Thalassemia (थैलेसीमिया) is an inherited blood disorder characterized by abnormal hemoglobin production. Symptoms depend on the type and can vary from none to severe. Often there is mild to severe anemia (low red blood cells). Anemia can result in feeling tired and pale skin. There may also be bone problems, an enlarged spleen, yellowish skin, and dark urine. Slow growth may occur in children. Considering the critical impact of thalassemia on health, Siddha Spirituality of Swami Hardas Life System appeals to readers to read this article and learn free Siddha energy remedies for wellbeing.
Thalassemia Types (थैलेसीमिया के प्रकार)
Thalassemias are genetic disorders inherited from a person’s parents. There are two main types:
- Alpha thalassemia, and
- Beta thalassemia
The severity of alpha and beta-thalassemia depends on how many of the four genes for alpha globin or two genes for beta-globin are missing. Diagnosis is typically by blood tests including a complete blood count, special hemoglobin tests, and genetic tests. Diagnosis may occur before birth through prenatal testing.
Thalassemia Meaning (थैलेसीमिया का अर्थ)
Any of a group of hereditary hemolytic diseases caused by faulty hemoglobin synthesis, widespread in the Mediterranean, African, and Asian countries.
Thalassemia Symptoms (थैलेसीमिया के लक्षण)
Iron overload (लोहे का अधिभार)
People with thalassemia can get an overload of iron in their bodies, either from the disease itself or from frequent blood transfusions. Too much iron can result in damage to the heart, liver, and endocrine system, which includes glands that produce hormones that regulate processes throughout the body. Excessive deposits of iron are the cause of damage. Without adequate iron chelation therapy, almost all patients with beta-thalassemia accumulate potentially fatal iron levels.
People with thalassemia have an increased risk of infection, which is especially true if the spleen has been removed.
Bone deformities (अस्थि विकृति)
Thalassemia can make the bone marrow expand, which causes bones to widen. This can result in abnormal bone structure, especially in the face and skull. Bone marrow expansion also makes bones thin and brittle, increasing the risk of broken bones.
Enlarged spleen (बढ़े हुए प्लीहा)
The spleen aids in fighting infection and filters unwanted material, such as old or damaged blood cells. Thalassemia is often accompanied by the destruction of a large number of red blood cells and the task of removing these cells causes the spleen to enlarge. Splenomegaly can make anemia worse, and it can reduce the life of transfused red blood cells. Severe enlargement of the spleen may necessitate its removal.
Slowed growth rates (धीमी विकास दर)
Heart problems (हृदय की समस्याएं)
Diseases, such as congestive heart failure and abnormal heart rhythms, may be associated with severe thalassemia.
Thalassemia Causes (थैलेसीमिया के कारण)
Both α- and β-thalassemias are often inherited in an autosomal recessive manner. Cases of dominantly inherited α- and β-thalassemias have been reported, the first of which was in an Irish family with two deletions of 4 and 11 bp in exon 3 interrupted by an insertion of 5 bp in the β-globin gene.
For the autosomal recessive forms of the disease, both parents must be carriers for a child to be affected. If both parents carry a hemoglobinopathy trait, the risk is 25% for each pregnancy for an affected child.
Evolution (क्रमागत उन्नति)
Having a single genetic variant for thalassemia may protect against malaria and thus can be an advantage. People diagnosed with heterozygous (carrier) β-thalassemia have some protection against coronary heart disease.
Normally, the majority of adult hemoglobin (HbA) is composed of four protein chains, two α and two β globin chains arranged into a heterotetramer. In thalassemia, patients have defects in either the α or β globin chain, causing the production of abnormal red blood cells (In sickle-cell disease, the mutation is specific to β globin).
The α-thalassemias involve the genes HBA1 and HBA2, inherited in a Mendelian recessive fashion. Two gene loci and so four alleles exist. The excess β chains form unstable tetramers, which have abnormal oxygen dissociation curves.
