I have a PIP assessment next week and really do not know how I am going to explain the Fibro fog. I was thinking of printing some information down and writing what I experience on a daily basis and some days are different if my anxiety sets in. I do find Fibro fog difficult more as I have got use to it 24 hours a day for 3 years. If I ovethink about the Fibro fog I would probably cry as I thought it was just something that comes and goes not continuously stays. The tablets do nothing what doctor gave me ? what does everyone think?