Ergomed Clinical Research is proud to introduce Keti Peeva, an extraordinary artist whose passion and creativity have become a beacon of hope for many. Living with Spinal Muscular Atrophy (SMA), Keti was diagnosed in 1993 at a US hospital—a turning point that set her on a transformative journey of self-expression and resilience.
A Life Transformed by Art
Despite the challenges posed by SMA, Keti has embraced her condition and transformed her experiences into powerful, evocative art. Each piece she creates is imbued with themes of love, hope, and determination. Her work not only reflects her personal journey but also serves as a medium through which she connects with others, sharing a message of strength in the face of adversity.
Art That Speaks to the Heart
One of Keti’s most compelling works is a heart-shaped hot air balloon carrying a couple—a poignant symbol of Rare Disease Day (RDD). This artwork captures the uplifting power of hope and the comfort that comes from unity and support. It’s a visual reminder that even in the midst of life’s trials, beauty and inspiration can flourish.
Keti Peeva’s journey is a testament to the transformative power of art and the resilience of the human spirit. Her ongoing commitment to spreading awareness about rare diseases inspires us all, and we are honored to be part of her remarkable journey.
Why This Matters to Ergomed
At Ergomed, our commitment to rare disease research goes beyond clinical trials—we strive to amplify the voices of those living with these conditions and foster greater awareness. Partnering with Keti Peeva allows us to highlight not only the scientific advancements in rare diseases but also the human stories behind them. Her art embodies the resilience, hope, and courage that drive our mission every day. By supporting Keti’s work, we reaffirm our dedication to improving the lives of patients living with rare disease—not just through research, but by helping to build a world that truly understands and supports them.