group fighting against this Government Policies and Acts worked together; that includes the millions of unemployed people, disabled people, redundant/retired ex Forces, Refugees & Asylum seekers, Older people, those against the dismantling of the NHS, those against the destruction of our Education System, people fighting for freedom of speech/Human Rights – I could go on.

I’m not suggesting the individual groups and campaigns should cease, the’re too important, but that their memberships should come together and recognise and accept the similarities – We are ALL estranged for Government and ALL striving for the same aim ultimately, a JUST & FAIR Society; ran by a democratic Government that was fully aware, we the people are scrutinising them.

This is my Dream, can WE make it a Reality?

We are all better as a group united
Then as separate groups who are divided
We’re more powerful in unity than alone
As we have combined power of all our souls

Chris Wayne – http://chriswaynepoetry.wordpress.com/2013/12/21/the-core-of-the-uk/

Attending ATOS? WE Can Help:

Disability Enabling and Empowerment Project (Leic’s) (DEAEP) was set up in 2013 in response to identified needs; disabled, chronically sick and vulnerable people are increasingly required to demonstrate their need for the financially support necessary to survive, both often in employment, as well as not.

DEAEP is a social not for profit business that offers accredited training to  sick and disabled people, unemployed, and other vulnerable individuals. The training experience enables participants to, knowledgeably and confidently, actively support others during times of extreme stress; this could be attending ATOS assessments and, or to participate in social and community engagement.

So far we have a 100% success rate with people we’ve represented

The rationale behind DEAEP:

Anyone who’s disabled or chronically ill in the UK 2013, is only to well aware of the devastating effects of The Welfare Reform Bill, whether it be someone on Incapacity Benefit (IB) waiting for the dreaded assessment onto Employment Support Allowance (ESA); a new claimant for ESA after losing their job, or a current ESA recipient  who’s almost at the one year cut off time. It might be a Disability Living Allowance (DLA) recipient waiting for the claim form to apply for the new  Personal Independence Payment (PiP)

These are just some of the ways that Welfare Reform is affecting those of us too ill to work or live with the ever increasing costs of being disabled.

What these changes all have in common is the growing number of ‘assessments’ we’re all forced to undergo.

Many of us who have already experienced the cold, inhumane and in some cases, downright dangerous process of being assessed by ATOS,  know the associated costs these visits have on our health; from waiting for that now dreaded brown envelope, the energy it takes to complete the overly long complex claim form, the stress caused by actual ‘assessment’, through to the wait for the decision made at the DWP by a low level civil servant who might have had two days training in disability!

None of this is news to many of us, and many more disabled and sick people will soon be au-fait with this ever rotating process.

Many people on social networks like Facebook & Twitter have expressed the view that when  having someone to help them through this experience,  be it form filling, support at ‘assessments’ or at appeal it has helped them; and it is this what we at DEAEP aims to do.

We  offer free accredited training for people to skill them up, to then act as peer supporters for others going through this process.

We also can help with support at hospital/GP visits or in fact anywhere sick and disabled people feel having someone at their side to prompt them tell their story and get the truth across.

The training programme will also help participants in other areas, and can open doors to further education or even employment.

So if you are interested or require our help please contact us athttp://www.deaepleicester.moonfruit.com.

All personal and medical data disclosed is destroyed on conclusion of case

 

A Call for Impact Assessment on Disabled people to be debated by Parliament

It seems that every day there’s a new call to action, another petition to sign, a blog to RT, and so on; & I’m sure I’m not alone in having to make conscious decisions, often at an hourly rate about which new campaign to endorse.

Well for this one I’m making NO excuses, on Wednesday 10 July Labour is using Opposition Day to “debate the changes they have made that affect disabled people, and at about 16:00 we will force a vote to demand a Cumulative Impact Assessment by October  2013 at the latest

YES, at last the tireless work of Pat’s Petition, WOW, Spartacus and many many others has finally been recognised, but…this alone is not enough!

Between now & then we can all help make sure this debate is not lost; so please everyone

  • Write to your MP and ask them to back the motion
  • Write to your local paper and explain why we urgently need a cumulative impact assessment
  • Tweet your support using #MakeRightsReality

& do everything we can to make sure this vital motion is carried -“That this House believes that the Government should publish a cumulative impact assessment of the changes made by this Government that affect disabled people (to be published by October 2013).”

Dear Esther Mcvey – We’d like a reply please

Dear Esther McVey

We are very disappointed to find ourselves having to write once again to you after sending you our Open Letter on the 9th of May 2013, which was signed by over 800 disabled people, family and friends.

We find it astonishing that over a month later we have yet to receive an acknowledgement of receipt of the open letter let alone a reply. Are the opinions of over 800 disabled people, so unvalued by the minister for disabled peopled, that you think it is acceptable to fail to even acknowledge receipt of a letter from them?

