Vote With Your Hearts #wrb & Don't Leave Disabled People Out In The Cold

Vote with your hearts, and don't let the Welfare Reform Bill leave disabled people out in the cold...

Image shows a naked disabled woman lying on a snowy beach unable to reach the attendant wheelchair next to her

 

 

 Image taken by Graeme Lamb Media

Time Limiting ESA - Template Letter to Lords

Yesterday, I asked you all to write to a Lib Dem peer and plead with them to vote against time limiting ESA to just one year.

Today, I've written a template letter for you to use. Template letters are certainly less effective - many parliamentarians won't open more than one or two of them. However, they are better than not writing at all. For every peer who receives 5, 10, 50 template letters, at least they get to see the strength of feeling people have over an issue.

If you don't have the confidence to write your own, please use this one. Peers might also remember that I write for disabled people. Many cannot write a letter themselves. Due to physical or mental disabilities, I have often had comments from those so very grateful that a template letter I have provided allowed them to engage democratically.


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"Dear .........................

I am writing to you in the hope that you will vote against time limiting ESA to just one year in the coming welfare reform bill Report Stage and Third Reading.

-700,000 people with serious illnesses and impairments will be affected by this policy, many losing any right to an independent income. http://www.dwp.gov.uk/docs/esa-time-limit-wr2011-ia.pdf

-The means test is set at just £7,500 per year, meaning that a partner must support an unwell or disabled loved one if they earn more than this.

-Families already overwhelmingly living in poverty will lose £4661 per year. This is three times as much as higher rate taxpayers will lose in child benefit.

-This policy only affects working families and savers as it only applies to those who have contributed NI or have savings over £6000.

-It is a disincentive to work and will only encourage families to break down http://www.dwp.gov.uk/docs/esa-time-limit-wr2011-ia.pdf


-The only justification ministers have given for this policy is that "We can't afford it" Sick and disabled people with limited capability for work are conflated with jobseekers as ministers claim ESA must be brought into line with JSA

-Ministers admit that 94% of those affected will not have found work by the end of the year. They also insist that it is irrelevant whether or not they have recovered. http://www.dwp.gov.uk/docs/esa-time-limit-wr2011-ia.pdf


-People with serious, lifelong, and degenerative conditions will all be affected by this. People with MS, Cancer, Parkinsons, Bowel Disease, Kidney Failure, Heart Disease, Lung Disease, Schizophrenia, Bi-Polar and many many more conditions will lose benefits, left in limbo until they are judged unable to do any kind of work at all,. http://www.publications.parliament.uk/pa/cm201012/cmselect/cmworpen/1015/1015vw44.htm

At your annual conference this year, Liberal Democrat members voted overwhelmingly to oppose an "arbitrary time limit" on ESA. http://carons-musings.blogspot.com/2011/09/please-support-glasgow-norths-brilliant.html Please, please, stand by the wishes of your grassroots and of your party and oppose this cruellest of measures.

We are relying on you to help us. Only Liberal Democrat peers can provide a majority and ensure that a one year time limit on sickness benefits is not made law. Please, you promised to protect the most vulnerable and if ever a policy hit the most vulnerable the hardest, then it is time limiting ESA.

Many thanks

........................


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Here is a link to Lib Dem Peers. Simply click on it, pick a letter of the alphabet at random, and copy and paste in the letter. http://www.libdems.org.uk/peers.aspx
The more you can do, the more we can persuade. Thank you.

Finally, please keep up the pressure and RT, share on Facbook, email to friends and feel free to cross post this.

The Hardest Hit Protest, Leeds

Last Saturday thousands of ill and disabled people, their carers and supporters took to the streets in cities across the UK to protest against the cuts that are unfairly targeting them. This unprecedented event was The Hardest Hit October Action.

It takes a lot to make the disabled community take to the streets, mainly because its so difficult for us. If you had eavesdropped my twitter feed last week you would have seen my conversations and musings dominated by The Hardest Hit as we all shared protest survival strategies. We knew there would be a price to pay in our health for attending but as one of my friends put it, "protesting will hurt me but not protesting will hurt me more". 

For every one of us attending an event there were hundreds who were unable to go because they were too ill or disabled, too poor, too busy caring for someone or just couldn't use our inaccessible public transport. They sent messages of support, they were with us in spirit. 

I'm not an activist or a disability campaigner, I'm just an ordinary person struggling with some pretty serious mental health problems. I am, like most other ill and disabled people, one of the hardest hit by the cuts.
I travelled to Leeds to join the Hardest Hit protest because this Government wants to stop my benefits, remove my services, call me a scrounger and force me from my home. For many of us this protest is personal, we're not just fighting for fairness - we're fighting for survival. 

Over two hundred of us gathered in the sun in Leeds. We marched along The Headrow bringing the city centre to a standstill. Shoppers stood and watched as we marched with our wheelchairs, our Assistance Dogs, our mobility scooters, our carers, our children, our friends and our banners. Speeches were made by disability activists, charity sector workers, trade union members, NUS members, a local MP and ordinary people facing huge challenges. The message from all of them and the people listening was clear - these cuts are unfair, we are afraid and we are angry. 

There is a 'perfect storm' facing ill and disabled people. We are already struggling to survive from day to day. Our NHS services are being cut and the voluntary sector agencies who would offer us support are losing their funding. The benefits of those of us who cannot work are being cut or removed and those of us who do work are losing the practical and financial support necessary to make working possible. The additional cuts proposed in the Welfare Reform Bill will leave us and our carers more impoverished, isolated and vulnerable. On top of this, ill and disabled people are being labelled as scroungers and benefit cheats, vilefied by the media and treated with suspicion by the public. Disability hate crime is increasing, people are facing abuse and harassment on a daily basis and many are afraid to leave their homes. 

This Government has promised to support disabled people who are in genuine need - but only if THEY can define 'support', 'disabled', 'genuine' and 'need'. This is a cynical disability denying ploy to remove support from the people who need it. This Government is merely transferring funds from ill and disabled people and carers to private companies making millions from 'welfare reform'. 

One of the most disturbing things is how badly informed most people still are about this. The public still think that disability benefits are a 'lifestyle choice' and believe we are all driving around in BMWs. Sadly many disabled people and their carers are still unaware of quite how badly the cuts will affect them. The media is not listening to the disabled community, some of the Hardest Hit events attracted over a thousand protesters but there was barely any BBC television or radio coverage. The future for society's most vulnerable is bleak. We are 'all in it together' its just that some of us are deeper in it than others. 

Attending the protest left me with mixed feelings. I was proud to stand in solidarity with the hundreds on the streets of Leeds, the thousands in cities across the UK and the tens of thousands who were there in spirit.

But I was also sad and angry that this country should need an event like The Hardest Hit at all.

Guest Post by Vanessa Teal