Does it cost anything to join?
No. The community runs on LINE OpenChat, so anyone with the LINE app can join. There are no fees or dues of any kind.
Community
—Does any of that sound familiar?
This community is run in Japanese. Conversations take place in Japanese, so some reading ability is needed to take part.
This is a relaxed space for people who find faces hard to remember, people who suspect they may have prosopagnosia (face blindness), and people who have been diagnosed — somewhere to talk about everyday struggles and the workarounds that help.
Prosopagnosia is a condition in which memory for faces alone does not work as it should. It is thought to affect roughly 1 in 50 people. Yet it is barely known in Japan, and many people are misread as rude or uninterested in others, and end up carrying it by themselves.
No diagnosis is required. “I don’t know whether I have prosopagnosia, but I struggle to remember faces” is reason enough to join. If speaking up feels hard, reading along is completely fine.
These are some of the topics that come up day to day.
This community is run in Japanese. Conversations take place in Japanese, so some reading ability is needed to take part.
Questions we often hear from people deciding whether to join.
No. The community runs on LINE OpenChat, so anyone with the LINE app can join. There are no fees or dues of any kind.
Yes. A diagnosis is not required. If you are unsure whether you have prosopagnosia but struggle to remember faces, you are welcome. In practice, most members have not been formally diagnosed.
Yes. LINE OpenChat lets you set a name and icon separate from your everyday LINE account, and your friends will not be notified that you have joined.
Absolutely. Reading along is welcome. Many people find that simply seeing others describe the same experiences brings real relief, so there is no pressure to post.
It is run by the Name Mnemonic Research Institute (NMRI), which works to raise awareness of prosopagnosia. The organizers have prosopagnosia themselves. NMRI is not a medical institution and cannot provide diagnosis or medical advice.
All resources below are in English.
Whether you suspect you might have prosopagnosia, want to share thoughts on the site or our products, or have a media or writing inquiry — we take everything by DM on X or Instagram.
We cannot provide medical diagnosis or advice. If you are considering seeing a doctor, please consult a specialist. Replies may take some time.
Here is what we are looking for right now. For any of these, a one-line DM is all it takes.
We are looking for people interested in trying our prototype under development. See the AR Glasses page for where things stand.
Be on our list for the next survey of people living with prosopagnosia. See the research report for what we have asked so far.
We publish first-person stories under flower-name pseudonyms. See the Voices page for the stories published so far.