I've just had my assessment which I feel did not go well. My form was filled in very well, with real life examples, frequency/fluctuations, taking into account the 'reliability' criteria and all she seemed to fixate on was how long it takes me to chop a carrot, how long can I stand up for, can I speak to the click and collect driver at Tesco and how often do I have flares (I have MS) . I feel she will fixate on the fact that my last relapse on MRI was in 2018. I explained, and have explained on the form, that I am progressing without relapses but that my neuro has not amended my diagnosis 'type' because he wanted to get me on a particular drug to try and slow progression and needs the relapsing/remitting diagnosis to get the funding approved. There is so much that she seemed to miss out too. Do the decision makers *actually* read your forms or do they just agree with assessors?
Because the quality of information the assessor gathered, based on the questions she asked, is really poor and this worries me greatly