Sickle cell disease (SCD) is a complex group of inherited blood disorders associated with debilitating pain and complications that can affect every organ in the body.
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What Causes SCD?
SCD is a genetic disorder that is passed down from parent to child. It is caused by a defect in a gene.
How is SCD Diagnosed?
A Blood test is used to diagnose SCD. In the US, this blood test is part of a newborn screening program. Click here to learn more.
What are the complications associated with SCD?
Pain episodes, infection, hand-foot-syndrome, eye disease, Acute Chest Syndrome (ACS), and stroke are some of the most common complications of SCD.
How can SCD complications be prevented?
- Stay up-to-date on vaccines to prevent infections
- Annual eye checkup
- Regular health checkup
- Management of pain episodes
Lifestyle Behaviors to Prevent Pain Episodes
- Drink plenty of water
- Do not get too hot or too cold
- Avoid high altitude
- Proper and frequent hand washing
- Safe food preparation and handling
- Manage stress