Leber hereditary optic neuropathy (LHON) Community

Meet, discuss & support other patients or families living with Leber hereditary optic neuropathy (LHON). Contribute to topics, or just share what's on your mind.

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Welcome to the LHON community

Take a moment to introduce yourself in this section. If you see a post in a language you don't know, click on the link at the end of the post to have it translated into your language.

When you have a moment, write your story through the link in your profile and share your experiences with people around the world.

Write me with any questions: team@rareconnect.org