Sunday, July 18, 2010

Sarcoidosis (sar-koy-DO-sis)

Sarcoidosis

Sarcoidosis (sar-koy-DO-sis) is a disease of unknown cause that leads to inflammation. It can affect various organs in the body.

Normally, your immune system defends your body against foreign or harmful substances. For example, it sends special cells to protect organs that are in danger.
These cells release chemicals that recruit other cells to isolate and destroy the harmful substance. Inflammation occurs during this process. Once the harmful substance is destroyed, the cells and the inflammation go away.
In people who have sarcoidosis, the inflammation doesn't go away. Instead, some of the immune system cells cluster to form lumps called granulomas (gran-yu-LO-mas) in various organs in your body.


Skin granulomas

Overview
Sarcoidosis can affect any organ in your body. However, it's more likely to occur in some organs than in others. The disease usually starts in the lungs, skin, and/or lymph nodes (especially the lymph nodes in your chest).
The disease also often affects the eyes and the liver. Although less common, sarcoidosis can affect the heart and brain, leading to serious complications.
If many granulomas form in an organ, they can affect how the organ works. This can cause signs and symptoms. Signs and symptoms vary depending on which organs are affected. Many people who have sarcoidosis have no symptoms or mild symptoms.

Lofgren's syndrome is a classic set of signs and symptoms that is typical in some people who have sarcoidosis. Lofgren's syndrome may cause fever, enlarged lymph nodes, arthritis (usually in the ankles), and/or erythema nodosum (er-i-THE-ma no-DO-sum).
Erythema nodosum is a rash of red or reddish-purple bumps on your ankles and shins. The rash may be warm and tender to the touch.


Treatment for sarcoidosis also varies depending on which organs are affected. Your doctor may prescribe topical treatments and/or medicines to treat the disease. Not everyone who has sarcoidosis needs treatment.
Outlook
The outcome of sarcoidosis varies. Many people recover from the disease with few or no long-term problems.
More than half of the people who have sarcoidosis have remission within 3 years of diagnosis. "Remission" means the disease isn't active, but it can return.
Two-thirds of people who have the disease have remission within 10 years of diagnosis. People who have Lofgren's syndrome usually have remission. Relapse (return of the disease) 1 or more years after remission occurs in less than 5 percent of patients.
Sarcoidosis leads to organ damage in about one-third of the people diagnosed with the disease. Damage may occur over many years and involve more than one organ. Rarely, sarcoidosis can be fatal. Death usually is the result of complications with the lungs, heart, or brain.

Poor outcomes are more likely in people who have advanced disease and show little improvement from treatment.
Certain people are at higher risk for poor outcomes from chronic (long-term) sarcoidosis. This includes people who have lung scarring, heart or brain complications, or lupus pernio (LU-pus PAR-ne-o). Lupus pernio is a serious skin condition that sarcoidosis may cause.
Research is ongoing for new and better treatments for sarcoidosis.


Bernie Mac dies of Sarcoidosis
What Causes Sarcoidosis?
The cause of sarcoidosis isn't known. More than one factor may play a role in causing the disease.
Some researchers think that sarcoidosis develops when your immune system responds to a trigger, such as bacteria, viruses, dust, or chemicals.
Normally, your immune system defends your body against foreign or harmful substances. For example, it sends special cells to protect organs that are in danger.
These cells release chemicals that recruit other cells to isolate and destroy the harmful substance. Inflammation occurs during this process. Once the harmful substance is destroyed, the cells and the inflammation go away.
In people who have sarcoidosis, the inflammation doesn't go away. Instead, some of the immune system cells cluster to form lumps called granulomas in various organs in your body.