You continue to use statistics that have been widely condemned by fellow Mps, Unions and even the Clergy. Once again we ask that you refrain from twisting the statistics about DLA and make some effort to re build confidence in both your department, and government statistics that have become devalued by your department consistent misuse.

When our ministers cannot be trusted to tell the truth about benefits that affect so many vulnerable people and the public at large can no longer trust the statistics that drive reforms, it becomes vital that ministers do everything in their power to rebuild the trust of the public.

If they fail to do so, it becomes incumbent on the systems set in place, to ensure that ministers adhere to the rules placed upon them. And we will endeavour to ensure that process takes place.

Thank You Once Again for Your Time

Jayne Linney and Debbie Sayers

Dear Esther McVey, your ‘facts’ aren’t True! UPDATE

Dear Esther McVey MP

We the undersigned have been shocked and appalled at you and your Minister’s persistent use of dubious facts and statistics regarding DLA. We ask that you make use of  the raft of factual statistics and desist from twisting evidence; your misrepresentation presumes some sort of illegal activity regarding DLA claimants, this is particularly disturbing when the DWP’s own figures for fraud of DLA is 0.5%.

Jonathan Portes, director of the National Institute of Economic and Social Research and a former chief economist at the DWP, said ‘it was part of a “consistent pattern” which threatened to undermine public confidence in official statistics…”I think it is very unfortunate. These statistics are very important. Government analysts, economists and statisticians work very hard to produce them and they provide important information to the public,”…”It is very important that ministers should not seek to misrepresent what those stats actually do or don’t show. That detracts from the public’s faith in the analysis produced by government statisticians. “This is, I am afraid, a consistent pattern of trying to draw out of the statistics things which they simply don’t show.”’

No evidence for Iain Duncan Smith benefit cap claim, says research chief 13.04.13

Your persistence that DLA requires few face-to-face medicals and little or no additional medical evidence to obtain DLA, is untrue. The government’s own figures show that just 16% of awards relied on the form only and a mere 9% of DLA funding was spent on this basis

Your claims that  DLA is awarded without a medical;  is simply not true, many claimants have to undergo a face to face medical assessment, as part of their application as the DWP website shows: Medical assessments You might get a letter saying you need to attend an assessment to check your eligibility. Further the DWP statistics report of November 2011 also clearly demonstrates Medical Examinations did form part of the assessment process for claims. http://statistics.dwp.gov.uk/asd/asd1/adhoc_analysis/2011/dla_evidence_award_values_nov11.pdf Table 2:

Savi Hensman’s blog in Ekklesia also disproves your claims –  Government minister Esther McVey’s untrue claims about Disability Living Allowance

‘Disability Living Allowance is an “outdated benefit” for which “around 50 per cent of decisions are made on the basis of the claim form alone – without any additional corroborating medical evidence,” stated UK minister for disabled people Esther McVey on the BBC and elsewhere this morning (8 April 2013).

This is completely untrue – the government’s own figures show that just 16 per cent of awards relied on the form only and a mere nine per cent of DLA funding was spent on this basis. McVey was trying to justify the controversial replacement of DLA by Personal Independence Payment (PIP) from today, to be paid to fewer people.’

Savitri Hensman Ekklesia

The latest figure you used in you BBC interview that of 50% of claimants not presenting any additional medical evidence, may in fact be due to medical evidence being sought directly, via the consent form on page 7 of the DLA form, which gives the DWP permission to contact the claimants GP and other medical professionals directly for further information.

You also state that 71% would “stay on it for life” without further assessments, but there have been no lifetime awards for sometime now, therefore your statement made on the BBC on the 8th of April 2013 is misleading. The new term ‘Indefinite Award’ requires claimants to undergo reassessment at any time at the whim of the DWP is it therefore the fault of the claimant if the DWP fail to exercise that right?  However, they announced a few months ago that they would not be testing those with indefinite claims at all until after the next election. Indefinite awards make up nearly 70% of all DLA awards and the government claim over and over that it is this group who have been “left to languish” yet they’ve decided to do nothing about it at all.

‘She also referred to the claim that, under DLA, 71 per cent of people get support for life without checks. This, again, is misleading. The figure refers to ‘indefinite’ awards, which means that their period may vary according to needs. Recall is possible if circumstances change. This is appropriate. There are many people who have permanent and unalterable disabilities. Moreover, while benefit may be awarded for a non-fixed period, that does not mean it is necessarily ‘for life’. The total number who still get DLA excludes those who have had it on fixed awards and now no longer get it.’

