Jul 172014
 

DPAC have had an odd kind of non-relationship with DRUK. We’ve disagreed about many things. For example, DPAC is for saving ILF, DRUK’s Sue Bott suggests this is something we should probably forget about, and that ‘Whilst the ILF has benefited many disabled people, claims that it has been at the forefront of independent living are a little exaggerated’[1]. This is not the view of ILF users. See their stories, their lives, their experiences  It is amazing that anyone can believe that passing ILF to local authorities who already say that without ring-fenced funding many ILF users will lose support and/or be institutionalised is something we need to accept while we all get together to talk about ‘new visions’.

 

The DRUK conference dedicated to a ‘new vision’ for independent living is also a confusing affair, not only are they embracing Simon Steven’s approach[2] ( He who accused DPAC of murdering disabled people and was dropped from Leonard Cheshire’s sponsor program because of his outright abuse to other disabled people[3]), but one of their advertised partners for this conference are Craegmoor .

 

Craegmoor are part of the Priory Group owned by Avent International which is a US Equity Company- changing times you may say-and you’re right. Maybe that’s what these new visions are about: capitalising on the market, private equity companies taking public money, and disability organisations getting in on the act- maybe neo-liberalism rather than disabled peoples’ rights and equality now make up ‘new visions’ of independent living

 

Craegmoor ‘s target market are those labelled with autism, learning difficulties and mental health issues. They take 85% of their funds from public funds[4]. Craegmoor’s  web site boasts of its residential homes:

We provide understanding and support for people with learning disabilities, autism and mental health problems in a variety of settings based on the individual’s abilities and needs. Our nationwide residential care services support people to develop the skills they need to live as independently as possible’.

 

Wait, since when were residential homes part of independent living? Weren’t these the very oppressions that early activists fought to get out of, and current activists (and ILF users) are fighting to stay out of?

 

Their brochure[5] goes further:

Craegmoor is part of the Priory Group of Companies. From education to hospitals, care homes and secure facilities, the Priory Group of Companies offers individually tailored, multidisciplinary treatment programmes for those with complex educational needs or requiring acute, long-term and respite mental healthcare’.

 

Treatment programs? Not sounding very independent living or social model. As well as residential homes, secure ‘hospitals’ and segregated schools. It all sounds very daunting.

 

But there’s much more on the Priory group of companies too which is even less palatable concerning cover-ups and abuse. Until July 2013 Phillip Scott was Chief Executive if the name isnt familiar, he was also the Chief Executive for Southern Cross. Itself a subject of inquiry on institutional abuse and 19 unexplained deaths[6] Craegmor say they transform lives, but in what way?

 

In May 2013 there was Melling Acres, ‘where inspectors reported major concerns about the care and welfare of its seven residents – care plans were poor, with scant information about physical health needs, there were limited activities and a lack of advocacy to enable people to express concerns about their care’. In September 2012 ‘following an anonymous tip, inspectors found residents at risk of abuse in Lammas Lodge, a home for young adults. There were not enough staff and what staff there were, inspectors found, were not properly trained to meet residents’ complex needs. There were six major areas of concern, including care and welfare, medication and safeguarding. The home, which was warned it must improve or face closure, has since been given a clean bill of health by the regulators’. Both homes were registered under Parkcare Homes’ so neither Priory or Craegmoor got the fall-out despite ownership[7].

 

This was not the case in 2012 when concerned relatives hid CCTV cameras in the room of Highbank hospital in Bury Manchester to reveal abuse by staff[8], not so with the Bentley Court home in Wolverhampton suspended by the council for what it called ‘safeguarding issues’ in 2010, a council that stopped sending those with dementia to Bentley Court[9], and not so in 2012 when what was described as the ‘Priory mental hospital’ in Windes on Bennet Lane was closed due to not meeting 10 standards of Government quality and safety including: Patients not being fully protected from the risk of abuse and their privacy, dignity and independence not being respected, staff not receiving necessary training, a lack of systems to assess and monitor the quality of the service provided, care plans did not always cover patients’ needs. There were also reports of patients attempting to escape during supervised visits into Widnes town centre[10].

 

So as said definitely NOT independent living.

 

In 2004 the then CEO of the Priory group Chai Patel said ‘My view is, if there is ever a conflict that involves choosing between care and profit, then we should not be involved in that environment,’[11] Given the examples above it seems profit is the defining factor.

 

It didn’t take long to find this information, it didn’t take long to realise that these are not the partners who should be with any organisation claiming to support independent living, even ‘new visions’. So maybe the question that needs to be asked is what exactly do DRUK support?

 

There are a few clues, in a recent blog piece by DRUK (dated 16th July) mentioning a very good Guardian piece by independent living activist John Evans[12], an ILF user, the last paragraph says: ‘Sue Bott, Director of Policy and Development at Disability Rights UK, has written a new blog which also discusses the role of the ILF but proposes that disabled people should concentrate their campaigning towards achieving a single integrated system that assesses people’s needs and allocates assistance and support based on the outcomes people could achieve in their communities and contribute to society’.

 

John Evans says everything we need to know-we have a vision for independent living and we already have a model forged by international independent living activists. There is nothing wrong with that model. There is no reason to stop fighting for it, abandon it or develop ‘visions’ or hallucinations of lesser systems in which we divide disabled people by perceived contributions to society-all disabled people are of value, all deserve to be supported. It is the ILF model that needs to be built upon and expanded to all-something that promotes real independent living.

 

The fact that a so-called user led organisation is putting forward anything different with the spectra of institutionalisation added to the mix is a tragic condemnation of all that disability activists have ever worked and fought for. We are appalled that DRUK are willing to sacrifice disabled people’s futures in this way and sadly can only assume this is to ensure on-going funding from the government.

follow @dis_ppl_protest for more

If you want to email DRUK you can do so by emailing:  liz.sayce@disabilityrightsuk.org

 

[1] http://disabilityrightsuk.blogspot.co.uk/2014/07/we-need-new-vision-for-independent.html

[2] http://disabilityrightsuk.blogspot.co.uk/2014/07/we-need-new-vision-for-independent.html

 

[3] http://davidg-flatout.blogspot.co.uk/2014/07/inclusion-forgotten-ambition-lost-i.html?spref=tw

[4] http://www.craegmoor.co.uk/library/files/Craegmoor%20Locations%20&%20Services%20Brochure(1).pdf

[5] http://www.craegmoor.co.uk/library/files/Craegmoor%20Locations%20&%20Services%20Brochure(1).pdf

[6] http://www.bbc.co.uk/news/uk-24581693

[7] http://beastrabban.wordpress.com/2013/07/20/private-eye-on-failure-of-care-at-more-care-hospitals-owned-by-american-private-equity-firms/

 

[8] http://www.dailymail.co.uk/news/article-2227229/Nurses-quizzed-police-abusing-patient-Priory-Hospital-concerned-family-hid-secret-camera-room.html

 

[9] http://www.expressandstar.com/news/2010/01/15/elderly-will-no-longer-be-sent-to-care-home/

 

[10] http://www.runcornandwidnesweeklynews.co.uk/news/health/failed-priory-mental-hospital-widnes-5875608

 

[11] http://www.managementtoday.co.uk/news/432103/Man-Priory/?DCMP=ILC-SEARCH

 

[12] http://www.theguardian.com/society/2014/jul/16/independent-living-fund-closure-disabled-people-residential-care

Jul 032014
 

 Hello comrades 

ALLFIE  (the Alliance for Inclusive Education) would like to put together some short and snappy videos on disabled peoples experiences of having Disabled Students Allowance and the impact it has had in helping them benefit from higher education on our lovely website – 

In particular we would like to focus on inclusion and participation whilst recognising that for some disabled students having the DSA means the potential of getting higher grades or getting a qualification whilst studying at university.  Also it be great to hear how DSA has supported disabled students who benefited from higher education even if they have not ‘passed’ their course.  

We would like to interview disabled people (young and old!) who  are thinking twice about going to university as a result of Government’s DSA reforms.

If anyone wants to know more about the DSA reforms please follow the link – http://www.allfie.org.uk/   Please scroll down to ALLIFE’s june briefing. 

If you are going to be around for the ILF tea party on Friday  – please let me know as I will have a small video camera to do the interview with.    I will be wearing an ALLFIE teashirt.     If you want to have a chat please ring me on 0207 737 6030 during Tuesday and Thursday.

 See u there, Simone Aspis.

Jun 192014
 

The ILF has transformed People’s lives.  The Independent Living Fund does what it says on the tin – it liberates people who wouldn’t otherwise be able to, to live independently.  It lets them make choices about how they live – things we often take for granted: when to get up or go to bed, what and when to eat.  It allows them to work, to be active in the community and to live in their own homes.

 

I challenge the Minister today to guarantee that those currently in receipt of ILF won’t become less independent as a result of his decision to close it in June 2015. Because that’s what people fear.  That’s what they are frightened of.  They fear losing their jobs, losing those staff they employ to support them and losing their independence.  They fear being forced out of their homes and into institutions.

 

The Minister may say he’s passing the monies and responsibility to Local Authorities but this will not ease their fear.  And he is rather naïve if he thinks that absolves him from his responsibilities for this decision.  I’m afraid he can’t get away with devolving responsibility and blame for the consequences of his decision to others.  That’s why I ask him for these guarantees today.  For a start Disabled People Against Cuts calculate the current annual cost of support at around £288 million yet the government only identified £262 million to transfer to local authorities.   And it gives no reassurances that this money will be ring fenced to be spent only on supporting disabled people to live independently rather than absorbed into broader council budgets.

 

According to SCOPE £2.68 billion has been cut from adult social care budgets in the last 3 years alone, equating to 20 per cent of net spending.  This is happening at a time when the numbers of working-age disabled people needing care is projected to rise by 9.2% from 2010 to 2020.  In a recent survey 40% of disabled people reported that social care services already fail to meet their basic needs like washing, dressing or getting out of the house.  And 47% of respondents said that the services they receive do not enable them to take part in community life.

 

So it’s not surprising that people are desperately worried about their future.

The worry is that continued underfunding of social care will mean the care system will simply not be able to support disabled people to live independently.  The lack of reference to ‘independent living’ under the definition of the ‘well-being principle’ in the Care Bill which local authorities will need to take into account when providing care further fuels this anxiety.

 

And it’s not just people in receipt of ILF who are worried – it’s their friends, their carers and their families too.  The cases of two of my constituents illustrate this well.

 

 

Ashley Harrison is a Scunthorpe United fan like me cheering on the Iron at Glanford Park. At 10 months old he was diagnosed with cerebral palsy.  He will turn 30 this year.  Ashley has lived in his own bungalow since 2006.  The ILF allows him to employ his own team of carers.  Ashley is an inspirational man, a fighter but he is worried that the control over his future is being taken away from him.

 

His mother says:

 

‘The closure of the ILF would be nothing less than devastating for us as a family. Since Ashley was awarded his ILF allowance the whole family’s lives have changed for the better. ILF understands Ashley’s needs and always do everything they can to constantly improve Ashley’s life and enable him to live independently.

As a family naturally all we have ever wanted is the best for Ashley, which the ILF has helped us achieve. The ILF has always seemed to be the leading and positive force at meetings ensuring that social services match and meet Ashley’s needs. Without the ILF we all face a very uncertain future. The uncertainty that Ashley faced in his early years prior to receiving his ILF award have been daunting, frustrating and of course a constant battle with social services.

The alleged “smooth transfer” over to social services is already proving to be nothing of the sort.  Each and every meeting we hold (which are incredibly frequent) leave us having to justify Ashley’s needs as a disabled person.  The assessments they ask us to complete are totally unsuitable for the severely disabled.

All of the disabled people living independently with the help of ILF are living their lives to the full. The fear is that if ILF closes these people will lose their human rights and dignity to live their lives as they should.

As a mother who’s fought the last 30 years for Ashley to have the life he wants and of course deserves, I dread to think what the next generation of disabled people will have to endure without the positive support of the ILF.

I beg you to listen to myself as a mother of a disabled son and also listen to all those disabled voices who deserve to be heard.

Give each and every person the ability to live and achieve their dreams just as you and I can.

The Paralympics just proves how amazing disabled people can be!!!’

 

 

Jon Clayton is also in receipt of ILF.  Like Ashley he has carers whom he employs who understand his disability.  His sister writes

 

‘My brother Jon is quadriplegic having been involved in an accident which was not his fault at the age of 18. He is now 54. 

He is one of life’s truly inspirational people; an accomplished mouth artist – a gift he only knew he had after his life changing accident-  living independently in his own home. He freely gives his time mentoring other disabled persons, helping them come to terms with another life. A life without limbs. A life without walking.


He has always sought to live as normal a life as possible. Having gone through marriage, divorce, being a step father, losing a partner.

He is both ordinary and extraordinary.

He relies heavily on his full time carers. Carers who he personally has ensured are trained to an appropriate and exceptional level to look after a person with specific and defined needs. One false move and he could (and has) spent 18 months bed bound with a pressure sore at the expense of some ill trained nurse.


His carers are trusted to ensure and give a high level of care, entrusted with the most personal of tasks from catheter changing, toileting, dressing etc.  This has been part of Jon’s life since his accident. Something he has taken on with humour and dignity.

If the ILF is removed Jon will be unable to live independently. Being able to engage in what you and I would consider a normal life. He will be unable to travel, have holidays, visit family, visit friends. 

The ILF has enabled independence. Given life, where life seemed over.

I would therefore urge you to do all you can to prevent this life enabling function – the ILF – from being eroded’

 

A fundamental concern for Jon, Ashley and others is whether they will be able to employ their specialist staff in the future.  North Lincolnshire Council’s responded to this question on 9th June 2014:

 

‘We appreciate this situation may cause you concern as an existing Independent Living Fund customer and would wish to reduce any worry or anxiety you may have.