Genetics also may play a role in sarcoidosis. Researchers believe that sarcoidosis occurs if:
You have a certain gene (or certain genes) that raise your risk for the disease
—And—
You're exposed to something that triggers your immune system
Triggers may vary depending on your genetic makeup. Certain genes may influence which organs are affected and how severe your symptoms are.
Researchers continue to try to pinpoint the genes that are linked to sarcoidosis
Who Is At Risk for Sarcoidosis?
Sarcoidosis affects people of all ages and races. However, it's more common among African Americans and Northern Europeans. In the United States, the disease affects African Americans somewhat more often and more severely than Whites.
Studies have shown that sarcoidosis tends to vary in different ethnic groups. For example, eye problems due to the disease are more common in Japanese people.


Lofgren's syndrome, a type of sarcoidosis, is more common in people of European descent. Lofgren's syndrome may involve fever, enlarged lymph nodes, arthritis (usually in the ankles), and/or erythema nodosum. Erythema nodosum is a rash of red or reddish-purple bumps on your ankles and shins. The rash may be warm and tender to the touch.
Sarcoidosis is somewhat more common in women than in men. The disease usually develops between the ages of 20 and 50.
People who have certain jobs also may be at higher risk for sarcoidosis. Examples include:
Health care workers
Elementary and secondary school teachers
People whose jobs expose them to agricultural dust, insecticides, pesticides, or mold
Suppliers of building materials, hardware, or gardening materials
Firefighters
People who have a family history of sarcoidosis also are at higher risk for the disease.
What Are the Signs and Symptoms of Sarcoidosis?
Many people who have sarcoidosis have no symptoms or mild symptoms. Often, the disease is found during achest x ray done for another reason (for example, to diagnose pneumonia).
The signs and symptoms of sarcoidosis vary depending on which organs are affected. Signs and symptoms also may vary depending on your gender, age, and ethnic background.
Common Signs and Symptoms
In both adults and children, the disease most often affects the lungs. If granulomas (inflamed lumps) form in your lungs, you may wheeze, cough, feel short of breath, or have chest pain. Or, you may have no symptoms at all.
Some people who have sarcoidosis feel very fatigued (tired), uneasy, or depressed. Night sweats and weight loss are common symptoms of the disease.
Common signs and symptoms in children are fatigue, loss of appetite, weight loss, bone and joint pain, and anemia. Children who are younger than 4 years old may have a distinct form of sarcoidosis. It may cause enlarged lymph nodes in the chest (which can be seen on a chest x ray), skin lesions, and eye swelling or redness.

Other Signs and Symptoms
Sarcoidosis may affect your lymph nodes. The disease can cause enlarged lymph nodes that feel tender. Sarcoidosis usually affects the lymph nodes in your neck and chest. However, the disease also may affect the lymph nodes under your chin, in your armpits, or in your groin.


Sarcoidosis can cause lumps, ulcers, or areas of discolored skin. They may itch, but they don't hurt. These signs tend to appear on your back, arms, legs, and scalp. Sometimes they appear near your nose or eyes. These signs usually last a long time.


Sarcoidosis may cause a more serious skin condition called lupus pernio. Disfiguring skin sores may affect your nose, nasal passages, cheeks, ears, eyelids, and fingers. These sores tend to be ongoing. They can return after treatment is over.
Sarcoidosis also can cause eye problems. If you have sarcoidosis, it's important to have an annual eye exam. If you have changes in your vision and can't see as clearly or can't see color, call 9–1–1 or have someone drive you to the emergency room.
You should call your doctor if you have any new eye symptoms, such as burning, itching, tearing, pain, or sensitivity to light.

Signs and symptoms of sarcoidosis also may include an enlarged liver, spleen, or salivary glands.
Although less common, sarcoidosis can affect the heart and brain. This can cause a number of symptoms, such as abnormal heartbeats, shortness of breath, headaches, and vision problems. If sarcoidosis affects the heart or brain, serious complications can occur.
Lofgren's Syndrome
Lofgren's syndrome is a classic set of signs and symptoms that appear in some people when they first develop sarcoidosis. Signs and symptoms may include:
Fever. This symptom only occurs in some people.
Enlarged lymph nodes (which can be seen on a chest x ray).
Arthritis, usually in the ankles. This symptom is more common in men.
Erythema nodosum. This is a rash of red or reddish-purple bumps on your ankles and shins. The rash may be warm and tender to the touch. This symptom is more common in women.


