pip assessment at home
Comments
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Hi,No it doesn't mean anything other than they've agreed to do a home assessment. Good luck.I would appreciate it if members wouldn't tag me please. I have all notifcations turned off and wouldn't want a member thinking i'm being rude by not replying.If i see a question that i know the answer to i will try my best to help.
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ok thanks are a good amount of people being moved from longterm dla too pip
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danny1986 said:ok thanks are a good amount of people being moved from longterm dla too pip
(1) How well you complete the claim form - PIP2
(2) How good the relevant evidence is that you send back with the claim form
(3) If you have a good working knowledge of how PIP works or you have a good advisor working with you supporting the application.
Apart from those three things you are then left with the luck of the draw as to whether you get a decent assessor.
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ok thanks just worried ii been on dla my whole life im completely house bound can barely walk across the room just hoping i get moved onto pip how strict are they being with longterm dla people
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danny1986 said:ok thanks just worried ii been on dla my whole life im completely house bound can barely walk across the room just hoping i get moved onto pip how strict are they being with longterm dla people
I had to fight to get that increased to Enhanced Mobility & Care. Again in 2015 the same happened after a re-assessment and had to fight once again to get it back up to Enhanced for both. Then in 2017 It happened again when I was given 0 points after a 3rd re-assessment. I tried to get it back to Enhanced for both but failed and my claim was closed. Since then I don't get any type of disability benefit.
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oh dear this has me very concerned are a lot of people getting knocked back by pip
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danny1986 said:ok thanks just worried ii been on dla my whole life im completely house bound can barely walk across the room just hoping i get moved onto pip how strict are they being with longterm dla peopleYour DLA award has nothing to do with your PIP claim even though you've been on DLA long term. PIP is different to DLA. Did you send evidence to support your claim? They very rarely contact anyone for evidence and the onus is on you to make sure it's sent.Lots of people claim PIP successfully and this includes those that transfer from DLA but we rarely hear about it. If someone's had a decision they're happy with they have no questions to ask so don't tell their story.Reading all the negative posts on forums won't help you feel any better. Good luck.I would appreciate it if members wouldn't tag me please. I have all notifcations turned off and wouldn't want a member thinking i'm being rude by not replying.If i see a question that i know the answer to i will try my best to help.
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@Yadnad I'm sorry but your negative comments on a lot of threads don't help other people that are currently going through a PIP claim. People come here because they're worried and stressed and need help, the last thing they want is negative comments from other people.
I would appreciate it if members wouldn't tag me please. I have all notifcations turned off and wouldn't want a member thinking i'm being rude by not replying.If i see a question that i know the answer to i will try my best to help. -
That’s why we have scope, to help.
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I had a home assessment inMay 2017 to transfer from DLA to PI P and I actually ended up better off and my review date of 2027.I must admit I had a lot of help from age UK.Finally I wish you very best of luck.
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@danny1986 wishing you the very best of luck with your home assessment.
I had my PIP assessment last week at one of their centres. XPoliteness costs nothing, but goes a long way in life.
Always look out for each other. Be kind.
Hugs and smiles mean the world. XX -
ok thanks really worried can barely stand and even need someone too wash me my health so bad
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Very best of luck with your assessment @danny1986, do keep us updated and let us know if we can be of assistance.
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poppy123456 said:@Yadnad I'm sorry but your negative comments on a lot of threads don't help other people that are currently going through a PIP claim. People come here because they're worried and stressed and need help, the last thing they want is negative comments from other people..
Let's all live in the make believe world of Alice in Wonderland then?
At least with others expressing their negative experiences it does show to the poster that they are not alone.
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I have to agree with Yadnad here. Just because his experience wasn't sunshine and rainbows, he gave his own anecdotal account of what happened to him, and even prefaced by saying he is only speaking about what happened to him.
