Showing posts with label disability. Show all posts
Showing posts with label disability. Show all posts

Tuesday, 13 December 2011

Now it's Real. First Cancer Patients, Now Government slash benefits for Disabled Children

Last night, the House of Lords failed to support an amendment put down by Tanni Grey-Thompson, the most successful paralympian of all time, to protect the benefits of disabled children once Universal Credit is introduced.

You can read more here http://www.family-action.org.uk/section.aspx?id=14225 but effectively, under universal credit, all but the most profoundly disabled children will only get half as much support. Child Tax Credit additions for disabled children will fall from £52.21 per week to £25.95 per week - a loss of £1366 per year, or £20,000 over the course of a childhood.

You might wonder what possible argument a government who promised to "protect the most vulnerable" could possibly make for this change. I myself was fascinated to see how on earth they had justified throwing disabled children to the wolves.

Ready? OK, if they didn't betray disabled children, it would just have to be disabled adults. After all, disabled children have parents to look after them. What's more, if they didn't cut money used to buy wheelchairs and incontinence pads for disabled children, they wouldn't be able to afford to address the hideous failures of ESA (Employment and Support Allowance or sickness benefit) and ensure that all those who qualify for long term support, get it.

Could there be a more disgusting example of divide and conquer? Each man for himself. The image of a Victorian gent throwing a handful of pennies on the floor and leaving the cripples to fight it out amongst themselves comes to mind.

And remember, this is no longer theory.

I've been writing about these issues for 18 months now, sadly my blogs have often contained doom and gloom predictions of horrors to come. Well last night they started to come in a first blaze of in-glory. The Welfare Reform Bill is now at Report Stage in the Lords. These votes will almost certainly decide what becomes law and what doesn't. For disabled children, now it's too late.

Shame on us.

There is one more session before Xmas. Then 4 sessions after Xmas, then the final no-going-back vote to pass the bill. There is still time to lobby peers. There is still time to stop the time limiting of ESA. http://diaryofabenefitscrounger.blogspot.com/2011/12/time-limiting-esa-template-letter-to.html There is still time to oppose PiP and abolishing Disability Allowance. http://onemonthbeforeheartbreak.blogspot.com/ There is still time to fight Clause 52 http://www.guardian.co.uk/commentisfree/2011/dec/08/conservative-compassion-disabled-sick and housing benefit changes that will leave thousands of sick and disabled people at risk of homelessness.

In a week where the government suggested all cancer patients undergoing chemotherapy ought to be assessed to see if they can work or not, I can only wonder where this will all lead. I can only hope history is no guide  the future

If I can find any tiny silver lining, it is that we only lost by 2 votes. That is the closest vote I have seen so far.

2 votes. 2 Lords. 2 letters, 2 emails, 2 tweets.

There is still all to play for, but sadly disabled children just fought the last stage of their fight. And lost.

Sunday, 4 December 2011

Dear UN : SOS!!!

The quite excellent John Pring at Disability News Service dug up this murky little nugget of breathtaking cheek from our delightful coalition. http://www.aboutaccess.co.uk/article.php?id=254&item=Government+rewrites+history+for+UN+report+

It seems that the government had to prepare a report for the UN disability convention. Apparently, the report was meant to describe


"measures that are being taken to implement each of the articles of the UN Convention on the Rights of Persons with Disabilities."


However, in a dazzling piece of collective amnesia, our very own UK government didn't seem to think it necessary to mention the eye-watering level of cuts to disability benefits, services and support. 


Despite an "Initial Report" running into a zzzzzzzzzingly epic 126 pages and an even more lengthily off-putting "Annexe" of 167 pages, there appears to be nothing at all discussing the impact £9.2 billion of cuts will have on disabled people's "rights"


One might think that up to 600,000 people losing Disability Living Allowance, for instance, might, you know, impact on how Disabled people erm, Live? That abolishing the Independent Living Fund might, well, have some impact on how Independently we can Live? That cutting Access to Work might make it, erm, harder to, well, Access Work? Cutting Social Care might make the care we receive a little less Social? Capping housing might, well, lead to some people losing trifling little things like, THEIR HOME??? Never mind the astonishingly sinister Disability Denial of ESA, where nearly 2 million people will miraculously be found "Fit to Work" after all, simply by pressing a few buttons on a LIMA computer screen? 


I can only hope that whereas misinformation, distortion, omission and double-think seem to be perfectly acceptable in the UK, the UN will take a rather more "Real-Life" view of our rights. 


SOS UN : UK disabled people here! You can skip the 293 pages of fantasy our government just sent you if you like. Send food packages!! Send tents! Send Peacekeepers! 

Tuesday, 29 November 2011

Europe Calls on Governments to Protect Disabled Citizens

I reproduce this letter on behalf of the European Disability Forum. On first reading, I'm not sure our UK government can claim to meet any of these demands. Except No.3 of course, which appears to be a particular obsession.... 
Despite the rhetoric, cuts to Access to Work even call No.3 into question.


