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Thalassemia Health Feed

Hi I am looking for bride for marriage, recently I got proposal from one girl who is suffering from thalassemia, how would be the life if I married this girl. Does she can lead a normal life or any medication required, what would be the cost if medication is required always?

Hi I am looking for bride for marriage, recently I got proposal from one girl who is suffering from thalassemia, how ...
It depends on what type. If she is thalassemia minor and you don't have it then it may not cause much trouble. If you both are then it can cause major trouble.
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I and my partner want to get married but we both have thalassemia minor. We are facing a lot of objections from our family and they say that we cannot have healthy children. Can you please advice?

I and my partner want to get married but we both have thalassemia minor. We are facing a lot of objections from our f...
Yes there is 25% possibility that the kid will be thalassemia major. But you can do following test during pregnancy to find out if your baby is at risk for thalassemia, you can have prenatal tests during pregancy to see if he has the condition. Prenatal tests are tests you get during pregnancy to see how you and your baby are doing. 1. Chorionic villus sampling (also called cvs). This test checks tissue from the placenta to see if your baby has a genetic condition. You can get cvs at 10 to 13 weeks of pregnancy. 2. Amniocentesis (also called amnio). This test takes some amniotic fluid from around your baby in the uterus. The test checks for birth defects and genetic conditions in your baby. You can get this test at 15 to 20 weeks of pregnancy.
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Thalassaemia - Know Forms Of It!

Thalassaemia - Know Forms Of It!

Thalassaemia is one of the most difficult hereditary diseases to live with. Even though there is no cure, parents can prevent their child from being born with this terrible disease if they are careful.

However, preventing the spread of disease in the world has proven difficult due to the lack of proper awareness about the condition. This is why the World Health Organization established May 8th as World Thalassaemia Day.

Importance of World Thalassaemia Day

8th May is dedicated to past and present Thalassaemia patients in the world, who are surviving with the condition. It is also a day when the medical organizations around the world come together to plan and raise awareness about the disease. Camps are set up in various cities and villages to educate people about the dangers of Thalassaemia and teach them about prevention measures of it. On World Thalassaemia Day, hospitals and clinics promote pre-marriage genetic testing that can help prevent hereditary conditions in the family. In India alone, 7,000-10,000 children are born with this disorder every year.

Aside from spreading awareness, there are other important reasons for celebrating World Thalassaemia Day. These include - 

1. To motivate healthy people in the world to donate blood regularly in order to reduce the suffering of patients of Thalassaemia

2. Motivating doctors to take care of the special needs of such patients

3. Motivating people suffering from the disease to undergo treatment, as soon as they can, to reduce complications

4. To motivate the government of various countries around the world to build better health care facilities for people suffering from Thalassaemia

5. To reduce Thalassaemia related deaths around the globe

Causes and types of Thalassaemia

Thalassaemia is a hereditary condition, passed on from parents to their children. The condition results in improper and insufficient red blood cell and haemoglobin formation. This causes anaemia in the body.

There are two main types of Thalassemia -

1. Alpha-thalassemia- In this type, up to four genes are involved. Two genes are passed down to you from each parent. In case of a single mutated gene, you will not suffer from the condition, but you become a carrier. In the case of two mutated genes, the symptoms of the disease will be mild. In the case of three mutated genes, the symptoms will be severe. Most children with four mutated genes are stillborn, while a few may survive for a short period after birth.

2. Thalassaemia minor- Two genes determine whether an offspring will suffer from thalassaemia minor or not. If one of these two genes is mutated, the child will have mild symptoms of the disease. If both the genes are affected, the child will be healthy at birth but will develop severe thalassaemia within the first two years of life.

Treatment for Thalassaemia

Treatment varies depending on the severity of the disease that affects you. For instance, people with mild Thalassaemia do not require frequent treatment. For these people, blood transfusion is necessary after surgery or childbirth.

