Archive for DIsabled People’s Direct Action Network

Celebrating The Best Of Our Year

Signs Of The Times

Signs Of The Times

 

I was put out a wee bit two weeks ago. A Community Champion expressed the view that there are good things going on and we should realise and celebrate it. I thought to myself well if that is your approach as a watchdog of health and social care then we are in trouble. I think he was referring to campaigning voices expressing discontent at a community event. We need to continue to voice our anger and dissatisfaction but maybe he has just a little bit of a point. So what was the best ting that happened to you this year?

Mine is such a simple pleasure that is built into a much bigger thing.

I got a new job this year at the Merton Centre for Independent Living and that’s well exciting. Travelling to work necessitates going through Kings Cross on the underground and every time I do I hear an announcement; “This station has step free access”. It fills me with pride. I think to myself, I was a part of that.

Back in the day, I campaigned with the Disabled People’s Direct Action Network (DAN) for accessible transport. We said it would be the first part of our drive for Independent Living. Today, we have more access on the underground, London Docklands Railway and London Buses. It’s not right yet but we’re getting there – ‘to boldly go where everyone went before’. We built an infrastructure for inclusion and its still going on around us. So, every time I hear “this station has step free access”, I smile.

I didn’t hear it last night but I travelled from Prince Regent to London Bridge with disabled poets; John O’Donoghue and Allan Sutherland and his partner, Vicky. They travelled on after I got off. The last time I travelled with so many disabled activists on the underground we took a circle line tube prisoner at St James’s, one stop before Victoria and faced down so much hostility from people going to work, shopping, heading to Gatwick for a holiday. They we’re so angry to be denied their independent lives. We we’re so smug and satisfied at handing out our lesson. So, on leaving these worthy, wordy friends I smiled again; replete with knowledge of secret histories.

What was best about 2013 for you.    

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Don’t Let The Jimmy Savile Thing Bring You Down

inverted picture of a badge stating that there is no excuse for child abuse

I received a message from a private facebook page asking members if the Jimmy savile thing was acting as a trigger to people experiencing mental health issues. My reply was as follows:

Nope!!!! The Savile thing is not a trigger for me. Its a source of pride. Last year I reprinted a press article on facebook about how DAN, the disabled people’s direct action network, had stopped Savile opening an accessible garden at Leeds British Rail – later one of our members came back and identified Savile as an abuser. He said that this had happened at Stoke Mandeville to some of our people. He was confident that the claim was true. We made this information available the day after he died and was getting the good obits and tributes for his charity work. We stood against him again. it’s a scarey thing to do to make a stand. We did our own in our own way. But like the Savile family i regret that this wasn’t done more eloquently and firmly during his life time. I was in Trafalgar Square on Saturday. A rally was happening. Its slogan was child abuse is no excuse. Hardly anyone was there. Survivors were speaking out. More pride, more recovery. Keep on speaking out. Let there be no excuse.

Lets stop child abuse.

Lets learn lessons from the collusion we believe might have happened in this scenario

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Service user training story

Warning!!! Warning!!! Difficult Service User.

Close your eyes and let me take you on a journey. You are going down your advocacy paths. Think of me like weather. Think of me like snow. I am here to interrupt your journey. I lie thick and sludgy dripping into your road, getting between your layers, turning to ice, and making holes in your advocacy journey.

Nothing here will be nice. Nothing will be friendly. I’m not hoping to be supportive. But I hope you take it as an opportunity for learning.

You can open your eyes now. You know where we are going. Let me tell you where I’m from.

