Life with Rare Coexistence of Systemic Lupus and Ankylosis Spondylitis

Hello, I just curious to find the other 8 - 10 individuals living with the Rare Coexistence of Systemic Lupus and Ankylosis Spondylitis (Axial for me ). Tbh, living with these crazy autoimmune conditions haven't made me a professor but the work to being as healthy as possible is grueling (it would be nice to gain some financially credible degree of some type of
consolation prize).

I don't have all the answers nor do I expect you to. I simply want to be able to ask a question and have someone understand me.
I have spent so much time trying to live that I forgotten how to to actually enjoy life without fearing what will happen in the next 5 minutes. Please 🙏🏿 is you're our there, comment and join the conversation