Inspiration from the Sidelines – University of South Carolina Athletics
Armani Latimer, a former captain of the South Carolina Dance Team and a Dallas Cowboys Cheerleader, has become a powerful voice for those living with alopecia. The Anderson, South Carolina native publicly shared her journey with the autoimmune condition in December 2024, performing with the Cowboys without a wig for the first time.
A Lifelong Journey with Alopecia
Latimer was diagnosed with alopecia areata at the age of 12. Alopecia, as she explains, encompasses any form of hair loss, with alopecia areata specifically causing hair to fall out in patches – which can vary in size. Her initial expectation was that the hair would grow back, a hope influenced by the fact that her father also lives with the condition.
Navigating alopecia during middle and high school presented challenges, as Latimer experienced unkindness from peers. Her mother provided crucial support, helping her find hairstyles to conceal the hair loss, and she began using extensions during high school pageants. Latimer’s father was also a key source of information and understanding.
From Carolina to Dallas
Latimer’s dedication to dance continued at the University of South Carolina, where she auditioned for and ultimately joined the Carolina Dance Team after significant preparation. She described the experience of stepping into “Willy-B” as unforgettable. She graduated from South Carolina in 2020 and returned to campus in August of the following year to choreograph for the dance team.
Dreaming of a professional dance career, Latimer set her sights on the Dallas Cowboys Cheerleaders. Despite initial feelings of being unprepared, she was encouraged by her parents to submit an audition video. She successfully navigated the rigorous audition process, including training camp and multiple rounds, to earn a spot on the team.
The Decision to Perform Without a Wig
During her second year as a Dallas Cowboys Cheerleader, Latimer experienced total hair loss. On December 9, 2024, she made the deeply personal decision to perform without her wig during a game against the Cincinnati Bengals. This act stemmed from a process of redefining her own beauty standards and recognising that her hair did not define her.
The response to her performance was overwhelmingly positive. Latimer shared that it was “incredible” to know so many people were interested in learning more about alopecia and that her story resonated with others who felt alone. She has since retired from the Dallas Cowboys Cheerleaders but continues to perform as a DCC All-Star and dedicate time to speaking engagements about alopecia.
Looking Ahead
Latimer plans to take the LSAT and attend law school in the future. She expressed a lifelong desire to be a role model, particularly for her two younger brothers, and finds fulfillment in inspiring others. She emphasizes the importance of building a strong community for those struggling with alopecia.
Frequently Asked Questions
When was Armani Latimer diagnosed with alopecia?
Armani Latimer was diagnosed with alopecia areata when she was 12 years old.
What prompted Armani Latimer to perform without her wig?
Armani Latimer performed without her wig after a period of redefining her own beauty standards and realising her hair did not define her.
What is Armani Latimer planning to do next?
Armani Latimer is planning to take the LSAT and attend law school, while continuing to work as a DCC All-Star and speak about alopecia.
How might increased visibility of conditions like alopecia impact societal perceptions of beauty and self-acceptance?