Monday, January 31, 2011

Call for interest

 

The uNclear Family ('Dis-Action Transfer')

 

Background: The 'uNclear Family' takes as a starting point a set of early 1980's dry (rub down) transfer architecture images used to illustrate designs for public spaces such as shopping developments, cityscapes, town planning designs and the 'Action Transfers' series that came complete with it's own themed panorama. These groups of images are conspicuous in that they show a hypothetical nuclear family type community who show no signs of disability.

 

What: A collaborative arts project for deaf and disabled artists/persons led by Bruce Davies artist in residence for  'IMPACT' – an 8 week residency established by Arts Council South West. The 'uNclear Family' is a context driven installation project that addresses issues of visual representation of the deaf and disabled community. The basis of the work will emerge from responses and research conducted during the residency at Holton Lee and through the establishment of an extensive on-line creative focus group.  The project uses audience participation to inform and develop  the projects outcome to create a mutually accessible platform for expression, enabling participants to translate and convey their own experiences and perspectives visually. 

 

Who: Deaf or disabled artists/persons who are interested in collaborating and contributing toward a visual debate that will lead to the production of a series of images that explore issues of representation of the deaf and disabled community. The results of this enquiry will then be placed together to create a new inclusive 'Dis-Action Transfer' community. Once the work is complete and installed the audience of the new work will be tasked with addressing issues of expectations, acceptability and representation of the deaf and disabled community in contemporary society. How they think they might fit into this new inclusive community will be part of this question.

 

How: Contributors are invited to respond to 'The uNclear Family' by submitting a drawing, image (jpegs) or short descriptive text illustrating how they might visualise themselves and/or life experiences that relate to this context. Responses should be submitted via email. The selected contributions will be translated, where appropriate, in the graphic style of the original set, or as originally conceived by the originator and inserted into a new 'uNclear Family' to create new ways of seeing this new  community. Responses are also welcomed in regard to the 3 proposed environments that will form the back ground on which these images will be presented.

 

Where: Holton Lee/On-line. Potential dates, sites and venues, as yet unconfirmed for presenting the work at Holton Lee. Public spaces and gallery settings both regionally and nationally will be explored.

 

When: Now

Final submission date for images February – March 15th 2011

Contact: Bruce Davies via email for more info/submissions: bruceisanartist@googlemail.com

 

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MS Trust statement on proposed Disability Living Allowance changes

31 January 2011

Author: MS Trust

The MS Trust is concerned that the change from Disability Living Allowance (DLA) to Personal Independence Payments (PIP), has a risk of disadvantaging people with multiple sclerosis.

The MS Trust calls on the government to:

  • Ensure that people with MS are not penalised for making personal efforts to manage their disabilities and increase their quality of life
  • Define what they mean by updating the definitions of disability.
  • Explain how aids and adaptations are to be taken into account in the new assessments. An aid or adaptation only assists - it does not solve the problem, the disability still exists.
  • Describe the assessment process so that it is clear whether they will be sensitive enough to accommodate the fluctuating nature of MS.
  • Define how they will handle those people who have currently been told they have DLA for life? MS is a long-term neurological condition and for life as there is no cure.
  • Ensure that PIPs encourage independence not just save money.
  • Clarify the proposal to remove mobility allowance for people in residential care to ensure people with MS, who may have been forced into residential care at a young age, do not have their ability to be part of the wider society removed.

Consultation

The government launched a consultation about the changes to DLA in December. The MS Trust would encourage anyone who hasn't yet responded to do so before the closing date of 14 February.

In the press release announcing the consultation, the Minister for Disabled People, Maria Miller, says the government "remain fully committed to the principles of DLA as a non-means tested cash benefit". However, DLA is also described as "a poorly targeted and unsustainable benefit", with attention drawn to the cost, estimated at £12billion, and the perception that it "can act as a barrier to work". As part of the process, the revised replacement for DLA will be called the Personal Independence Payment.

The consultation is asking about three areas:

  • Simplification of the purpose and eligibility for the benefit
  • Creating a more objective assessment process for new and existing claimants
  • How to prevent the benefit acting a barrier to a employment
Respond to the consultation on the Department of Work and Pensions (DWP) website
DWP press release
Benefits - Living with MS

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Sunday, January 30, 2011

Kidz in the Middle - Visitors FREE entry ticket attached!

 
'Kidz in the Middle'

Thursday, 10th March 2011 at the Jaguar Exhibition Hall, Ricoh Arena, Coventry

One of three of the largest FREE UK exhibitions totally dedicated to children and young adults with disabilities and special needs, their families, carers and the professionals who support them.

Thank you for your interest in our Kidz events. We are now pleased to attach a copies of the visitors' FREE entry ticket for this exhibition. Although the tickets are

not compulsory they do save time on registration, if completed beforehand.  They also include the timetable of all the FREE seminars taking place throughout the day, the exhibitors list and details of the fun and features running alongside the event so can help you plan your day. 

Attending the 'Kidz' events is more crucial now than ever before. The Government continues to commit to the investment of £340 million in equipment and wheelchair services, and has recently announced that they will be providing local authorities with £800 million to help fund short breaks for families with disabled children.

As  funding continues to be a major concern, the 'Kidz Team' have taken a proactive approach and introduced 'The Funding Point' offering advice and information on alternative funding streams for equipment and much more to all our Kidz events.

