About me? Mad, disabled, in debt, feminist, radical, angry, pacifist, warrior, radio 4 listener, geek, flower-power chick...
About Hippie blog? Ramblings, photos, fury, giggles and musings about love, peace, friendship, madness, happiness, the state of the world, my life, cool pics, my health and general ranting...
For a long time now, the links in my right side bar have been horribly out of date. They didn't represent the blogs I do read, they didn't represent the blogs I no longer read, and many no longer existed or had become password protected.
I used to use the right sidebar links as my way of keeping on top of which blogs I read, but now I read most blogs in google reader, and have been ignoring ---> for months and even years.
It got to the point where it was ridiculous, I wasn't linking to my favourite blogs and I was linking to lots of dead ones, so I set about the dreaded task of sorting it out.
So, for the last few days I have been going to each blog I linked to, and either adding it to google reader, or finding it was long gone, or finding it contained things I didn't want to read any more. So the blog list has been gradually shrinking - the more I did, the more I deleted.
And I have worked out a way to link to the blogs I like and read, without the sidebar getting so overwhelmed again, so now I have set up my blog list to be attached to my google reader account, but only the ten most recently updated blogs will show to the right.
I have also deleted a lot of the links that weren't blogs. The ones that remain are below the blog list. I should order them somehow, but I'll work that out in time. I have also changed my twitter feed, flickr feed and last.fm feed gadgets so they are more up to date, and look neater and fit in better, and added a 'most popular posts' thing right at the bottom of the page.
There will be a Sheffield Seed Swap on Sunday 20th February at The Old Sharrow School, S7 1DB
we invite you to take some of our saved seeds and share with us seeds that you have saved yourself. Its aso fine to come empty handed ! we would just ask for a donation for any seeds you would like to take...or perhaps there is something else you can swap? All the seeds saved here at the seed swap are organic and local.
This means that these seeds will be more suited to local climatic conditions and will be more suited to organic growing conditions.
Seeds are one of humanities greatest resources. We rely upon saving seeds for most of our food, and much of our clothes and our medicines. One seed can produce a plant that will produce many thousands of seeds, each with the potential to produce many more thousands...
seedysunday.org is a good resource for seedswaps nationwide.
There will also be information on local community food growing projects, and other local food events as well some plants, cups of tea, and cake! This event is free. We welcome donations to keep this event going into the future.
What Do They Know? is a fascinating website. You can submit Freedom of Information requests through it, and view the requests submitted by others, as well as the responses from the various public sector organisations. So you can do a search for, say, work capability assessment and see all the requests and responses made through the site, or search for your local area, or hospital, or a government department.
With your department aiming to remove the benefits from 25% of DLA claimants, and deem 91% of ESA claimants as fit for work, please could you inform me what provisions have been made for those disabled and sick people to choose a quick and painless death in preference to slow and painful death by starvation, neglect or homelessness.
and goes on to ask whether ATOS will therefore be providing suicide kits.
The same man has made a video of telephone calls to ATOS asking for the same information.
Mozaz, aka Mark Wallis, was angry, unpredictable, stubborn and inconsistent.
But he was also passionate. And way more sensitive than many people gave him credit for. He was supportive, when he liked you, though whether he liked you or not could change at a moment's notice. But when he was on your side, he would back you up every step of the way, whatever the kind of support you needed was. Emotional support, practical support, and advice. He offered, and he meant it.
Mozaz was a great photographer who, like me, didn't see any contradiction in finding beauty as much in abandoned, derelict buildings as in the rolling countryside. And he found much beauty in both. He adored Sheffield and was certainly one of its characters.
And Sheffield, despite itself, will miss him.
As an anarchist, and a troublemaker, and with strong feelings about almost everything, he was often to be found at demonstrations and protests. As a person he found solace in hugging trees, he wasn't ashamed to admit he cried.
The last time I saw him he was proud to have spent the past few hours in a police station. He felt proud that he was considered to be enough of a threat to the state to be worth arresting. Before being released without charge he had made sure to inform all of the coppers of their union rights, urging them to seek advice about whether they should be enforcing fascist government policy. He was exhausting to be with. Everything had the potential to make him rant, often in unexpected ways. But there was an anarchist rave hidden behind every possible situation which could arise, and he never failed to provide it. He was a prolific blogger and was @ur32daurt on twitter.
Mozaz was hard work, but if you looked beyond what was immediately visible he was sensitive, supportive, intense and warm-hearted.
He died in the early hours of this morning after a time in Intensive Care with pneumonia. Through the last few days, since becoming aware of his being ill, I kept hold of the fact that he was surely indestructible. But sadly this proved not to be the case, and he has left this city a little quieter, he has left the police force with a little less work to do, and he has left many people, myself included, reeling.
I love writing letters and cards, and I have phases of doing lots, then not doing any for ages.
The 52 Weeks, 52 Letters challenge for 2011 has inspired me. I aim to write a letter or card each week this year.
What a lovely challenge! There's nothing quite like receiving a hand-written, personal note from a friend through the door, and I hope I can bring 52 smiles to others throughout the year.
I am struggling to see their logic. Is it aimed at women who they believe were somehow planning to be abused, yet on seeing the poster they will see the error of their ways, and decide against it? How else can it be understood?
Raising awareness of domestic abuse is very important. The quote provided makes good points: “Christmas is meant to be a happy time for families but for many living in our districts it will be a time of fear and pain,” said Sarah Hill, Director of Independent Domestic Abuse Services.
“The pressure builds up as people spend more time together than normal - which can often be a flash point for abuse. But we are here and ready to help – to listen or to provide some shelter.”
But how does this equate to the victim blaming, completely missing-the-point poster.
If anyone is going to urge anyone to do anything, we need to urge abusers not to abuse. It is so screamingly obvious that it frustrates me immensely that we have to write about this again and again and again.
Nobody wants to be abused. A woman seeing a poster telling her not to 'be on the receiving end' does not stop her partner 'being on the giving end'. It may just make her feel even more powerless and vulnerable.
Provide helpline numbers, sure. Provide advice and support, absolutely. But point the advice in a way that does not make it her fault. In a way that does not put the onus on her to not be punched or kicked or raped.
Because believe me, she already does not want to be on the receiving end. She does not need a patronising poster campaign to tell her that.
If you are experiencing domestic abuse, please call the National Domestic Violence Helpline on 0808 2000 247, or find a service local to you through the Women's Aid website.
And remember, it is not your fault. Ever.
I wish we did not have to keep saying this, but as long as people keep putting out information like that, we will.
Companies like A4e, who are paid by the government to get benefit claimants into work, are treated with at best suspicion, and at worst fear and loathing, by many disabled people, especially following TV programmes such as Benefit Busters.
The DWP currently have a shortlist for other companies who are bidding for contracts to carry out government compulsory back-to-work schemes, and worryingly one of the shortlisted companies is the dreaded ATOS, who carry out the ESA medicals, and G4S (formerly Group 4 Security).
However, apparently also on the shortlist, according to benefitsandwork.co.uk, is a consortium consisting of a group of 7 charities, who have called themselves Disability Works UK.
Disability Works UK is a collaboration of national third sector disability organisations including Leonard Cheshire, Mencap, Scope, Mind, Action for Blind People, United Response, Pure Innovations, Advance UK and Pluss.
They boast about their £654.4 million turnover, and cash surplus of £15.6 million, which makes me feel a little queasy. As someone who has donated to more than one of these charities in the past, I will certainly never do so again if that is going to be used in a bid for them to gain their place in what is one of the most oppressive parts of the government's new benefit regime.
For charities and voluntary sector organisations who have done some campaigning against the punitive measures put in place within the benefit system, to now want to play an active part in that system, is disturbing. For them to use money donated by people in good faith as part of that, sickening.
And where does it leave our chances of major disability charities campaigning on our behalf against punitive benefit reforms? If they are hoping to profit from the legislation, I cannot see how we can expect adequate support or representation from them.
If Mind, Scope, Mencap, Leonard Cheshire et al win these contracts, will these charities, who are seen by many as the voice of disabled people, be playing a part in benefit sanctions? Will they be working with ATOS as colleagues? Will we ever trust them again?
Other disability blogs and websites have already done some great posts on this subject, and I wanted to draw attention to some of what is being said around the interwebz on the reform proposals.
I don't know whether I'll be able to make my way through reading the consultation document myself without breaking things and / or having a complete meltdown, but if I do I will try to summarise it in a blog post when I have.
For those readers on qualifying benefits, you can check whether or not you are yet eligible for any Cold Weather Payments on this direct gov website.
Payments are made when the average temperature for where you live is recorded as, or forecast to be, zero degrees Celsius or below over seven consecutive days.
Also from direct.gov, who qualifies for Cold Weather Payments:
If you are in receipt of Pension Credit, Income Support, Income-based Jobseeker's Allowance or Income-related Employment and Support Allowance (ESA), you may also be able to get Cold Weather Payments.
You get £25 for each seven day period of very cold weather between 1 November and 31 March and it is paid automatically, you do not need to apply for it.
