Australia Alopecia Areata Foundation

Information

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.

Website: http://www.aaaf.org.au
Members: 153
Latest Activity: May 12, 2017

Discussion Forum

About AAAF

Started by Vesna Devcic Sep 18, 2010. 0 Replies

Hi All our AAAF supporters, please visit our Facebook page https://www.facebook.com/aaafonline/Or visit our website should you require further…Continue

Comment Wall

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You need to be a member of Australia Alopecia Areata Foundation to add comments!

Comment by Vesna Devcic on August 14, 2012 at 6:14am

The Adelaide Lunch went really well and lots of new people attended! One supporter even drove from a couple of hours away and was so glad she did to have met some wonderful ladies!

Just a note that some of our supporters are holding their own events to raise awareness - see

Facebook -
https://www.facebook.com/aaafonline?ref=hl#!/AlopeciaAwarenessCycle

or via Go Fundraise
http://makingadifference.gofundraise.com.au/page/JMiller
and
http://personalchallenge.gofundraise.com.au/page/AlanT

If you are interested in creating your own fundraising event - drop us a line on info@aaaf.org.au to see how we can help!

Comment by Vesna Devcic on August 6, 2012 at 8:54am

Adelaideans - don't forget the luncheon on 11th August at 12 noon - Café Primo, Glynburn Road, Firle. RSVP to liz@aaaf.org.au by Wednesday 8th August

Comment by Vesna Devcic on August 6, 2012 at 8:53am

We are still looking for people to join in the Victoria University Survey has been given Ethics Approval and is being released this week. 100% confidential, and results will help everyone on there Alopecia journey. Whether you have AU, AT AA or your hair has grown back you can participate. If you are 13 -25 and have yet to register please contact louise.borg@live.vu.edu.au for participation. Thank you for making a difference.

Comment by Vesna Devcic on August 6, 2012 at 8:51am

Hi Everyone,
For those of you that have children at school that have alopecia, this could be a way to raise awareness!

http://www.aaaf.org.au/uploads/AAAF%20Crazy%20Hair%20Flyer2012.pdf

Comment by Chel Campbell on July 30, 2012 at 6:44pm

Victoria University Survey has been given Ethics Approval and is being released this week. 100% confidential, but results will help everyone on there Alopecia journey. Whether you have AU, AT AA or your hair has grown back you can participate. If your 13 -25 and have yet to register please contact louise.borg@live.vu.edu.au for participation. Thank you for making a difference.

Comment by Chel Campbell on July 27, 2012 at 12:53am

S.A. Group Luncheon Saturday 11th August at 12 noon. Café Primo, Glynburn Road, Firle. RSVP to liz@aaaf.org.au by Wednesday 8th August.

Comment by Vesna Devcic on July 24, 2012 at 6:24am

Hi Eveyrone
For those that are creative - take a look at how to create your own head scarfs!

http://www.aaaf.org.au/uploads/AAAF%20How%20to%20Make%20a%20Head%20...

Comment by Chel Campbell on June 28, 2012 at 5:52pm

We need you. Victoria University Psychology Researcher is seeking individuals between the ages of 13 to 25 with all forms of Alopecia Areata to participate in an 100% anonymous research study. The results of this study will be used by the support groups in Australia to assist those newly diagnosed or needing coping strategies. The study needs a minimum of 50. We have 36 registered. Please email louise.borg@live.vu.edu.au - Thank you Chel

Comment by Vesna Devcic on June 28, 2012 at 5:31am

Judy I am sure you will enjoy the experience as everyone that has had the head painting done loved it! For those in Melbourne we are doing this at our November Awareness Week.....watch this space :)

Comment by Judy 1612 on June 26, 2012 at 4:01am

Love the lyrics for this song. Can't wait to listen to it.
Looking forward to taking park in the Turning Heads project. My turn 21st July. so excited to be a part of getting the word out about Alopecia.

 

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