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A day in the life
A day in the life
A day in the life: Josiah’s diagnosis with familial cold autoinflammatory syndrome
By CONTRIBUTOR
28 June 2023
RARE News
102,000 newborns could be saved every year if proper screening were in place – celebrating International Neonatal Screening Day
By admin
28 June 2023
RARE News
Rare Care Centre Australia impact report
By admin
26 June 2023
RARE News
Pioneering polar adventurer and charity CEO of The Muscle Help Foundation charity to be awarded MBE for services to people with muscular dystrophy
By admin
26 June 2023
RARE News
An important milestone for the Duchenne community
By admin
23 June 2023
Charity & advocacy
Dee and Nadia’s journey with Kawasaki disease
By CONTRIBUTOR
21 June 2023
RARE News
Charity survey shows 60% of people with PSP and CBD are misdiagnosed
By admin
17 June 2023
RARE REV-inar
Gene therapies: a new age of care in rare diseases?
By editor
14 June 2023
RARE News
Cure Mito Foundation launches resource on Leigh syndrome
By admin
9 June 2023
Charity & advocacy
Global Genes and Cure JM Foundation: expanding mental health support for the rare disease community
By CONTRIBUTOR
7 June 2023
RARE News
DNA sequencing in newborns reveals years of actionable findings for infants and families
By admin
5 June 2023
RARE News
Global Genes’ RARE-X issues open call to researchers to participate in the Inaugural Xcelerate RARE Challenge
By admin
31 May 2023
Patient voice
Together—every step
By CONTRIBUTOR
31 May 2023
RARE News
American Kidney Fund will host cystinosis camp as part of national virtual camp for children and teens with kidney disease
By admin
25 May 2023
A day in the life
A day in the life: Cathy Moughton, PSPA helpline care navigator
By CONTRIBUTOR
24 May 2023
Charity & advocacy
GACI Global: circulating hope for families affected by a rare genetic disease that primarily affects the circulatory system
By CONTRIBUTOR
17 May 2023
Patient voice
Generalised arterial calcification of infancy (GACI): Ruben’s story
By CONTRIBUTOR
17 May 2023
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