Archive for the ‘Uncategorized’ Category

Crippen hears that charities have called on Government to prioritise those who are more vulnerable to the virus

Three ‘disability’ charities have called on the Government to ensure that disabled people, including those with learning difficulties and autism, as well as their families and support workers, receive prioritisation for the new COVID-19 vaccination.

The call from Mencap, Sense and the National Autistic Society, is in response to interim advice from the Joint Committee on Vaccination and Immunisation (JCVI), which the Government are using to steer their approach to vaccination. The advice is heavily biased towards older people aged 65 or over, and they feel does not give sufficient prioritisation to disabled people.

Last week, Public Health revealed that COVID-19 deaths for people with a learning disability in England are six times the average.  The review found that those aged 18-34 with a learning disability were 30 times more likely to die with the virus than their counterparts in the general population.

According to the Office for National Statistics published in September, 59% of all deaths involving COVID-19 from March 2 to July 14 were of disabled people.

Richard Kramer, Chief Executive of Sense, said: “The needs of disabled people have been consistently forgotten by Government and this can’t continue as we look to find a way out of the pandemic.”

This was echoed by Edel Harris, Chief Executive of Mencap, who said:

“People with a learning disability have experienced shocking discrimination during the pandemic. They have been subjected to blanket ‘Do Not Resuscitate’ notices, refused admittance to hospital and left in lockdown long after everyone else.”  

And Caroline Stevens, Chief Executive of the National Autistic Society, stated: “Our research shows the pandemic has left people with Autism and their families stranded.”

Description of cartoon for those using screen reading software

Two figures in lab coats and wearing PPE are stood in the Covid 19 Research Laboratory. Behind them are three disabled people, two with Downs Syndrome and another with Autism Rules on his top. One of the Lab technicians has just noticed them and is saying: “You know you said that we needed some guinea pigs!”

Crippen and the surgeon who hops to it after losing his own legs

Having worked so hard at challenging the ‘tragic but brave’ stereotype of disability, it still persists, although this time with a rather ironic twist.

A surgeon who carried out hundreds of amputations before losing both of his own legs has accepted an award for being one of the bravest people in Britain at the Amplifon Awards for Brave Britons 2020. Although he has redeemed himself by launching a one-man mission to improve after-care for fellow amputees in the South West of England.

Dr Neil Hopper, a vascular surgeon from Cornwall who lost both his legs after developing sepsis after a camping trip with his children last April, has returned to work at the Royal Cornwall Hospital at Treliske in Truro with a mission.

Dr Hopper who has performed hundreds of amputations, spoke to Cornwall Live about his bid to improve post-hospital support and care for fellow amputee patients after his own experience. Specifically, he’s fighting for better care for amputee patients after they leave hospital.

He said: “…if they were cancer patients, the lack of support would be seen as a national disgrace!”

Dr Hopper added:

“The thing that made me worry was that I was getting the red carpet treatment. People were bending over backwards for me, a colleague, so I started imagining what it would be like for other patients.”

He added: “The thing I think we can easily change is that eight weeks between leaving hospital and getting legs. That’s the black hole nobody really thinks about. It’s fair to say we’ve spent decades improving amputee care in hospital. We’ve got that bit right now, but it’s that next bit that doesn’t seem to be as good.”

Changes have already been made thanks to Dr Hopper’s determination and you can read about these in the full Cornwall Live article.

Description of cartoon for those using screen reading software

Dr Hopper, wearing a rabbit costume, is seen ‘hopping’ down a hospital corridor on prosthetic blades. A voice from a speaker on the wall is saying: “Dr Neil Hopper please report to Theatre C please”

Crippen looks back 25 years to his cartoons of that era

As you’ll have seen, there’s been a lot of talk about it being 25 years since the launch of the Disability Discrimination Act 1995. I was even persuaded by our over-worked Editor Colin to throw in my own two-penny worth (that’s old money to you youngsters out there!) with an article about the event.

The impact it’s had on me, however, has been to have a quite a few requests from various people to use the cartoons that I created at the time. Unfortunately, these ‘toons were drawn back in the dark ages when black and white imagery was the norm, with an equally low resolution mainly for the printed page. These were created at the time for such publications as Disability Arts In London (DAIL) magazine and the newsletter of the Trades Union Disability Alliance (TUDA News). I now create in colour with a much higher resolution more suited to t’ tinternet.

A couple of the organisations that requested permission to use the cartoons, like the BBC, have in fact, gone ahead and used them despite the poor quality. This has left me with mixed feelings, as these old images don’t really represent the Crippen that has evolved, if you see what I mean.

