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Geographic atrophy has a notable disease burden for patients and for those who care for them. The loss of vision can be traumatic and impacts many aspects of a patient\u2019s financial and social life, including relationships, hobbies and daily activities.1<\/sup><\/p>\n<\/div><\/div>\n\n\n\n\n
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Patients & caregivers<\/h2>\n<\/div>\n\n\n
Geographic atrophy has a notable disease burden for patients and for those who care for them. The loss of vision can be traumatic and impacts many aspects of a patient\u2019s financial and social life, including relationships, hobbies and daily activities.1<\/sup><\/p>\n<\/div><\/div>\n<\/div>\n<\/div>\n\n\n
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Geographic atrophy is a leading cause of legal blindness<\/strong> and is estimated to account for around 25%<\/strong> of all cases attributed to AMD.2<\/sup><\/p>\n<\/div><\/div>\n\n\n\n\n
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Prevalence of late AMD is expected to increase further<\/strong> with the aging population, and it is predicted there will be over 18 million cases<\/strong> by 2040.3<\/sup><\/p>\n<\/div><\/div>\n<\/div>\n<\/div>\n\n\n
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Devastating emotional and financial impact on both patients and their caregivers, and a substantial negative impact on an individual\u2019s ability to perform essential and enjoyable daily activities.1,4\u20136<\/sup><\/p>\n<\/div>\n\n\n
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A new survey of those living with geographic atrophy reveals that this disease comes with a large emotional burden and loss of independence.6<\/sup><\/h2>\n<\/div>\n\n\n
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The global Geographic Atrophy Insights Survey (GAINS) (N=203), conducted by The Harris Poll and sponsored by Apellis Pharmaceuticals, found that for nearly 7 in 10 (68%) of people living with GA, the impact of vision decline on their independence and quality of life is worse than they expected.6<\/sup><\/p>\n<\/div>\n<\/div><\/div>\n\n\n
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(35<\/sub>%) withdrew<\/strong> from their social lives<\/strong> due to vision loss6<\/sup><\/p>\n<\/div><\/div>\n\n\n\n\n
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agree the impact<\/strong> of vision decline on quality of life (QoL) <\/strong>and independence<\/strong> is worse than they expected<\/strong>6<\/strong><\/sup><\/p>\n<\/div><\/div>\n\n\n\n\n
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(77<\/sub>%) agree their vision was impacted faster than they expected<\/strong>6<\/strong><\/sup><\/p>\n<\/div><\/div>\n<\/div>\n<\/div>\n\n\n
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of those who have difficulty recognising faces feel frustrated<\/strong> when they cannot recognise the faces of friends or family<\/strong>6<\/strong><\/sup><\/p>\n<\/div><\/div>\n\n\n\n\n
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of people living with GA agree that prior to their diagnosis, they attributed their vision loss<\/strong> to a natural part of ageing<\/strong>6<\/strong><\/sup><\/p>\n<\/div><\/div>\n\n\n\n\n
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wish they had understood the irreversible impact geographic atrophy would have on their vision<\/strong>6<\/strong><\/sup><\/p>\n<\/div><\/div>\n<\/div>\n<\/div>\n\n\n
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Living with geographic atrophy can take a deep emotional toll. Of those who have difficulty recognising faces due to vision loss (n=61), 49% feel frustrated<\/strong> when they cannot recognise the faces of friends or family. Furthermore, out of all respondents, ~1 in 3 (35%) withdrew from their social lives because of geographic atrophy. These hardships also often come as a surprise, as most (77%) people living with Geographic Atrophy agree that the impact on vision is happening faster than they anticipated<\/strong>.6<\/strong><\/sup><\/p>\n<\/div>\n\n\n
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People living with GA report feeling:<\/strong>6<\/strong><\/sup><\/p>\n<\/div><\/div>\n<\/div><\/div>\n\n\n
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Despite these challenges, those living with geographic atrophy wish there were more educational materials for patients and caregivers (86%). There is a meaningful opportunity to empower them by providing more support as they navigate a future living with geographic atrophy.6<\/sup><\/p>\n<\/div>\n\n\n
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want more information and options<\/strong> about geographic atrophy to feel empowered to take control of their disease6<\/sup><\/p>\n<\/div><\/div>\n\n\n\n