On the other hand, people suffering from severe Thalassaemia rely on frequent blood transfusions. In a small number of cases, if you are able to find a proper donor, you can also take advantage of stem cell transplant to treat Thalassaemia. After such surgery, you no longer need blood transfusions for the rest of your life. Therefore, prevention and genetic testing before conceiving is the best way to combat Thalassaemia in the long run.

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I am suffering from hemoglobin e-beta thalassemia. My spleen has enlarged very badly. Also I have fatty liver. Also I am suffering from hypothyroid. Also I am suffering from stomach heaviness after my daily lunch in the left side of my stomach. And also I am suffering from sleep paralysis. So, doctor please help me.

I am suffering from hemoglobin e-beta thalassemia. My spleen has enlarged very badly. Also I have fatty liver. Also I...
Dear user. I can understand. Please don't be panic but be serious about the symptoms. Consult your physician for physical investigation. Please provide more information so that we can start the diagnosis process and the treatment. I am here to help you in every aspect of your mental and physical health. Any sexual or psychological problems can be cured with the help of various methods and therapies. I suggest you to post your query with every detail here. I will help you in overcoming your problems certainly. Take care.
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What Does Thalassemia Do To Your Body?

What Does Thalassemia Do To Your Body?

Thalassemia is a genetic (i.e., passed from parents to children through genes) blood disorder. People with Thalassemia disease are not able to make enough hemoglobin, which causes severe anemia. Hemoglobin is found in red blood cells and carries oxygen to all parts of the body. When there is not enough hemoglobin in the red blood cells, oxygen cannot get to all parts of the body. Organs then become starved for oxygen and are unable to function properly.

There are two types of Thalassemia disease- 

  1. Alpha Thalassemia disease: There are two main types of Alpha Thalassemia disease. Alpha Thalassemia Major is a very serious disease in which severe anemia begins even before birth. Pregnant women carrying affected fetuses are themselves at risk for serious pregnancy and delivery complications. Another type of Alpha Thalassemia is Hemoglobin H disease. There are varying degrees of Hemoglobin H disease.
  2. Beta Thalassemia disease: Beta Thalassemia Major (also called Cooley's Anemia) is a serious illness. Symptoms appear in the first two years of life and include paleness of the skin, poor appetite, irritability, and failure to grow. Proper treatment includes routine blood transfusions and other therapies.

Causes of Thalassemia-

Thalassemia occurs when there’s an abnormality or mutation in one of the genes involved in hemoglobin production. You inherit this genetic defect from your parents.

If only one of the parents is a carrier for thalassemia, the child may develop a form of the disease known as thalassemia minor. If this occurs, the born child probably won’t have symptoms, but he/she will be a carrier of the disease. Some people with thalassemia minor do develop minor symptoms.

If both of your parents are carriers of thalassemia, you have a greater chance of inheriting a more serious form of the disease.

Symptoms-

The symptoms depend on the type of thalassemia:

  • Thalassemia Minor: Thalassemia minor usually doesn’t cause any symptoms. If it does, it causes minor anemia.
  • Beta-thalassemia: Beta-thalassemia comes in two serious types, which are thalassemia major, or Cooley’s anemia, and thalassemia intermedia. The symptoms of thalassemia major generally appear before a child’s second birthday. The severe anemia related to this condition can be life-threatening. Other signs and symptoms include:
    • fussiness
    • paleness
    • frequent infections
    • a poor appetite
    • failure to thrive
    • jaundice, which is a yellowing of the skin or the whites of the eyes
    • enlarged organs

This form of thalassemia is usually so severe that it requires regular blood transfusions.

  • Alpha-thalassemia: Alpha-thalassemia also has two serious types, which are hemoglobin H disease and hydrops fetalis. Hemoglobin H disease can cause bone issues. The cheeks, forehead, and jaw may all overgrow. Hemoglobin H disease can cause:
    • jaundice, which is a yellowing of the skin or the whites of the eyes
    • an extremely enlarged spleen
    • malnourishment

Hydrops fetalis is an extremely severe form of thalassemia. It occurs before birth. Most individuals with this condition are either stillborn or die shortly after being born.