You can help ensure the parents, children, and the professionals who work with them have access to the most up to date information on equipment, products and services by circulating the enclosed information on the Kidz events. We are more than happy to send more tickets if you can circulate.  Please contact the Kidz Team on the number below.

Thank you

Carmel Hourigan

Admin & Exhibitions Manager

0161 214 5959

Breaking news!!!

You can now follow the Kidz events on Facebook.....

Kidz up North/Kidz in the Middle/Kidz South....... follow the link or graphic below

http://www.facebook.com/pages/Kidz-up-NorthKidz-in-the-MiddleKidz-South/178174555543123

Disabled Living, Redbank House, 4 St Chad's Street, Cheetham, Manchester, M8 8QA
Tel: 0161 214 5959 Fax: 0161 835 3591
Email: info@disabledliving.co.uk
Website: www.disabledliving.co.uk

Established in 1897, Disabled Living is a Registered Charity No 224742

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There is an Alternative! A NW TUC Conference Liverpooll 11 February 2011

As part of our countdown to the TUC's national demonstration in London on the 26 March we are holding this conference in Liverpool:

There is an Alternative! A NW TUC Conference

10.00  - 1.00 Friday 11 February 2011

Liner Hotel, Liverpool

We know that cuts will damage public services and put more than a million out of work. The poorer you are, the more you lose. But ministers say there is no alternative. Speakers at this conference will  explain that the cuts are political choices, not economic necessity. We will set out the alternatives.

We are inviting to the conference trades union officers and activists and representatives from a range of community and voluntary sector organisations.

Please reserve the date, we will confirm speakers and final agenda shortly but I would be grateful if you could consider appointing delegates from your organisation,  just e mail name and contact details to me.

Best wishes

Alan

Alan Manning

TUC Regional Secretary

0151 236 5432

www.tuc.org.uk/northwest

Charities say sickness benefit assessment reforms will cause further misery at taxpayer's expense

Charities say sickness benefit assessment reforms will cause further misery at taxpayer's expense

Papworth Trust is leading a coalition of national charities concerned that government reforms to the Work Capability Assessment, which examines people's fitness for employment, will cause further misery to Britain's most vulnerable people.

Charities are being overwhelmed by evidence showing the Assessment to be inaccurate. The government's independent review of the Assessment, published in November 2010, made recommendations for improvements which were widely commended by industry experts. However the government now plans to firstly implement recommendations from their October 2009 internal review, which charities believe will worsen the Assessment.

The October 2009 review was far less comprehensive than the independent one which followed. It did not include evidence from the high percentage of successful appeals which show the common failings of the Assessment. Many of the internal recommendations, in particular around how to recognise mental health conditions and learning disabilities, have been contradicted by the later independent review.

Matthew Lester, Work and Learning Director of Papworth Trust says that "The inaccuracy of the Assessment is already causing unnecessary expense because over a third of those found fit to work are appealing the decision. Implementing questionable reforms from the earlier review will waste further resources, diverting from those needed to implement the independent review.

"Worst of all, it means that vulnerable people will continue to be put through an inaccurate Assessment, causing unnecessary distress to highly vulnerable people."

---Ends---

Notes:

There are 42 organisations in the coalition including Mind, RNID, Crisis, Scope and Remploy. They submitted evidence to Professor Harrington's independent review and have now issued an open letter to the Minister for Employment Chris Grayling to share their concerns about the Assessment reform plan. Please email helen.sampson@papworth.org.uk if you cannot download the letter from the link above.

About Papworth Trust:

Papworth Trust provides a wide range of services for disabled people. It has doubled in size over the last three years.

Each year the Trust helps over 17,000 people from the East of England and beyond through a wide range of services covering Employment, Vocational Rehabilitation, Housing, Personal Support and Learning for Life and Work. The Trust also works with the Government, employers, service providers and commissioners to promote disability equality and good practice.

 

Registered Charity 211234, Registered Company 148906 England, Registered Social Landlord LH1648

Registered Office Address : Head Office, Papworth Trust, Papworth Everard, Cambridge CB23 3RG

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Turn2us News January 2011: New Year, new projects; DLA news; Frank Field's strategy to end child poverty

 

Welcome to the January issue of Turn2us News - the first one of 2011. Read on to find out what exciting projects are in the pipeline and news about Turn2us.


New Year, new project – joining forces with Turning Point to help more people in need

Turn2us are kicking off 2011 with an exciting new partnership with Turning Point - a  leading UK health and social care charity - to deliver our e-learning and free online tools to their project /support workers across the UK. 
 

Read on to find out more about this new partnership

 Turning Point initiative article

Article on the Personal Independence Payment  
Government plans to replace Disability Living Allowance

The Department for Work and Pensions has announced a consultation on a proposal to replace Disability Living Allowance (DLA) with a new benefit called Personal Independence Payment (PIP) in 2013/2014. This would be a non means-tested, extra costs benefit, like DLA.

Read more about Personal Independence Payment


Read our new section on benefits and people who are working but on a low income

Are your clients working for an employer or self employed but on a low income?

Help may be available through welfare benefits, depending on the hours a week worked, their earnings and other income they may have.

