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The Sunshine Within: Josefina's Nevus Journey

Girl with arms raised stands before a sunset with silhouetted palm trees. Nevus Outreach logo in corner. Warm, tranquil mood.

From the moment she entered the world, Josefina has radiated her own sunshine. Her mother, Mariana, describes her as “a girl full of light, with an endless curiosity about the world around her… and a smile that lights up every space she enters.” She loves to dance, sing, and discover new things. But what makes Josefina truly special isn’t just her joy for life- it’s her remarkable way of facing life with courage.


A toddler is smiling up to the left, with multiple small congenital melanocytic nevi on her arms and face.  Her hair is brown and about shoulder length. She is posing in a little white ruffled top with a sense of wonder in her brown eyes.

A Journey That Began at Birth


Josefina was born in 2017 in Argentina with a visible difference- a giant congenital melanocytic nevus. Her nevus extends from her lower back, stomach, down her thighs- often referred to as a “trunk nevus.” The rest of her body is sprinkled with smaller nevi, like tiny stars scattered across the sky.


In the early days, her parents immersed themselves in learning everything they could about her condition.

“At first, everything was confusing,” her mother recalls. “There were so many new words, so many questions, and a deep uncertainty about what lay ahead. I didn’t know what it meant- there was a mix of wonder, concern, and an overwhelming desire to understand.”
A little girl, about age 2, is sitting on a stool wearing a white dress and angel wings. She has a big smile on, as if she is laughing. She has congenital melanocytic nevi scattered on her legs, arms and face. Her brown curly hair is bouncy and her brown eyes are looking directly into the camera.



Surrounded by a dedicated team of dermatologists, neurologists, and

psychologists, Josefina received holistic care aimed at supporting her overall well-being. Yet for her family, the most meaningful guidance came not just from experts, but from the heart.




“Every decision was made carefully, always putting Josefina’s well-being first,” her mother explains. “We listened to the specialists, but we also trusted our intuition as parents.”

While biopsies have been performed, no surgeries were pursued- her parents chose to focus not on aesthetics, but on nurturing her happiness and self-esteem.


Love, Family, and Emotional Growth


The family’s emotional journey has been one of transformation. “We went from fear to acceptance, and from acceptance to the purest love. As a family, we grew stronger,” her mother shares.

A girl with long brown curly hair is laughing and pointing off to the right. She is standing in front of green foliage, in the summer sunshine. She's wearing a bright red top with blue jean overalls, and the biggest smile- showing all her teeth. She is freckled with congenital melanocytic nevi on her face, chest and arms.

Josefina herself has embraced her story with confidence beyond her years. “She speaks naturally about her skin. She knows her body is unique and that makes her special. There’s no shame or pain in her gaze; there’s pride and confidence.” Frequently advocating for herself and the nevus community, by sharing the facts about her unique skin.

“We explained that her skin was different, and that this difference made her beautiful and brave. We never hid her condition; we embraced it as part of her identity.”

Lessons in Strength



A girl dawning a white ballerina dress poses for the camera. Her brown hair is up in a bun with white bows decorating her hair. She has a closed mouth smile and is gently bowing with her arms stretched across her tutu. She has congenital melanocytic nevus on her face, chest and arms.

The hardest part, her mother admits, is the risks GCMN can carry, such as melanoma. “We don’t know exactly how her skin will evolve or what decisions would be necessary in the future.” But every medical milestone has brought gratitude and hope. “Every checkup where everything is fine is a cause for celebration.” 


Through Josefina’s journey, her family has learned profound lessons about love, resilience, and what truly matters.

“This journey taught me that resilience is born of love and that true beauty lies in authenticity. Being Josefina’s mother transformed me: I learned that accompanying is not controlling, but trusting; that loving is accepting.”


Finding Connection and Building Awareness



Two girls are celebrating on the beach. Both girls are mid jump with big smiles on their faces. They are on a beach in Argentina, and the water is shallow below them- with a warm sandy brown hue to the ripples in the water.

The family found immense strength in community- connecting with others who truly understood their experience.

“Sharing our journey with other families made us feel seen and supported,” they say. “It reminded us that we are not alone.”

Social media soon became another source of connection and empowerment. “It allowed us to share our story, challenge misconceptions, and raise awareness about congenital nevi. Through it, many reached out with empathy, and other families found in our voices a reflection of their own and a source of comfort.”


Josefina’s mother hopes the world learns to view visible differences with greater compassion. “They are not flaws to be corrected or hidden,” she explains, “but unique parts of who we are. Behind every mark is a story, a life, a human being who deserves to be seen beyond their appearance.”


Hopes for the Future


Looking ahead, Josefina’s mother dreams of a world that embraces diversity wholeheartedly.

"I hope Josefina grows up free, safe, and happy. May she find a world that embraces her without judgment, where diversity is celebrated.”

And to other parents just beginning a similar journey, she offers a message full of tenderness and wisdom:

“Breathe, hug, and trust. Fear is natural, but love is stronger. You are not alone. Your children are a gift, not for what they carry on their skin, but for what they awaken in our hearts.”

A girl with long brown hair is posing for the camera with her arms tucked behind her head. She looks directly at the camera with her big brown eyes and has a gentle smile on her dace. She has several small congenital melanocytic nevi on her face. She's wearing a red and white long sleeve shirt with racing flags and checkers all over it.

💡 Want to connect with other CMN families, find trusted resources, or support research? Visit Nevus Outreach to learn more, join our community, share your story, or make a gift today.

Get in touch:

Phone:  501-500-1932

Email: info@nevus.org

Address:

361 Southwest Drive, #353

Jonesboro, AR 72404

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Our Mission:

Nevus Outreach is dedicated to driving awareness, fostering a supportive community, and advancing research for people affected by congenital melanocytic nevi and related conditions.

EIN: 59-3455128

Nevus Outreach is a registered 501(c)(3) nonprofit organization dedicated to supporting individuals and families affected by CMN and NCM.

Medical Disclaimer: The information provided on this website is for educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider regarding medical concerns.

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