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Kelly Kashmer is the founder and Executive Director of NothingPink, a nonprofit organization dedicated to raising awareness about hereditary breast and ovarian cancers while providing personalized support to individuals at high risk. Her journey began with a life-altering diagnosis of Stage II Triple Negative Breast Cancer, just two weeks after learning she carried the BRCA2 gene mutation.

 

Following intensive chemotherapy and enduring 11 surgeries, Kelly channeled her experience and determination into founding NothingPink as a 501(c)(3) organization. Since then, she has tirelessly led the organization with a mission to empower others through education, advocacy, and support, making a profound impact on the lives of women in her community.

At NothingPink, we are committed to empowering individuals

and families affected by hereditary breast and gynecological cancers.

~Kelly

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About Us

NothingPink supports individuals and families affected by hereditary breast and gynecological cancers. We provide education, resources, and compassionate care—including support groups, workshops, and guidance on genetic testing—to help people take informed, proactive steps for their health.

My Story

Founded in 2015 by Kelly Kashmer in Fort Mill, South Carolina, NothingPink was born from a deeply personal journey of resilience and hope. At the age of 31, Kelly was diagnosed with Stage II Triple Negative Breast Cancer due to the BRCA2 gene mutation. Genetic testing not only saved her life but also inspired her to create an organization dedicated to supporting others on similar paths.

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What is NothingPink?

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