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I have recently been diagnosed with ppms and have also tested positive for the jc virus and still refused esa, the medical assessment was pathetic, I had to move my hands and forearms up and down, failed because I was sat longer than 10 minutes (although I also have austeo arthritis and have to sit with my legs straight) and I can use an ipad, so my sympathy goes out to all who are wheelchair dependable that order their food shopping online. Not once was I asked about mobility or general day to day living, as far as I see it, your assessment should be done via your neurologist or your own g.p and not by someone who is obviously under qualified.