What are the affects of Alzheimer on a person

What are the affects of Alzheimer on a person

http://www.chacha.com/question/what-are-the-affects-of-alzheimer-on-a-person

The disease course is divided into four stages, with progressive patterns of functional impairments: Pre-dementia, Early dementia, Moderate dementia, Advanced dementia. During this last stage, the patient is completely dependent upon caregi…

How does Alzheimer Disease affect a person?

http://www.alzheimer.oxford.on.ca/ad/overview.html

Alzheimer Disease affects a person’s ability to understand, think, remember and communicate. At first, small subtle changes may not be apparent. However, as the disease progresses, the person gradually becomes unable to:･ learn new things m…

How Alzheimer’s affects a person:

http://www.nemahealth.org/programs/nac/

Alzheimer disease affects a person’s ability to think, understand, reason, remember, and communicate. Many of the changes that occur early are so subtle you may not notice them or think they are remarkable. But gradually, you will notice th…

Related Questions Answered on Y!Answers

Religiously… Why do we experience mental diseases that rob us of our memories (like Alzheimer)?

Q: When Alzheimer’s affects a person it doesn’t stop there. It effects the whole family. It not only robs the patient of their memories where they are diluted to the mental capacity of a 5year old, but it ruins the good memories that the family has of that person. I know this from personal experience. I barely remember my grandma before she had Alzhiemers. And fear is put into the family that not only that it could happen to them but it could happen to their dearest family members like their mom. I have a hard time with my faith when I start thinking of the “Why is this happening”, but I pray about it still.A lot of bad things were released on this world when Eve at the apple, but what is the point of Alzhiemer. Why such a cruel disease? I’m aware of others but lets just focus on this one. If you do not believe in God then keep your opinions to yourself I want a religious explanation.J: do you know anyone who has moderate to sever Alzheimer that you spent a week with?A week is all it takes to clean up human waste. To listen to the yelling at the tv. To have to dress them because they don’t remember how. To have to shower them because they’ve forgotten to A) Do it and B) to scrub everywhere. To have to show them how to hold a dinner utensil every time they eat because they don’t remember how. Sometimes they don’t even remember that the “bathroom” feeling is and just lets it go, never mind the missing the toilet or not going to it and going on a random space in the floor.

A: I don’t know. Alzheimer’s is not a punishment for wrongdoing, it’s just a confusing, heartbreaking disease that people get. I have been spending a couple of hours a week for the past six months with people who have Alzheimer’s and while it is tiring and frustrating, it is also very rewarding to spend time with them. There are people there who I wish I could consider friends because I really do get to care about them just from playing Bingo and listening to music with them, but I realize that they likely don’t remember me from week to week, and it’s difficult to deal with. I’m not even related to any of them and it’s hard. I think that it’s a trial for the family and friends and the individual with Alzheimer’s to have to deal with it, but I do believe that somehow some amount of good comes from the experience. We can see miracles and learn patience and love and compassion because of it. I think that God sees how we deal with these trials, whether we’re the one with the disease or a caretaker or friend or daughter or grandson or whatever, and remembers the good we do and the effort we put forward to handle it, and we’re blessed because of it.

Which genetic condition should I choose for a biology project?

Q: AgammagoblulinemiaAlbinismAlcaptonuriaAlzheimer’sCharcot-marie-ToothCleft lip/palateClubfootCoffin Lowry syndroneColorblindnessDiabetes mellitusDown’s syndromeFragile X syndromeGalactosemiaGlaucomaHereditary deafnessHereditary cataractHurler’s syndromeHypercholesterolemiaHypertensionMaple syrup urine diseaseMarfan syndromeMuscular dystrophyPhenylketonuriaProgeriaPyloric stenosisSpina bifidaThalassemiaTrisomy 9Trisomy 13Trisomy 18Turner syndromeTuberous sclerosisXeroderma pigmentosaThese are the genetic conditions that I have to choose from, but I may choose a genetic condition not on the list as long as there is enough information for me to use to answer a couple of questions. These questions are about the affects of the condition, symptoms, treatment, inheritance pattern and a lot of other genetic information, genetic cause, diagnosis, cures or research for a cure, expected life span of a person w/ condition, frequency, and a punnet square to represent possible outcomes of offspring, etc.If anyone would like to know what the exact questions are, please feel free to post a comment letting me know, and I will try to post up the questions ASAPWhich genetic conditions will allow me to find significant information? please give me a few conditions as I might now get my first choice, and please explain why you recommend it. Thank you

