- dandelion tea for sickle cell anemia
dandelion tea for sickle cell anemia
3 plants against sickle cell disease
Sickle cell anemia is a type of inherited anemia. The basis of the disease is an abnormal hereditary point mutation which develops on chromosome 11. Among the hereditary hemoglobinopathies where the hemoglobin molecule is abnormal, it is the most common disease.
African herbal remedy for sickle cell disease
The treatment we offer you to cure sickle cell anemia consists mainly of natural herbal teas.
Herbal tea is a natural remedy made from plants. The active principles are prevented the appearance of painful crises in children 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.
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Infusions and decoctions for the treatment of sickle cell anemia
For the treatment of sickle cell anemia, herbal preparations and one-component decoctions of medicinal plants are used
Medicinal dandelion roots and leaves (6 g) pour 200 ml of water and boil for 10 minutes.
After half an hour of infusion, you can take 1 tablespoon three times a day before meals.
Birch leaves and nettle
Mix birch and nettle leaves in equal proportions. In 1.5 cups of boiling water, steep 2 tbsp. mixture and insist for an hour.
After straining, mix with half a glass of freshly squeezed beet juice. Drink the composition in a day in 2-3 doses before meals. The duration of taking the drug is 2 months.
Mix in equal proportions the inflorescences of yarrow, medicinal dandelion root and dioecious nettle leaves. In 1.5 cups of boiling water, steep 1 tsp. mix and insist for 3 hours. Drink in a day in small portions (3-4 doses half an hour before meals). Treatment with a decoction lasts from 1.5 to 2 months.
Pour peeled garlic cloves (300 g) into a half-liter bottle and fill it with medical alcohol. Insist for 3 weeks. Add 20 drops of the product to half a glass of milk. Take three times a day.
How is the disease diagnosed?
The medical history of the patient and his family may already raise suspicion. Symptoms may be characteristic of other conditions associated with anemia or hemolysis, but if both are present, there should also be a suspicion of sickle cell anemia.
After a thorough examination and physical examination of the patient, a routine blood sample in the laboratory confirms anemia and hemolysis. Special laboratory processing of the blood sample taken from the patient (hemoglobin electrophoresis) accurately confirms the presence of HbS and the disease itself. Imaging exams, mainly abdominal ultrasounds, show an enlarged spleen or liver, possible infarction. Any complaint may require imaging of this organ.
Under the microscope (after proper preparation) red blood cells take on the characteristic sickle cell form from which the disease is named.
Living well with sickle cell anemia
People with sickle cell disease can live fully and enjoy most of the activities others do. The following tips will help you, good health.
- Seek good medical attention
Sickle cell disease is a complex disease. Good quality medical care from doctors and nurses who know a lot about this disease can help prevent some serious problems. Often the best option is to see a hematologist (a doctor who specializes in blood diseases) who works with a team of specialists.
- Get regular checks
Regular check-ups with a primary care physician can help prevent some serious problems.
Babies from birth to one year old should be seen by a doctor every 2 to 3 months.
Children 1 to 2 years old should see their doctor at least every 3 months.
Adults and children 2 years of age and older should see the doctor at least once a year.