Sickle cell anemia is caused by mutations in genes inherited from both parents (must be both) or called autosomal recessives. In children who inherit the genetic mutation from only one parent, they will be carriers of sickle cell anemia and will not have any symptoms. Genetic mutations that occur in people with anemia cause various disorders in the body. This happens because of the production of red blood cells in an abnormal shape.

How can it be diagnosed?

The diagnosis of sickle cell disease is made by examining the Hb test for the presence of hemoglobin S or defective hemoglobin that causes sickle cell anemia. To determine the severity of the anemia, the amount of normal hemoglobin will also be checked, so that it can be referred to other tests to see possible complications. While sampling amniotic water to look for the presence of sickle cell genes, can be done to diagnose sickle cell anemia in the fetus from the womb.

What is Anemia?

Anemia is a complex of signs found as a result of clinical symptoms and laboratory blood tests. The disease is characterized by a decrease in the level of red blood cells and hemoglobin per unit volume of blood. The anemic syndrome can manifest as a separate disease or accompany some diseases.

Icb code 10 D50-D89: blood diseases, hematopoietic organs, and certain disorders involving the immune mechanism.

According to generally accepted criteria, anemia in men is indicated by:

• hemoglobin reduction of 130 g / l;
• erythrocyte level is less than 4 * 1012 / l;
• hematocrit is below 39%.

In women, these indicators are as follows:

• hemoglobin below 120 g / l;
• erythrocytes less than 3.8 * 1012 g / l;
• hematocrit - 36% and below.

A separate group includes pregnant women in whom a decrease in hemoglobin below 110 g / l and a hematocrit of less than 33% is considered abnormal.

Natural Herbal Treatment

If you are looking for a natural way to cure sickle cell anemia, then this natural treatment is for you. Here is the world's best natural remedy for sickle cell disease. Herbal tea is a natural remedy made from medicinal plants. The active ingredients it contains prevent the onset of painful attacks in children as well as in adults. Thus, it works by reducing the number of red blood cells deformed by sickle cell disease and by promoting the production of new normal red blood cells.
It also straightens red blood cells that are deformed by disease and prevents them from blocking small blood vessels and causing severe pain. This will allow you to regain normal blood circulation. This herbal tea is a very effective remedy and has already helped many patients prevent their sickle cell attacks. Its success far exceeds that of the leading drug against sickle cell disease.
To discover our natural treatment for sickle cell anemia, click on the image below

Sickle cell anemia and moringa

Moringa leaves can help the body absorb more iron, thereby increasing the number of red blood cells in the body. Moringa leaf extract is considered to be very useful in the treatment and prevention of anemia and sickle cell disease  (SCD) or also called sickle cell disease.

How do you use moringa?

While there is no fully scientifically proven dose yet, some studies suggest that intake can reach up to 400 mg per day to provide all of the benefits mentioned above.

Moringa tea is the most widely used form of consumption because it is quick and easy to prepare and can be consumed at any time of the day.

Ingredients

• 250 ml of water;
• 10 g (1 tbsp.) Moringa leaves.

Method of preparation

Place the water in a saucepan over medium heat until it boils, add 1 tablespoon of moringa leaves, cover and let stand for 5 minutes. Filter and drink 2 cups of tea per day. 

The health benefits of moringa

Moringa has various properties that could provide health benefits. According to some studies, it could be used for:  

• Increase respiratory capacity,   helping to fight diseases such as asthma;
• Prevents diabetes  because it has properties that help regulate oxidative stress, which reduces blood sugar levels, improving protection against cell damage; 
• Protect the heart,  avoiding the absorption of cholesterol in the intestine and the formation of fatty plaques in the arteries, thus reducing the risk of cardiovascular disease; 
• Regulates blood pressure,  as it improves blood circulation due to its vasodilator effect; 
• Helps in weight loss   by containing fiber and a large amount of protein that helps increase the feeling of fullness;
• Prevent and fight anemia,  because its leaves contain a large amount of iron (105 mg per 100 g), promoting the increase of red blood cells;
• Increases the body's defenses  because it contains antioxidant substances such as polyphenols, vitamin C and beta-carotene which stimulate the immune system;
• It has an anti-inflammatory and analgesic effect  because it contains isothiocyanates, quercetin, and chlorogenic acid,   which are substances that help to slow down the inflammatory process, which can alleviate the symptoms of diseases such as rheumatism, osteoarthritis or inflammation of the prostate, for example;
• Protects and moisturizes the skin,  as it contains vitamins B1, B2, B3, B6, C, E, and A, promoting healing of the skin;
•   Improves the health of the digestive system by  preventing or treating stomach ulcers and helping to fight constipation due to its high fiber content;
• Helps to treat hemorrhoids, as it improves blood circulation, causing vasodilator effect;
• Improve vision  thanks to its high content of beta-carotene, which is a precursor of vitamin A;
• Helps decrease the effects of menopause as it helps maintain levels of inflammation and oxidative stress during this stage, promoting a natural balance of hormones that are affected during this phase.

For more information contact our expert on Telephone/whatsapp: +229 90 43 17 26

What is sickle cell anemia?

Sickle cell anemia (FA), sometimes called sickle cell anemia, is a blood disorder that causes your body to make an unusual form of hemoglobin called hemoglobin S. Hemoglobin carries oxygen. It is found in red blood cells.

