More Stupidity

The Coalition Government plans to scrap DLA in favour of a new objective benefit called Personal Independence Payments and will include a medical assessment in order for a claimant to prove entitlement according to a public consultation paper into DLA reform.

So the attack on sick and disabled people is set to continue! Please share this frightening information with as many people and groups as possible so that a proper campaign against scrapping DLA can be coordinated. I can see these changes bringing out a huge number of people onto the streets in protest to show the government that ENOUGH IS ENOUGH!!!

The full consultation can viewed and downloaded here;

http://www.dwp.gov.uk/docs/dla-reform-consultation.pdf

The following comes from that said report;

THE GOVERNMENTS APPROACH TO DISABILITY BENEFIT REFORM

We propose to replace Disability Living Allowance (DLA) with a new cash benefit – Personal Independence Payment – which will contribute to the extra costs of overcoming the barriers faced by disabled people to lead full and active lives.

The benefit will reflect changes in society, such as legislation. Disabled people are rightly not prepared to accept being restricted from playing an active part in society. We need a benefit that helps contribute to the extra costs of living independently, in a way that is right for each individual.

The benefit will continue to take account of the social model of disability. The assessment will be objective, reflect the impact of the barriers disabled people may experience, and make sure they are treated as individuals.

Central to Personal Independence Payment will be a new, fairer, objective assessment, which will allow us to identify those who face the greatest need, in a more consistent and transparent manner. We are developing the new assessment in collaboration with a group of independent specialists in health, social care and disability, including disabled people.

Personal Independence Payment will be based on need not income and will be a more active benefit, recognising changes to individuals’ situations and taking account of the support that disabled people can access to help them live independently. Where possible, we will signpost individuals to support that may help them manage their condition. We will ensure that the award continues to reflect the individual’s changing needs over time by building in periodic reviews.

The new benefit will be introduced in 2013/14, so there will be further opportunities to feed in views on how we might deliver it. We are already involving disabled people in developing the new benefit and will continue to do so.

We will introduce a Bill that will set out the high-level legal framework underpinning the new benefit, with the detailed requirements set out in secondary legislation.

Responses to this consultation will be used to inform secondary legislation on this detailed design, including the new assessment process. Where possible, and in particular on the new assessment, we will be publishing draft regulations during the passage of the Bill.

WHAT WILL STAY THE SAME

We want to be clear about what we propose will remain the same under the new system. We recognise that there are a number of features of DLA which many disabled people value, in particular the ability to spend the money in a range of ways to meet their personal circumstances. That is why Personal Independence Payment will remain an extra-costs benefit, providing cash support and allowing disabled people to spend the benefit in the way which best meets their individual needs.

The new benefit will not be means-tested or taxable, and payment will not depend on having paid National Insurance contributions. It will continue to be available to those who are in work, as well as those who are out of work.

Support will continue to be provided to children and adults up to the age of 65. Individuals who receive the benefit before reaching 65 may continue to receive Personal Independence Payment if their needs continue. We will keep the upper age limit for receiving the new benefit under review, given the changes being made to the State Pension age.

We will continue to support those in the most difficult circumstances by
maintaining special rules for people who are terminally ill. Claims submitted under these rules will be fast tracked to provide financial support as quickly as possible.

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I can not stress the importance of getting this information to as many people as possible. If you run a group which has interests in protecting disabled people please copy this message and forward it on to others.

If you are a member of such a group or organisation please forward this message onto whoever runs the group or organisation or anyone else who may be interested.

This shocking treatment of disabled people can not be permitted to continue!

This I took from the facebook page Welfare Rights. With thanks to Steven Preece.

I am again seeking legal adivce about my benefits. I have been told by several people including my own MP Sir Peter Soulsby, that they think that I should be on the higher rates. The DWP have said I am not able to work yet they are saying im not disabled enough to get the higher rates. I now have the support of my local councilor Ross Grant.

I dont choose to be disabled I dont think that anybody would. I would love to be able to go out and work again. That way I wouldnt get comments like im being greedy or lazy.

Most of my family go out and work and it seems that I am the only one not able to. I have to watch every single penny I get coming in. Sometimes my account gets overdrawn and my accoun accours charges.

The government are now going to cut benefits for people yet again. Will we be going back to Victorian times and having poor houses. Pick Pocketing is susposed to be illegal yet with the government cutting peoples money surely thats what they are doing? More people will be turning to crime to be able to live. Then again I suspose that people would be better off in prison. They would get 3 meals a day, no bills to pay and more human rights.

Acceptance

Children seem to be more accepting of disabled people than adults. I go to visit my friends and their daughter Shannon runs up to me and gives me a hug. She doesn’t care about anything I have wrong with me. She just wants me to play with her.