Savitri Hensman Ekklesia

In the press you have continued to indicate the reason for the change from DLA to PIP is the rapidly accelerating growth of DLA claimants up by some 35% in the last ten years, from 1.1million to 3.3million, a figure we do not contest. However we would like to examine the context of the 35%; the reform of DLA is only affecting working age claimants, with children and Pensioners being exempt from the changes (for now). Given this, when analysis of the increase in claimants in undertaken discounting those exempt,  you get a significantly different figure of 13%. Why then are you insistent on using the wholly inaccurate 35% figure if not only to make your claim seem more urgent?

Sue Marsh co author of the Responsible Reform Report states:“…the government have constantly misled the public over the new benefit, claiming a 35% rise when Spartacus Report showed clearly that the rise is only 13% for the working age group who will be affected. Physical conditions have remained totally stable, whilst the 13% rise is almost all due to a rise in mental health conditions and learning disabilities, a trend seen worldwide, not just in the UK.”

Sue Marsh Diary of a Benefits Scrounger.

Or if you prefer Disability News Service

 “DWP released a “statistical update”, which it said showed the number of successful claimants of DLA had risen by 15,000 between February and May 2012.

But analysis of DWP figures by Disability News Service (DNS) has shown that the rise in claimants is due to increases in the number of children and older people receiving DLA, while the number of claimants aged 16-64 actually fell by more than 1,600. This is important because the reforms and cuts will only affect working-age claimants…”

Disability News Service

Alternatively

“To quote the DWP 2013 report Fulfilling Potential: Building a deeper understanding of disability in the UK today, “There are 11.5 million people in the UK who are covered by the disability provisions set out in the Equality Act… six per cent (0.8 million) of children, 15 per cent (5.4 million) of adults of working age and nearly half (45 per cent, 5.3 million) of adults over State Pension age are covered… Only around half (six million) of the 11.5 million people covered by the disability provision in the Equality Act are in receipt of disability-related benefits.”

Savitri Hensman Ekklesia

Finally

Anne McGuire, Labour’s shadow minister for disabled people, said it was “yet another example of the DWP manipulating the figures on DLA to suit their agenda of abolishing DLA”.

This brings us to another disturbing trend of recent weeks, statements being made by yourself and MR ID Smith MP which strongly suggest people are rushing to claim DLA in order to avoid the new harsher PIP assessment criteria…

“We’ve seen a rise in the run-up to PIP. And you know why? They know PIP has a health check. They want to get in early, get ahead of it. It’s a case of ‘get your claim in early’.”

IDS 8/4/13

Hufffington Post

And you yourself have similarly claimed…

The Mail on Sunday this week reported that McVey believed coalition plans to abolish working-age DLA had led to a huge increase in applications by people desperate to claim the benefit before it was replaced by the new personal independence payment (PIP), which will come with a tougher assessment.

The Mail on Sunday article – based on an interview with McVey – stated: “The decision to introduce new tests has produced an extraordinary ‘closing-down sale’ effect, with rocketing claims as people rush to get their hands on unchecked ‘welfare for life’ before McVey’s axe falls on April 8.”

A spokeswoman for McVey told Disability News Service (DNS) that, although she did not use the phrases “closing-down sale” or “welfare for life”, “everything in the article was a fair representation” of the interview.”

John Pring DNS

We have a number of  issues with these statements not least of which, the inescapable fact that no one can escape the changeover to PIP; every single DLA claimant, whether they have been on it for years or for five days will have to reapply for PIP in the next few years, therefore no one will be able to ‘get ahead’ of it and any ‘last minute’ claim for DLA would simply delay the inevitable. Ergo the suggestions in your statements that recent claims are an attempt to escape PIP appear convoluted . Our assertion is further supported by , Declan Gaffney Tue, 04/09/2013 in his article Did claims for DLA increase in the run-up to PIP? analysed statistics produced at https://www.nomisweb.co.uk/ which appear to refute these statements.

He States: “I presume Mr Duncan Smith has some basis for this claim, but it’s not supported by the published data on DLA. The changes only affect people of working age, so I’ve charted the number of claims by people age 16-64 with a duration of three months or less, using the data available on Nomis. A sudden increase in people claiming should show up in these figures: I don’t see it. On the contrary, the latest figures are the lowest on record.”

Given our concerns outlined above we request that you officially retract your recent comments with regard to DLA and PIP and issue a fairer balanced statement, based upon accurate data and one which maintains the integrity of Ministers in Government. We request you include the facts  that PIP only applies to working age DLA claimants; that there has been only an average increase in overall working age claimants, and there has been no significant rush to apply for DLA .

If you agree with the above and want to add you name to the latter please follow the link below and SIGN https://docs.google.com/document/d/1n2QVXOKKSfkn9dwXOvmQ74Vzbhyx7HXEbid8EpEb674/edit?usp=sharing

This letter will close for signatures at midnight 21/04/13

Co Author – Debbie Sayers  – Ramblings of a Fibro Fogged Mind ramblingsofafibrofoggedmind.wordpress.com