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Message preview	Hi there, You are invited to a Zoom webinar. When: Apr 15, 2021 04:00 PM Pacific Time (US and Canada) Topic: Treatment and Support for Children with Alopecia Areata Register in advance for this webinar: https://us02web.zoom.us/webinar/register/WN_UkeYVIIbTkiKT3dZJSs5Vw After registering, you will receive a confirmation email containing information about joining the webinar. ---------- Webinar Speakers Dr. Leslie Castelo-Soccio & Jeff Woytovich Dr. Leslie Castelo-Soccio is a board-certified dermatologist and Assistant Professor of Pediatrics and Dermatology at the University of Pennsylvania Perlman School of Medicine. She also serves as Head of the Pediatric Hair Clinic and Director of Research in Pediatric Dermatology at the Children’s Hospital of Philadelphia. Her research focus is on pediatric hair disorders. Jeff Woytovich has been married since 1994 and has four daughters. A proud veteran of the United States Marine Corps, Jeff is owner of Woytovich Consulting, LLC and A Woytovich Motion as well as the founder and director of the Children's Alopecia Project (CAP). Jeff founded CAP after his second oldest daughter lost her hair to alopecia. Deeann Graham & Mimi Rivard Deeann Graham is a published author of Head-On, Stories of Alopecia and podcast host Alopecia Life as well as a volunteer and mentor for the the Children's Alopecia Project. She works as an alopecia life coach for clients and their families to help them find answers and reclaim their power. Deeann also presents alopecia workshops in the beauty and medical industries to provide patient-centered resources and support. Mimi Rivard is a Nurse Practitioner with over 30 years’ experience in serving marginalized populations. She spent the bulk of her career working in urban settings with individuals living with HIV and AIDS. Mimi is currently the Director of Gender Affirming Care at Equitas Health and also maintains a robust practice providing gender affirming and HIV care. Angela Boes & Glenda Moore Angela Boes co-leads the Bay Area Children's Alopecia Group with her daughter (age 7). Angela was diagnosed with alopecia when she was five and her daughter shortly after her first birthday. They're on a mission to continue to choose not to suffer from their autoimmune condition and focus their energy on connecting and providing support for children and their families also living with alopecia.

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