PIP Refusal
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I dont get it??? I was asked to attend an interview for PIP and it was refused No news there then - However the following week I went for ESA assessment and was put into the Support group with the GP who carried out the assessment writing that I will be wheelchair bound in approx eighteen months and that I would need an electric wheelchair as my arms are of little or no use to me already due to pain and that I would not be able to self propel in a standard wheelchair???? How can my PIP be refused when a DWP doctor seen my Fibromyalgia as bad as it is???
0 likes, 9 replies
ChrisA15 wendidly643
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wendidly643 ChrisA15
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SteV3 wendidly643
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ChrisA15 wendidly643
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ChrisA15 wendidly643
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SteV3 ChrisA15
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It took a USA Professor of Neurology and his own team flown in from New York to London, where I met them every 3 months for nearly 2 years, before they could find what was my problem/disorder. I had to sit in the middle of a huge round room with my wife, and we were with the Professor, all his teams were sat around in the circular room. Basically, I was quizzed by numerous US neurologists, and the Professor.
Even now, I am seen by the British President of Neurology - he is well known in the UK by many Neurologists. If I mention something I done recently, and I did not know I was not supposed to do it, he makes all phone calls to various departments, to make sure anything that is required is provided, and funded by the correct departments.
They have started sending me all carbon copies of letters to my doctors, so I can back up any claim for PIP with dates and where injections were given and by which Neurologist. They did not used to do this, only recently, and all referrals are carbon copied as well.
Regards,
Les.
SteV3 wendidly643
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It is nothing new, the DWP is doing many strange things, ESA maybe granted and PIP refused, the whole system is in a mess. They are trying to make out to people they have less appeals and new claimants than what was initially stated. Course many people knew it was untrue, so the DWP started putting through some cases quicker than others, the fact is they still have a huge back log, which will take years to clear, even now.
The truth of the matter is if you get DLA Mobility Component Low Rate now, then after the PIP change you will not even get anything!! How does that work?? The PIP Mobility side only has two sections, the chance of you obtaining enough points is virtually "nil", yet it has only 2 questtions both of which can give you a possible maximum of 24 points, where as the Care side as a maximum of 72. The chances of receiving Care is higher than Mobility.
I'm on Contribution-based Employment and Support Allowance (Support Group), I had no "face-to-face" interview, but this only happens if you have a disorder that will never improve, and only becomes worse, which is very depressing to actually state, since I been like this since my 20's! My main Neurologist states I have Generalized Dystonia, but my team Neurologist states I have Cervical Dystonia amongst many other things. Most people think Cervical is to do with the Cervix, with Dystonia this is actually the neck, and where I have 6 injections every 10 weeks. But I have many disorders as well, and I haven't yet been changed from DLA to PIP, it's due, just don't know when.
I would appeal on your PIP, especially since your ESA now completely contradicts your PIP status. Do it, they won't like it - but unless you fight them you never win on your first assessmentt anyway.
Regards,
Les.
wendidly643 SteV3
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I will let you know how court hearing goes but I am not holding out for anything positive x
ChrisA15 wendidly643
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