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Community Networks

There’s a KC community ready to help

There are several KC community forums and message boards online dedicated to better understand this disease. These are the most common places that patients go to seek out information about their diagnosis and build relationships with members of the KC community.

Here are a few groups you can join to participate in the conversation.

Keratoconus Group (Follow)
Keratoconus Group (Join)
Keratoconus Community
Keratoconus on Reddit

The following is a list of resources for current or potential patients and their families. If you have a specific medical question, it is best to consult your doctor.

National Keratoconus Foundation
Alliance for Eye and Vision Research
Cornea Research Foundation of America
Prevent Blindness

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