Happy Alopecia Awareness Month.
When I lost my hair due to alopecia totalis, there were innumerable private struggles. But the hardest part was experiencing a transformation not of my choosing while on a public stage for all to see.
Every day, women in public life are scrutinized and judged for our appearance – and choosing to walk this path without a wig certainly disrupts the societal norms of what is professional or beautiful.
The bullying and name-calling compounded my insecurities, but the support of my family, the A-Team, the alopecia community, and my Squad straightened my crown when I needed it most.
Nearly 7 million Americans are living with alopecia — an autoimmune disease that attacks the hair follicles. We all deserve to show up in the world, to occupy space as our full and authentic selves, and we have a moral obligation to create space for others to do the same.
Bald is beautiful, and I am continually grateful to my family, the A-Team, the alopecia community, and each and every one of you.
With love and gratitude,
Ayanna
If you or someone you know is living with alopecia and is in need of resources, or wants to learn more, please click here: https://www.naaf.org/find-support
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