
04/06/2025
These photos show the first time Lupus started to show on the outside of my body—
I lost hair. My face broke out into swollen patches and butterfly rashes. I felt like a stranger in my own skin. I thought beauty only lived on the surface, and suddenly, I didn’t recognize mine anymore.
The diagnosis felt like a betrayal—my body, my health, my energy… all slipping. And the loneliness that followed? It was just as painful.
But I held onto God, and He held onto me.
💜 “He gives power to the weak and strength to the powerless.” – Isaiah 40:29 (NLT)
To anyone newly diagnosed with Lupus or living through a flare right now:
I see you. You’re not alone. Your body is not your enemy.
Healing takes time. Grace. And community.
If this touched you, comment below or tag someone who needs this reminder. 🦋