The two cartoons that have been requested the most have been the one with two vicious looking dogs, representing employers and service providers confronting a little puppy identified as disabled people. As you’ll see, I’ve recreated that one for the DDA article I mentioned earlier. The other one was a cartoon of a young female wheelchair user encased in a box with just her head showing out of the top. She’s saying to a companion: “When I realised that they treated the mail with more respect, I decided to travel as a parcel!”

So, here’s that one, recreated for this blog posting, but this time in glorious colour. And who knows, maybe in another 25 years, this image will be considered outdated?

Keep safe.

Description of cartoon for those using screen reading software

A young female wheelchair user is traveling inside of an old style train’s guard’s van. She is encased in a large box with just her head showing out of the top. She is saying to a companion: “When I realised that they treated the mail with more respect, I decided to travel as a parcel!”

Crippen revisits the subject of disability hate crime

This is the second year running that the National Police Chief’s Council (NPCC) has refused to provide any explanation for why police forces are passing significantly fewer cases of disability hate crime to the Crown Prosecution Service (CPS).

The number of disability hate crime cases referred to prosecutors by police forces has now fallen for the fifth year in a row, and it is now only about a third of the level it was in 2014-15 (924 cases).

The Home Office has also refused to offer any explanation for the fall, or to say if it was due to a fall in police numbers, or even if it was concerned about the issue.

This week, an NPCC spokesperson refused to answer questions put to them by the Disability News Service (DNS) about the figures, other than cutting and pasting answers his office had produced in response to completely different hate crime figures obtained by a charity earlier this month (Ed: figures!).

Disabled members of the Disability Hate Crime Network this week expressed alarm at the police failings.

Sue Groves, chair of Medway Independent Police Advisory Group and an independent critical incident advisor to Kent Police, said the drop in police referrals to CPS was “very worrying and will only serve to increase the concerns victims of disability hate crime have around reporting incidents to the police that they will receive an appropriate response”.

Sue was herself a victim of a disability hate crime, in London, and the four-week delay before it was investigated as a hate crime – after originally being told by the Metropolitan police that it was “just an on-street altercation” – meant any CCTV evidence was no longer available and the investigation failed to progress.

She said: “I have been able to use this experience to feed into improvements within Kent Police, but others are not so fortunate, and thus there is a desperate need for a concerted national push to ensure all disability hate crime reports are correctly flagged from the outset …”

Another disabled network member, David Gillon, said he was particularly concerned by reports that some officers were removing the “tags” or markers that show that offenses should be treated as disability hate crimes, which he said not only affects those cases but also “potentially distorts the statistics about how common this is, and the margin of police failure”.

You can read the full report in Disability News Service.

Description of cartoon for those using screen reading software

A white shaven headed thug in a bright red tracksuit is grabbing the shirt of a young black guy and is lifting him off of his feet. The young guy is holding a clipboard with survey written upon it and a broken crutch lies at his feet. He’s saying to the thug: “Final question Sir – do you hate me because I’m Black, disabled or Gay?!”

Crippen hears about people with Autism experiencing undignified and inhuman care

Once again, it has fallen to the Disability News Service (DNS) to expose how disabled people are still being treated throughout mental health units in England.

You’d be forgiven for thinking that we still lived in the middle ages when you read the Care Quality Commission’s (CQC) report into the use of restraint, seclusion and segregation for autistic people and people with learning difficulties and mental health conditions in mental health units in England.

People with Autism have told the care regulator about the “undignified and inhumane” care they have been subjected to in mental health units, including the frequent and traumatising use of segregation and restraint in England.

In the report, Out of Sight – Who Cares?, CQC says it found “too many examples of undignified and inhumane care, in hospital and care settings where people were seen not as individuals but as a condition or a collection of negative behaviours”.

The response to this was often to “restrain, seclude or segregate them”.

DNS tell us that the review calls for “fundamental change in the way care is planned, funded, delivered and monitored”, so it is “underpinned by a firm foundation of human rights”, and restraint, seclusion and segregation “are no longer accepted …”.

Many of those subject to restraint described to CQC its “lasting and traumatising effects”, with one saying about being restrained:

“It makes me feel …dehumanised. I don’t feel like a real human being.”

One patient with autism identified as Alex described how she sought help from mental health services because of a lack of appropriate community care. During an initial 72-hour admission to hospital, she experienced a “catastrophic clash” between her autism and the lighting, noise and chaos of the “box” she was kept in, and quickly became “overloaded”.

In the following months, she was restrained 97 times and secluded 17 times, was forcibly drugged, and her body was left “battered and bruised”, and her identity “fractured”.

She told the review: “They didn’t like the autistic part of me. I tried to tell them that autism is all of me, it’s who I am.

After three-and-a-half years, she was eventually able to flee to Africa where she created a new routine and set up an autism-friendly home, weaned herself off the drugs she was taking, received private treatment from a psychologist, and, after six weeks, started to work as a teacher again.

