Category: Satistics


A few nights ago after six pm, I received an urgent cry for help and advice from a lady I know, who has herself faced major health issues with her son and is disabled herself. When completely out of the blue her brother who is also a vulnerable adult with health problems received a accelerated eviction notice from his landlord stating he had to leave the property the next day.

She desperately needed advice on whether the landlord could do this. Having had issues with private renting, I advised her about his rights re his section 21notice and googled some info on accelerated evictions, as well as who else might be able to advice such as Shelter and her local councils housing department. As well as advising that she spoke to a solicitor first thing in the morning…

This has seriously stressed two vulnerable disabled adults trying to sort this out…

Thankfully they managed to get hold of a solicitor, and their agency agreed he had not been given a section 21 along side not meeting the terms of an accelerated eviction notice so his landlord has to go back to the courts before anything can happen giving them more time to find him a new place…

And what caused all this? Yep you guessed it… the ESA backlog, it had taken so long for his claim to be sorted that his landlord decided he didn’t want him as a tenant even though his benefits had been sorted and his rent paid…

I can only image what would have happened to the vulnerable man if he hadn’t had a loving sister to help him out…

the solicitor who is helping this lady out also deserves a shout out and has been highly recommended by the lady in question as being very supportive and helpful re benefits and the BT as well as other things and works with legal aid is… Laura Webster… http://www.hopkins-solicitors.co.uk 01623 460460

This is what your propaganda and welfare reform fiasco has wort Mr IDS you are beyond saving and you will be judged one day…

#impeachDWP #NowPetition

So say we all… Dxxx

Thursday i had the dubious good fortune to be looking through twitter during and after the #WOW debate…
I came across some long and varied tweet between several campaigners and Mr S and as you might of guessed there was plenty of mud slinging. Some of which i felt was way more extreme than was necessary or healthy and probably has had lasting consequences for at least one participant. ..
Anyway what struck me apart from all the completely out of proportion accusations where several interesting views of Mr S…

Firstly Mr S is convinced all campaigners have been sending death threats to ATOS… personally I can say that I don’t think any of the campaigners I know would do that, least i would hope they wouldn’t after all despite their involvement I believe the fault lies with the DWP even if ATOS are complicent and should be held accountable. Death threatening the company and staff is counter productive to getting public opinion on our side… Most of us have been to busy helping individuals and trying to effect useful change at the DWP to engage with individuals at ATOS.

Secondly Mr S seems to think that all people who are not paraplegics or born with some form of life limiting physical or mental disability are not disabled and are therefore workshy… as someone with a hidden disability/illness who works and runs my own business  as well as having a disabled partner who also works full time in a skilled job it would seem that that assumption is on shaky ground… and this evening I was just celebrating with a friend who has had to give up a job because of her ME who has been successfully employed by another employer full time but more suited to her needs before she has had a single day unemployed… So maybe Mr S is showing his prejudice in demanding to know why we want money taken from the ‘real disabled’ (his words) to fund people he perceives as workshy when people who are chronically sick can and often are to sick to consider working in an employment market that has little understanding of their needs and no intention of employing them… and the so called mechanisms designed to help disabled people in to work to manage work and to retain work function so poorly see my previous blog about Access to Work here… But those of us who can find such employment are more than willing to do so if our health allows…
Sometimes having work and being willing to work still doesn’t always make it possible for you to actually work…

Thirdly Mr S seems to think that the WOW petition and other campaigns are about shutting disabled people away out of sight… or in one of his more colourful responses thinks we campaigners want all ‘real disabled’ people ‘gassed’ to leave more money for the ‘fakers and workshy’… this shows a deeply disturbing truth and I think fear that Mr S has… could it be his agressive defence of the welfare changes is his way of kinda wearing camouflage… hiding in plain sight from a system that is destroying disabled peoples lives… im on your side so dont attack me im a ‘real disabled’ person…

And his oppinion about us couldn’t be further from the heart of what campaigners want, in fact what we are fighting for is exactly the opposite…
We absolutely believe those that are well enough and who can and want to work should get as much support to do so as possible but thats not what the Work Capability Assessment does. It doesn’t say ok what work can you do or what work would you like to do and what do you need, how can we support you to be able to achieve that ambition… The WCA asks can you work on any or all jobs whether appropriate or available and even hypothetical jobs that may or may not exist… and it does it in a way that is hostile, unsupportive, adversarial, terrifying and damaging to both self esteem and mental well being, having a devastating effect on the claimant… There is little provision to help those found fit to actually get the work they can apparently do and no safety net if after trying work they find they cant do it or get sicker or have new disabilities develop.They just have to reapply and go through the whole nightmare again… I fully expect cases of WCA/PTSD to be recognised in the coming years…

