Firefly Fund

Firefly Fund

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We fund research and education to accelerate cures for rare genetic diseases that affect children.

03/02/2026

Last week, the Zevra team had the honor of attending the Firefly Dreams Gala, a powerful evening dedicated to supporting rare disease research and education, specifically Niemann-Pick disease type C (NPC).

This year’s cowboy chic theme brought energy and heart to an unforgettable night. Most importantly, it was a moving reminder of why raising awareness for rare diseases like NPC matters so deeply.

We’re proud to stand alongside this community and support the mission.

02/27/2026

In recognition of Rare Disease Awareness Month and Rare Disease Day (Feb 28th) Firefly Fund honors the more than 300 million people across the world living with a rare disease (National Institutes of Health).

We stand united with rare disease patients, families, clinicians, researchers and advocates supporting early diagnosis and those advancing research and life-changing, life-saving treatments.

Learn more about our core programs serving the community – patients, families and clinicians – with essential resources and support, advancing knowledge about the complexities of rare diseases: https://fireflyfund.org/our-programs/

02/15/2026

💛💛💛 Love to our amazing Firefly Dreams Platinum Sponsors — LLK LLC, Cyclo Therapeutics, and Laura & Kyndel Bennett — for helping this night shine brighter.

Cyclo Therapeutics, a Rafael company
cyclotherapeutics.com

LLK LLC
llkllc.com

02/14/2026

We’re so grateful to our presenting sponsor Zevra Therapeutics for helping bring our annual gala Firefly Dreams to life. ✨

Zevra is a rare disease therapeutics company with therapies approved in the U.S. for the treatment of Niemann-Pick disease type C (NPC).

Learn more
https://zevra.com

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