424- Thalassemia Natural Thalassemia Treatment

Thalassemia Treatment: Natural Thalassemia Remedy is effective against this inherited blood disease. Discover the composition of our natural thalassemia treatment. Indeed, thalassemia is a hereditary genetic disease and there is no serious remedy in the medical field. We have developed a natural thalassemia treatment that addresses blood diseases associated with thalassemia.

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Thalassemia Natural Remedy For Thalassemia

What is Thalassemia?

Thalassemias are genetic blood diseases that affect red blood cells. Indeed, they are characterized by a defect in the production of haemoglobin. This is manifested by a quantitative and qualitative decrease in red blood cells. In the most severe, there is chronic anaemia that can be fatal.

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Natural Remedy For Thalassemia

We have developed a natural treatment to treat thalassemia naturally with plants that help in the quantitative and qualitative production of red blood cells. Natural remedy for thalassemia cures a large number of alpha and beta-thalassemia

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Prevalence of Thalassemia

Thalassemia affects more people from countries around the Mediterranean, Southeast Asia, China, India and the Middle East.

Cause of Thalassemia

Thalassemia is a genetic blood disorder caused by a defect in the gene that controls haemoglobin production. The disease is an inherited form of anaemia that most commonly affects children of Mediterranean, African, and Asian descent. Thus, for a child to be affected by the pathology, each of his parents must transmit a diseased gene to him.

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Symptoms of ThalassemiAnaemia

Anaemia is the first manifestation of thalassemia without forgetting the other symptoms which are:

pallor and splenomegaly
bloating and intestinal discomfort
fatigue, fever, headache
growth and bone tissue disorders.
shortness of breath, heart murmur
increase in the size of the liver and spleen,
asthenia, weakness, exaggerated fatigability
tachycardia, palpitations
exertional dyspnea, polypnea
mucocutaneous pallor
dizziness or ringing in the ears

Prevention of Thalassemia

The disease being of genetic origin with a gene from both parents, prevention must be done upstream. This relies on genetic counselling when a diagnosis of thalassemia arises in a family. Gecounsellingseling consultations exist in all university hospitals as well as in some large general hospitals. There are several kinds of thalassemia

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Alpha or beta thalassemia?

Haemoglobin is made up of four protein chains: two alpha chains and two beta chains. Thalassemia is caused by an abnormality in one or more genes that code for the manufacture of these chains. We speak of alpha-thalassemia if an alpha chain is abnormal. When it comes to a beta chain, it is called beta-thalassemia

Beta-thalassemia

The most common and serious type of thalassemia (abnormal beta chain) is beta-thalassemia. It can be minor, intermediate or major depending on the number of genes affected. The major form is the most formidable. Also known as Cooley'sanaemiaa. It manifests as profound anaemia and often occurs between 6 and 24 months of age. In the intermediate form, the anaemia is less severe and appears later. The minor form, or Rietti-Greppi-Micheli disease, causes almost no symptoms. It is most often discovered incidentally. Beta-thalassemias are exceptional in the population of French origin, except in Corsica, where 3% of carriers are found.

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Alpha-thalassemia

The severity of alpha-thalassemia depends on the number of alpha genes carrying the disease: the minor form is most often mild, while the severe form results in the death of the child at birth or a few months later. In the case of alpha-thalassemia, the symptoms depend on the number of genes affected. If the woman is pregnant, the fetus may die. We sometimes note the isolated increase in the volume of the spleen with deep anaemia

Symptoms of thalassemia major

Beta-thalassemia major is manifested by profound anaemia from early childhood, discolouration of the skin, enlargement of the liver and spleen, an abnormally shaped skull and face, as well as impaired growth and bone tissue.

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Thalassemia and pregnancy

If you have thalassemia and your partner is a carrier of thalassemia traits, your baby is at risk of inheriting the disease. In addition, the stress associated with pregnancy aggravates the symptoms of thalassemia. This can lead to complications such as anaemia and stress on the heart. The pregnancy of a thalassemic woman is a high-risk pregnancy that must be closely monitored. The birth weight of the child may be lower than normal. Namely that genetic counselling centres allow you to be advised and accompanied in the face of certain genetic and/or hereditary diseases such as thalassemia, especially before considering pregnancy

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Diagnosis: blood test, electrophoresis, ultrasound

Diagnosis of thalassemia is made through a blood test. Thus, the complete blood count (NFS) makes it possible to evaluate the appearance and the number of red blood cells, and thus to know the total quantity of haemoglobin. Then, biochemical analyzes of haemoglobin can distinguish alpha-thalassemias from beta-thalassemias. Haemoglobin electrophoresis can identify the types of hehaemoglobinsresent and their distribution in the blood. Genetic analysis is also possible and often recommended. Abdominal ultrasound can assess the size of the liver and spleen

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Thalassemia Medical Treatment

The medical treatment of thalassemia is based on blood transfusion in severe cases. But punctual in the intermediate forms. Often, these transfusions are frequent in the major forms. Prescribing medication for elevated ferritin is helpful because iron overload is one of the complications of thalassemias. These treatments control the disease, but the only cure for thalassemia is bone marrow transplantation.

Correction of anaemia

When the lack of haemoglobin is too great, regular blood transfusions are necessary. They consist of injecting the person concerned with blood or red blood cells taken from a donor to maintain an acceptable level of red blood cells in the blood.

Vitamin B9 supplementation

It may be recommended to start a daily vitamin B9 supplementation because the need for this vitamin is increased in the case of thalassemia. Vitamin B9 is involved in the production of red blood cells.

Splenectomy

A splenectomy is the surgical removal of the spleen. This operation can be considered when the anaemia is very important

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Treatment of iron overload

People with thalassemia have an iron overload in their bodies. This accumulation can lead to different complications. This is why iron chelators are proposed to eliminate excess iron.

Bone marrow transplant

Bone marrow transplantation is the only treatment that can permanently cure thalassemia. This is a heavy treatment that is only offered in the most severe forms of the disease.

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Thalassemia Natural Treatment

We have a good remedy that eliminates anaemia and regulates iron in the body

Herbal Tea 424: Thalassemia Natural Thalassemia Treatment

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Treatment of Thalassemia: Natural Remedy Against Thalassemia effective against this hereditary blood disease.

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