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sickle cell

Transcript: Sickle Cell Anemia Sickle cell disease is a group of disorders passed from parents to children (genetic) that includes sickle cell anemia. Sickle cell anemia is condition that makes the red blood cells curved. The red blood cells start out normal, but when they are stressed they become curved, hard, and sticky. The sickle cells have a hard time trying to move through the bloodstream. Sickle cells are small but they damage blood vessels they make it harder for the blood to flow right and they cause pain to the carriers. This disease shortens the carries life over all but if taken care of properly then the carrier should be able to live a normal life. This disease can be fatal. Sickle cell anemia is a recessive gene. thats all i have work cited http://www.medicinenet.com/sickle_cell/article.htm http://www.seattlecca.org/diseases/sickle-cell-disease-overview.cfm?gclid=CPyw3aj1_KwCFUOo4AodeAvzSQ http://library.thinkquest.org/17109/diseases.htm http://sickle.bwh.harvard.edu/sickle_trait.html The end sickle is a big problem in africa

sickle cell

Transcript: Sickle cell anemia is inherited from both parents. If you inherit the sickle cell gene from only one parent, you will have sickle cell trait. People with sickle cell trait do not have the symptoms of sickle cell anemia. Almost all patients with sickle cell anemia have painful episodes (called crises), which can last from hours to days. These crises can cause pain in the bones of the back, the long bones, and the chest. Some patients have one episode every few years. Others have many episodes per year. The crises can be severe enough to require a hospital stay. Treatment for a sickle cell crisis includes: Blood transfusions Pain medicines Plenty of fluids Other treatments for sickle cell anemia may include: Hydroxyurea (Hydrea), a medicine that may help reduce the number of pain episodes (including chest pain and difficulty breathing) in some people Antibiotics to prevent bacterial infections, which are common in children with sickle cell disease Ariana Boudoin Biology 1010 Sickle cell anemia is a disease passed down through families in which red blood cells form an abnormal sickle or crescent shape. Red blood cells carry oxygen to the body and are normally shaped like a disc. Treatments . sickle cell anemia Sickle cell anemia is caused by an abnormal type of hemoglobin called hemoglobin S. Hemoglobin is a protein inside red blood cells that carries oxygen. Works Cited A.D.A.M. Medical Encyclopedia. "Sickle cell anemia" 2012, A.D.A.M., Inc. February 7, 2012. http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001554/ What is sickle cell anemia? Causes Symptoms . symptoms & treatments

Sickle Cell

Transcript: Purpose Goal Upon completion, incidents of sickle cell emergencies will be reduced by 65% within a year of the program, for those who attended the program. 16 week program 5Major cities Implementation: Week 10-Convention Pre-test given to all partisipants Day 1-What is Sickle Cell Anemia-SCDAA Day2- Guest Speaker :Tionne “T-Boz” Watkins Day 3- Nutrition tips/ Help sooth symptoms Day 4- How to help: Community Attack Back Day 5- Vender day/Q&A Post-test given to partisipants Learning Objectives Objectives I think this is about facts! Radio Broad Cast Flyers Social Media Twitter Facebook Press Release After participating in small group discussions, the majority of participants will disagree or strongly disagree with the statement; “There’s no way I can avoid having any sickle cell complications.” After attending a presentation on sickle cell anemia, 75% of the participants will be able to identify their personal risk factors for having a sickle cell attack. Hard Match: 6000.00 By the third month of the program, participants will be able to distinguish the pain of a possible sickle cell attack. Within 5 months of the program, 45% of the community will be able help a person having a sickle cell attack get to help. Evaluation Total amount requested: $24,079.94 I think this is about data! Different perspectives What is Sickle Cell Anemia Six months after the completion of the program, at least 50% of the participants will be more conscious of sickle cell patient’s body signals and likely to help them when needed. Marketing Total Cost: $27,345.40 Indirect Cost: $2,734.54 I think this is about feelings! Total: $30,079.94 (cc) photo by theaucitron on Flickr Topic Behavior/Environmental Objective: Process Impact Outcome After attending lectures and presentations on sickle cell anemia complications, 35% of the participants in the program will be able to list 3 of their body signs and symptoms’ indicating their body is having a sickle cell attack. (cc) photo by theaucitron on Flickr Program Design

