M4RD: RDI-Lancet commission for rare disease
18 August 2025
Interview by Emma Bishop, RARE Revolution insider,
featuring Lucy McKay, chief executive officer, and Megan Pullein, research project manager,Medics for Rare Disease (M4RD)

“If we’re talking about meeting the basic standards of human rights law, then the [rare] community isn’t a problem. It’s society that is creating the problem, rather than the rarity creating the problem.” Lucy