This study demonstrates that patient advocacy groups significantly enhance medication availability and improve diagnosis of hereditary angioedema (HAE), particularly in emerging economies within the Asia-Pacific region. This study supports integrating patient advocacy group involvement into management guidelines, emphasising their role in improving access to diagnostics and treatment for HAE.
Keywords: Asia–Pacific; advocacy; hereditary angioedema; patient support groups.
© 2025 The Author(s). Clinical & Experimental Allergy published by John Wiley & Sons Ltd.