Dear 43 Things Users,

10 years after introducing 43 Things to the world, we have decided we have met our last goal: completing the incredible experience that has been 43 Things. Please join us in giving one last cheer to all the folks who have shared their goals with the world, as well as all the people who have worked at The Robot Co-op to build this incredible website. We won a Webby Award, published a book, and brought happiness to a lot of people.

Starting today, 43 Things users can export their goals and entries from the site. Starting August 15, we will make the site “read only”. 43 Things users will still be able to view the site and export their content, but we won’t be taking any new content from users. We hope to leave the site up for folks to see and download their content until the end of the year. Ending on New Year’s Eve takes us full circle.

It has been a long ride (one of our original goals was to "build a company that lasts at least 2 years” - we beat that one!) While we wish the site could live on, it has suffered from a number of challenges - changes in how people use the site, the advertising industry, and how search engines view the site. We wish the outcome was different – but we’ve always been realistic about when our goals are met and when they aren't.

As of today, you will be able to download your goals and entries. See more about that on the FAQ page. Thanks for 10 great years of goal-setting and achieving.

- The Robots.

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MEAW 2011 (read all 10 entries…)
The Social Model of Disability - text from The Red Cross UK

Because awareness campaigns such as this should ultimately aim to reduce how disabling an illness or an impairment can be, I thought it was right to end the week with an essay about the social model of disability. I have made one or two amendments in square brackets, and if you don’t want to read it you could watch a short video about the subject here. Society should work for its members, not against them. Your awareness potentially helps to enable impaired people, even if just a little. Thanks again for your support!

The social model of disability is a different way of thinking about disability. It has been developed over years by academics and campaigners. The idea is to replace old-style thinking with a very different perspective.

Why is a social model of disability needed?

The standard way of thinking about disability in the past was the so-called medical model. That remains fine for doctors, but it is less useful for others. The medical model, naturally enough, concentrates on disease and impairments. It puts what is wrong with someone in the foreground. It is concerned with causes of disease. It defines and categorises conditions, distinguishes different forms and assesses severities.

All these are important in diagnosis, prognosis, devising treatment programmes and in prevention but they are not very relevant to the way that someone with a disability lives their day-to-day life. If you have epilepsy, you know what your seizures are like. It isn’t necessary to know whether doctors regard them as mild, moderate or severe. It may be interesting for someone to know that the Latin name for their movement disorder is hemiplegia, but the chances are they are concentrating on more practical things.

Perhaps the most important consequence of the medical model is that bringing the impairment into the foreground risks pushing the person into the background. They become less of a person, and more a collection of symptoms.

What is unhelpful about the medical model?

It is likely to inspire pity, or even fear. Pity is not a useful commodity. Many people are scared of impairments, sometimes irrationally so. The model risks objectifying people, lumping them together because of their condition, not because of who they are. It is not nice to be told you are a typical case of something or other – and even worse to be viewed like that.

What is more, it doesn’t have very much to say about people’s lives and how they live them.

How is the social model of disability different?

Instead of emphasising the disability, the social model puts the person at the forefront. It emphasises dignity, independence, choice and privacy.

A key concept of the social model is that society disables people. Another way of saying that is that disability is a social construct. How we organise things in our culture limits and restricts what some of its members can do. That takes some understanding, so first it is worth clarifying some terminology.

Words are important, not because of the need to use the fashionably correct terms, but because the terminology reveals the thinking behind them. Here are some definitions of two key words:

Impairment. Having an impairment means there is something not working properly with part of the body, mind or senses. Someone who has had a leg amputated has an impairment. So does someone whose learning disability makes it difficult for them to remember things. So does someone is partially blind, or deaf, or who has epileptic seizures, or who has unwanted muscular spasms, or any number of things that don’t work properly.

Disability occurs when a person is excluded, because of their impairment, from something that other people in society take for granted. That might be the chance to attend an event, access some service or get involved in an activity. It might be to live independently, to earn a living, to be kept informed, or just to make choices for themselves.

You might assume that the impairment [always] causes the disability. Wrong. It is the choices society makes that causes someone to be disabled [or more disabled]. Organise things differently, and they are suddenly enabled – though the impairment hasn’t changed.

An obvious example might be a deaf person wanting to attend a conference. If no sign language interpreter is there, or no loop for a hearing aid, there is not much point in going. The person is excluded – disabled. But with a signer operating alongside the speakers, or a loop, the person can take part just the same as anyone else. They still have the same hearing impairment. But they are not disabled.

The same applies to a wheelchair user wanting to get on a bus. If it has room and access for wheelchairs, they are fine. If not, they are disabled. And so with a visually impaired person wanting to find out what the council is doing. If information is available on tape, they are enabled. If not, they are disabled.

So the impairments themselves don’t matter?

Obviously, they still matter. Not being able to see, hear or walk, has an important effect on people. The idea of the social model of disability is to give them a chance, to remove barriers that society places.

So impairment does not have to lead to disability?

That is right. Think about people who are have poor vision – short sight or astigmatism. Without spectacles or contact lenses very many would have a much reduced quality of life. They could not join in many events and activities, and may even be a danger to themselves and others in certain circumstances. But society provides an ophthalmologist on every high street, and a system of getting affordable corrective lenses. As a result, people with bad eyesight don’t have to be excluded from anything. If we ordered life differently, the same could be true of people with other conditions we think of as “disabilities.”

Isn’t using aids and adaptations for everyday life still a disability?

No. Or if it is, we are all disabled. We all rely on aids and adaptations of some sort in our daily lives. We use motor vehicles for transport, electronic aids for entertainment and accessing information. We rely on flushing toilets and water on tap for comfort and hygiene. We need electrical gadgets for cooking and washing clothes. Our society would disable everyone if these were not so readily available.

What does the social model mean for disabled people?

The logic is that only disabled people – as individuals or groups – know how their ability to participate in society in the way that they want to is affected. It is not something you can easily identify from outside. So, to find out what needs to be different, disabled people need to be listened to. That puts them at the centre of things, replacing the paternalistic “we know what’s best” approaches of the past.



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