I say all this from experience the only support is through the work related activity group which doesn’t apply if your found fit for work and even if do end up in this group the system is so badly floored you might fare better out on your own… As a Job Seeker there is the Work Choice option which i talked a little about in my previous blog… but it is far from successful and if it fails you have to start all over again…

Simply put the WCA tests for the wrong thing in the wrong way and will therefore never achieve its goal… assuming that is, that the goal is not just to cut the numbers and save money… if its about getting the disabled and those with chronic illness back in to work where possible then it has to start with the right question. Which in many ways is not a question at all but a dialog individual and tailored... what work can you do or would like to do and how can we help you do it…

My fourth observation is more worrying and yet for me the hardest as I hate criticising personal choice and believe that every individual is entitled to their opinion assuming it doesn’t hurt anyone else… but reading the comments on twitter Mr S made to several activists and campaigners I found myself deeply disturbed that Mr S thought it was appropriate for an adviser and self proclaimed voice for disabled people to speak to members of the public in this way… to accuse them of terrorism and to accuse them of murdering ‘real disabled’ people and wanting them gassed. Is deeply hurtful, I was shocked that anyone would think that of people I know who are passionate about the lives of disabled people being about choice and inclusion and I was shocked that someone who says they want the best for disabled people could be so far off track and so hurtful… I think the tweets from Mr S should be investigated by twitter by the police as he must have come very close to braking both the rules and the law…
As a disabled working person and a human being who tries to see the good in all things I was disgusted and appalled by his behaviour on Thursday and call upon the powers that be to investigate his twitter activity…
Dxxx

Hi peeps this is a post about Access to work inspired by Kaliya Franklin’s blog post

The ‘Scrounging Scum’ to ‘hard working, tax credit claiming, socially acceptable scrounging’ journey 

But it’s also a way for me to get some stuff out there so it’s not only in here anymore… *Warning* it will be long…

As most of you know I have Fibromyalgia among other things…

In 2009/10 I first realised something was going to happen to my Incapacity benefit… that I would at some point in 2010 be reassessed for something called ESA… Having a fluctuating condition, I quickly came to realise, having listened to accounts of the process my friends had gone through that it was unlikely  I would get through as I had been working on higher permitted work for three years so I started to look for alternatives.

I came up with the idea of starting my own business as a designer maker and keeping the teaching job I was doing… So I signed up for work choice that was a rocky road to say the least they where just not set up for self employment… My business has yet to make any money… sigh…

During this time I made my first application to Access to Work… to find they couldn’t help with my job because I had found it myself and hadn’t used Job Center Plus to get it so I fell at the first hurdle.

Next came the application for help with my business… I phoned Access to Work to start the ball rolling but because I was with Work Choice they wouldn’t accept my application and re directed me back to Work Choice. Work Choice said they didn’t deal with Access to Work and knew nothing about it… Fell again at the second hurdle…

In October 2011 I went P/T self employed, I had no funding and no stock so spent the winter months making work as and when I could afford materials and doing small local craft shows.

Towards the end of my first year in which I had made lots of work and had managed to go to several craft shows I decided I really needed support from Access to Work so contacted them again. This time they passed me to an adviser who asked to have details of the travel I expected to do in mileage and cost as well as time I might need a support worker and approximate cost along side any equipment needs I might have, I came off the phone thinking how am I going to work all that out… I was at a bit of a loss…

During this year my partner  J had developed a painful knee and had been in and out of hospital for tests and scans, some of them in Oxford, we live in Cornwall.

Then J was diagnosed with bone cancer (2012) a very rare one and he had to have a serious operation to remove his knee and a big chunk of his upper thigh bone and some of his shin bone and have them replaced with prosthetic metal implants the upper rod almost reaching his hip and the lower rod going half way down his shin bone… (*try to remember this description for later)

Access to Work and pretty much every thing else was forgotten at this point, though I kept my job going as I realised my two and a half hr job and my P/T business would soon be the only income we would have.

