Thank you for your interest in SAF and welcome to this wonderful community!
Simply complete the contact form and you’ll be connected to the only patient organization dedicated to all things scarring alopecia. You will receive access to SAF’s newsletter, e-news blasts with the latest and greatest information, invitations and announcements to patient support meetings and conferences, and inspirational member stories to fill your heart.
Knowing that you are not alone is reassuring…
And, becoming a part of a collective, active group of patients supporting each other is empowering…
And, contributing your voice to the world of science and medicine so doctors and researchers can learn more, find better treatments, and eventually a cure, is life-changing.
Disclaimer: SAF does not sell, distribute, or share the contact information of its members with any person, company, marketing service, or healthcare entity. Your contact information is solely used at the discretion of SAF’s board and staff for SAF-related activities and will never be shared unless otherwise requested or noted.