Who We Are

Rare Million is committed to providing invaluable support and resources for individuals with rare diseases and chronic illnesses. Our platform is a beacon of hope and knowledge for those navigating the challenges of rare conditions.

At Rare Million, we believe in empowering individuals through education, community engagement, and personalized support. We strive to create a safe space where individuals can find solace, information, and connection. Join us in our mission to make a difference!

What We Believe

  • Every diagnosis deserves community.

  • Accessibility isn't optional.

  • Disabled voices belong in every room.

  • Hope and realism can coexist.

Meet Sarah

Sarah Mumper

Founder | Disability Advocate | Speaker

Born and raised in Sacramento. I'm a 3o year old disability advocate, amusement park lover (Universal and Disney), reader, and creative. Diagnosed with a rare genetic disease (McCune Albright Syndrome/Fibrous Dysplasia - FD/MAS) at a young age, I wanted to create a space with resources that are easily accessible for those living with and caring for those with a disability no matter physical or invisible.

I believe information for resources to help in a person’s quality of life should be free and accessible. I may not be an expert in all things, but through my connections to the disabled community, I believe we can learn from one another.

Available for consulting and speaking engagements.

Please email for availability.