Description
Thalassemia is one of the most challenging form of
hematological disorders. Ninety percent of the children develop
symptoms of anemia in the first two years of birth, requiring blood
transfusions for rest of their lives.
About **0,**0 babies worldwide are born with severe forms of
the disease each year. Thalassemia occurs most frequently in people
of Italian, Greek, Middle Eastern, South Asian (Indian
Sub-continent) and African ancestry.
Approximately **0,**0 children born with Thalassaemia in the
world, among them about *0,**0 cases are in India. In certain
Indian population like Assamese, Bengali, Gujarati, Maharashtrian,
Marwari and Punjabi, as high as *5% of the population are silent
carriers of a defective Thalassaemia gene, while mildly anemic are
not otherwise affected by the illness. In Gujarat itself
Thalassaemia is very common in some castes like Bhanushalis,
Lohana, Sindhi, Meman, Khoja, Jain and Brahmin.
Thalassemia is also known as Mediterranean anemia or Cooley's
anemia is a genetic blood disease. People born with this disease
cannot make normal hemoglobin, which is needed to produce healthy
red blood cells.
The two main types of thalassemia, alpha and beta, are named
for the two protein chains that make up normal hemoglobin. The
genes for each type of thalassemia are passed from parents to their
children. There are mild and severe forms of the disease, the
latter often called Cooley's anemia.
ALPHA THALASSEMIA:
Alpha thalassemia occurs when one or more of the four genes
needed for making the alpha globin chain of hemoglobin are variant
or missing. Moderate to severe anemia results when more than two
genes are affected. Alpha thalassemia major can result in
miscarriages.
BETA THALASSEMIA:
Beta thalassemia occurs when one or both of the two genes
needed for making the beta globin chain of hemoglobin are variant.
The severity of illness depends on whether one or both genes are
affected, and the nature of the abnormality. If both genes are
affected, anemia can range from moderate to severe.
People with mutation only in one gene are known as carriers or
are said to have thalassemia minor. Thalassemia minor results in no
anemia or very slight anemia. People who are carriers do not
require blood transfusion or iron therapy, unless proven to be iron
deficient.
Price of 1 Unit
US $**2.*5
FRIEGHT CHARGES EXTRA
Duration of 1 unit of Treatment:
3 Months
GENERAL SYMPTOMS OF THE DISEASES:
- Children born with thalassemia major usually develop the
symptoms of severe anemia within the first year of life.
- Symptoms Lacking the ability to produce normal adult
hemoglobin, children with thalassemia major are chronically
fatigued, fail to thrive, and, do not grow normally.
- Prolonged anemia will cause bone deformities and eventually
will lead to death within the first decade of life. The only
treatment to combat severe anemia is regular blood
transfusions.
TREATMENT PROCEDURE:
[A] Internal Ayurvedic Medicine to manage general
symptoms of thalassemia as well as the iron overloading
disorders.
[B] Result oriented and clinically proven **0% Ayurvedic
standardized herbal medicine. The clinical trial of this medicine
has been done successfully on more than **0 patients. The
polyherbal medicine is free from adversities.
ADVANTAGES OF TREATMENT:
The polyherbal formulation improves quality of life as well
can give relief in the general condition of the Thalassemics.
Patient may need transfusions comparatively less than normal
condition.
- Improves intellect, sharpens memory.
- Normalize the Renal and Liver functions.
- Strengthens the cardiac cells.
- Also helps to maintain the blood sugar level.
- Checks chronic fatigue and patient feels more energetic.
- Also very effective on iron overload. See details in iron
overloading diseases.
SAFETY PROFILE:
The drug is a mixture of time tested and safe herbs. No any
side effects reported till today.
PRECAUTIONS TO BE TAKEN:
No any special precaution is needed thus precaution varies
from individual to individual depending upon the constitution of
the body. Hence, it will be sent along with the medicine.
RECOMMENDED DURATION OF THE
COURSE:
Depending upon the severity of the disease.
SPECIAL ADVICE:
Please check serum Ferritin level at regular
interval.
PRESENTATION:
**0 tablets and **0 sachets of herbal tea.
Expertise doctor for Thalassemia Treatment is Dr. Joban
Modha.
QUALITY ASSURANCE:
We know that our products deal with human lives and therefore
with utmost faith in nature, we believe in only highest quality
standard products and under strict quality processes which are non-
hazardous & non-toxic without any side effects. Absolute herbal
medicine.
PAYMENT METHOD:
Orders may be placed: on-line, either using the shopping cart
from our website or the quick-order form, through the mail, via
fax, or over the phone
SHIPPING & DELIVERY TIME:
We Ship world wide to most of the countries by offering door
step delivery within five business days.
