An Open Letter to David Cameron & Ian Duncan-Smith(47 Posts)
An Open Letter to David Cameron & Ian Duncan Smith.
Hitler would have been proud of your treatment of the Disabled. Since you came to power you have both vilified and marginalized us. You started what is tantamount to a witch hunt because of the few bad apples that abused the system and you have tarred us all with the same brush and the media has played its part in this. Headline news when disability benefit fraud is reported, but the news never reports when those who desperately need, and have legitimate claims are denied help, unless that is, it affects wounded military personnel.
When you came to power and announced these reforms you stated that those in genuine need of help would get it, and yet you have devised a medical assessment that is not fit for purpose. If the medical assessment is fit for purpose then why are 40% of appeals overturned in favour of the claimant? Instead of saving money, your medical assessment is costing you more in the long run because of the sheer number of appeals, because it has failed those who really need the help, the same people that you told they had nothing to fear.
I am a single parent and a Carer and Im also disabled, I have Chronic Fibromyalgia Syndrome. I have two sons, one is 19, Autistic with a speech & language communication disorder who needs 24/7 care. My elder son is 20, he suffers from Grand Mal Epileptic Seizures and has a recurrent type 1 dislocation of his right shoulder, the damage to his socket is such that he needs surgery but cannot have the surgery because his epilepsy is treatment resistant and should he have post op seizures it would rip the repairs to his shoulder apart.
Because of this we have been told that unless the seizures come under control he will NEVER have the operation. This leaves my son in the situation of having an arm that has a 90% risk of dislocation performing everyday tasks and a 99% risk of dislocation when he has a seizure.
I am also his carer as he needs 24/7 supervision, but I am not recognised as his carer as I am already the named carer of my younger son, you can only get carers allowance for one person, which I receive for my younger son. And just so as people are clear on this issue, that carers allowance is classed as an income so it gets deducted from my income support.
You also state that the bill for Disability payments has to be cut and yet the Carers of this country save the Government £119 BILLION a year. If this is the case then why cant the money we save you as carers go to those who desperately need it?
You also say that the DLA system has to be changed because it is open to so much abuse, making it sound like anyone can get it, you never go into how many genuine people were denied it.
When I first applied for DLA on behalf of my epileptic son he was denied as the decision maker stated He was not at risk of epileptic seizures
I myself was also denied until my consultant wrote a very strong letter to them about their decision and how debilitating my condition is.
I also had to appeal for the mobility component of DLA for my Autistic son, because despite the reams of information Id sent them from Ed psych, Social workers, Learning Support and the Learning Disabilities Clinic & his Clinical Nurse, they chose to use a statement from his head teacher who had only been in the school for six months and didnt know him very well as their evidence. Even the judges at the appeal were disgusted with this and overturned the decision in favour of my son, there and then after only 5 mins deliberation, it was unprecedented to be given a decision on the day, normally it is sent in writing.
My eldest son had to have his ATOS medical assessment in June. Up until Monday 20th August we did not know the result. It was only after phoning the DWP about another matter that we were told they had sent us the decision on Aug 2nd. My son had failed the assessment, we were told he had only scored 6 pts. Apparently he is fit for work despite QUALIFIED doctors saying he isnt fit for work. At no point during this assessment did ATOS or the DWP contact any of my sons doctors or specialists
We were informed by welfare rights that he only has a month in which to appeal, but we still have not received the decision letter or appeal forms. During the phone call on Monday they said they would resend everything and it should take three days to get to us, I had to phone again on Friday to say we had still not received them. I therefore am wondering if this another ploy by the DWP to put people beyond the appeal date?
My eldest son spent two years training to be a plumber, he had his career all planned out, but he had to give up as his epilepsy got worse and the damage to his shoulder was revealed after an MRI.
Now he is literally housebound, he cannot go anywhere without someone with him, he gets no warning to his seizures, they occur regularly both night and day, and when his arm dislocates, which is frequently, he needs to go to A&E. It is not the life of a normal 20 year old.
This is just one example: On the 24th July at 12 a.m he had a seizure luckily this time his shoulder stayed in, but the following afternoon at 1.15 p.m he had another and his shoulder dislocated. I took him to A&E, they relocated the arm and then had another. It took five of the A&E staff to get him on a trolley and into resus. We didnt leave the hospital that day until 8pm.