I was born with a physical impairment. Leaving my mother’s womb I was struggling to survive due to my impairment. I was given to the NHS. Are you proud of the NHS? A lot of you are aren’t you? Maybe we are all their service users. But do you know what they do to disabled people? they poke us they prod us, they drug us, test us, experiment upon us. They want to fix, treat and cure and then they find they can’t so they drop us. And through all this time they are telling you and everyone around you in your communities, in your societies that we are bad, we have something wrong with us. Its not enough that they gave you a label for your condition, they have to go slap a value on it and those values are being used now. the deserving poor, the undeserving poor. The ones we will give benefits to, the ones we won’t. Us scroungers, us work shysters, we who broke Britain, and caused the sick note culture. So, they and their administrators, their leaders they are always getting rid of us. Hitler had some very effective strategies for this didn’t he?

The next thing they did was to wrap me up and post me off to a very special school or as they called it then a school for delicate children. They have done this for me because I am a delicate, withering flower and I need to be cared for. See how they value me. See how they send me away from family, away from friends, away from community. See how they send me to a new hierarchy. Heads of this, heads of that, teachers, house masters, house mistresses, dormitory leaders, table monitors. thugs. Every single one of them. See how they oppress you, see how they give you tasks they know you can’t do, just to undermine you, make you red-faced, cause you grief, cause you pain. See how they treat the first vegetarian I ever met. See how they forced meat into his mouth and see how some of them shove other pieces of meat into other holes and understand the dilemmas. Understand that they won’t let you speak, that they tell you that you cannot tell, for if you tell the most awful thing yet will befall you and consider how you might best survive this. Me. I used to run and hide, abscond, spend the night beneath the stars, close to trees, testing my body to survive the rain that was falling down, all around me.

And let me tell you about the education they give you about the way they equip you for the outside world. Well you can pray to god, you can be thankful there are others worse off than you, you can go and dig the garden or run about on the sports field before coming in for lunch, then spend time sleeping on camp beds set up for you in the gymnasium, before fitness tests, blow ping-pong balls up sloping tables, blow feathers in the air, press ups, touch ups. Wind ups.

I got by, I survived. I got out. I mainstreamed. The only disabled child in the new school. And I was fun. It was great fun to poke fun at me, a wonderful fun packed time to be spat at, to be slapped, to be punched, to have my ears flicked. The best part of all this fun and laughter, the great thing was I would never, well not for a few years anyway, fight back. And when I did fight back, I would never lose. I might hardly ever win but if you get knocked down the best thing is to just get up again. Take it on the chin again.

See the system for what it is. See how they want to impair you further, see how they take your voice away and drive you into mental distress and turmoil see how they want to make you stupid, see how they want to lead you into abuse and violence. Understand what it means to survive, understand what it does to us. Understand what it means to you as advocates when the society that you live in, the class systems that you are a part of, the professional groupings that you are becoming qualified to join through your certification, understand what all that does and what it leaves you with.

People like me. the undermined, the beaten, the betrayed, the stupid, the de-skilled, the disenfranchised, the disabled people, the ones who sink like i sank, the ones who drowned, the ones who died, the ones who came back, with anger and pride driving them, the ones who drove themselves, proving daily in every way that we are as good if not better than you, Because we got this from you and we came back with better. Understand why we challenge and understand why we are challenging.

And understand that you need to check who you are and where you are going now. Because if you want to say you’re sorry, then i can only seek to piss on pity and best check the choices too, the options that you are opening up to me as a disabled person as I become older, whilst our independence/freedom movements are under attack. Because I tell you this. I don’t want to die in a nursing home. I’d rather go to jail than die in a nursing home.

And wonder finally why you weren’t there as Advocates when I needed you, ask yourselves why I never knew you existed. It’s not enough to say you didn’t even exist then. Because someone, somewhere was being incredibly irresponsible and all I want from my Advocates are Advocates who will be responsible. Advocates who take responsiblity for where they are on the journey, Advocates who understand the real story and Advocates who use it to enable my people to move forward.

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A Letter to the Activists

Hi Sue, Clare, Nick and Mike

Could you take the time to have a look at this link please

http://www.facebook.com/topic.php?topic=276&post=864&uid=116511635036942#post864

Its about housing actions coming up in December and January.

