Analysis Of Prader Willi Syndrome, A Very Low Incidence Disability

Jeannette and her siblings adapt to self- sufficiency from a young age, from being emotionally and physically neglected by their parents. The children don’t expect anything so they learn to work with what they have and what opportunities come their way. Jeannette saw the suffering of the family and took this leadership for the family guiding her sibling in the correct path.

I enjoyed the activity learning about my family and how my family’s unique characteristics could be different than another individuals. Using this knowledge, I can enter every clinical session with an open mind and explore what makes the individual, couple, or group their own personality. Everyone has a story and many of those stories begin within a family system.

As a result, the daughter suffered in her formative years. She didn’t have the money to hire a nanny or a husband to support her while she stayed to take care of the baby. Aside from being sickly, her relationship with her mother suffered. At times she was emotionally detached from her mother and her capacity for learning was somewhat hindered.                

During our lives, serval blissful, traumatic, culture event that established the transformations during cognitive, social, physical, and characteristic changes in our lives from the time of birth through our death. A person’s existence is shaped and molded by the experiences that have set us physically and mentality. The interview conducted for this project for an understanding of, Mrs. Candi Jones, is a mother, daughter, and sister. She was the middle child of in a physically disable household where father and sister hearing-impaired; a mother who is deaf. They are a mixture of a sibling through birth, adoption, and foster. During the interview with Ms. Jones, she discusses experienced numerous events in her life that play a major influenced

Jon Owens was born on March 1, 1960. Jon’s parents feared of having a child with mental retardation. Jon family members are, mom is a psychotherapist and dad is a psychiatrist. Jon had two sisters Jennifer and Jennice and a brother Charlton. Jennifer is a filmmaker. Jennifer says Jon is a spiritual teacher. Jennice is a keynote speaker. Charlton is a lawyer and a doctor. When Jon was born, a pedestrian told his parents he would never reach age 5. Jon’s parents spoke with a fellow friend and doctor who had a brother with Downs’s syndrome. The family friend expressed the grief of putting brother in an institution and how it ruined his family lives. Jon’s parents thought it would best to put him in a nursing home. Jon was in a crib all his life. Jon lived in a nursing home for 6 ½ years until his caregiver died. Jon’s parents had received a call to make decisions about Jon’s care. Jon was diagnosed with having Down’s syndrome. Jon was more than a little slow, but mentally retarded. Jon had limited intellectual and physical abilities.

I wanted to make sure that I asked Cuyler’s mom a positive question about how Cuyler and how his disabilities have affected their family. I asked “What strengths have developed in your family because of Cuyler’s disabilities?” She said that because of his disabilities they have developed trust and learned how to depend on one another. Since Cuyler cannot leave the house at least one of his parents needs to be around the house. She also said that as their other children have become older they

Our family’s life is completely different than others due to my mom’s disease, but I have known no other way of living. My mother has had M.S. since she was in college, so I was born into a world with motorized scooters and walkers and extra precautions. This is my norm. And while other people may pity my mother and our family, I see no reason to be down. I could spend all my time harping on the drawbacks and my ”missed opportunities,“ but what fun would that be? I will always find the silver lining.

Although Lydia learned to accept her mother’s disability, the family as unit still needs to work together. As a family they must continue to experience the stages of grief, as it is a cycle. There may arise challenges as John and Tom’s respective careers and Anna’s children occupy their time but they still need to be involved within their family. As Alice had supported them, they must work to support Alice as she progressively loses her memory. It is through remaining together in support and love, that all of the members can grow and develop. As a family, the Howards can build proper copying techniques, which can help in other aspects of their

How people are changing these individuals lives because they are not thinking the same as regular people. Some of these individuals did not put on any medication to calm themselves down. The families and the individuals have a hard time to deal with ASD. However, they deal with it in the best way they can.

The arrival of a new baby brings excitement, joy, and anticipation. The Robertson family was certainly no exception to these feelings when their son Steven was born. Ida and John Robertson were like most new parents when it came to expectations and interactions with their son on a daily basis. This nuclear family of three soon realized their way of life would be altered as they struggled to adapt to Steven’s condition. As their little boy continued to grow, the parents would enquire about genetic testing, search for a school conducive to Steven’s needs, and learn to embrace a lifestyle in which Steven would thrive.

As explained in my essay, my brother’s condition did truly take a toll on my parents and myself in our daily life. My brother’s condition was never predictable, which made it much more difficult of a situation to deal with. There were times where he would not have a seizure for a few days. Yet, on other days, he would have about ten seizures a night. I remember clearly how somedays I had to stay home rather going to school just incase we had to take my brother to the hospital. Being the only English speaker in my family, I had to be present in such situations. I remember sitting on the side of his bed with my mother next to me, just waiting for him fall asleep so we could get some rest ourselves. There were times where I would go to school without getting much rest the night

Interviewee Billie Ragon gave me the opportunity to hear the story of her life and how her color and disability has affected how she has lived. Family values and the region, in which she lived, played a huge part in how she lived daily life. Different groups of people, whether it was family or just individuals from the community impacted her life greatly. Finally, Mrs. Ragon out of the kindness of her heart wanted to conduct this interview so maybe it could help others that may be suffering or feeling any kind of pain.

Addiction is a word that many people would associate with the body and its craving of a substance of any kind. Many individuals feel as if being dependent upon a substance is something that could be preventable and that the human body can live without. Though most substances an individual is addicted to are not needed to live a healthy life, the addiction could potentially kill that individual. Other substances such as food, one cannot live without. Food, unlike other additions, is a substance that the human body needs to survive. In recent years, there has been an upcoming epidemic regarding the obesity rate and the need for individuals to understand that lack of exercise and the increase in amount of unhealthy food is killing them. However, in some cases it may not be the lack of exercise and the unhealthy food choices alone that is keeping some individuals in a category labeled obese; conversely it could be a genetic condition keeping them that way.

The story focuses that regardless when things don't appear to go your direction, you have to remember the significance of family since they will acknowledge you for your identity. This

The story is based on a child named Emily that has a physical disability. Emily lived in a family of five children. "She always had a reason why we should stay home" (Olsen 601). Emily is lonely. When she was a toddler, she was left in a day care so Emily's mom could bring income to the house. Emily is a child that, as many others, grew up mostly on day care. Emily was