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
We use cookies to help us provide you with a better service, but do not track anything that can be used to personally identify you.
If you prefer us not to set these cookies, please visit our Cookie Settings page or continue browsing our site to accept them.
Close