 

Allocation of future monies will be based on your updated assessment and support plan and on future Local Authority funding so at this stage we cannot give any specific guidance on the amount of monies that you may receive from us or cannot give guarantees on the future employment status of any Personal Assistants you may currently employ.’

 

As you can imagine such ‘reassurance’ only serves to heighten anxieties and build mistrust!

 

So I return to my central question – will the government guarantee that Ashley Jon and all those currently in receipt of ILF will not lose their independence as a result of their decision to close it.  A decision I believe is aimed at saving money but might end up costing more in other budget areas such as health.  A better way forward would be for government to engage with ILF recipients learn from their experience and find ways of shaping future services that are cost effective but continue to deliver true independence.

 

As Disabled People Against Cuts points out for the 17,500 people in receipt of ILF ‘the closure of the Fund will have a devastating impact on the lives on these individuals and their families.  It also has a much wider significance because at the heart of this is the fundamental question of disabled people’s place in society: do we want a society that keeps its disabled citizens out of sight, prisoners in their own homes or locked away in institutions, surviving not living or do we want a society that enables disabled people to participate, contribute and enjoy the opportunities, choice and control that non-disabled people take for granted?’

Or in Mahatma Ghandi’s words “A nation’s greatness is measured by how it treats its weakest members.”

 

People like Jon and Ashley are not weak but strong.  The ILF gives them independence and liberates their strengths. Now is the opportunity for the Minister to guarantee their future independence will not be compromised by the closure of the ILF.

 

http://www.nicdakin.com/ilfspeech.html

 

DPAC would like to thank Nic and all the supportive MPs at the adjournment debate on ILF on 18th June 2014

 

See the ILF debate at: http://www.bbc.co.uk/democracylive/house-of-commons-27884690

 

 

May 162014
 

We are asking all local council candidates to pledge their support for developing inclusive education practice if elected onto the council.

For DPAC members not standing, we want your local council candidates to pledge their support for inclusive education practice.

We would like to have a photo of candidate with his or her party rosette, name, borough and ward and a sentence or two on why she or he is supporting ALLFIE’s manifesto demands.

We would like to aim for every candidate to offer his or her support for inclusion.

Please follow link: http://www.allfie.org.uk/pages/work/manifesto.html

Send photos to simone.aspis@allfie.org.uk

 

May 082014
 

“An Inclusive Education and a Fulfilling Life” Conference Saturday 7th June 2014 10am until 3.30pm
Email: afulfillinglife2012@gmail.com
Accessible Venue Kahawa Café 163 New Union Street
Coventry CV1 2PL

Purpose: This conference sets out to bring together disabled people, the parents of disabled children and those with SEN, and their non-disabled allies to explore common ground, opportunities and choice with regard to independent living and enjoying an education alongside their peers.

The conference will:
• Be respectful and accessible
• Be informative and participatory
• Use cooperative learning approaches
• Give examples of where things are working
• Discuss why life is getting harder for disabled people.

Refreshments: Lunch provided

The charge will be: £2.00 disabled people and family members
£4.00 for allies (professionals etc)
This in a not-for-profit event; all proceeds are to cover the cost of the conference. Please pay on the day but we do need a definite commitment that you are coming so we can make arrangements.

Interested in attending or want more information?

Please book a place: Email: afulfillinglife2012@gmail.com
Organisers: Elaine Hill, Rob Punton, Keith Venables, Caroline & Maresa MacKeith
Advisors: Katie Clarke, Steve Cooper & Tara Flood
Text or call: 0780 587 8729

For more information about ALLFIE: http://www.allfie.org.uk

 

May 042014
 

People who don’t use the spoken word have a great deal to say about communication. People who do use the spoken word have a great deal to learn about communication from people who don’t.

Quiet Riot is a group of young adults who don’t use the spoken word. Quiet Riot had their first meeting four years ago. They meet in Manchester but come from around the UK, with members in Holland and Ireland.
They are:

Paul-Thomas Allen
Judathan Allen
Raphael Allen
Danian Allen (1984-2005)
Heathar Barrett
Nadia Clark
Gareth Donnellon
Thiandi Grooff
Josh Harris
Anthony Kletzander
Maresa MacKeith
Dan Stanton
The communication used by many members of Quiet Riot is known as Facilitated Communication Training (FCT) a strategy introduced into the UK by Marion Stanton, who is currently lead UK Assessor and trainer:

,http://www.candleaac.com/staff.htm

Marion invited Rosemary Crossley, from Australia to meet with families in the UK almost fifteen years ago, who in turn introduced many of the Quiet Riot members to FCT.
http://www.annemcdonaldcentre.org.au
FCT is now used very effectively as a primary means of communication by many people around the UK. Using a key board on which to type, a trusted assistant (facilitator) supports the person to manage their body’s motor movements, which can be impaired as a result of sensory overloads/invasions as well as a wide diversity of other body motor issues.

FCT has fundamentally changed the opportunities for members of Quiet Riot:
” I am a man with no speech. I am a user of the pointing method of communication. I listen well and understand what is said… I am operating a perfectly weird body. I am wonderfully made..”

Raphael Allen
” I’m wondering if using Facilitated Communication will help to understand me better and give me some respect. I wish more people were given the chance to use facilitated communication it is great to be given a voice”

Anthony Kletzander.

“Having no voice is not great but at least I can type good things. Being in good company like kids who talk. Talking with me makes me happy.”

Heathar Barrett

http://www.heatharashley.co.uk/Home.html
“Trust your belief in your child. FC opens doors for those of us whose voices deny us use. People have to listen to our voices in the wilderness of disability. I can do things you elevate your expectation to. Look beneath the surface of appearance and see the qualities that are within”

Josh Harris.
I think FC is such a part of me that its difficult to think of it as an entity in it’s own right. I feel very lucky to have been surrounded by people who respected my communication giving me a limited experience of negativity around FC. I do however know that there are those who dismiss FC, I see this in their faces and reactions. My concerns are for those young disabled people who, for whatever reason, are affected by such situations.

Blake Williamson
Too bad I was seen as dumb of mind as well of mouth. Words offer all the possibilities of fine choices switching from a non-being to educated in the eyes of the world. The route to my intellect is now open”

Paul-Thomas Allen.
” in the end the funny woman from Australia ( Rosemary Crossley) gave direct explanations, we ran away as slow as could be. Facilitation was a map just to find out about going A.W.O.L. I was not seen as a thinker with reason until I used typing. I type to talk differently. It is very good being able to communicate.”

Judathan Allen
” I am aware that you don’t realise how I am able to type. I go to university. Perhaps one day I will have a part on T.V. And you will have the opportunity to read my fan’s praises.”

Danian Allen (1984-2005)
“To be able to express myself as full as possible, without the correct method my answers are limited ” and “To be recognised as intelligent enabling me to live an independent life in my own home ”

http://www.contactcandle.co.uk/about_dan_stanton.htm
Dan Stanton
“(FC ) allows me to communicate ,to have a voice.
Way in which it changed my life
I gave my opinion on my medical treatment
I Am Real
I am Real
Not a malfunctioning person with a confused mind
Just a normal thinking person
Who laughs, complains, shows sadness and happiness.

I am real”

Gareth Donnellon.

Funding, Quiet Riot and the ODI
Quiet Riot campaigned for three years with no funding. Members financed their own attendance at the meetings in Manchester. They were brought together by a commitment, to talk with each other in a safe place, to plan campaigns and enjoy their Right to Communication: a right for every human being. The long term aims of Quiet Riot are to change the ways in which society welcomes and values people who do not use the spoken word.

Quiet Riot has been hosted and given hospitality by Greater Manchester Coalition of Disabled People (GMCDP), since the first meeting. ACE North, have also provided a venue for larger gatherings, again free of charge.

In our fourth year the The Edge Fund, a creative and democratic funding body, offered funding to Quiet Riot* which is being used to enable Quiet Riot to develop a customised website where they can reach out to local and global connections giving more people an understanding of FCT and an opportunity for the many people around the world who are needlessly denied their voice.

Funding for groups, at the “cutting edge” in societies, like Quiet Riot, is an important political issue. Given that the very existence of Quiet Riot provides a powerful reflection of people who have been failed within their own society. Quiet Riot has emerged despite statutory organisations who have failed to serve their legitimate support requirements.

The name of Quiet Riot appears to be a challenge for some, which was illustrated when Quiet Riot considered making a funding application to Office for Disability Issues (ODI), a government, established body to orchestrate the voice of disabled people in the UK. Quiet Riot was invited to change the name, to one less controversial ! – perhaps F— O– might be more appropriate! We have no funding from any government agency, which allows a freedom to critically question and challenge government and it’s agents, which has to be an essential feature of any campaigning group.

Quiet Riot members now in their twenties and thirties have each had the powerful support from their families, to have their voice heard, often against significant opposition from schooling authorities. An important lesson for schooling services to learn is that labels attached to any individual cannot convey anything of value about an individual. Such labels lead teachers into a cul-de-sac about an individual, requiring a great deal of time trying to find a way out.

Meaningful appreciations of another person’s skills, contributions and qualities will emerge via a mutual and respectful relationship. Such relationships can start with mutually respectful communication. The early schooling experience for many QR members was in segregated settings and very far from respectful :

Segregated Education

“Special education is a cruel solution to educate people like me. I had the label (PMLD ) evil! I asked real people if they are aware of atrocities in school. Ask and ask again was anyone aware how awful it was doing stuff in special school. Emphasise it. The school system was a a vert (lawn) where seeds of alarm flew away. No one sussed what a serious affaire was swept away under the alters of Abraham . I was a walled prisoner in my own world dying slowly. When I returned from school each hour I sat thinking- give me a tool to communicate”

Judathan Allen.
“Special school you think is bad. It is the nondescript way they teach is dull. They only had lots of detritus to share.”

Paul-Thomas Allen.
The health service starts the process of diagnosis and categorisation of disabled people by creating labels that the schooling system uses to segregate and devalue disabled people. Authorities engage in convoluted assessments, measuring and testing the “capacity” of individuals. The disabled person is incidental to this process: it is an institutional response to legitimise prejudice and discrimination against a disabled person.

“I have no sex no gender apparently I only have this alleged affliction. reports and labels are the sum of my parts. There was never a label beyond disabled.i am just punk I am just an allocation of resources.”

Paul Thomas Allen
Institutions continue to segregate and devalue the human being as they have done for many decades.
” I have sorrow in my heart for you not learning the proper inclusion of me.”

Heathar Barrett
Segregation at school age will tend to lead to more segregation in adult life – feeding the “services” that exist for the maintenance and protection of the institution and its processes.

Labels of “deficit” are attached to the individual and reflect the approach of an institution. We need to shift these labels away from the individual to the institution. Therefore, the constant need for institutions to measure and categorise people could be described as Obsessive Compulsive Disorder (OCD). Some Schools, Colleges and Universities have Profound and Multiple Learning Disabilities (PMLD) because they have failed to welcome and learn from people they continue to reject and exclude based upon the negative differences the institutions have determined and cultivated. This is particularly true of people who do not use the spoken word for their communication.
“In my pupil days at home I learned children whose bodies operated differently were not welcome really anywhere in the high schools in the myopic time we lived in. I thought then real choice was just for those talking people”

Raphael Allen
“Being alone I feel Dead”

Heathar Barrett
It is soul destroying to continually have your contributions and efforts for participation thwarted by systematic indifference, ignorance and rejection. Such an approach to people is abusive and a total denial of their human rights. There continues to be a disturbing amount of confusion around the language and practice of inclusive education. We cannot give people inclusion, people have to Feel included.
” I invite experts to ask how we feel and our opinions. Autism really offers the world a fine lesson in humanities We require understanding, respect trust and love. In return we test the worlds ability to accept differences that exist between people ”

Josh Harris.
http://www.communitycare.co.uk/2008/01/16/josh-harris-autism-and-the-ambition-to-become-a-rabbi/#

qr pic 1

We know inclusion is working up and down the country in schools, colleges and universities for people with the diversity of impairments. We know people are included when we change the way we offer support in response to an individual’s particular requirements and when there is a welcome of difference and different voices for people to participate and contribute to the learning environment they are an integral part of.
” I would like to take this opportunity to say thank you for your accommodating and satisfying subject in question. There was very much calm and confident re-assurance surrounding me when in your real lecture of thought and wisdom. For me acceptance is from within a massive heart. Please have diversity bring you good joy in real life. With very fond and great thoughts for life – To Lesley Groom University Tutor from Heathar Barrett.

Hope and acceptance are a luxury I do enjoy. I feel very immense greatness about the university of my love and life in the making of a good great free future. We are moving forward.

Heathar Barrett.

My School
By

Maresa MacKeith
“Taking The Time”
www.inclusive-solutions.com
http://www.one-for-all.org.uk/

The thought of starting was ecstatic,
I wanted to learn so much.
To me the building was magic,
With life in its crumbling husk.

The thought of being ordinary,
Filled me with a joy I can’t tell.
Still the thought of that building keeps memory,
For me of pure water: a well.
It was because I had ordinary teachers, who recognised that I had skills, that I am where I am now, doing English at university. The special education system did not do that for me; it endlessly measured my incompetence.

Maresa MacKeith

 

However, when a school refuses to change, to welcome and accept different ways of learning, it cannot be overstated just how oppressive it is to be seen as different, when your difference is devalued by the organisation that claims to be a place of learning!
“It should be perpetuated that I have no differences. I just need really cool people to understand my ways. I am in my difference the despoiler of your pattern”

Paul Thomas Allen.