I think its a good chance to get  some things going again

I’ve just looked for you on my facebook friends but see that some of you are missing (i did lose half of them recently). I’ll try to reconnect with you that way to.

You might also want to have a look at my facebook groups

Brent CHIEF Campaign for Housing Independence Equality and Freedom

http://www.facebook.com/group.php?gid=116511635036942
and BIG CHIEF. campaign for housing independence & freedom

http://apps.facebook.com/#!/home.php?sk=group_179857192028023&ap=1

Brent CHIEF was a small local group that we started up with the support of very few local advice agencies. We started with a chat from the Disability Law Service that we invited our members  with housing problems to.

Brent CHIEF grew out of this. Within 12 months we have met with each other, laid out a manifesto for change to housing provision featuring a set of demands, set a host of questions that we want housing providers in Brent to answer to and sketched a heap of strategies to take the issue further.

We set up the facebook group above and our first expressions of interest came from Scotland, Hastings and Warwick. Disabled People across the country are having major housing problems and this is impacting on our independence, freedom and equality.

Linda Burnip, Clare Glassman and myself pressured Disability Lib to host a first Disabled People’s Housing Consortium and it was from this that BIG CHIEF came.

I think we have a major opportunity here to push the free our people agenda. Alan Holdsworth once told me that the accessible transport campaigns was the first step to independent living. I felt that worked because the public could understand it. I don’t think they were ready to understand the free our people stuff but I think they could understand houses are essential to independence.

Anyway, I wanted to bring this to your attention so a) you were up to speed with what is going on, b) you can consider joining in, c) you can talk to other people about it, d) you can join the facebook pages and follow a developing story.

Thanks for your time

rich

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How i gOT cOMIC rELEIF cOMPLETELY wRONG

Sorry my mistake but i just love the look of that title. So that’s what happens when you press the caps lock.

As the creator of the We All Shot Pudsey Bear Facebook Group I should think my position on the sad, drab, charitable telefon is pretty clear. But Comic Relief failed to get my agitator’s juices flowing this year. I didn’t mind the build up on the beeb with each and every programme foaming to get a red snout on. I just ignored it when Bill Turnbull and his equally rubbish co-presenters across the beeb salivated with perceived goodness. optionally i just turned the box over or off. it’s really easy – especially in these golden lazy days of the tv remote.

I’d have liked to have got more wound up when traversing the streets i suppose. My bank had a dress down day to celebrate the ghastly day. I wouldn’t have noticed if i hadn’t heard a customer berating the illegal immigrant teller (trafficked in to make profits from glamour during the credit crunch) (that attempt at humour is beneath me – not) for not wearing red and then being flashed her shoes. No one seemed that bothered.

But i had a major pleasure last night. I was out. I didn’t watch tv at all. i didn’t have to surf around the beeb. I went to see Martin Carthy, Norma Waterson and Chris Parkinson at the Kings Head, Crouch End. Now i have to say this about Martin Carthy. It dawned on me how strong his commitment to the craft is. I find commitment a very interesting word this week when my commitment to my craft is wavering. What happened between me and DAN this week?  Why isn’t We All Shot Pudsey Bear getting more of my attention? Why is my vacillation vacillating?

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Action against welfare reform. Proclaimed in the Queens Speech. Whilst DAN Protested

DAN take to the streets again

DAN take to the streets again

12.3.08 – Whitehall, London International Day Of Disabled People

DAN. The Disabled People’s Direct Action Network Protest and block traffic outside Downing Street to object to Welfare Reforms proclaimed in the Queen’s speech – this day

 

DAN’s Sick Note – Press Release

 

Instead of celebrating the International Disabled Day of Disabled People today the Disabled People’s Direct Action Network (DAN) are in central London protesting against the governments “Employment Support Allowance” and “Work Capability Assessment” which are replacing Incapacity Benefit. This punitive economic attack will hit thousands of the poorest in society, forcing them further into poverty and a discriminatory job market, while thousands more are losing their jobs due to the deepening recession.

