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Living with one of the World's Rarest Syndromes (The Story of Sweet P)
24:05
YouTubeSpecial Books by Special Kids
Living with one of the World's Rarest Syndromes (The Story of Sweet P)
P is diagnosed with a form of primordial dwarfism that only she is known to have. As a child, she loved to make silly sounds and play hide and seek with her friends ...
4.8M viewsMay 9, 2024
Primordial Dwarfism Stories
5K views · 79 reactions | Primordial Radio is the evolution of rock and metal radio. A community where you can hear the best music, connect with friends new and old and be yourself. Grab your 30-day FREE trial from the link below and join the evolution落 | Primordial Radio | Facebook
1:01
5K views · 79 reactions | Primordial Radio is the evolution of rock and metal radio. A community where you can hear the best music, connect with friends new and old and be yourself. Grab your 30-day FREE trial from the link below and join the evolution落 | Primordial Radio | Facebook
FacebookPrimordial Radio
5.1K views2 weeks ago
Nick is the third oldest known individual living with primordial dwarfism | Journal Stories
Nick is the third oldest known individual living with primordial dwarfism | Journal Stories
FacebookJournal Stories
720 views7 months ago
Is Jyoti Amge Still the Shortest Person Alive Today? - Epic World Record Holders
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Is Jyoti Amge Still the Shortest Person Alive Today? - Epic World Record Holders
YouTubeEpic World Record Holders
3 months ago
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Primordial Dwarfism Facts
Finn lives with Primordial Dwarfism, which means she grows below average size. While her and her family do their best to lead a normal life, it is a condition that requires a lot of special attentions, one of them being the visits to the hospital. She is getting an ultrasound to make sure everything is normal. Additionally, we follow Fin in preparation for her first day of school as she has to have an uniform specially made for her size. From: Britain's Tiniest Toddlers | Real Families
4:04
Finn lives with Primordial Dwarfism, which means she grows below average size. While her and her family do their best to lead a normal life, it is a condition that requires a lot of special attentions, one of them being the visits to the hospital. She is getting an ultrasound to make sure everything is normal. Additionally, we follow Fin in preparation for her first day of school as she has to have an uniform specially made for her size. From: Britain's Tiniest Toddlers | Real Families
FacebookReal Families
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more fun facts: he’s the only person with dwarfism in his family, his type of dwarfism is called spondyloepiphyseal dysplasia congenita (SED), and he uses a segway to get around in real life#greenscreen | Aubrey Smalls
1:40
more fun facts: he’s the only person with dwarfism in his family, his type of dwarfism is called spondyloepiphyseal dysplasia congenita (SED), and he uses a segway to get around in real life#greenscreen | Aubrey Smalls
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Dwarfism Myths Vs. Facts: 4 Things You Should Know About Little People
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