
For if you or your loved one has been recently diagnosed
Everything you need to know, and how the AAAF is here to support you
What is Alopecia Areata?
The word “Alopecia” means hair loss. The word "Areata" means "patchy" or "in areas". Alopecia Areata is an autoimmune disease that results in patchy hair loss on the scalp and elsewhere on the body. It can range from small, individual smooth patches of hair loss to the total loss of all hair on the body—including ear and nose hair.
Alopecia Areata is not uncommon; current estimates suggest that 2% of the population will be affected by the condition at some point in their lifetime. It can affect people of all ages, genders and ethnicities, but most commonly presents during childhood.
Alopecia Areata is not uncommon; current estimates suggest that 2% of the population will be affected by the condition at some point in their lifetime. It can affect people of all ages, genders and ethnicities, but most commonly presents during childhood.
There is currently no cure, however AAAF is on a mission to do all we can to work towards a cure.
There are three main types of Alopecia Areata. Alopecia Areata, which means one or more patches of hair loss on the scalp. Alopecia Areata Totalis refers to total loss of hair on the head. Alopecia Areata Universalis means complete hair loss of the entire body.
In all forms of alopecia areata, the hair follicles remain alive and are ready to resume normal hair production whenever they receive the appropriate signal. In all cases, hair regrowth may occur even without treatment and even after many years. It is not currently known exactly what causes Alopecia Areata. It is believed to be a complex combination of genetic and environmental factors.
Alopecia Areata… It’s life changing.
There are three main types of Alopecia Areata. Alopecia Areata, which means one or more patches of hair loss on the scalp. Alopecia Areata Totalis refers to total loss of hair on the head. Alopecia Areata Universalis means complete hair loss of the entire body.
In all forms of alopecia areata, the hair follicles remain alive and are ready to resume normal hair production whenever they receive the appropriate signal. In all cases, hair regrowth may occur even without treatment and even after many years. It is not currently known exactly what causes Alopecia Areata. It is believed to be a complex combination of genetic and environmental factors.
Alopecia Areata… It’s life changing.
Looking for something in particular?
What to expect on your journey
Created based on the experiences of many members of the AAAF community, this is what to expect in the coming stages of your Alopecia Areata journey.
Health care professionals
Each link alongside will take you to directories to find a health care professional in your local area.
To Know
The SALT scale and Alopecia Areata Severity Scale
On your initial diagnosis for Alopecia Areata, you may have received a SALT or AASc score.
The Severity of Alopecia Tool (SALT) quantifies scalp hair loss in Alopecia Areata on a 0–100 scale, with scores of 50 or above denoting severe disease. Although valuable, the SALT score is limited to the scalp; it excludes body, eyebrow, and eyelash involvement. Furthermore, this clinical metric fails to account for the significant emotional and psychological burden experienced by patients.
How the SALT Score is Measured? The test divides the scalp into four regions, calculating the percentage of hair loss in each and multiplying it by a specific weighting factor. 0 means no scalp hair loss, and 100 means complete (or 100%) scalp hair loss. With a score of 50 or greater is typically classified as severe.
How the SALT Score is Measured? The test divides the scalp into four regions, calculating the percentage of hair loss in each and multiplying it by a specific weighting factor. 0 means no scalp hair loss, and 100 means complete (or 100%) scalp hair loss. With a score of 50 or greater is typically classified as severe.
The Alopecia Areata Severity Scale (AASc), introduced by researchers in 2022, evaluates hair loss percentages across the scalp and body while integrating the psychological effects of the condition. By capturing these broader clinical and emotional dimensions, the scale guides physicians in prescribing highly individualised treatment plans.
Treatments
There is no cure, but there are options if you’d like to explore them…
While the cause is unknown, there is currently neither a cure nor a single standard treatment for Alopecia Areata. Navigating this can feel incredibly overwhelming, but please know that we’ve got you—you do not have to walk this path alone.
There are many options available if you would like to explore them. While scientists continue to study what causes the condition, researchers are making massive leaps in understanding genetics, hair follicle development, immune treatments, and skin stem cells. In the meantime, some people find success with existing medical treatments—including medications approved for other health conditions—which can help hair grow back, at least temporarily. We are here to help you navigate these choices whenever you are ready.
There are many options available if you would like to explore them. While scientists continue to study what causes the condition, researchers are making massive leaps in understanding genetics, hair follicle development, immune treatments, and skin stem cells. In the meantime, some people find success with existing medical treatments—including medications approved for other health conditions—which can help hair grow back, at least temporarily. We are here to help you navigate these choices whenever you are ready.
Further reading

