On the recordSeptember 21, 2022
Finally, Mr. Speaker, I rise to recognize September as Alopecia Awareness Month. Across the country, approximately 7 million people have alopecia, an autoimmune disease, which I live with, that attacks one's hair follicles. People of all ages, genders, races, and from every walk of life are living with this condition. Thankfully, although this does not threaten our lives, it does not mean that it does not impact it. Collectively, we are fighting for bold investments in skin disease research, comprehensive medical coverage, and meaningful public education to combat the stigma, discrimination, bullying, and, indeed, even depression and suicide ideation that so many of us experience. Whether we are sharing a meal in the heart of the Massachusetts Seventh or sharing our stories, to someone who is newly diagnosed, we choose strength over shame and purpose over pain. I can personally attest to the fortitude that defines our community each and every day. Although there is no cure, there is community. We work to create space so that all of us may show up in the world as our full and authentic selves. This transformation that I live with is not one of my choosing, but it is one that I have learned to embrace unapologetically with the support of my loved ones, team, and broader community in my decision to not wear a wig, recognizing the power of that representation for the 7 million-strong alopecia community in this country.…