EU SUMMIT: OUR LETTER TO HEADS OF STATE: WE DON'T WANT TO BE EXCLUDED MORE THAN WE ALREADY ARE


To the Heads of State and Government of the European Union,

RE: IMPACT OF THE ECONOMIC CRISIS ON PERSONS WITH DISABILITIES

persons with disabilities wants to keep their rights
The European Disability Forum (EDF), the voice of 80 million persons with disabilities and their families in Europe, calls on all the Governments of the European Union to ensure that the needs of people with disabilities and their families are taken into account all the way through economic, political and social policies.


Austerity measures undertaken by governments in the European Union could undermine progress towards the realisation of the rights of persons with disabilities enshrined in the UN Convention on the Rights of Persons with Disabilities as well as the social targets of the Europe 2020 strategy and the European Disability Strategy 2010 – 2020. Poverty, social exclusion, discrimination, marginalisation, illiteracy and negative stereotypes of people with disabilities can be the sad legacy of the economic, social and political reforms if implemented without duly consideration of the rights of people with disabilities.
 
 
The EDF calls on the European Council and all the Governments of Europe to ensure that people with disabilities are not socially, economically or politically excluded. In order to make sure  that the rights of persons with disabilities are not undermined by current responses to the economic crisis, we must consider that: 
 
1. People with disabilities might freely move in European societies, live independently and included in society: no action restricting these capacities should be envisaged in any social protection reform. Personal assistance and other community support services should not be undermined by austerity measures.

2. Education of persons with disabilities will be respected and reforms in the education systems will not mean reduction in education support policies in mainstream education and should not lead to segregation to special schools.

3. The right to work and employment is fully respected: Measures for full inclusion in employment including reasonable accommodation and supported employment should not disappear from the national employment policies.

4. Access to health services for people with disabilities is not put into question and health services for people with disabilities do not consider their health as secondary in respect to non-disabled people.

5. That Social habilitation and rehabilitation is considered an investment for European societies ensuring that all capacities are collected and fully participate in the construction of Europe after the crisis. The quality of social services should remain a pre-condition for respecting the human rights of people with disabilities.

6. Adequate living standards and social protection are ensured. This will mean that no measures are taken that will have the effect of leading people with disabilities into poverty, social exclusion or reduction of his/her living income.

7. Freedom of expression and opinion and access to information is not restricted by reforms of public and private services.

8. Respect for family life is ensured by guaranteeing to all people with disabilities and their families adequate family policies. These policies should remain a priority.

9. Organisations representing people with disabilities should be consulted in regard to any action that could have an impact on the rights of people with disabilities.

10. Raising the awareness of the needs of persons with disabilities should take place in order to ensure that the portrayal of persons with disabilities in the media and other relevant stakeholders is done correctly and does not lead to social stigmatisation.
 
Yannis Vardakastanis
President of the European Disability Forum

Friday, 14 October 2011

New Shadow Minister for Disabled

Yesterday, Kaliya Franklin spoke to Ed Miliband while I suffered through a birthday party for my just-turned-7 year old. All morning, we rehearsed lines as I baked cocktail sausages and planned strategy while I stuffed plastic party bags with plastic rubbish.

I'm sure Kaliya will be writing up an article later today, so I won't go into details, but the conversation went very well and Ed did a lot of listening and asked a lot of questions.

Late yesterday evening, John Pring from the excellent http://www.disabilitynewsservice.com/ ** heard from the new Shadow Minister for Disabled People. Anne McGuire was confirmed in the role and sent him this statement  :

“I’m delighted to have been appointed as Shadow Minister for Disabled People. There is a responsibility on all of us to care for those in need. However, many disabled people feel that they are unfairly being portrayed as scroungers and are feeling very vulnerable"

“Labour will be the voice for those in genuine need, who need extra help to live a full life. The introduction of the Universal Credit will see support for disabled children halved, while the Severe Disability Premium is to be scrapped with nothing appropriate put in its place. We believe there can be reforms made to the system, but this is the wrong way to do it, and we will do all we can to stop these changes.”


I'm sure sick and disabled people will be encouraged by this comment and very pleased that Labour appear to finally be listening to campaigners and most importantly, to them, the people affected by this government's eye-watering cuts to disability support.


** If you haven't bookmarked John's site, please do. He is the only investigative journalist focused solely on reporting disability issues and his weekly updates are invaluable.

















Monday, 5 September 2011

Template Letter to Lords Re: Welfare Reform Bill

So, with the welfare reform bill about to have its second reading in the Lords, I've written this template letter to send and DarkestAngel32 blog http://darkestangel32.wordpress.com/  have produced this brilliant list of email addresses to send it to.

Obviously feel free to send your own letter about the things that matter most to you, but if you'd like to send mine, you're very welcome. Email addresses are at the end and whether you send the letter to one peer or everyone on the list, it all makes a difference.

Please do join in. The more letters and emails they receive, the more chance we have of making a difference. The bill is already facing difficulties because of the brilliant work we did while it was in the commons. Now we need to build on that and make sure that as many peers as possible know about the issues.

Finally, please share this article, tweet, link and send to friends. Thanks.