How is thalassemia diagnosed?

Thalassaemia is often detected during pregnancy or soon after birth.

  1. Screening during pregnancy: Screening to check if a baby is at risk of being born with thalassemia is offered to all pregnant women.
  2. Testing after birth or later in life: Newborn babies aren't routinely tested for thalassemia because the test used isn't always reliable soon after birth and the condition isn't immediately dangerous. However, the main form of the condition – beta thalassemia major – is often picked up as part of the newborn blood spot test (heel prick). A blood test can be carried out at any point to diagnose the condition if a child or adult has symptoms of thalassemia and the condition wasn't picked up earlier on.
  3. Testing for the Thalassemia Trait- A blood test can be done at any time to find out if you have the thalassemia trait and are at risk of having a child with the condition. This can be particularly useful if you have a family history of the condition or your partner is known to carry thalassemia.

If your child has thalassemia, blood tests may reveal:

  1. A low level of red blood cells
  2. Smaller than expected red blood cells
  3. Pale red blood cells
  4. Red blood cells that are varied in size and shape
  5. Red blood cells with uneven hemoglobin distribution, which gives the cells a bull's-eye appearance under the microscope

Blood tests may also be used to:

  1. Measure the amount of iron in your child's blood
  2. Evaluate his or her hemoglobin
  3. Perform DNA analysis to diagnose thalassemia or to determine if a person is carrying mutated hemoglobin genes

Treatment for Thalassemia-

The treatment for thalassemia depends on the type and severity of disease involved. Your doctor will give you a course of treatment that will work best for your particular case.

Some of the utilized treatments include:

  • blood transfusions
  • a bone marrow transplant (BMT)
  • medications and supplements
  • possible surgery to remove the spleen or gallbladder
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Hi, Husband and wife both thalassemia carrier. Wife is pregnant of 17 weeks. Is the child affected by thalassemia or not. How I detect before born that the baby is thalassemia affected or not. Is abortion possible?

Hi, Husband and wife both thalassemia carrier. Wife is pregnant of 17 weeks. Is the child affected by thalassemia or ...
Yes there are high chances of having thalassemia. You should consult your gyencologist for proper test and guidance for the early diagnosis.
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Thalassemia - Know More About It!

Thalassemia - Know More About It!

Thalassemia is a genetic (i.e., passed from parents to children through genes) blood disorder. People with Thalassemia disease are not able to make enough hemoglobin, which causes severe anemia. Hemoglobin is found in red blood cells and carries oxygen to all parts of the body. When there is not enough hemoglobin in the red blood cells, oxygen cannot get to all parts of the body. Organs then become starved for oxygen and are unable to function properly.

There are two types of Thalassemia disease- 

  1. Alpha Thalassemia disease: There are two main types of Alpha Thalassemia disease. Alpha Thalassemia Major is a very serious disease in which severe anemia begins even before birth. Pregnant women carrying affected fetuses are themselves at risk for serious pregnancy and delivery complications. Another type of Alpha Thalassemia is Hemoglobin H disease. There are varying degrees of Hemoglobin H disease.
  2. Beta Thalassemia disease: Beta Thalassemia Major (also called Cooley's Anemia) is a serious illness. Symptoms appear in the first two years of life and include paleness of the skin, poor appetite, irritability, and failure to grow. Proper treatment includes routine blood transfusions and other therapies.

Causes of Thalassemia-

Thalassemia occurs when there’s an abnormality or mutation in one of the genes involved in hemoglobin production. You inherit this genetic defect from your parents.

If only one of the parents is a carrier for thalassemia, the child may develop a form of the disease known as thalassemia minor. If this occurs, the born child probably won’t have symptoms, but he/she will be a carrier of the disease. Some people with thalassemia minor do develop minor symptoms.

If both of your parents are carriers of thalassemia, you have a greater chance of inheriting a more serious form of the disease.

