Hi everyone...
Its been a while...I was curious if anyone has had any issues with pleurisy since being diagnosed with UC. I have had several bouts lately, on and off for months. I thought the first bout was due to a virus and cough but once it has resolved and months later have pleurisy again!!! Its painful and annoying. I read that its common in people that have autoimmune diseases but wondered if anyone else had this problem and what they did for pain. Its tough since I can only take tylenol!
Thanks for your input and I hope everyone is staying positive!!!
Amy