Don't understand M.E. either. Even urban does not allow the type of language which would do some of the assessors justice.Health fucking professionals!
Don't understand Cerebral Palsy, don't understand Multiple Sclerosis.
Cunts
They think M.E. is a me me problem that doesn't exist.Don't understand M.E. either. Even urban does not allow the type of language which would do some of the assessors justice.
Sod the falling asleep - I'd be more intrigued to see the reaction to somebody who begins slurring, stuttering, and looking confused when asked a very short and simple question.They think M.E. is a me me problem that doesn't exist.
What would they do if someone feel asleep during the ass essment ?
ATOS are clearly fuckwits. Even those without medical training understand that CP isn't a condition that improves.
Health fucking professionals!
Don't understand Cerebral Palsy, don't understand Multiple Sclerosis.
Cunts
Sod the falling asleep - I'd be more intrigued to see the reaction to somebody who begins slurring, stuttering, and looking confused when asked a very short and simple question.
Just WTF
Amy Jones, Cerebral Palsy Sufferer, Given Prognosis By ATOS That Her Disability 'Expected To Improve'
In my job as a support worker I look after a couple of people with cerebral palsy. I have absolutely no expectation of their condition improving anytime soon.
Panda, this side of the herring pond it's "physiotherapy" not "physical therapy". I agree with the rest of that though.Also, most of us without medical training understand that for some people with CP, it's only their commitment to a regime of painful physical therapy that keeps them as mobile as they are.
this is a email address of a UN official she wants to hear storys of how atos and dwp have effected disabled people, and she is doing an investigation into the breach of human rights by atos, please send her your storys of the awful experiances you have recieved via atos srhousing@ohchr.org
This nonsense HAS GOT TO STOP!
Will no fucking MP pick it up and run with it?
They could 'make a name for themselves'.
Investigate ATOS - It's methods, it's income strategy, it's software and why "we" don't own it,
it's recording policy.
Plus Yardbird DEMANDS to know the name and qualifications of the "Healthcare Professional" interrogating him.
Sorry, I'm just so angry.
I am not reading this thread at the moment as it just makes me too anxious and I am doing a bit better over all and don't want to spoil it, but, just wanted to pop in and say much much strength to you all, you are in my thoughts and thank you so much for your help in the past.
Love from me x x
UNABLE to walk, talk or feed himself, Ryan Norman has needed round-the-clock care since he was four months old.
Now, at the age of 20, Government bureaucrats say he must have a medical to see if he is fit for work before he can claim the benefits his mother relies on to care for him.
Ryan’s mother, Ceneta, his sole carer, claims she is in serious financial difficulties after Ryan’s child benefit and tax credits automatically stopped on his 20th birthday on September 1 – with a wait of several weeks before he is assessed for adult benefits....
If the MP's can't be arsed to do anything then we need to shut ATOS down.This nonsense HAS GOT TO STOP!
Will no fucking MP pick it up and run with it?
They could 'make a name for themselves'.
Investigate ATOS - It's methods, it's income strategy, it's software and why "we" don't own it,
it's recording policy.
Plus Yardbird DEMANDS to know the name and qualifications of the "Healthcare Professional" interrogating him.
Sorry, I'm just so angry.
If the MP's can't be arsed to do anything then we need to shut ATOS down.
Everyone needs to report the 'HCP' to their appropriate body and get then struck off. ATOS can't operate if no one willilling or able to do the assessments.
I like the idea of this -
In the absence of a guarantee that you will provide recording equipment, I shall be bringing a stenographer with me.
A court stenographer - I trust that this is acceptable.
That just shows how thick the HCP's are then. When you appeal and get sent a copy of your forms and the WCA report from the DWP, the WCA report has the HCP's name in full on the first page.I foresee a slight problem, comrade W.
That problem is that there's already a considerable amount of anecdotal evidence of HCPs refusing to give "clients" either their credentials or their full identities at assessments.
It's almost like they have something to hide...
Well, I'm out of all this bollocks for a now, being an OAP. Just hope that I'll be better by the time I'm re-assessed in a few years time.Ouch! A court stenographer, being an officer of the court, would present pretty much an unimpeachable version of events.
Bit of a simplistic (verging on insulting) viewpoint - that if you *just* get help you'll sail into the support group. It is not that simple. It might have worked for you but there is still evidence that there is more too it than just getting help.Doesn't matter whether the DWP or ATOS understand ME. DWP rules say it's a neurological condition, so the WCA is conducted by a doctor. If you prepare well and use the resources at benefitsandwork. co.uk you can sail into the support group. I did. The snag is that if your ME is too bad for you to be able to work, you won't be capable of preparing well. So you need LOTS of help. If you don't get help, you're fucked.
I didn't know that, that's disastrous. So nothing I said applies any more.CFS/ME no longer mandates neurological assessment or even assessment by a doctor, which it did up to DWP guidance amendment in June.
Yep. Goalposts have moved, or at least aren't publically visible.I didn't know that, that's disastrous. So nothing I said applies any more.
Was re-checking the DWP guidance for someone on this thread and noticed that where they'd previously stated the assessment had to be carried out by a doctor, it had been changed. Checked the date and saw it was June this year.How did you find that out?