My name is Kimberly
I'm a 10-year-old full of life, creativity, and determination. I love art, hanging out with friends, and showing off my sticker collection. I have every kind, from glittery to glow-in-the-dark.
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But every night, when it's time to go to sleep, I struggle. I suffer from relentless itching caused by my condition, congenital melanocytic nevus (CMN).
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I wake up scratching until I bleed, desperate for relief that never comes. My parents have spent 10 exhausting years trying everything—cooling rags, a fan by my bed, even a vibrating mattress—but nothing stops the unbearable itching.
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My parents were so sad to watch me suffer like that and not know how to help.
That is what brought me and my parents to Nevus Outreach. At one of our events earlier this year, they found something they had been missing for years: hope.
For the first time, they met others who understood exactly what they were going through.
And something amazing happened at the conference in July. I was surrounded by kids just like me, I found confidence. I told my story and made new friends, and this fall, I felt so inspired that I even ran for class president!
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But my struggle isn’t over. I still fight every day with overwhelming discomfort. And the worst part? We don’t yet know why some people with CMN suffer so much more than others—or how to help.
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Will you help Nevus Outreach learn more?
Your support will mean so much.
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Love,
You can help create sweet dreams for people like Kimberly
Where do the funds go?
Donate to support those living with CMN, NCM, and related conditions
Your donation to our Sweet Dreams Appeal could help towards:
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Groundbreaking research to bring clinical trials to the United States for CMN, NCM, and related conditions.
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More patient-centered resources for new parents of children with CMN, NCM, and related conditions.
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Essential support services as families navigate the challenges of living with CMN and NCM.
We've been changing lives since 1997
In the past 27 years, Nevus Outreach has achieved amazing things. We support a global community with members in 33 different countries and 6 continents. We raise our voices for equality and advocacy for those with rare conditions like CMN and NCM. We are a founding partner of the Nevus Owners Outcomes Registry (NOOR), where we hope to further research and improve the health and well-being of all those affected by CMN, NCM, and related conditions.
Will you help us continue our vital work?