Sarcoidosis Signs and Symptoms


The illustration shows the major signs and symptoms of sarcoidosis and the organs involved.

How Is Sarcoidosis Diagnosed?
Your doctor will diagnose sarcoidosis based on your medical history, a physical exam, and the results from tests. He or she will look for granulomas (inflamed lumps) in your organs. Your doctor also will try to rule out other causes of your symptoms.
Medical History
Your doctor may ask you detailed questions about your medical history. For example, he or she may ask whether you have a family history of sarcoidosis. Your doctor also may ask whether you've had any jobs that may have raised your risk for the disease.
Your doctor also may ask whether you've ever been exposed to inhaled beryllium metal. This type of metal is used to make aircrafts and weapons. Your doctor also may want to know whether you've had contact with organic dust from birds or hay.
Exposure to these substances can cause inflamed lumps in your lungs that look like the granulomas from sarcoidosis. However, these lumps are signs of other conditions.


Physical Exam
Your doctor will examine you for signs and symptoms of sarcoidosis. Signs and symptoms may include red bumps on your skin; swollen lymph nodes; an enlarged liver, spleen, or salivary glands; or redness in your eyes. He or she will check for other causes of your symptoms.
Your doctor also may listen to your lungs and heart. Abnormal breathing and heartbeat sounds may be a sign that sarcoidosis is affecting your lungs or heart.
Diagnostic Tests
You may have tests to confirm a diagnosis and to find out how the disease is affecting you. Tests include chest x ray, lung function tests, biopsy, and other tests to assess organ damage.
Chest X Ray
A chest x ray is a painless test that creates pictures of the structures inside your chest, such as your heart and lungs. The test may show granulomas or enlarged lymph nodes in your chest. About 95 percent of people who have sarcoidosis have an abnormal chest x ray.


Lung Function Tests
Lung function tests measure the size of your lungs, how much air you can breathe in and out, how fast you can breathe air out, and how well your lungs deliver oxygen to your blood. These tests may be used to find out whether sarcoidosis is affecting your lungs.


Biopsy
Your doctor may do a biopsy to confirm a diagnosis or rule out other causes of your symptoms. A biopsy involves taking a small sample of tissue from one of your affected organs.
Usually, doctors try to biopsy the organs that are easiest to access. Examples include the skin, tear glands, or the lymph nodes that are just under the skin.
If this isn't possible, your doctor may use a positron emission tomography (PET) scan to pinpoint areas for biopsy. For this test, a small amount of a radioactive substance is injected into a vein, usually in your arm.


The substance, which releases energy, travels through the blood and collects in organs or tissues. Special cameras detect the energy and convert it into three-dimensional pictures.
If lung function tests or a chest x ray shows signs of sarcoidosis in your lungs, your doctor may do a bronchoscopy (bron-KOS-ko-pee) to get a small sample of lung tissue.
During this procedure, a thin, flexible tube is passed through your nose (or sometimes your mouth), down your throat, and into the airways to reach your lung tissue.


