At 62, Flashdance icon Jennifer Beals is still turning heads
2:06
At 62, Flashdance icon Jennifer Beals is still turning heads
1 month ago
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Callie Truelove is diagnosed with Williams syndrome, a rare genetic condition known to cause a joyful demanor. She loves everybody and even sees hearts in common objects all around her. Callie's parents consider her positivity a blessing, but also try to teach her not everbody can be trusted. | Special Books by Special Kids
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Callie Truelove is diagnosed with Williams syndrome, a rare genetic condition known to cause a joyful demanor. She loves everybody and even sees hearts in common objects all around her. Callie's parents consider her positivity a blessing, but also try to teach her not everbody can be trusted. | Special Books by Special Kids
1.1M viewsJan 28, 2021
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Jennifer Beals on life after death, loving Campbell Scott, and The L Word
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Jennifer Beals’ Parents Rarely Admitted Their Mixed Ethnicity
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Steven is diagnosed with Marfan and Beals syndrome. His body is growing faster than his frame can support. At 13 years old he is 7 feet tall, blind and unable to walk. Despite facing rejection Steven still believes he is worthy of love. His only concern is that others may not feel the same. | Special Books by Special Kids
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Steven is diagnosed with Marfan and Beals syndrome. His body is growing faster than his frame can support. At 13 years old he is 7 feet tall, blind and unable to walk. Despite facing rejection Steven still believes he is worthy of love. His only concern is that others may not feel the same. | Special Books by Special Kids
7.7M viewsJul 15, 2019
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Steven is diagnosed with Marfan and Beals syndrome. His body is growing faster than his frame can support. At 13 years old he is 7 feet tall, blind, and unable to walk. He has faced rejection but still knows that he is worthy of love. Steven just hopes that others feel the same. | Special Books by Special Kids
14:20
Steven is diagnosed with Marfan and Beals syndrome. His body is growing faster than his frame can support. At 13 years old he is 7 feet tall, blind, and unable to walk. He has faced rejection but still knows that he is worthy of love. Steven just hopes that others feel the same. | Special Books by Special Kids
2.3M viewsJan 9, 2021
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“ I push through the pain of living with congenital contractural arachnodactyly (Beals syndrome), severe Scoliosis, and Clubfeet. Congenital contractural arachnodactyly (Beals syndrome) is an extremely rare genetic disorder that is identified by certain joints such as my fingers, elbows, knees, and hips. I have severe Scoliosis that is so bad that my spine sticks out. That’s a hump on the right side of my back. I have club feet so I walk inward (pigeon-toed). I used to have to deal with my ribs
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“ I push through the pain of living with congenital contractural arachnodactyly (Beals syndrome), severe Scoliosis, and Clubfeet. Congenital contractural arachnodactyly (Beals syndrome) is an extremely rare genetic disorder that is identified by certain joints such as my fingers, elbows, knees, and hips. I have severe Scoliosis that is so bad that my spine sticks out. That’s a hump on the right side of my back. I have club feet so I walk inward (pigeon-toed). I used to have to deal with my ribs
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Special Books by Special Kids on Instagram: "Steven is diagnosed with Marfan and Beals syndrome. His body is growing faster than his frame can support. At 13 years old he is 7 feet tall, blind, and unable to walk. He has faced rejection but still knows that he is worthy of love. Steven just hopes that others feel the same."
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