forms of dementia can affect the way an individual communicates. All forms of dementia can affect the way a person communicates‚ so in time they may have to find different ways of expressing themselves and their feelings. As a carer your non-verbal communication will become important‚ your body language‚ facial expressions‚ gestures‚ eye contact and tone of voice will have to be taken into account when you are communicating with a sufferer. In the early stages of some forms of dementia people may
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The range of an organism and its dispersal is limited or affected by many things in its surroundings. These things can be slightly different in their specifics from organism to organism but generally‚ for all organisms‚ these are the main restrictions to their range and dispersal (either natal or breeding). The first limiting factor to the distance they can travel from their population or parent is the resources available. One artificial barrier is habitat fragmentation by humans and their use of
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Nephrotic syndrome is a group of symptoms including protein in the urine‚ low blood protein levels‚ high cholesterol levels‚ and swelling. The urine may also contain fat‚ which can be seen under the microscope. Nephrotic syndrome is caused by various disorders that damage the kidneys‚ especially the basement membrane of the glomerulus. This causes abnormal excretion of protein in the urine. This condition can also occur as a result of infection‚ use of certain drugs‚ cancer‚ genetic disorders
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Understanding Dementia and Alzheimer’s Disease Dealing with Dementia and the progression of Alzheimer’s disease through its three stages is often a daunting and distressing task. Most often relatives feel isolated and without help as if they were to be left alone‚ having no help to deal with the "unknown". They are also afraid of having to watch their loved ones become more and more distant‚ potentially losing a horrible battle with this disease. In order to help with this fear of the "unknown"
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and this is what we called Dementia. Along with this health condition some problems arises too‚ they tend to have more likely to suffer depression as they were brought to the healthcare facility‚ they have a new environment and/or cannot cope if tragic events arise in their past life. In this case study‚ I will be discussing a patient who is presently admitted
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My condition 3is called ITB syndrome Explanation: ITB syndrome stands for Iliotibial Band Syndrome. This is a common thigh injury generally associated with running. The band is crucial to stabilizing the knee during running. The irritation usually occurs over the outside of the knee joint‚ at the lateral epicondyle. The iliotibial band crosses bone and muscle at this point; between these structures is a bursa‚ which should facilitate a smooth‚ gliding motion. However‚ when inflamed‚
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Alagille Syndrome Abstract Alagille syndrome is a genetic disorder passed either by the parents or due to a genetic mutation(s). The liver is the affected region of the body. The liver has a lower count of bile ducts within the liver resulting in liver damage due to buildup of bile. If the liver stops working a transplant is needed for the patient to survive. This disorder also affects many other systems of the body. Treatment options include either use drugs or a liver transplant. There is
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Tourette Syndrome is characterized by several indicators including muscular tics‚ vocal or phonic tics‚ disinhibited thoughts‚ emotional differences including difficulties in emotional regulation‚ obsessive compulsions and rituals. The characteristics and frequency of indicators can change throughout a “Touretter’s” life time. The onset of Tourette Syndrome is usually in childhood between the ages of 5 and 10 (average 7) years old. People with Tourette Syndrome have little or no control over the
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Hunter Syndrome Hunter syndrome is a rare genetic disease that almost always occurs in males. This incurable disease is also called mucopolysaccharidosis II (MPS II). This disorder is caused by the deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). This enzyme is needed to successfully break down glycosaminoglycans‚ as part of the body’s normal recycling and renewal process. In a person with Hunter syndrome‚ enzyme I2S is missing or not working correctly. It is the accumulation
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01/29/2003. The SSA granted disability benefits because of borderline intellectual functioning and pervasive developmental disorder. She had a history of Apert’s syndrome
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