The key to success, she told the review, “is creating the right environment and treating psychological differences with dignity and respect”.

You can read more about this disturbing report in the Disability News Service article online.

Description of cartoon for those using screen reading software

A young white male is strapped to a reclining chair whilst a white, bald thug in a quasi-uniform is shining a strong light in his face. The thug is holding a hypodermic in his other hand and at his feet is a large box with a skull and cross bones and the words drugs printed on it. On the wall, in the shadows is a sign that says Mental Health Unit. The thug is saying: “We have ways of curing you!”

Crippen hears of funding that will be used to build evidence of DPO crisis

New research will seek crucial evidence of the “serious crisis” facing Disabled People’s Organisations (DPOs) across England.

Inclusion London told the Disability News Service (DNS) that they have secured £80,000 from the National Lottery Community Fund to research the state of England’s “chronically under-resourced, fragmented and precarious” DPO sector.

It will produce proposals for long-term improvements to the regional and national DPO infrastructure and build a “clear picture” of the support the DPO sector needs. The research will also be used as the basis for future funding applications.

The new funding follows calls by DPOs during April’s national conference of the Reclaiming Our Futures Alliance – of which Inclusion London is a member – for more to be done to ensure the voices of disabled people and their user-led organisations are heard at both regional and national levels.

Inclusion London told DNS that about a quarter of DPOs have closed since 2015, while many others are “hanging on by a thread”.

It says that life for disabled people “is getting worse not better”, with “exclusion and discrimination coupled with rising poverty and inequality as a result of austerity, welfare reform and cuts to public services”.

The lack of resources means DPOs cannot carry out vital projects, such as outreach work with disabled people in institutions, developing the skills of its members, and tackling the “systematic exclusion” disabled people face.

Inclusion London warns that it is still “culturally acceptable, indeed the norm, to have non-disabled people representing us with funding disproportionally going to the large disability charities that are not run or controlled by disabled people and do not represent or even amplify our voice”.

To understand just how dire the situation is then please click here to read the full DNS article.

Description of cartoon for those using screen reading software

A white male and a white woman both smartly dressed in business suits are receiving a large sack of cash from Boris Johnson who represents the government. They carry a sign that identifies them as ‘groups for the disabled’. Behind Boris and trying to attract his attention, are two disabled people; a young white woman using a wheelchair and an Asian man who is wearing dark glasses and carries a white stick. They are both looking angry. They are identified by a sign that reads ‘groups of disabled people’. The male charity worker is saying to Boris: “Groups FOR and groups OF – it’s just a matter of semantics don’t you think?!”

Crippen pays tribute to the irreplaceable Sian Vasey

Disabled activists have paid tribute this week to Sian Vasey – a much-loved, “multi-layered activist” who played a “pivotal role” in the disabled people’s movement for more than 40 years – who died last week.

A stream of messages on social media mentioned her contributions as a disabled activist, a pioneering member of the disability arts movement, a BBC producer, a writer, a campaigner on issues such as accessible transport and independent living, and as a Labour party and union activist.

Writing in the Disability News Service (DNS) John Pring comments that many mentioned her wit, her contribution as a role model for other disabled people, and the part she had played in protests as an activist with the Disabled People’s Direct Action Network (DAN) and Not Dead Yet UK (NDY UK).

Mandy Colleran described Sian as “the warrior queen of the disability movement”, and “a role model, a thinker, a leader, an activist, a writer, and a great friend”, and said she was “irreplaceable”.

The DNS article goes on to mention that Sian’s activism with NDY UK often intertwined with her campaigning on independent living.

In November 2014, as NDY UK prepared for its latest protest outside the House of Lords to demonstrate opposition to a bill that sought to legalise assisted suicide, Sian said: “Many of us need support with our daily routine, washing, dressing, continence and going to the loo but this in no way affects our well-being, or diminishes our dignity. We get the help we need, but we have had to fight hard to get it. It is a tragic fact that this is a primary cause of such people wanting to end their lives prematurely.”

Sian was also a member of the pioneering Union of the Physically Impaired Against Segregation (UPIAS) in the 1970s, and played a key role in setting up another pioneering disabled people’s organisation, London Disability Arts Forum. She was later director of Ealing Centre for Independent Living (ECIL) and was awarded an OBE in 2009 for services to disabled people.

Description of cartoon for those using screen reading software

A caricature of Sian sat in her wheelchair with a cheerful smile on her face. She is wearing a dark pink top with blue tights and has a silver bracelet on her right wrist.

Crippen looks for the scheme that was designed to amplify the voices of disabled people

Do you remember two years ago when the government announced that they’d be setting up nine regional networks to “amplify” the voices of disabled people? Well, two years later and five of them haven’t even held a single meeting!

