This film is about preserving the stories of people with dwarfism, both past and present. Dwarfism has only been portrayed on screen through a narrow lens, and we hope to fix that with this film. I’m so excited to announce that thanks to your support, we have now crossed $42k raised. We are so close to reaching our next milestone goal, and being able to resume filming. As an independant film created by people with disabilities, your contributions are essential to bringing this film to life. This

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213K views · 12K reactions | October is Dwarfism Awareness month....

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

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