Jessica joined AAAF in the role of Tasmanian Branch Manager in April 2018 after being diagnosed with Alopecia Areata in November 2017. Jessica is enthusiastic about creating a more extensive support network within Tasmania and being Launceston based, believes this is a great starting point. Jess is passionate about building supportive relationships, creating understanding and awareness as she understands the need for support and assistance locally. Jess has worked as an Early Childhood Educator and enjoys playing social netball.
Jessica can be contacted at firstname.lastname@example.org
TAS Support Group
Support groups are a fantastic way to get in touch with other people who are living with Alopecia Areata, to ask questions and find new friends. Our Facebook groups are closed groups and you will be contacted by an administrator to ensure you are joining the correct state group and are part of the alopecia community.
AAAF runs a wide range of events, from Open Days and Trivia Nights, to pizza dinners and casual catch ups over coffee. These events all aim to provide a supportive atmosphere and chance to socialise with other people who have Alopecia Areata and their families. See the events page to find upcoming events near you.
State Providers Supporting AAAF
For information about wigs, including what subsidies may be available to you, refer to our our Wigs Document via this page.
|Company Name and Contact||Phone||Site||Specialty|
|Wigs On Wheels||Contact Carmen
0424 920 025
|Website||Friendly free and discreet mobile wig service specialising in wigs for medical conditions|