Other Tests To Assess Organ Damage
You also may have other tests to assess organ damage and find out whether you need treatment. For example, your doctor may recommend blood tests and/or an EKG (electrocardiogram).
Everyone who is diagnosed with sarcoidosis should see an ophthalmologist (eye specialist) for eye tests, even if they don't have eye symptoms. This is important because eye damage can occur without symptoms.
How Is Sarcoidosis Treated?
Not everyone who has sarcoidosis needs treatment. In some cases, the disease goes away on its own. Whether you need treatment and what type of treatment you need depend on your signs and symptoms, which organs are affected, and whether those organs are working well.
If the disease affects certain organs, such as your eyes, heart, or brain, you'll need treatment even if you don't have any symptoms.
In either case-whether you have symptoms or not-you should see your doctor for ongoing care. He or she will want to check to make sure that the disease isn't damaging your organs. For example, you may need lung function tests to make sure that your lungs continue to work well.
If the disease isn't worsening, your doctor may watch you closely to see whether the disease goes away on its own. If the disease does start to get worse, your doctor can prescribe treatment.
The goals of treatment are to:
Relieve symptoms
Improve organ function
Control inflammation and reduce the size of granulomas (inflamed lumps)
Prevent pulmonary fibrosis (lung scarring) if your lungs are affected
Your doctor may prescribe topical treatments and/or medicines to treat the disease.
Medicines
Prednisone
Prednisone, a type of steroid, is the main treatment for sarcoidosis. This medicine reduces inflammation. In most people, prednisone relieves symptoms within a couple of months.


Although most people need to take prednisone for 12 months or longer, your doctor may lower the dose within a few months after you start the medicine.
Long-term use of prednisone, especially at high doses, can cause serious side effects. Work with your doctor to decide whether the benefits of this medicine outweigh the risks. If your doctor prescribes this treatment, he or she will find the lowest dose that controls your disease.
When you stop taking prednisone, you should cut back slowly (as your doctor advises). This will help prevent flareups of sarcoidosis. Cutting back slowly also allows your body to adjust to not having the medicine.
If a relapse or flareup occurs after you stop taking prednisone, you may need a second round of treatment. If you remain stable for more than 1 year after stopping this treatment, the risk of relapse is low.
Other Medicines
Other medicines, besides prednisone, also are used to treat sarcoidosis. Examples include:
Hydroxychloroquine. This medicine works best for treating sarcoidosis that affects the skin or brain. Your doctor also may prescribe this medicine if you have a high level of calcium in your blood due to sarcoidosis.
Methotrexate. This medicine works best for treating sarcoidosis that affects your lungs, eyes, skin, or joints.


Your doctor may prescribe these medicines if your sarcoidosis worsens while you're taking prednisone or if you can't handle prednisone's side effects.
If you have Lofgren's syndrome with pain or fever, your doctor may prescribe nonsteroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen.
If you're wheezing and coughing, you may need inhaled medicine to help open your airways. You take inhaled medicine using an inhaler. This device allows the medicine to go right to your lungs.
Ongoing Research
Researchers continue to look for new and better treatments for sarcoidosis. They're currently studying treatments aimed at the immune system. Researchers also are studying antibiotics as a possible treatment for sarcoidosis that affects the skin.
Living With Sarcoidosis
Sarcoidosis has no cure. However, you can take steps to manage the disease. Get ongoing care and follow a healthy lifestyle. Talk to your doctor if you’re pregnant or planning a pregnancy.


Ongoing Care
Getting ongoing care is important, even if you don't take medicine for your sarcoidosis. New symptoms can occur at any time. Also, the disease can slowly worsen without your noticing.
How often you need to see your doctor will depend on how severe your symptoms are, which organs are affected, what treatments you're using, and whether you have any side effects from treatments. Even if you don’t have symptoms, you should see your doctor for ongoing care.
Your doctor may recommend routine tests, such as lung function tests and eye exams. He or she will want to check to make sure that the disease isn’t damaging your organs.
Discuss with your doctor how often you need to have followup visits. You may have some followup visits with your primary care doctor and others with one or more specialists.
Lifestyle Changes
Making lifestyle changes can help you manage your health. For example, follow a healthy diet and be as physically active as you can. A healthy diet includes a variety of fruits, vegetables, and whole grains.
It also includes lean meats, poultry, fish, beans, and fat-free or low-fat milk or milk products. A healthy diet is low in saturated fat, trans fat, cholesterol, sodium (salt), and added sugar.
If you smoke, quit. Talk to your doctor about program and products that can help you quit. Also, try to avoid other lung irritants, such as dust, chemicals, and secondhand smoke.
Emotional Issues
Living with a chronic disease may cause fear, anxiety, depression, and stress. It’s important to talk about how you feel with your health care team. Talking to a professional counselor also can help. If you’re feeling very depressed, your health care team or counselor may prescribe medicines to make you feel better.
Joining a patient support group may help you adjust to living with sarcoidosis. You can see how other people who have the disease have coped with it. Talk to your doctor about local support groups or check with an area medical center.
Support from family and friends also can help relieve stress and anxiety. Let your loved ones know how you feel and what they can do to help you.


