Sickle cell disease is an inherited disorder that is caused by a mutation in the DNA sequences that codes for the beta chain of the hemoglobin protein. Red blood cells are, normally, flexible and round, but with the sickle cell anemia the red blood cells become sticky, rigid, and crescent shaped. The Hemoglobin protein carries oxygen in the red blood cells throughout the body. With the disease, the blood cell’s shape can cause them to get lodged in the blood vessels resulting in the obstruction of blood flow, especially in the smaller arterial vessels in the body This occurrence not only reduces oxygen content to the area of concern, but can be a very painful experience for the victim. People who inherit this disease have two abnormal hemoglobin…
I am in support of the “Sickle Cell Disease Research, Surveillance, Prevention, and Treatment Act of 2015.” Sickle Cell is a serious blood disorder that causes red blood cells to become misshaped. These abnormally shaped red blood cells can get clustered into blood vessels and block blood flow to areas of the body. According to the center of disease and control the number of people with sickle cell in the united states is unknown, but it is prevalent amongst African-Americans occurring in 1 out of 365 births.…
Pain crisis is the primary symptom of SCD; it is caused by sticky, sickle cells forming blood clots resulting in ischemia. Acute chest syndrome is a potentially life-threatening complication that occurs when blood clots collect in the small blood vessels that supply the lungs. Symptoms include fever, chest pain, dyspnea, chills, and hemoptysis. Pulmonary infiltrates are common as well as pulmonary hypertension, and the majority of patients are hypoxemic (Paul, Castro, Aggarwal, & Oneal, 2011). Splenic sequestration is another common complication; rising when the sickle cells become clogged and are trapped in the spleen causing rapid splenomegaly and pain (National Heart, Lung and Blood Institute, 2015).…
To prevent sudden painful attacks and a trip to the ER from the blockage, a person with Sickle Cell drink a lot of water, try to keep at a moderate temperature, avoid high altitudes and low oxygen levels. Adults that experience these sudden attacks can take medicine to stop or prevent them. Infection, which children with the disease often experience more of, can be prevented by washing your hands as you should anyways, but vaccines can also prevent…
Identify one intervention that can be taken by the RN to reduce the stigma and improve management of acute and chronic pain associated with Sickle Cell Disease, (SCD). One intervention that comes to my mind after reading the articles would be recognizing the cues to an acute pain episode and responding appropriately and in a timely manner (Jenerette & Ataga, 2014). By doing so, it could help manage the chronic pain associated with sickle cell disease. Patients with SCD are often stigmatized as addicted to opioids, disbelieved or mistrusted regarding reports of pain and not being allowed to participate in their own health care (Jenerette & Ataga, 2014).…
Barbie dolls with distorted arms, cheap bedazzled jewelry, cherry-flavored chap stick or stolen makeup from Mom: things you can find in a little girl’s drawer. But not mine. My drawer consisted of test strips, alcohol pads, syringes and lancets. At the age of eight, I was diagnosed with type 1 diabetes. Given this news, I felt isolated and my future became a blur.…
In many family households the main provider for the family would often be the male, but in my family there was a different circumstance. Because my dad got kidney stones and when the time he had found out he had kidney stone it was too late for any treatment and was immediately given the choice of a kidney transplant. Which cause a lot of money and also there are risks of not succeeding in the surgery. As my dad's name on the long waiting list of needing a kidney transplant, he had to take medicine prescribed by the doctor, but also go to the hospital once a week to get kidney treatment so the condition would not get worse. As my dad staying at home all the time and going to the hospital once a week to get his treatment, my mom would keep going…
I still remember my Junior year like it was yesterday. I was so blind to how the real world worked. I was stuck in a fantasy. One day I was diagnosed with a life changing disease. A couple of days later I lost all my friends.…
How did Sickle Cell made an impact on my life, Sickle Cell made and big impact on me in different ways it taught me to be true to myself that i shouldn 't care what others think about me i was made to be like this and I have to accept that this is who I am, this is me. My whole life I have always put this on God, always asking “why me” “why pick me”. I really didn 't think about it until I got older that God is’t the problem nothing is the promise that if I want to fight this I have to accept that this is who I am and nothing can change that, I never had a good life when I was a little kid always getting bullied and it never stoop that no will understand me or that no one will accept me. But who care that no one will accept me, if I believe…
A sickle cell client who was admitted was placed on a Patient Controlled Analgesic (PCA) pump. The suspected that the client had tampered with the pump and had received more medication than was ordered by the physician. The tampering could lead to an opioid overdose and would have legal ramification for the hospital. Once it was determined that the patient was tampering with the pump, it was removed and sent to engineering for analysis. The client was in need of pain management and oral medications were not strong enough to cover his pain.…
Everyday is meaningful for me not only meaningful but lucky that I’m living and chasing dreams because of one person my mom who saved my life by giving me a kidney at the age of three. I was born with kidney failure I so small for age and for some reason I never ate so the kidney transplant team put a G-tube or gastrostomy tube in me it was another way so I get all the needs to grow without eating food. Then the kidney transplant team told my mom why I was so sick and that i needed a kidney transplant so mom took the offer to give her kidney to me and mine went to my mom the transplant went very well I went to school but as a weak kid I got sick alot so I was in and out of the hospital because of my weak immune system. But there was a good and bad thing about being in the hospital…
Growing up, my heath has always been a factor that would I consider, it could either break me or make me. I was born with Sickle Cell Disease, and over the years it has been tough for me to keep up with my social and academic life. I have to always worry about taking my medications, staying fit and hydrated in order to avoid a crisis. My mother also has Sickle Cell Disease, and when I was born she passes it down to brother and I. During middle school and high school my parents were very active in making sure I got the right medical attention that I needed.…
Sickle cell anemia is a genetic blood disorder that causes normal red blood cells to form into an irregular shape, called sickled-cells. The sickle cell gene causes the body to produce abnormal hemoglobin. After a while, the hemoglobin will then cluster together anywhere in the body causing the blockage of blood flow through the blood vessels. This blockage deprives the tissues and blood of oxygen which can lead to many difficulties and problems. SCD becomes life-threatening when the damaged red blood cells begin to breakdown, when the spleen does not work properly or at all, or when it is unable to prevent infections from coming in.…
The first thought I had when I was retrieving the wheelchair, for my turn, was that it was heavy and extremely awkward to carry. The pedals were carried separate and it didn’t collapse very well. It took a lot of work to get it into the back seat of my car. My friend pulling from one side of the car and I shoving it in from the other side. I had played around in a wheelchair before.…
My Fathers illness has equally effected all of my siblings and I significantly. It is most difficult hearing stories from my family members about my father before he became ill and depressed. He was often considered the center of each conversation. It is difficult to type these words about my father considering that the last time my father and I have shared a laugh is beyond my memory. My mom always tells me that I am very similar to my father in terms of his stubbornness and positivity.…