Symptoms-

The symptoms depend on the type of thalassemia:

  • Thalassemia Minor: Thalassemia minor usually doesn’t cause any symptoms. If it does, it causes minor anemia.
  • Beta-thalassemia: Beta-thalassemia comes in two serious types, which are thalassemia major, or Cooley’s anemia, and thalassemia intermedia. The symptoms of thalassemia major generally appear before a child’s second birthday. The severe anemia related to this condition can be life-threatening. Other signs and symptoms include:
    • fussiness
    • paleness
    • frequent infections
    • a poor appetite
    • failure to thrive
    • jaundice, which is a yellowing of the skin or the whites of the eyes
    • enlarged organs

This form of thalassemia is usually so severe that it requires regular blood transfusions.

  • Alpha-thalassemia: Alpha-thalassemia also has two serious types, which are hemoglobin H disease and hydrops fetalis. Hemoglobin H disease can cause bone issues. The cheeks, forehead, and jaw may all overgrow. Hemoglobin H disease can cause:
    • jaundice, which is a yellowing of the skin or the whites of the eyes
    • an extremely enlarged spleen
    • malnourishment

Hydrops fetalis is an extremely severe form of thalassemia. It occurs before birth. Most individuals with this condition are either stillborn or die shortly after being born.

How is thalassemia diagnosed?

Thalassaemia is often detected during pregnancy or soon after birth.

  1. Screening during pregnancy: Screening to check if a baby is at risk of being born with thalassemia is offered to all pregnant women.
  2. Testing after birth or later in life: Newborn babies aren't routinely tested for thalassemia because the test used isn't always reliable soon after birth and the condition isn't immediately dangerous. However, the main form of the condition – beta thalassemia major – is often picked up as part of the newborn blood spot test (heel prick). A blood test can be carried out at any point to diagnose the condition if a child or adult has symptoms of thalassemia and the condition wasn't picked up earlier on.
  3. Testing for the Thalassemia Trait- A blood test can be done at any time to find out if you have the thalassemia trait and are at risk of having a child with the condition. This can be particularly useful if you have a family history of the condition or your partner is known to carry thalassemia.

If your child has thalassemia, blood tests may reveal:

  1. A low level of red blood cells
  2. Smaller than expected red blood cells
  3. Pale red blood cells
  4. Red blood cells that are varied in size and shape
  5. Red blood cells with uneven hemoglobin distribution, which gives the cells a bull's-eye appearance under the microscope

Blood tests may also be used to:

  1. Measure the amount of iron in your child's blood
  2. Evaluate his or her hemoglobin
  3. Perform DNA analysis to diagnose thalassemia or to determine if a person is carrying mutated hemoglobin genes

Treatment for Thalassemia-

The treatment for thalassemia depends on the type and severity of disease involved. Your doctor will give you a course of treatment that will work best for your particular case.

Some of the utilized treatments include:

  • blood transfusions
  • a bone marrow transplant (BMT)
  • medications and supplements
  • possible surgery to remove the spleen or gallbladder
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Prevention From Genetic Diseases!

Prevention From Genetic Diseases!

