Thank you to everybody on this site – I have found it very helpful. I was diagnosed with GCA in September. I have to say my GP and Bath Hospital were excellent though it was a shock. My sight tested OK in the Eye Clinic. I started on 60 prednisolone reducing, and I am coping quite well, but I am paranoid about a flare and losing my sight so my worries are twofold:
Firstly I have an astigmatism in one eye so have always had some distortion in focus especially when I am tired - I am anxious to know how will I know if there is a flare? I know the visual symptoms but is it more likely when I get down to lower doses, or when I have just reduced, or? Will the headache also return before or when I get visual disturbances, or other symptoms?
Secondly my eyes are very watery – is this the prednisolone? I am a bit reluctant to tell the drs as I am on enough meds already and do not want to take more or change what seems to be working but it does make my vision blurry.