u/Triplet-momma

Has anyone with lupus ever had Botox? I’m generally not a fan of putting foreign substances in my body, but I’d like to also try to go a non-surgical route to look younger. But I don’t want to use Botox and then have a flare. In the past when my disease was less controlled. I didn’t feel well after getting Kybella but that was many years ago before I was diagnosed with lupus. Now my lupus is pretty well controlled. Anyone have well controlled em autoimmune disease and get
Botox? What was your experience?

How do I educate my teenagers about my Lupus? 8 years ago when I was diagnosed I got the kids a children’s book about lupus but I think they still really don’t understand.