Pregnancy
Many women who have sarcoidosis give birth to healthy babies. Women who have severe sarcoidosis, especially if they’re older, may have trouble becoming pregnant. In some cases, sarcoidosis may get worse after the baby is delivered.
If you have sarcoidosis and are pregnant or planning a pregnancy, talk to your doctor about the risks. Also, if you become pregnant, it’s important to get good prenatal care and regular sarcoidosis checkups during and after pregnancy.
Some sarcoidosis medicines are considered safe to use during pregnancy; others are not recommended.
Life style change can stop Sarcoidosis !


Sarcoidosis takes its name from the Greek words, sarx, meaning "flesh" and osis, meaning "condition." Hence, sarcoidosis is nothing but a flesh (skin) condition and as I have always said, any disease or condition of the flesh is a blood disorder, for as the Bible states in Leviticus 17:11 "for the life of the flesh is in the blood." Said another way, the condition of the flesh is manifested in the blood and the condition of the blood is manifested in the skin.
Clearly, sarcoidosis affects the glands, the inner and outer skin, and the lymphatic system.
Sarcoidosis is a degenerative disease and is therefore due to improper diet. A degenerative disease is a preventable and reversible disease.
People with sarcoidosis, such as actor Bernie Mac and actress Tisha Campbell, suffer from TOXIC BLOOD and MUCOIDAL OBSTUCTION of the lymphatic system and mucous membranes (internal skin). While most of us suffer from toxic blood and mucus or mucoidal obstruction also, everybody's body is different and our diseases manifest differently and in areas where we have weak or deficient energy.

Tisha Campbell-Martin American actress and singer

So Western medical doctors may call the disease sarcoidosis, but in reality it's nothing but a skin condition predicated upon obstruction of the mucous membranes and lymphatic system.
Sarcoidosis can be reversed by first modifying the diet. Meat, dairy and simple starches should be greatly reduced if not outright eliminated from the diet (which is greatly recommended).
Junk foods (refined grains/pastries, soda pop, candy and chocolate, processed food stuffs, coffee, alcohol and beer, etc.) should be entirely eliminated.
Next, the blood should be purified. The first initial step in purifying the blood is by detoxifying your whole body. When you cleanse your blood you automatically cleanse your lymphatic fluid.
However, since the blood and lymph fluid run or travel in opposite directions but are adjacent to one another, I prefer to deal with them together or congruently with certain herbs that have an affinity for these vital fluids.
The human body actually has three times the amount of blood in lymphatic fluid. Yes, we have more lymph fluid than blood in our bodies. The ration is 3 to 1. However, whereas the blood circulates ten times per minute, the lymph only circulates once a day. Based upon this, I think we will all concur that our lymphatic circulation is greatly stagnant and obstructed.
Lymphatic (and blood) stagnation and impurity can be reversed with herbs.


Herbs that cleanse, strengthen, revitalize and nourish the lymphatic system and lymph fluid include
OCTILLO, LOBELIA, MULLEIN LEAVES, GOLDENSEAL ROOT, ECHINACEA ROOT, CLEAVERS, RED ROOT, BURDOCK ROOT, and WILD INDIGO.
Blood purifying, building, nourishing, revitalizing, and strengthening herbs include
STRAWBERRY LEAF, BURDOCK ROOT, DANDELION ROOT, YELLOW DOCK ROOT, CAPSICUM (CAYENNE) FRUIT, NETTLE LEAF, OREGON GRAPE, MANJISTHA, ALMA (AMALAKI FRUIT), CRANSEBILL, ECHINACEA ROOT, CERASEE, ELDER BERRIES, BAY BERRIE, and GOLDENSEAL ROOT.


