Welcome!

Welcome to Love, Alopecia!

If you’re here, you’re most likely one of the millions of people in the world who make up our alopecian community.

Perhaps someone in your family, maybe your child or partner or sibling, has joined the alopecian tribe.

Maybe you work with someone with alopecia, perhaps as a hairdresser or wigmaker or doctor or psychologist or teacher, and you want to know more about alopecia in order to help them the best you can.

Welcome. 

Love, Alopecia is a place for all people who make up the alopecia community. If that sounds like you, you can keep up to date by following us for email updates, or by following AAAF on Facebook.

This is a place for the sharing of stories, information, advice and support. Our writers are all experts on alopecia – we’ve been living with it for years.

Stef has been a Support Ambassador with AAAF for several years. Stef has hosted numerous awareness talks at schools, conferences, and business events and has featured on TV and radio, all aimed at improving awareness of alopecia through education. She has had alopecia since she was six  years old.

Georgia (AKA George) is also Support Ambassador, in addition to her main role as the AAAF Secretary. Her background is in media and business, and has had alopecia for as long as she can remember.

Our other writers are, well, you. We have Guest Writers from within all different areas of the alopecia community. They may be blog writers already or may just have a single story to tell, but all are a vital part of what we do here.

Our philosophy is about approaching alopecia as an experience and as an identity, not as a disorder to be overcome. As well as discussing alopecia-specific experiences and advice, we focus on wider issues of image, identity and lifestyle. We’ll be posting articles, opinions and stories centred around the many ways AA affects our lives and impacts who we are.
This project has been proudly developed and supported by the Australia Alopecia Areata Foundation Inc.

If you’re looking for information about Alopecia Areata, how and why it occurs and how to manage the condition, click here to access the AAAF site. If you’re looking for support for people with Alopecia Areata within Australia, AAAF has state based support groups, Support Ambassadors and a variety of tools and resources you can access from here. For parents seeking resources for a child with alopecia, click here to access the AAAF Parents Support Page, which include links to our School Pack and Parents Brochure.

Please feel welcome to browse the site, chat with us in the comments and follow us to stay up to date. If you’re interest in writing for us, we’d love to hear from you! Please drop us a line at lovealopecia@gmail.com

 

 

Advertisements

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

Powered by WordPress.com.

Up ↑

%d bloggers like this: