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Editor's picks
Editor's picks
Let’s talk about sex, baby!
By admin
25 October 2023
Editor's picks
Marie Curie: the inspiring legacy of a great woman of science and our RARE inspiration
By admin
16 August 2023
Editor's picks
RARE Revolution Magazine publishes new impact report – The impact of RARE diseases on sibling experience
By Rebecca Pender
23 January 2023
Editor's picks
World Orphan Drug Alliance (WODA): bringing therapies to underserved patients around the globe
By Rebecca Pender
6 July 2022
Charity & advocacy
Married on a mountain with a collapsed lung
By Rebecca Pender
23 June 2022
Editor's picks
Saarah’s Foundation: a fitting legacy to Saarah Ahmed—daughter, sister, star student, aspiring neuroscientist, Miss Universe GB contestant and kEDS warrior
By Rebecca Pender
20 May 2022
Editor's picks
Building a bridge between patient and pharma: the CMT story
By Rebecca Pender
9 May 2022
Editor's picks
What can we learn from European rare disease policies to future-proof our health systems?
By Rebecca Pender
4 April 2022
Editor's picks
Brace! Brace! Brace… for burnout!
By Rebecca Pender
2 March 2022
Editor's picks
Everyone, on the bus!
By Rebecca Pender
28 January 2022
Editor's picks
Reframing the conversation around grief
By admin
6 October 2021
Editor's picks
RARE Revolution’s bereavement survey
By admin
6 October 2021
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