 

We are sick of

 

  • Politicians who attack minorities – that they see as easy targets – for public spending cuts and biased media / press coverage that negatively portrays Disabled People as lazy scroungers and benefits cheats

     

  • Lack of access to meaningful education and training, leading to a lack of qualifications and job skills.

 

  • Work in hostile environments where employers continue to discriminate; i.e. Against disabled employees that need part time and flexi-time work due to impairments, and don’t have mechanisms that allow Disabled People to be absent without prior notification, for their impairment / condition.

 

  • The lack of support to help us get to work and function in the workplace; e.g. regular breaks , shorter hours and a working week that can be adapted to suit our needs.

 

DAN says Disabled People want:

 

  • Politicians, press and media to wake up to the damage their words do

  • Access to meaningful education and training, leading to proper qualifications and job skills

  • Justice in the workplace with real penalties for discriminatory employers

  • A positive approach to the inclusion of Disabled People especially those with invisible or fluctuating impairments / conditions

  • Solutions to poverty rather than policies that compound it

  • A fair and just system that enabled Disabled People who seek work and a non punitive system for those Disabled People who cannot currently work.

  • Decent jobs with adequate incomes

 

Comments from the action; A DAN activist said: “the action was short and sweet. A symbolic action outside Downing Street showing that even on the day of the Queens Speech we can get close to parliament and government, The strength of disabled activists strung out along Whitehall continues to illicit the support of the public and sets a marker for a future of real; rights in Britain for Disabled People.

 

DAN’s Sick Notes are a response to political jibes about Sick Note Britain. They are distributed by disabled activists on actions to inform the public about the reasons for our continuing discontent. They are freely available for use.

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Documenting DAN – Sex and disabled people

I was recently asked by Roof Magazine (Shelter’s rag) to present JPEGS from DAN’s Free Our People Campaigns. Free Our People demands accessible housing. I guess that’s what the article will be about. Sadly, i don’t have any JPEG’s. I’m still confounded by negatives, contact sheets and the like.

However, as i had been asked i did look just in case whilst also tipping off other DAN members who may have JPEGS. In reviewing some of my photos I was struck by ideas of friendships and couple-dom. I think of at least four partnerships involved in DAN. Just thought of another two. That’s six and if i put my mind to it.

I went to the office today to pick up the digital as I will be seeing one half of one of the couples tonight and if he’s carrying a photo of his partner i had an idea for a photo.

I may be able to develop another exhibition from this idea. But it also strikes me in retrospect what a cauldron of hot sex DAN was on national actions. I never saw any of it myself. I’m a sober early to bed kind of guy. But, I’ve heard stories since.

Sex and disabled people. I’m sitting here wondering how i feel about this. I know many of these couples. I celebrate most of the partnerships that i know of.  Some of them have children. I am a disabled person myself. I have campaigned for life which implies i campaign for sex too. I am watching the embryology bill with interest. I have told disabled people about dating agencies. But, i feel some kind of prudence stirring. A part of me is saying it shouldn’t be allowed. I am hooked into some kind of concern about vulnerable people. This is really strange. I’ve never felt like this before. What is going on? Promoting the social model is about challenging myths. Disabled People don’t have sex. Disabled People have weird sex. They tie themselves on. If disabled people have sex they will have disabled children. They only want children so they will someone to care for them. These are some of the sex myths i know about disabled people. As myths i recognise them all to be wrong. I think what is needed now is to spend more time with disabled people who are in a relationship. I hope to see another two people tonight who fit within this criteria. Blimey that’s seven DAN couples.

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Sick Note Britain – What Disabled People are sick of

Watch out for news and media stories concerning the return of the Disabled People’s Direct Action Network.

