Friday, 13 February 2015

Photos: Meet 100cm Girl Who Is Looking For Love, Wants To Start A Family

19-year-old Hannah Kritzec, who was born with primordial dwarfism, is determined to find love and start a family Minnesota, USA.

Hannah suffers from an extremely rare condition called primordial dwarfism which means she is only 99cm tall. 

The condition is so rare only 100 people in the world are believed to have it. Such form of dwarfism causes short stature and dozens of other health problems including the threat of brain aneurysms and a shortened life span.

Hannah, was adopted by Jackie and Larry Kritzeck at birth and grew up in Minnesota, USA
Hannah, was adopted by Jackie and Larry Kritzeck at birth and grew up in Minnesota, USA.

The girl also has two titanium rods in her back after developing scoliosis and dental implants because her teeth and mouth are too small. Despite her diagnosis Hannah leads healthy and active lyfestile, she loves singing, ballet and dancing to hip-hop.
Hannah shows off her singing, dancing and acting skills at a class in Minnesota
Hannah shows off her singing, dancing and acting skills at a class in Minnesota

Now the teenager prepares for graduation from high school, choosing a career, dreaming about boys and even starting a family. 

Speaking about her plans for the future, she says,“Everyone thinks I’m five-years-old when they see me and it’s frustrating because I’m not a baby. 
Hannah Kritzeck tries to live as a normal teen but finds it difficult to find clothes and shoes that fit
Hannah Kritzeck tries to live as a normal teen but finds it difficult to find clothes and shoes that fit

Just because I’m smaller, doesn’t mean I’m any different. My ideal man would be someone with blue eyes, brown hair, and a Mohawk – and someone who would protect me. Looking to the future, I’d like to get married and have my own family. I would like to have two kids, a boy and a girl.”
Hannah Kritzeck was born with the condition that affects just 100 people worldwide
Hannah Kritzeck was born with the condition that affects just 100 people worldwide

Jackie, Hannah’s adoptive-mother, says,“We’re just going to I’ve each day like there isn’t one tomorrow. That’s all you can do. Live to the fullest. My advice to anyone living with the condition would be to never give up on your dream, and keep trying.” 
Hannah does not let her size stand in her way
Hannah does not let her size stand in her way...
Follow @maryamwokiliblog BBM Pin- 2AD7BD2D and BBM Channel- C003F8977

1 comment: