I am a mother of a son with Alopecia Areata. He is extremely confident and comfortable in his body. I am the President of the Australia Alopecia Areata Foundation. The foundation was established to bring awareness of the condition into the general public and this is being achieved by running media campaigns, public events and social events with the various support groups around Australia.
Thank you for your response.. Do you have much support here in Australia with Alopecia? Do you think it workthwhile getting the story across on national TV or do you believe there to be a better forum.. As you know, I'm new to this, however after seeing a story on trichotillomania, it got me thinking about Alopecia and how hard it is to get info
Hi Chel, you have such a beautiful name. If you could pass on the youth ambassadors details that would be great. Will you be holding any meetings or catch ups any time soon? :)
Tracey
Thank you for your response.. Do you have much support here in Australia with Alopecia? Do you think it workthwhile getting the story across on national TV or do you believe there to be a better forum.. As you know, I'm new to this, however after seeing a story on trichotillomania, it got me thinking about Alopecia and how hard it is to get info
Thanks Tracey
Jun 23, 2010
StillHere
Oct 12, 2011
Pams
Hi Chel......where are the meetings in Brisbane? Are tbey for all types of alapecia.....mine is frontal fibrosing alapecia.
Feb 19, 2015