food that helps to fight against anemia


    Understanding sickle cell anemia

    Sickle cell anemia, also known as sickle cell anemia, is an inherited disorder of red blood cells (RBC). It is the result of a genetic mutation that causes deformed red blood cells. SCA gets its name from the crescent shape of red blood cells that resemble a farm tool called a sickle. Usually, red blood cells are shaped like discs. Red blood cells carry oxygen to organs and tissues in your body. It is more difficult for red blood cells to carry enough oxygen.

    Sickle cell disease can also get stuck in your blood vessels, obstructing blood flow to your organs. This can cause a painful condition called a sickle cell crisis. It can also contribute to the development of 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

    Organic African herbal tea for drepacytosis dawabio

    Telephone/whatsapp: +229 90 43 17 26

    Organ damage

    ACS causes the blood to have less oxygen, and it's usually not bad enough to cause organ damage. But if sickle cell disease gets stuck in a blood vessel and blocks blood flow to an organ, it can cause permanent damage to organs, including the kidneys, liver, and spleen.

    Although organ damage is not reversible, you can slow down the process if you catch it at an early stage. This is one of the reasons why regular check-ups are important for people with ACS.

    Acute thoracic syndrome

    Acute chest syndrome results from sickle cell anemia blocking the blood vessels that lead to your lungs.

    Its symptoms include:

    • cough
    • chest pain
    • difficulty in breathing

    If you have ACS and notice these symptoms, seek medical attention immediately. Acute chest syndrome can be fatal

    Hand-foot syndrome

    Hand-foot syndrome, sometimes called dactylitis, occurs when sickle cell patients block the blood vessels in the hands or feet. For some, this could be the first noticeable symptom of ACS.

    It is marked by painful swelling of the hands or feet. It can also cause fever in some people.

    Treatment for hand-foot syndrome usually involves a combination of drinking more fluids and pain medication.

    Stunted growth

    Red blood cells support the growth of your body by providing oxygen and other nutrients necessary for development. When they do not contain oxygen and nutrients due to SCA, it can lead to a slower growth rate in children and the onset of puberty later in adolescents. In men, it can also lead to infertility.

    Loss of vision

    Over time, the small blood vessels that supply blood to your eyes can become blocked with sickle cells, damaging your retina. Some people also develop additional blood vessels due to the reduction in oxygen. Both of these factors can contribute to vision loss.

    That's why doctors strongly recommend that people with ACS have annual eye exams.


    When your liver breaks down red blood cells, your body makes a substance called bilirubin. Sickle cells break down faster than typical red blood cells, resulting in an increase in bilirubin. Too much bilirubin can form gallstones in the gallbladder, a small organ that stores bile and helps digestion.

    Symptoms of gallstones include:

    • pain in the upper right part of the abdomen
    • pain in the center of your abdomen just below your breastbone
    • back pain between the shoulder blades
    • right shoulder pain
    • nausea and vomiting

    In some cases, gallstones can be dissolved with medication. In others, it may be necessary to remove them surgically.

    Splenic sequestration

    The spleen is an organ responsible for filtering the blood to remove cell waste, maintain fluid balance, and activate white blood cells for the immune system. Splenic sequestration occurs when the splenic vessels are blocked by a large number of sickle cell patients.

    Symptoms of splenic sequestration include:

    • pale lips
    • rapid breathing
    • extreme thirst
    • rapid heartbeat
    • sudden weakness
    • pain in the left abdomen

    Splenic sequestration requires immediate treatment, usually by blood transfusion. If this happens regularly, you may need to remove your spleen.


    The spleen also helps filter the blood and fight off potentially harmful bacteria. Sickle cell disease can damage the spleen, making you more vulnerable to infections, including the flu, pneumonia, and meningitis

    These types of infections can quickly become serious in people with ACS, so it's important to see a doctor if you have:

    • a fever
    • stiffness
    • cough
    • fatigue

    Leg ulcers

    Leg ulcers are open sores in the skin on your leg. People with ACS are more prone to developing them.

    Symptoms of a leg ulcer include:

    • swelling
    • the feeling of pain in the legs
    • the feeling of heaviness in the legs
    • irritated skin surrounding the open wound

    Leg ulcers are treated with compression bandages and topical ointments. In some cases, you may need an antibiotic to prevent or treat a wound infection.


    A blockage in one of the blood vessels in your brain can lead to a stroke. This is a serious condition that can have lasting consequences.

