Movement mourns father of social model

The disability movement is mourning the death of one of its pioneers, an academic and anti-apartheid campaigner whose work “transformed people’s understanding of disability” and laid the basis for what became known as the “social model”.

Vic Finkelstein’s ideas influenced a generation of disabled activists to join what he described as a struggle against oppression.

Finkelstein wrote about how being imprisoned for anti-apartheid activities in his native South Africa in the 1960s helped influence his understanding of disability.

The only time that things were ever made accessible for him, he said, was when he was in jail, adding: “Somehow, when the state has a need it does make things accessible!”

After becoming disabled following a pole vaulting accident as a teenager, he had come to believe that disabled people “face the most prevalent, world-wide, persistent, resistant to change and endemic form of apartheid, to put it mildly, of any human group throughout the world”.

After leaving South Africa in 1968, he came to Britain as a refugee and linked up over the next few years with members of its youthful disability movement, meeting activists such as Ken and Maggie Davis, Paul and Judy Hunt, and Sian Vasey.

In 1972, Finkelstein helped found the Union of the Physically Impaired Against Segregation (UPIAS) with Paul Hunt, who had spent much of his life in Leonard Cheshire residential homes and campaigned against institutional discrimination.

UPIAS took what was then seen as a radical new approach, arguing that the main issue facing disabled people was their oppression by society, rather than seeing disability as “a personal tragedy”.

Finkelstein’s redefinition of the fundamental principles of disability was later described by the disabled academic Mike Oliver as “the social model of disability”, the key to understanding disabled people’s oppression.

What was “paramount”, Finklestein wrote later, was “our focus on the need to change the disabling society rather than make us fit for society”. He and his fellow UPIAS members were seen as “extremists” by the established disability charities.

Vasey, then in her early 20s, and now director of Ealing Centre for Independent Living, says she had been “in awe” of Finkelstein, who was “a force to be reckoned with”.

She says he made a “huge” contribution to the disability movement. “He changed how we think about disability. He challenged you to be more radical and didn’t tolerate anything that wasn’t.”

In 1975, Finkelstein helped influence the thinking behind Link, a new television programme about disability, and wrote a script for a cartoon, Very Crossroads, which ran on the show for a year and illustrated how attitudes and the environment create disability, rather than people’s impairments.

“Overcoming apartheid,” he would write later, “involved turning the racist world upside down and in my story disabled people living in an apartheid-like village become the dominant group, design the social and physical environment exclusively for themselves and then oppress people who deviate from themselves.”

Rosalie (now Baroness) Wilkins, who presented Link, says Finkelstein made a “huge” contribution to the disability movement.

She says: “It feels like the end of an era with his death. He was the person who first gave life to the idea of the social model. He was a very compassionate man but a very tough one and a fantastic family man.”

Finkelstein also played a major part in setting up the British Council of Disabled People (BCODP) and was its first chair, studied psychology and teaching, taught on the Open University’s (OU) ground-breaking disability studies course, and later helped set up the London Disability Arts Forum.

In 1981, he represented Britain at the first world congress of Disabled People’s International in Singapore and was elected onto its world council.

He also helped set up Disabled People Against Apartheid, and campaigned successfully for the exclusion of the South African team from the Stoke Mandeville games for disabled athletes, at a time when the country was already barred from mainstream international sport.

Professor Jan Walmsley, a former OU colleague, says Finkelstein had “an enormously powerful influence not only on the way the OU taught and continues to teach in health and social care, but also on UK disability policy”, including the Disability Discrimination Acts and the personalisation agenda, and put the OU “at the forefront of teaching and thinking about disability”.

She adds: “As a colleague he was enormously generous to me, encouraging me in every conceivable way to develop my ideas, writing and research. [He was] a great fighter for what he believed in.”

After leaving the OU in 1994, Finkelstein was invited by Professor Colin Barnes to become a senior visiting lecturer at the Centre for Disability Studies at the University of Leeds, and continued to be involved with the centre until his retirement in 2008.

Barnes, another hugely influential figure in the movement, had first written to Finkelstein in the early 1980s as part of his research into disability discrimination.

He was sent a copy of Finkelstein’s Attitudes and Disabled People, which explained clearly “why disabled people are discriminated against in Britain”.

