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Know Rare
How We Help
Journal App
Research Finder
Rare Blog
How It Works
FAQs
Get in Touch
How We Help
Journal App
Research Finder
Rare Blog
How It Works
FAQs
Get in Touch

Video & Podcasts

Featured
Accepting Help is Hard
Accepting Help is Hard
Choosing What to Care About When Navigating a Rare Disease
Choosing What to Care About When Navigating a Rare Disease
Sharing the Silver Linings of Living with a Rare Disease
Sharing the Silver Linings of Living with a Rare Disease
Worst Thing to Say to Someone Living with a Rare Disease
Worst Thing to Say to Someone Living with a Rare Disease
Why Rare Disease Patients Fight So Hard for Clinical Trials
Why Rare Disease Patients Fight So Hard for Clinical Trials
Having a Rare Disease is a Full-Time Job
Having a Rare Disease is a Full-Time Job
The Waiting Game in a Rare Disease Clinical Trial
The Waiting Game in a Rare Disease Clinical Trial
The Loneliness of a Clinical Trial
The Loneliness of a Clinical Trial
What I Didn’t Know About The Clinical Trial Selection Process
What I Didn’t Know About The Clinical Trial Selection Process
Getting Treatment and Dealing With Insurance
Getting Treatment and Dealing With Insurance
In the Shadow of Rare: Growing Up as the Healthy Sibling
In the Shadow of Rare: Growing Up as the Healthy Sibling
Finding Your Voice: Writing About Your Rare Disease Story
Finding Your Voice: Writing About Your Rare Disease Story
Announcing Know Rare’s New Podcast Series: Rare Insights
Announcing Know Rare’s New Podcast Series: Rare Insights
Know Rare Connect: Living With Myositis
Know Rare Connect: Living With Myositis
A Rare Mom's Take on Living with Refractory Seizures
A Rare Mom's Take on Living with Refractory Seizures
Journaling Your Journey
Journaling Your Journey
Connect with Members of the Know Rare Team
Connect with Members of the Know Rare Team

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