HOW  TO PREVENT TRANSMISSION OF  Autism, Thalassemia, Muscular Dystrophy, Dysphasia, CANCER, DOWN SYNDROME  & other GENETIC DISEASES?
Rare diseases are a diverse set of over 7,000 different conditions that afflict an estimated 1 in 20 Indians and 350 million people worldwide, which are incurable with 40% mortality. Put simply, it means that every bus on the road with a full complement of passengers possibly has two people with a rare disease. : In terms of estimates of IORD [Indian Organization For Rare Diseases-with Indo American sponsorship] we have [in India] 10 million children/adults suffering from 700 rare diseases, which are incurable. Muscular Dystrophy, Autism, Thalassemia, Parkinson’s Syndrome, Cancer, Brain & Spinal Cord affected Disorders, Down Syndrome, etc., are some such genetically transmitted incurable diseases. Only 10% of offspring may be affected by predecessor-victims. 
1. ADHD is a neurodevelopmental disorder characterized by inattention and disorganization, with or without hyperactivity-impulsivity, causing impairment of physiological functioning. ADHD persists into adulthood in approximately 20 percent of individuals.
2. Autism spectrum disorders (ASDs) are conditions in which people have difficulty developing normal social relationships, use inappropriate language, and behave in compulsive and ritualistic ways.
3. Intellectual disability (ID) is significantly sub-average normal intellectual functioning present from birth or early infancy, impaired cognitive functioning and deficits in two or more adaptive behaviors. Rett syndrome.
4. Learning disorders involve an inability to retain, or broadly use specific skills or information, resulting from deficiencies in attention, memory, or reasoning which affects academic performance.
5. Rett syndrome is a rare neurodevelopmental disorder that affects a female child who had normal development in the initial 6-month period of her life.

ROOT CAUSE: FIRST & FOREMOST SYMPTOM: DELAYED MILESTONES IN INFANTS & CHILDREN.

Prevention & Remedy

1.PREVENTION: 
A.  No sex with a pregnant mother after formation of the fetus in the 3rd month of pregnancy. Because, in coitus, there shall be severe vibrations in the mother’s uterus affecting the brain and spinal cord of the fetus in the offing. [7]. In the  3rd month of pregnancy, the fetus takes full shape and PRANA is infused by the Gods [BRAHMA, VISHNU & MAHESHWERAHA] through Brahma Randhra-an aperture in the middle of the head. What Indian Mythology says that @ that auspicious time, somebody must read out loudly epics like Ramayana, Bhagawata, Siva/Vishnu Puranas, Bhavadgeeta,etc. so that the 3 Gods shall be pleased to implant the best seed with “no genetically transmitted disorders” into the fetus in the offing. So that genetic diseases can be prevented. Mothers of other religions like Christians/Muslims/Jainism/Buddhism, etc., can seek benefit from Bible, Quoran, preachings of Vardhan Mahaveer, Gautam Buddha, etc., respectively.
B.  The first & foremost symptom is 'delayed mile-stones' in a growing infant/child. 

C. Instant Remedy for Delayed Milestones:
For any INFANT/CHILD/PET* ANIMAL- ACUPRESSURE RENDERS IMMENSE BENEFITS: Acupressure techniques may be applied safely to every human/animal, right from 1-day old infant to a 100 years old man. Acupressure may come to rescue infants/kids + growing children. There are more than 1000 acupressure points [remote control points to regulate the functioning of all internal organs/systems] spread on the human body. Take 1 or 2 tsp of Johnson &Johnson Baby massage oil/olive oil [til oil, mustard/soybean oil in winter], massage the entire body with your thumb & fingers and then give a bath with warm water. Acupressure is more helpful for infants/children suffering from ‘delayed milestones’ & all-around improvements [including constipation issues] can be noted in his/her metabolism. If feasible, any mother can do massage, a lady from barber’s community maybe engaged, since she is, genetically, trained. 
Benefits: All internal & external organs shall be grown up to produce handsome/pretty boys/girls with robust health. In India, women from Barber community are genetically trained to apply professional massages. 

HOMOEOPATHIC THERAPEUTICS

Homeopathy is known to act on patients of different constitution, temperament and diathesis. There are many medicines in homeopathy which produce and hence cure various mental symptoms. Acting on such constitutions and affecting such mental state it can cure many neurodevelopmental disorders when given along with psychosocial therapies.

A. Agaricus Muscaris: These children are late in learning to talk and walk, but it is due to mental defect, a slowly developing mind. Other indications for giving Agaricus being, children with twitching and early fainting or nervous girls prior to puberty who have convulsions from being scolded, or from excitement and shock. Children are slow in learning, make mistakes and cannot remember. They are nervous patients who find out mistakes in writing and spelling after going over their own manuscripts.