A: Hard to really say but if I was doing it I would chose Tay-Sachs disease (abbreviated TSD, also known as GM2 gangliosidosis or Hexosaminidase A deficiency).It is an autosomal recessive genetic disorder. In its most common variant known as infantile Tay-Sachs disease it presents with a relentless deterioration of mental and physical abilities which commences at 6 months of age and usually results in death by the age of four.Research in the late 20th century demonstrated that Tay-Sachs disease is caused by a genetic mutation on the HEXA gene on chromosome 15. A large number of HEXA mutations have been discovered, and new ones are still being reported. These mutations reach significant frequencies in several populations. French Canadians of southeastern Quebec have a carrier frequency similar to Ashkenazi Jews, but they carry a different mutation. Many Cajuns of southern Louisiana carry the same mutation that is most common in Ashkenazi Jews. Most HEXA mutations are rare, and do not occur in genetically isolated populations. The disease can potentially occur from the inheritance of two unrelated mutations in the HEXA gene. Which is one of the reasons that it is so interesting because generally you need the same mutation.Until the 1970s and 80s, when the molecular genetics of the disease became known, the juvenile and adult forms of the disease were not always recognized as variants of TSD. Post-infantile Tay-Sachs was often mis-diagnosed as another neurological disorder, such as Friedreich ataxia.[5] Patients with LOTS frequently become full-time wheelchair users in adulthood, but many live full adult lives if psychiatric and physical difficulties are accommodated. Psychiatric symptoms and seizures can be controlled with medications.If you want to do it on this and need any help please let me know.

can you rephrase this essay?

Q: Scientists should have an obligation to explore every avenue of genetic make up because Human Genome Project has allowed researchers to understand the blueprint for building a person. As researchers learn more about the functions of genes and proteins, this knowledge will have and has a major impact in the fields of medicine, biotechnology, and the life sciences said in the article Genes, Dreams, and Reality: The Promises and Risks of the New Genetics from the Indiana law journal. English professor at university of Memphis stated on his blog daredreaam.com that it allows doctors and scientists to look for any flaws in the human genes and DNA in order to find out if people will have any future diseases or conditions that could affect them. It will be possible for mothers of new born babies to find out the risks of diseases or conditions as they get older. The successes of the human genome project have even enabled researchers to pinpoint errors in genes that cause or contribute to disease. The ultimate goal is to use this information to find new ways to treat, cure, or even prevent the thousands of diseases like Alzheimer’s, and cancers that afflict humankind In the article what can the New Gene Tests Tell Us? From Judges’ Journal of the American Bar Association, stated that Gene testing already has improved lives. Certain gene tests can be used to clarify a physician’s diagnosis, as well as determine the appropriate treatment for the patient. In addition, parents can have the option of knowing whether or not their children will be born with devastating medical disorders. Those who are at risk for preventable diseases may also find out before the disease has struck.please?im desperate… thanks!!!!

A: The Human Genome Project has allowed researchers to understand the blueprint for building a person. Now, Scientists should have an obligation to explore every avenue of genetic make up. Researchers are learning more about the functions of genes and proteins. Genes, Dreams, and Reality: The Promises and Risks of the New Genetics, an article in the Indiana law journal, claims that this knowledge has had, and will continue to have, a major impact in the fields of medicine, biotechnology, and the life sciences. (name of professor), a professor of English at the University of Memphis agrees. He stated on his blog daredreaam.com, that it allows doctors and scientists to look for any flaws in the human genes and DNA in order to find out if people will have any future diseases or conditions that could affect them. It will be possible for mothers of new born babies to find out the risks of diseases or conditions as they get older. (name of article author), states in New Gene Tests Tell Us? From Judges’ Journal of the American Bar Association, that Gene testing already has improved lives. Certain gene tests can be used to clarify a physician’s diagnosis, as well as determine the appropriate treatment for the patient. In addition, parents can have the option of knowing whether or not their children will be born with devastating medical disorders. Those who are at risk for preventable diseases may also find out before the disease has struck. The successes of the human genome project have even enabled researchers to pinpoint errors in genes that cause or contribute to disease. The ultimate goal is to use this information to find new ways to treat, cure, or even prevent the thousands of diseases like Alzheimer’s disease, and cancers that afflict humankind.