Alopecia Areata and the Battle Against Bad Information
Handling Questions – Alopecia Tips for Kids
Resources

Alopecia, Teens and Mental Health
Knowing the signs, how to start a conversation and where you can get support can change the lives of young people going through hard times.

Support for Family and Friends
A resource guide built for those in your inner circle to help them understand what you need and that mentioning Alopecia Areata is not off limits.

Youth Brochure
The “Teens Talking to Teens” brochure draws on their experiences of teens with Alopecia Areata from around Australia.

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.
FAQ
No. Alopecia is a broad medical term for hair loss of any kind, and there are many types. Using it precisely matters, because the wrong term can lead to the wrong diagnosis, the wrong support, and confusion when raising awareness. AAAF focuses specifically on Alopecia Areata and its variants, including Alopecia Totalis (complete scalp hair loss) and Alopecia Universalis (complete loss of all body hair).
No. You cannot “catch” it from another person. Alopecia Areata is an autoimmune condition, where the immune system mistakenly attacks the hair follicles. It is not infectious, not caused by poor hygiene, and not something that can be passed on through contact.
It’s complicated, and many people in our community are surprised to find there’s no simple yes or no. Sometimes, Alopecia Areata appears with no family history and no clear explanation. As one person shared: “The reason you have Alopecia can’t always be explained.” The fuller picture is that Alopecia Areata is polygenic, meaning a combination of changes across many genes appears to be involved, including genes that function in the hair and skin and in the immune system. It also shares genetic risk factors with other autoimmune conditions, which is why people with Alopecia Areata may also develop other autoimmune disorders, including vitiligo, lupus, and autoimmune thyroid diseases.
The risk of developing Alopecia Areata is greater for first-degree relatives of affected individuals than in the general population, but having a family member with the condition does not mean you will develop it, and many people have no family history at all. In short: genes play a role, but they are not destiny, and Alopecia Areata cannot be traced to a single inherited cause.
The risk of developing Alopecia Areata is greater for first-degree relatives of affected individuals than in the general population, but having a family member with the condition does not mean you will develop it, and many people have no family history at all. In short: genes play a role, but they are not destiny, and Alopecia Areata cannot be traced to a single inherited cause.
It depends on the type and extent of the condition. For many people hair does regrow, sometimes naturally and other times through treatment. For others, the loss is permanent, and the extent of the loss can change over their lifetime. The unpredictability is part of what makes Alopecia Areata so difficult to live with, and comments like “at least it will grow back” can be hard to hear when you simply don’t know.
Not yet. Research is ongoing and AAAF actively funds and supports studies into new treatments, working alongside some of the world’s leading dermatologists.
No, it’s so much more than that. Hair is tied to identity, to how we present ourselves to the world, and to how we feel in our own skin, and how we navigate the world. It is not just hair.
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,
+ 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,
+ 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.
'No Hair we Care' packs
‘No hair we care’ packs are a curated personalised pack filled with items to support one living with Alopecia Areata.
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No Hair We Care Package – Adult
Once-off purchase; includes headwear, skincare, books, DVDs, makeup, jewellery, games and more, plus support resources. Limited to one pack per person with alopecia; contents subject to change. Not sold outside Australia. -

No Hair We Care Package – Teen
Once-off purchase; includes headwear, skincare, books, DVDs, makeup, jewellery, games and more, plus support resources. Limited to one pack per person with alopecia; contents subject to change. Not sold outside Australia. -

No Hair We Care Package – Kids
Once-off purchase; includes headwear, skincare, books, DVDs, makeup, jewellery, games and more, plus support resources. Limited to one pack per person with alopecia; contents subject to change. Not sold outside Australia.
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.
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.
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
Stay up to date
Stay up to date with the latest news and happenings in your local area.