So, if you want to check whether you are due to receive one, you can do so here.
There are plenty of must-read articles and blog posts which I haven't had the time or the spoons to cover. All of the following are well worth a look.
Scope are running a survey about the real costs of being disabled, which you can fill in here.
"On the Shoulders of the Vulnerable", an article from Morning Star with information about ATOS and how ESA medicals are failing disabled people, especially those of us with mental health problems.
Laurie Penny in the New Statesman writes Strictly Come Scrounging, Anyone?, about The X Factor vision of society [which] blames the poor for their predicament.
Hopi Sen and Left Futures point out the contradiction in David Cameron criticising those claiming over £20,000 in housing benefits, compared to his own expenses claims for his second home.
Crisis, a national charity for single homeless people, have created a comprehensive, myth-busting press release full of information on how the government are 'peddling myths' to sell the Housing Benefit cuts.
The same article is looked at on This Is My Blog, who looks in depth at 'abandoned claims' and why they might really happen.
Susannah posts a plea for help, describing how the removal of the Mobility Component of DLA from people in residential care will directly affect her brother.
I am touched and moved that so many people have contacted me, and commented, in such a supportive way. It was a very scary thing to do, but it also felt very important. Thank you everyone.
The last few days I've watched the videos from BendyGirl at Benefit Scrounging Scum, and I loved them, I thought they were brilliant. But I never thought it was something I could do, until in her second video she pointed out how important it is for everyone to speak out.
Like many, many people I am frightened by the proposed changes, the cuts, to disability benefits, and what's going to happen to services and the third sector.
The thought of withdrawing mobility rate... the thought of withdrawing the mobility section of DLA for people in care homes is disgusting. The thought that just because somebody was living in a care home, they no longer need to go anywhere, they no longer need mobility equipment, is just obscene.
The changes in housing benefit rules so that people under 35 in private rented accommodation can't get full housing benefit if they live on their own is disgusting.
And limiting ESA to one year, when so many people were fighting against the very principle of ESA at all, and now to have to change that fight to at least, it was perhaps better than nothing, and if people are going to be put on it because they are considered fit to work, even though we know that many, many people who are not fit for work are being put on ESA, the fact that that's now limited to one year, and nobody seems to know what would happen after that.
When we are in a recession, and people – everybody who isn't working is finding it difficult to find jobs, and the strange assumption that the few jobs that there are will go to disabled people, is just not unfortunately how this society works. Disablism means that disabled people are discriminated against every day, and that includes the disabled person who is well enough to work can find it more difficult to find that job because employers are frightened, or don't want to make changes, or don't know what it means.
I'm frightened. And I'm also, like many other people, very confused. I watched the budget on Wednesday, and I was thankfully using twitter at the same time because there were many aspects that I didn't understand, or that I thought I must have misheard. And that there was a group of us all watching and using twitter at the same time made it more accessible to me, I guess.
But there are many unanswered questions. I've heard of people ringing the DWP to say, 'What's this about ESA being stopped after a year?' and the DWP not being able to answer, because they don't know.
The Housing Benefit cuts, I've heard so many different stories about who it's being cut for. So it's not just that the changes are frightening, it's that they're very unclear, and people don't know where they stand.
When I first became ill and went on benefits, I just got Income Support, and it was a horrible time. With paying part of my rent out of that, and with making debt repayments out of that, I had £15 a week for food, and electricity, and transport. For months I lived on... I used to buy these tins of Irish Stew from Kwik Save, and they were disgusting, but they were really cheap, and I figured it was as close to a balanced diet as I could get because it had meat and potatoes in it. And for months, every day, I had one meal a day, and that consisted of Kwik Save Irish Stew and as much bread as I could eat. Every day. For months. I couldn't afford sanitary towels, I couldn't afford shampoo.
I didn't know about other benefits. And someone told me about DLA and I applied for it, and I eventually got it, and it was one of the key... it was key for me, it was vital. Because my health was bad enough anyway, it was vital for me because I could afford to eat more than Irish Stew. I could afford to go to places on the bus. And I'm talking medical appointments. Before that I was missing medical appointments because I couldn't afford to get there. I could get taxis. I could get ready meals when I wasn't well enough to cook.
Getting DLA literally changed everything for me. And makes, still makes, such a difference. It means that I can afford the extra things I need because I'm disabled. Like taxis. Like ready meals when I can't cook. Like mobility aids, and other aids I use. DLA, along with everything, is being threatened. With ATOS taking over the medicals. And after what they've done with the ESA medicals that's frightening, and many people who need DLA are going to lose it.
