Australia Alopecia Areata Foundation


Australia Alopecia Areata Foundation

Established to be the national Australia body supporting research to find a cure or acceptable treatment for alopecia, support those with the disease and their families, and inform the public about all forms of alopecia areata.

Members: 152
Latest Activity: Jul 14

Discussion Forum

About AAAF

Started by Vesna Devcic Sep 18, 2010. 0 Replies

Founded in 2010, Australia Alopecia Areata Foundation (AAAF), is established to be the national Australia body supporting research to find a cure or acceptable treatment for alopecia, support those…Continue

Comment Wall


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Comment by Chel Campbell on July 14, 2014 at 7:43pm
Reminder the W.A. Quiz night is on 2nd August  Don't forget to book your tickets.
• Phantom of the Opera tickets $15 ph  enquiry
• Family passes to Rottnest
• Hair and beauty vouchers – including salons who already service those with Alopecia
• Day Spa Vouchers
• Signed E...agles products
• Bounce Voucher
• Perth Mint Tours
• Dockers merchandise
• Penguin and Lion Sea Cruize
• Books donated from Dymocks
• Adventure world passes
• Surfing lessons
• A $1375.00 photography session
• $100 Harvey Norman gift certificate and many, many more!
Comment by Chel Campbell on July 14, 2014 at 7:37pm

If you are in Victoria and want to come to the pizza night - don't forget to RSVP to

Comment by Chel Campbell on July 11, 2014 at 2:30am

With International Alopecia Day fast approaching check out our events calendar for the activities happening in your state.

Comment by Fascinatinrythm on July 11, 2014 at 2:06am

Hi all, My story began when I was 11-12 years of age,(1979-80), this was the first time I suffered from Alopecia. Back then it was called Alopecia Nervosa Type A. At the time I was a child actor. An Australian film I did called Mystery Island (1980), shows the hair loss in certain scenes. My hair did grow back after a few years. Now 35 years later I am experiencing alopecia (areata) hair loss again. It seems to be far more aggressive although I did not shave my head back then as I have done on this occasion. All signs show that it is the areata variety although the hair loss is also on my chin and around my mouth,(the goatee area).

Comment by Vesna Devcic on June 16, 2014 at 11:42pm
SA - sorry I forgot to add the date for the dinner! 6th July at 6.30pm :)
Comment by Judy 1612 on June 16, 2014 at 3:39pm
Hi Rebecca, the picnic day is Sunday 29th. Would love to see you there.
Comment by dianna on June 16, 2014 at 9:20am

thank you for the invite .i read you profile and thank you  for the help you give to those people and me you are a great  woman .

Comment by Rebecca Goldsworthy on June 15, 2014 at 4:47am

What date is the Family day at Logan Central???

Comment by Vesna Devcic on June 15, 2014 at 12:04am

SA - AAAF Family Dinner

Café Brunetti - 187 Rundle St, Adelaide at 6pm

Liz our AAAF SA Support Group Manager has organised a get together Dinner for all.

To ensure you all will have a seat, please RSVP to

As always these dinners are always great for a catchup with old friends and welcomes new friends!

Comment by Vesna Devcic on June 15, 2014 at 12:03am

QLD - AAAF Family / Kids Get together & Play Day

AAAF have organised a Family day for children with Alopecia Areata and their families and friend s at Logan Gardens, Civic Parade, Logan Central - 10am

It's a great day for children to make new friends, and meet others that have the same condition. Its also a great forum for parents to share their journeys and meet new friends or catchup with old ones!

Please email our QLD state manager -,  if you are intending to come along - Judy will update you where to meet!

Look forward to seeing you there


Members (152)





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