Read our comprehensive new section on Benefits for people who are in work but on a low income 

 Information section on benefits for people who are in work but on a low income

Article about Frank Field's child poverty report 

Frank Field proposes new strategy to end child poverty

An independent review into poverty and life chances, led by Frank Field MP, recommends a new approach to tackling child poverty – one that does not just view poverty as a lack of money and focuses in particular on the crucial first five years of life. A public consultation on child poverty is now running until 15 February.

Find out more about Frank Field's child poverty strategy


Turn2us London workshop - 22 February

Are you an adviser working in London? Would you like to know more about Turn2us online tools and services for intermediaries?

Why not attend one of our free workshops for intermediaries. The next one will be held in London (Hammersmith) on 22 February from 11.00 am - 3.00 pm.

Click here for more information about our intermediaries workshops and register for this workshop

Information about Turn2us intermediaries workshops 

With best wishes until next month,

The Turn2us team.





Join our online networks:

http://www.facebookloginhut.com/facebook-login/http://www.facebookloginhut.com/facebook-login/http://www.facebookloginhut.com/facebook-login/

Visit us: www.turn2us.org.uk
Call us: 0808 802 2000
Email us: info@turn2us.org.uk

Elizabeth Finn Care is a charity registered in England and Wales: 207812 and Scotland: SC040987. Turn2us is part of Elizabeth Finn Care.

 

Elizabeth Finn Care Logo

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human rights

Following the threat of direct action against EHRC who had promised to speak to me before Christmas but still hadn't they have now telephoned me to arrange a meeting in the Midlands with DPAC and asked what would be the most important thing we would want them to do. I said that this should be maintaining or improving access to independent living, choice and control for disabled people as I think that more or less sums up what the problems with all the cuts are including WCA etc

They told me a lengthy list of things they are currently doing plus dome planned things they will be doing including monitoring specific local councils so suggested Kensington and Chelsea due to removal of nighttime care as now a standard practice and Birmingham moving to extra-critical care only.

Not 100% sure that EHRC will be an enormous amount of help but think they should indeed be supporting disabled people to have human rights and just wish it wasn't so difficult to get them to do anything.

Linda

disability arts online - newsletter

  

Disability Arts Online

Listings newsletter

DAO National Disability Arts Bulletin

DAO logo

This bulletin is a free bi-monthly service promoting details of the most recent events and jobs / opportunities within the disability arts field.

For more events and jobs / opportunities, please go directly to the listings pages on the DAO website

If you would like to take advantage of this service, please post your listings via the online form

National events listings:

Fittings Multimedia Arts, in collaboration with Sounds of Progress present: Raspberry

01/02/2011 - 19/02/2011

Raspberry - a Musical, inspired by the life and times of Ian Dury - makes its London debut Oval House Theatre, after a hugely successful tour earlier in 2010 - at Oval House Theatre, London

Supporting children and young people with learning disabilities and mental health needs

02/02/2011

Conference exploring the overlap of challenging behaviour and mental health disorders, and the lack of understanding of the nature and manifestation of mental health disorders - at the ORT House Conference Centre, London

Project Volume: Intonation

04/02/2011

Modern Art Oxford hosts a residency for artists and dancers to exchange their physical and visual vocabularies in response to the current sculptural exhibition, Thomas Houseago: What Went Down

Exhibition: Artists/Curators

07/02/2011 - 09/04/2011

A very exciting exhibition of portraits made by Henshaws Art Makers in Knaresborough, North Yorkshire

Deafinitely Theatre present 4Play

10/02/2011 - 12/02/2011

Watch a showcase of four new short plays by the winners of last summer's Deafinitely Creative playwriting competition at the Drill Hall, Central London.

Disco Fever

10/02/2011

Monthly disco for adults with learning difficulties/disabilities at Henshaws Arts & Crafts Centre, Knaresborough, North Yorkshire

Mind the Gap present Of Mice & Men - National Tour Spring 2011

10/02/2011 - 28/05/2011

Mind the Gap is showcasing their award-winning adaptation of John Steinbeck’s classic ‘Of Mice & Men’ at Mind the Gap Studios, Bradford

Anjali Dance Company in Resolution! 2011 at The Place

17/02/2011

Anjali's professional company of dancers with learning disabilities perform Fruit For Thought at The Place, London in Resolution 2011

Light and Movement Workshop

19/02/2011 - 20/02/2011

Play Time with Digital Media and Dance: Have lots of fun exploring and playing with digital media and movement: Shrewsbury, Shropshire

CoolTan Arts Largactyl Shuffle: Celebration of LGBT History

19/02/2011

Celebrate LGBT History month with CoolTan Arts Largactyl Shuffle, a fun guided cultural walk for mental and physical wellbeing, on Saturday 19th February, 12noon at Maudsley Hospital, Denmark Hill, SE5 8AZ

National jobs and opportunities listings:

Disability Arts Cymru: GO GET STARTED!

Location: Wales | Closing date: 31 January 2011

Go get started is an opportunity for emerging visual artists to exhibit across Wales.

uScreen Community Fund 2010-2011

Location: South East | Closing date: 31 January 2011

Remuneration: Up to £7500

The uScreen fund is open to festival and community events, workshops as well as production bursaries and international exchange bursaries.

