My name is Peyton and I am a little girl with a lot of attitude! I was born with a rare genetic condition called Nager Syndrome. My blog is my way of telling my family and friends about life with this complex syndrome. I have a tracheostomy, a g tube, severe bilateral hearing loss, aortic valve disease, craniofacial, hand, arm and shoulder anomolies. Despite all that I am a normal toddler...