The glandular system also needs working on and the following herbs greatly help the glandular or endocrine system –
SARSAPARILLA, LICORICE ROOT, KELP, MACA and GINSENG (all varieties).
The mucous membranes also need attention in cases of sarcoidosis. Herbs that are beneficial and healing for the mucous membranes include
MULLEIN LEAVES, MARSHMALLOW (ALTHEA), LOBELIA, RED RASPBERRY, SLIPPERY ELM BARK, and IRISH MOSS
People suffering from sarcoidosis would be amazed at what happens with the constant cleansing and purifying of the body, especially the blood. By converting to a mostly vegan-vegetarian diet and consuming vast amounts of green foods (green, leafy vegetables) and fruit, the body would alkalize and greatly speed up the healing of its internal organs.
Alkalizing baths consisting of sea salt (one whole box or package added to the water) proves very therapeutic in cases of sarcoidosis.
Putting more oxygen into the body via ozone or oxygen baths and/or liquid oxygen drops would also help to cleanse and alkalize the body, greatly enhancing the natural healing effect of the body.
Elimination of meat (dead, slaughtered animal flesh) and dairy products (liquefied cow snot and pus) would prove most beneficial in healing of sarcoidosis.
Remember, since sarcoidosis is a flesh disease or condition, a flesh condition is nothing but a blood condition. A blood condition usually represents or denotes toxicity so with the cleansing of blood automatically comes the cleansing of the organs. Plain and simple!


Contrary to what you have been told and/or irregardless of what you may think, sarcoidosis is 100% healable. You do not have to live out your entire life with this insidious disease, unless you choose to do so, which would be unwise, very unwise.
Key Points
Sarcoidosis is a disease of unknown cause that leads to inflammation. It can affect various organs in the body.
Sarcoidosis is more likely to occur in some organs than in others. The disease usually starts in the lungs, skin, and/or lymph nodes (especially the lymph nodes in your chest). The disease also often affects the eyes and the liver.
In people who have sarcoidosis, immune system cells cause inflammation and cluster to form lumps called granulomas.
If many granulomas form in an organ, they can affect how the organ works. This can cause signs and symptoms. Signs and symptoms vary depending on which organs are affected. Many people who have sarcoidosis have no symptoms or mild symptoms.
Some researchers think that sarcoidosis develops when your immune system responds to a trigger, such as bacteria, viruses, dust, or chemicals. Genetics also may play a role in sarcoidosis.
Sarcoidosis affects people of all ages and races. In the United States, the disease affects African Americans somewhat more often and more severely than Whites. The disease also is slightly more common in women than in men. It usually develops between the ages of 20 and 50.
In both adults and children, the disease most often affects the lungs. If granulomas form in your lungs, you may wheeze, cough, feel short of breath, or have chest pain. Some people who have sarcoidosis feel very fatigued (tired), uneasy, or depressed. Night sweats and weight loss are common symptoms of the disease.
Lofgren's syndrome is a classic set of signs and symptoms that appear in some people when they first develop sarcoidosis. Signs and symptoms may include fever, enlarged lymph nodes, arthritis, and erythema nodosum (a rash of red or reddish-purple bumps on your ankles).
Your doctor will diagnose sarcoidosis based on your medical history, a physical exam, and the results from tests. He or she will look for granulomas (inflamed lumps) in your organs. Your doctor also will try to rule out other causes of your symptoms.
Whether you need treatment and what type of treatment you need depend on your signs and symptoms, which organs are affected, and whether those organs are working well.
Your doctor may prescribe topical treatments and/or medicines to treat the disease. Not everyone who has sarcoidosis needs treatment. In some cases, the disease goes away on its own.
If the disease affects certain organs, such as your eyes, heart, or brain, you may need treatment even if you don't have any symptoms.
Sarcoidosis has no cure. However, you can take steps to manage the disease. Get ongoing care and follow a healthy lifestyle. Talk to your doctor if you're pregnant or planning a pregnancy.
Getting ongoing care is important, even if you don't take medicine for your sarcoidosis. New symptoms can occur at any time. Also, your condition can slowly worsen without your noticing.
The outcome of sarcoidosis varies. Many people recover from the disease with few or no long-term problems.
Rarely, sarcoidosis can be fatal. Death usually is the result of complications with the lungs, heart, or brain. Poor outcomes are more likely in people who have advanced disease and show little improvement from treatment.
Chinese herbs can play a big role for healing Sarcoidosis

