Orang Utan
Psychick Worrier Ov Geyoor
Brilliant, fishfinger
Anytime. Least we can do for all the kind birthday threads you doThanks to all of you for the messages of support
Also, is a PIP award based on the support a person actually gets or on the need for support whether they get it or not?
I'm not an expert but that is absolute bullshit.Question for ViolentPanda or other benefits experts:
My PIP assessment says I don't need any assistance because Toggle assists me. Can they use support provided by a partner as a reason to deny me PIP. They've denied me any PIP and ended my DLA and my appeal is being heard on February 13, only about ten days away.
Also, is a PIP award based on the support a person actually gets or on the need for support whether they get it or not?
Question for ViolentPanda or other benefits experts:
My PIP assessment says I don't need any assistance because Toggle assists me. Can they use support provided by a partner as a reason to deny me PIP. They've denied me any PIP and ended my DLA and my appeal is being heard on February 13, only about ten days away.
Also, is a PIP award based on the support a person actually gets or on the need for support whether they get it or not?
My IT mind kicked in when I read this post. And what it said was "race condition"Question for ViolentPanda or other benefits experts:
My PIP assessment says I don't need any assistance because Toggle assists me. Can they use support provided by a partner as a reason to deny me PIP. They've denied me any PIP and ended my DLA and my appeal is being heard on February 13, only about ten days away.
Also, is a PIP award based on the support a person actually gets or on the need for support whether they get it or not?
Question for ViolentPanda or other benefits experts:
My PIP assessment says I don't need any assistance because Toggle assists me. Can they use support provided by a partner as a reason to deny me PIP. They've denied me any PIP and ended my DLA and my appeal is being heard on February 13, only about ten days away.
Also, is a PIP award based on the support a person actually gets or on the need for support whether they get it or not?
My sister has reapplied for PIP after being turned down and ATOS told her point blank that they don't even bother contacting your doctor or specialist they leave it down to the HCP. Yes my sister did record that phone call.They need evidence, not just a feeling or your word. They do take doctor's opinions into account obvs...
My sister has reapplied for PIP after being turned down and ATOS told her point blank that they don't even bother contacting your doctor or specialist they leave it down to the HCP. Yes my sister did record that phone call.
They're supposed to, whether or not they do is another matter. There was certainly an overreliance on the outputs of the software they used up to a few years ago, above any other evidence.Yeah, but they take evidence from doctors into account, don't they? Evidence you provide, I mean, like letters from them and scans and so on.
There's a lot of truth in what you say, but there's a downside, too.Thinking again we might be able to give you more assistance if you tell us more about how your original assessment was conducted. If you don't want to do it here (though here is semi-private) then I'm going to volunteer equationgirl to read a PM as well as me and anyone else you might want to include.
There's a line from Tom Jones (book, not singer) that I've thought of for years:
“It is not enough that your designs, nay that your actions, are intrinsically good, you must take care they shall appear so.”
For disability assessments it is not enough that you actually are disabled, nor that all your actions are affected by your disability, but you must show that they are. This is not only because ATOS et al are despicable, but because they are not you. They need evidence, not just a feeling or your word. They do take doctor's opinions into account obvs but a lot of it is stuff that your doc won't necessarily know, or will be guessing at, esp if it's stuff not on scans or blood tests etc. For example, if you can't reliably travel by public transport alone then give examples of times you've tried (including times you even thought about doing it). Make it concrete - give them something hard to butt their heads against.
The silver lining in all this is that it does actually make you assess what help you need. In theory you could realise that you could manage without PIP if a few changes were made, but that's not for this thread really. Realising how much help you need can be depressing at first but getting the help you need is so much more of mood lifter that it's worth the mental process.
There's a lot of truth in what you say, but there's a downside, too.
For many people coping with long-term conditions, part of the process of coping is normalising their disability as far as they can, and just using the resources they do have to get on with life the best they can. But when they are forced, on a periodic basis, not just to enumerate every difficulty their disability or illness causes them, but to do so to a patently sceptical audience, who is quite likely simply to dismiss it out of hand, that has its own effects.
A very large percentage of the clients I see at the surgery have been, or are going, through the DWP assessment/appeal process. It's bad enough for those with physical disabilities or chronic pain, but for those with mental health problems, where having to think through just how awful your mental state makes your life, it is really harmful. A lot of people relate that the process leads them into a state of mind where they're thinking "fuck, if it is really this bad, why am I even bothering to try and carry on?". I am not remotely surprised that the rate of suicide attempts amongst benefits claimants is so much higher than amongst the population in general, and I think this is a classic example of the old truism that measuring things always affects the things being measured.
There has to be some kind of evaluation process, I accept that. But it should be enabling, not punitive. An assessor saying "so, if you're suicidal, why haven't you killed yourself yet?" should simply never happen - that's a question that can be asked, but only by the right people, in the right context, and not in a situation where the "wrong" answer can mean someone being deprived of their only means of support.
I in turn shall apologise for any suggestion that my post was critical of yours . It was meant only to be a perspective from the other end. I agree that, as the system stands, it is necessary to do things the way you described; my (probably off-topic) comments were born of my frustration at a system that wilfully does so much harm beyond what has already been done by disability, sickness, or mental ill-health.I don't disagree with any of that. I'm disabled, the parent of a disabled person, and have been posting on this thread for years. I do not need educating about what it's like to claim disability benefits.
I think that trying to phrase everything in concrete terms is very helpful for the box-ticking forms and assessments and can make a difference between a claim succeeding and being denied. That there is one upside to this - that it can help you identify what support might help you - does not mean that the many downsides cease to exist. So I said "silver lining" because that usually means "one good side of a shit situation," not "I love this and think it's all wonderful." If my post came across the latter way then I apologise.
I in turn shall apologise for any suggestion that my post was critical of yours . It was meant only to be a perspective from the other end. I agree that, as the system stands, it is necessary to do things the way you described; my (probably off-topic) comments were born of my frustration at a system that wilfully does so much harm beyond what has already been done by disability, sickness, or mental ill-health.