At the moment i keep playing my symptoms down to my rhuemy because i am terrified about trying new medication. A year ago i was on methotrexate which at first seemed to help but then i ended up having a migraine that would last 4 to 5 days every week and my partner had to take time off of work to take care of the children as i was too ill. Recently things are becoming bad again with the nerve pain and swelling etc but im scared ill have a bad reaction to anything new and end up in more pain making it harder for my family. i hate feeling like a burden to them although they are wonderful and never complain. ah and lupus fog, does it get any better or worse as time goes on. Im forgetting even simpler things at the moment but we do still try to laugh it off.
I hope everyone is having a none flare day x