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

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

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

Finn, Liam and Alex live with Primordial Dwarfism Type 2, which means they never grow taller than 3 feet. This puts them at risk of developing serious brain conditions such as moyamoya, which consists of blocked arteries at the base of the brain - an area called the basal ganglia. Still, they all live extremely fulfilling lives with certain precautions. From: Britain's Tiniest Toddlers | Real Families

This moving and inspiring film is about three young British primordial dwarves: Liam, Finn, Alex, and their families. Primordial dwarfism is extremely rare and the body stays proportionate but tiny. Only one in five million children suffer from the condition and it is believed fewer than 200 people have the condition worldwide. From: Britain's Tiniest Toddlers | Real Families

Do you recognize Jyoti? She has a form of dwarfism called primordial dwarfism! #history #education #learning #disability | Aubrey Smalls

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

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