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Q&A Sickle Cell Disease Podcast by Leading Pediatric Hematologist, Amber M. Yates, MD

Sickle Cell Disease is an abnormality caused in haemoglobin, a protein in our red blood cells which carries oxygen throughout the body. Those who suffer from this rare disease are more likely to experience deformed blood cells that are sickle-shaped, and an overall lower quantity of red blood cells which can result in blockages of blood circulation and lack of oxygen.

The most common complication of this disease is pain which is likely to occur any time without warning. The pain is caused when less blood is circulated to the bones, and other significant complications may include acute chest pain, kidney problems, and strokes.

In this modern healthcare podcast on Sickle Cell Disease, (SCD), we are going to elaborate on the treatment to monitor or manage sickle cell disease. Whereas healthy red blood cells last 90 to 120 days, red blood cells affected by Sickle Cell Disease last only 10 to 15 days and often result in complications such as anaemia, poor health, and a shortage of breath. Although he healthcare complications are certainly challenging, there are several options available for treatment. Many leading doctors specializing in SCD recommend customized treatment, such as regular blood medication for pain, blood transfusions, and even a bone marrow transplant.

How should one proceed? Diagnosing Sickle Cell disease can be difficult because it requires proper screening, and the lack of effective programs for early detection places a significant burden on children and parents at a later stage in life.

Hence, it becomes imperative to know all the facts about SCD so that you may proceed with deep understanding and with proper guidance. To know exactly what Sickle Cell disease is and what, as a parent, you can do for its prevention, do stop by at https://gethealthy360.com/amber-m-yates-md-pediatric-hematologist-sickle-cell-disease-podcast. The Sickle Cell disease podcast uncovers prudent insights by Dr Yates, the co-director of the Sickle Cell Center at the Texas Children’s hospital in Houston, who answers the most common questions on SCD.

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