B, Baryta Carbonica: These children are late in coming into usefulness, with their studies, to take on their activities and to do their work. They are late in learning to talk, to read, to make the combinations that enter into life; to take in images and form perceptions etc. They have late in learning how to walk, even with good limbs. Baryta carbonica, Borax and Natrum muriaticum, all three have “late learning to walk”  due to a peculiar kind of tardiness in the development of the brain, so that they are late in learning to do things; late in developing. But Baryta carbonica leads them in this late coming into the activities.

C. Calcarea Carbonica: These children have “Late learning to walk,” because the legs are so weak. Actually, it is not late learning to walk, but it is late walking. A child knows how to walk, but it can’t walk due to a defect in bone or weakness. Calcarea carbonica has very weak limbs, flabby muscles and poor bones, and hence he is late in learning to walk.

D. Calcarea Phosphorica: Here the child is losing flesh along with slow learning to do things and walk, or the legs are not strong enough to support the body, or it is due to defective mental development.

E. Medorrhinum: These children are rachitic, stunted in growth, dwarfed and mentally dull and weak. They usually have constitutional effects of maltreated and suppressed gonorrhea.

F. Natrum Muriaticum: These children have “late learning to walk” but this is actually because of brain trouble due to which child is late in learning to do things.

G. Phosphorus:  Phosphorus is suited to feeble constitutions, who have been born sick, grown-up slender and too rapidly. They are emaciated or are rapidly emaciating; especially children who are going into marasmus, and in persons who have a tubercular history.

H. Silicea Terra: These children are slow in learning to walk due to deficient nutrition not because the food is lacking in quality or quantity but from improper assimilation.

CONCLUSION

After using Homoeopathy for various acute and chronic diseases, we should focus on the present scenario of genetic and lifestyle disorders, where other systems of treatment do not have many roles to play. Homeopathy works well both as a therapeutic and constitutional approach. We may select different homeopathic medicine according to the type of developmental delay and cause behind it. Developmental disorders of few medicines and their probable causes have been described below in Table 1.

Table 1.Summary of various developmental disorders in different medicines and their causes

MEDICINES    DEVELOPMENTAL DISORDER    CAUSE
1. Agaricus muscarius - Late in learning to talk and walk, Due to mental defect3
2. Baryta carbonica - Late in learning to talk, to read, late in learning how to walk, even with good limbs. Tardiness in the development of the brain
3. Calcarea carbonica - Late learning to walk. Because the legs are so weak
4. Calcarea phosphorica - Slow learning to do things and walk. Legs are not strong enough and defective mental development3.
5. Medorrhinum Rachitic, stunted in growth, dwarfed and mentally dull and weak. Suppressed and maltreated gonorrhea3
6. Natrum muriaticum - Late learning to walk. Because of brain trouble3
7. Phosphorus - Born sick, grown-up slender, grow too rapidly, are emaciated or are rapidly emaciating. Tubercular history3
8. Silicea Terra - Slow in learning to walk. Due to deficient nutrition from improper assimilation
 

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थैलेसीमिया का इलाज - Thailesimia Ka Ilaj!

थैलेसीमिया का इलाज - Thailesimia Ka Ilaj!

