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Website title: Love, Alopecia – All about alopecia, All by alopecians.
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My name is Kylie, and I’ve been living with alopecia since I was six years old. Now at 39, people often say, “you must be used to it by now.” But the truth is, you never really get used to it. There are still quiet moments where I catch myself wishing, “what if it just grew back?”
It started with something small—hair on my pillow. Then more,...
“Hi, I’m Mila. I’m 5 years old. I was diagnosed with alopecia areata when I was 2 years old, and I lost 80% of my hair. I also lost one eyebrow, and if asked where it was, my reply was, “It’s gone on holidays to Hungry Jack’s!”
If people ask where my hair is, we like to educate them on what alopecia is.
My hair has since grown back, though ...
“Thank you to the AAAF for this sponsorship – that has enabled me to continue my dancing.
Dancing is my favourite activity to do. It is not just the physical activity – but all aspects, the hard work and training to improve, the confidence of performing on stage in front people, whether it’s at home with my family or on live television in front of thousands of...
The last few months have mainly been about starting year 10 and training hard for the big competitions coming up. School is going well this year. I feel more confident with how I look. I’m currently in a growth stage. I have a few small patches of hair growing on top of my head, but I still shave my head as I have gotten used to it being short. I have also star...
Hello, my name is Hayley. I would like to thank the AAAF Team for awarding me the sponsorship gold program.
At age 5, I was diagnosed with Alopecia. Initially, I had tried some treatments which I stopped due to side effects. In the beginning, I would wear wigs as many people would make inappropriate comments and bully me in school.
My famil...