How can we help you?
HeadsUp Association provides a warm home for thousands of alopecia areata patients and their families – we are a community that understands you. In the association you will find advice and a listening ear for all the difficulties you encounter – you are not alone.
Personal Advice
Contact us to receive advice from our personal experience. You can speak with people who have experienced the same difficulties you are experiencing. You can contact us through the contact page, or by phone at 058-5652177 (also via WhatsApp).
Tools for Parents
Use the tools for parents we prepared to support children with alopecia.
Support Groups
Join active support groups on social networks. The groups are closed to patients and their families only, and the information is not exposed to anyone who is not a member of the group.