He says: “His work has influenced everything I have done ever since. He was there at the very beginning. He transformed people’s understanding of disability.”

He says that, thanks to Finkelstein’s work, “every country in the world now recognises that disability is a political issue”.

Barnes is another who points to his influence on UK disability discrimination legislation, as well as the UN Convention on the Rights of Persons with Disabilities, with tributes to Finkelstein and his work coming from disabled activists, writers and academics across the world, including Japan, South Africa, the US and Canada.

Rhian Davies, chief executive of Disability Wales, described after hearing of Finkelstein’s death how she heard him speak at a conference 25 years ago.

She wrote on her organisation’s website how hearing him talk about how “people with impairments are disabled by society, that disabled people should control their own organisations and develop their own culture… instantly illuminated” the experiences she had had since acquiring an impairment.

She said: “Instead of blaming myself for not trying hard enough to fit in with the ‘able-bodied’ world, I realised that it was society that had failed to accommodate the reality of people with impairments.”

She said Finkelstein was a “great man with an extraordinary vision”, and added: “Championing the social model of disability has been one of the main driving forces in my life; to have learned about it directly from the person who devised it was a huge honour and privilege.”

Colin Barnes admits that he was initially “in awe” of Finkelstein, and found him “very intimidating”.

But he adds: “As I got to know him, he was a very warm-hearted human being. The more you got to know him, about him, the more you realised he was a truly special individual.

“There is no way you could not look up to Vic Finkelstein, for his clarity of thought, his wisdom, his humanity. In many respects, we all stand in the shadow of Vic Finkelstein.”

News provided by John Pring at www.disabilitynewsservice.com

TUC protest: Disabled people send powerful messages to government

Disabled people who took part in the huge TUC protest march and rally in London have sent a series of powerful messages to the government about the impact of the cuts on their lives.

They told Disability News Service during Saturday’s event why they had joined the hundreds of thousands of other protesters who took part in the March for the Alternative.

Linda Burnip, a founder of Disabled People Against Cuts, which played a big role in supporting disabled people to take part, said: “I am hoping to send a really powerful message to all politicians, including Ed Miliband [the Labour leader], that we are not going to be messed around with.”

Stuart Bracking, a member of the Unison union, said he was demonstrating to protect services and to protest about cuts to disability benefits.

He said: “I have been on demonstrations over the last 20 years and the visibility of disabled people is much higher on this demonstration than it has been over the last 20 years.”

Doug Whalley, who lives in a residential home, said he believed disabled people were being “unfairly punished” for “something that wasn’t our fault”.

He said the proposal to stop paying the mobility component of disability living allowance (DLA) to people in residential care was “really sick”.

And he appealed to the government to “stop making up stuff about disabled people and tax the bankers, not the people who can afford it least”.

Deborah Sowerby said she felt as if she was “among friends” on the protest, and added: “There has not been enough of this coming together. There are a lot of us and we are not going anywhere and that is why we are here today.”

Adrian Whyatt, from the London Autistic Rights Movement, said: “We need to try and get them to see these cuts are not working.”

He said disabled people were being “targeted” by the government, and pointed to the mobility component decision, and problems with the notorious work capability assessment.

Sian Vasey, director of Ealing Centre for Independent Living, said she was worried about cuts to social services, and added: “If they dismantle everything they are only going to have to rebuild it again.”

Marian O’Brien, coordinator of Ealing User Involvement Service, said her message to the government was to not privatise services.

She said: “We want to keep our welfare state. The ‘big society’ will not happen because they are cutting back on funding. They are dismantling the welfare state bit by bit.”

Anne Pridmore, chair of Being the Boss, which supports disabled people who employ personal assistants, said she believed the cuts had put disabled people’s rights back 20 years, while the government’s reforms were about “trying to get big businesses rich”.

She said: “I am so angry. In three years’ time it looks like I will end up in an old people’s home. Without support, people will not be able to get up in the morning. If disabled people have not got the support packages they will not be able to go to work anymore.”

Her colleague Jan Turner said: “I am here because of the service cuts, because of all of the money they are spending on the census and the Afghan war and the Gaddafi war and all the tax evasion.

