Know Rare Connect: Leben mit Myositis
Journalist Lindsay Guentzel describes navigating a diagnostic odyssey and how she manages day-to-day life with myositis in an impactful webinar.
Die Sichtweise einer Mutter auf das Leben mit refraktären Anfällen
Rare mom Samantha Deschenes gives us an unfiltered look into life as a parent to a child with refractory seizures.
Tagebuch über Ihre Reise
Join Know Rare in a heartfelt exploration of the profound impact of journaling on the lives of those touched by rare diseases. In the “Know Rare Connect: Journaling Your Journey” webinar.
Verbinden Sie sich mit Mitgliedern des Know Rare Teams
In this recap of our first live Know Rare Connect event, we meet some incredible members of the Know Rare team and hear their stories.