We’re thrilled to celebrate an incredible milestone – 15 years of AAAF! It’s been an extraordinary journey filled with hope, growth, and connection.

Over the past 15 years, we’ve worked tirelessly to raise awareness about Alopecia Areata, break down Continue reading →

📅 When: Wednesday, 8th January 2025

⏰ Time: 10:00 AM

📍 Where: Timezone Cavill Avenue entrance

👉🏻 Full details: https://www.facebook.com/events/1134447428204515/

Start the year with a cracking good time! We’ve got 1 hour of games and activities lined up, and Continue reading →

Have you ever paused to reflect on how much has changed for you over the years?

We’re inviting you to take part in our Then and Now Challenge! This is your opportunity to showcase your transformation and inspire others Continue reading →

We’re excited to bring you an update from our recent Annual General Meeting (AGM)! Our team enjoyed a fantastic weekend together, sharing ideas, celebrating our achievements, and planning for the future. We discussed some truly exciting opportunities, and we’ll be Continue reading →

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 →

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:

1. AbbVie/Upadacitinib Study
   • Age Range: Continue reading →