“I’m really tired of being different”

Anthony Kletzander
For people who do not use the spoken word there can be a continual and exhausting struggle to have your voice heard. For many people with the label of autism who use FCT, there can be a massive amount of time and energy required to overcome or manage their bodies’ sensory changes in order to type each and every word.

ice cream
I am finding it very hard to be a free fast user of FC when I am not focused on feeling anxiety free”

Heathar Barrett-
communication board in hand doing ordinary things like buying an ice cream. This does not require a “transition plan” or “a service delivery audit” Or a specialist training programme to create a team of ” Whippy Therapist”

QR fell walking
Heathar using her communication aide on a walk across the moors.
Again no “specialist service” getting in her path.
“I am an individual with my own wants. Sometimes my neurons do screw up and it takes time to fix them.”

Paul Thomas Allen
” being autistic causes sensory problems like bright lights which makes me feel dizzy and they burn my eyes. I also have problems with loud noises. They really scare me and make me feel really nervous”

Anthony Kletzander.
“People inspire me all the time. It’s the easy things I envy like people who are pain free”

Josh Harris

The only way we can get near to understanding what is required for an individual to type whilst having to manage the permutations of sensory invasions, which could relate to all the senses and more within any given learning environment, is by being respectful and responsive to the individual. Having a mutually respectful communication is essential.
As for what we can do to encourage change in Universities, I think there is a wider issue here. If FC is not accepted as a means of communication during examinations, as it was when I did my GCSE’s and A levels, then the next generation of disabled academics are thwarted in accessing university through such academic routes. The universities are poorer places for not having a fair representation of all students in their Halls and of course where we are never seen we are never easily accepted nor understood

Blake Williamson.
Professionals have a responsibility to shift their lack of understanding or toleration of ignorance about different ways of communication and recognise that the denial of a person’s communication is not simply the denial of a learning experience but the consequences can be life threatening.

Anthony Kletzander from independent living to institutionalization

Anthony Kletzander, one of the founder members of Quiet Riot lived independently in Dublin in his own flat, with his own 24hr support. Because people, uninvited came into his life and chose to deny his FC, he was forced into an institution after he had experienced a full life living independently, with his own support staff. Within days he was given antipsychotic medication against his wishes, this resulted in emergency hospital treatment. Anthony’s voice continues to be denied at the institution.
“Tell them to stop giving me medication. I have no choice it makes my head feel strange”

“I would love to be in independent living. It is much better than residential.”

“Really trying to be accepted into society is very difficult and I am really saddened by this”

This is the clip about university. Nua Health Care in Ireland refuse to accept Anthony’s communication. They have also refused his right to independent living. Anthony was hospitalised twice from this institution over a period of three weeks. Anthony’s struggle continues made more difficult by Nua Health Care continuing to deny Anthony’s voice.

https://www.dropbox.com/s/oxh98ewgf54qthq/MVI_0121.MOV

 

qr anthony typing
Anthony Kletzander. Typing with Marion Stanton just half hour after meeting with her. Nua Health Care refused her offer of support.
Fear

A poem
by
Maresa MacKeith

He watches, and you are scared.
Mute and Flalling
If he could talk he would tell.
So you silence him.

 

qr grad pic

Maresa uses facilitated communication on her graduation day at Nottingham Trent University.
People who are prepared to deny a person’s communication when they don’t offer a meaningful alternative are abusing a person’s Human Rights.

It is an abuse of the power and authority of a psychologist or therapist to * deny a person’s means of communication, then have the effrontery to accept, a large fee, to carry out an “assessment” and make judgments and recommendations about the person’s life with whom they insist they cannot communicate!

” I have spent every day since birth when people think my head is bad like my body. Top physicians from all over came to inspect the Allen family, every one of them you imagine a certified genius. They ran me through their tests prosecuting me with steal augers. Pain like real despicable pain. Played with and investigated all facts collated their only conclusion was to find I was guilty. I was dense and better as a doorstop. I inhabited my own head just watching, I had to live the isolated life. I had to wait …. It did not occur to the world I am not retarded and a vicious anger I was cultivating. In my egg I stayed. In my soft manner to wither, it was sometimes insanity”

Paul -Thomas Allen.
I am unable to pronounce what thoughts are in my mind. When I use facilitation I am able to let others know how I feel. This is undoubtedly beneficial for my peace. Past appearances of the disabled are wrong. What people pronounce does not show how clever they are. I think it is because writing allows people to say exactly what they want. People make assumptions

Damian Allen ( 1984-2005)

Quiet Riot, DPAC and challenges powers and practices
Quiet Riot is an organisation that offers a much more powerful future for the person who does not use speech but insists that their voice is heard.
There is also a growing new network of organisations of disabled people in the UK and internationally who are challenging the oppressive practices and asserting the human rights of disabled people. It is co-ordinated by Disabled People against the Cuts (DPAC) This New Democratic and transparent approach is not seeking to justify the participation of disabled people around the UK but fundamentally challenging the powers and practices that seek to prevent their contribution and participation.

Facilitated Communication has enabled members of Quiet Riot to challenge the powers and practices that seek to silence people that do not use the spoken word.

http://www.centreforwelfarereform.org/who-we-are/fellows/nadia-clarke.html

Nadia Clarke
Quiet Riot are engaged in subjects like: Biology, English literature, Creative Writing, Poetry, Philosophy, Jewish Religious Studies, Music, Geology, Ethics and Human Rights at Universities around the UK, Ireland and Holland. Thiandi Grooff a member of Quiet Riot and uses FC is in her final year of undergraduate study at a University in Amsterdam. She has been been engaged in a detailed qualitative study into group identity.

This study shows that a safe place for discussions is very important: the participants are welcomed, without threat by opponents who reject their way of communicating or the State, and every effort is made to overcome barriers to speaking. In this study the benefits of the collective identity for the members of the group ( Quiet Riot) were clear: a more powerful personal identity and self-esteem that led to more courage to speak up and to engage in relations and actions outside the group.”
Thiandi Grooff
FCT is used by increasing numbers of people around the world and with whom there is a growing connection via the internet. A powerful collective voice is emerging and demanding their space to be heard. It is a voice to reckoned with

Joe Whittaker April 2014

With many, many thanks to the great guys at Quiet Riot for putting this together and to Joe-DPAC fully support Quiet Riot and FCT.

This piece has been put together for the European Independent Living Day May 5th created by ENIL to celebrate independent living and to highlight the impact of cuts on independent living- we want to add that those who reject FCT also reject independent living –please add your support

For donations and support for Quiet Riot, FCT or any of the issues mentioned in this piece please contact: whittakerjoe5@gmail.com

For those fighting for inclusive education please contact the Alliance for Inclusive Education (ALLFIE) http://www.allfie.org.uk/

 

Apr 212014
 

DPAC would like to thank everyone for making last week’s (April 12 2014) National Conference such a huge success. There was a huge turnout with over 150 disabled activists from all over the UK including many new DPAC members attending, but just as important there were hundreds of members and supporters beyond the venue taking part through social media – watching the video live-stream, tweeting and sharing comments, views and sending messages of support. This was fantastic work by everyone and a truly inspiring collective effort.

DSC_1030 con

Here’s a brief outline of how it went.

Programme
The day was timetabled into sections beginning with practical reports and voting on policy motions. This was followed by two workshop sessions and then a closing session for everyone to feedback on the day. Four workshops were available to choose from in each Workshop session. Detailed reports on these will follow later.

John McDonnell MP, a longstanding friend and supporter of DPAC, gave a rousing opening speech to encourage everyone and remind us of the victories achieved so far. He congratulated disabled people and DPAC for fighting back, along with our sister organisation Black Triangle and WoW Petition initiators

As he finished he mentioned his own recent health condition which he said he felt brought him closer to our movement. Ellen reacted quickly by giving him a DPAC t-shirt and declaring him a full DPAC member to instant applause and cheers.

photo1jm tshirt

Finances
The Finance Report showed a healthy state of affairs for the time being thanks to individual donations, t-shirt and badge sales plus grants from the Edge Fund, the Network for Social Change, Trust for London  and the Andrew Wainwright Trust. More fund-raising is necessary going forward.

Motions
1. Government Honours
This proposed that any future candidates for the DPAC Steering Group could thwart the network and collective ethos of DPAC if they had received a national honour like an OBE or MBE. The ‘BE’ refers to the imperialist British Empire which is still celebrated despite what we know of the suffering and oppression this caused. The motion conversations also suggested that any media attention would be focused on those with honours and titles, rather than on the collective network ethos that DPAC ascribes to. The motion was put forward as a rejecting of this possibility and that of the honours system more generally. This was defeated.

2. Discrimination
This motion stated DPAC opposition to discrimination on the grounds of gender, sexuality, age, faith, disability, ethnicity or status. It also empowered the Steering Group to terminate the membership of anyone who supported a party which holds discriminatory policies, like UKIP. This motion passed based on an appeals process being put in place

3. Steering Group Size
This motion sought to expand the Steering Group from 8 members to 12 in order to respond to increased activity and maintain a broad, diverse and inclusive profile. This was passed.

Steering Group
There were 11 nominees for the Steering Group. Conference took a vote on whether to vote for accepting all 11 nominees, or vote for them one by one. Conference voted to accept all 11 nominees. The new steering group are currently reviewing co-opted places and will get back to the additional people that applied past the deadline as soon as possible

Steering Group:
Andy Greene
Bob Ellard
Ciara Doyle
Conan Doyle
Debbie Jolly
Eleanor Firman
Ellen Clifford
Linda Burnip
Paula Peters
Roger Lewis
Sabina Lahur

It was highlighted that the working groups are important in taking DPAC forward. The co-chair said she hoped those who did not stand for the Steering Group but were still interested in getting involved would join these as soon as possible.

Finally, a big thank you to the Conference Organising group and Workshop leaders who worked so hard to make this wonderful event a reality.

Links to videos from the day are here with thanks to Occupy for live streaming on the day to make the conference inclusive to all are here

Links to pictures can be found on DPAC flicker here
Thanks to Pete Riches, Szucs Gabriella and Rob Peters

The powerpoint on highlights of the last year can be found DPAC Report
A link to 2013 and some of the things DPAC did is here

See you on the streets!

DPAC www.dpac.uk.net
Twitter: Dis_ppl_protest
Also find us on Facebook with a group and open page under ‘Disabled People against Cuts’

contact: mail@dpac.uk.net

 

Apr 192014
 

“You have to love your own baby becos everone says they are a nusance”

 Sally age 8

I have come to recognise another truism! – If you are a parent of a disabled child. The school will give whatever support, you believe, is necessary for your child – as long as it matches with what the school is prepared to offer.If you want something different ,You! “The parent”  who is typically the mother, become “A problem” . The more articulate you are the more you are seen as “bloody awkward”.Colourful labelsgrow, the more you persist : “too pushy”, “in denial”, “neurotic”, “deranged”,”obsessed”, “too emotional”, “irrational” “naive” are a few of the polite names given to parents.

 

The rhetoric from schools and education authorities promoting partnership, between parents and professionals is common. This laudable aim, if realised,could save a great deal of pain and heartache for all concerned. The ultimate goal for most parents is for their child to feel safe welcomed and a belonging to the school. This is “gold dust” one parent said. Initially parents will “bend over backwards” to keep on the “good side of school” they are motivated by the desire to make this goal a reality for their child to experience. However, because there currently exists an unequal distribution of power and authority between parents and professionals the potential for “partnership” is only likely to happen when parents conforms to the plans of professionals.

 

After twenty five years being with parents advocating for their disabled child, I have not met a parent who had wanted conflict with the school. It is however, the professional who has the responsibility to change what they are doing to ensure the child can feel safe welcome and belongs to the school.A consequence of seeing the parent as a problem is that it is a distraction from supporting the child. There is a shift to devaluing and marginalising the parent ,which generates a struggle that can continue for weeks, months and sometimes years.

 

One mother said:

 

“They (the professionals) made me a monster. At first, I was totally compliant with everything they told me about my son. I would have balanced on my head if they wanted me to . Then I realised they lied to me and started bullying me- now professionals are having to manage the monster they created.”

 

The very act of questioning the practice of a school or an authority by a parent can result in unleashing of an assault that can leave the parent exhausted. The struggle increases if the parent challenges more than one statutory service and therefore multiple professionals. Such a position can overwhelm parents, with formal letters, procedures , phone calls ,e-mails, and now texts. The communications often contains implied threats or advice encouraging the parent to simply accept that which is being offered by professionals, even when they know this will go against what the parents believe is not in the interests of their child.

 

Does this mean that parents are always right and professionals wrong about a child’s support requirements? Such an assertion would be absurd. However, when a parent lacks confidence in the support provided by the school or when they are unable to influence the schooling experience for their child,when parents  witness their child is disrespected, denied important opportunities, with no friendships the parent is likely to be propelled into demanding change. When a parent is forced to take such an exposed yet principled position, they will be subject to scrutiny and interrogation, by a number of professionals who will hold a different position, at a case conference or annual review. Whilst such formal settings are routine for professionals for parents they can be traumatic.

If individual professionals were subjected to the same degree of scrutiny and interrogation before a panel of critical parents they would, quite rightly, be calling upon their professional associations to represent their position.

 

The professional in a protracted dispute with a parent will have access to supports throughout the process : they have time away from work, they can hand over to another colleagues, they can have someone to type letters,make phone calls, arrange meetings, they get travelling expenses, they get time off in lieu if they work beyond contracted hours, they can even move to another job whilst in the middle of a serious dispute with a family, and they receive a salary- Professionals have protection from a school or system culture, where professionals will protect each otherkeeping internal disagreements behind closed doors, allowing them to present a united front.No such accommodations are available to parents engaged in the same protracted dispute not of their initiation. When the professional decision is made it becomes bizarrely impenetrable. Parents are patronisingly encouraged to follow the ” Complaints Procedures” if they are “‘unhappy” with the decision. This would be another professional procedure that can take months, with little expectation of changing the original decision.

