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Video instructions and help with filling out and completing Can Form 8854 Nationality

Instructions and Help about Can Form 8854 Nationality

Music. People assume that I am a lot older than I am. I think they do when they ask my age. My name is Michelle Elizabeth Ches and I am 20 years old. I have a condition called Holloman syndrome, which has 28 characteristics. I have 2,605 children that I don't have. I think they are here in this world for 20-year-old Michelle. I was born with Holloman Street syndrome, a condition so rare that at the time of my birth, there were only 250 known cases worldwide. It feels surreal because there's a lot of rise that I want to go up. It's frustrating that I can't go in the water because I risk being a burly headless. When I was pregnant with Michelle, everything was normal. There was no issue at all throughout the pregnancy or delivery. Michelle was diagnosed by geneticists who had recognized the syndrome from pictures in their medical books, but they had never seen it in person. The fact that my child had a rare genetic disorder, occurring only once in every five million births and every five generations, devastated me. The main symptoms of Holloman's Streif syndrome are cranial-facial disorder, bilateral cataracts, frontal bossing of the forehead, a recessed chin, a small beak-like nose, a small airway stenosis, ear canals, and dental anomalies. Michelle also has some of the secondary characteristics such as dwarfism, cardiomyopathy, chronic pulmonary lung disease, mitral gastrea, fragile bones, skin atrophy, and alopecia. Now, Michelle is a smart and happy 20-year-old young lady. She's as happy as ever and one of the happiest 20-year-olds I know. Her favorite things to do are playing on her computer, watching movies on her iPad, and playing with her dog Piper. She got her job four years ago, but unfortunately, she hates it. Despite her happiness,...