Victoria Gibbs is a #lupuswarrior. She powered through her illness and realized the benefits of self-care.
"The good news is that being diagnosed with #lupus wasn’t the end of the world, but a new beginning." Read her story: ow.ly/aBny50L2yxZ
A3. I tell my doctors right away about any side effects. Calling them or via E-mail. Especially after having to go to the ER 5 times since March for lupus-related dehydration and dizziness. #LupusChat
A3: I tell them how I feel & the side effects I experienced. I also look lab trends. If they don't listen I fired them like how I did one rheumatologist bc ultimately this is my body and they will just sleep comfy at night whether I was in pain or not. H3ll nawl. Lol
#LupusChat