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I had my face to face assessment 6 weeks ago. It took about 45 to 50 minutes . I took my sister with me for support, as I don`t like meeting strangers when I`m alone and thought that the assessment would be stressful. far from it. The lady was very friendly and sympathetic. She apologised for running ten minutes late and explained that it is because she`d read through the report letters from my GP and Rheumatology nurse. She said that they were very helpful.
She asked me questions which were related to the answers that I gave in the application form and some of them, she asked me again a few minutes later , I presume that is to catch out people who are lying. She also asked my to lie on the examination table ( sit in my case, as I cannot lie on my back. She asked me to lift each leg as far as I could ( not far with my left) and bend my knees ( again, a lot less with my left). She asked me to grab her fingers and pull back, my right hand soon let go! She also asked me to turn my head and nod my head, I can do neither. I explained to her what extra aids that I have in my Motability car ( extra swivelling mirrors are a DVLC requirement to help me drive safely) . I was encouraged by the fact that she did a lot of typing and therefore wrote a long report.
4 weeks later, I had the letter telling me the results. I`d been awarded enhanced rate for daily living and mobility , which is more than I had before when I was on DLA ( I got middle rate care and high mobility for life). The only disappointment was that she didn`t write down that my conditions that affect my abilities to carry out everyday tasks properly are chronic and will never get any better, so I was awarded PIP for 4 years. I intend to have a chat with my rheumy nurse and GP to ask if they`d write letters telling the DWP that my conditions are incurable. That way I may get a ten year award . Good luck with your claim, be honest with them, tell them how it is and keep positive .
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AnksponPete said:
I had my face to face assessment 6 weeks ago. It took about 45 to 50 minutes . I took my sister with me for support, as I don`t like meeting strangers when I`m alone and thought that the assessment would be stressful. far from it. The lady was very friendly and sympathetic. She apologised for running ten minutes late and explained that it is because she`d read through the report letters from my GP and Rheumatology nurse. She said that they were very helpful.
She asked me questions which were related to the answers that I gave in the application form and some of them, she asked me again a few minutes later , I presume that is to catch out people who are lying. She also asked my to lie on the examination table ( sit in my case, as I cannot lie on my back. She asked me to lift each leg as far as I could ( not far with my left) and bend my knees ( again, a lot less with my left). She asked me to grab her fingers and pull back, my right hand soon let go! She also asked me to turn my head and nod my head, I can do neither. I explained to her what extra aids that I have in my Motability car ( extra swivelling mirrors are a DVLC requirement to help me drive safely) . I was encouraged by the fact that she did a lot of typing and therefore wrote a long report.
4 weeks later, I had the letter telling me the results. I`d been awarded enhanced rate for daily living and mobility , which is more than I had before when I was on DLA ( I got middle rate care and high mobility for life). The only disappointment was that she didn`t write down that my conditions that affect my abilities to carry out everyday tasks properly are chronic and will never get any better, so I was awarded PIP for 4 years. I intend to have a chat with my rheumy nurse and GP to ask if they`d write letters telling the DWP that my conditions are incurable. That way I may get a ten year award . Good luck with your claim, be honest with them, tell them how it is and keep positive .
She was visibly beyond fatigued, and even fell asleep in the waiting room while we waited, but I still fear this will affect her award.
Congrats on your award though. You must be very relieved. -
Thanks PIP. To balance matters and though this is not relevant to this thread, Poppy and her daughter obtained their respective correct PIP awards with no issues because they sought out good advice from at least two agencies and were able to complete the PIP2 forms fully giving the correct information and arranged for the correct relevant evidence to be sent.
Poppy is an example where everything went according to plan. Shame that a lot of others don't have that same experience. -
"Arranged for the correct relevant evidence to be sent"? That's not correct, i gathered the evidence myself and sent it, not anyone else.
I would appreciate it if members wouldn't tag me please. I have all notifcations turned off and wouldn't want a member thinking i'm being rude by not replying.If i see a question that i know the answer to i will try my best to help. -
poppy123456 said:"Arranged for the correct relevant evidence to be sent"? That's not correct, i gathered the evidence myself and sent it, not anyone else.
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