Why is Ayurveda trusted to cure sickle cell Anaemia?

What is sickle cell anaemia?

Sickle cell anaemia or sickle cell disease is a genetic condition related to red blood cells. Normally, RBCs shape spherical, which allows them to travel across the smallest blood vessels. However, in sickle cell anaemia, these cells grow or shape like a sickle. This change in their shape makes them rigid and sticky and prone to get stuck in small vessels. This slow or block the blood flow and oxygen to parts of the body and eventually cause pain and damage the tissues.

Sickle cell anaemia is an autosomal recessive disorder. In order to be affected with SCA, one must have two copies of the gene to have the disease. In case a person has only one copy of the gene, it is called the sickle cell trait. However, ayurvedic medicine for sickle cell anaemia is recommended to the patients in order to normalise the shape and texture of red blood cells (RBCs).

It is assumed by medical science that there is no cure available for people with this disease. But ayurvedic treatment for sickle cells anaemia can help relieve pain and prevent morbidities associated with the disease.

What are the symptoms of sickle cell anaemia?

Signs and symptoms of sickle cell anaemia may appear around infancy after they have turned four months. While there are multiple types of sickle cell anaemia, they all have similar symptoms, which vary in severity among individuals. These include: –

• excessive fatigue due to anaemia (low RBCs)
• fussiness in babies
• bedwetting if kidney disease is also associated
• swelling and pain in hands and feet
• jaundice
• frequent infections
• pain in the chest, back, arms, or legs

When to see a doctor –

Sickle cell anaemia is diagnosed after a baby is born. If you or your new – born develops these symptoms, rush to your doctor for a sickle cell anaemia ayurvedic treatment to restore the normal working of red blood cells properly.

What are the major types of sickle cell anaemia?

There are four main types of sickle cell anaemia caused by different mutations in alpha and two beta chains. These genes are present in haemoglobin, a type of protein that carries oxygen.

1. Haemoglobin SS disease –

This is the most prevalent type of SCD. It develops when a baby inherits copies of the haemoglobin S gene from both parents. This forms haemoglobin known as Hb SS. As it is the severity of the four types of SCD, the complications may be experienced at a higher rate.

2. Haemoglobin SC disease –

It is the second most prevalent type of SCD. This type develops when you inherit the Hb C gene from one parent and the Hb S gene from another. The signs that appear with Hb SC are often similar to Hb SS.

3. Haemoglobin SB+ (beta) thalassemia –