Completely sick of the way welfare reform has been managed by the government and their lap dog media allies i asked disabled people what they are sick of. This is what they said;

Sick of Adjustments not being made to allow disabled people to access the workplace

Sick Of Employers getting away with not making adjustments.

Sick Of Poverty

Sick Of Not being able to afford to eat a healthy diet.

Sick Of Standards of living that put a strain on human relationships

Sick Of Standards of living tearing our families apart.

Sick Of Pregnant women given no chance to meet disabled people

Sick Of Pregnant Women being told disabled children will be a burden

Sick Of Young disabled women being sterilized without consent.

Sick Of Young disabled people being given no sense of self-worth and
respect.

Sick Of Hypocrisy. Organisations recognising equality and access, but failing to deliver.

Sick of Companies failing to implement best practise

Sick Of Businesses not complying with legislation

Sick Of People not asking me how they may best assist me.

Sick Of Business not being able to recognise diverse disabled people

Sick Of Local authorities’ falsehoods about equality for disabled people.

Sick Of disabled people failing to demonstrate for equality

Sick Of Disabled People not campaigning against bad welfare reforms

Sick Of Pathways to Work not employing disabled people

Sick Note Legislation enabling employers to keep us out of work

Sick Note Disabled people compromising the social model to suit themselves

Sick Of Fair Access to Care criteria being the precise opposite of what they say

Sick of Fair Access To Care ensuring unfair, unequal lack of access to services

Sick Of Fair Access to Care showing no discernable level of care

Sick Of Residential cesspits called nursing homes charging more than the Ritz hotel

Sick Of Residential Cesspits locking us away from the rest of the community.

Sick Of Community Care charges taxing our right to go to the toilet, eat, get dressed.

Sick Of Residential Cesspits stopping independent living let alone having a life!

Sick Of Segregated education

Sick Of less than 0.1 percent of all housing being accessible

Sick Of other residential accommodation not being accessible

Sick Of Widespread, institutionalised discrimination against poor people

Sick Of discrimination in all social, political, economic and personal aspects of life.

Sick Of A complete lack of accessible information in society.

Sick Of Privatisation in general and of the health service in particular.

Sick Of Exclusion of Disabled People from most aspects of the job market
Sick Of Prejudicial government claims about lazy scrounging cripples

Sick Of Prejudicial media claims about lazy scrounging cripples on benefit Sick of Prejudicial claims reinforcing and justifying stereotypes and myths about us.

Sick Of Prejudical claims justifying and legitimatising hate crimes against us.

Sick Of Ingrained institutionalised discrimination against Disabled People

Sick Of Ingrained institutionalised discrimination in the criminal justice system

Sick Of the criminal justice system disregarding hate crimes against Disabled People.

Sick Of the criminal justice system sanctioning murderers of disabled people

Sick Of Scope, Mencap, Mind, RADAR, Leonard Cheshire, RNIB, RNID

Sick Of Social Workers (bless ‘em)

Sick of people who say they speak for us because of the belief that we can’t speak for ourselves

Sick Of Oppressive people (and oppressive organisations)

Sick Of Organisations which claim to represent us but can’t get more than the number of a football team along to their AGM’s.

Sick Of People who claim to be apolitical but are really supporters of the status quo

Sick Of People who treat other people as less than human because of the colour of their skin, their sexuality or their gender.

Sick Of People who express discriminatory views without knowing the facts

Sick Of People who call for asylum seekers and refugees to be sent back to “where they came from”

Sick Of People who used campaigning work to get their snouts in the trough.

Sick Of People who work for service providers, carry out assessments – inc; financial ones

Sick Of People who defend the criteria used to exclude most disabled people

Sick Of People who excuse themselves by saying “I’m only doing my job.”

Sick Of Rules, Regulations, Bureaucracy.