Wednesday, January 27, 2010

Anemia .. different types & how to treat

What is Anemia?


Anemia is a condition where there is an abnormally low number of red blood cells circulating in the body. It is the most common disorder of the red blood cells, affecting about 3.5 million Americans.


Anemia is not a disease. It is a condition that results from below-normal levels of hemoglobin in the red blood cells. Hemoglobin is the iron-containing pigment of the red blood cells that carries oxygen from the lungs to the tissues.


There are many different kinds of anemia, each with its own cause. For example, a poor diet can cause anemia. The more severe types of this condition are often inherited.
Why Does Anemia Occur?
To understand why anemia occurs, it's important to understand the function of blood itself. Blood is a mixture of plasma (the fluid part of the blood) and cells. Its red color comes from the predominant cells found in the blood, called erythrocytes.

A healthy person has about 5 million red cells in every cubic millimeter of blood. Each cell contains a protein (hemoglobin) that carries oxygen through the body.
The process of creating and recycling red blood cells is exceptionally complex. Trouble can occur at any point in this process. If the red blood cells fail to effectively transport oxygen throughout the body, anemia can result.

Facts About Anemia

The word anemia is Greek for "without blood."
Anemia is a common problem for menstruating women because their iron supplies are depleted monthly.

In young children, marrow in all the bones produces red blood cells. As a person ages, red blood cells are eventually produced only in the marrow of the spine, ribs, and pelvis.
The life span of a red blood cell is between 90 and 120 days.
Old red blood cells are removed from the blood by the liver and spleen, and the iron is returned to the bone marrow to make new cells.

A person with anemia will feel tired and weak because the body's tissues are being starved of oxygen. In fact, fatigue is the main symptom of most types of anemia. The severity of symptoms is in part related to the severity of anemia. Mild anemia can occur without symptoms and may be detected only during a medical exam that includes a blood test.

What Are The Symptoms Of Anemia?



Symptoms of anemia include:
. Fatigue
. Weakness
. Fainting
. Breathlessness
. Heart palpitations (rapid or irregular beating)
. Dizziness
. Headache
. Ringing in the ears (tinnitus)
. Difficulty sleeping
. Difficulty concentrating

Common signs include:

. Pale complexion
. The normally red lining of the mouth and eyelids fades in color
Rapid heartbeat (tachycardia)
. Abnormal menstruation (either absence of periods or increased bleeding)

. Other signs depend on the cause of the anemia. These can include spoon-shaped finger nails and toenails in iron-deficiency anemia, mild jaundice in hemolytic anemias, and leg ulcers in sickle cell anemia .


What Causes Anemia?

There are three general causes of anemia:

. Decreased red cell production by the bone marrow
. Increased red cell destruction, or hemolysis
. Blood loss from heavy menstrual periods or internal bleeding

When you're anemic, your body either produces too few healthy red blood cells, or destroys them faster than they can be replaced or loses too many of them. If your diet lacks certain vitamins and minerals, the production of hemoglobin can slow down.

Types of anemia caused by decreases in red cell production include iron deficiency anemia and vitamin deficient anemia.