With my condition Neurofibromatosis, it causes me to have tumours all over my body. She asked me why are you so spotty. She’s only 5 years old. I explained to her in simple terms and that was that.

It’s the adult population who change the kid’s minds. Children don’t see the wheelchair they seem to see the person that is in it. If people teach their kids to accept others more then they will grow up understanding everybody is different.

Just because a person looks different on the outside or has different abilities they still have feelings. I remember a quote from somewhere I forget where, “if you cut me do I not bleed”. A disabled person still has feelings. Disabled people are not second class citizens if you got to know them you may find that you have things in common with them.

It’s the same with people of different races and sexuality. In this day and age most countries are multicultural and have people with different sexual preferences. If a child is brought up to accept this as normal then they will grow up to treat all people the same.

I don’t see a person for their colour or sexuality I just see them for the person they are. Why should a person be judged for being different to his neighbour or friend?

Update

Again I reapplied for Disability Living Allowance at the middle rates. Again I have been turned down. In basic terms because I have coping methods it makes me less disabled. They don't take into account I can never work again.

I have also lost some of my housing and council tax benefit. They seem to let Asylum seekers have no trouble having money, yet people who have lived in the country all their lives get shafted. In London an asylum seeker gets paid £2000 a week in housing benefit, after being moved from a house only costing £800 a week housing benefit because she didn't like the area. I am not a racist but they need to think about the people in this country who need help first before helping others.

There is people who get high rate disability for having an addiction or just being depressed. If they have an addiction surely giving them more money gives them more money to spend on it. If someone is depressed, they should go out and get a job perhaps that would stop them feeling so depressed.

I have been told by people to stop complaining and be grateful for for what I get. If I could work I would are they or anybody out there, willing to find me a job that I can do for 3 hours a week for a full weeks wages then I would work.

I read in a news paper about a war hero who lost a leg. He has been told hes not entitled to some benefits. This is completely wrong. He was fighting for our freedom he deserves all the help he can get.

This government and the last seem to think if you can cope your not entitled to help. It needs sorting!

Benefit Changes

Following recent releases from the Government and the DWP it has become clear that they intend on making it far more difficult to successfully claim Income Related Benefit's.

This will be partly done by forcing sick and disabled people back into work by working out exactly what they believe those people would be capable of doing. Many Welfare and Disabled charities have shown contempt and dread at these prospect's pointing out that sick and disabled people in the work place poses a real risk of injury to both themselves and others. Not to mention the probability that forcing such people back to work to early, or when they are clearly unable, will only aggravate their conditions causing them to go back onto sick and disabled benefit's; if they can get them.

So what happen's if they can't? It's simple really; they will simply plunge even further into poverty, possibly losing their homes and maybe even loved one's because of the mental and financial stress it would put on the family structure. Either that, or they will have to work, making their health even worse and possibly end up in an early grave. I could be critical and say that the Government would welcome this because of saving's to the NHS and the Welfare System, but then that could get me in trouble, lol. But this is how it comes across. A kind of discreet Social Genocide, and if any Government personal are reading this don't bother suing because I ain't got nothing, lol. Unfortunately it looks as if it won't matter which party is in power after the election as both major parties look set to cut welfare and reduce the number of people claiming them.

Britain has the highest rate of Sick and Disabled benefit claimant's in Europe but maybe they should start looking at the reason's behind this. It is not necessarily down to people being "work shy", but more to do with the poor quality of living standard's in many communities like overcrowding or housing that poses a health hazard to their occupant's. This is the link to crime too! Instead of throwing money at constant welfare research and reform they should pump it into improving the quality of living for so many of Britain's citizens. Only this can improve people's health, where applicable, and will eventually bare fruit in the form of less people off work sick and improved life for all. Those saving's could then be put into improving the lives of disabled people by providing better services and standard of care as well as making the job of carer's much easier.

The problem is those in a position of power have mostly lived a financially stable life and have never had to learn how to live on nothing. Program's life "Tower Block of Commons" on channel 4 have tried to address this matter and in my own personal opinion, very successfully. Politicians who have volunteered to participate in the program have finally seen just how difficult it is to live of state benefit's and are also beginning to realise that the majority of those people DO NOT do so through laziness or simply to get some "free" cash. Of course there are those who choose not to work but they are in the minority and at a time when unemployed people out number available job's by as much as 10 to 1, it is both irresponsible and unfair to label unemployed people in such a manner. If you haven't yet seen this program on channel 4 I would definitely recommend it. You can view the episodes here;

http://www.channel4.com/programmes/tower-block-of-commons/4od#series-1

So let's see where some of that wasted money is going. The following research probably cost the tax payer more than your average sick or disabled person per year, and show's how the Government and the DWP see falling number's in those claiming Income Related benefit's. One of the most frightening of which is the one on Pension Credit. If they think our mature citizens will not be claiming the money on which they depend, just where exactly will it be coming from. You surely can't expect these people to work,....can you?!

http://www.dwp.gov.uk/docs/projections-of-entitlement-to-incomerelatedbenefitsjune2008.pdf

With thanks to Steven Preece for sending this to me.