Beta-thalassemia (बीटा थैलेसीमिया)
Beta thalassemias are due to mutations in the HBB gene on chromosome 11, also inherited in an autosomal, recessive fashion. The severity of the disease depends on the nature of the mutation and on the presence of mutations in one or both alleles.
Beta thalassemia most often occurs in people of Mediterranean origin. To a lesser extent, Chinese, other Asians, and African American can be affected.
Just as with beta-thalassemia, mutations that affect the ability of this gene to produce delta chains can occur.
Thalassemia Diagnosis (थैलेसीमिया का निदान)
Thalassemia can be diagnosed via a complete blood count, hemoglobin electrophoresis, and DNA testing.
Thalassemia Prevention (थैलेसीमिया की रोकथाम)
The American College of Obstetricians and Gynecologists recommends all people thinking of becoming pregnant be tested to see if they have thalassemia. Genetic counseling and genetic testing are recommended for families who carry a thalassemia trait.
A screening policy exists in Cyprus to reduce the rate of thalassemia, which, since the program’s implementation in the 1970s, has reduced the number of children born with the disease from one of every 158 births to almost zero. Greece also has a screening program to identify people who are carriers.
Large scale awareness campaigns are being organized in India both by government and non-government organizations in favor of voluntary premarital screening to detect carriers of thalassemia and marriage between both carriers are strongly discouraged.
Thalassemia Management (थैलेसीमिया का प्रबंधन)
People with β-thalassemia trait should be warned that their condition can be misdiagnosed as the more common iron-deficiency anemia.
They should avoid the routine use of iron supplements; iron deficiency can develop, though, during pregnancy or from chronic bleeding. Counseling is indicated in all persons with genetic disorders, especially when the family is at risk of a severe form of the disease that may be prevented.
Thalassemia Anemia (थैलेसीमिया एनीमिया)
People with severe thalassemia require medical treatment. A blood transfusion regimen was the first measure effective in prolonging life.
Iron overload (लोहे का अधिभार)
Multiple blood transfusions can result in iron overload. The iron overload related to thalassemia may be treated by chelation therapy with the medications deferoxamine, deferiprone, or deferasirox. These treatments have resulted in improving life expectancy in those with thalassemia major.
Deferoxamine is only effective via daily injections which makes its long-term use more difficult. It has the benefit of being inexpensive and decent long-term safety. Adverse effects are primary skin reactions around the injection site and hearing loss.
Deferasirox has the benefit of being an oral medication. Common side effects include:
It, however, is not effective in everyone and is probably not suitable in those with significant cardiac issues related to iron overload. The cost is also significant.
Nausea, vomiting, and diarrhea are relatively common with the use of Deferiprone use. It is available in both Europe and the United States. It appears to be the most effective agent when the heart is significantly involved.
Bone marrow transplantation (बोन मैरो प्रत्यारोपण)
Bone Marrow Transplantation (BMT) may offer the possibility of a cure in young people who have an HLA-matched donor. Success rates have been in the 80–90% range. Mortality from the procedure is about 3%. There are no randomized controlled trials which have tested the safety and efficacy of non-identical donor bone marrow transplantation in persons with β- thalassemia who are dependent on blood transfusion.
In a study of 31 people, the thalassemia-free survival rate 70%, rejection 23%, and mortality 7%. The best results are with very young people.
Thalassemia Research (थैलेसीमिया रिसर्च)
Gene therapy (जीन थेरेपी)
Gene therapy is being studied for thalassemia. The procedure involves collecting Hematopoietic Stem Cells (HSCs) from the affected person’s blood. The HSCs then have a beta-globin gene added using a lentiviral vector. This potentially results in a progressive increase in hemoglobin A2 synthesis in all subsequent developing red blood cells, with the resultant resolution of the anemia.
While one person with beta-thalassemia has no longer required blood transfusions following treatment within a research trial, it is not an approved treatment as of 2018.
