Posted 5/29/2017 2:19 PM (GMT -7)
I was looking up Uc and entropathic arthritis, and one of your old posts came up when you were enquiringly about it.
It's been a few years since, & just wanted to ask how have your joint symptoms been? Did you end up treating symptoms with biologics?
Initially I suffered from sacriolitis about 4 years after UC diagnosis, whereby I was suspected to have AS. But since then it's effected my knees, hips, & hands occasionally. So I've been labelled as reactive arthritis.
Just wanted to talk to someone in a similar position, & what worked best for treatment?
Thanks in advanced for a response, not sure if you still post on here.