Just before his op I contacted Access to Work as I realised I was going to need help because not only would I need to keep my job but my Partner would no longer be able to care for me or my son I was going to have to do it all…

When I phoned my adviser there was a message saying he no longer worked for Access to Work and I should contact the main office… I had to start all over again… I phoned and was told an adviser would phone me back…

They never did…

After the op J came home it had been hard coping on my own with a little help from social services, while he was away but having him home was hard to as he could hardly walk and was on a lot of pain medication…We settled in to a routine when two weeks later he developed symptoms of a tummy bug… I had to fight the GP to get him to come out… My partner was rushed to hospital with pneumonia and two blood clots on his lung, he was in hospital for another week…

Christmas was just round the corner so I had to do some craft fairs as this is one of the busiest times of year and I needed to try to make some money…. Once again I considered contacting Access to work but I just didn’t have the time. J was still on Statutory Sick Pay so we where doing ok…

January  2013 came and J started to feel cold all the time we thought it was just the weather, then he lost his appetite after a few days I said you need to see the Dr, so we booked an appointment… The morning of the appointment J collapsed in the kitchen his leg had gone very red, I rushed him to the surgery and the Dr saw him straight away… she called an ambulance which we had to wait an hr for they where all busy… in that hr J went from sick to very sick and in extreme pain… when we got to the hospital they kept him in A&E for several hrs, then suddenly started rushing about giving him meds they thought he had an infection… over the space of the next ten days we nearly lost him a couple of times he was delirious with the pain because they couldn’t get it under control even with very strong meds and their was little to nothing I could do to help except be there as much as I could trying to share his pain… he had two wash outs to try to get the infection under control… they basically opened up his scar and jet washed the tissue and prosthetics to get the muck out… it didn’t work and he got sicker again… at this point they transferred him to Oxford, I knew how sick he was and how close it had come to losing him so this was really hard as I couldn’t go with him… I had to try to keep things as normal as possible for our son and try to keep my job going… He was in Oxford for a further twenty odd days and had another wash out… The bone infection specialists devised a treatment of combination antibiotics administered via pick line, which started to work and he started to recover, we managed one visit while he was there but it was very hard on us all being so far apart…

J was in hospital for just over a month, leaving me to manage on my own… just as I need to be doing my tax returns lol… it doesn’t rain less it pours…

When J came home he still had the pick line in and had nurse visits every day to administer his meds… they sent a large box of meds with him id never seen so may boxes of injections and tablets, our kitchen trolley looked like a chemist shop… he was very weak and it took a lot of time for him to recover but the med combination worked and he eventually started to pick up and they removed the pick line and put him on meds by mouth…  a combination of two antibiotics twice a day specialised ones to combat the bone infection that likes to live on prosthetic implants… He’s still taking them now a year later…

By this time it was April 2013 and J’s SSP ran out and he applied for ESA, he was very quickly sent an ESA50 (within a couple of weeks) we went through the process of gathering his info and sending it off (exhausting)… the new crafting season was beginning… I had been trying to make new work all this time but it was difficult to get as much done as I would have liked… the notion of Access to work crossed my mind again but to be honest it seemed like more work than I could handle having to do all the leg work myself just wasn’t possible…

I had also started the Stats Campaign with Jayne Linney during the last couple of months as I needed a way to channel my anger and frustration at our misfortune and the treatment of the disabled…

In July J Drs decided his knee wasn’t bending as well as it should , as he could only bend it 35 degrees… So they decided to do a Manipulation Under Anesthetic (MUA). This was done in Oxford again and was supposed to take three days… unfortunately the op went badly and his scar was torn open and his quads tendon was damaged this is the one that keep your thigh muscles in place with out it your muscles would be like a rubber band rolled up round the top of your leg… our physio is good at graphic descriptions…lol  they had to open his scar up and repair the damage… he was in hospital for another week…

When he came home he wasn’t allowed to bend it for a few weeks and had it in a full leg splint… at the end of August a year after diagnosis he was allowed to start physio and began to bend it in a bending full length splint…

In Sept 2013 over two yrs since his first problems J went back to work, still on two crutches with a full leg splint…having never heard any more from ESA, he hadn’t been placed in either group and hadn’t had a WCA… J’s work offered a sit down day job, as part of his reasonable adjustments because his job involved standing for eight hours (*remember the description of his prosthetics) and walking about but they assured him they would find him a sit down job and on days as he could no longer ride his bike to work to get to work on the evening shift. He would be allowed a graded return all of which sounded possible… The works Drs assessment stated this was how it should be done…

