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Pip reduced

Hi I have signed up today in the hope for some help if possible. I have been on ESA for 4 years now and was awarded PIP about two years ago. I suffer depression, anxiety, artritues, asthma, syatica and gout. 3 weeks ago I had another Pip assessment done and was also ask change to my heath since last assessment. The answer was yes I now also now have spondylitis type 2 diebetise, high colestral, B12 defecity and IBS. My pip was due today put was lot less then I have been getting. I have not had a letter to give me the results of my assignment. Dose anyone no why it has been reduced.
Replies
Senior online community officer
What does the letter say?
The first time people find out that they had got an award is when the money hits the bank. Hang in there - a letter will be on it's way to let you know what is happening.
Hope you manage to get it sorted tracy2244
The DWP/assessing company should obtain these as they have an agreement with the NHS to pay the GP for this information.
Given that you have to do your best to get an award and as much as it goes against the grain I would suggest you comply with the request.
Not right at all.
https://www.communities-ni.gov.uk/articles/esa-information-healthcare-professionals
https://www.gov.uk/government/publications/esa113-interactive-for-use-by-healthcare-practitioners
Personally I believe that even if they do look at it they would take it all with a pinch of salt as anybody can write anything on a form.
You have had good experiences both with your daughter and yourself so obviously that would colour how you view the system.
Your experiences are at the other end of the spectrum when compared to mine.
But I did notice a very strong point why have so many of us not received the results of the claim form.
When I first applied for Disability Living Allowance. I received the results form showing how many points was allocated for each section.
Mobility cooking dressing talking.
However when I was sent the claim for Pip which shocked me at 68 years old and not working If we do not get the results we can not contest the results. I lost around £130 a month with their results of my pip application . but it left me in such a frail mess. figures of authority scare the hell out of me. Its wrong but even though know in my heart they are wrong.it has left me terrified of those damned forms and the process.how much did you get in that year or another year.
I'm sorry Poppy if I don't jump around with the joys of spring given what I have been through with PIP since 2013.
I'm sorry I simply don't accept that anyone is trying to scare anyone here and that this is the place to talk about the problems we have been having so we can relate to one another and feel supported. stree I don't think you will find many with positive experiences with the DWP since the coalition government in 2010. What really isn't helpful is calling out individuals for being 'negative' when they are discussing problems with benefits on a disability forum. We are talking about how it is being made needlessly more and more difficult to just get what we are entitled to. There is justice, but people shouldn't be put through all of this with assessments and forms and appeals we are just stating it as a fact. There is enough to worry about in life, especially for those viewed as 'disabled' thing could be made easier and pretending its not going on doesn't help or change anything either. I also stand by my belief that bureaucrats must stop being allowed to over rule the decisions made by our doctors. They are the ones that are best placed to say how someone's condition affects them. Its an insult to the profession. Don't worry Yadnad I agree. The DWP under this gov are failing in epic proportions, this is the reality we are hear to be realistic and help each other find practical solutions to get over these barriers that are needlessly being put in front of people that quite frankly need it the least - this is exactly the place to talk about all of that - as long as your not being offensive or personal toward anyone else, which your not, then please continue to vent here - tracy2244 hang in there it really is tough if I know first hand how daunting these assessments can be and the whole ESA and PIP process, I hope you have someone that can go with you to the assessment..
Even that plus other pain relief meant nothing for my PIP assessments - it was described as low dosage mild pain relief!
It was the first assessor that put that in the report.
In a way I can understand all of the comments and insinuations that she made - in fact the second report was damn near identical in all ways - same terminology, same phrases and the same dismissals.
As I have said before two issues that I have come to realise will always go against me - the first is something that you mentioned a while back about assessors not being too keen in trying to be fair with a claimant that can become awkward, argumentative and vocally aggressive during the assessments. As I have said before I will always treat people with respect but in exchange I expect the same in return. The first assessor did not help the situation in the way that she dismissed my explanations demanding a yes no answer. Her demeanour was something to be desired and her overall attitude from the start was aggressive - 'do as I tell you as I can close this assessment at any time'.
Secondly and I have mentioned this before also, when I meet strangers, in fact anybody, I am always polite, articulate, and self conscious of how I feel inside but will not show it. Emotion is something that I can only show to people I trust. I may well come over as capable, officious and determined. Put it another way, no one including friends would have any idea as to the turmoil that goes on in my head. I would not be able to do the voluntary job I do.
So with that level of medication, the side effects are now reduced to the extent that I no longer walk around in a zombie state.
Yes I know I may give out the wrong impressions and signals - that is entirely down to will power, determination as well as fight or flight I use the fight mode - running away never solved anything in my life hence how and why I ended up in this state both physically and mentally! Most people would run a mile if someone started pointing a gun in their face - my reaction was to take the guy down except that I didn't realise that there were two of them.