"Seeking individuals between the ages of 13 to 25 with all forms of Alopecia Areata to participate in an anonymous research study. Research is being conducted by a student researcher, Louise Borg as part of an Honours Degree in a Psychology course,…"
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Chel Campbell replied to Taylor's discussion mmm in the group Australians with alopecia"Hi Taylor,
I think most activities occurring under the Australia Alopecia Areata Foundation Group. There are many people from Melbourne on that group. I'm from Victoria - mornington peninsula."
Chel Campbell commented on Vesna Devcic's group Australia Alopecia Areata Foundation"Also for those in W.A., don't forget the Activity Day On Sunday from 1:00pm. It will be an action pack day with hands on demonstrations and a chance to speak to our youth ambassador. Liz will be on hand to answer any questions having had…"
Chel Campbell commented on Vesna Devcic's group Australia Alopecia Areata Foundation"The W.A. Support group is running an Activity day on Sunday March 25th 2012, at Leederville Town Hall starting at 12:30pm, to introduce Georgia Gardner the Youth Ambassador along with Greg O’Rourke the newly appointed W.A. Branch Manager. The…"
Chel Campbell commented on Vesna Devcic's group Australia Alopecia Areata Foundation"I am pleased to advise that at its meeting on 10 February 2012, the Board of Directors were happy to accept the offer of the AAAF Grant The AAAF Grant is made annually by the Australia Alopecia Areata Foundation Inc for the development of a…"
Chel Campbell commented on Vesna Devcic's group Australia Alopecia Areata Foundation"AAAF has secured honour student Louise Borg from the University of Victoria under the guidance of Associate Professor. Gerard A. Kennedy to complete her thesis on, “How to cope living with Alopecia Areata”. Our resolve is to have some…"
Chel Campbell commented on Vesna Devcic's group Australia Alopecia Areata Foundation"Hi Holly,
We are currently organizing an event for Sunday 25th March in Perth. The AAAF does most of its correspondence via email, if you would like to be included please register here http://www.aaaf.org.au/index.php?page=alopecia-areata-registry"
Chel Campbell commented on Goody's group Aussies with Alopecia"Hi Stru,
The AAAF group is a little more active in communication."
Chel Campbell commented on Vesna Devcic's group Australia Alopecia Areata Foundation"For all those in QLD interested in going to a cocktail party, with nibbles, live music, silent auction- all for a gold coin donation - bring a group or a friend as there is plenty of time to plan - the event is Nov 25th at Little Beans Cafe 2215…"
Chel Campbell commented on Vesna Devcic's group Australia Alopecia Areata Foundation"SA Support Group Xmas Dinner
Date: Sunday 27th November
Time: 6pm
Venue: Café Brunelli, Rundle Street (next to the entrance to the car park which is above Hungry Jacks)
RSVP: At least a week before for booking purposes
Contact: Liz…"
Chel Campbell left a comment for StillHere"Our Youth ambassador Shea can be contacted on shea@aaaf.org.au. She is on AW as well"
StillHere left a comment for Chel Campbell"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? :)"
Chel Campbell posted an eventAAAF - Free - Natural Therapy Awareness Night at Victoria Australia
October 14, 2011 from 6pm to 10pm
9 Guest Speakers include:KinesiologyThought Field TherapyReikiFusion HealthGripper WigQi GongWig Styling, Eyebrow and Eyelash sytlingSee More
Profile Information
- Relationship Status:
- Married
- 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?
- 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 (5 comments)
- 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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