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Finding Myself in the Mirror: My Story of Growing Up With CMN

Smiling person in yellow sweater stands outdoors with blurred greenery. Text: "Meet Naava" and "Nevus Outreach" logo. Bright, cheerful mood.

Growing Up Different

I am Naava, Growing up in a small village in Kampala, Uganda, I was born with a congenital melanocytic nevus (CMN) on my face. It was a constant reminder that I was different, and it seemed like the world was always staring back at me. People would gawk, point, and whisper to each other, making me feel like a spectacle, not a person.

Smiling person wearing a black and pink bonnet, black top, with a distinct birthmark. Background of polished wood creates a warm atmosphere.

The Weight of Being Seen but Not Understood

As a child, I struggled to understand why God had made me this way. I felt like I didn’t fit in, like I was an outsider looking in. The constant attention and scrutiny took a toll on my self-esteem, and I began to believe the negative voices in my head. I felt unloved, ugly, and like I didn’t belong.


Searching for Purpose in the Pain

But somewhere along the way, something in me began to shift. I started questioning the idea that my difference made me “less.” My CMN was a part of me, yes, but did it define me? Did it get to write the narrative of who I was and what I could become?

Smiling person in a red "Happy Days 1976" shirt and jeans poses with hand on face. Background has a building, plants, and clear sky.

The Turning Point

As I grew older, I began to see myself more clearly. I realized I was so much more than my appearance. I was smart, kind, talented, and full of potential. I had a perspective shaped not by shame, but by resilience.


Then one day, I looked in the mirror and saw someone beautiful—someone strong, someone who had endured more than most and was still standing.


In that moment, I understood that God had created me this way for a reason. My nevus wasn’t a flaw; it was a part of my story. It wasn’t a punishment; it was a path. A reminder that I was unique, valuable, and deeply loved.


My CMN Is Part of My Story — Not My Identity

Today, I embrace my uniqueness and celebrate my differences. I know now that I’m not alone. So many others struggle with feeling like they don’t belong or aren’t enough.

Person with dreadlocks and facial design makes a peace sign. Wears black top and gray jacket. Background has patterned stone wall. Smiling.

To you, I say this:

You are beautiful. You are loved. You are enough. The opinions or reactions of others do not determine your worth.

A Message to Anyone Who Feels ‘Different’

I share my story because I know how heavy it can feel to hide or doubt yourself. You don’t need to shrink to make others comfortable. You don’t need to change to belong.


Your uniqueness is an asset, a part of your brilliance, and the world needs exactly who you are.



A person smiling and standing outside in front of a window on a textured wall, wearing a gray shirt and jeans on a red brick walkway.

Why I Share My Story

My journey to self-acceptance has been long and winding, but it has taught me so much about love, compassion, and resilience. I have learned to love myself—flaws and all—and to see the beauty in what makes me different.


If you’re struggling to find your place in the world, remember:

You are loved. You are valued. You are enough.

Your light matters, and your story has power. You are a precious gem, and the world needs your shine.

-Navaa

💡 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.

 
 
 

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Get in touch:

Phone:  501-500-1932

Email: info@nevus.org

Address:

361 Southwest Drive, #353

Jonesboro, AR 72404

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

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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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