Sick Of Having to still campaign for things we asked for 25 years ago

Sick Of Still having to campaign for access

Sick Of Still campaigning for the right to live where we like with whom we like

Sick Of Still campaigning for the right to go to the loo when we want

Sick Of Still having to campaign to eat what we want,

Sick Of Still campaigning for accessible housing

Sick Of Still campaigning for an adequate income

Sick Of Disabled people’s groups that still don’t take up race, gender, sexuality issues

Sick Of Lists!!


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Institutions are no Solutions

The Jersey children homes scandal is of course horrific and a source of pain to many but what gets my goat is the sense of shock.

Abuse in institutions is well documented. The disabled people’s direct action network ran a ‘free our people’ campaign. It sought the closure of institutions and demanded the creation of independent living centres. Some danners still support this call. Royal commissions have been set up to investigate abuse of elders in nursing homes. There have been numerous court cases and dramas on tv about abuse in childrens homes.

Disabled people don’t necessarily want to be seen as vulnerable people. But we are sometimes vulnerable in different circumstances – as are we all. The social model of disability would suggest to some that we are particularly vulnerable in institutions. It suggests that the institutions depend on systems that grind down the best of us – staff and users. It causes familiarity and familiarity breeds contempt and contempt leads to abuse.

Only yesterday i was talking to a friend who told stories of personal abuse. He has been attacked many times on the streets just for being a disabled person. I reminded him the first time i met him he was complaining that a member of staff in an institution had kicked him in the head. He remembered this story and confirmed it. Which interested me greatly has i know he has been hiding it for years. When i asked him all those years ago if he had been kicked in the head he denied it. He didn’t want to get in any more trouble. This is how the wall of silence develops. this is how the institutions get away with it. the other tool they use is the idea of reliable witnesses. We are not treated like reliable witnesses. Policies and procedures are another good tool. Some agencies use them to defend their staff. You can normally spot them by how they respond to complaints.

Against this we need to balance the risks of independence. My friend was attacked more on the streets than he ever was in an institutional setting. Hate Crime is new on the police agenda and new to the legislation. What the social model might suggest here is that we know the risks of life outside. We need to talk to the policy makers and develop strategies for minimising the harm that it might cause. But more than this each and everyone of us needs to take personal responsibility. If we see it happening we need to intervene at a level that is best for us. Not all of us can stand up to what is happening but we can create diversions, we may be able to shout for help, we may be able to use our mobiles.

Abuse is bad. We have to stop it.

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Yakety Yak I talk back

I have been reflecting of late on the day i learned to speak.

I wasn’t always able to do it easily.

Speech had been taken from me.

The institution really was no solution for me. (paraphased DAN Slogan)

But in spite of my newly acquired impairment i tried to deny my experience of disability. I mainstreamed. I got a job.The role disabled people were allowed way back then.  A lonely scene. Me and the computer. A mainframe. Air conditioned. Cut off. Isolated.

I got promotions. I got wage increases. Year in. Year out. No problem.

But then it came to the point, 9 promotions on, when the next step meant meeting the public. The boss said they would be embarassed to see me, redfaced at my stammer. If i wanted to do it I needed to learn how to talk.

So i took the step. Engaged with the medical model and at the end of the day found a temporary, then contemporary cure. I changed. The introverted extrovert became an extroverted introvert. I couldn’t shut up. I spoke without hesitation, without stumble. The elusive perfect speech settled upon me like billy-ho. The boss offered me the job. I said stick it. I’m off and off i went. New in a new world.

 I came to long for myself to be back. The fellow i knew. The shyer person. The one that people had a real interest in talking to, telling problems to. They loved me for i could not speak and that meant they could and here i was now out on a limb. Not yakety yak. That wouldn’t cover it. More like yikety yekity yakity yak. The gas that bubbled.

Eventually the temporariness of the solution faded and my friendlier self returned. But i knew something new about myself. I could cope with the world. I had the speech i wanted and i could represent. I also knew i really didn’t mind myself too much either. I am. I contribute. I have purpose.

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