Everything that is happening since the new government came in is frightening to disabled people. And I'm not a Labour supporter. I know that various important Labour politicians have come out and said that they would be doing what the Conservatives are doing with regard to disability benefits. So I'm not falling into the trap of saying, 'the coalition government is awful, Labour is the answer', because they are... although they are fighting some aspects of the budget, they are supporting the disability benefit cuts.
I feel like I'm being punished for being disabled. The press and the government are doing a really good job at the moment of whipping up hatred, whipping up this image of disabled people being scroungers, of disabled people not really being disabled, and being workshy and lazy. The government and certain parts of the press are promoting this strongly and I can feel, in the atmosphere, that this is affecting people's views. And with the further cuts, this gets worse and worse.
What depresses me is not my illness. What depresses me is not my impairment. What depresses me is how I am treated because of it. That's what makes everything so much harder. We do need to speak out. Because disabled people are being scapegoated and it's horrible. And for non-disabled people, you don't know what's round the corner. I became disabled. Many people become disabled. It could be you in a few years, with no care packages, with no benefits, with no support. With people thinking... with people thinking you're lazy or can't be bothered, or exaggerating. Nobody's immune from disability. And there are some people in the government, the Prime Minister included, who really should know that through their own lives. I am so... I'm frightened, and I want to give a message of hope, but at the moment it's hard to find one.
So I'll agree with BendyGirl that the hope... maybe we have to get hope from each other... from knowing it's not just us, it's not just me that's frightened, it's not just me that's confused, who doesn't know what's happening and what's going to happen.
Scope are running a campaign to email your MP to ask them to take action immediately to oppose the cuts to the public services and benefits that many disabled people in the UK use and rely on.
All you have to do is fill in your contact details, then your MP's email address is automatically found and you can read and alter the proposed message before you confirm that you would like it to be sent.
It's impossible to overstate how terrified some disabled people are, in Britain right now.
The fear of benefit cuts is so high, and so real, and attitudes like those of Nadine Dorries add to the climate of terror.
Already people are scared to leave their house for fear of being reported to the DWP for faking their illness, now those who find networks like twitter to be a lifeline are becoming frightened to post.
If you are stuck in bed, and you've found a way to use your laptop lying down, or you can use a phone or iPad, sites like twitter are perhaps the only way for many to actually communicate with others. It may be the only conversation someone has for a week.
One purpose that these threats serve is, I suspect, to keep us all quiet. We can't complain about the process of reapplying for DLA, or of the ATOS assessments, if the very complaints we type will be used as an additional stick to beat us with. Even if typing those 140 characters used up so much energy that we then had to sleep for an hour to recover. Or hurt our eyes so much that we have a migraine for 3 days.
On days that I can't leave the house, and can't use the phone, the internet is the only tool I have to communicate with the outside world. I don't want to lose that. But the fear affects me as much as anyone, and right now so many of my outlets feel threatening.
This is what the threats to disability benefits are doing to me. It is worsening my madness significantly, which, ironically, will make me less and less able to work, not more.
Balding said the word "dyke" was "too often used as a pejorative and insulting term". She said her sexuality was irrelevant to the programme and the hurt had been compounded by the columnist's mock apology for previously saying that she looked "like a big lesbian".
As you might expect, Stonewall has released a press release on the judgement, however it has used offensive and racist language in that press release to make its point.
Using racist language, to highlight how bad homophobic language is, is never the way forward. Holly's post on Oppression Olympics explains this clearly, and insulting Meera Syal and Vanessa Feltz's ethnicities is as offensive as the original AA Gill comment. Doing this in the guise of supporting a decision against offensive language is ridiculous.
I don't want to directly quote the language they used, but the screenshot above of the press release will show you what they said. The 'P' word in particular is one which makes me feel sick. Using it as an example of what The Sunday Times would never have said is misguided at best, and I do wonder what Ben Summerskill was thinking when he thought this was appropriate.
I've lately started getting a lot of spam comments on my old posts, so I've been deleting them as they come in (Hint to spammers, don't bother writing a convincing looking comment for the context when your username is GenericViagra).
But as the problem is getting worse by the week I have now changed my settings so that comments left after a post has been up for 14 days will have to be moderated. Hopefully this won't be too annoying for regular or legitimate commenters, and it will save me time and energy I could better spend, I dunno, pissing about.
