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Atos Medicals - Questions, Answers and Support

Just fucking unbelievable, someone deserves to suffer for this and not Amy.

I think the U.N rapporteur has now extended her remit and is looking at ATOS/Govt disability benefits issue from a human rights perspective, I don't have the email to hand but she is accepting evidence, etc.
 
This is the website I got the info from - it's the public DWP guidance for a range of medical conditions:
http://www.dwp.gov.uk/publications/specialist-guides/medical-conditions/a-z-of-medical-conditions/

It does say this is used by Decision Makers for DLA/Attendance Allowance decisions, but I would be very very surprised if the DWP Decision Makers aren't using it for ESA decisions in conjunction with the LIMA software output. I think this because of the amendments that have been made over the past few months effectively 'downgrading' the assessment requirements for conditions such as ME and traumatic brain injury. Obviously I haven't been through every condition to check changes, I have noticed these ones as questions were raised about these specifically and I had used them before June 2013.
 
well I heard yesterday that they haven't changed their decision because of "lack of evidence":( and my case is to go to tribunal.

I didn't really think they would change it at this stage.
 
This is the website I got the info from - it's the public DWP guidance for a range of medical conditions:
http://www.dwp.gov.uk/publications/specialist-guides/medical-conditions/a-z-of-medical-conditions/

It does say this is used by Decision Makers for DLA/Attendance Allowance decisions, but I would be very very surprised if the DWP Decision Makers aren't using it for ESA decisions in conjunction with the LIMA software output. I think this because of the amendments that have been made over the past few months effectively 'downgrading' the assessment requirements for conditions such as ME and traumatic brain injury. Obviously I haven't been through every condition to check changes, I have noticed these ones as questions were raised about these specifically and I had used them before June 2013.
I've followed all the links but I can't find anything about a doctor no longer being required for the WCA. I can't even find a single mention of assessment requirements. Am I looking in the wrong place? :confused:

I also searched the news section of benefitsandwork and couldn't find anything.
 
well I heard yesterday that they haven't changed their decision because of "lack of evidence":( and my case is to go to tribunal.

I didn't really think they would change it at this stage.

They seldom do, tribunal is where it all happens. Hope it goes your way.
 
I've followed all the links but I can't find anything about a doctor no longer being required for the WCA. I can't even find a single mention of assessment requirements. Am I looking in the wrong place? :confused:

I also searched the news section of benefitsandwork and couldn't find anything.
Look for the medical condition you are interested in for example ME. It used to say that a doctor had to do the assessment, since June that bit has been removed. That means the assessment can be done by a HCP which could be a nurse or a physio with no experience of that condition.
 
So you've assumed that doctors no longer do assessments just because that site doesn't say anything about who does them. :hmm:

It's a valid assumption though, given that it's often through such revisions and/or omissions of decision-maker and "hcp" advice that Benefits & Work get their first clue as to what the DWP is up to with regard to particular policies. I'd be inclined to treat eqg's assumption as valid until further notice.
 
It's a valid assumption though, given that it's often through such revisions and/or omissions of decision-maker and "hcp" advice that Benefits & Work get their first clue as to what the DWP is up to with regard to particular policies. I'd be inclined to treat eqg's assumption as valid until further notice.

I disagree. It needs checking out before announcing it as a fact. Given the way that CFS, stress, depression and suicidal thoughts feed off each other, I wouldn't dream of posting something so alarming without verifying it. It's heartless and irresponsible, and it needs editing to tell people that it's just a suspicion with an explanation of how that suspicion was arrived at, and an assurance that it's being researched further.
 
I disagree. It needs checking out before announcing it as a fact. Given the way that CFS, stress, depression and suicidal thoughts feed off each other, I wouldn't dream of posting something so alarming without verifying it. It's heartless and irresponsible, and it needs editing to tell people that it's just a suspicion with an explanation of how that suspicion was arrived at, and an assurance that it's being researched further.

Wind your neck in.

The original assessment was:

there's been some sly updates to the DWP medical conditions guidance and previously some of those that mandated assessment by doctor no longer do so. Head injury is one such example - I checked recently. CFS/ME no longer mandates neurological assessment or even assessment by a doctor, which it did up to DWP guidance amendment in June. It also helpfully notes that CFS/ME 'predominantly affects young people'.

That appears to be accurate.

It doesn't say doctors no longer do assessments: it says their use is no longer mandated in those documents.

If you or others misread it, that's not the poster's fault.
 
You don't understand the point, you haven't familiarised yourself with the context and you don't have any relevant knowledge to share.

I'll come back to this thread when I have some facts. In the meantime I suggest that anyone looking for guidance here should double check the 'information.'
 
I disagree. It needs checking out before announcing it as a fact. Given the way that CFS, stress, depression and suicidal thoughts feed off each other, I wouldn't dream of posting something so alarming without verifying it. It's heartless and irresponsible, and it needs editing to tell people that it's just a suspicion with an explanation of how that suspicion was arrived at, and an assurance that it's being researched further.
I think we can reasonably accept that a web forum isn't exactly hardcore legal advice. Equationgirl has a pretty good track record on this stuff, and - whatever assumptions may have been made - I don't think her comments warrant the kind of attitude you're giving her on this. If you really think she's barked up the wrong tree, an "Are you sure about that?" might be a little more tactful than the way you have gone about it.
 