According to Justin Tomlinson, the so-called minister for disabled people, the aim of the networks was to bring the views of disabled people and local disabled organisations across England closer to government.

It actually took them over a year to name the new chairs of the nine networks, and it is only six months since the government’s new Disability Unit announced that the networks had finally started work across England. Although it’s boss, Justin Tomlinson appeared to have misled MPs on the women and equalities committee about the success of the networks.

He told them the networks were allowing “all voices, particularly of all sizes of disability organisations” to “share their real lived experience and help us improve our policies, our communications”, and that he found it “a very, very rewarding part of my role”.

At that point, only two of the nine networks – those in the north-west and in Yorkshire and Humber – had held any meetings!

Two of the four networks that have met – those for London and the north-east – only had their first meetings towards the end of last month, according to a freedom of information (FOI) response to Disability News Service (DNS).

The Disability Unit has also been forced to admit in the FOI response that it has not even seen the minutes of the few network meetings that have taken place.

You can read more about this in the Disability News Service article written by our colleague John Pring.

Description of cartoon for those using screen reading software

An empty table and chair are located beneath a sign that reads ‘disability regional network’. The sign is hanging crookedly from the wall by one screw. A giant spider’s web covers everything with a large black spider sat up in the corner of the room. The whole scene looks abandoned and forgotten.

Crippen discovers that the new Secretary of State for Work and Pensions is planning to … er?!

As most of us are aware, face-to-face assessments for Personal Independence Payment (PIP) and other healthcare benefits have been suspended since March and the onset of the Covid 19 pandemic.

In its place telephone and paper-based assessments have been used to determine how much support a claimant needs which in turn, influences the award, if any, somebody receives.

Taking questions from the Work and Pensions Committee on how the DWP will continue to respond to coronavirus over the coming months – including PIP assessments, Thérèse Coffey, Secretary of State for Work and Pensions was asked how the telephone and paper-based assessment process was working and if they were considering changing to video conferencing any time soon?

Ms Coffey responded somewhat vaguely: “In terms of going forward, we’re still working on some plans in that regard and I’m not at the stage yet where we can share exactly what it is we’re going to be doing …”

Neil Coyle, Labour MP for Bermondsey and Old Southwark then asked what the DWP was going to do in the long-term about “tackling the complexity of the assessment process and other barriers that seem to prevent disabled people from accessing support.”

Once again Ms Coffey was unable to give a clear answer saying that it was part of a policy formulation that the DWP is still working on and hopes to publish … er, soon.

So, there we are, yet another Secretary of State for Work and Pensions unable to say what it is they are actually doing, or to give a clear answer to any questions raised … nothing new there then!

Description of cartoon for those using screen reading software

Theresa Coffey is standing in front of a row of seated officials in the office of the works and pensions committee. The committee members are all looking at her expectantly. She is saying: “Erm …”. Behind her is Dominic Cummings with pieces of paper around his feet which read ‘false facts’, ‘more false facts’ and ‘even more false facts’. He is whispering to her: “Stall them Theresa – I’ve just dropped all of the crib sheets!”.

Crippen despairs as new boss of DWP carries on their callous tradition

Whilst giving evidence to the Work and Pension Select Committee Dr Thérèse Coffey MP, the new boss of the Department for Works and Pensions (DWP) casually claimed that the department does not have a legal duty or statutory requirement to safeguard vulnerable benefit claimants.

Referring to a letter Dr Coffey had sent the Committee following her appearance before the committee on 22 July, Labour MP Debbie Abrahams, a former Shadow Work and Pensions Secretary asked: “I notice in the second page of this letter a backtracking on [your position in the evidence session on 22 July 2020] when you say the DWP does not have a duty of care or a statutory safeguarding duty. Given that you provide services to vulnerable people … should there be? And shouldn’t there also be a moral obligation under the government in recognition of the services they provide to vulnerable people?”

In her response, Coffey stated that she did not think it was the responsibility of the DWP to have that statutory duty. “We are not the local council, social services, the doctors and other people …” she added dismissively.

Not only does Coffey’s response show a lack of concern over the well-being of disabled claimants, it also means that their safety is not at the forefront of DWP policy and that any harm they cause to vulnerable people is not their responsibility!

It certainly explains their reluctance to engage with the issue of the deaths of disabled claimants due to draconian DWP policies and procedures.

Description of cartoon for those using screen reading software

Theresa Coffey and Iain Duncan-Smith (IDS) are sat at a table. A plaque on the table reads ‘Department of Works and Pensions’. In front of Coffey is a piece of paper with ‘DWP has no duty to safeguard clients’. Another piece of paper is in front of IDS and reads ‘DWP do not accept any responsibility for deaths of benefits claimants’. IDS is saying: “Good to see that Ms Coffey is continuing our proud tradition of not giving a toss!”