Unveiling Unicorns is a nonprofit organization dedicated to raising awareness for rare and chronic illnesses, reducing isolation, and providing resources that empower individuals and families navigating diagnosis and life after diagnosis. Our programs begin with awareness campaigns, accessible drives, and storytelling, and will expand over time to include advocacy, peer support, accessibility reviews, and ultimately a medical program that bridges gaps across specialties.
Unveiling Unicorns is dedicated to raising awareness of rare and chronic illnesses, reducing isolation, and providing practical resources for navigating diagnosis and daily life. Through community engagement, accessible drives and programs, and the amplification of real stories, we support individuals and families facing the unique challenges associated with rare and chronic illnesses.
We envision a world where individuals with rare and chronic illnesses are understood, supported, and empowered at every stage of life. Our long-term goal is to expand from awareness and community programs to comprehensive solutions: building inclusive campus accessibility networks, creating peer support systems, developing an accessibility review platform, and ultimately establishing an integrated medical team that bridges gaps across specialties.
Ellie Melamed has been diagnosed with several mast cell disorders, Narcolepsy type 1, POTS, rheumatoid arthritis, hypermobile Ehlers-Danlos syndrome, and numerous other rare and chronic conditions. In fact, the word “anomaly” is listed as a condition on her medical chart. As someone who grew up with multiple rare and chronic illnesses, she saw a need for resources that would:
As a result, Ellie founded Unveiling Unicorns Inc. and incorporated the company at the age of 19. Ellie continued to work on Unveiling Unicorns throughout college, earning her Bachelor of Science in Business. She is also professionally certified in project management, digital marketing & e-commerce, and IT automation with Python. Ellie hopes to make a difference in the lives of those affected by rare and chronic illnesses and provide the resources and support she wished she had as she navigated her diagnostic journey and adjusted to life afterwards.