Help us improve Access @ the Edinburgh Fringe Festival

Location: Edinburgh | Closing date: 31 January 2011

We want to get your perspectives on how accessible you think the Fringe is to disabled people. Please help us by filling in a survey. It will take no more than 5 minutes to complete.

RIBA launch photo competition titled In With The New

Location: South East | Closing date: 31 January 2011

RIBA South/South East is launching an exciting competition to showcase your images of the south east's diverse architecture

Call out for work for artwork for exhibition and book

Location: UK-wide | Closing date: 4 February 2011

Practising artists with autistic spectrum conditions or Asperger syndrome in the UK are invited to submit work towards a book that will be published to coincide with an exhibition at G2 Solihull Gallery in April 2011.

Online Exhibition Opportunity - Drake Music In Translation

| Closing date: 7 February 2011

Remuneration: Each artist will receive a fee of £320

For Drake Music In Translation, we are seeking to commission 2 artists with personal experience of disability to collaborate with Drake Music artist / curator in residence, Melanie Clifford, on a new online commission investigating translation and interpr

Outreach Director

Location: London | Closing date: 13 February 2011

Remuneration: Voluntary

PanicLab dance-theatre looking for outreach director

Call out for work for artwork for exhibition

Location: West Midlands | Closing date: 25 February 2011

Practising artists with autistic spectrum conditions or Asperger syndrome in the West Midlands region are invited to submit artwork towards a small scale exhibition at G2 Solihull Gallery taking place in April 2011.

Making Events Accessible Wiki

| Closing date: 1 March 2011

Social Care Institute for Excellence invite you to tell them what you think makes an event accessible.

Impact Arts Fair

Location: Candid Arts Trusts, London | Closing date: 1 March 2011

Creative Future are calling for submissions for the UKs 1st national marginalised art fair with works only by socially excluded arts practitioners at the Candid Arts Trusts, London

www.disabilityartsonline.org.uk

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Birmingham students facing disciplinary action after protest



Support the 12 University of Birmingham students facing disciplinary procedures that could result in the termination of their degrees. One of them who is facing disciplinary action was too ill to get out of bed at the time.

The students are facing the disciplinary action after a peaceful occupation on Monday 17th January. The group undergoing disciplinary action, some of them disabled supporters of DPAC,  were part of a larger group opposing the University’s plans for department cuts and staff redundancies. 

Unreasonable force was used at the end of the occupation by university security staff that resulted in several injuries against peaceful protestors. The university refused to allow for concerned staff members and union members to enter the building to oversee the eviction as impartial witnesses.

The University should drop all disciplinary charges agsinst the students who were protesting peacefully, should make a statement apologising to students and staff for the use of unreasonable force and ensure impartial witnesses are allowed access during any future occupations.

Please sign the petition and  circulate widely - disabled students facing disiplinary action after protesting on National day of Action 
http://www.ipetitions.com/petition/defendbirminghamstudents/
 
 For more information contact Claire at  cxl736@bham.ac.uk  and mobile number 07772585794.

 

Wednesday, January 19, 2011

Music Organisation Offers Mentoring To Young Disabled Musicians

  
Drake Music is pleased to announce they have 5 places on their pioneering music mentoring programme in partnership with Sound Connections.

Young disabled musicians aged 15-30 in London have the opportunity to work with one of our three music mentors for 10 hours over 5-10 weeks. Our mentors are all highly experienced musicians.


The mentor programme helps to: 
• Set goals
• Encourage areas of talent
• Build confidence
• Development as an artistic
• Support progression in music


Whether playing an instrument, sing, use Assistive Music Technology or compose, either as a solo artist or as a band or collective, the mentoring programme supports young musicians (for example in highlighting areas for development, making connections and networking, setting up gigs or music installations, broadening existing influences or listening, widening audience, career development and personal development).
Nick Wilsdon, Advanced Mentor at Drake Music says ' The music mentoring programme offered by Drake music is a great opportunity for disabled musicians to explore and develop their artistic potential under the guidance of experienced musicians' .

This FREE opportunity is open to disabled musicians who:
-- Are aged 15-30
-- Play a musical instrument (including Assistive Music Technology such as Soundbeam or switches), or sing or compose music
-- Have a keen interest in their own development as an artist
-- Are considering music either as a career or as a route to personal development, or both
-- Are either a solo artist or a group
-- Are passionate about music

To apply for a place on the programme or to apply on behalf of someone you work with please request an application form by email annathorpetracey@drakemusicproject.org

For more information on Drake Music visit www.drakemusicblog.blogspot.com  or

www.drakemusic.org (you will be redirected to Drake Music’s former website until the new one is launched in early 2011).

Ends

Notes to editors

High resolution images and interviews with key artists are available.

For further information please contact Chardine Taylor-Stone at Drake Music on

020 7739 5444 or

chardinetaylorstone@drakemusic.org.

Out of hours please contact 07896793059

 

 

About Drake Music:

Drake Music is a dynamic music and technology hub, founded in 1988. For over twenty years they have pioneered the use of assistive music technology to make music accessible and have developed a wealth of innovative and imaginative approaches to teaching, learning and making music. Central to their work is the belief that everyone can fulfill their creative and musical potential given the right opportunities. 

Non-disabled people can make music in many ways and at many different levels. Drake Music’s vision is a world where disabled musicians have this same range
 of opportunities, and a culture of integrated music-making, where disabled and non-disabled musicians work together as equals.

