Should my baby sleep in the bed with me? I have asked this question to myself in preparation for our baby’s arrival. In my opinion‚ this is not a controversial topic‚ it is simply an individual’s opinion based on beliefs and instinct as a parent. I know there is so much information out there and decided to research the specifics. The forms of co-sleeping‚ bed sharing‚ or the family bed is a widely discussed topic around the world. In my opinion‚ sleep sharing includes any sleep arrangement within
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Mental Illness Research Questions - Munchausen Syndrome What illness are you researching? Factitious Disorders Munchausen Syndrome Ganser Syndrome What is the definition of your disorder? What might be physical/noticeable characteristics of this disorder? Munchausen syndrome is a mental disorder where a person repeatedly pretends to have severe illnesses‚ when they actually are the ones causing the illness to themselves. Those who have this illness will mostly complain of physical pain‚ as opposed
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Turner Syndrome It was first described in 1930‚ and first diagnose in 1959. Now a days‚ 1 of 2‚000 females are born with this syndrome. Turner syndrome (also known as TS) is named after the famous endocrinologist Henry Turner‚ who was the first person to described and published any findings about this syndrome. This condition is also known as Bonnevie-Ullrich syndrome‚ Gonadal dysgenesis‚ and Monosomy X. The syndrome is a non-inherited chromosomal condition that only occurs in females. It’s cause
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thoroughly? yes Corrie Nicholas Sedita English 101 November 25‚ 2012 Stockholm syndrome: Cause and Effect Stockholm syndrome; an issue that lends it name from a 1973 robbery of Kreditbanken in Stockholm‚ Sweden‚ in which two robbers held four bank employees hostage from August 23 to 28. These robbers shared a space with their victims and became emotionally attached and even defended them after. Today this syndrome is viewed as a psychological response to a situation where the victim has had their
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Care for Babies CHCCN5C Element 1: Respond to babies/infant cues and needs Cues and needs Infants cues and needs are met by the way we respond to them in their first two years of life‚ which can influence their ability to form trusting relationships for the rest of their life In Pairs discuss possible cues and needs and their meaning……. Familiar infant cues Cue Gurgling Laughing Pointing Possible Meaning Content Happy Needing/wanting something Fidgeting Grizzling Smiling Sobbing Crying
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Asperger’s Syndrome Today there are many different types of disabilities and syndromes. When you have a child to be diagnosed with a disability or a syndrome life can suddenly become overwhelming. This is especially true if they have been diagnosed with Asperger’s Syndrome. Parents sometimes feel guilty because their child has a disability or syndrome. Parents may feel that they are responsible for their child’s disability or syndrome. Parents may feel guilty about their child being diagnosed
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is like that. Have you ever heard of something called Marfan syndrome or MFS? It is a genetic disorder that about one in every five thousand people have and there is a fifty percent chance that it can be passed on to the next generation ("What Is Marfan Syndrome?"). Marfan syndrome is an abnormal condition characterized by elongation of the bones‚ and abnormalities in the cardiovascular system and the eyes (Hamilton). Marfan syndrome is a genetic disorder that can be inherited from ancestors and
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METABOLIC SYNDROME LEARNING OBJECTIVES At the end of lecture students should know – Definition of Metabolic Syndrome – Visceral obesity is an indicator of the syndrome and an independent marker for CVD – Current and some potential future treatment options. METABOLIC SYNDROME CONCEPT (Not New) • 1923 - Kylin first to describe the clustering of hypertension‚ hyperglycemia‚ hyperuricemia • 1936 - Himsworth first reported Insulin insensitivity in diabetics • 1965 - Yalow and Berson
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Case Discussion Beal’s syndrome (OMIM # 121050) is a disorder of connective tissues. The syndrome was first explained by Beal’s and Hecht in 1971. It is inherited as an autosomal dominant disorder that is characterized by multiple flexion contractures‚ arachnodactyly‚ severe kyphoscoliosis‚ abnormal pinnae and muscular hypoplasia. It is caused by a genetic mutation in FBN2 gene (encoding the extracellular matrix micro fibril fibrillin 2) on chromosome 5q23. The FBN2 gene provides instructions for
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Angelman Syndrome By Ciera Carr Dr. Glimps 2006 Carr 1 Ciera Carr Dr. Glimps Research Paper Angelman Syndrome Angelman syndrome is a genetic disorder that is caused by a couple of different attributes. The first one is “a deletion on chromosome 15 of maternal origin or paternal uniparental disomy”(Curfs‚ 2004‚ p. 1263). There has also been found that some people with the disorder have no deletion on the chromosome at all. Angelman syndrome was first discovered in 1965 by a doctor
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