We contacted Access to work about his transport and mentioned he’d need a in work assessment…

J started work and was put straight back in to his old job…

On his feet for the half a shift he was doing and they supplied a chair on wheels that J found dangerous to maneuver with one leg as it was like paddling with one paddle he kept going in circles… this continued… J complained that he couldn’t do the job… his work just said your not using the chair enough and that he was his own worse enemy… all this was done on evening shift… Slowly his hr increased to full time over a month, so did his pain and swelling, preventing his knee from bending at all… In September J applied for Personal Independent Payments… here at the tail end of February we still have heard nothing from the DWP about his PIP application…

Access to work sorted paying his transport but failed to do an in work assessment…

We phoned… they said we needed to re apply… Aaagghhh… We reapplied weeks went by nothing… We where told they couldn’t contact the company to do the assessment, J told them not to bother… he had lost hope, hope that they could help and hope that the company he had worked for over ten years would let them help because they clearly didn’t care about the pain and damage they had caused him… he got really low… so did I but I couldn’t show it…

In November we went to London to visit Parliament… 🙂

January 2014 came and we learned that we had been massively over paid by Housing Benefit despite offering to give them everything they needed and giving them everything they asked for , the same week J was told he was up for redundancy, just five months after getting back to work and being tortured by his boss who happily told him one day ‘I had a bit of knee trouble once it got better”…

During this last year our son has been assessed for sensory issues and is now being assessed for Autism… his OT thinks we have to work a lot harder as parents than someone with kids that don’t have his problems. As parents of an only child we thought all kids where this difficult… bless him we are still fighting to get him the help he needs at school…three years and counting…

and then my computer died… 😦

So we have had no assessment for ESA, limited help from Access to work and no news from PIP… and plunged in to huge debt by HB…

The support system for helping the sick and disabled work… doesn’t work!

Now it’s close to a new crafting season… Do I apply for Access to Work?

I know this was long I make no apologies, some things just have to be said out loud, I never want to forget what theses past two years have been like because it drives me to fight for others.

I want to say thank you to the staff of Tralisk Hospital Truro a hospital that often gets bad press but saved my J more than once and me and our son in the past, and The staff of the Nuffield Tumor team and the Bone infection Unit for saving J from the cancer and the bone infection… with out the NHS J would not be here…

I want to thank J family and my family for all their support and help this would have been a lot tougher with out them…

To his boss and his company I want to say Agghhh you ass holes… but I doubt ill get the chance… 🙂 And just so there are no doubt about the pain they caused him ive just found this lovely pic of his prosthetics… its not the full leg which is a shame but you get the picture…

J's Prosthetics

J’s Prosthetics

There are new things a foot… the stats campaign is ongoing… I’ve started a new Fibro campaign with fibrogirl called for the moment FibroMe ForAction, and I’m working on something I think might have been over looked, I need to work on that…

Thank you for staying with me I need to go wipe away my tears there hasn’t been much time for them in the last two years and I needed to acknowledge in some way how crappy its been so I can move forward… J continues the meds and is slowly getting stronger… I’ve been in a massive flair since Christmas and quite low but I’m beginning to come back so watch out IDS I’m not done with you yet… Dxxx

PS i believe the National Service Bill gets its second reading tomorrow lets hope it dies…

I know ive not been around since london but to be honest ive been wiped out both physically and mentally and unable to really get it together. On top of which my sons been ill just a virus but it takes its toll on sleepless nights… Anyway this piece is Written by Sue Marsh. and Cross posted in the interests of viralness.

I can hardly bear it any more. Day after day after day. Terrible stories of suffering, despair and suicide.

I’m know you don’t believe it. I know what you’re told. “It’s getting better, we’re taking action, we’re improving the process, these people don’t try hard enough, they’re not really sick enough.”

People say I shouldn’t beg. But I’m not proud. If getting down on my knees and begging you would make a difference, I’d do it gladly. I promise you now, you’ll be remembered for this. If you’re sitting at home right now, thinking about your legacy, I promise you it will be this. It will be that you turned away from the pain and suffering before your very eyes. I’ll make sure of it if it takes me 20 years.

It will be that you allowed your Department for Work and Pensions to lie and cheat and mislead whilst people – millions of people – suffered.

