Pip

Well after much thought my daughter rang dwp to tell them my condition has got worse and new medication and new condition which was hard because I was awarded it for 10 years on going which was 4 years ago but it was standard for both got 10 points for mobility ,she filled the forms in and it was received in March with another Drs letter about stress and no phone assessment .only home visit if needed ,but think she should ask for a paper based assessment ,should my daughter contact dwp or assessment provider who the forms are with .also get esa support again this was home visit Thank you for any help so stressful my Dr thinks it's awful how we have to go through all of this .

Would also like to say how good this site is ,and any help in this plp claim would be a great comfort has I'm finding it very stressful Thank you .

Thank you for your reply it was only about pip a change in conditions because since I was awarded pip for at least 10 years on going I have arthritis in more places and on lots more medication my Dr wrote a letter explaining the stress of a telephone assessment and any assessment would have to be done at home ,my daughter did ring and it was sent to assessment provider in March and waiting for a telephone assessment my daughter was going to ring and ask for a paper based decision what do you think my esa support is fine they are aware and done home assessment has did pip in 2017 ,they ask you to tell them of a change and when you do it causes so much stress my Dr is very good but even she says they don't read most of the forms and letters I've sent in ,I had to give up my nursing job in 2017 with a bent spine and arthritis now in neck im she 55 Thank you for taking time to read this .

Thought that would be the case but conditions have got worse neck and back of head coming from spine so can't turn my head without pain twisting is so painful too ,my Dr wrote another letter saying no phone assessment due to stress and sleep most of time did to pain killers ,my report from a paramedic who came to my home said it's a life long condition has I was born with it so why can t they do a paper based assessment I know it's classed has a new case but it's all still dwp es a support was ok with all my not and no phone call it makes you so ill on top of feeling so I'll everyday Thank you for your understanding my daughter was going to email capta what are your thoughts please .