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Sickle Cell Powerpoint Template

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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. 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

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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.) Title: sickle cell anemia prognosis health information The End! 3.) Title:Sickle Cell Anemia Websites! SICKLE CELL ANEMIA Is Sickle Cell Anemia A Curable Disease? Another Definition! 4.) "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.) 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?

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