I know, I don’t usually click on video links either. But you found time to watch Strictly Come Dancing,you said so at the Downing St charity reception. And we know you loved Fruit Ninja. And you have time to take countless holidays.

So even if you’re convinced I’m wrong, absolutely certain I’m just a trouble making leftie, please, I’ll beg you, I’m not proud, find ten minutes – just ten minutes to watch

This film. 

Work Capability Assessments have been found in law to discriminate against people with mental health conditions. Your government appealed but the appeal was overturned. Not only are you on the wrong side of the argument, you’re on the wrong side of the law.

You have to stop this. You can pause the migration of Incapacity Benefit claimants until the process can be made safe. YOU can do it. Today if you chose to. You could stop this dreadful social crisis unravelling before our eyes.

And I’m begging you. For what it’s worth.

Well, we finally did it! We submitted the petition on Monday 18th at 2pm and here’s the article in the Mirror as proof… keep your eyes peeled for an article in the Independent on line as well… Thank you all so much for helping us to get there, we are forever in your debt… when i get a chance to catch my breath I’ll tell you a bit about the day… D and Jxxx http://www.mirror.co.uk/news/uk-news/how-iain-duncan-smiths-inaccurate-2809297

It seems such a long time since that day at the beginning of April when i said to Jayne Linney on FB ‘you know someone should write that woman (Esther McVey) a letter’ and Jayne said something like ‘You up for it Deb’… This was in response to yet another out pouring of bile and spin from our erstwhile minister for the disabled who not only left her post but took the post with her… :$

Well, since then not only have we written an open letter to McVey that received 866 signatures. Several follow-up letters as well a dozens of emails to various Mps. We’ve done lots of blog posts that I hope you’ve been following and we have tweeted ourselves in to flare ups… 🙂

The Petition to hold Ian Duncan Smith Mp to account for his use of stats, which grew out of our open letter,  has reached 105.053 signatures and will be hand delivered to Lis Kendell Mp and Kate Green MP at 2pm on Monday at Portcullis House main entrance… We would love to see some of you there if you feel up to it 🙂

At this point I would like to say a few thank you’s

Firstly to Jayne Linney for kicking me in to action and for all her work with me on the open letter and petition it will be lovely to finally meet you.

To Beth Gregson without whom none of the letters would have been written and who has held my hand through many a scary day in the last year. I’m also looking forward to meeting you… My son is very excited about meeting BETH… lol

To Jayne Young for amazing Grammar skills and disability knowledge I bow to the vastly more experienced… 🙂

To Declan Gaffney who made sure all our stats where ship-shape and bristol fashion, how I envy you math types… I haven’t a clue, we are so in your debt for keeping our stats straight and coherent… 🙂

To Michael Meacher MP, Anne Begg MP Sheila Gilmore MP, Liz Kendell MP and Kate Green MP and any I’ve missed out, who have advised on procedures, kept us up to date on what’s happening or who have demanded answers from the DWP on all of our behaves… Thank You…

To John Bald, Allan R Williamson, Patricia White, Helen Sims, Sandra Martin, James Ventham and Jayne Linney again for letting me abuse your images in the name of campaigning ill be using them again soon lol…

And last but defiantly not least to Everyone who signed our open letter, who signed, shared and RT our petition as well as those that donated to the cost of going to London… with out any of your support I would not be making a six-hour journey to London…  so EEK! thanks for that 🙂 lol

This is YOUR petition and as we know IDS is scheduled to meet with the Work and Pensions Committee Select Committee on Dec 9th…

I know I will not be alone in watching with interest… Dxxx

Hi folks

Well as you know we are going to meet with Liz Kendal and Kate Green on the 18th of November.

To submit our Petition about the DWPs use of stats asking the Work and Pensions Select Committee to hold Ian Duncan Smith to account, for his and his ministers use of stats to paint a dark and inaccurate picture of those on benefits, especially those on DLA and ESA.

Well, we thought as well as inviting you those who signed our petition all 104,696 of you to attend the hand over.

We would like you to make a comment about how the use of Stats by the DWP has effected you, whether that’s emotionally, physically or if you have been a victim of hate crime.

How has the picture that is being painted of you by the media fuelled by the use of stats coming out of the  Dwp, affected your life.

