Supporting the Alopecia Areata Adventure Camp in Western Australia!

We are excited to announce that the funds collected through various schemes this coming year will support next year’s Alopecia Areata Adventure Camp for children. At AAAF, we are dedicated to meeting the needs of individuals affected by Alopecia Continue reading →

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Jessica B has stepped into the role of NSW Branch Manager for AAAF

Jessica’s alopecia journey began at the age of 12 with small patches of hair loss, which later became more aggressive. Earlier this year, she lost all of her hair and has embraced her uniqueness, often rocking some incredible wigs! 💇‍♀️ Continue reading →

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Meet Yasmin: Championing Change and Embracing Identity Beyond Hair

Yasmin, a dynamic 23-year-old from Brazil, has transformed her lifelong journey with alopecia into a powerful movement for change. Born without hair, Yasmin once believed that her identity was tied to her appearance. However, she soon realized that true identity Continue reading →

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We are currently looking for participants to join TWO significant studies aimed at advancing our mission of awareness, support, and research towards a cure for Alopecia Areata.

Study Inclusion Criteria:

Diagnosis of severe alopecia areata (AA) with 50% scalp hair loss
No spontaneous scalp hair regrowth over the past 6 months
Current episode of AA lasting less than 8 years

Study Details:

AbbVie/Upadacitinib Study
- Age Range: Continue reading →

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Corporate Volunteering: Make a Difference with AAAF

At AAAF, we believe in the power of community and the impact of lending a hand. As an entirely volunteer-run and community-supported organization, we thrive on the generosity and skills of individuals who are passionate about making a difference.

Continue reading →

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“From Hair to There: Life with Alopecia”

The episode we were hosted on for “From Hair to There: Life with Alopecia” is live!

Join Global Healthy Living Foundation Australia and our AAAF to discuss the importance of resources and community support for patients and their families.

Episode Continue reading →

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Exclusive Alopecia Areata Australia Updates

We are excited to announce that the Raise Issue 18 – May 2024 is now available!

In this latest issue, you’ll find exciting features, inspiring stories, research update and valuable insights that you won’t want to miss.

To Continue reading →

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Navigating Safety Concerns: Understanding the Risks of JAK Inhibitors

A comprehensive safety study on the JAK inhibitor tofacitinib, used for rheumatoid arthritis, revealed concerning risks compared to tumor necrosis factor inhibitors. These risks include major cardiovascular issues, various cancers (particularly lung, lymphomas, and non-melanoma skin cancers), severe infections, and increased mortality Continue reading →

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ASAMI Study: Findings from a worldwide expert agreement on factors influencing Alopecia Areata severity.

What are the key factors that determine Alopecia Areata severity?

IMPORTANCE:

Current measures of alopecia areata (AA) severity, such as the Severity of

Alopecia Tool score, do not adequately capture overall disease impact.

OBJECTIVE:

To explore factors associated Continue reading →

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Revamped Grant a Wig Program: $700 Grant Offered for Young Wig Recipients

Since 2012, the Australian Alopecia Areata Foundation (AAAF) has provided crucial support to young individuals and families dealing with alopecia through their Grant A Wig for Kids program.

The program has expanded to assist various demographics, including university students Continue reading →

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