What more in the name of love?
Issy Clegg examines healing with pride: What LGBTQ+ activism gave to healthcare – and what’s still missing Despite a history of oppression members of the
In rare diseases, patients aren’t on the sidelines – they are central partners. Their lived experience fills critical evidence gaps and shapes what “meaningful outcomes” truly are. Rare Disease Networks bring together patients, clinicians, regulators, and pharma to create smarter, more feasible development pathways. We explore how and why in our latest blog, written by […]
Issy Clegg examines healing with pride: What LGBTQ+ activism gave to healthcare – and what’s still missing Despite a history of oppression members of the
This year, World Vitiligo Day 2025 will be celebrating its 15th anniversary at an AI-focused summit in Toronto, Canada. The theme is ‘Innovation for Every
While removing NHS England will eliminate some bureaucratic overhead, it won’t solve the system’s deeper issues. Without substantial investment, meaningful workforce support, and a coherent
LDA Research has recently welcomed Julia Heck to our team as Senior Research Manager. Market research holds a special place in Julia’s heart as she
Erin Paterson shares her experience of being gene positive for the rare Huntington disease, and how she is on a mission to positively impact other
Our Research Consultant Andrew Grant advocates for awareness of the physical and mental issues patients face while their condition remains undiagnosed Getting a diagnosis when
