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THE FLAGELLA VISION FOUNDATION 

Empowering Vision, Illuminating Lives

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Progress to a Cure

The urgent mission of The Flagella Vision Foundation is to make positive impact on the lives of individuals suffering from blindness due to rare ciliary retinal disease. The Foundation is a 501(c)(3) not-for-profit charitable organization founded in 2023 by a passionate family driven to find support and treatment for their loved one's blindness due to IFT140-related retinal dystrophy. Flagella is committed to accelerating life changing outcomes by advancing research and advocating for individuals and families facing the challenges associated with retinal disease. Ciliary Retinal diseases encompass a group of rare genetic blinding disorders that affect the cilia, tiny hair-like structures in the retina responsible for vision. These conditions can cause a range of visual impairments and vision loss. Flagella is committed to drive the research that will lead to treatments and cures for blinding retinal ciliopathies and build advocating communities of support.

WAYS WE HELP

The Focus of Our Efforts

RESEARCH

The Flagella Vision Foundation;s goal is to drive the research that will lead to treatments and cures for those suffering from blinding retinal ciliopathies. 

ADVOCACY

The Foundation's premise is that making a real difference is not only possible but vital.  Creating communities of support and shared information is essential in this rare retinal ciliopathy

disease journey to a cure.  

VOLUNTEER

The Foundation is in need of dedicated advocates to help raise funds and increase awareness.  For more information about how you or your organization can help, please contact saurin@flagellavision.org. 

PARTNERSHIPS

Pending National Organization for Rare Diseases memember application.



 

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©2024 by The Flagella Vision Foundation. All Rights Reserved. The Flagella Vision Foundation is a qualified 501(c)(3) non-profit organization and all donations are tax deductible. EIN 93-1699094

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