A determined teenager is showing remarkable resilience after being diagnosed with a challenging health condition.
Olivia Young, a 13-year-old described as “amazing and courageous,” was diagnosed with alopecia in May. Despite trying various treatments, her hair loss has been rapid.
“When I started thinking deeply about my situation, I realized that many others might be struggling to even get out of bed due to alopecia or an autoimmune disease,” said Olivia, who is known as Liv. “I felt the need to share my story and let people know that there will be days when you might feel unattractive or like you don’t fit in.”
Liv emphasized that while hair can be a significant aspect of one’s identity, it’s what’s inside that truly matters. “Hair was important to me, but trust me, no matter how someone looks—whether they have hair or not—it’s what’s on the inside that counts,” she said.
To support Liv during this challenging time, a Givealittle page was created by Shannon Ellison. The page reads: “Although Olivia absolutely rocks no locks, like any 13-year-old girl, she has had to put on a brave face and endure what most never have to.”
The page seeks donations to help the Young family purchase a wig made of human hair and to cover ongoing medical and wellness costs. “With the support of her amazing family and fabulous friends, we’re raising funds to help Liv cover the expenses needed to live her best life while conquering alopecia,” the page states.
Liv admitted that the diagnosis was a significant shock. “It started with one small patch. It wasn’t until we visited the doctor that we noticed there were several patches,” she recalled. “I realized I was losing my hair rapidly. It was more than hurtful to find out. For my family, it was a big shock.”
She added, “It was tough for them to deal with, and especially hard for me, thinking that this could be the last time I have my natural hair.”
As her condition progressed, Liv, a student at Macleans College, decided to get a wig. At the time, she had a mullet hairstyle and only a quarter of her hair left. The Young family began researching where to find “comfortable and affordable real hair wigs” and discovered Freedom Hair in Dunedin.
“There, I met an amazing family who showed us a lot of support, explained the costs, how the wigs are made, and how they should be worn,” Liv said. She noted that there’s a long wait for a high-quality, custom-made wig—anywhere from six months to two years.
The family also visited Hair Creations in Eden Terrace, Auckland, where they purchased a lace wig that Liv now wears. “I always tell myself, ‘whatever happens, happens.’ I have to live every day like it might be my last, so I try to be very inspirational,” Liv said.
Liv has been uplifted by the support from her community. “I felt very alone when I first found out about my alopecia. Now, I feel so supported and loved,” she shared. “I never realized how many people were there for me until my story went online. Words can’t express how grateful I am for all this love.”
Expressing her gratitude for the donations and kindness she’s received, Liv said, “I’m very thankful for every donation, kind comment, and hug. I couldn’t have done it without the people who’ve shown me love and supported me on this journey.”
Liv’s mother, Joanne Young, noted that the government offers a $1200 subsidy for under-18s, which can be claimed every three years. “While helpful, it’s a drop in the bucket considering the lace wig cost $3500, and the Freedom Wig will be around $6000,” Joanne explained. “Being human hair, they only last two to four years before needing to buy another.”