Dear ..........[insert name of peer]

On the 13th September, the welfare reform bill will have its second reading in the House of Lords.
Rather unusually, many aspects of the bill are yet to be finalised or fully detailed. This in itself will, I'm sure, make your job rather difficult as you consider the many, many details and changes proposed.

However, I'm writing to you with some very specific concerns that sick and disabled people have and I've linked to some articles and research which I hope you will find helpful.

1) Removing Disability Living Allowance mobility payments from adults in residential care.
An adult who needs to live in residential care will have extensive needs and are often amongst the most severely disabled. The mobility component of DLA afforded them their only freedom, allowing them to choose to fund a power wheelchair otherwise unavailable on the NHS, or to pay for taxis or transport to get out now and then. Taking this away would leave the most vulnerable disabled people effectively housebound. There is no support for this change anywhere - charities, independent benefit reports and even the government's own advisers have called for this to be removed from the bill.

2) Scrapping DLA entirely and replacing it with Personal Independent Payments (PIPs).
DLA is a very effective benefit with fraud rates of less than 1% (DWP own figures) It is already incredibly hard to claim and the qualification criteria are very narrow. The government have announced that DLA claimants will also soon face assessment and that the overall number of claimants will be reduced by at least 20%. The government's own advisory committee concluded that they could find no justification for this reform and have asked for clarification from the government.
If a benefit is already very efficient, yet a government announce a 20% cull before a single assessment has even taken place, we conclude it can only be a cost cutting measure that will ignore genuine need.

3) Time limiting Employment Support Allowance (ESA, previously Incapacity Benefit) to 1 Year
Many people who need to claim ESA have "long term variable" or chronic illnesses such as MS, Parkinson's, Bowel Disease, Leukaemia or severe Mental Illness. These conditions often do not go away after a year and sadly, often get worse over time. A high percentage of those with these conditions are being found "fit for work" under ESA but after 1 year, even those who have been found unfit for work will receive no state assistance whatsoever if they have a working partner. All of their benefit will be stopped, a loss of just over £5000 a year.


4) ATOS assessments are "unfit for purpose" and a better way of assessing need must be implemented. 

ATOS are the private company charged with assessing over 1.5 million sick and disabled people during this parliament.

-Up to 40% of rejected claims are going to appeal with up to 70% of those decisions being overturned with representation.
-Assessments are humiliating and degrading causing great anxiety to those genuinely in need.
-Just 7% of previous claimants are being found unfit to work on a long term basis.
-Testimony from Consultants and GPs is often ignored entirely.
-People are dying before lengthy appeals can be heard.
-Even the professor who designed the structure of ESA calls them a "complete mess"

There are other problems with the bill - capping housing benefit; re-classifying "mobility" so that those who use their wheelchairs too efficiently can be classed as "fully mobile"; removing an age related payment from ESA; scrapping the Independent Living Fund; cutting community care provision; cutting the Access to Work programme and many more - all of which will hurt sick and disabled people disproportionately, but the four points above MUST be addressed before the Welfare Reform Bill is passed.

They are causing or will cause real hardship.
They will not achieve savings as pressures will only be shifted to the NHS or social care provision.
They will increase homelessness, mental illness and poverty amongst this most vulnerable group of all
They will leave many in genuine need without support
They reduce the independence, standard of life and dignity of those we have a basic duty to protect.

I urge you to give these issues your time and consideration. Please, help us to make sure that amendments to the bill are passed ensuring that these 4 issues are addressed.

Yours sincerely,

...............[add your name]

List of contact details :


Baroness Thomas of Winchester
thomascm@parliament.uk
Baroness Stowell of Beeston
stowellt@parliament.uk
Lord Bishop of Hereford
bishop@hereford.anglican.org
Countess of Mar
marm@parliament.uk
Lord Feldman of Elstree
chairman@conservatives.com
Lord Freud
freudd@parliament.uk
Lord German
germanm@parliament.uk
Lord Addington
addingtond@parliament.uk
Lord Adebowale
adebowalev@parliament.uk
Lord Beecham
beechamj@parliament.uk
Lord Boswell of Aynho
boswellte@parliament.uk
Baroness Campbell of Surbiton
campbelljs@parliament.uk
Baroness Greengross
greengrosss@parliament.uk
Baroness Grey-Thompson
greythompsont@parliament.uk
Baroness Hayter of Kentish Town
hayterd@parliament.uk
Baroness Healy of Primrose Hill
healyab@parliament.uk
Baroness Hollis of Heigham
hollisp@parliament.uk
Baroness Howe of Idlicote
howee@parliament.uk
Lord Kennedy of Southwark
kennedyro@parliament.uk
Lord Knight of Weymouth
knightja@parliament.uk
Lord Low of Dalston
lowc@parliament.uk
Lord Mackay of Clashfern
mackayjp@parliament.uk
Lord Mckenzie of Luton
mckenziew@parliament.uk
Lord Morris of Handsworth
morrisw@parliament.uk
Lord Ramsbotham
ramsbothamd@parliament.uk
Lord Touhig
touhigjd@parliament.uk
Lord Whitty
whittyl@parliament.uk
Baroness Wilkins
wilkinsrc@parliament.uk