Thalassemia & Free Siddha Energy Remedies (थैलेसीमिया और नि:शुल्क सिद्ध ऊर्जा उपचार)
1. Siddha preventive measures (सिद्ध निवारक उपाय)
Everybody must practice Siddha preventive measures, whether a person is affected with thalassemia or not, but preventive measures are the primary steps for switching on to any other Siddha energy remedies, and hence they are important. It helps in one’s capability, effectiveness, and productivity, decision making power, intellectuality and removing minor health problems. There are three types of preventive measures:
- Earthing – performed for earthing the negativity of our body
- Field Cleaning – cleans energy field (Aura) of our body
- Siddha Brain Exercise/Energizing – energizes our brain for proper functionality
Everybody’s tendency is to get attracted toward the word ‘free‘, however, don’t neglect even these Siddha preventive measures are free. Avail the benefits by practicing them sincerely, and regularly. For the ease of understanding Siddha preventive measures, please watch a video for a live demonstration.
2. Siddha Shaktidata Yog (सिद्ध शक्तीदाता योग)
This unique Siddha Shaktidata Yog of Siddha Spirituality can solve the problems related to thalassemia with free Siddha energy remedies. There is no compulsion of training of ‘Swami Hardas Life System’ methods. This not only gives benefits to self but also it can be used for other affected persons, whether a person is in the same house, distantly available in the same city, same nation or may be in any corner of the world, however, both the procedures have been explained here.
3. Siddha Kalyan Sadhana (सिद्ध कल्याण साधना)
Recite this Sadhana with a Sankalp “My problems of thalassemia are solved as early as possible and I should gain health”, which should be repeated in mind 3 – 3 times every after each stanza. Any person irrespective of caste, creed, religion, faith, sex, and age can recite this Sadhana for free, which should be repeated at least twice in a day. To know more, please click on this link.
4. CCPE products (CCPE उत्पाद)
These products work on the concepts of ‘Conceptual Creative Positive Energy’ (CCPE) within the provisions of ‘CCPE Life System’ and the theory of Quantum Technology to a certain extent. However, the products get activated only whenever touched by a human and then they become capable of solving the problem and achieving health. However, please use these products for thalassemia as mentioned below:
CCPE Extractor: The CCPE Extractor should be gently moved over the Agya Chakra in a circular motion at least for 30 to 60 seconds, thereafter, follow the same process on the head, heart, liver, naval for another 30 to 60 seconds, which finishes within almost 3 – 6 minutes.
CCPE Booster: Keep one Booster over the Agya Chakra and another one each over the head, heart, liver, naval for 6 – 12 minutes. You may need to have 5 Boosters, which establishes positivity.
5. A daily routine for Thalassemia (थैलेसीमिया के लिए एक दैनिक दिनचर्या)
In general, a daily routine to manage thalassemia:
- Carry out all medical checks as suggested above and follow the advice of your doctor
- Apply free Siddha energy remedies minimum 3 times a day, as explained above
- In case, if someone wishes to learn advanced methods of Swami Hardas Life System, undergo unique training
Ensure to sprinkle in some fun during the day: Don’t forget to relax and laugh in between. Laughing is a great way to boost your immune system and help you.
Along with all the above activities, apply above explained free Siddha energy remedies minimum 3 times a day, the more is good. Just try the methods of Siddha Spirituality of Swami Hardas Life System. I am confident that you will surely find improvements within 15 days.
Training of Swami Hardas Life System (स्वामी हरदास लाइफ सिस्टम का प्रशिक्षण)
Any problem with regard to health, peace, and progress can be solved independently without money and medicines by undergoing training of Swami Hardas Life System. Any person irrespective of religion, caste, creed, faith, sex, and age can undergo this unique training.
In view of the above, I am confident that you have learned about thalassemia, symptoms, causes, diagnosis, precautions, management, and treatments. You also learned free Siddha energy remedies. Now, you have become self-sufficient, hence its right time to use your acquired knowledge for solving problems as per the provision available in Siddha Spirituality of Swami Hardas Life System.
After reading this article, what are your thoughts? Would you please put more efforts into enhancing or updating your knowledge? Let me know your precious thoughts.
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