We actually ended this week back down A&E at 5 a.m.
And this is someone you expect to go out and find full time work? His seizures are aggressive and in the words of his Neurologist epilepsy can prove to be fatal thats why we try to treat it with medication unfortunately in my sons case he is in the 20% of epileptics that prove to be treatment resistant.
How can he look for work when he can not go anywhere alone? How can he work with his right arm dangling out of his socket and being in constant pain? How can he work with uncontrollable epilepsy?
I shouldnt have been surprised really after ATOS & the DWPs track record..the man with the heart condition declared fit for work who died 39 days later, a man with motor neurone disease declared fit for work as he lost use of his limbs..what chance did my son have?
How can you sit there and condone this system and what it is doing to people? It takes the likes of someone dropping dead for it to become a newsworthy story, how many more will this happen to?
You sit in your ivory towers completely out of touch, you strip us of our dignity labelling us all as malingerers and liars blaming us for costing the tax payer so much money, causing hatred against us.
How about telling the taxpayers how much money the Carers save you? But then that would have to be telling the truth and that is something that Politicians seem to be allergic to.
It seems to me and many others that I have spoken to that this Government would like nothing more than to see us all eradicated. You have made sure that the entire country sees us a burden.
My carers allowance is £58.45 per week, I care for my sons for 168 hours per week which equates to 0.34p per hour, but thats just for one of them, divide that 0.34 by two and I am being paid an astonishing 0.17p per hour, well I would be if they didnt deduct it from my income support.
I do not get any respite, I do not get to go on holiday, I do not get to retire I rarely even get any sleep, and yet what I do goes completely unrecognised by this Government.
So for all those people who seem to think those on DLA have an easy life and are swanning around on holiday all the time nothing could be further from the truth, and its about time they realised this.
I have had to fight tooth and nail for the past 19 years for any help at all, the education system, the care system and the benefit system, Ive had to fight them all. I used to be fit and healthy but now I am one of 625,000 people to suffer mental and physical ill health as a direct consequence of the stress and physical demands of caring long term, not to mention the additional stress that you, the government put us under.
I, like many others in my situation, am at the end of my tether, sick to my stomach at your treatment of us and this nightmare world you have created for us. Whats next? Put us all in workhouses??
I find it abhorrent that in this civilised society that you are crucifying the most vulnerable people of all, and subjecting us to emotional and psychological abuse.
Yours Most Sincerely Distressed
Pen - have you received any advice about appealing against the decision? I have no personal experience of the system, but from reading posts on here it does seem that getting support from someone like the CAB can make a big difference!
Also, it might be an idea to ask to have this thread moved to the SN boards, you'll find the people there a lot more friendly and knowledgeable.
I'm really sorry to hear about your plight. Have you written to your MP or No 10? I doubt Cameron & Osbourne will be reading MN.
Secondly just wanted to point out that the ATOS system was introduced under the last Labour government, not the coalition.
That's not to say I think the current tests are good. I think it's obvious to most people that there are huge flaws in the current testing processes.
So should the coalition improve the testing, yes. Is it some Tory witch hunt? No.
Pen I fully support your letter to DC and ID-S
I have as some will know adopted 8 children with SN (sadly 3 have died) all 5 remaining have high needs, 3 deaf, 1 blind, 2 tube fed, 2 epilepsy, 2 complex heart conditions, 2 in wheelchairs, and only 1 with a colostomy. We have saved this country ovar £6,000,000 in the last 30+ yeare.
DD attended an ATOS examination she has Down Syndrome, heart defect with pacemaker poorly controlled asthma OK probably not helped by her learning difficulties she too has to look for a job despite her cardiologist writing that any work would add to her morbidity!! I have appealed
Hitler would have been very proud Well done Pen for such a good post
Thank you for your responses @flatpackhamster, firstly I really don't care about Godwins law, I say things as I see them and when the boot fits..well need I say more? @SaskiaRembrandtWasFramed, yes I have had advice and have a welfare rights worker on board, not to mention some very astonished doctors & specialists supporting us. @niceguy2 this letter has been sent to No.10, I've also emailed it to every newspaper I could find. It doesn't really matter who introduced the test as all politicians are the same and the flaws are on a scale of the grand canyon, and no one is admitting it, they just constantly defend it. I also did not say a Tory witch hunt, I said a Government witch hunt, because that is what it feels like for me and many others because nobody balances out the argument, nobody defends the legitimate claimants.