Drake Music takes an active role the wider cultural activity of re-imagining (dis)ability and diversity via arts and music.

Drake Music is a small organisation with a national office based at Rich Mix Cultural Foundation in East London, and teams of musicians and project managers who deliver work in London, Bristol/SW and Manchester/NW in conjunction with a wide range of associates. They work in partnership with schools, universities, arts organisations, local authorities, music services, software & hardware developers as well as musicians, technologists, composers and artists from other disciplines. The organisation is regularly funded by the Arts Council England. 

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Tuesday, January 18, 2011

Petition the Minister for Disabled People to Recall the Public Consultation on DLA Reform

We, the undersigned, urge the Minister for Disabled People to recall the Public Consultation on Disability Living Allowance (DLA) reform, and to cease work on reform of this benefit, due to serious flaws in the consultation paper. As such, the consultation questions are deeply skewed and any answers will be likely to support wholesale reform. This is both unfair and unwise, and will cause hardship for many disabled people.

The case for reform has been criticized, and then completely demolished, by the various disability rights groups fighting reform. They accuse the DWP of building their argument without sufficient evidence. The claims that DLA can act as a barrier to work, in particular, are robustly questioned. Questions are also raised concerning the accuracy of the representation of supporting data. For example, the claim is made that DLA claims have risen by 30% in eight years - without accounting for population growth of 5% in this period, a pronounced demographic shift, and increased awareness of DLA.

Most devastating to the case for reform is the critique of proposed amendments, leading one to ask whether augmenting DLA might not be a better, cheaper way of improving employment opportunities, rather than launching an entirely new benefit. It would seem that the costs of such rebranding are only justified when savings are made by cutting the DLA caseload by 20%. This figure is, in and of itself, questionable – how is it possible to know that this many people can be removed?

The Personal Independence Payment (PIP) appears to be a case of cuts dressed as positive reform. Disability rights groups and charities have uniformly condemned the proposals, warning of dire consequences. The list of those affected includes: people who are mobile with aids; people with disabilities so severe that they are unable to be very active; care home residents; those who receive local authority care packages. Most other disabled people will suffer through needless reassessments upon the introduction of PIP, and re-testing every few years even when a condition cannot be treated.

There is a strong feeling amongst people with disabilities that the Coalition Government have declared war on us, with a continual ratcheting of pressure on us since the Emergency Budget in June 2010. Announcements on Employment and Support Allowance, Incapacity Benefit, and Disability Living Allowance have made us feel that the Government is scapegoating us and removing the support on which we depend. Iain Duncan-Smith's comments to The Sun newspaper [01/12/2010) suggesting that Incapacity Benefit claimants were partly to blame for a large fiscal deficit caused by a recession, a bail-out of the banks and quantitative easing. Whilst there may be ways to improve DLA, they do not involve replacing it with a new benefit, and neither do they involve removing anyone from the claimant caseload.

Paralysed man told he's fit to work

 
A PARALYSED car crash victim who requires round-the-clock care faces financial and emotional turmoil after being told by benefits bosses he is fit to work.
Severely disabled Simon Powell has been stripped of his disability benefits and will soon lose his mobility car following an assessment by a doctor on behalf of the Department of Work and Pensions (DWP).

Despite the 45-year-old being wheelchair-bound, unable to stand without the aid of crutches and needing help to the toilet, Simon and his partner and carer, Val Bolan, 51, will now miss out on their desperately-needed £120-a-week Disability Living Allowance (DLA).

A tearful Simon, who is also unable to wash and dress himself, said: "We just can't believe it.

ATTACK AGAINST ATOS

  

Press release January 2011     

 

ATOS ATTACK- Second National Day of Action Against Benefit Cuts

Where- London - starting at Triton Square, NW1    -  January 24th from - 2pm

PHOTO OPPORTUNITY

  

Anne Novis MBE a member of DPAC says “ society is allowing the government to implement the most discriminatory and harshest attacks on disabled people ever seen. Those that stand-by and allow this are the same as those who stood-by when disabled people were targeted by the Nazi’s for annihilation. For anyone who thinks that is too harsh I want to say clearly that it is our lives we’re fighting for, some have already killed themselves due to what is happening to us and many more are considering it.”

 

Disabled people and their supporters angry at the way they are being exploited by ATOS healthcare who are making ever increasing profits off the backs of disabled people’s misery plan to mobilise around the country for the second National Day of Action Against Benefit Cuts.

 

The anger against ATOS is now so widespread that dissent has spread to even rural locations such as Lydney in Gloucestershire, hardly the sort of place one would imagine being a hotbed of resistance and revolt.

 

Protestors are angry that in spite of the well documented criticisms of the Work Capability Assessment by the government’s own review carried out by Professor Harrington as well as by CAB and Disabled People’s own Organisations ATOS have once more been awarded a £300 million contract by DWP to keep carrying out these flawed assessments which ruin lives and lead to suicides.

 

Another DPAC supporter recently wrote “My Uncle committed suicide last summer. He tried to get ESA and succeeded in getting it by appealing at a tribunal. However, the DWP had him go for another medical assessment through ATOS healthcare and they, again, awarded him 0 points. He hung himself a few days after receiving the papers for the second appeal tribunal.”

