National vitiligo day came and went June 25th, but those of us affected by this autoimmune disease live wth it daily. Two years ago my symptoms began. Took courage, and a few tears to tell my husband when I figured out was going on. To tell him it would spread, and continue with no end it sight to the pigment loss. Cause unknown, no cure. I feared he would no longer find me attractive. That it would challenge us in ways I could not predict. I cried and held my head down feeling defeated without any control of my destiny. He simply said "It will make you look exotic ❤️". ☺️ Some days I struggle with #acceptance. Today is one of those days. Frustrated with the lack in interest by the medical community to research what for many like myself is deeply painful, on a psychological level. Most days I embrace what makes me different, or as my husband puts it "makes you look exotic". 🙌🏻 #vitiligo #vitiligonation #vitiligoawareness #tryingtofindthesilverlining #fuckvitiligo #itsnotcontagious