The EHN Patient Advocacy Handbook is designed to empower patients living with cardiovascular disease (CVD) by providing the knowledge, skills, resources, and practical guidance needed to advocate effectively for their rights, quality care, and supportive policies.
Developed by the European Heart Network (EHN), with the essential input and contribution of EHN member organisations and patient advocates that are part of the EHN Patient Network, this handbook aims to enable individuals to engage with decision-makers, actively shape policies, and drive positive change in cardiovascular health.
Advocacy efforts transform patient experiences and needs into meaningful policy reforms and legislative actions. Effective advocacy bridges the gap between evidence and action, helping to create healthcare systems that are fair, accessible, and focused on outcomes that matter to patients.
By sharing their expertise, patients with CVD can inspire researchers, policymakers, and funders to prioritise better access to care, increased research, and stronger prevention.
Advocacy empowers individuals and drives collective change for improved cardiovascular health across communities.
If you’d like to get in touch on this, please contact:Mehitabel HollerPatients and Research Managermholler@ehnheart.org+32 488 51 41 26