 

Disabled people are further dismayed that ATOS seem to be the preferred choice of the coalition government to be paid yet more huge sums of money to throw disabled people off Disability Living Allowance.

 

 DPAC co-founder Eleanor Lisney said “ ATOS’s assessment methods have been proven to be flawed with as many as 70% of disabled people disallowed ESA having it re-instated at appeal. The 8,000 appeals a week against refusal to award ESA are swamping the Tribunal system at goodness knows what cost to the taxpayer.”

 

DPAC say that although they have no idea yet how the government plans to reduce the number of claimants for Disability Living Allowance by 20% what they are sure of is that those disabled people refused DLA are not going to experience a miracle cure but will instead be left without the vital financial support they need to meet the additional costs of being disabled.

 

ENDS

 

press liason - Linda Burnip 01926 842253/0771 492 7533 Disabled People Against Cuts ( DPAC)  mail@dpac.uk.net

                                                       

Anne Novis MBE ( contactable through press liaison)

 

Notes for editors

 

http://benefitclaimantsfightback.wordpress.com/

 

Disability Living Allowance ( DLA)

This has 2 components Care and Mobility. It is a benefit paid to both those in and out of work and is designed to meet the additional costs of disability.

 

Extra costs of disability to households

DWP’s  own research quotes figures that show poverty rate rises from non disabled households to disabled households from 4.5 to 29.7 percentage points per household.

 

Saunders calculated that the extra cost of having at least one household member with a disability is about 37 per cent of disposable income; that is, a household containing one member who is disabled would need 37 per cent more income than a comparable household without such a person to reduce the incidence of hardship to the same level. Source: Sanders (2006) in DWP Research Report No 542 Review of international

evidence on the cost of disability David Stapleton, Ali Protik and Christal Stone

 

Extra costs of disability to individuals

A Rowntree report (2004) found that the weekly income of disabled people who are solely dependent on benefits is approximately £200 below the amount required for them to ensure an acceptable, equitable quality of life’

 

However, even if receiving maximum benefits, disabled people still experience a substantial shortfall in income. The income of disabled people solely dependent on benefits, irrespective of the type or level of their need, is approximately £200 less than the weekly amount required for them to ensure a minimum standard of living.

 

Source: Disabled people’s costs of living: ‘More than you would think’ (2004) by Noel Smith, Sue Middleton, Kate Ashton-Brooks, Lynne Cox and Barbara Dobson with Lorna Reith, is published by the Joseph Rowntree Foundation (ISBN 1 85935 236 7,

 

Employment

 

The employment rates of disabled people are around 48% compared with around 78% of non-disabled people Source Labour Force Survey, Quarter 2,2010

 

Only 20% of those with mental health problems are in employment- Source- Labour Force Survey, Jan-March 2009.

 

Suicide Cases

A disabled Scottish poet and writer who killed himself after receiving 2 letters one saying his Incapacity Benefit had been stopped and another that his Housing Benefit had been stopped –

http://www.heraldscotland.com/comment/obituaries/paul-reekie-poet-writer-icon...
A disabled woman fighting for re-housing for over 5 years as well as having her social care cancelled left a suicide note saying “No human or animal should ever have to go through life as I did.”

http://www.camdennewjournal.com/news/2010/mar/jennyfer-spencer-‘when-you-read...
attempted suicide by ex-school caretaker who had brain tumour and was unable to sleep, had weakness down one side of his body and was having fits. His GP deemed him unfit to work but the 15 minute Atos medical declared him fit for work. This would have led to his benefits being cut by over £60 per week.
what one disabled woman says about the cuts  “I could go on and on, about the misery it would cause, to remove DLA. It would lead to a slow death painful death. Worth adding here, I have spoken to many in my situation, who are discussing mass suicide, rather than suffer more health miseries, for which there are no cures! They are not depressed, but just pragmatic about the fate that awaits all of us.”

A Push Too Far

I am a disability activist, you know one of those people who will complain, (how dare I?), when facing discrimination, challenge inequality wherever I find it and advocate for other disabled people.

Oh one of those you might say, YES! one of those who believes in the human rights of every single person, those 'rights' so many take for granted as they have not had them taken away yet.

I have fought, yes fought, for nearly twenty years for disabled people to be believed about their experiences of targeted hostility, harassment and abuse, hate crime and for an appropriate response from society.

Within all this I also fight for myself as a wheelchair user who needs care to live independently.
One of those who relies on benefits to live, to carry on having a family life, to practise my faith and be safe.

Oh I hear it already I am 'burden on society', 'work shy', a 'fraudster' and should have been 'killed at birth', I have actually been told this when attacked on a local high street and read it every day in the media .

I would love to get paid for the volunteering I do, for the contribution I have made to this society, for caring for my children and 23 foster kids, for advocating and counselling, advising and supporting other disabled people.

But hey I am part of the Big Society, one of those who does all this for free, you know like David Cameron wants you all to do now.

I am qualified up to my eyeballs, have attempted to get paid work many times often just a couple of hours here and there as that's all I can commit to due to my body not being as active as my mind.

Most employers don't want those who are sick, disabled a burden, work shy and fraudsters to work for them you know?

Now I face cuts in my personal care, the ILF which funds half my care package is scrapped and I will only get 5 more years of such support, that's if I still qualify of course.