 

Being a parent who is knowledgeable about the education system,aware of legislation and particular policies, is not a  guarantee that your child will get the support you believe to be  appropriate for your child. Being the “Parent” you can be positioned so that your contributions are devalued if they differs from professionals ” in charge” because it is they who the system invests the authority. A mother of a disabled child, who was extremely knowledgeable and articulate about the complexities of her child’s support requirements, she was aware of different teaching methods,  how to differentiate curriculum, adapt resourcesfor particular children. This woman wasfamiliar with the range of external agencies able to enhance the support available in school. In addition she was familiar with internal workings of thelocal education authority, where her child attended school. This mother started her professional career as a teacher in the same authority, served eight years as a special educational needs co-ordinator(SENCO), followed by seven years as a deputy head teacher, finally taking on the roleof education advisor. But now she was positioned as a “parent” again she was asking for something different from that which the school was prepared to offer. She was described as being “too involved” and “too emotional” and no longer “objective” This mother was forced into a conflict with the professionals, from the authority she had served as a senior educationist.

 

How can such exhausting disputes be minimised? Professionals have to learn to listen and listen then listen again first to the child and the parent advocating for their child.

 

The professionals will have had training, they may well have many qualifications, they can have much knowledge about a particular impairment and yet know nothing about the support requirements of Heathar who may have that particular impairment. Professionals can only support Heathar effectively if they are able to develop a relationship with Heathar. The parent, advocating for their child can be a valuable introduction to Heathar.

 

If professionals ask questions, to which they don’t already assume the answer they are more likely to develop a meaningful understanding with the child and learn about the child. When  a person is genuinely listened too, good relationship happen. This is far more likely to lead to the parent having confidence in the actions of the professionals who are there to serve their child. Professional can also build on a good relationship with the parent when they don’t:

 

Tell ​a parent their child is not the only one in the school!

 

Tell a parent the school does not have the resources to support their child!

 

Tell a parent that support to their child – will result in support being removed from other children.

 

Tell a parent that you are an extremely busy person!

 

Tell a parent that you are an expert in this type of condition, when referring to their child.

 

Tell a parentthe date and time of a meeting without first checking on their availability.

 

Tell a parent to come to a meeting on their own

 

Tell a parent you have to leave their meeting early because you have an important                       appointment to attend.

 

Tell the parents of an important decision, just before you go on school holidays.

 

Give the parent a patronising smile and nod of your head, when you totally disagree with them.

 

George Bernard Shaw suggested that it was the reasonable person who adapts themselves to the world as it exists. However, it is the unreasonable person who persists in adapting the world to accommodate a different way of thinking. GBS concluded, that all progress depends upon the “unreasonable” person orthe ” bloody awkward” parent?

 

Joe Whittaker

April 2014.

 Posted by at 19:22
Apr 182014
 

We read with interest the piece in the Independent by Rachel Reeves and Kate Green regarding Labour’s response to the Work Capability Assessment [1]

Labour should realise that disabled people are deeply distrustful of any Labour reform of a Work Capability Assessment system, which Labour introduced in the Welfare Act of 2007 with the stated aim of removing 1 million claimants from the benefit system [3].

Our position has been and will be that the Work Capability Assessment is deeply flawed in its basic concept, not just in terms of the details of its delivery, and inclusion in the workplace for disabled people cannot simply be achieved by a ‘back to work’ test.

manifesto

In the Reclaiming Our Futures, Disabled People’s Manifesto [4], we state that a priority demand from government is that:

A comprehensive and strategic plan of action is developed with disabled people and our organisations to tackle the discrimination and exclusion disabled people face in work and employment including: increasing quality and range of personalised support available to disabled people, strengthening disabled employees rights and tackling employer discrimination and poor practice

Other key demands include that:

Economic productivity must not be the only measure of people’s worth and value, volunteering offers as much value to society as paid employment. While we recognise that volunteering can offer additional skills, it should not be the default option for disabled people because of our exclusion from paid work

There must be policy and media recognition that there will always be disabled people who are unable or too ill to work. These individuals must be supported by a publically funded system. They should not be penalised or demonised as they are currently.

For true inclusion in the workplace for disabled people a wider approach is necessary including but not limited to:

• Will Labour commit to the restoration of Disabled Student’s Allowance,
• Will Labour commit to the restoration of the Independent Living Fund,
• Will Labour commit to the extension of Access to Work (AtW) to include unpaid voluntary positions,
• Will Labour commit to the reversal of the reduction of people who currently receive DLA, but will not receive PIP and also lose their Motability access,
• Will Labour commit to the reinstatement of the requirement for councils to produce equality schemes on employment and access
• Will Labour commit to the provision of accessible transport.
• Will Labour commit to the reinstatement of “day one” protection from unfair dismissal in employment law
• Will Labour commit to the provision of Employment Tribunals enforcing mandatory organisation-wide measures on preventing disability discrimination
• Will Labour commit to the provision that all government contracts, at a national, regional and local level, are only awarded to companies that are fulfilling measurable equality targets for the employment of disabled people

(for further points see reference 2)

These currently are some of the barriers to inclusion in the workplace for disabled people, and they will not be fixed by simply amending the WCA. The issue must be seen within the context of the wider interconnected system of barriers in place. It must be seen in terms of what a large majority of disabled people have already identified as key problems.

In terms of inclusion we also need from Labour, a recognition that for many disabled people to be able to work there has to be a nationally transportable social care system with a guarantee that people would keep the same levels of funding wherever they needed to move to work.

We need recognition that there is an onus on government and employers to fully accept the spirit of the Equality Act 2010 [4] with its requirement to the opening of work opportunity to disabled people. Without this, no “fit for work test” aimed at cutting disability benefits will make any impact whatsoever on the numbers of disabled people who can attain and sustain employment.

We also need from Labour a stronger recognition that there are many disabled people who cannot enter the work place and should not have to live in fear of being pressured into doing so.

There is much that the article leaves out and that leaves us with a number of serious concerns and questions.

While we are not yet prepared to endorse in any way Labour’s new approach to the Work Capability Assessment, we do see the article by Rachel Reeves and Kate Green as a helpful starting point for discussions on the future of inclusion of disabled people, who want and are able to work, in the workplace and we would welcome an opportunity to meet with them and discuss this further. We would like meet with Kate Green and Rachel Reeves to ask the following questions:

1. Will Labour commit to stop spending public money on private
contractors and return any assessments of disabled people back to GPs
with medical evidence taken into account as well as give a commitment to
look at the barriers to work for disabled people who can and want to
work (in line with the social model of disability)?

2. Will Labour commit to a time and date to talk with DPAC, My Legal,
the Mental Health Resistance Network, Black Triangle, Deaf activists,
those with learning difficulties ( with an outreach of ½ a million
disabled people) to listen to the views of the largest network of grass
roots disabled people on the WCA and ESA?

3. If Labour are committed to scrapping the WCA when will Deaf and
disabled people, and those with mental health issues have sight of the
detail of any alternative Labour is proposing?

4. If Labour accepts the harm, devastation and premature deaths that have
been an outcome of the WCA why have they chosen to suspend their
prospective parliamentary candidate for St Austell and Newquay, Deborah
Hopkins for speaking out in public about the harm caused by the WCA.

5. Will Labour address the disproportionate harm that the WCA and
sanctions on ESA and JSA are causing to all disabled people, in
particular those with mental health issues and learning difficulties?

6. We along with many others insisted that a centralised Independent Living Fund
for Scotland be established and it has been done. They have also promised to re-open ILF to new users, with a commitment of additional funds and recognition of its importance to independent living and obligations to article 19 of the UN Convention on the Rights of Persons with Disabilities. Why has the Labour
Party not promised to re-establish it south of the border?

Many of the Statements included in this response are taken from the UK Disabled Peoples’ Reclaiming our Futures Manifesto and are endorsed by a UK network of disabled people and Deaf and Disabled Peoples Organisations, including: ALLFIE, Inclusion London, Equal Lives, DPAC, Inclusion Scotland, Disability Wales and the TUC Disabled Workers Committee [2], who between them reach several million disabled voters.
References
1. How Labour would reform the Work Capability Assessment http://www.independent.co.uk/voices/comment/how-labour-would-reform-the-work-capability-assessment-9265479.html
2. The Reclaiming Our Futures, Disabled People’s Manifesto http://disability-studies.leeds.ac.uk/files/library/UK-Disabled-People-s-Manifesto-Reclaiming-Our-Futures.pdf
3. The Green Paper: The new deal for welfare: Empowering people to work. 2006 http://webarchive.nationalarchives.gov.uk/+/http://dwp.gov.uk/docs/a-new-deal-for-welfare-empowering-people-to-work-full-document.pdf
4. Equality Act 2010 http://www.legislation.gov.uk/ukpga/2010/15/contents

 

Apr 072014
 

DPAC_coloured_Logo_2__biggerWe are very much looking forward to seeing everyone who can come to our national conference on Saturday but it is also important that those of you who can’t get there in person are able to take part. There are a number of ways you can do this:

  • Send messages of support and your ideas for what DPAC should focus on over the next year to mail@dpac.uk.net or @dis_ppl_protest.These will be put up on the graffiti wall at the conference and included in the notes from the day.
  • Watch the conference live on:

http://bambuser.com/channel/OccupyLondon and http://bambuser.com/channel/DPAC

  • Live tweet your questions and contributions to @dis_ppl_protest

  Or email: mail@dpac.uk.net

 The program for the day is at DPAC Conference 2014 Saturday 12th April – Conference Programme

Apr 042014
 

We’ve had a great response to bookings for the DPAC conference on Sat 12th April in London, but places are now running out. Please email:  dpacfightback@yahoo.co.uk

with your details, number of places needed and any access needs.

12th April 2014 – 11am until 5pm

London Met University, Tower Building, 166 – 220 Holloway Road, London, N7 8DP

Since we started in October 2010 Disabled People Against Cuts has been at the forefront of the fight against austerity. With Atos on the run, and the bedroom tax on the ropes we are seeing the results of hard campaigning. But there is much more to do to ensure disabled people’s rights to live independently and with an adequate income.


The national conference is a chance for DPAC members to come together, to share experiences and discuss your ideas for moving forwards.


DPAC are working hard to bring to conference a surprise guest, a person who, if anyone has, has been the catalyst for the re-emergence of disability activism in the last few years, someone DPAC has enjoyed a close relationship with from visiting him at home to donating underpants to supporting his select committee appearances.


Workshops will look at: –  Where Now for the Independent Living Fund campaign,  – Developing a Social Model of Distress,  – Winning the Argument,  – Disability, Art and Protest,  – Building a National Network of Disabled People’s Organisations and Direct Action practical skills among others.

 Please note places are limited so priority will be given to DPAC members. For information about joining please contact mail@dpac.uk.net

The venue is wheelchair accessible. BSL and a note taker will be provided. For access information go to: http://www.disabledgo.com/access-guide/islington-council/london-metropolitan-university-tower-building

For access queries including booking parking please contact DPACfightback@yahoo.co.uk
To book places or for more information please contact DPACfightback@yahoo.co.uk

 

 

 

Apr 042014
 

Dozens of young people with learning difficulties and their families have hit out at a decision to slash foundation learning courses for pupils with profound or moderate learning difficulties – from five days a week to three at One, formerly known as Suffolk One, in Ipswich. the link to the article in the East Anglian Daily Times is below.

Suffolk DPAC will be working with them to try to prevent this as the only other alternatives for their education are at special school sixth forms.

http://www.eadt.co.uk/news/ipswich_angry_parents_claim_education_of_children_with_learning_difficulties_will_be_damaged_after_one_cuts_foundation_courses_1_3478573#sharinganchor

As we know segregated classes within mainstream settings do not count as inclusive education. But neither does the forced placement of disabled learners in fully segregated settings of so called special schools, colleges, universities or any other learning environment. DPAC opposes both!

We refer all to our allies ALLFIE (The Alliance for Inclusive Education) for a better understanding of what inclusive education means and how it can be achieved-DPAC strongly supports Inclusive education as a fundamental principle of independent living and as the only way to achieve full equality and inclusion for all disabled people.

Please see the ALLFIE web site for more informaion on inclusive education and get involved in their campaigns

http://www.allfie.org.uk/

also please see the valuable comment from Joe Whittaker below

 

 

Mar 102014
 

There are many different ways to be involved in the work of DPAC. All are equally valuable. We all have a role to play in campaigning for disabled people’s rights and a fair society, in whatever way we can from taking part in protests to tweeting, from administrative tasks to writing poems, from making banners to conducting research. Every contribution is important, formal or informal. Some ways to get involved are:

 

       Joining as a member. You will receive occasional urgent action and information updates from us and have the right to vote at our general meetings.

 

       Signing up to the website for regular information

 

       updates every time something new is added to our website.

 

       Following DPAC on twitter: @Dis_Ppl_Protest and Facebook or the quieter Facebook page

       Joining or setting up a local group. Local groups need to follow the DPAC constitution. Local activity is really important for raising awareness about the impact of austerity on disabled people and leading the way in the fightback. For a list of local groups see HERE

       Or contact mail@dpac.uk.net

 

       Linking between DPAC and other campaigns and unions, for example Occupy, UK Uncut, the Anti Bedroom Tax and Benefit Justice Federation, Reclaim the Power, Fuel Poverty Action, Boycott Workfare, the People’s Assembly, local anti cuts groups, local trades councils and trade unions branches.

