Diagnosed about 6 months ago, I've been on Sulphasalazine and Naproxin/omeprazole but not making much of a difference, Tried to make a follow up (3 month) appointment with Rheumatologist but they're not making any appointments at present due to consultant shortages.
I only went on Sulphasalazine to try and target the cause as opposed to the symptoms to prevent joint damage.
I am considering stopping Sulphasalazine as it seems to make me lethargic but continuing with anti-inflammatories.
Any thoughts anyone?
Posted Tue 24 Jan 2017 05.16 by ohwell
Yes a big one.
My skin went haywire August 2016, don't know why. Today is Tuesday 24th. I was to to see a dermatoligist in March 2017. I said that was not close to good enough. My GP agreed. They told me how to make a complaint, but they made it anyway on my behalf.
Am now under a consultant at a London teaching hospital, one of the best. seeing her again in a couple of weeks. And yes am on stuff. four or five creams, stuff for the bath, a pill - god knows.
Its incurable and nobody knows what causes it. Try and get referred to a specialist..
Do not take no consultants as an answer. I am under one. You may want to have a word with your GP - they refer