To qualify for ILF you must be on the high rate care component of DLA and need more then £200 plus pounds worth of care from your local authority.

But DLA is to be scrapped too , the local authority has no money and will be implementing increased charges for care and cuts in care as soon as possible.

I will be reassessed for the Severe Disability Allowance I get and probably have this taken away and be put on Job Seekers Allowance, after all I should be in paid work you know.
It does not matter about my health issues, regardless I must be in paid WORK!

Yet if I lose my care I cannot function, get up, get dressed, shop, socialise, practice my faith, in fact do nothing let alone be in paid work in some sort of ideal world where priority is given to sick and disabled people to get into work first before all those others sacked, made redundant, not sick, more experienced employees out there seeking work too.

I may get a basic income but I will have to jump through hoops, attend interviews, training and more and if I don't ? Well I will be punished of course, the finance will be lessoned and eventually stopped.

Yet if I have no care support I cannot get up, dressed, eat, go out, and attend interviews or training.

But that does not matter I should make more effort as I am work shy, a fraudster and a burden on the state and 'unsustainable' as government ministers keep telling me.

So how will I survive? I will not.

But that's ok too as then there will be less disabled people and we will save the government some money and all these incentives will have been shown to work as I, and so many others, will not exist.

And if we do mange to 'exist' it will be in residential care, or in bedsits, living on the scraps of funding society can 'afford' or deem reasonable for us to live on, we will return to begging on the streets then everyone will be happier as I will not be a 'burden' or a 'fraudster'.

Yet once upon a time I had a dream, to own a home, have a career, travel and enjoy my retirement.
I was in paid work, as was my partner, we contributed to society by it's current definition.

But oops! One day my body gave out, my back ripped apart and I entered the world of spinal injury, discrimination, inequality and prejudice.
Overnight I was unable to move from a bed, lost my work, my foster children, my partner and myself.

I did not choose this,it happened to me, as so many illnesses and accidents do.

One day you may find you or a member of your family becomes sick or injured, be born too early or face being different.

Now I face increased poverty, for no matter what you think disabled people on benefits are not rich, I face medical tests (many of them)  by unqualified people who will decide whether I am too ill/disabled or not to be in paid work.

I face serious cuts in my care package, lose the five personal assistants I employ to help me, lose my wheelchair adapted car, lose DLA which was meant to help with some of the extra costs of being a disabled person.

Once I fail the ESA medical, which most do, I will become one of the invisible disabled, those not on anyone's radar. I will face sanctions for not complying with job seeking requirement's and lose even more of the pittance I am meant to survive on.

I will lose myself again.

Not due to an injury that was no ones fault but due to a society that is allowing a government to implement the most discriminatory harshest attacks on disabled people this generation has faced.

A society that is allowing those who can fight least to be targeted as the scapegoats for the financial mess they and the succeeding governments got us into.

Yes you, and you and you, all of you who stand by and say nothing or encourage such vicious and undeserving attacks are just as responsible for what is happening.

Those who stand by and allow this are equivalent to those who stood by when disabled people and Jews were targeted by the Nazi's for annihilation.

Too harsh for you?

Its our lives we are fighting for, our very lives, some have already killed themselves due to what is happening, many more are considering it.

Will you stand by?


Anne Novis MBE

Protests against benefits cuts

We'll be sending out our normal newsletter next week.  But in the meantime, we want to let you know about protests happening right now, or in the near future, against cuts which affect claimants.

The Broken of Britain are holding a blogswarm, beginning today and lasting over the weekend, entitled One Month Before Heartbreak.  It's intended to highlight the fact that the unusually short consultation about the abolition of disability living allowance, and its replacement with personal independence payments, ends in just one month's time.

More details about the blogswarm, which involves mass postings about the issue on blogs, at One Month Before Heartbreak and from Bendygirl writing in the Guardian.


You can take part in the DWP consultation about abolishing DLA and/or contribute to the Broken of Britain submission.

There's also a petition you can sign.


A National Day of Protest Against Benefit Cuts is taking place on 24 January, with events already arranged in London, Livingston, Leeds, Lydney, Burnley and Hastings.  Organisers are hoping that many more people will arrange events in their own local area.

Justice for All is a coalition of, so far, over 1,300 advice agencies, community groups, lawyers, members of the public and others.  They are campaigning against the slashing of the  legal aid budget, which could see hundreds of advice services close and a massive reduction in the availability of free advice about issues such as welfare benefits, debt and housing problems.

Justice for All launched with a lobby of the House of Commons on 12 January and have managed to get an Early Day Motion against the legal aid cuts tabled which you may want to ask your MP to sign. 

Justice for All are hoping that many more people will sign up to join the fight against legal aid cuts.

These may be small beginnings, but we hope that you'll find something here that you can support.  We'll do our best to keep you updated on any further actions in the coming months.

This information is also available online at www.benefitsandwork.co.uk/news/latest-news/1285-protests-against-benefits-cuts.

The Beginning

Mary

 

If your a regular follower of my News Blog through my site, www.disabilitydirect.org (or read my entries on facebook or twitter), you will know that I have been reporting and reproducing disability news for a couple of years.  I had always thought, that while it was important to always try and present a positive slant about disability issues in the choice of stories I presented, actually writing the news myself was never really part of plan.
 
