RARE Youth Revolution
RARE Revolution Magazine's youth platform empowers young adults and their families within rare disease communities. If you're 25 years old or under, email [email protected] to become a contributor.
RARETalks - Necrotising Enterocolitis (NEC) Part One
RARETalks - Necrotising Enterocolitis (NEC) Part Two
My life, my genetics: understanding my genetics
RARETalks - Spinal Muscular Atrophy (SMA)
RARETalks - Xeroderma pigmentosum (XP)
RARETalks - Bardet-Biedl Syndrome (BBS)
RARETalks - Cavernoma
My life, my Genetics: newborn screening
My life, my genetics: prenatal screening
My life, my genetics: family planning
My life, my genetics: genetic counselling
My life, my Genetics: genetic inheritance
Five in Ten: An interview with Carly about Huntington's Disease
RARETalks - Huntington's disease
RARETalks - Cystinosis
BPSU Symposium - Engaging young people in healthcare
RARETalks - X-linked Ichthyosis
Personal Stories Series - Eddison
Personal Stories Series - Katrina
Personal Stories Series - Amelia
Personal Stories Series - Barney
Personal Stories Series - Zainab
RARETalks - Lupus
Illuminating RARE Youth Talent Internship Programme
Personal stories Series - Aoife
Personal Story Series - Joe
Personal Stories Series - Katie
RARETalks - Ehlers Danlos Syndrome (EDS)
Personal Stories Series - Chelsea
#RAREfest22 Rare Quiz and Mythbusters