Kenadi Jordin-Brumley was born February 13, 2003. At birth she weighed a little more than a kilogram, and the doctors did not expect that the girl will survive. But she survived. First, experts had difficulty with the diagnosis, but when Kenadi was 8 months old, the parents learned that she suffers primordial dwarfism – a very rare type of mutation. People diagnosed with growth usually does not reach more than 75 cm and weigh about 3 kg.
Now Kenadi 4 years. From his illness, she does not feel any discomfort – on the contrary, the girl has already become famous in America as “little angel” and a model for several well-known photographers. And all the difficulties associated with short stature, compensates for the care of parents – they love their daughter and are confident that their family lives a little miracle.
Now Kenadi 4 years. From his illness, she does not feel any discomfort – on the contrary, the girl has already become famous in America as “little angel” and a model for several well-known photographers. And all the difficulties associated with short stature, compensates for the care of parents – they love their daughter and are confident that their family lives a little miracle.
However, as recognized by Briand and Jordin Court Brumley – mother and father Kenadi – the only problem for them – financial. Due to the unusual growth of the daughter, the parents will have to spend a lot of money and time trying to buy special furniture, clothing, and, in fact, to rebuild your entire home. But even these difficulties – nothing compared to the joy that brings Kenadi and parents, and all others. She has a gift to warm the hearts of men, – says Brian. – After talking with her, you feel as if touched with God.
