Sickle-cell/Hb-C disease with crisis Save
ICD-10 code: D57.21
Chapter: Diseases of the blood and blood forming organs and certain disorders involving the immune mechanism
Sickle-cell/Hb-C Disease with Crisis
Sickle-cell/Hb-C disease with crisis is a genetic blood disorder that affects millions of people worldwide, mostly those of African descent. It is an inherited condition that causes abnormal hemoglobin molecules to form, leading to the sickling of red blood cells. This sickling can cause a range of health problems, including pain, organ damage, and a compromised immune system.
Those with sickle-cell/Hb-C disease have a combination of the sickle cell and Hb-C genes, which causes a milder form of sickle-cell disease. However, some people with this condition may still experience severe symptoms, known as sickle-cell crisis. During a crisis, the sickled red blood cells can block blood flow to various parts of the body, causing intense pain and increasing the risk of organ damage.
If you or someone you know has sickle-cell/Hb-C disease, it is essential to manage the condition carefully. This may involve regular check-ups with a healthcare provider, taking medication to prevent complications, and making lifestyle changes to reduce the risk of triggering a crisis. Some lifestyle changes that may help include staying hydrated, avoiding extreme temperatures, and getting enough rest.
It is also important to have a support network of friends, family, and healthcare professionals who understand the challenges of living with sickle-cell/Hb-C disease. They can provide emotional support, help with managing symptoms, and offer advice on how to live a healthy and fulfilling life with this condition.
- Regular check-ups with a healthcare provider.
- Taking medication to prevent complications.
- Making lifestyle changes to reduce the risk of triggering a crisis.
- Staying hydrated.
- Avoiding extreme temperatures.
- Getting enough rest.
Living with sickle-cell/Hb-C disease with crisis can be challenging, but with the right care and support, it is possible to manage the condition and live a full and active life. If you or someone you know has sickle-cell/Hb-C disease, speak to a healthcare provider for more information on how to manage the condition and reduce the risk of complications.