Osteogenesis Imperfecta is a disease that impairs bone marrow making bones brittle and easily breakable. For young kids, this is the end of the world. They aren’t able to jump on the trampoline, ride a bike, or participate in any athletic activities. This not only holds them back from having an active and exciting childhood but also from making friends. Kids with osteogenesis are withheld from the high points of childhood, but one boy diagnosed with OGI is still living his life to the fullest. His excitement about his everyday life that most people might believe is shortcutted is rather encouraging and inspirational.
Scott D Henry, a grown male tiktoker who has three million followers and gets up to twelve million views on select videos, posted a video with a young boy named Kevin Gabor who has Osteogenesis Imperfecta. After watching this, viewers were inspired by Kevin’s natural charisma and joyfulness. Now Kevin Gabor has over a million followers on Tiktok and shares his life with Tiktok and other media platforms. His online viewers enjoy watching his updates on his life full of fun! Kevin travels often. Just recently he visited Vienna and Romania and shared all of the views, meals, and tours on his Tiktok page.
Even when just at home, Kevin shares the food at his dinner table with his family or the recent Lego set he bought. Sometimes he is so excited about his pizza or trip to the store that he sings to his video audience. Just viewing the joy that he finds in his everyday life is inspiring. Most people with his condition might feel sorry for themselves their whole lives, but instead, Kevin uses his story to share his joy in life with anyone who might come across his page.
https://urldefense.com/v3/https://www.tiktok.com/@k3vingabor?_t=8fr38RwtvLf&_r=1;!!GNU8KkXDZlD12Q!6UuDjY7eSanjTnhXRWyluE53Ea5YgeLkbZrpaYMFoP_uaQS83Ao-sLfxdlv89HuW3W9pGwm0WnCCn-AcLop_69p5Qg$
Above is the home page of Kevin’s tiktok where he entertains his viewers and shares his story.