थैलासीमिया एक प्रकार का ब्लड डिसऑर्डर है, जो आपके शरीर में असामान्य हीमोग्लोबिन और रेड ब्लड सेल्स के उत्पादन के लिए जिम्मेदार होती है. थैलासीमिया विभिन्न प्रकार के होते हैं ‘जैसे अल्फा-थैलासीमिया, बीटा-थैलासीमिया इंटरमीडिया, कोली एनीमिया और मैडिटरेनियन एनीमिया. हीमोग्लोबिन ऑक्सीजन ले जाने में रेड ब्लड सेल्स की सहायता करता है. रेड ब्लड सेल्स और हीमोग्लोबिन में कमी के कारण एनीमिया हो सकता है. इसके परिणामस्वरूप कमजोरी और थकावट महसूस करते हैं. इसके अलावा, आप पेट में सूजन, डार्क यूरिन या पीले रंग की त्वचा का भी अनुभव कर सकते हैं. यह एक अनुवांशिक स्थिति है जिसका उपचार बचपन में किया जाना चाहिए. यदि आप थैलासीमिया के पूरी तरह से ग्रसित नहीं है तो इसके उपचार की जरुरत नहीं होती है. लेकिन यदि आप थैलासीमिया से गंभीर रूप पीड़ित हैं, तो आपको नियमित रूप से ब्लड की जरुरत पड़ सकती है. इसके अलावा, थकान से निजात पाने के लिए आपको स्वस्थ आहार का सेवन करना और रोजाना एक्सरसाइज करने को अपनी रूटीन में शामिल करना चाहिए. इस लेख के माध्यम से हम थैलेसिमिया का इलाज कैसे किया जा सकता है इसके बारे में जानेंगे.

थैलेसिमिया के लक्षण-
थैलेसिमिया के लक्षण यदि किसी व्यक्ति में नजर आयें तो आपको तुरंत चिकित्सक से संपर्क करना चाहिए. इसके लक्षणों में थकान, कमजोरी, पीलापन और धीमा विकास प्रमुख हैं. आइए अब थैलेसिमिया के लक्षणों पर एक नजर डालें –

  • एनेमिया यानि खून की कमी होना
  • विकास का अवरुद्ध होना
  • त्वचा का पीलापन
  • थैलेसिमिया में कमजोरी भी इसका एक आम लक्षण है
  • श्वसन संबंधी परेशानी
  • आँखों में पीलापन
  • आयरन की अधिकता


थैलेसिमिया का इलाज-
थैलेसिमिया के हल्के रूपों में उपचार की आवश्यकता नहीं भी हो सकती है. लेकिन इसके गंभीर रूपों में रक्त संक्रमण या दाता स्टेम-सेल प्रत्यारोपण की आवश्यकता हो सकती है. आइए थैलेसिमिया के इलाज के विभिन्न संभावनाओं पर एक नजर डालें.

  1. विटामिन की उचित खुराक दें: - थैलेसिमिया के मरीजों को विटामिन की उचित खुराक देनी चाइए क्योंकि विटामिन हमारे शरीर की विभिन्न गतिविधियों, वृद्धि एवं विकास को प्रोत्साहित करते हैं.
     
  2. रक्तसंचार को प्रोत्साहित करना: - जिन लोगों को थैलेसिमिया की समस्या है उनके रक्तसंचार को लगातार प्रोत्साहित करते रहने की आवश्यकता होती है. ताकि तमाम अवरोधों को कम या खत्म किया जा सके.
     
  3. आयरन की अधिकता को खत्म करना: - जाहीर है थैलेसिमिया के दौरान हमारे शरीर में आयरन की मात्रा बढ़ जाती है. इसलिए इस दौरान आपको ऐसे उपाय करने चाहिए जिससे शरीर में आयरन की कमी आए.
     
  4. शीघ्रता से चिकित्सकीय जाँच कराना: - बच्चों या टीनएजर्स में इसके लक्षण दिखाई देने पर उन्हें तत्काल चिकित्सकीय परामर्श दिलवाएँ ताकि समस्या नियंत्रण में आ सके.
     
  5. प्राथमिक चिकित्सा केंद्र: - यदि आपके आस पास अस्पताल नहीं है तो नजदीकी प्राथमिक चिकित्सा केंद्र में जाकर भी इसे दिखा सकते हैं. इसके बाद किसी अस्पताल में ले जा सकते हैं.
     
  6. रक्तदोषों की जाँच: - थैलेसिमिया के मरीजों में विभिन्न प्रकार के रक्तदोषों में वृद्धि की संभावना होती है. आपको चाहिए कि आप रक्त दोषों की उचित जाँच कराएं या चिकित्सक के परामर्श के अनुसार कदम उठाएँ.
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