If you would like to make a comment please use the same email as before thats disabilitywatch@gmail.com and we will try to print out as many as we can to take with us to the hand over…

Lets tell the committee how we feel about what is happening… Please keep it clean we don’t want to edit, we want it to be in your own words but we don’t want to lose the sympathy of the committee by being abusive…

With out you guys, this campaign wouldn’t be going anywhere, it’s your voices that are important to us…

Jayne and Debbie xxx

At last we finally have a date to submit our petition for the Work & Select Committee to hold IDS to Account for his persistent misuse of statistics; on Monday 18th November @ 2pm

  • We are meeting with both Liz Kendall – Shadow Secretary for Care and older people and
  • Kate Green – Shadow spokesperson for Disabled people at Parliament.

From there Liz will place the petition in the Petition Bag (which hangs on the back of the Speaker’s Chair), and after presentation The Votes and Proceedings publication will record:

  • The petition’s subject matter.
  • Description of the petitioners.
  • That the petition was presented formally.

The full text of the petition will then be printed in Hansard. A copy of the petition will be sent to the DWP who are expected to offer observations which will also then be printed in Hansard.

This process guarantees we will receive a response which should be that IDS is attending the Select Committee on December 9th and there he will be challenged on his untruths.

If anyone wishes to join us in submitting our petition please let us know by commenting below before Monday 11 November.

Jayne and Debbie 🙂 xxx

Back in June we had reason to feel positive our petition asking the work and pensions select committee to hold IDS to account for his use of statistics had reached 100,000 and we had been told that the committee wanted to tie it in to the end of year review of the DWP so they had all the facts at their disposal. A date would be forthcoming…

Time dragged on  and in June we were told MR Smith had cancelled because the end of year review was still not ready…

Time dragged on…

and once in July again the appointment was cancelled with the promise of something in the autumn…

Time dragged on…

and in September we were told November but…

Time is still dragging on and now on the 31st of October 2013, and we’re told it will be December…

That means the end of 2013, the 2011/12 Annual Report from the DWP will be eight months late… Yes that’s right EIGHT MONTHS late why is nobody shouting about this… well I guess we are…

I’m wondering why the press aren’t wondering what’s going on, why MPs aren’t asking questions…

So I’m calling on everyone for help can we start making a noise about this can we tweet #whereisIDS #DWPLateReview 

Also I want everyone to start writing to their MP asking why the DWPs end of year review is nearly six months late… and asking when he will be seeing the Work and Pensions Select Committee in person. We don’t want his juniors to be answering questions we want him to explain what is going on Ultimately Mr Smith is responsible for his deaprtment not Mr Penning or Ms Mcvey…

When a whole department can’t be held responsible and circumvents the balance and checks process we should all sit up and pay attention

Perhaps MR Smith thinks he is above answering questions… Perhaps he’s busy… either way time should be made to get the review in and discuss its good points and short comings… that’s the process that’s the job if he doesn’t like it perhaps he should resign…

Thank you all for your continued support of Jayne and myself we are doing all we can to push for this and MPs like Sheila Gilmore who is also fighting to get IDS to committee is very much appreciated I’d just like to take this opportunity to once again thank all those that have helped with the campaign fund… We are hoping to be able to use some of it soon 🙂 Dxxx

We are being misled again this time by our new “Minister of

State for Work and Pensions” Mike Penning

Mike Penning has begun his career as the new Minister of state for work and pensions, by using the same misleading tactic of his predecessors…
Manipulating stats to make all DLA/PIP claimants look like they do not deserve their benefit because they haven’t been assessed in a face to face with the DWP… In an article in the Daily Mail with the extremely misleading head line “Disabled benefits farce: 94% of new claimants have never been assessed by a doctor” 

He said “Only 6 per cent of new disability benefit claimants have a face-to-face assessment with a medic, it has been revealed.”

 Implying that only a small amount of claimant are getting benefits they are entitled to…

But the truth is far more revelling…

DWP “Medical Examination Report states that:

6% of claimants were actually seen face to face by a DWP engaged assessor.

40% by a GP,

10% on the claim form they submitted alone. Often clearly the most disabled 

45% on “other evidence” perhaps a community psychiatric team or a consultant

Getting the full picture is important

Ministers that continue to misuse stats, show us that they cannot be trusted to work for us as disabled people or care about us as voters.

It seems the Stats campaign has another member to add to the list. A growing list of ministers and MPs that regularly mislead the public and parliament in order to justify their cuts that disproportionately hit the sick and disabled.

Sue Marsh has done an excellent blog about this at Diary of a benefit scrounger.

The fight goes on… Dxxx