IRDs are rare diseases, and the number of people affected by these conditions, and their impact on the greater population has remained largely undocumented – both at a national and global level.
In addition to vision loss, IRDs can affect patients, their families, and caregivers in a number of ways – including financial burden and poorer wellbeing. However, there is a lack of holistic data that represents these far reaching impacts.
This in turn hinders the development and funding of supports, clinical services, treatments, and clinical trials for IRD patients.
To address the large data gap surrounding the impact and occurrence of IRDs, Deloitte Access Economics was engaged by Retina International, together with a consortium that included patient-led organisations and industry partners.
The study carried out aimed to estimate the societal disease burden, and economic impact of IRDs in the United States of America (USA) and Canada – a cost-of-illness study. This study collected data from patients in the form of surveys.
Here are some key data:
You can download the files below: