What is sickle cell anemia?

The sickle cell anemia (FA), also called sickle cell disease is a blood disorder that makes your body makes an unusual form of hemoglobin called hemoglobin S.L'hémoglobine carries oxygen and is found in red blood cells (RBCs ).

Although red blood cells are usually round, hemoglobin S shapes them into a C shape, which makes them look 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 ACS have lower oxygen levels and fewer red blood cells. Both can cause a range of complications.

Fortunately, there are natural remedies that are much more effective. Indeed, certain medicinal plants allow to definitively cure the symptoms of sickle cell anemia. 

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: 00229 90 43 17 26

Is AF preventable?

Sickle cell anemia is a genetic disease that people are born with, which means there is no way to infect it. Still, you don't need to have FA for your child to have it.

If you have FA, it means you've inherited two sickle cell genes (one from your mother and one from your father). If you don't have AF but others in your family have it, you may have only inherited one sickle cell gene. This is called the sickle cell trait (TD). People with TD carry only one sickle cell gene.

Although TD doesn't cause any symptoms or health problems, it does increase the chances that your child will have AF. For example, if your partner has AF or TD, your child might inherit two sickle cell genes, causing AF.

But how do you know if you have a sickle cell gene? And what about your partner's genes? This is where blood tests and a genetic counselor come in.

How do I know if I carry the gene?

You can tell if you carry the gene for sickle cell disease from a simple blood test. A doctor will take a small amount of blood from a vein and test it in the lab. They will look for the presence of hemoglobin S, the unusual form of hemoglobin involved in AF.

If hemoglobin S is present, it means you have either AF or TD. To confirm which one you have, the doctor will follow up with another blood test called hemoglobin electrophoresis. This test separates the different types of hemoglobin from a small sample of your blood.

If they only see hemoglobin S, you have AF. But if they see both hemoglobin S and typical hemoglobin, you have TD.

If you have a family history of AF and plan to have children, this simple test can help you better understand your chances of passing the gene. The sickle cell gene is also more common in some populations.

According to the Centers for Disease Control, TD is the most common Trusted Source among African Americans. It is also found more often in people with ancestors of:

• Sub-Saharan Africa
• South America
• Central America
• the Caribbean
• Saudi Arabia
• Mediterranean countries, such as Italy, Greece and Turkey

If you are unsure of your family history but think you might belong to one of these groups, consider getting a blood test just to be sure.

Is there a way to make sure I don't pass on the gene?

Genetics is a complex subject. Even if you and your partner are tested and both carry the gene, what does this actually mean for your future children? Is it always safe to have children? Should you consider other options, such as adoption?

A genetic counselor can help you navigate both your blood test results and the questions that will arise afterward. By looking at the test results of you and your partner, they can give you more specific information about your child's chances of having TD or FA.

Finding out that any future child with your partner might have AF can also be difficult to deal with. Genetic counselors can help you navigate these emotions and consider all of the options available to you.

The essential

AF is an inherited disease, which makes it difficult to prevent. But if you're worried about having a child with AF, there are a few steps you can take to make sure they don't have AF. Remember that children inherit genes from both partners, so make sure your partner follows these steps as well.

For more information, please contact our experts at:

Telephone/whatsapp: 00229 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 is also broken 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 of 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 main drug against sickle cell disease.
To discover our  natural treatment for sickle cell anemia,  click on the image below

Telephone/whatsapp: 00229 90 43 17 26

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 some 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 a disease who died within a certain time frame. For example, one study mentions that a disease has a 5% death rate 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 fallen 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.

Do people with sickle cell anemia 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 of 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 probably due to the lack of access to quality health care among adults with FA.

What affects a person's prognosis?

Many things play a role in determining the lifespan of a person with AF. But experts have identified a few concrete factors, especially in children, that may contribute to a less favorable prognosis:

• having the hand-foot syndrome, which is painful swelling in the hands and feet, before the age of 1

• having a hemoglobin level of less than 7 grams per deciliter

• have a high white blood cell count with no underlying infection

Access to nearby and affordable health care can also play a role. Regular follow-up with a doctor can identify complications that may require treatment or symptoms. But if you live in a rural area or don't have health insurance, that's easier said than done.

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 or older.

FA can also cause a  stroke if the sickle cells block a blood vessel in the brain. You can get a better idea of ​​your child's risk by having them do 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 reveals 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 FA 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 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 decades.

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

What is sickle cell anemia?

The  sickle cell anemia  is an inherited blood disease. It can cause a series of serious complications such as anemia, respiratory failure, but also very painful attacks that occur in different parts of the body.
Those most affected by sickle cell disease are people of African or Middle Eastern descent, as well as South and Central America.
The  symptoms of sickle cell anemia  include periods of intense pain, rapid heart rate, yellowing of the skin, jaundice, vision problems, skin ulcers, confusion, urinary tract infections, bone lung and / or gallbladder biliary and others.
Sickle cell disease is difficult to treat. Conventional medicine is generally aimed at managing and controlling symptoms, often with hydroxycarbamide, as well as pain relievers. Hydroxycarbamide inhibits DNA replication, which can slow down sickle cell production and worsen symptoms of sickle cell disease.
These drugs also cause a number of unwanted and toxic side effects, including toxicity to the bone marrow, liver, nausea, vomiting, diarrhea, constipation, mucositis, hair loss, blood problems. blood urea and creatinine.
Fortunately, there are natural remedies that are much more effective. Indeed, certain medicinal plants allow to cure definitively the symptoms of sickle cell disease. Here are the 6 best natural remedies for sickle cell disease:
 
1- African herbal medicine

If you are looking for a natural way to cure sickle cell disease, 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 main drug against sickle cell disease.
To discover our natural treatment for sickle cell anemia ,  click on the image below
 

Telephone / whatsapp: 00229 90 43 17 26    

2- Cajanus cajan

The Cajanus cajan, Pois d'angole in French, is a shrub 3 meters high, growing in tropical or subtropical regions around the world. The leaves and seeds do not have the same chemical composition, with different indications as a result. The leaf contains tannins and sterols. The seed, carbohydrates (the main constituent), proteins rich in amino acids such as phenylalanine, lipids, phenolic acids and some vitamins.
The leaves have no activity in sickle cell disease, they are antibacterial. These are the seeds that have anti-sickle cell activity, reducing the level of sickle red blood cells. Cajaminosis prolongs the time it takes for red blood cells to sickle.

3- Fagara zanthoxyloids

Zanthozyloid Fagara is commonly called the Fagarier. The Fagarier is a tree which is found in Senegal, in Benin as well as in Cameroon. It is one of the components of VK 500, a medicine for sickle cell anemia. One gram of powder from the root of this plant drunk by a very sick sickle cell patient three times a day makes seizures completely disappear. Fagara prevents hemolysis of red blood cells. The active ingredients responsible for the antidepanocytic action are acids, the main one being hydroxymethyl-benzoic acid and also zanthoxylol. How do you use fagara against sickle cell disease?
-Mix the fagara and calotropis powders in equal quantity
-Take a teaspoon of the mixture, mixed in a glass of hot water
-drink 3 times a day (morning, noon and evening).
 
4- Calotropis procera

Calotropis procera, also called "Apple tree of Sodom", grows in desert and even semi-desert areas of the coastal regions of the Red Sea and the Indian Ocean, on soils which can be considered as degraded, always close to dry streams. They are also found in Morocco, especially between Rissani and Agdz. In Morocco, it is called the satan tree. To use it against sickle cell disease, it must be mixed with Fagara (see above)
 
5-  Moringa Oleifera

A small tree that can measure up to 10 to 12 m, the moringa is a very fast growing tree (2.5 m after three months) which requires very little water. Moringa leaves are very effective in relieving sickle cell disease.
Infuse the leaves and drink like tea several times a day, or take the powder a spoonful twice a day cold or hot in the meal or other drinks work very effectively
 
6-  Sugar cane

Mixing sugar cane with the white and red flowers of Mesembryanthemum is very effective against sickle cell disease.
Ingredients:
-Sugar cane
-The white and red flowers of Mesembryanthemum (still called bonjour
bonoir ) -Plain water
Preparation:
-Cut the sugar cane into pieces and add the two red and white flowers that you rinse properly.
-Make the infusion with plain water for 07 minutes.
Take this herbal tea with a beer glass morning and evening for two good weeks.

For more information, please contact us at:

Telephone / whatsapp: 00229 90 43 17 26