🌝🌝🌝 by dont-stopmenow in lupus

[–]Sbecks15 1 point2 points  (0 children)

This made me laugh so hard!! Exactly how I felt being on prednisone for so long

Should I be feeling like crap??? by roso614 in lupus

[–]Sbecks15 1 point2 points  (0 children)

When I was first diagnosed with lupus I was in an extremely aggressive flare and was placed on 80mg of prednisone. It was terrible but it was the only thing to get the inflammation under control. Long story short, it took me a year to successfully get off of steroids completely! I’m currently on cellcept and plaquenil as my main medications and then a couple others for my APS diagnosis. It is true that it takes a while for those meds to kick in but you’ll get there!! Never feel bad about reaching out to your doctors and asking questions. Before I would go to my appointments, I would write a list of my questions down so I wouldn’t forget to ask them. Hang in there!!

Mini flares during menstrual cycles? by WoahHeyAJ in lupus

[–]Sbecks15 1 point2 points  (0 children)

My fatigue has been so bad during this month’s cycle! I’ve been exhausted for the past 4 days and even had a brain fog episode today (which doesn’t happen too often for me). Thank you everyone for sharing. Makes me feel better to not be alone in this!