Herbal Tea 424: Thalassemia Natural Remedy For Thalassemia
Thalassemia Treatment: Natural Thalassemia Treatment effective against this hereditary 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 Treatment
Natural Thalassemia Treatment effective against this hereditary 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.
Click here to Contact us about Natural Thalassemia Treatment
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Thalassemia Natural Thalassemia Treatment
What is Thalassemia?
Thalassemias are genetic blood diseases that affect red blood cells. Indeed, they are characterized by a defect in the production of hemoglobin. This is manifested by a quantitative and qualitative decrease in red blood cells. In the most severe, there is a chronic anemia that can be fatal.
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Natural Thalassemia Treatment
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
Click here to Contact us about Natural Thalassemia Treatment
Prevalence of Thalassemia
Thalassemia affects more people from countries around the Mediterranean, Southeast Asia, China, India and the Middle East.
Causes of Thalassemia
Thalassemia is a genetic blood disorder caused by a defect in the gene that controls hemoglobin production. The disease is an inherited form of anemia 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 Thalassemia
Anemia 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 counseling when a diagnosis of thalassemia arises in a family. Genetic counseling 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?
Hemoglobin 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's anemia. It manifests as profound anemia and often occurs between 6 and 24 months of age. In the intermediate form, the anemia 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.
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 anemia
Symptoms of thalassemia major
Beta-thalassemia major is manifested by profound anemia from early childhood, discoloration of the skin, enlargement of the liver and spleen, an abnormally shaped skull and face, as well as impaired growth and bone tissue.
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 anemia 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 counseling centers allow you to be advised and accompanied in the face of certain genetic and/or hereditary diseases such as thalassemia, especially before considering pregnancy
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 hemoglobin. Next, biochemical analyzes of hemoglobin can distinguish alpha-thalassemias from beta-thalassemias. A hemoglobin electrophoresis can identify the types of hemoglobins present 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
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 anemia
When the lack of hemoglobin 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 needs for this vitamin are increased in case of thalassemia. Vitamin B9 is involved in the production of red blood cells.
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 anemia
Symptoms of thalassemia major
Beta-thalassemia major is manifested by profound anemia from early childhood, discoloration of the skin, enlargement of the liver and spleen, an abnormally shaped skull and face, as well as impaired growth and bone tissue.
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 anemia 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 counseling centers allow you to be advised and accompanied in the face of certain genetic and/or hereditary diseases such as thalassemia, especially before considering pregnancy
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 hemoglobin. Next, biochemical analyzes of hemoglobin can distinguish alpha-thalassemias from beta-thalassemias. A hemoglobin electrophoresis can identify the types of hemoglobins present 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
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 anemia
When the lack of hemoglobin 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 needs for this vitamin are increased in case of thalassemia. Vitamin B9 is involved in the production of red blood cells.
Please reach us at http://wa.me//+22967546677
Click below to order clove oil
Book an appointment with lady feranmi on
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