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Resources for Youth

Facing the teenage years with Alopecia Areata comes with its own unique set of personal and social challenges

This space helps you navigate the real-world stuff—like talking to new people, nailing your first job interview, dating with confidence, and finding the right support whenever you need it. 

Resources

Many of these brochures were created following psychological research undertaken by AAAF
Alopecia, Teens and Mental Health
Knowing the signs, how to start a conversation and where you can get support can change the life of someone like yourself when going through hard times.
Youth Brochure
The “Teens Talking to Teens” brochure draws on their experiences of teens with Alopecia Areata from around Australia.
Common things you’ll hear
A resource with common statements people make, intending the best but may be hurtful or frustrating, with alternatives. This is perfect for sharing with loved ones and friends.
Grief and Alopecia Areata
This brochure includes information on how the grieving process can accompany hair loss, and how this can impact people of various age groups, including teens.
Coping with Alopecia Areata
“Coping with Alopecia Areata” brochure includes information about the most helpful strategies for managing the impact of Alopecia Areata on your life.
Job Interviews
Job Interviews with Alopecia Areata
You may be unsure what to wear, whether or not to tell your story, and what your interviewers will think. Preparing yourself for all of this will help you ace your interview, regardless of whether or not you choose to disclose your story.
Click Here
Dating Advice
Dating and Alopecia with Shayna
She brings such a light, easy energy to these important conversations that AAAF wanted to share even more of her story! Below we cover a little more about Shayna and her most important tips for dating!
Click Here
Travel
Alopecia Travel Tips
Whether you’re hitting the snowy slopes or heading north to escape the winter chill (or planning a euro summer), this time of year is amazing for travel. But travelling with Alopecia Areata can have some new complications and considerations.
Click Here

Video Resources

These are a small selection of some of our most commonly viewed resources from YouTube

Wig Styling & Care Advice

Makeup Tutorials

Alopecia, Dating and Relationships Chat

Eyelashes & Eyebrows

How to tell your friends

Donate

Make a Donation

Everything AAAF does is community funded. No government support, no corporate backing. If this community has helped you, or you want to help others find it, your donation goes directly to the work that matters: support, education, and research.

Our Programs

As a foundation we run multiple programs to be involved in…
Our Programs

Sponsorships

This Sponsorship Program provides financial support for individuals and families living with Alopecia Areata, wanting to undertake skill development and participation in activities.
Our Programs

AAAdventure Camps

A super fun weekend, filled with memorable experiences, and a fantastic opportunity to meet other kids with Alopecia Areata. Plus, it’s a chance to have an absolute blast!
Our Programs

Grant a Wig

AAAF’s Grant A Wig for Kids Program provides grants which support children with Alopecia Areata and their families. 
Peer and Mental Health Support Resources

I’m looking for Peer & Mental Health Support

Alopecia Areata… it’s life changing, but you are never alone. Here we’ve curated a collection of resources to make the more difficult days easier and have them occur less often. Many of our community members learn to love their Alopecia Areata. On this page find:

+ Mind body Mindfulness Practices,
+ Tips and advice for the bad days,
+ Community Support Networks,
+ Mental health support networks,
Get Involved

I’d like to get involved

Join our mission to support, educate, and advocate for the alopecia areata community. Every contribution makes a meaningful impact. Here you’ll find:

+ How to individually volunteer or become a corporate sponsor,
+ How to fundraise,
+ How to get involved in donating hair,
Donate

Make a Donation

Everything AAAF does is community funded. No government support, no corporate backing. If this community has helped you, or you want to help others find it, your donation goes directly to the work that matters: support, education, and research.

Products curated for you

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Connect with our Support Ambassadors

Our Support Ambassadors are people living with Alopecia Areata who have been where you are. They're available for one-on-one conversations when you need to talk to someone who genuinely understands

Yasmin

Support Ambassador
Yasmin turned her lifelong experience with alopecia into a powerful platform for change. Born without hair, Yasmin spent years believing that her identity was tied to her hair, However, she soon realised that hair doesn’t define her, leading to a profound transformation in her life. Her journey as a model and influencer is marked by her unwavering commitment to helping others live confidently with alopecia.

Vanessa

Support Ambassador
Vanessa’s daughter was diagnosed with Alopecia Areata at age 6 and now is a teenager with total hair loss. Vanessa understands the emotional impact on parents when their child suddenly and unexplainably loses their hair – not having the answers, wanting to access treatment but not knowing where to start, feeling powerless and confused.Joining the AAAF community and attending the Kids Adventure Camps with her daughter gave Vanessa a strong network of wonderful caring parents and volunteers. Gaining knowledge and confidence to help her daughter embrace her condition and live a confident and happy life with Alopecia.Vanessa is passionate about helping families to access information and supports to navigate their way through the uncertainty of hair loss and help bring connection within the community for kids with hair loss to support each other.

Mental Health Support Organisations

If you need help or support immediately, we recommend reaching out to the following organisations.
Beyond Blue
Find helplines and support through their Australia wide network.
Kids Helpline
Specialised for kids aged 5-25.
Headspace
Providing early intervention mental health services to 12-25 year olds.
Australian Psychological Society
For connecting directly to psychologists.
Discover our peer support and mental health resources

Connect on our support groups

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. AAAF has support groups, run as a closed group on Facebook, in most states. They are a key way that AAAF communicates new projects, support resources and events within the community, so joining is a fantastic way to stay in the loop.

For our state-based groups, please only request to join the group for the state that you live in. The Men’s Support Group and Teen’s Support Group are open Australia-wide. 
ABN: 14 104 820 346 | Charity Registration No. A0057033E

© Australia Alopecia Areata Foundation Inc.

Personal and health information collected by AAAF is protected under the Privacy Act 1988 (Commonwealth) as amended by the Privacy Amendment (Private Sector) Act 2001 (Commonwealth) including the National Privacy Principles and the Health Records Act 2001 (Victoria). AAAF being national in collection, is required also to comply with any other relevant state or territory privacy legislation (the Law). In this policy, a reference to ‘information’ in general is a reference to both personal and health information.

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