My Sickled Cells.
My-Sickled-Cells.pdf
ISBN: 9781777881900 | 196 pages | 5 Mb
- My Sickled Cells
- Page: 196
- Format: pdf, ePub, fb2, mobi
- ISBN: 9781777881900
- Publisher: Revee Agyepong
Google google book downloader My Sickled Cells English version
Revée Agyepong was 12 years when she typed in the words Sickle Cell Disease into the google search bar. Her heart sank, jaw dropped and eyes swelled up with tears when she saw the life expectancy of 14 years flash across the screen. Over the years she experienced everything from crippling pain crises, pulmonary embolism scares, high powered blood transfusions and multiple surgeries. Feeling forgotten by God, she found herself hopeless and running out of options. Revée was amazed when she passed the age of 14; she truly had no idea that God had a bigger plan for her life. With the help of her sister, she pushed for an opportunity to be cured of sickle cell disease via stem cell transplant. With only a 14% chance to have a donor match in her family, Revée and her entire family were overjoyed when they found that her older sister was a 10/10 perfect match! She became one of the first adults in Western Canada to undergo a stem cell transplant to cure sickle cell disease. God blessed Revée with a second chance at life and this time she gets to do it sickle cell free! Despite her challenges, she didn't allow herself to give up. She became a fierce advocate for herself and others and continues to dedicate her life to paving the way for those that follow. Come along with Revée on this triumphant story of determination, grit and the power of God.
What is Sickle Cell Disease? | CDC
In someone who has SCD, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle”. The sickle cells die early,
Know Your Sickle Cell Trait | NCDHHS
All tissues within the body are at risk for damage because of the obstruction of blood flow. Common chronic complications of sickle cell disease include:.
Sickle Cell Disease in Children - Health Encyclopedia - URMC
Healthy red blood cells with normal hemoglobin are round and move easily through blood vessels. When a child has SCD, the red blood cells are hard and sticky.
Sickle Cell Crisis: Symptoms, Causes, Treatment, Prevention
The stuck cells slow or even totally block blood flow, so some parts of your body don't get the oxygen they need. That can cause intense pain
Home - Sickle Cell Disease Association of America Inc.
Official website of Sickle Cell Disease Association of America Inc. Sickle cell disease is an inherited blood disorder that affects red blood cells.
Frequently Asked Questions | Sickle Cell Anemia
Hemoglobinopathy is a term used to describe disorders caused by the presence of
Sickle Cell Trait - StatPearls - NCBI Bookshelf
This is in contrast to sickle cell disease (SCD), in which the affected individual has two abnormal hemoglobin beta gene alleles. Unlike
My Friend Has Sickle Cell Disease. How Can I Help? - Kids
The pain can last for a few hours, a few days, or sometimes longer. People with sickle cell disease have a low number of red blood cells, called anemia. This
Sickle cell anemia - Symptoms and causes - Mayo Clinic
So Your Baby Has The Sickle Cell Trait
As a carrier of this gene your baby has red blood cells that contain some sickle hemoglobin, but far less than the person with sickle cell
sickle cell anemia | Symptoms, Sickle Cell Trait, & Treatment
sickle cell anemia, hereditary disease that destroys red blood cells by causing them to take on a rigid “sickle” shape. The disease is characterized by many
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