Here is a brief update for anyone who it would help.
I went to CAB who were lovely and I have filled out an appeal form to ESA, so hopefully it will help.
I went to hospital today for the results of an MRI and the spinal consultant has told my that I have suspected 'cervical myelopathy' and could be facing a rather risky operation and now need more MRI's, tests and to see a neurologist.
I would just like to warn other Fibro sufferers NOT to put all symptom or problems down to the syndrome and to get something checked out if they are not sure what is or isn't connected to the fibro. I just thought that the awful dizziness was another side effect, which in part it might be; it is not the whole picture.
Gentle hugs to all and take care of yourselves