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danny1986 said: ok thanks are a good amount of people being moved from longterm dla too pip
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 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 .
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 .
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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