I had a follow up appointment a few days ago things haven't improved much since taking predisolone. The predisolone has been reduced slightly and I've now been started on a low does of Colchicine I just wondered if this has helped anyone with there pain? My mouth ulcers and styles have become less frequent since taking predisolone but the pain over my body is just getting worse and worse and becoming to effect my sleep. I've always got headaches every now and then but a couple times recently I've had headaches possibly migraines that have been so painful my head feels like it's pulsating then I would feel sick and get shaky which I explain to my doctor and he sent me for a MRI on my brain today and I asked why and he said with behcets you can't take any chances. Does anyone know what they look for in MRI's for behcets?