Chel Campbell
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  • Victoria
  • Australia
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About Me
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.
Do you have alopecia? (Choose appropriately)
Parent or guardian of child with alopecia
Are you age 18 or older?
Yes - I am 18 or older
Your Website (Leave blank if you don't have one):
http://www.aaaf.org.au

Comment Wall (6 comments)

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At 1:31am on February 19, 2015, Pams said…

Hi Chel......where are the meetings in Brisbane?  Are tbey for all types of alapecia.....mine is frontal fibrosing alapecia.

At 8:38am on October 12, 2011, StillHere said…
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? :)
At 1:13am on June 23, 2010, Tracey said…
Hi Chel

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
At 12:36am on May 24, 2010, Michelle L said…
Hi Chel - just a question - why is the Support Group for AA only? What about other forms of Alopecia? Is there a group in Perth?

Thanks :-)
At 3:49am on September 26, 2009, Cherylnz said…
Hi Chel,

Welcome to Alopecia World

Cheryl :)
At 12:36am on September 24, 2009, Tracy and Amanda said…
Hi Chel,
How are you? I also have a child with AA. I hope to be talking to you soon.
Tracy
 
 
 

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