 

       Joining or being involved in the running of campaign sub-committees. We currently have sub-committees at different stages of development in the following areas:

o   Atos and the Work Capability Assessment

o   Independent Living Fund

o   Access to Work

o   Reclaiming the Social Model of Disability

o   Disability, Art and Protest

o   Direct action

o   Inclusive Education

o   Communications and social media

o   Research

o   Local groups

o   Working with Disabled People’s Organisations – building a national voice

At the DPAC conference workshops will be held in each of the different campaigns and there will be a chance to sign up if you are not already involved.

       Being on the Steering group. At the conference we need to elect our steering group for the next year. There is more information about this below.

Steering group

One of the roles we have to make sure we run in a way that follows our aims and principles and is accountable to DPAC members is being on the Steering Group.

Being on the Steering Group is a big time commitment and is often a difficult job because there is so much to do.

For this reason in order to stand for nomination to the Steering Group we need people who can sign up to:

·         Minimum of 5 – 10 hours commitment per week

 

·         Corresponding regularly by and checking emails to stay in touch with developments and inputting to the development of DPAC initiatives

 

·         Co-ordinating particular areas of work, involving members widely and working with allies

 

·         Being involved in at least two sub-committees

 

·         Taking responsibility for either co-ordinating or providing an active and supportive link to at least two local groups

 

·         Representing DPAC at meetings, events and conferences sometimes at short notice

 

·         Working collectively and positively within a team of people with contrasting access needs

 

·         Following DPAC principles and values at all times:

o   Social model of disability

o   Rights not Charity

o   Inclusive Education (no ifs no buts)

o   Working within the broad left

o   Equal opportunities and social justice for all regardless of ethnicity, sexuality, gender, disability, age, faith, employment status, resident status. No to scapegoating of any kind.

 

It is important we have a diverse steering group covering a range of impairments, equalities strands and areas of the country. We also recognise that due to fluctuating impairments people may need to step back from activity for temporary periods.

The current DPAC constitution sets the number of steering group members at 8 but the current steering group will be putting forward a motion at the conference for members to vote on enlarging the steering group to 12.

All those wanting to put themselves forward for the steering group must be full DPAC members. If you would like to put yourself forward for the DPAC Steering Group please send a 500-700 word statement to mail@dpac.uk.net

 explaining why you would like to be on the Steering Group, how you are able to meet the commitment and any existing political/group affiliations before the 31st March 2014.

This text will be put on the DPAC web site-you do not need to be able to come to the DPAC conference on the 12th of April to be considered for election to the steering group, but we’d appreciate it if you could.

 

We’d like to say a big thank you to the past DPAC steering group for all their work, and invite them to apply again if they wish to

Dec 302013
 

As a grassroots campaign group DPAC wouldn’t exist without the dedication of all those who give their time to exposing what is happening: coming out on the streets, writing reports, researching, writing web content and policy critiques, heading up and being part of the growing number of local DPACs, organising events, engaging with social media and a whole set of other stuff that keeps DPAC vibrant, active and strong – its thanks to you that DPAC exists.  DPAC also want to thank the growing number of grassroots groups, individuals, academics, supporters, unions and organisations we’ve worked with in 2013.

2013 began with DPAC being awarded campaign of the year for our work in 2012 the year ends with DPAC being named as ‘people of the year’ by Owen Jones. In 2013 DPAC supported many local based protests on transport, the bedroom tax, ILF, local authority cuts and privatisation. We blocked roads protested against fuel poverty, fracking, the loss of legal aid, the bedroom tax, the closure of ILF and more. We set up Reclaiming our Futures 7 days of action joined by hundreds to celebrate the gains of the disabled peoples’ movement and to protest at the effects of imposed austerity on disabled people. DPAC launched the UK Disabled Peoples’ Manifesto which was followed by an EDM.We also published a number of reports.

There was cause to celebrate: the Government were ruled to have made the decision to close the Independent Living Fund unlawfully. Mental Health Resistance network succeeded in winning both case and appeal by the Government on the discrimination of the WCA. DPAC were approached by the UN prior to Raquel Rolnik’s UK visit to feed-in –her findings on the bedroom tax were devastating for the Government. DPAC led a whole range of events and join events on benefit justice to join together and fight the evils that this Government have imposed. While every protest, every campaign, every new network and every exposure of this Government is a success, we received growing numbers of emails from those left without money, food, homes and suffering cuts to their support.

In 2014 we must continue to fight and take all actions we can to change and expose the devastation this Government is causing to disabled people.

You can subscribe to receive all DPAC web posts or become a DPAC member at www.dpac.net.uk join us on twitter @Dis_PPL_Protest or on Facebook

 Key highlights of DPAC actions from 2013 below….

January

DPAC were awarded campaign of the year (2012) by Lipstick Socialists. They said: The fight back by disabled people as the Con/Dem Govt stripped some of the most ‘vulnerable’ sections of the community of their benefits. Their campaign against Atos (who made the decisions) during the Paralympics was inspiring and they have led the way in the fightback against the Con/Dem Govt. – See more at: http://www.internaldpac.org.uk/DPACClone/2013/01/#sthash.tEoKp2ds.dpuf

Co-op Campaign: stop the Atos Contract! Launched to publicise that Co-op were thinking of renewing a three year Atos contract for occupational health-Eventual outcome Co-op publically state they wouldn’t renew the contract with Atos.

DPAC call Vigil on Judicial Review initiated by Mental Health Resistance Network on WCA

Benefit Justice organising meeting by Tenants, DPAC unions and others held in London. We also live streamed London DPAC meeting so that everyone could access it. Annie Howard exposed Atos and DWP in relation to the data protection Act http://www.internaldpac.org.uk/DPACClone/2013/01/dwp-and-atos-make-a-mockery-of-the-data-protection-act/ Alan Shellbrooke a Tory MP said he wanted to introduce US style cards for those on benefits. We also linked with Fuel Poverty Action for the first of the 2013 actions on Fuel Poverty. We urged everyone to have their say on the Care Bill and to mention the ILF issues and posted advice on the Bedroom Tax and Discretionary Housing Payments and how to access them ahead of this inhuman misery. Condemn Love anti-Atos song by the excellent Kevin Robbins got it’s first airing

February

Victory for Daniel Roque Hall and Winvisable as Daniel is released from prison. Annie and Bob uncovered The Atos and DWP’s Land of make Believe http://www.internaldpac.org.uk/DPACClone/2013/02/atos-and-dwps-land-of-make-believe/

Owen Jones donates some of his prize from young writer of the year (donated by Lord Ashcroft) to DPAC http://www.internaldpac.org.uk/DPACClone/2013/02/thank-you-owen-but-we-wont-count-on-the-money-until-lord-ashcroft-puts-it-in-our-account/

We publicised the workfare cases The judgment on cases brought by Cait Reilly and Jamie Wilson mean that all but one of the Government’s workfare schemes (Mandatory Work Activity) that force unemployed people to work unpaid or lose benefits have been deemed unlawful. As we know IDS went off and rewrote the law- See more at: http://www.internaldpac.org.uk/DPACClone/2013/02/#sthash.jZLw1k5A.dpuf

We publicised an update on the Bedroom Tax, unfortunately not rewritten by IDS or anyone else. The post by Frank proved to be an unfortunate prediction of what was to come.

On ILF we produced a template letter for MPs and our collected FoIs on what Local authorities responses were to the ILF consultation http://www.internaldpac.org.uk/DPACClone/2013/02/what-local-authorities-said-about-the-closure-of-ilf/

Whitehall Traffic was brought to a standstill outside the Dept of Energy and Climate Change http://www.internaldpac.org.uk/DPACClone/2013/02/whitehall-road-block-brings-traffic-to-a-standstill-outside-dept-of-energy-climate-change/

Unum were finally nailed on driving Governments’ on welfare cuts http://www.internaldpac.org.uk/DPACClone/2013/02/unum-finally-nailed-through-bragging-on-driving-government-thinking/

DPAC and Inclusion London issued a statement on ILF while our National English DPOs remained silent http://www.internaldpac.org.uk/DPACClone/2013/02/defend-independent-living-save-the-independent-living-fund/

Annie Howard exposed the myths around the support group and ESA http://www.internaldpac.org.uk/DPACClone/2013/02/11-was-never-intended-to-be-the-number-of-people-in-the-support-group-dwp-big-blunder-annie-howard/

Atos and the treatment of mental health users and survivors was further exposed through You Tube, while  Kate Belgrave asked where were the MFCs at Atos – we’re still looking… http://www.internaldpac.org.uk/DPACClone/2013/02/harrowing-atos-assessment-and-where-are-the-mental-health-champions/

A letter from Ed Miliband was publicised after it was sent to us by a supporter http://www.internaldpac.org.uk/DPACClone/2013/02/letter-from-ed-miliband-on-atoswca-but-is-it-enough/

DPAC joined the campaign against the privatisation at Barnet and the great Crapita takeover http://www.internaldpac.org.uk/DPACClone/2013/02/urgent-stop-captia-10-years-plus-contract-for-council-services-in-barnet/

We launched a campaign against Colin Brewer who said that disabled children should be put down – he later resigned, but tried to put himself forward in a subsequent election process. http://www.internaldpac.org.uk/DPACClone/2013/02/urgent-stop-captia-10-years-plus-contract-for-council-services-in-barnet/

We published an email from one of our supporters which asked SCOPE what it was doing to save ILF , SCOPE suggested they get in touch with  DPAC http://www.internaldpac.org.uk/DPACClone/2013/02/scope-and-ilf/

March

We reposted the excellent Nick on ESA Process in Chaos and the Government cover-up http://www.internaldpac.org.uk/DPACClone/2013/03/dwps-esa-process-in-chaos/

As DPAC is on the working group of the European Network on Independent Living (ENIL)  against European austerity and its effect on disabled people we asked you to write to your MEPs to support  a push to get this debated in the European Parliament

March 13th was the court case on ILF in which 5 ILF users took the DWP to court against the proposed closure of ILF in 2015 We stepped up the campaign to publish stories of ILF users and those that would have benefited from ILF if it hadn’t been closed to new users in 2010 by Miller without even a dodgy consultation process. http://www.internaldpac.org.uk/DPACClone/independent-living-fund/

 The Benefit Justice Summit co-organised by DPAC in London brought together unions, grassroots groups, lawyers and tenants groups

We publicised news for parents of disabled children in the private rented sector and how they could claim money back from the DWP http://www.internaldpac.org.uk/DPACClone/2013/03/urgent-news-for-parents-of-disabled-children-renting-in-private-sector-money-back-from-dwp/

Beth Tichbourne was fined £745 plus costs for saying that David Cameron had ‘blood on his hands’ in an outrage that we should never forget  http://www.internaldpac.org.uk/DPACClone/2013/03/bethan-tichborn-cameron-has-blood-on-his-hands5503/

We publish an update on ILF court case with video http://www.internaldpac.org.uk/DPACClone/2013/03/ilf-court-case-update-and-implications/

 

DPAC and our sister org Black Triangle issue a joint statement on Labour and Bedroom tax http://www.internaldpac.org.uk/DPACClone/2013/03/joint-statement-and-petition-by-dpac-and-black-triangle-anti-defamation-campaign-in-defence-of-disability-rights-on-the-labour-party-campaign-against-the-bedroom-tax/

DWP and Government lies on ILF closure are exposed by DPAC in previously classified papers and memos from the DWP to ministers http://www.internaldpac.org.uk/DPACClone/2013/03/summary-of-secret-correspondence-from-the-dwp-to-mcvey-on-the-ilf-closure/

ESA appeals increase by 70% DPAC reposts Nick’s analysis http://www.internaldpac.org.uk/DPACClone/2013/03/more-chaos-esa-appeals-up-by-70/

Disability charities consistent apathy for disabled peoples’ lives, but not for their high salaries for directors was highlighted yet again http://www.internaldpac.org.uk/DPACClone/2013/03/how-the-big-disability-charities-let-down-disabled-people-again/

DPAC supported local protests and campaigns and also protests against staff cuts on railways and transport protests

April

April was the month that the condemns brought in more of their cuts for ordinary people the hated bedroom tax, the end of council tax support, the benefit cap and more http://www.internaldpac.org.uk/DPACClone/2013/04/the-nasty-party-go-on-the-offensive-against-disabled-people/

DPAC and UKUncut served eviction notices on our ‘favourite’ MPs –they had too many bedrooms –a complaint was put into You Tube who were told to remove the videos of IDS’ mansion http://www.internaldpac.org.uk/DPACClone/2013/04/eviction-notice-for-ids-and-oh-my-what-a-big-house-you-have/ http://www.internaldpac.org.uk/DPACClone/2013/04/ids-home-occupation-videos/

The TUC disabled workers refuse to join the Government sponsored Disability Action Alliance hosted by Disability Rights UK (DRUK) http://www.internaldpac.org.uk/DPACClone/2013/04/the-disability-action-alliance-or-whatever-happened-to-the-disability-strategy/

After news that the 5 ILF users that took the DWP to court had lost the case processes began to appeal the decision and still not a word of support from the big Disability charities or the aforementioned DRUK  http://www.internaldpac.org.uk/DPACClone/2013/04/claimants-to-appeal-high-court-decision-concerning-closure-of-the-independent-living-fund/

DPAC learns of a man who was arrested and tried in a secret court and jailed due to Atos –DPAC launches a campaign http://www.internaldpac.org.uk/DPACClone/2013/04/man-arrested-and-tried-in-a-secret-court-after-atos-assessment-support-needed-in-nottingham/