I suppose (naively) I thought I could remain aloof, dispassionate about it all and just report what came across my desk, or more accurately what came in to my inbox. But no. Because sometimes, sometimes you read something that just gets to you, and both challenges and changes your thinking.
 
So here is the email from Mary, virtually as it appeared in my inbox about a week ago, spelling mistakes an all.
 
 

Dear DD

Great to read your web site and that we, the disabled have a strong voice through your web site.
ILF Cuts. 4 years will pass quickly.
I am 64 yrs, own my converted home, severely disabled and totally human and power chair dependent due to have chronic rheumatoid arthritis. I have difficulty swolling so it takes 3/4 to eat my meals. My care package is 18 hrs per day including sleepovers.  I cannot do anything for myself, but thanks to my ILF i can lead a active and produced life.
If the ILF is taken away, and my local council do not implement any cuts, they are working within NICE, i will be left with 2200/0800 Sleepover. 1200/1300 lunch 1800/1900 tea.   Added to this 1 1/2 hrs for shopping, 7 hrs per week for social care. 1/2 ironing and 3/4 for housework. 15 min shower
The outcome of such a care package will be, dehydration, i cannot use my hands to hold a cup unless i have the cup locked into my thumb.  I can drink a cold drink from a straw.  Only 1 hr for lunch means in that hour i will have to be changed as i will be wet, given a sandwich and a drink.  No afternoon drink, dehydration again.  Pressure sores will appear. Heated up meal for tea, when i am to get this meal cooked? washed because i shall be wet.  Drink.  As i will be wet my night staff will have to wash me before putting me to bed.  I am told that it only takes 1 1/2 to get me up where in fact it takes 3 hrs.
To sum up.  I will have three options.  Live with this terrible care package. This i cannot and will not do.  Go into care.  Kill myself.  The latter seems the best option.
Please keep me up to date with what you are doing.
Mary L
 
 
This is Mary .... and this is what she does...
 

 
Yes, Mary is a world record holder!

 

Please see http://powerwheelchaire2e.blogspot.com/ for more.

 

 

I have to admit when I read Mary's message I cried.  There must be something very wrong with the world if the proposed changes to the benefits system for disabled people and the Independent Living Fund, should cause someone to consider taking their own life!
 
While I understand that not all disabled people who receive help from the state are in such a desperate position, Mary's message does highlight a major concern:
 

Provision of care and services that support disabled people is not a luxury that can be removed as soon as the economics get difficult.  For some their care and support is essential to their very survival an wellbeing.

 

In 2009 the previous Labour administration finally signed up to the UN Convention on Human Rights for Disabled People. Perhaps the new coalition government should read it!
 
 
For more about the UN Convention on Human Rights for Disabled People please click "What' This About" above.

Show your support for Young Carers

So many people contacted me last year saying how they had gone through similar experiences to us. When their child had gone to school they had realised that their life was different to that of their peers. They had felt sad and alone coz their peers were too young to understand and empathise what their life as a young carer was like. It led me to start researching how much support there was in schools for young carers, and how much was taught about young carers issues.
Over the past 6 months I have liaised with many carers charities, people working with young carers, aswell as people working high up in local Education, the Children's Commissioner for Wales and Welsh Assembly Govt.

I have discovered that there is a 'hit and miss' situation going on. It is currently left up to individual schools to decide how much is taught about young carers issues with social education (PSE) lessons, which is leading to some schools offering amazing support, whilst others are offering very little support.

The Princess Royal Trust for carers and the Children's Society recently created a fantastic schools resource pack which is a free to download online resource, it offers guidance for teachers on how best to support young carers in their schools, and is a brilliant resource to use to teach pupils about young carers issues. If it was used within schools it would lead to greater empathy and understanding within the school's community.

So far we have managed to get a link to this resource added to the Welsh Assembly Government's PSE website and we hope to get similar links added to the equivalent websites for England, Scotland and N.Ireland.

My next step after that is to contact the Government and Dept for Education.


Our main goal is to get it made compulsary for all schools to support young carers and raise awareness of young carers issues so that young carers will be identified earlier on in their school lives and given the support they need to enable them to achieve their full potential...which is every child's right according to the UN Rights of a child!!

This is where you can help us!!

We have created a petition and we need people to sign it and share it amongst their friends and family. When we have enough signatures we will be sending it to No 10 Downing Street.

It will back up what I am saying ... that the general public feel that there needs to be more support for young carers.

If you think that young carers deserve to be recognised and supported within ALL schools then please follow the link to the petition, sign it and share the link with your friends and family.

http://www.petitionbuzz.com/petitions/youngcarersawareness

Thank you so much for taking the time to read this.

We really apreciate it!

Victoria Taylor.

P.S. There was a TV programme on last week about young carers, here's the link if you missed it, and would like to watch it.
aa
http://www.itv.com/news/tonight/episodes/tooyoungtocare/

There is a movement starting of charities and young carers support workers who have been working for years to try and get more support for young carers finally being heard and people are beginning to realise just how much young carers do, and how much they save local councils every yr...millions of pounds...so surely they should be supported?! This is why I am reaching out to you and asking for your help... if we could get lots of signatures on this petition it will really help when I contact the Government.


Thank you so much!

Posted via email from Editor's posterous

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