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In this episode of the Pediatric Retinal Research Foundation podcast, Hannah, a content creator, discusses her journey with vision loss and how she has utilized social media as a therapeutic outlet. Hannah began creating videos on TikTok and YouTube in 2023 to cope with her vision loss, which started around three years prior. With the tool of humor, she transformed the challenges of her condition into clever videos, receiving laughs and positive feedback from friends and family. This creative process helped Hannah manage her difficulties while making others laugh, serving as her personal therapy. Despite her initial reluctance to acknowledge her vision impairment, Hannah found solace in the supportive community that her videos fostered, and she continues to share her experiences candidly and humorously.
Hannah also delves into her background, explaining that she was born with cone dystrophy, a rare genetic retinal disease that gradually worsened her vision. Initially, she maintained a near-normal life, working as a professional photographer for 13 years. However, in 2019-2020, her condition rapidly deteriorated, leaving her with only a pinhole of vision in one eye. This transition was tough, especially during the pandemic, but her family and friends provided crucial support. Hannah shares that joining online communities and connecting with others who have similar experiences was invaluable. She stresses the importance of communication and patience, advising those newly experiencing vision loss to seek support and be open about their needs.
In this episode of the Pediatric Retinal Research Foundation podcast, Hannah, a content creator, discusses her journey with vision loss and how she has utilized social media as a therapeutic outlet. Hannah began creating videos on TikTok and YouTube in 2023 to cope with her vision loss, which started around three years prior. With the tool of humor, she transformed the challenges of her condition into clever videos, receiving laughs and positive feedback from friends and family. This creative process helped Hannah manage her difficulties while making others laugh, serving as her personal therapy. Despite her initial reluctance to acknowledge her vision impairment, Hannah found solace in the supportive community that her videos fostered, and she continues to share her experiences candidly and humorously.
Hannah also delves into her background, explaining that she was born with cone dystrophy, a rare genetic retinal disease that gradually worsened her vision. Initially, she maintained a near-normal life, working as a professional photographer for 13 years. However, in 2019-2020, her condition rapidly deteriorated, leaving her with only a pinhole of vision in one eye. This transition was tough, especially during the pandemic, but her family and friends provided crucial support. Hannah shares that joining online communities and connecting with others who have similar experiences was invaluable. She stresses the importance of communication and patience, advising those newly experiencing vision loss to seek support and be open about their needs.