We also supported and co-organised a number of Benefit Justice summits across the country, supported more protests on transport and privatisation and continued to support the Barnet crisis

May

We supported CSRF in protesting at the |PCS conference and their refusal to refuse to implement benefit sanctions http://www.internaldpac.org.uk/DPACClone/2013/05/civil-service-rank-and-file-protest-at-pcs-conference/

We joined with False Economy in the search for the elusive Mental Function Champions at Atos , Dr Greg Wood  quits Atos and turns whistle blower http://www.internaldpac.org.uk/DPACClone/2013/05/where-are-the-mental-function-champions-at-atos-and-other-atos-type-things/

DPAC publishes info on Hardship payments and budgeting loans as we get more and more emails from people caught in the poverty and sanction traps set by the DWP –the post has been shared over 36,0000 times  http://www.internaldpac.org.uk/DPACClone/2013/05/hardship-paymentsbudgeting-loans-and-short-term-advances/

Black triangle meet with Scottish Government to discuss regulations regarding Atos and GPs http://www.internaldpac.org.uk/DPACClone/2013/05/esa-regulations-25-and-31-campaign-black-triangle-to-meet-with-scottish-parliament-welfare-reform-committee-chief-this-thursday/

The Mental Health Resistance Network win against Government on WCA , but spectra of legal aid cuts is raised too http://www.internaldpac.org.uk/DPACClone/2013/05/will-legal-victory-by-mhrn-against-atos-tests-be-our-last-we-need-to-act-now/

DPAC and the TUC disabled workers block Tottenham Court Road in an act of solidarity http://www.internaldpac.org.uk/DPACClone/2013/05/dpac-and-tuc-members-in-direct-action-of-solidarity/

DPAC publishes a critique of UKIP http://www.internaldpac.org.uk/DPACClone/2013/05/why-the-rise-of-ukip-is-dangerous-for-disabled-people/

DPAC’s own Ellen Clifford talks to real fare http://www.internaldpac.org.uk/DPACClone/2013/05/ellen-clifford-talks-to-real-fare-on-welfare-reform-and-protest/

June

June 1st marked a day of UK wide protests against the bedroom tax attended by DPAC

DPAC publishes stats by Nick that show the huge hike in sanctions under the Coalition  http://www.internaldpac.org.uk/DPACClone/2013/06/jsa-benefit-sanctions-sky-rocket-under-coalition/

DPAC holds a Birthday party protest for ILF http://www.internaldpac.org.uk/DPACClone/2013/06/press-release-independent-living-fund-birthday-protest/

The fight against the Bedroom tax continues with protests and new groups springing up and supporting each other across the country http://www.internaldpac.org.uk/DPACClone/2013/06/updates-the-fight-against-the-bedroom-tax/

DPAC publishes Lies, Damn IDS and Statistics  http://www.internaldpac.org.uk/DPACClone/2013/06/lies-damn-ids-and-statistics/

July

DPAC releases its program for 7 days of action, campaigns and protest: Reclaiming Our Futures http://www.internaldpac.org.uk/DPACClone/2013/07/reclaiming-our-futures-7-days-of-action/

DPAC joins protest at Downing Street against the bedroom tax

DPAC joins Justice Alliance to protest against cuts to legal aid

DPAC joins vigil for case against bedroom tax outside the Royal Courts of Justice

DPAC posts a list of advice and legal resources as emails from people in severe hardship escalates further http://www.internaldpac.org.uk/DPACClone/2013/07/advice-and-legal-resources/

Sisters of Frida go to Geneva to challenge the situation for disabled women at the UN http://www.internaldpac.org.uk/DPACClone/tag/sisters-of-frida/

We list the MPs that voted against a cumulative impact assessment http://www.internaldpac.org.uk/DPACClone/2013/07/for-fellow-extremists-everywhere-how-your-mp-voted-on-the-cumulative-impact-assessment/

Southwark DPAC challenge local politicians http://www.internaldpac.org.uk/DPACClone/2013/07/sdpac-challenge-local-politicians/

Government Issues ministerial statement on Atos http://www.internaldpac.org.uk/DPACClone/2013/07/government-issues-ministerial-statement-over-atos/

Bromley/Croydon DPAC join UKUncuts Stuff the Banks http://www.internaldpac.org.uk/DPACClone/2013/07/bromleycroydon-dpac-stuff-the-banks-update/

DPAC takes part in the anti-fracking protests at Balcombe where Caroline Lucas is arrested

August

Updates for Reclaiming Our Futures 7 days of Action http://www.internaldpac.org.uk/DPACClone/2013/08/reclaiming-our-futures-29th-aug-4th-sept-updates/

UK Disabled peoples’ Manifesto launched http://www.inclusionlondon.co.uk/UK%20Disabled%20peoples%20Reclaiming%20Our%20Futures%20Manifesto

John McDonnell puts forward an Early Day motion on the UK Disabled Peoples’ Manifesto put together by DPAC, Inclusion London, ALLFIE and Equal Lives Norfolk

Early Day Motion 483: Disabled People’s Manifesto
That this House warmly welcomes the launch of the UK Disabled People’s Manifesto, Reclaiming our Futures, developed by disabled people and their organisations across the UK, which sets out the shared vision of disabled people for an inclusive and equal society free from economic, social and cultural barriers; and urges all political parties represented in this House to engage in a constructive dialogue with the disabled people’s organisations promoting the manifesto with the aim of achieving its objectives. – See more at: http://www.internaldpac.org.uk/DPACClone/2013/09/early-day-motion-483-disabled-peoples-manifesto/#sthash.VWGXvrlo.dpuf

 

DPAC are asked by UN to assist Raquel Rolnik UN Special Rapporteur on Housing prior to her visit to the UK . The visit and her findings that the bedroom tax is regressive and unfair cause Tory ministers to say she should sort her own country out, she is a Marxist and produce other ridiculous statements in the right wing media http://www.internaldpac.org.uk/DPACClone/2013/09/un-investigator-recommends-for-bedroom-tax-to-be-scrapped-immediately/

DPAC block the front entrance of BBC for non reporting of the true situation in the UK under welfare cuts as part of the Reclaiming Our Futures 7 days of action http://www.katebelgrave.com/2013/09/disabled-people-against-cuts-block-front-entrance-of-bbc-portland-place/

DPAC host art exhibition and night of entertainment, plus a day debate on the continued relevance of the Social Model with Anne Rae, Colin Barnes and Debbie Jolly

The Brilliant Kate Belgrave writes on protests and Government Extremism, protests are held outside the DWP, the Department for Education, the Department of Energy, and the Department of Health before moving on to Parliament to host the launch of the UK Disabled People Manifesto: ‘reclaiming our Futures on the UK Freedom Drive day part of the Reclaiming Our Futures week of action

http://www.internaldpac.org.uk/DPACClone/2013/09/protests-and-government-extremism-kate-belgrave/

 

DPAC posts UK Freedom Drive film by Reel News http://www.internaldpac.org.uk/DPACClone/2013/09/uk-freedom-drive-the-film/

 

See also http://www.internaldpac.org.uk/DPACClone/2013/09/dpacrof-4th-september-highlights/

 

 

September

 

DPAC works with Just Fair on Independent Living Issues ahead of a planned visit by the UN special rapporteur on disability http://www.internaldpac.org.uk/DPACClone/2013/09/dpac-works-with-just-fair-on-independent-living-issues/

We publish George Berger from Sweden report on Atos, KPMG and the NHS http://www.internaldpac.org.uk/DPACClone/2013/09/atos-kpmg-and-the-nhs-be-afraid-be-very-afraid/

DPAC launches a new report on the WCA http://www.internaldpac.org.uk/DPACClone/2013/09/dpac-report-work-capability-assessment/

Two of the DPAC co-founders go to Strasbourg to join the European Network on Independent Living for the 6th ENIL Freedom Drive to march to the European Parliament and tackle MEPs. Debbie Jolly is elected to serve another term on the ENIL Board and presents on behalf of DPAC on protest and what is happening in the UK under imposed austerity http://www.enil.eu/campaigns/freedom-drive/

DPAC co-organises with Wow Petition for 10,000 Cuts Memorial for those that have died through Atos and in solidarity with all suffering under Cameron’s regime of imposed austerity http://www.internaldpac.org.uk/DPACClone/2013/09/10k-cuts-and-counting-video/ see also http://www.internaldpac.org.uk/DPACClone/2013/09/10000-cuts-and-counting-linda-burnip/

Dr Alison Wilde discusses the Paralympic Legacy http://www.internaldpac.org.uk/DPACClone/2013/09/paralympic-legacy-but-which-one/

DPAC supports the Ontario Coalition against Poverty who Government want to follow the lead of the UK in denying people their entitlements http://www.internaldpac.org.uk/DPACClone/2013/09/call-out-to-support-ontario-coalition-against-poverty/

October

IDS found misleading again http://www.internaldpac.org.uk/DPACClone/2013/10/ids-found-misleading-again/

DPAC and Black Triangle consider legal action against GPs who refuse to provide evidence for disabled people and those with long term health issues http://www.internaldpac.org.uk/DPACClone/2013/10/legal-action-has-your-gp-refused-to-provide-further-medial-evidence-for-your-dwp-appeal/

Anita Bellows write another stunning piece exposing the bedroom tax http://www.internaldpac.org.uk/DPACClone/2013/10/bedroom-tax-the-policy-which-could-only-succeed-if-it-failed-anita-bellows/

DPAC organises vigil for Mental Health Resistance WCA case appeal by DWP http://www.internaldpac.org.uk/DPACClone/2013/10/vigil-for-wca-case-support-mental-health-resistance-network-21st-october/

DPAC joins UKUncut to protest to save Justice

DPAC join in protests against staff cuts on London Tubes http://www.internaldpac.org.uk/DPACClone/2013/10/boriss-latest-attacks-against-accessibility-and-safety-on-london-transport/ also see http://www.internaldpac.org.uk/DPACClone/2013/10/unions-unite-with-campaigners-on-tube-and-station-cuts/

DPAC publicises Punishing Poverty a report on Sanctions by Manchester CAB http://www.internaldpac.org.uk/DPACClone/2013/10/sanctions-punishing-poverty-new-report-by-cab/

DPAC publishes info on mandatory reconsideration http://www.internaldpac.org.uk/DPACClone/2013/10/some-information-on-mandatory-reconsideration-in-force-from-october-28th-2013/

UK Disability history month kicks off http://www.internaldpac.org.uk/DPACClone/2013/10/uk-disability-history-month-launch-event/

November

ILF users win appeal, Government say they won’t fight decision –a success but we wait for the Government next moves http://www.internaldpac.org.uk/DPACClone/2013/11/gov-will-not-appeal-court-ruling-on-closure-of-ilf/

http://www.internaldpac.org.uk/DPACClone/2013/11/victory-for-independent-living-rights-in-english-appeal-court/

DPAC reposts the critique of the Henwood and Hudson report as some in the disability field still claim that ILF should close http://www.internaldpac.org.uk/DPACClone/2013/11/why-the-henwood-and-hudson-report-failed-in-justifying-the-closure-of-the-independent-living-fund/

DPAC ask members and supporters to write to Penning on ILF http://www.internaldpac.org.uk/DPACClone/2013/11/write-a-message-to-penning/

Anita Bellows asks why Litchfield as ‘independent’ assessor of the WCA when he was involved in its design http://www.internaldpac.org.uk/DPACClone/2013/11/dwp-tactics-ask-litchfield-designer-of-the-wca-to-review-it-anita-bellows/

DPAC publishes info on fuel poverty as we receive more emails from people without heating or electricity due to sanctions and welfare cuts http://www.internaldpac.org.uk/DPACClone/2013/11/fuel-poverty/

Independent Living rights News is published on DPAC http://www.internaldpac.org.uk/DPACClone/2013/11/independent-living-rights-news-17-november-2013/

http://www.internaldpac.org.uk/DPACClone/2013/11/independent-living-rights-news-edition-2/

Paddy Murphy writes on the apparent idiocy of DECC http://www.internaldpac.org.uk/DPACClone/2013/11/disabled-people-and-fuel-poverty-what-does-decc-know-anyway/

DPAC attends the bedroom tax lobby at Parliament http://www.internaldpac.org.uk/DPACClone/2013/11/report-on-the-bedroom-tax-lobby-meeting-westminster-tuesday-12th-november-2013/

DPAC , Fuel Poverty Action and the London Pensioners are joined by hundreds on the streets to protest at unacceptable fuel poverty and deaths while the energy companies continue to make huge profits http://www.internaldpac.org.uk/DPACClone/2013/11/hundreds-protest-at-big-six-energy-companies-over-fuel-poverty-deaths/

http://www.internaldpac.org.uk/DPACClone/2013/11/npower-protest-against-31000-fuel-poverty-deaths-this-year/

DPAC supports ALLFIE’s campaign on no return to segregated education http://www.internaldpac.org.uk/DPACClone/2013/11/no-return-to-segregrated-education-please-sign/

DPAC and Inclusion London hear heartbreaking testimonies from disabled people affected by the cuts. We send them to the special rapporteur on disability.

DPAC and Inclusion London hold an Emergency  lobby at Parliament on Independent living to launch the DPAC report on Independent Living http://www.internaldpac.org.uk/DPACClone/2013/11/independent-living-and-the-cumulative-impact-of-cuts-from-the-streets-to-the-commons/

Mary Laver and ILF user film on life without ILF is posted http://www.internaldpac.org.uk/DPACClone/2013/11/an-important-request-on-ilf-from-mary-laver/

The Disability Crime Network write to the attorney General on disability hate crimes  http://www.internaldpac.org.uk/DPACClone/2013/11/disability-hate-crime-network-letter-to-attorney-general/

December

Anne Novis writes on hate crime http://www.internaldpac.org.uk/DPACClone/2013/12/a-life-less-valid-when-is-a-hate-crime-not-a-hate-crime-by-anne-novis-mbe/

Belgium vote yes on euthanasia for minors now accepted as law http://www.internaldpac.org.uk/DPACClone/2013/12/belgium-vote-yes-on-euthanasia-for-minors/

DPAC urges members and supporters to join Boycott Workfare in online action against workfare http://www.internaldpac.org.uk/DPACClone/2013/12/take-online-action-against-the-workfare-conference/

We publicise Habinteg’s report on the effect of the bedroom tax on independent living  http://www.internaldpac.org.uk/DPACClone/2013/12/what-price-independent-lives-a-new-report-on-bedroom-tax/

Government lose appeal against decision that WCA discrimates against those with mental health issues.  The Mental Health Resistance Network (MHRN) who instigated the case against the WCA celebrate another victory. MHRN a grassroots group were later joined by the charities, but without MHRN the case would not have got to the courts. http://www.internaldpac.org.uk/DPACClone/2013/12/victory-against-wca/

DPAC joins Boycott Workfare in targeting companies replacing paid work with workfare http://www.internaldpac.org.uk/DPACClone/2013/12/target-the-companies-replacing-paid-work-with-workfare/

DPAC support ALLFIE’s call for action http://www.internaldpac.org.uk/DPACClone/2013/12/educate-dont-segregate-allfies-call-for-action-on-the-10th-december-1pm/

We publicise Equal Lives’ video on how the cuts effect at the local level http://www.internaldpac.org.uk/DPACClone/2013/12/our-lives-equal-lives-norfolk-and-the-cuts/

DPAC posts video by Colin Barnes on the importance of the social model by UCU http://www.internaldpac.org.uk/DPACClone/2013/12/interview-with-colin-barnes-what-are-the-origins-of-the-social-model-of-disability-and-why-is-it-so-important-to-equal-rights-campaigners/

DPAC attends open meeting with Mike Penning http://www.internaldpac.org.uk/DPACClone/2013/12/feedback-from-todays-meeting-with-mike-penning/

DPAC publicises the case of Anthony  Kletzander’s  treatment in Ireland at the hands of ‘professionals’ as he is denied basic rights http://www.internaldpac.org.uk/DPACClone/2013/12/update-anthony-kletzander-needs-your-help/

Owen Jones names DPAC as one of his ‘person of the year’ choices for 2013 http://www.independent.co.uk/voices/comment/who-is-your-person-of-the-year-9018337.html

 

 

 

 

 

 

 

Dec 052013
 

Crippen Gove is in bed with the ghosts of segregation past  and future

ALLFIE WILL BE VISITING THE DEPARTMENT FOR EDUCATION on the 10th DECEMBER TO DEMAND THE GOVERNMENT BANISHES THE GHOSTS OF SEGREGATION PAST BY WARNING ABOUT THE NEW GHOSTS OF SEGREGATION FUTURE

CALL FOR ACTION on the 10th DECEMBER!  

WHERE & WHEN:

Date:      10th December @ 1 pm

Meeting place: the Café in Abbey Centre, 34 Great Smith Street, Westminster London SW1P 3BU

Contact:  Simone/Tara at ALLFIE – 0207-737-6030                               simone.aspis@allfie.org.uk / tara.flood@allfie.org.uk  / www.allfie.org.uk

ALLFIE logo

THE FACTS:

Since 2010 the numbers of disabled children and young people being forced into segregated education is on the increase, despite the Government’s UNCPD Article 24 (Right to Inclusive Education) obligations to develop a fully inclusive mainstream education system. This year the Government is pushing through SEN reforms that will increase, even further, the numbers of disabled children and young people being forced into segregated education – this is despite David Cameron, in 2010, promising parents of disabled children he would do all that he could to support their choice of inclusive education.

Time and time again, the Government have refused to listen to disabled people and our allies about the damaging impact the SEN reforms will have on the rights for disabled students and pupils to be included in mainstream education –
ENOUGH IS ENOUGH!!

We must ACT NOW to tell Michael Gove (Secretary of State for Education) and the Coalition Government that there must be no return to segregation!!

Today we are presenting the following DEMANDS to Michael Gove and the Coalition Government:

  • Disabled children and young people MUST have a right to be included in mainstream education.

 

  • Disabled children and young people MUST have a right to receive support to participate in mainstream education in accessible buildings.

 

  • The Local Offer of services MUST support disabled children and young peoples’ access to mainstream education.

 

  • Local Authorities MUST continue to have a strategic duty to promote and develop the capacity of mainstream schools to deliver inclusive education practice as set out in the Inclusive Schooling Guidance.

    Join ALLFIE’s “EDUCATE DON’T SEGREGATE” Campaign now!
     
Dec 022013
 

ALLFIE WILL BE VISITING THE DEPARTMENT FOR EDUCATION on the 10th DECEMBER TO DEMAND THE GOVERNMENT BANISHES THE GHOSTS OF SEGREGATION PAST BY WARNING ABOUT THE NEW GHOSTS OF SEGREGATION FUTURE !

WHERE & WHEN:
Date: 10th December @ 1 pm
Meeting place: the Café in Abbey Centre, 34 Great Smith Street, Westminster London SW1P 3BU
Contact: Simone/Tara at ALLFIE – 0207-737-6030 simone.aspis@allfie.org.uk / tara.flood@allfie.org.uk / www.allfie.org.uk

THE FACTS:
Since 2010 the numbers of disabled children and young people being forced into segregated education is on the increase, despite the Government’s UNCPD Article 24 (Right to Inclusive Education) obligations to develop a fully inclusive mainstream education system. This year the Government is pushing through SEN reforms that will increase, even further, the numbers of disabled children and young people being forced into segregated education – this is despite David Cameron, in 2010, promising parents of disabled children he would do all that he could to support their choice of inclusive education.
Time and time again, the Government have refused to listen to disabled people and our allies about the damaging impact the SEN reforms will have on the rights for disabled students and pupils to be included in mainstream education –
ENOUGH IS ENOUGH!!
We must ACT NOW to tell Michael Gove (Secretary of State for Education) and the Coalition Government that there must be no return to segregation!!
Today we are presenting the following DEMANDS to Michael Gove and the Coalition Government:
• Disabled children and young people MUST have a right to be included in mainstream education.

• Disabled children and young people MUST have a right to receive support to participate in mainstream education in accessible buildings.

• The Local Offer of services MUST support disabled children and young peoples’ access to mainstream education.

• Local Authorities MUST continue to have a strategic duty to promote and develop the capacity of mainstream schools to deliver inclusive education practice as set out in the Inclusive Schooling Guidance.

Join ALLFIE’s “EDUCATE DON’T SEGREGATE” Campaign now!

 

View the petition

Nov 282013
 

ALLFIE NEEDS YOU!

Please sign our petition calling for

Lord Nash and the Govt to put back

the guidance on Inclusive Education

into the SEN Code Practice

The Government are threatening to turn back the clock for disabled children and young people with SEN by placing them back into special schools – BREAKING AN ELECTION PROMISE to parents who were told by David Cameron that he would do all that he could to help parents who want their children included in mainstream. Disabled people know through experience that segregated education does not work if we want to live together in society as respected adults.

The Government have removed all the guidance for Local Authorities and schools on inclusive education in their revised SEN Code of Practice which accompanies the new Children and Families Bill. The Guidance helps schools to do inclusion well.

WE KNOW INCLUSION WORKS, enabling thousands of disabled children to access a mainstream education where they can learn, make friends and feel they belong in their local communities – something which is impossible in even the best resourced special schools. Removing this guidance will waste over 20 years of painstaking development in the field of inclusion, leaving the coast clear for the rapid expansion of separate and privatised schools and colleges which is already underway. Parents will lose confidence in the ability of the mainstream to make safe and appropriate arrangements for their children and young people, and will feel they have no option but to accept segregation.

We must stop them now!

Lord Nash has responsibility for steering The Bill and the Code through the House of Lords where amendments can still be made before the final vote. ALLFIE has been trying to get a meeting with Lord Nash but he has either ignored or denied our requests – our patience has now run out! Let us take thousands of signatures to Lord Nash on the 10th December and show him that we will not accept a return to the mistakes of the past which are now threatening a whole new generation of young disabled people and those with Special Educational Needs.

PLEASE Sign the petition and say NO RETURN TO SEGREGATION!

Lord Nash, Department for Education: Government must put back all the guidance on Inclusive Education in the Special Educational Needs Code of Practice so Schools and College can be better at including disabled children and young people<http://www.change.org/en-GB/petitions/lord-nash-department-for-education-government-must-put-back-all-the-guidance-on-inclusive-education-in-the-special-educational-needs-code-of-practice-so-schools-and-college-can-be-better-at-including-disabled-children-and-young-people?utm_source=guides&utm_medium=email&utm_campaign=petition_created>
Once you have signed it please forward to all of your networks.

Alliance for Inclusive Education

Nov 122013
 

Add your voice to DPAC’s survey–what needs to change? What are the key issues for disabled people under this Government? We know most of them-but what about specific barriers: education, transport, building more accessible housing-are they getting worse or better?…Tell us…so it’s not just us arguing for change…

 https://www.surveymonkey.com/s/WYZVQXV

Oct 152013
 

The Equality and Human Rights Commission is engaging with disabled people and disabled people’s organisations on the key issues under the Disability Convention (UNCRPD).

You can find the questionnaire here http://www.equalityhumanrights.com/human-rights/our-human-rights-work/international-framework/un-convention-on-the-rights-of-persons-with-disabilities/the-un-disability-convention-participation-questionnaire/

DPAC is calling on disabled people to tell the EHRC about the impact of this stigmatising government and the concerns we have about the replacement of the social model of disability with the bio psycho social model.

see for more on biopsychosocial model: http://www.internaldpac.org.uk/DPACClone/2012/04/a-tale-of-two-models-disabled-people-vs-unum-atos-government-and-disability-charities-debbie-jolly/

 

Sep 172013
 

Based on the advice and guidance given by Just Fair Consortium members during the 11th July evidence gathering meeting, the Just Fair Consortium is currently working with disabled people and DPAC to produce a report examining the right to independent living in the austerity era. 

 Just Fair will launch the report in the Houses of Parliament in late November 2013.

 Within this remit, the report will analyse the following issues:

 * Personal Independence Payment (PIP);

* Under-occupancy penalty (“Bedroom tax”/”Spare room subsidy”);

* ‘Benefit cap’;

* Employment and Support Allowance (ESA) and the Work Capability Assessment (WCA);

* Universal Credit;

* Cuts to social care; and

* Closure of the Independent Living Fund. 

 Disabled people are leading on all elements of the research and advocacy work, including selection of the report theme and sub-issues, submission of real-life case-studies, contribution of hard-hitting statistical analysis and presentation of testimony evidence at the November report launch. 

 DPAC have sent Just Fair a number of reports and case studies. We will keep you updated, in the meantime if you have anything you’d like included, please email us at: mail@dpac.uk.net

The Just Fair website can be found at http://just-fair.co.uk/

 

Aug 292013
 

Scope charity says they care about disabled peoples’ rights to access universal services close to their homes as part of their high profile ‘Britain Cares’/ ‘I Care’ campaign.

At the same time Scope is fundraising and asking the state to continue funding their institutionalised and segregated residential and educational services for disabled people.   

Throughout history special residential educational and care institutions have claimed to provide the education and care that disabled people need.  

We are here to dispel the myth of segregated ‘care’ and education services that are provided without our consent.  

do not:

·        Support disabled people’s choice and control over their lives.

·        promote disabled peoples inclusion in their local communities  

·        Support disabled people’s aspirations in education, training and employment.  

·        Support positive relationships between disabled and non-disabled people.  

·        Challenge the unacceptability of disability-related bullying and hate crime.

Scope is one of range of big business disability charities that are funded by the state to provide segregated education and care services at the expense of providing funding for independent living and inclusive education- things that are wanted by disabled people, their organisations and allies to provide proper independent living.

SCOPE supports the full implementation of the UN Convention of Persons with Disabilities that includes disabled peoples’ rights to inclusive education (Article 24) and Independent Living (Article 19).    

If SCOPE truly believes in disabled peoples’ human rights to be included in their local communities then they must stop the patronising caring campaign and be prepared to make fundamental changes to their paternalistic services.   

DISABLED PEOPLE WANT SCOPE ‘TO DARE’ TOO…..

We dare SCOPE to close their special schools and colleges.

We dare SCOPE to develop alternative services that will support disabled peoples access to mainstream education.

We dare SCOPE to support ALLFIE’s Inclusive Education manifesto demands. 

We dare SCOPE to close residential institutions and develop real independent living alternatives for disabled people

We dare SCOPE to stop all segregated services such as day care to enact the full inclusion of disabled people

We dare SCOPE to stop claiming that they work ‘with’ disabled people while they continue to gain service contracts from local authorities when there are active user-led disabled organisations in that area.

It’s not only Scope but all the other disability big charities who claim to support disabled peoples human rights that must be challenged and be prepared to dare to do what disabled people want: a right to be supported, to be educated, and to live in their local communities, free from the possibility of state sanctioned institutionalisation.    

Please join DPAC’s Reclaiming Our Futures campaign….. We Launch the ‘I Dare’ Campaign against Segregation and the Removal of our Rights online campaign on the 3rd Sept

disabled extremist i dare

With thanks to Ania for pic

‘I Dare’ Day 3rd Sept

This is not just about SCOPE but all those other big disability charities Leonard  Cheshire, MENCAP, MIND you name them- they all do it-they all claim to speak in our name. Add to this, this Government and we ‘dare’ to campaign against it all.