So you've assumed that doctors no longer do assessments just because that site doesn't say anything about who does them. :hmm:
With respect, I've been involved in this thread and doing research on the LIMA software and the DWP approach to medical assessments for well over a year. I made the notification about the use of a doctor no longer being mandated because to me it is a significant change by the DWP to their assessment approach. I gave a link to the DWP website (primary source) and notified the thread of when the change took place. I have never tried to make out I am an absolute authority on ATOS or assessments in general, but thought this change was significant to talk about.

I am both hurt and annoyed at your response as I have never tried to do anything but support those affected by the whims of the DWP, and present any information I find accurately and with links to the primary DWP source where possible.

Thanks to those posters who appreciated what I posted and why, and who stuck up for me - ViolentPanda, laptop, existentialist to name but a few.

ETA: Appeals have been won because the claimant hasn't been assessed by a doctor as mandated by the DWP themselves for their condition(s). That's why this set of changes is so important - it removes that appeal argument for the claimant. Not a good thing.
 
Looks like the DLA have accepted the tribunals decision as they have sent me a form asking where to deposit my DLA and back pay. :)

They already have these details on record. :facepalm:

TBF, they send a note asking that because a lot of people have their DLA paid into a Post Office Card Account, and they're not able to remit your backpay to a POCA, only as a bank transfer or (which they may not do anymore) as a cheque.
 
I disagree. It needs checking out before announcing it as a fact. Given the way that CFS, stress, depression and suicidal thoughts feed off each other...

You're having a pop at someone for making assumptions, and then post this shite making assumptions about the nature of ME/CFS, that all those with ME/CFS will be prey to "stress", and that this will necessarily cause "depression and suicidal thoughts". :facepalm:
Guess what? Not even close.

...I wouldn't dream of posting something so alarming without verifying it. It's heartless and irresponsible, and it needs editing to tell people that it's just a suspicion with an explanation of how that suspicion was arrived at, and an assurance that it's being researched further.

You do realise that Atos has been using basic HCPs rather than doctors for neuro conditions since the inception of WCAs, don't you? Have a look on epilepsy-specific boards, or boards for Parkinsons. They regularly use OTs to assess people with Parkinsons. The "use a doctor for claimants with neuro conditions" is "best practice" guidance by the way, no longer regulation or mandated policy. It's not "must use", it's "should use", unfortunately for us.

I know you get off on being precious and self-righteous, but frankly you should wind your neck in and do a bit more research yourself.
 
Wind your neck in.

The original assessment was:



That appears to be accurate.

It doesn't say doctors no longer do assessments: it says their use is no longer mandated in those documents.

If you or others misread it, that's not the poster's fault.

Yup. Basically they've given themselves a "get out of jail free" card that has nothing at all to do with:
a) The low ratio of doctors to other healthcare workers that Atos use,
b) The BMA pretty much anathematising Atos and the DWP, and
c) The fact that they've found doctors to be a bit less pliable than nurses, physios and OTs when it comes to getting them to "revise" WCAs.

Honestly. :)
 
And on the basis of equationgirl's last post, I wish to retract any qualifiers I made about assumptions. It's pretty obvious to me now that her statement on the question of doctors doing assessments is unimpeachable.

I think that it might be politic and tactful to consider offering her something of an apology, Frumious B.

It might be.
I'm expecting a Jeremiad against Urban's monothought clique, myself. :D
 
TBF, they send a note asking that because a lot of people have their DLA paid into a Post Office Card Account, and they're not able to remit your backpay to a POCA, only as a bank transfer or (which they may not do anymore) as a cheque.
My DLA has always been paid into a bank account. They already have those bank account details on record. IIRC they also ask what bank account you want your DLA paid into on the DLA form as well. :facepalm: @ DWP

I think they are just using it as a delaying tactic so they can hang onto it for a few more weeks and earn a bit more interest on it. :(
 
My DLA has always been paid into a bank account. They already have those bank account details on record. IIRC they also ask what bank account you want your DLA paid into on the DLA form as well. :facepalm: @ DWP

I think they are just using it as a delaying tactic so they can hang onto it for a few more weeks and earn a bit more interest on it. :(

No, seriously, it's a pro forma they send out because a majority of people get their DLA and/or other benefits paid to a POCA, so they just mail out the pro forma to everyone. My dad got one when he got given Attendance Allowance, even though he had his pension paid into his bank account.
 
I have an ATOS assessment tomorrow. Saturday. At home, without me having to request it. Got the letter yesterday, on the same day as the letter saying "we will send you a letter with the date soon." All seems very odd.
 
I have an ATOS assessment tomorrow. Saturday. At home, without me having to request it. Got the letter yesterday, on the same day as the letter saying "we will send you a letter with the date soon." All seems very odd.
Good luck. BTW take your time answering the door or get somebody to do it for you. Your walk to and from the door may be observed and included in the assessment by the so-called healthcare professional.
 
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