Dejana Backo’s story is one of perseverance, strength, and boundless love. Born without arms, she never let her disability define her. Instead, she pushed past every obstacle, proving that limitations exist only in the mind. Today, she is not only a celebrated athlete and artist but also a devoted mother who cares for her child with incredible skill—using only her feet.
Her journey is a testament to human resilience, showing that challenges can be turned into stepping stones toward greatness. From excelling in para taekwondo to becoming a mother, Dejana has redefined what it means to live a full and meaningful life.
Embracing Her Unique Identity
Born on December 9, 1994, in Novi Sad, Serbia, Dejana grew up questioning why she was different. As a child, she often asked her mother why she didn’t have arms. However, as she matured, she realized that her body was not a limitation but a unique gift. She chose to embrace it and live life with confidence.
Her positive outlook and strong character helped her achieve incredible success in multiple fields. Nicknamed the “Girl with Wings”, she became a symbol of empowerment in Serbia, proving that strength comes from within.
An Extraordinary Athlete and Artist
Dejana’s achievements are nothing short of inspiring. At the young age of nine, she joined the Society of Mouth and Foot Painters, a move that ignited her passion for art. Determined to refine her skills, she later pursued a degree at the Academy of Fine Arts in Novi Sad, where she honed her talent and showcased her work across multiple Balkan countries.
Video : Mom withouth hands – playing with baby Lara – good morning – lets rock this day
But her passion didn’t stop at art. Dejana had always dreamed of competing in the Paralympic Games, leading her to take up para taekwondo in 2016. Her dedication paid off when she won the K41 women’s -47 kg division at the World Para Taekwondo Championship in Turkey in 2019—making history as Serbia’s first world champion in this category.
From Champion to Motherhood
In February 2023, Dejana embraced an entirely new role—motherhood. Choosing to step away from competitions, she prioritized preparing for her baby’s arrival, even deciding to skip the 2024 Paralympic Games in Paris. While she may not be competing in sports for now, she remains active in spreading inspiration through social media.
Motherhood comes with its own set of challenges, but Dejana has once again proved that she is unstoppable. She has mastered using her feet for everyday tasks, including feeding, dressing, and caring for her child. With the same resilience she showed in sports and art, she is tackling motherhood with grace and determination.
A Love Story Rooted in Strength and Support
Dejana is not alone in her journey—she has a strong and supportive partner. Her husband, a fitness instructor, has been by her side, providing encouragement and love. Their relationship is a powerful reminder that love transcends physical limitations.
The couple enjoys traveling and sharing their experiences online, proving that their bond is built on mutual admiration and shared adventures. On February 22, 2024, they took their love to the next level and officially tied the knot. In a heartfelt social media post, Dejana wrote:
“When you love without boundaries, unconditionally and completely pure. 22.2.2024—the day these two beautiful people swore before God for eternal love!”
Their wedding was not just a celebration of their love, but also a moment that showed the world that true love knows no physical barriers.
Facing Motherhood with Confidence
For many new mothers, taking care of a child can feel overwhelming, but Dejana has adapted in extraordinary ways. She changes her baby’s diapers, clothes, and even walks with her by holding hands—using only her feet. Her ability to care for her child in such a unique way is nothing short of extraordinary.
In an interview, she spoke about the realities of being a disabled mother, admitting that there are challenges but emphasizing that self-worth and a positive mindset help overcome any difficulties.
“We all have some difficulties as people with disabilities,” Dejana shared. “But if you have a good picture of yourself, if you know who you are and what your worth is, you can overcome anything and focus on the positives.”
A Life That Inspires Millions
Dejana’s journey is more than just a personal success story—it is a source of inspiration for millions around the world. She has shown that no obstacle is too great, no dream is too big, and no challenge is impossible to conquer.
- As an artist, she has defied expectations by painting breathtaking pieces with her feet.
- As an athlete, she has shattered records and proved that physical disabilities do not define one’s capabilities.
- As a mother, she is proving that love, creativity, and perseverance are more powerful than any physical limitation.
Conclusion: A Story of Courage, Love, and Strength
Dejana Backo’s life is a shining example of what can be achieved with courage, determination, and self-belief. From an inquisitive little girl questioning her differences to a world champion, artist, and loving mother—her story is nothing short of miraculous.
Video : Don’t look at what I don’t have, see what I can do ❤️ Girl With Wings
Her ability to embrace motherhood, overcome challenges, and live a fulfilling life is an inspiration to all. Whether she is painting, competing, or caring for her child, she continues to prove that with the right mindset, anything is possible.
Dejana’s journey reminds us that true strength is not measured by physical abilities, but by the heart, resilience, and spirit of a person. She is not just an athlete, an artist, or a mother—she is a living testament to the power of perseverance and love.
How Tessa Evans is Turning a Rare Condition into a Source of Inspiration and Change
The human body’s ability to adapt and overcome challenges is truly remarkable. Tessa Evans, born on Valentine’s Day in 2013, exemplifies this resilience. Diagnosed with Bosma arhinia microphthalmia syndrome—a rare genetic condition—Tessa has not only become a symbol of medical advancement but also a beacon of hope and inspiration.
Understanding a Rare Genetic Condition
Bosma arhinia microphthalmia syndrome affects the development of the nose, eyes, and puberty, and can also influence brain structure. With fewer than 100 documented cases worldwide, the condition is exceptionally rare. First identified in Vietnam in 1981, evidence suggests its existence may date back even further. Tessa Evans is one of the few individuals living with this condition, representing a unique story of courage and progress.
A Trailblazing Journey
Tessa’s parents, Grainne and Nathan Evans from Maghera, Northern Ireland, were unprepared for the diagnosis, as no abnormalities were detected during pregnancy. Despite the shock, the couple embraced their daughter’s uniqueness and embarked on a mission to enhance her quality of life through groundbreaking medical treatments.
Groundbreaking Treatments
At just two weeks old, Tessa underwent her first surgery to receive a tracheostomy tube, enabling her to breathe and eat more easily. By the age of two, she made history as the youngest patient to receive a cosmetic nasal implant. Utilizing advanced technologies such as 3D printing and medical tattooing, doctors are working to create a permanent nasal structure for Tessa as she grows. These innovations are designed to reduce the need for future surgeries and provide her with a more natural profile.
Challenges Beyond Appearance
Living without a sense of smell presents unique safety challenges for Tessa. Without this critical sensory warning system, she is more vulnerable to dangers like fires or spoiled food. Her parents remain vigilant, ensuring her safety and emphasizing the importance of raising awareness about her condition.
Inspiring Change and Progress
Tessa’s courage and her family’s determination have sparked hope for others facing similar diagnoses. Her groundbreaking treatments have inspired another child in the UK to pursue similar procedures. Described as “charming” and “fearlessly courageous,” Tessa continues to challenge perceptions and drive innovation in medical science. Her family’s Facebook page, Tessa; Born Extraordinary, documents her incredible journey, inspiring nearly 10,000 followers.
A Legacy of Resilience
Tessa Evans’ story is one of love, resilience, and medical breakthroughs. Despite the extraordinary challenges posed by her rare condition, she exemplifies what is possible with determination and the support of a dedicated family. Tessa’s journey is not only reshaping lives but also redefining the boundaries of medical science.
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