“I think they are doing unnecessary cuts to people who are vulnerable. I am doing it for other people who can’t protest.”

Sheila Blair, also from Being the Boss, said: “I volunteer with a lot of organisations. What I don’t want is for a lot of organisations like the ones I volunteer for to get to a position where they have no staff and everything is done by volunteers in the name of the ‘big society’, which is a lot of shit. I just get very angry about it all.”

Frank Lerner, a retired head teacher, said: “Everything I have ever worked for in my life is being destroyed. I just think that this government is out to destroy the infrastructure of our society for their own easy ends.

“The cuts are nothing to do with what is needed, they are to do with what they want to achieve. It is dogma rather than necessity.”

Raymond Johnson, from People First (Self Advocacy), said he believed the banks should be forced to make cuts rather than disabled people.

He said: “Obviously there are lots of people here against the stupid cutbacks. Saying ‘we are all in this together’, I don’t think so. There are a hell of a lot of people here.”

Sandy Marks said she was protesting “because I can and because when they have finished with us I will not be able to”.

Sarah Fisher, from Knutsford, Cheshire, said: “The banks got us into this mess but it is the ones who are least able to cope with cuts who are going to be paying for it. There is no fairness in what is happening.”

She added: “I am hoping that this will help. I think if nothing else it will give a wake-up call to the government in that not everybody is behind this ‘we are all in this together’.”

Lisa Egan, co-founder of the Where’s the Benefit? blog, said she was there “to protest against the cuts, because I need the welfare state and the NHS in order not to die”.

Louise Hickman, from Hackney, said she had joined the protest because of the “vulnerability of support for disabled people in further education”.

Olcay Lee said: “We are here to stop the cuts if we can.”

Her husband, Andrew, director of People First (Self Advocacy), said: “Disabled people didn’t actively put us in this mess.

“We are very concerned that cutting services for disabled people, there is no logic to where the cuts are actually being made.

“Yes, we need to get the country into a better shape but disabled people need the right support. Without the right support there will be more money [needed] to clear up the mess.”

Andrew Hart said he was at the protest as a disabled trade union member, the trustee of a voluntary organisation that was suffering from the cuts, and the father of a son with autism, who was facing the loss of education maintenance allowance (EMA) as he prepared to start sixth form college.

Riven Vincent, from Bristol, the disabled mother who caused a media storm after saying she had asked her council to take her disabled child into care because of a lack of respite, called on the government to rethink its DLA reforms, and its plans to remove the mobility component from those in residential care.

She said: “I am marching because of the cuts that will affect disabled people, including my daughter Celyn (Williams).

“I have met David Cameron and he promised none of his cuts would affect disabled people and he has lied.”

Dean Thomas, from Nottingham, said he was on the march “because I can be here. For other people who can’t be here. The cutbacks are focused on the most vulnerable people in society. They are completely wrong.”

John, who asked not to give his surname, said he had joined the march because services were under threat.

He was scornful of David Cameron’s “big society”, and said: “The expectation that there will be all these volunteers to do the jobs is a bit false. There are already volunteers in society. How many more are there going to be?”

Margie Hill, from Knowsley, Merseyside, a member of the Unison union who works in local government, said she believed the government wanted to target disabled people, and was going to “try to pick them off, get rid of them” and “scupper our benefits”, while any new jobs would go to non-disabled people.

Catherine Callaghan, also from Knowsley, has been made redundant from her job with Greater Merseyside Connexions Partnership, which she said had cut more than 40 per cent of its workforce.

She had worked there with disabled young people, and said the loss of EMA meant young people would be “dropping out in their droves from education, hanging round the streets and there will not be people like us to interact with them to get them back on track”.

Jonathan Bartley, who is not disabled but cornered David Cameron in front of TV cameras before last year’s general election about his battle to secure a mainstream school place for his disabled son, Samuel, said his wife had lost her job at Sure Start.

He added: “Clearly it is affecting our family, our whole community, and it is very important that the government understands that this is not what the country voted for.

“What seems to be happening is the poorest and the most vulnerable are paying the price for the financial crisis they didn’t get us into.”

News provided by John Pring at www.disabilitynewsservice.com