@2old2beamum thank you so much you my dear deserve a medal, and I take my hat off to you, its just beyond ridiculous about DD, I hope common sense prevails at the appeal...if there is any left in this country!! All the best to you all
Man in coma loses DLA. Nothing these fuckers do surprises me anymore.
Posted too soon. 32 people die every week after being cured by Atos.
@flatpackhamster, firstly I really don't care about Godwins law, I say things as I see them and when the boot fits..well need I say more?
Say what you like. Don't think for a minute that comparing our colossal welfare state to the extermination of the disabled by Nazis advances your argument one iota.
I agree it's a good letter, you are being appallingly treated and more people need to shout about this.
But I had to force myself to read it after you started with Hitler. He actively murdered people. Using him to advance your own cause is horribly disrespectful to and dismissive of the lives he ended in pain and torture.
Annie, if you read my second link you'll see that the Tories are killing people.
OP, I would try to make letter shorter, which will mean that more people actually read it, and remove the reference to Hitler.
Sorry, but as Jew I take particular offence to anyone involved in anything short of a real holocaust playing the Hitler card. I do think what the government is doing to the disabled is despicable, I rant about it all the time to anyone who will listen. I wish I could actually do something useful about it.
But I think the fact that many posts on this thread are now about the inappropriateness of referencing Hitler instead of discussing how to make the government stop screwing the disables kinda proves my point that it's an unnecessary distraction from the real issue and should be removed.
Annie, if you read my second link you'll see that the Tories are killing people.
That's correlation, not causation. There's no verifiable link between being assessed for work and dying. And really, citing an opinion piece in The Mirror...
Annie I too am Jewish and perhaps the disbelievers of the holocaust could explain where my Grandparents siblings and families went, nothing heard from them since 1940.
This however does not alter the fact that this fucking government cares nothing about the vulnerable.
Note for Pen66 thanks for your lovely comments but please remember we asked for our DC's you didn't so respect should be yours. I wish all of us
goodluck we will need it!!
Are you going to refute that with a link to The Heil saying disabled people are being feted with flowers then FlatPack?
No, because you can't. Even one of their own is saying the demonisation of the disabled is wrong. You may claim they're benefit scroungers, I say they deserve their hard won reward. Never forget, it only takes a second to become disabled.
I remember the 'debate' in the House of Commons where various Tory MPs described disabilities as 'lifestyle choices'. How do you explain that?
My son is 10 and has ASD and quite a few other disabilties, I am so worried for his future our next battle and it will be, is to secure him a place in a special school for his secondary education, we cannot send him to mainstream as they will tear him limb from limb ( I have two other boys in mainstream secondary). OP I hear you and I understand, the disabled are treated like scum these days, as if they are workshy and benefit frauds, yet the reality is they really cannot do what is being asked of them.
Nicholas - Flatpack hasn't said anything about the disabled being scroungers or argued that what is happening isn't awful. Only that the Hitler references aren't appropriate. Not sure what you're picking her up on.
The Tories are not killing anyone. If you were to sit down and go through stats of the morbidity rate of the working population I think you would find there is nothing unusual or causative about 32 people dying after being taking off DLA.
Nicholas* which Tories are actually carrying out these murders? I don't like the bastards but hyperbole like yours helps nobody. It might even be the lib dems who are carrying out the alleged killings.
Well it looks as though the shrills are out tonight then
I am not offended by the Hitler comparison, I have Jewish heritage and lost a lot of my family during the holocaust and more during the war.
It is eugenics plain and simple, so the comparison is fair imo. Hitler started with the disabled and mentally ill first. Im sure at the time most people looked the other way, Similar is happening nw actually. Also the use of propaganda is somewhat reminiscent of The Third Reich.
We afford illegal wars and bailouts yet deprive our own to the point where they lose all means to support themselves. People are driven to homelessness and suicide because of this.
Nay sayers are also out of touch a little. The effects that these changes have on the individuals that they are affecting are huge, and rather than discussing our disgusting government people would rather pick nits about comparisons and being offended ffs
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