Sept 3rd is DPAC ‘s ‘I Dare’ day, a day of online action on twitter and Facebook , with a few surprises too.

We want to see people tweeting and spreading the word across social media against all those that try to take our rights away – that segregate us, that say they speak for us-we want to show them that we dare to fight back.

Flood twitter and Facebook with ‘I dare’ messages –here’s some we made earlier…..

I dare campaign

 

#I dare: speak up and campaign for independent living and to save ILF

#I dare: speak out about the lost of support for disabled people

#I dare: speak out on the increasing suicides and premature deaths from Atos assessments

#I dare: speak out on the increasing number of disabled people left without food because of cuts

#I dare: to tell the truth about what is happening in this country to disabled people under this Government

#I dare: to say that its not ‘care’ disabled people want, but the right to make our own choices

#I dare: to say I want rights not charity

#Britain dares #I dare #We dare

Inclusive Education NOT segregated Education for Disabled children and young people

#I dare to experience mainstream education!

# I dare the Govt to implement the education related recommendations in the EHRC Hate Crime reports – what are they afraid of!

#I dare the government to give disabled people choice of mainstream provision – what have they got to lose other than a few quid invested in segregated ed!

And why not send an ‘I dare’ Picture to SCOPE to let them know what you think http://www.britaincares.co.uk/ show them #Britain Dares, better send us a copy too at: mail@dpac.uk.net

 

 

 

 

 

Aug 242013
 

National protest to defend disabled people’s rights and freedoms and demand equality and inclusion

Last year we shamed Atos and occupied the Department for Work and Pensions in opposition to the injustice and distress caused by the Work Capability Assessment. A year later and the only Paralympic legacy most disabled people have seen is one of more cuts and more anger.

Research has shown that cuts are targeting disabled people. Meanwhile government and the media misrepresent figures and statistics to label disabled people as benefit scroungers.

We say this isn’t right.

We say we need to unite and fight against injustice.

 Join us for the final day of the Reclaiming Our Futures Disabled People’s week of action as we protest in Westminster.

 Four themed ‘blocks’ will meet at 4 Government departments, central to the lives of disabled people. After handing over our demands, blocks will then move towards Parliament where we will formally launch the UK Disabled People’s Manifesto and present our demands to our elected representatives.

 Choose your ‘block’ and meet at 12.45pm at one of:

 Department for Education to oppose government attacks on inclusive education and a return to segregation

(SanctuaryBuildings, 20 Great Smith Street, London, SW1P 3BT)

 Department of Energy and Climate Change if you’re angry about the numbers of disabled people living in fuel poverty while the energy companies rake in ever growing profits

(3 Whitehall Pl, City of Westminster, SW1A 2AW)

 Department for Transport to challenge inaccessible transport, the opening of new inaccessible stations for Crossrail and proposed cuts to rail staff further reducing customer assistance

(Great Minster House, 33 Horseferry Rd, London SW1P 4DR)

 Department of Health to defend our NHS and demand our right to levels of social care support enabling choice, control, dignity and independence

(Richmond House, 79 Whitehall, London SW1A 2NS)

LOBBY OF PARLIAMENT:

5 – 6pm – launch of the UK Disabled People’s Manifesto

#dpacrof

reclaiming our futures

 

Aug 132013
 

dpacxx

Reclaiming Our Futures UK

 

Join this year’s week of action to protest against austerity, fight for our rights and celebrate disabled people

 

From 29th August – 4th September DPAC and other campaigns will offer a range of activities you can get involved in. These events will bring together our anger at what is happening now, and celebrate our victories won, both in the past and to come.

 

 

Our rights are being stripped away day by day, by the neo-liberal policies being imposed on us all by the Condems, leaving us without much hope for our futures – or our children’s.

 

We have been here before. Our history is littered with examples of how our community has come together when under attack to fight – and win. From the early campaigns of NLBDP (National League of Blind and Disabled People) through to the founding and manifesto of UPIAS (Union of

 

the Physically Impaired Against Segregation) and on to DAN (Direct Action Network)- Now we have DPAC leading direct action and a host of other key grass root campaigns working towards reclaiming our rights and futures.

 

We have fought our corner over 3 centuries. And those fights have brought victories; the Independent Living Movement, our early CILs (Centres for Independent Living) and early active DPO’s (Disabled Peoples Organisations) and the significant rights for disabled people (which are now under attack). They represent big victories, brought about by mobilizing in our communities around our common cause – and having the will and determination to see our demands met without compromising our rights. We have consistently united in anger and celebration.

  

Download easy read information about the week here:

DPAC easy read (2)

 

DPAC Reclaiming our Futures Action

 

This autumn, we are asking our community to come together in anger, and celebration again – and to unite around our demands

 

We will be launching the UK Disabled People’s Manifesto setting out our vision of how the resources, structures and institutions of our society today can be re-designed to empower disabled people to take part in life on our terms. Disabled people are, and always will be, the experts on our lives and our self-determination. It will be a vision and practical plan that we can take forward in our communities, workplaces and lives to reclaim our futures.

 

In the build up to the manifesto launch, DPAC is leading The ‘Reclaiming Our Futures’, seven days of action to protest against the targeting of disabled people by austerity measures, to fight for our rights for inclusion and independence as equal citizens and to celebrate the value, pride and self determination of disabled people.

 

From 29th August – 4th September DPAC and other campaigns will offer a range of activities you can get involved in. These events will bring together our anger at what is happening now, and celebrate our victories won, both in the past and to come.

 

The plan below is only half the story. We want YOU, your Deaf and Disabled People’s Organisation, your campaign group, your community, your friends to put on events and get involved too. Can’t get to our exhibition? – then put on your own. Can’t get to our direct action? – then do your own. Barbecues, debates, quiz nights, family days, picnics – whatever! ACT – in celebration or in anger! (PS don’t forget to let us know what you’re doing).

 

 

Day by Day: 29th August-4th September

 

 

Thursday 29th August – YOU launch our 7 days of action

 

A range of resources will be available for your use as we ask all supporters to start our week of action with an online blitz. You will be the ones creating the buzz and the hype sending letters and twitter messages to targets of your choice ranging from MPs to disability charities to the media. We will be producing twibbons and memes but make and circulate your own. If you haven’t got a Social Media account (such as Facebook & Twitter) set one up now, link to DPAC ( twitter: @Dis_PPL_Protest) and let’s create a cyber wave. #dpacrof

 

The launch will coincide with Transport for All’s Day of Action to make CrossRail accessible: http://www.internaldpac.org.uk/DPACClone/2013/07/day-of-action-to-make-crossrail-fully-accessible-thursday-29th-august-2013/

 

 

 

Friday 30th August – Local Protests

 

Last year during the ATOS Games over 30 local actions took place around the UK Local actions mean you get to choose the target of your choice. You could take the Reclaiming Our Futures manifesto to present at your local MP’s constituency office, spread it through social media, protest on the streets against segregated education, the proposed ILF closure or show solidarity at your local Remploy site (for those few factories in their last weeks of operation). Alternatively, you might want to lobby your local Council on the Bedroom Tax and cuts to local services/support. Oh, and as we know ATOS offices are still around too….we’re sure you have other great ideas to add… Remember to let us know what you are doing so we can promote your actions. We will be producing local action resource packs but any materials you develop please send us copies to share with other protests and online.

 

 

Saturday 31st – Disability, Art & Protest Exhibition and Fundraising Gig

 

An exhibition and sharing of work exploring disability, art and protest followed by a ticketed fundraising gig run in partnership with Madpride and Tottenham Chances. Come during the day and join in our banner making workshop to prepare for the big Freedom Drive on the 4th September. If you would like to nominate an artist, collective and/or piece of work please let us know (including any links) and we will try to get them involved. If you want to do a local, street or online art protest too-this could be the day to do it.

 

Venue: Tottenham Chances, 399 High Road, London, N17 6QN Times:

 

12 – 7pm Exhibition: disability, art and protest

1 – 3.30pm Banner and placard making workshop

 

4 – 6pm Work Sharing

7.30pm till late Gig

 

 

Sunday 1st September – Reclaiming the Social Model: the social model in the 21st Century

 

Anne Rae: former UPIAS and current chair of the Greater

Manchester Coalition of Disabled People (GMCDP),

 

Colin Barnes: Professor of Disability Studies at Leeds Centre for Disability Studies

 

 

As government and the private sector increasingly use a so-called ‘modern understanding of disability’ to redefine who is and who isn’t disabled it is more important than ever that we understand, defend and promote the social model of disability. This isn’t helped when the social model is not fully supported within our movement. This event will be a chance to hear from a range of speakers and to discuss why the social model is still relevant today to our lives and our futures and to map out what we need to do to fight for it. The event will be live-streamed with the opportunity for people to participate in the discussion virtually. We will also be promoting a range of resources around the social model.

 

Venue

UNITE House, 128 Theobald’s Road, Holborn, WC1X 8TN

Time: 12.30 – 4.30pm

 

 

Monday 2nd September – Direct Action

 

Despite the huge efforts of thousands of disabled people throughout the country, it is increasingly difficult to find spaces where lies, inaccuracies and mis-use of statistics can be challenged. DPAC recently released a study into how the DWP uses all of these to vilify and demonize disabled people.

 

See more at: http://www.internaldpac.org.uk/DPACClone/2013/06/lies-damn-ids-and-statistics/#sthash.MAk5nTiU.dpuf

 

But why is this down to us? People should be presented with both sides of the story and this isn’t happening. Disabled people are having to find ways to make sure our truths will be heard. Watch this space…

 

 

Tuesday 3rd September – ‘I Dare’ day

 

A day of online action to reinforce that we want ‘Rights not Charity’, and a society where we are able to operate on our own terms as disabled people. Dare to ask for Rights not Charity. Dare to be an activist. Dare to ask more of ‘our’ organisations. We aren’t asking for Care, we want Power: Power to write the script for our own lives, and not to be written out or written off by others. A range of actions and captions will be available for you to capture in an image and circulate online.

 

 

Wednesday 4th September – UK FREEDOM DRIVE

 

A final-day march and events in and around Parliament. Four

 

themed ‘blocks’ will meet at 4 Government departments, central to the lives of disabled people. After handing over our demands, blocks will then move towards Parliament for a lobby where we will formally launch the UK Disabled People’s Manifesto and present our demands to our

 

elected representatives.

 

Choose your ‘block’ and meet at 12.45pm at one of:

 

·        Department for Education to oppose government attacks on inclusive education and a return to segregation (Sanctuary Buildings, 20 Great Smith Street, London, SW1P 3BT)

 

·        Department of Energy and Climate Change if you’re angry about the numbers of disabled people living in fuel poverty while the energy companies rake in ever growing profits (3 Whitehall Pl, City of Westminster, SW1A 2AW)

 

·        Department for Transport to challenge inaccessible transport, the opening of new inaccessible stations for Crossrail and proposed cuts to rail staff further reducing customer assistance (Great Minster House, 33 Horseferry Rd, London SW1P 4DR)

 

·        Department of Health to defend our NHS and demand our right to levels of social care support enabling choice, control, dignity and independence (Richmond House, 79 Whitehall, London SW1A 2NS)

 

Lobby of Parliament: 5 – 6pm – launch of the UK Disabled People’s

Manifesto

 

WE WANT EVERYBODY TO JOIN US FOR THE FREEDOM DRIVE ideally in person, but also online-this is for everyone everywhere. There will be accessible transport from a variety of towns and cities throughout the country (details to follow) and there is some funding available for transport but we will need your co-operation and patience to make this work for everybody, so please bear with us and note that while DPAC members will be given priority we want to support as many people as we can. If you can’t get there send a photo or your name and you can march with us.

 

This week of action is yours. Please take part at whatever level suits you – BUT MAKE SURE YOU TAKE PART. Share our events, resources and actions as far and wide as you can.

 

 

 

Let’s Reclaim Our Futures, together!

 

 

DPAC web site: www.dpac.uk.net

 

DPAC facebook:

 

https://www.facebook.com/pages/DPAC-Disabled-People-Against-Cuts/213545112011414?fref=ts(Open Community group- including allupdates from DPAC)

 

https://www.facebook.com/groups/DPAC2011/?fref=ts(original open groupDPAC page- faster paced and more opinion driven than community group )

 

DPAC Twitter: @Dis_PPL_Protest 

 

DPAC email: mail@dpac.uk.net

 

 

Remember if you need help with funding to get to London (4th Sept) email us at mail@dpac.uk.net with details. DPAC members will get first priority but we’re hoping to be able to contribute to all that want to come along. If you are unable to come but would like your picture carried send us a photo or message. Please get in touch with any other queries as well and we’ll try to help.

Download this as a PDF Doc: http://www.internaldpac.org.uk/DPACClone/wp-content/uploads/2013/08/Reclaiming-Our-Futures-call-out-long-w-logos-v2.pdf

 Download this as a Word Doc: http://www.internaldpac.org.uk/DPACClone/wp-content/uploads/2013/08/Reclaiming-Our-Futures-call-out-long-w-logos-v2-1.doc

 

 Reclaiming our Futures is supported by The Edge Fund, Andrew Wainwright Reform Trust, Network for Social Change, Black Triangle, Mental Health resistance network, Wow Petition, Fuel Poverty Action, Occupy London, TUC, UK UNCUT, Boycott Workfare, Right to Work, Just Fair, Unite Disabled Workers, BFAAWU, European Network on Independent Living, Anti-Bedroom Tax and Benefits Justice Federation, and more…..

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