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Author:
CONTRIBUTOR
RARE caregiving
The barista and the quiltmaker: life lessons from strangers
By CONTRIBUTOR
5 July 2023
A day in the life
A day in the life: Josiah’s diagnosis with familial cold autoinflammatory syndrome
By CONTRIBUTOR
28 June 2023
Reviews
RARE Reads: Thrive Rare: Embracing The Uniqueness Within
By CONTRIBUTOR
27 June 2023
Charity & advocacy
Dee and Nadia’s journey with Kawasaki disease
By CONTRIBUTOR
21 June 2023
Charity & advocacy
Global Genes and Cure JM Foundation: expanding mental health support for the rare disease community
By CONTRIBUTOR
7 June 2023
Patient voice
Together—every step
By CONTRIBUTOR
31 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
Turning the tide for rare disease
Changing the landscape for the differently-abled community one smile at a time. Dr Sai Kaustuv is our RARE Inspiration
By CONTRIBUTOR
10 May 2023
Industry Insights
COVID: Three years on—what has changed?
By CONTRIBUTOR
3 May 2023
A day in the life
A day in the life with hypokalemic periodic paralysis: Ralph Berthiaume
By CONTRIBUTOR
1 May 2023
Turning the tide for rare disease
Arianna’s Magic Boots: stamping out a taboo in children’s books
By CONTRIBUTOR
26 April 2023
Patient voice
Raymond: A “ray of sunshine” living with VAMP2
By CONTRIBUTOR
21 April 2023
Science & tech
Engaging patients to shape the research of the future
By CONTRIBUTOR
21 April 2023
Charity & advocacy
Ableism can hurt your confidence. Learn to use your voice to regain your personal power!
By CONTRIBUTOR
19 April 2023
Turning the tide for rare disease
FOP Friends: celebrating a decade of support for the fibrodysplasia ossificans progressiva community
By CONTRIBUTOR
19 April 2023
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