TINY teenager Hannah Kritzeck loves singing, ballet and dancing to hip-hop, despite being just 39in tall. The 19-year-old was born with primordial dwarfism, a rare condition that only affects about 100 people in the world, which causes short stature and health problems, including the threat of brain aneurysms and a shortened life-span | Born Different

35K views · 840 reactions | The dwarves and elves long held a deep relationship during the early ages. | The Lord of the Rings on Prime | Facebook

2.7M views · 10K reactions | The world's largest ever gathering of people with primordial dwarfism have come together to bond with other families effected by the condition | Born Different | Facebook

October is Dwarfism Awareness month. Nick's friend, Hannah has Primordial Dwarfism (MOPD2) She is 3’3” tall at 28 years of age. There are over 100 types of Dwarfisms. Hannah enjoys hip hop, singing and drawing. She also loves fashion. Her dog Echo is her Mini me. Family and friends and Jesus are important to her. Don’t be afraid to say hello when you see her. Engage in conversation. She loves people. She helps at Mosaic church with the 4th and 5th graders in MoKids. LOVE A LITTLE!!! | Nick Smith

Charlotte is a girl who lives with a loving family of 6. Almost at the age of 2, she is smaller than some 6 months old babies due to a condition called Primordial Dwarfism. It is unknown what type of this disorder she has, but this is something important for her family to figure out - type 1 means she could die before turning 3, whereas type 2 could mean she gets to live a more fruitful life. Her family is fighting against time itself to make sure Charlotte's life can be saved. From: The Tiniest