Headway

Headway is a fantastic organization.  When I first had my brain haemorrhage they came to see me in hospital.  They offered great support to me and my family.    I was visited in hospital by one of their staff Sue Hannam.  She helped me to get Disability Allowance forms filled and gave me the opportunity to do different things.

After I left the hospital I attended Headway House 1 day a week.  They encouraged me to try new things and teach me basic skills like cooking and craft.  They also help people build up their confidence.  There is different types of brain injury and some people are worse than others. 

I met many different people during my time there.  Each one of them has something to give to society.  It helped me to learn to accept people for who they are.  Headway provides a range of staff and volunteers who all have different skills. 

They encourage people to try new things and to try to do things for themselves.  This is good as it helps people to regain their independence. 

Headway send some of the clients to college courses in partnership with local colleges.  This is very successful and again gets people to meet others.  I did courses myself on cooking how independent living and one where we went out to different places each week.  This was a help to me and stopped me becoming isolated. 

When my time came for me to leave Headway House.  I was appointed an outreach worker Padma Ram.  Again she helped me to fill in forms and help me find some volunteer work which I still continue to do.  They also offer support in taking you to appointments and explaining things to you that you are having difficulties in understanding. 

Headway signed me off their books as I was managing on my own.  Recently they have got back in touch and they will be coming to see me again with a new worker Nicola Rowe.  They said that even though I am coping I could do with a little more support. 

I am really thankfull for the support they have given me an will do so in the future.  Headway see their clients with brain injuries as human and treat them with dignity. 

Disability

Just because a person looks "normal" on the out side doesn't mean they are normal on the inside.I appear normal on the outside but on the inside is where the problems lie.

People with certain conditions get a raw deal. The government would rather get everyone into work to save money. They do not think about the long term. If like the government preferred, everyone worked it would cost them billions in hospital costs.

When I was fit and able to work the manager employed someone on a trial with downs syndrome. The company I worked at had n problem employing disabled people. I have been told by someone I can sit on my computer so henceforth I can get a job. If I worked now I would find it very hard. I do a bit of volunteer work now and I struggle after 3 hours. People say im just lazy but I have to work twice as hard as most people. That's what makes me tired.

I already feel useless that I have nothing to contribute, but when people snipe about it that hurts more. I would love to be able to make a difference to at least one persons life but I cant. I did want to try and do a degree just to prove to people I may be disabled but im not thick.

People think having a brain injury means that you have mental health problems. That is not always true. It sometimes means you have to try a lot harder to do basic things.

When you look in the mirror
What do you see
Do you see a waste of space
Or the man I could be


Yes I have no purpose
I sit bored every day
Because I cannot work
Well so the dr does say

That short poem I wrote is basically how im feeling. I shouldnt I know but when you cannot contribute anything to life, you start to feel useless.

Disabled people are not useless. A lot of people with disabilities have things to offer. Just because a person has got limitations or its not safe for them to work they might have skills other people dont.

Dont stare at a person because they look different. Ask them questions. Most disabled people dont mind questions. It educates people. That way it makes people more tollerant of others.

My home town of leicester recently hosted the special olympics. The visitors were all welcomed with open arms. This was plesantly surprising.

No 2 people on this planet are the same so treat everyone as a human being.

Humanity

Disabled people have no rights. Disabled people are not allowed to be happy, Disabled people are all just lazy and could work if they wanted too.

These are some of the comments I have had when I explained i am disabled. We are all human. Just because a person has difficulties doing things doesn't make them any less off a person.

I have had the attitude "you can sit on your backside all day you can get a job with computers".

I sit down most of the day because it makes me ill to stand for a long time. I find myself getting tired sometimes after being awake for a couple of hours. Society would rather I worked then made my self ill. Surely this would cost the UK government more?

The disabled are people as well if you cut us do we not bleed? Just because a person faces different challenges in life to survive doesn't make them less human..

I'm a 30 year old man who can never work again It already frustrates me as when friends phone me up to invite me out, I cannot afford to go. I'm losing more friends by the day. I asked my doctor to help me with my benefit situation, he had the attitude cut down on drinking beer then. I wish I could afford to drink beer it might take some of the monotony of life away

Everybody has the right to be treated with respect.