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- 13 Mar 2003
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When they were in power the tories pushed lots of people on to IB instead of unemployment benefit so the umemployment figures didn't look so bad.
Already been done a few times. I've even had my consultant dermatologist write a letter and still they claim I'm not disabled enough. Funny thing is though, if I chop a a little finger off I'll be entitled to shedloads of cash even though it won't affect my employment possibilities.
Nothing we in the department can do about it though, except i have to listen to chavs scream at me down the phone sometimes because we arent paying them enough or what they deserve
if it's not too personal may i has how you both are?
Also what is ME?
I work for the DWP and actually process the IB claims, i feel very sorry for the people who are genuine and get treated unfairly by the department, when all the people who arent genuine manage to scam their way through medicals and so on and continue to receive things for years.
Nothing we in the department can do about it though, except i have to listen to chavs scream at me down the phone sometimes because we arent paying them enough or what they deserve
This is the trouble with the system. So many people that really need the help slip through the net, and are turned away, while fakers manage to scam their way to receiving benefits they don't deserve and manage to claim for years.
I suffer from CFS/ME, and despite meeting all the criteria required, not being able to cook a meal, unable to walk far and take care of personal needs, etc etc, ( i am barely able to get up and dressed most days) they say i am not eligible as i might get better... One person i spoke to at the DWP even told me that i would be better in a months time, to which i replied, "oh fantastic, can i have that in writing!" Unfortunately, i wasn't better in a months time, and i am still supposedly not eligible to claim.
That's ridiculous. It's awful that people who are genuinely ill have so much stress trying to get a little bit of help. I think having someone who understands the condition when making your application can make a huge difference, since you have to make a statement about what you can't do and they need to make it really clear that some illnesses aren't consistent.
I doubt many people on these forums would admit to claiming it, even if they were laid up in bed with a fractured back,
It costs the country £12.65bn every year
The other joke is that ME has only recently been accepted by the government as a REAL illness, and although their most recent documentation recognises it as such, they havn't adapted the regulations for claiming benefits, so the DWP don't accept it as a real illness, which makes claiming impossible... /QUOTE]
Sorry to hear you're suffering from it Becca
Re the DWP from what i've heard they do accept it, but usually after a fight, Iknow someone who has had major problems with them because it wasn't officially recognised, but managed to get IB/DLA mobility etc after several long fights (right up to tribunals which is the last thing anyone with ME/CFS or any other real illness really needs).
She hates not being able to work :/
I suffer from CFS/ME, and despite meeting all the criteria required, not being able to cook a meal, unable to walk far and take care of personal needs, etc etc, ( i am barely able to get up and dressed most days) they say i am not eligible as i might get better... One person i spoke to at the DWP even told me that i would be better in a months time, to which i replied, "oh fantastic, can i have that in writing!" Unfortunately, i wasn't better in a months time, and i am still supposedly not eligible to claim.