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The Corneal Dystrophy Foundation is a patient advocacy organization.

We are a US based 501 (c)(3) IRS approved Nonprofit Charitable organization founded to provide patients and the public with information and education about corneal dystrophies, potentially blinding genetic disabilities.

The Foundation provides biannual Corneal Dystrophy Symposiums, free literature, websites, online support groups and DVDs on the subject that are professional recordings of the leading corneal specialists in the US and overseas.   .  Our support communities currently have over 3000 active members who exchange information about their particular disability.

We maintain a Member Recommended Doctors' List as a reference guide.

We work closely with many corneal specialists in the US & Canada to make patients better informed so they may make better medical decisions.

Our presenters are Corneal Specialists, Genecists, Researchers and Eye Bankers who provide peer-level presentations and education at these events without charge.


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