Sharing Our Stories: Alopecia Universalis

Why should you stick around this blog?

I’d like to think of myself as that that trusted sister/mom/boss/mentor/friend/rock-of-Gibraltar, who can help guide you through the uncharted territory of life’s curveballs from dating to health to career. I think I’ve gotten pretty good at making true friends, managing autoimmune conditions, and navigating career changes during midlife and maybe I could say something here that might resonate with you.

*Note: It would NOT be good to use this to keep that wig on your head. ^

Here We Go!

So, join me on this wild ride of hair-loss, laughter, and self-discovery. We'll share stories, tips, and support each other along the way.  Please, please, please share your stories with us. I promise you, it helps you and it helps others, knowing that there are many of us going through something similar. We’ll do our best to always come back to the thought that hair may actually be temporary for some of us, but confidence and resilience are forever. 

(One Very Long Sentence Below...)

Let’s laugh about the uncomfortable moments in life, cringe at the all-out failures, revel in our successes and pretend that when we all put our heads together that we are the most amazing doctor/scientist/detective the world has seen as I try everything in my power to grow back this damn hair.  Let’s go… we got this.

And P.S. Seriously, I really do hope you'll add some comments here so we can talk!