For anyone dealing with claims, I recommend the Benefits And Work website which sets out the assumptions they make with each question and why you generally need to answer "no, because" when asked if you can do something - because if you cannot do it safely, repeatedly, reliably, to acceptable standard and in a reasonable time it does not count. But they have to interpret your answer as meeting all those unless you tell them otherwise.
So my PIP responses (on separate sheets) end up being about 20,000 words demolishing every assumption (copy and paste for each question as needed).
My assessor reports have ended up just copying parts of what I've said. I've had 2 PIP assessments now, each over two hours , but I went with a Dr (not a medical one but I didn't mention that), and the assessors were very grateful to have the words they needed.
Neither of them had seen any supporting evidence, just my form. Got the award I should, both times, but that is thanks to me being a civil servant and knowing how to work the system.
And being politely arsy when refusing to do anything medically inadvisable, and getting DH to phone up repeatedly, and getting my MP involved when I was expected to travel 100 miles to a centre (I live in London).
The system is not fit for any humane purpose, only for purporting to support 'the disabled' while actually aiming to cut costs at all costs.
Question for anyone in DWP: why does it take so long for PIP2 forms to be put in the post which then takes 3 weeks to arrive from Belfast, and why in this era of digital by default is there still no electronic version of the form available?