It makes for very depressing reading, and while it does not look specifically at disability benefits, it reports on the reductions and changes in Housing Benefit, JSA and tax credits, all of which are claimed by many disabled people. For instance,
From 2013/14 any claimant on JSA for more than 12 months will have their HB entitlement cut by 10 per cent. This will continue until they have “left the benefit system and been in work for a while”. This seems a crude measure as it appears that it will apply even where the tenant is fully complying with their JSA requirements to actively seek work. The cut will fall hardest on those who face disadvantage in the labour market, such as people in poor health or with a disability who have failed the harsher medical tests for incapacity benefit and employment and support allowance, and have therefore been moved onto JSA.
It also explains why changing benefit levels from rising in line with the Retail Prices Index, to the Consumer Prices Index, will result in a reduction in the value of benefits and tax credits.
At the end of the study the report highlights scenarios illustrating the impact of the cuts on specific households, and several of the case studies include the issues of people who are ill or disabled. For instance,
A 50 year old man with mild learning disabilities and literacy issues has done manual work all his life until arthritis in his knees, hips and shoulder forced him to stop work. He has worked and paid contributions all his life until that point. He pays rent of £110/week and council tax of £18/week. He claimed ESA but was found fit for work, so is now claiming JSA. The number of jobs he will be able to do is severely limited. He also has no access to his own transport and finds public transport very difficult because of the arthritis. His Jobcentre Plus personal adviser finds it difficult to suggest jobs for him. He has been out of work since his arthritis made it impossible to continue in his job two years ago and he has been claiming JSA for a year. After housing costs he has a disposable income of £65.45 a week (his JSA). After a year as a result of changes in up-rating of JSA and also the LHA rates, his disposable income is likely to drop in real terms to about £64. However he may well also lose a further £8 off his HB as the 30th percentile rate is used to calculate the LHA rate. If he is unable to find a job after a year he will lose a further £10 a week of his HB. If he can not find somewhere cheaper to live he will have a disposable income after housing costs of about £46, a 30% reduction. Even if he can find somewhere cheaper to live, his disposable income will drop to £54, a 17.5% reduction. If he had been allocated to the work-related activity group for ESA, his income would be £91.30 a week.
1. Making an unwelcome manifestation with disruptive or adverse effect.
2. (of a person) Disturbing another by one's uninvited or unwelcome presence.
Intrusive comments from strangers about my breasts began pretty much as soon as they grew. Intrusive 'are you anorexic?' questions happened when I was slim (and yes, some of that time, I was. Did you really want that answer?). Intrusive comments about my weight are different now, but still intrusive and rude.
But lately, the subject of the vast majority of intrusive questions I get asked are related to being disabled.
Practically every time I go out, someone asks me, "So, what've you done then?" and nods to the crutch. This happens disproportionately in the bus queue, oddly. But can happen anywhere - last week by the guy serving me in Subway, and he didn't even stop there.
I am never quite sure how to answer. In my head I come up with clever and funny stories to answer this question, involving shark attacks and being trampled by donkeys, but in reality these rarely come out of my mouth. I sometimes say, "I had an operation on my leg" which, while true, isn't entirely relevant. For what it's worth, regarding that actual question, I haven't done anything.
I could tell the truth of course, but it's a long, complicated and in depth story, and people wouldn't actually want to hear the whole thing. Not that I'd do this, because it's none of their business. If you are a complete stranger, you are not entitled to my medical history.
Some, like the Subway guy, go further. "What was the operation for?" "What does it feel like?"
Then there's the unsolicited advice that so frequently follows: "My mate had something like that and when he stopped eating *insert random food group here* it got better"; "Have you tried *insert unproven alternative treatment here*?"; "You want to be careful using that stick, you don't want to get reliant on it".
Look, I have a consultant on the case, and she knows a lot about this stuff. You don't. Just drop it.
Think about it this way, if you were waiting in your GP's surgery waiting room, and someone asked you what you were seeing the doctor for, you'd feel that that was an inappropriate and overly intrusive question. It's the same - perhaps worse - at a bus stop, or a sandwich shop, or in the park.
Just like telling me I have big boobs (as if I didn't know) is inappropriate, and telling me to eat less is inappropriate, and telling a slim woman to eat more is inappropriate, so asking a complete stranger about their impairment is also inappropriate.
Sometimes young kids ask me questions, and I don't mind that as much. They mainly want to know if it hurts. Then they get on with whatever they were doing before. Actual friends asking me questions is fine, and actual friends offering me advice based on something they've read can be helpful, because they know what I've already tried and what I'm likely to want to try.
But the man at the sandwich shop and the woman at the bus stop and every other stranger who feels entitled to know, it's not fine. My body is mine, in all its weirdnesses and failings and successes. Some of its details are visible to you, but it's still not ok to just tell me what you think because you can see that I have breasts, a big tummy, a limp, scars or a mobility aid.
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