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Wigs for kids program

Our Stories


Nalani – “Children in particular will blurt out statements, but Nalani will just reply with ‘I know but I don’t need any hair’.”

Kaethe – “I’ve been hoping for over 6 years now for my hair to grow back and I don’t know how much longer I have to wait for my dream to come true.”

Siarrah – ‘My true beauty comes from the inside and the people that truly matter to me understand that.’

Faye – ‘When people talk to me, I like it when they look at my eyes and my face not at my head. ‘

Sarah 2016  – Surviving the emotional rollercoaster of living with no hair. How I overcame my 25 year battle with Alopecia to help other women learn to love themselves again.

Susan  -Life is like a box of chocolates, ya never know what you’re going to get.

John D“No matter what you’re going through, there’s a light at the end of the tunnel and it may seem hard to get to it but you can do it just keep working towards it and you’ll find the positive side of things”


Cameron  …..If I had paid less attention to my physical attributes, I would have realised that I actually have a lot more to give to the world then my hair.

Andee _Gabrielle ……. At 4years of age, Ellie would ask me “why did it have to happen to me  Mummy”…..all I can say to her is we love her no matter what.

Martina…… Yeah I miss the visits to the hairdressers, the pampering that went along with it all, but I spend the money elsewhere – wigs are fun – today my hair was long and wavy tomorrow it may be a short bob style.

molly…… Coming to accept Alopecia, is not only a personal trek, but one of   informing others about differences that exists amongst us.

Maretta …….I get compliments daily on how beautiful my hair is and all I can say is in my mind ‘if only you knew what is under all that hair and how I feel about it’.

Alex_Alison  Alison tells her story on son Alex …….We have a resilient, positive, strong willed young man.  He may not have hair but he is healthy, wealthy and wise otherwise in his life – That’s the greatest gift of all!

Jess …… I’m not sure that I’m fully ok with it yet, but everything that has      happened has given me the backing to survive whatever happens next.

Grace …….I am brave  because I was forced into it. Let them stare, let them stare in admiration.

Ellie …….I would really like to meet other little kids who are like me and have Alopecia as well. Then we can play together and we can be the same and no one will tease us. That would be my Happy Ever After Story.

Trevor …. if tomorrow there was a cure I wouldn’t want it. Having Alopecia has made me who I am and damn it, I don’t want to have to shave everyday.

Linsey….I wouldn’t wish alopecia on anyone. But having alopecia has helped to shape who I am; I wouldn’t trade being me for anything. I am blessed.

Ryan …You think that you are use to it, come to terms with it all….but I don’t think you ever really do, you just push it aside and try to move forward.

Brigette …I’d live my life without a lie

Vesna ……I have so often heard the saying “Everything happens for a reason”…so for what reason did I get Alopecia Areata???

Alyssa  …..It’s not worth the stress, I know image seems like everything these days—especially with teenage girls.. Maybe even boys. But it is ok.

Nikki …..I hope it grows back and doesn’t happen again.

Linda ……It is true “we are more than our hair” but for a woman in our society Alopecia is life changing.

Michelle …Sharing this “secret” with friends, means they often feel safe to confide in me.

Victoria …….Nobody with Alopecia is alone and its nothing to be ashamed of.

Jozette In many ways, having to deal with alopecia has made Tess, and the whole family, more resilient, and appreciate what really matters in life.

Charlotte .In accepting who I am, I’ve moved from feeling like the bald girl, to Charlotte who just happens to not have any hair.

Debbie ….Never give up!

kathi …Alopecia story as a poem.

Brooke ….it really made me realise that its just another aspect of life, nothing to really stress about.

Lily I like to wear a wig to school rather than anyone seeing me with no or little hair.

Pauline….I just hope one day there will be some magical cure for this disease.

Mel Why fit in when you are born to stand out.

Laura  As women we often stress so much about our appearance when in reality it is only us that is noticing a change.

Judy    I really missed my eyebrows and eyelashes much more than I missed my hair.

Stephanie I explained about alopecia. They all watched as I had my head shaved…. I wasn’t nervous … I could feel the support and love from everyone…

Stella 10 I’m VERY happy now in my school and I have a great family and friends and I’m happy to live a very bald and happy life!!!!!

Jane  I decided to make friends with Alopecia. …I believe that talking about Alopecia Areata more and revealing our patchy and bald heads is the way forward.

Violeta  Alopecia sculpted me into a very strong and confident woman that doesn’t believe that life has to be restrained by your hair.

Jack 8 What I like about my alopecia is that my friends get a good laugh when they say things like, ‘you’ve got a butterfly on your head’

Alex  I enjoy my life now as I made the choice to “don’t worry be happy !!!”



Julia Having Alopecia doesn’t have to be just bearable or just manageable. It will be part of you, but you can move on and it will not define you!

Heidi – Alopecia isn’t something we should feel embarrassed or ashamed about..

Heidi – I probably missed out on a lot because of my insecurities but I did have a great group of girlfriends who didn’t care that I didn’t have hair

Catherine 21,  Whether I have hair or not I am always thankful for what I have, rather on concentrating on what I don’t have.

Daneyl ” the strands of me”

Stef 16 telling her story through a poem.


Michell hair loss is something to be embraced. I’m ready for openness; I’m ready for people to be challenged; and I’m ready for bald women to feel empowered. I don’t want to spend my life merely surviving as a bald woman. I’d much prefer to live.

TEDxSouthBankWomen speaker Michelle Law performed ‘A Bald Woman’s Guide to Survival’ on Saturday December 1 at the independently organised event.  http://www.abc.net.au/unleashed/4404420.html

Video link:

Natalie, I am 25 and I have Alopecia Universalis. I have been wearing human hair wigs for the past 2 years and although there are tough days, I am more confident inraising awareness of this condition and telling people my story.

James Miller Imagine you are 10 years old, and one morning you wake up to find you have a bald patch at the back of your head the size of a golf ball,this is what happened to me.

Cam O’Rourke, 12, I first got AA in early 2010. It was a massive shock because it started off as
just one tiny patch, and in about four weeks, it had all gone, apart from a couple of tiny patches. My mates all helped me out by shaving their heads to show support, which was awesome.

Kylie Baker tells her story on how she mihgt not have a single strand of hair, but felt every inch the beautiful bride. Congratulations Kylie and Matthew.

Sarah P I’ve had ups and downs, I’ve been self conscious and I’ve been brave. I don’t know where I will be this time next year, or what my head will look like. But it’s an adventure, and its all part of my story.

Eliza & Ben In 2009, at the age of 3, Ben first experienced Alopecia.Ben’s elder sister Eliza realised how fortunate she was. She decided to grow her hair long enough so she could donate it to make a wig for another girl to enjoy.

Danielle K Who you are is about the inside not about what you look like on the outside, love
yourself no matter what for everything you are, inside and out.


Danielle – Danielle Bear, 28, accepts that being bald can be beautiful…….

Kylie – I have my ‘moments’ about Alopecia, but being constantly reminded of how beautiful I look is very supportive.

Joanne & Kylie – Living with no head coverage.

Georgia – Georgia Gardner, 17, I have plans for a very full, very fun, very bald life.

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