E-book

Records pile up, then become a book. Hard time becomes an asset

The everyday experience you live through isn't in hospital charts, clinical trials, or papers. vivome binds that record into an e-book and passes it to the next person walking the same path.

How it differs from ordinary health apps

·
Ordinary health apps
vivome
Where records end up
Locked in the app, forgotten
Published as an e-book
My experience
Only I ever see it
A map for someone on the same path
The data
Common everywhere
Daily experience found nowhere else
Reward
None
70% of sales goes to the author
Publishing
None
Opt-in · anonymized · after review

Data found nowhere else

What you live every day, “my stomach turned two hours after the medication,” “I always have trouble digesting on stressful days”, this daily experience is in no clinical trial, no hospital EMR, no paper. The most urgently needed record, yet one gathered systematically nowhere.

임상시험

통제 환경 · 소수

✕ 일상 경험 빠짐

병원 기록(EMR)

의사 관점 · 진단 중심

✕ 일상 경험 빠짐

학술 논문

일반화된 결론

✕ 일상 경험 빠짐

비보미, 병원 밖, 매일의 경험

“약 먹고 2시간 뒤 속이 뒤집혔어”, “스트레스 받은 날은 늘 소화가 안 돼”, 가장 절실하지만 어디에도 모이지 않던 기록.

전자책, 어디에도 없는, 당신만의 일상 경험 데이터

A record becomes the next person's map

The 60 or 90 days of real life in vivome, the nausea of Day 3, the first shower of Day 17, the hope of Day 42, are records of the process, not a summary of results. They become an e-book, passed from someone who walked the path first to the next person on it, what one person learned in the body, made readable for another.

📒

진짜 하루

60·90일의 과정

📖

전자책

결과 요약이 아니라

🧭

다음 사람의 지도

같은 길 위에서

공개는 전적으로 당신의 선택, 옵트인, 원문은 올라가지 않고 익명화, 검수를 거쳐 승인된 것만.

전자책, 한 사람의 기록이, 다음 사람의 지도가 됩니다

You're not alone

The record of someone who walked the path first fills what doctors can't. The relief of “so it wasn't just me,” the hope of “they made it, so maybe I can too,” a real answer to “when will this get better?”, things the averages of clinical data can't give.

🫂

“나만 그런 게 아니었구나”

같은 경험을 가진 사람이 있다는 안정감 (정상화)

🌱

“이 사람도 해냈으니, 나도”

먼저 걸은 사람이 보여주는 회복의 가능성

🧭

“언제쯤 나아질까”에 답

임상 데이터의 평균이 못 채우는, 현실의 시점

전자책, 같은 길을 먼저 걸은 사람의 기록이 주는 것

Hard time becomes an asset

Sell an e-book made from your records and 70% of the revenue goes to you, the author. Publishing costs are included in the subscription, so anyone can turn their experience into a book. And publishing is entirely your choice, opt-in, with raw text never uploaded but anonymized, and only what passes review going public. Hard time doesn't simply pass; it becomes an asset.

🪞

개인

나의 패턴 발견, 자기 이해

🧭

다음 사람

같은 길을 먼저 걸은 사람의 지도

💰

저자

판매 수익의 70%가 저자에게

전자책, 아픈 시간이 그냥 흘러가지 않고, 자산이 됩니다

Share experience, never prescribe

An e-book is a place to share “how I did it,” not “how you must do it.” “Here's what I did” is a record; medical suggestions like “you should do this too” get filtered out. Sensitive details like hospital names and diagnoses are masked automatically, exaggerations and guarantees like “miracle cure” are blocked, and only what passes review goes public. There's no room for ads or sponsors.

O“저는 이렇게 했습니다” · 내 경험의 기록
X“당신도 이렇게 하세요” · 의료 제안은 차단
익명화 (병원·진단명 제거)검수 후 공개과장·보장 표현 차단스폰서·광고 없음
전자책, 경험은 나누되, 의료 판단은 분리합니다

Features can be copied, but the experience one person lived through in the body cannot.

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