Akeilla’s Alopecia Wig

Hi, my name is Akeilla, and I’ve been living with Alopecia Areata since I was 3 years old. That means for nearly 14 years, I’ve battled with losing my hair — and with it, a lot of the confidence many people take for granted.

Growing up, I’ve been called names, stared at, and made to feel “different” in ways no child should have to. Alopecia isn’t just about losing hair — it’s about losing a part of your identity, and constantly feeling like you have to hide or explain yourself.

For as long as I can remember, I’ve only ever been able to wear my hair down to try and hide my bald patches. Even then, they can still be seen if the wind blows or I move a certain way. I’ve never been able to style my hair freely like other people my age, and it’s been a constant reminder of something I wish I could change.

I’ve always wanted to feel the same confidence others have, to feel normal when I look in the mirror. A high-quality wig would mean the world to me. It wouldn’t just be hair — it would be a piece of my self-esteem, a shield from cruel comments, and a step toward loving myself again.

Unfortunately, I haven’t been able to get a job yet, and wigs that look natural and last a long time are expensive. That’s why I’m turning to the kindness of others. Your support — whether big or small — will help me take a step toward feeling comfortable in my own skin again.

Thank you for reading my story, and for any help you can give. Even sharing this page means more than you know.