hello everyone!
So I’ve had sle since I was 13- it was rough then but then it was mild all along. I tested positive for Covid about 3 days ago - annoying sore throat, congestion and body aches, now feeling better but I’m starting to feel like my joints, specially my elbow and knees are aching. I’m a little scared of a lupus flare up, my lupus has been quasi dormant since I was 15, but last year I got Covid. 3 weeks later I had this throbbing headache and I could not see for a couple of minutes. I went to the eye hospital on marylebone and they said that my optic disc was swollen after which I was diagnosed with intracranial hypertension that resolved on its own… I saw my rheumatologist after that and for the first time in my life I had a positive lupus anticoagulant test even after repeating it.. anyone else had something similar or a sudden lupus flare up after Covid? I’m a little anxious as I don’t want to go through the same experience. I’ve asked my rheumatologist for a consultation in order to see if I can avert that as I’m currently not on any medication but was wondering if anyone out there has suffered something similar following Covid recently! In 2019 - Christmas Day 2019 I suddenly had this unbelievable headache it turned out to be meningitis and encephalitis.. doctors back then had a very hard time determining cause of my illness but mentioned SARS and MERS.. thankfully I recovered but now I think maybe I had Covid then as well but no one knew much about it.. any advice or shared experiences are welcome? I read somewhere that this could be a response to hypercoagulable state induced by Covid and was wondering what people are taking for that- heparin, or baby aspirin… want to see what I can tell my doctor next week!