Human rights

8th July 2026

Rare Disease Is a Health Inequality: It’s Time for UK Policy to Reflect That

Lucy McKay Healthcare policy, Rare Disease Advocacy Core20PLUS5, Health Equity, Health inequalities, Human rights, medical education, NHS, patient advocacy, rare disease, Rare Disease Action Plan, Rare disease policy 0

I’ve been levelling up I have been a Commissioner on the Lancet Commission for Rare Disease for two years and we are fast approaching the point of writing up our findings […]