The last flare put me in A&E for a few hours while they sorted out some treatment - steroids. That was 6 weeks ago.
I went down to 15mg last Friday and the symptoms started to re-emerge - my burning pelvis in particular. And then last night a potential big flare started. For me the symptoms of a flare starting are like the onset of flu (real flu ladies, not man flu). But a call to 111 got me speaking to a doctor within an hour and we agreed I should take another 15mg that evening and stay on 30 mg a day till I see my rheumy next week.
The extra 45mg of prednisolone yesterday evening and this morning has made a huge difference already and it looks like we may have headed off another major flare. My GP took bloods this morning to check CRP / ESR but she said "It's only a a tool. If you say you feel rough that's the important factor.'
Roll on Humira. It has to be soon..........
I am very impressed with the 111 service - in our area it seems to work very well. We have had cause to use it twice in the last few weeks with excellent service both times.
Off to the accupuncturist now for a blast of endorphins......
Paul Barrett
Hexham - Northumberland - Loads of spectacular walks - all I need now are the joints to go with them! :)
Enthesitis (2012)
Ulcerative Colitis (1990)