    Seek emergency treatment if you experience:

    • speech disorders
    • inability to raise an arm
    • falling to one side of the face
    • numbness, often on only one side of the body
    • difficulty walking or moving your arms
    • confusion
    • memory problems
    • difficulty speaking or understanding the spoken language
    • headache
    • loss of consciousness or coma

    Lifestyle changes to reduce the risk of complications

    ACS complications are not always preventable. But a few important lifestyle changes can lower your risk or decrease their severity.

    Get moderate exercise

    It is important for adults and children with ACS to exercise regularly.

    Experts recommend that people with ACS get a total of 150 minutes of moderate aerobic activity, such as biking or walking, per week. You might consider dividing this recommended total time into five 30-minute sessions per week.

    The CDC also suggests performing light strengthening activities, such as lifting weights, at least two days a week.

    While it is important to be active, try to avoid strenuous exercise or strenuous activity, as these can cause breathing difficulties.

    Eat balanced

    To help your body make more red blood cells, eat a diet rich in colorful fruits, vegetables, and whole grains. Try to limit your intake of refined sugars and fried foods.

    You can also consider taking a  supplement of  folic acid  . The bone marrow needs folic acid to make new red blood cells.

    Drink water

    You need to drink plenty of fluids throughout the day, especially in hot weather or during exercise. Dehydration increases your risk for a sickle cell crisis. Aim for 8 to 10 glasses of water each day. Plan to have a little more if the weather is hot or if you are going to be exercising more than usual.

    To manage stress

    Stress can also trigger a sickle cell crisis. While it is impossible to avoid all forms of stress, some stress management practices   include:

    • stay organized and plan your day
    • take the time to relax and rest
    • get enough sleep
    • breathing exercises
    • practice yoga or tai chi
    • write in a journal
    • talk to a friend
    • listen to music
    • take nature walks

    Try to keep an eye on how you feel throughout the day. This can help you identify the situations that stress you out so you can work on avoiding or reducing them.

    Be aware of temperature and altitude

    There is less oxygen in the air at higher altitudes. This lack of oxygen can trigger a seizure. If possible, you avoid traveling to high altitude areas.

    If you have SCA, you should also try to avoid sudden changes in temperature, like jumping into a pool or lake with cold water. When you go out, make sure you have dressed appropriately for the weather and remember to keep an extra layer on hand.

    Reduce your risk of infection

    Keep in mind that people with ACS may have a higher risk of infection. Therefore, it is important to take steps to reduce your exposure to viruses, bacteria, and fungi.

    Reduce your risks by:

    • washing your hands often, especially after using the toilet and before eating
    • avoiding contact with people who have an active infection and spending time in crowded environments
    • cook and store  food properly, especially  meat, to prevent food poisoning
    • making sure you are up to date on your vaccinations, including a  flu shot
    • take any antibiotics prescribed by your doctor
    • take extra precautions when traveling abroad, such as drinking bottled water or bringing antibiotics if your doctor recommends it
    • avoiding interactions with reptiles, including turtles, snakes, and lizards, as they can carry   harmful Salmonella bacteria 

    You should contact your doctor immediately if you think you have an infection. Early treatment can prevent a full-blown sickle cell crisis.

    Avoid smoking

    While smoking is bad for your overall health, it is very risky if you have ACS. It can increase the trusted source of your risk of acute chest syndrome, which can be fatal in some cases.

    It can also contribute to the development of:

    • a sickle cell crisis
    • leg ulcers
    • pneumonia

    Knowing when to see a doctor

    If you have ACS, it's important to see a doctor as soon as you think you might be having complications. The sooner you can treat the problem, the better your chances of preventing long-term problems.

    ACS complications can come on suddenly, so make sure you know who to call and where to go for medical treatment. Also consider sharing this information with your close friends and family.

    You should see a doctor immediately if you experience any of the following signs and symptoms:

    • fever above 101 ° F
    • unexplained and severe pain
    • dizziness
    • torticollis
    • difficulty in breathing
    • severe headache
    • pale skin or lips
    • a painful erection lasting more than four hours
    • weakness on one or both sides of the body
    • sudden vision changes
    • confusion or speech
    • sudden swelling of the abdomen, hands or feet
    • yellowing of the skin or whites of the eyes
    • capture

    Regular check-ups with a doctor are also essential to prevent serious problems. Babies with ACS should see a doctor every three months. Children 2 years of age and older, as well as adolescents and adults, should see their doctor at least once a year, even if they have no symptoms.

    The essential

    Sickle cell anemia can cause a whole range of complications, but there are several things you can do to reduce your risk of developing them. Make sure you see your doctor at least once a year so you can get a head start on treating any issues that arise.