While red blood cells are usually round, hemoglobin S makes them C-shaped, like a sickle. This shape makes them more rigid, preventing them from bending and flexing as they move through your blood vessels. As a result, they can get stuck and block the flow of blood through the blood vessels. It can cause a lot of pain and have long-lasting effects on your organs.

Hemoglobin S also breaks down faster and cannot carry as much oxygen as typical hemoglobin. This means that people with AF have lower oxygen levels and fewer red blood cells. Both can cause a range of complications.

What does all this mean in terms of survival rate and life expectancy? AF is linked to a shorter lifespan. But the prognosis for people with AF has become more positive over time, especially over the past 20 years.

Natural herbal treatment

If you are looking for a natural way to cure sickle cell anemia, then this natural treatment is for you. Here is the world's best natural remedy for sickle cell disease. Herbal tea is a natural remedy made from medicinal plants. The active ingredients it contains prevent the onset of painful crises in children as well as in adults. Thus, it works by reducing the number of red blood cells deformed by sickle cell disease and by promoting the production of new normal red blood cells.
In addition, it straightens red blood cells deformed by disease and prevents them from blocking small blood vessels and causing severe pain. This will allow you to regain normal blood circulation. This herbal tea is a very effective remedy and has already enabled many patients to prevent their sickle cell attacks. Its success far exceeds that of the leading drug against sickle cell disease.
To discover our  natural treatment for sickle cell anemia,  click on the image below 

Telephone/whatsapp: +229 90 43 17 26

Do people with sickle cell disease have shorter lives?

Although advances in medicine and technology have reduced the death rate from ACS in children, the condition is still linked to a shorter lifespan in adults.

One study looked at over 16,000 AF-related deaths between 1979 and 2005. Investigators found that the average life expectancy for women with AF was 42 years and 38 years for men.

This study also notes that the fatality rate from AF in adults did not decrease the way it did for children. Investigators suggest that this is likely due to the lack of access to quality health care among adults with FA.

What is the survival rate for sickle cell anemia?

When discussing a person's prognosis or outlook, researchers often use the terms survival rate and death rate. Although they look similar, they measure different things:

• Survival rate refers to the percentage of people who live for a period of time after receiving a diagnosis or treatment. Think about a study of new cancer treatment. The five-year survival rate would show how many people were alive five years after starting study treatment.
• Death rate refers to the percentage of people with an illness who died within a certain time frame. For example, one study mentions that a disease has a death rate of 5% for people aged 19 to 35. This means that 5% of people in this age group with this disease die from it.

When talking about the prognosis for people with AF, experts tend to look at death rates.

AF's death rate for children has dropped dramatically over the past few decades. A 2010 review refers to a 1975 study showing a 9.3% death rate for people with FA under 23. But in 1989, the death rate for people with FA under the age of 20 fell to 2.6%.

One compared the death rates of children with AF from 1983 to 1986 to death rates in the same group from 1999 to 2002. She found the following declines in death rates:

• 68% for 0 to 3 years old
• 39% for 4 to 9-year-olds
• 24% for 10 to 14-year-olds

Researchers believe that a new pneumonia vaccine released in 2000 played an important role in reducing the death rate in children aged 0 to 3. FA can make people more vulnerable to serious infections, including pneumonia.

What can I do to improve my prognosis?

Whether you are the parent of a child with AF or an adult living with the disease, there are several things you can do to reduce the risk of complications. This can have a big impact on prognosis.

Tips for children

One of the easiest ways to improve the prognosis of a child with FA is to focus on reducing their risk of infection. Here are a few tips:

• Ask your child's doctor if they need to take a daily dose of penicillin to prevent certain infections. When asking the question, be sure to tell them about any infections or illnesses your child has had in the past. 
• Keep them up to date on vaccinations, especially for pneumonia and meningitis.
• Follow up with an annual influenza vaccine for children 6 months of age or older.

FA can also lead to stroke if sickle cells block a blood vessel in the brain. You can get a better idea of ​​your child's risk by having them have a transcranial Doppler ultrasound every year between the ages of  2 and 16. This test will determine if they have an increased risk of stroke.

If the test shows it, their doctor may recommend frequent blood transfusions to help reduce the risk.

People with AF are also prone to vision problems, but these are often easier to treat when caught early. Children with AF should have an annual eye exam to check for any problems.

Tips for adults

If you are an adult with AF, focus on preventing episodes of severe pain, known as a sickle cell crisis. It happens when abnormal red blood cells block small blood vessels in the joints, chest, abdomen, and bones. It can be very painful and damage organs.

To reduce the risk of sickle cell anemia:

• Stay hydrated.
• Avoid strenuous exercises.
• Avoid high altitudes.
• Wear lots of layers in cold weather.

You can also ask your doctor to take hydroxyurea. It is a chemotherapy drug that can help reduce sickle cell attacks.

The essential

People with AF tend to have a shorter life expectancy than those without the condition. But the overall prognosis for people, especially children, with AF has improved over the past few decades.

Regular follow-up with a doctor and awareness of any new or unusual symptoms is essential to avoid potential complications that could affect your prognosis.

For more information contact our expert on Telephone/whatsapp: +229 90 43 17 26