healthcare equity Archives - Medics For Rare Disease

healthcare equity

21st May 2026

Impact Storytelling

Lucy McKay Healthcare education, Impact Stories, Rare Disease Advocacy charity leadership, healthcare equity, healthcare inequality, impact storytelling, medical education, Medics for Rare Disease, NatWest SE100, patient advocacy, rare disease, social enterprise, storytelling 0

Paying for Medicine In 2010 I was offered a place at medical school! I had managed to secure a coveted place on the Graduate Entry Programme (GEP) at Barts and […]

14th May 2026

Medics for Rare Disease Recognised in the NatWest SE100 Top Social Enterprises Index

Megan Pullein Healthcare education, Impact Stories, Rare Disease Advocacy charity leadership, healthcare equity, healthcare inequality, impact storytelling, medical education, Medics for Rare Disease, NatWest SE100, patient advocacy, rare disease, social enterprise, storytelling

We are incredibly proud to share that Medics for Rare Disease has been recognised in the NatWest SE100 Index of the UK’s top social enterprises. A celebration of the country’s […]

26th February 2026

Global Launch of ‘Rare Disease 101 (Nursing)’

Jo McPherson ELearning, Nurses, Rare Disease 101 global health, healthcare equity, midwifery education, Nursing education, nursing workforce, professional development, rare and undiagnosed conditions, rare diseases

The Global Nursing Network for Rare Diseases (GNNRD), in collaboration with Medics for Rare Disease, has announced the launch of ‘Rare Disease 101 (Nursing)’, a free, foundational eLearning course designed […]