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