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The Bald and Beautiful
The Bald and Beautiful
Story
My name is Stephanie, I'm 20 years old. I suffer from Alopeica Areata and this is my story. I was two years old when I experienced my first episode, throughout my whole preschool life I never had hair. It wasn't until I was five and beginning primary school did my hair grow back; throughout these years without hair mum was constantly looking for answers and a cure but unfortunately there was not one then and still not one now. When I was fourteen my hair began to fall out again, as you could imagine being a teenager who is trying to navigate their lives, friends, boys and school; I had an extra burden. One of the worst parts about my hair loss at this age was other people didn't understand what was happening to me, My hair continued to fall out. The doctors told me their was nothing more they could do I just have to see what happens. I then decided to shave my hair for the World's greatest shave, someone close to me passed away from leukemia and I thought if my hair is going to fall out anyway I may as well make it help someone else. Still to this day my hair has not grown back, there are many people around the world who have worse issues that they are facing but for me not having hair now for six years has been one of the most challenging things I have had to deal with. I was fourteen and going shopping with my mum when a young girl walked a complete 360 around me and then turned to her mum and said "mum why is she bald, it's weird". This is when I realised that I'm always going to look different but that's fine it's who I am and I can't change that no matter how many wishes I make. A few months back I met a girl the same age who suffered from Alopecia when she was younger but she was always able to cover her patches and she said something that has stuck with me. Some people have told me before that I was brave but I never see it that way I just see myself being dealt a difficult hand in life and I'm just trying deal with it the best I can. So I have decided to help others by raising money for Alopecia Areata Australia which helps to educate school kids on what Alopecia is and that not all bald people are sick; they also provide affordable wigs to kids in school. I am doing this by creating a team and participating in the City to Surf. So please dig deep and donate for this charity so close to my heart.
Australia Alopecia Areata Foundation Inc
Australia Alopecia Areata Foundation Inc. (AAAF), is established to be the national Australia body supporting research to find a cure or acceptable treatment for all forms of Alopecia Areata, support those with the disease and their families, and inform the public about all forms of Alopecia Areata.
Our Service philosophy is to give each person the best chance of managing their alopecia journey positively, the whole family and each individual needs to be supported to manage their unique experience. By reducing the financial and emotional stress and enabling children, young people, adults and their support networks to develop their strengths and skills, AAAF assists the whole family to achieve that positive journey.
https://makingadifference.gofundraise.com.au/page/AAAFBaldTea - Boldest Bald Tea Event
https://aaafhairdonation.gofundraise.com.au AAAF general donation page.
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