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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
Started by Vesna Devcic Sep 18, 2010. 0 Replies 0 Likes
Hi All our AAAF supporters, please visit our Facebook page https://www.facebook.com/aaafonline/Or visit our website should you require further…Continue
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It's fantastic that AAAF has received this grant that will help provide a wig for a child. Well done Vesna :)
Had a great day at the AASA Open day and lovely to meet you Artemis and Dana!! Only sorry I didn't have time to chat more!!
Hopefully you found it an informative day and met some new friends as well :)
Hope to catch you both again soon!
SA - Dont forget the SA Support Group Xmas Dinner :)
https://www.facebook.com/event.php?eid=298015433561029
27 November · 18:00 - 21:00
Location
Café Brunelli, Rundle Street (next to the entrance to the car park which is above Hungry Jacks)
Dates for NSW is this weekend 26th Nov at 2pm as well - sorry I forgot to add that in the comment below :)
VIC - AASA's Open Day information - it is this weekend!
https://register.eventarc.com/event/view/5976/tickets/aasa-annual-o
Hope to see some of you there!
NSW - Note the next NSW Support Group Open day
The venue for the meetings and open day is:
Ryde-Eastwood Leagues Club, 117 Ryedale Road, West Ryde.
You can contact Linda Phone: 9874 – 4392 or E-Mail: info@alopecia-sydney.com for further information.
Hope some of you will make it!
take care
Ves
If you are considering purchasing a wig you may like to checkout AAAF's support guide
http://www.aaaf.org.au/index.php?page=alopecia-areata-registry
If you have any form of Alopecia Areata come and register yourself on our website if you haven't done so already :)
AAAF has been awarded $6025. This Community Grant will establish the Wigs For Kids initiative, which will act as an introductory program for kids newly diagnosed with any form of Alopecia Areata and now wishing to wear a wig.
How great is that!
Artemis
I will be there so it will be great to meet you! I know a few of our followers will be there as well!
See you there!
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