Sickle Cell

Transcript: Sickle Cell By Cole Wicker and Ashley Phillips http://www.nlm.nih.gov/medlineplus/ency/article/000527.htm How do you get this? http://www.nhlbi.nih.gov/health/health-topics/topics/sca/ Symptoms No official cure http://sickle.bwh.harvard.edu/scd_inheritance.html http://learn.genetics.utah.edu/content/disorders/whataregd/sicklecell/ What is it? Work Cited http://www.nhlbi.nih.gov/health/health-topics/topics/sca/treatment.html en.wikipedia.org Treatments More Facts 1 out of every 500 African American Babies are diagnosed with Sickle Cell Blocks blood flow bbc.co.uk Most Common http://sickle.bwh.harvard.edu/sickle_inheritance.gif Damali and Ameil Reid

Sickle Cell

Transcript: Dr. James Herrick found it in 1904 His intern noticed sickle shaped “Red Blood Cells” In there patient who was a 20 year old black man complaining of pain in his Spleenal area. It is inherited if 1 parent has it. There offspring has a 25% (1/4) chance of getting this Recessive gene. It is the Autosomal chromosomes which are affected. Who it effects Most The Sickle Cell disease affect the African American group the most but the disease can effect anyone. Characteristics/ symptoms Have Hemoglobin “S” and Hemoglobin “A” There’s pain in muscles in the arms, legs, and chest. There’s also pain in the Liver, Heart, and Spleen. Life The life expectancy is normal for most people which is the age of 60-90. Sickle cell disease can be life threatening if it is not noticed or maintained, it can cause a stroke, blood clots, and it can increase the levels of iron in the body to toxic levels(DEADLY). ORGANIZATIONS TO HELP The FDA and the SCDAA have been collecting funds to proceed in genetic research to make the red blood cells from sickling to each other. For this to happen they must create a beeter for of Hydroxyurea which is

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Sickle Cell Anemia Powerpoint

Transcript: The damage of sickle cell disease occurs because the capillaries slow the flow of blood and reduces the supply of oxygen to various tissues. About 100,000 americans are thought to be living with sickle disease , and every year another 1,000 babies are born with the disease. Where And Who Does sickle Cell Mostly Occur? 2.)http://health.nytimes.com/health/guides/disease/sickle-cell-anemia/overview.html?WT.z_gsac=1 Title: sickle cell anemia prognosis health information The End! 3.)http://emedicine.medscape.com/article/205926-overview Title:Sickle Cell Anemia Websites! SICKLE CELL ANEMIA Is Sickle Cell Anemia A Curable Disease? Another Definition! 4.)http://www.ehow.com/how_2091958_prevent-sickle-cell-anemia.html "Sickle-Shaped" crescents! What Is Sickle Cell Anemia? "Sickle-shaped" means that the red blood cells are shaped like a crescent. gracias por ver mi presentación Is Sickle Cell Anemia Contagious? No,sickle cell anemia isn't a contagious disease. People are born with it however, it does not develop into adulthood. it is a genetic disorder that is passed down from parent to child. Byeee!! Yes,there are three main subsets of sickle cell disease. The most common form, which accounts for at least 60 percent of all cases, is sickle cell anemia.. Another form is sickle - Hemoglobin C disease and sickle beta thalassemia. Sickle cell anemia is the most common form of sickle cell disease (SCD). (SCD) is a serious disorder in which the body makes sickle- shaped red blood cells. Sickle cell Anemia Mostly Occurs In African Americans . Although Whites And other Races Can Also develop Sickle Cell Disease , It Is Most Common In African Americans. 1.)http://www.nhlbi.nih.gov/health/healthtopics/topics/sca What Is the Most Common Genetic Disorder In The United States? Sickle Cell Anemia is a type of disorder that occurs when the sickle cell gene causes the body to create abnormal hemoglobin. How does the damage occur? Thank You For watching My Presentation! What Do They look Like? Jade Swink Yes, Sickle Cell Anemia can be a potentially curable disease in a few patients who can receive a hematopoietic stem cell transplantation from a adequate match donor. Parental diagnosis is Also Available . The Laboratory procedures employed in parental testing must be accompanied with genetic and physiological children with sickle cell disease (SCD). Are there different types of sickle cell disease?

Sickle Cell

Transcript: DelayedGrowth www.sciencedaily.com/articles/s/sickle-cell_disease.htm A: When I was very young. Bone Pain Heredity Non-Infectuious Disease Q: How long have you lived with sicklle cell? Treatments Refrences Penicillin Symptoms Q: What type of sickle cell do you have? Body systems affected Causes of Sickle Cell Interview Circultory System www.wrongdiagnosis.com/specialst Sickle cell 101 A: A long time. Painful Crisis Sickle cell leading to silent strokes in children www.nhlbi.nih.gov/health/dci/disease/sca Genetics Interviwer: Aaron Hart Latest Reasherch Q: At what age did you get sickle cell? A: I have the sickle cell trait. Person Interviewed: Momma

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