so i’ve been tracking my lupus symptoms for yrs now and i’ve noticed a pattern with my fatigue. it’s not just the usual ‘i’m tired all the time’ thing, it’s more like my body has a mind of its own. some days i’m fine, others i can barely get out of bed.
i’ve been trying to figure out what triggers it and i think it’s related to my med schedule. anyone else notice that their fatigue gets worse after certain meds or at certain times of the day? i’ve been using careclinic to log my symptoms and meds, and it’s been helpful to see the patterns.
btw, logging a dose from my apple watch is a small thing that removes enough friction that i actually do it. has anyone else found any correlations between their med schedule and fatigue?