Lupus changed my life. My diagnosis flipped my entire world upside down.
Hearing my diagnosis back in May (2019) was heartbreaking, yet gave me clarity.
The cosplayer in me finally understood why I was struggling so hard to survive conventions.

I have had to slow waaaay down on my cosplaying and modeling, but I’m not quitting. Nope.

Lupus may take certain things from me, but cosplay is not one of them.

Currently, I’m not making any new cosplays or props. Its just too much for my body to handle while my immune system shuts down (such a joy that is 🙄).
So I am only working with cosplays I have already completed.
I’m also only attending local conventions. My first con since being diagnosed will be in November.
I’m anxious and worried about it, but also excited, as it has become one of my favorite cons to attend.

Slow me down? Yeaaaah. Its just the fact of how Lupus rolls.
But bring me to a full stop?
HEEEEELL NO.

I’ll see you all at Neko Con 2019!
✌🏻😜 #lifewithlupus #cosplayer #cosplaylife #autoimmune #SLE #SystemicLupusErythematosus #Lupus #LupusWarrior