Every young artist dreams of taking the stage, lights, music, and applause. For most children, this dream is limited only by imagination and opportunity. For Kayley Da Costa, the journey to the stage required something more: an extraordinary fight against her own body.
Kayley is a rising star in Trinidad and Tobago’s performing arts scene. She has trained in jazz, ballet, folk, and contemporary dance, performing on some of the country’s most celebrated stages through her work at Lilliput Children’s Theatre. Her original solo piece, “Fusion of the Isle”, showcased a maturing choreographic voice and a deep connection to Caribbean performance traditions.
She was recently awarded a full scholarship to attend New Waves 2025, an intensive dance and performance training programme presented by The Dance & Performance Institute in Port-of-Spain, Trinidad. Among the youngest in her cohort, Kayley distinguished herself through her commitment, focus, and artistic presence throughout the programme. But behind the curtain and the spotlight lies a story that very few see.
A Diagnosis at Five
Myasthenia Gravis (MG) is a rare autoimmune condition that causes weakness in the voluntary muscles of the body. Everyday activities that many take for granted, walking, climbing stairs, speaking, swallowing, and even smiling, can become challenging for those living with MG. At just five years old, Kayley Da Costa received this diagnosis. “It was scary,” recalls Kayley’s mother. “We didn’t know what the future would hold. Would she be able to dance? Would she be able to live a normal life?” The condition brought many uncertainties. There were moments of fear, hospital visits, and questions about what was possible. But from the beginning, Kayley showed a spirit that belied her young age.
Despite her diagnosis, Kayley never stopped dancing. “I didn’t want to stop,” Kayley says. “Dance is my happy place. When I’m on stage, I forget about everything else.” Her journey has required strict discipline. Proper nutrition, adequate rest, and faithfully taking her prescribed medications are non-negotiable parts of her daily routine. These treatments help manage her symptoms and allow her to remain active in the activities she loves.
Through it all, Kayley has been supported by her family, doctors, teachers, and friends, a village that has stood beside her every step of the way.
An Inspiration
to Others
June is Myasthenia Gravis Awareness Month, and Kayley has a message for others living with chronic illnesses: “Don’t let your condition define you. You are stronger than you think. Keep chasing your dreams, no matter what obstacles you face.” Her story is a testament to courage, resilience, and the power of never giving up. Looking to the future, Kayley dreams of achieving remission so she can continue living a healthy, fulfilling life, one where she can dance, act, and inspire others without the limitations her condition sometimes imposes. “Challenges can be transformed into opportunities for growth and success,” she says. “With faith, determination, and support, anything is possible.”
From the stages of Lilliput Children’s Theatre to the prestigious platforms of Trinidad and Tobago’s performing arts community, Kayley Da Costa is proving every day that the human spirit cannot be measured by medical charts or diagnoses. She represents exactly the kind of young artist programmes like New Waves were designed to support: disciplined, curious, collaborative, and unrepentantly ambitious. And as June brings attention to Myasthenia Gravis awareness, Kayley’s journey shines as a beacon of hope: a reminder that even the most challenging circumstances can be transformed into extraordinary achievements through perseverance and passion.
The stage is hers. And the story is just beginning.
Mary Cuffy is an educator and local children's author of the Ladybug series. Cuffy believes the best investment we can make in children is in the early years.
Email mary.cuff@yahoo.com . IG:marycuffy . FB: mary cuffy/Lola and the Dancing Ladybug
