top of page
Home
About us
Blog Posts
Contact Us
Five minutes with...
My Life, My Genetics
Resources
RARE Recruitment
More
Use tab to navigate through the menu items.
RARE
Youth
Revolution
Empowering young adults and their families within rare disease communities
All Posts
News and Events
Charity and Advocacy
Women in RARE: Next Gen
Letters to my Younger Self
Science and Tech
Our Voices
Letters of Love
Coordinator Corner
Five Minutes with...
The World of Work
Columnists
Internships
News and Events (Kids)
Charity (Kids)
Our Voices (Kids)
Science and Tech (Kids)
Columnists (Kids)
Youth Spotlight
Search
RARE Talks Xeroderma Pigmentosum
In the second edition of our #RARETalks series, Katie Callaghan and Esther Hula, two members of our RARE Youth team, speak to Eddison...
RAREYouth
Jul 30, 2021
RARE Talks Ehlers-Danlos syndrome.
The first video in our #RAREtalks Series features an interview with Katie and Esther, two members of our RARE team, both of whom have...
RAREYouth
Mar 25, 2021
Back to Top
bottom of page