If something in the body destroys or attacks red blood cells, the bone marrow tries to produce more blood. If the destruction of red blood cells is rapid, the marrow can't catch up. This problem is often inherited. The resulting anemia is called hemolytic anemia.


Hemolytic Anemia

A severe bleeding episode can result in temporary anemia until the body has had time to make up the blood that was lost. But even small, persistent losses of blood may cause anemia if you have a poor diet. A healthy person whose diet contains plenty of iron and vitamins can produce large amounts of new blood, reducing the risk of anemia

The Different Kinds Of Anemia
There are different kinds of anemia. Some forms of this condition are inherited, while others are brought on by poor nutrition.

Iron Deficiency Anemia
The body needs iron to produce the hemoglobin necessary for red blood cell production. In general, most people need just 1 milligram of iron daily. Menstruating women need double that dose.

Vitamin Deficiency Anemias
Vitamin B-12 is also essential in hemoglobin production. Normally, a chemical secreted by the stomach helps the body absorbs this vitamin. However, some people can't readily absorb B-12. The result is B-12 deficiency (pernicious anemia). Because the symptoms develop gradually this condition may not be immediately recognized. Those with thyroid disease or diabetes mellitus are at increased risk for this type of anemia. The condition occurs most often in 40- to 80-year-old northern Europeans with fair skin.

A lack of folic acid, another one of the B vitamins, can also lead to anemia. Folic acid deficiency is a particular problem for alcoholics.



Food rich in iron and vitamins

Hemolytic Anemias
Anemia caused by the premature destruction of red blood cells is known as hemolytic anemia. In this type of anemia, antibodies produced by the immune system damage red blood cells. This condition is sometimes associated with disorders such as systemic lupus, or lymphoma.

Toxic materials such as lead, copper, and benzene can also cause the destruction of red blood cells.

Blood transfusions may be necessary for some people with this kind of anemia. Hemolytic anemia can be acquired or inherited. Sickle cell disease and thalassemia are both inherited types of hemolytic anemia.

Sickle Cell Anemia


Sickle cell anemia is also known as Hemoglobin S disease. This is a serious, life-threatening inherited form of anemia. Persons with this disease have sickle-shaped red blood cells that are stiff and unable to squeeze through blood vessels.
Persons with this disease often suffer from pain in the joints and bones. Infections and heart failure can also occur.
The disease occurs in just 0.6 percent of the population, usually in African Americans.
Thalassemia
This is a group of anemias due to the defects in the genes producing hemoglobin. It is most common in people of Mediterranean descent. There are two major forms: thalassemia minor and thalassemia major.

As its name implies, thalassemia minor is mild and those suffering from this condition go on to live a full life. Treatment is often unnecessary. Thalassemia major can be serious, but it is very rare. Transfusions or bone marrow transplants are usually required. Thalassemia major is also called Cooley's anemia, named after the doctor who first described it in 1925.
Aplastic Anemia
This is one of the deadliest and most rare forms of anemia. Only two to six people per million have this type of anemia. The condition results from an unexplained failure of the bone marrow to produce all types of blood cells. Instead, fat cells replace bone marrow.
Aplastic anemia is usually found in adolescents and young adults. Symptoms can include bleeding in the mucous membranes. Chemicals such as benzene and certain pesticides can also cause this type of anemia.


Favism, G6PD Deficiency, Fava Beans and Legumes



What is Favism?

Favism describes the susceptibility to, and clinical presentation of, acute haemolytic crises as a consequence of eating broad beans in a subgroup of patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency. It can be potentially life-threatening. Broad beans are derived from the plant Vicia fava, hence the condition's name. Susceptible patients may also experience the syndrome when exposed to the plant's pollen.


Favism is associated with some severe variants of G6PD Deficiency. It is called favism because the consumption of broad beans, sometimes called fava beans, causes. oxidative stress and hemolytic anemia In some cases eating any legume causes some degree of hemolysis.
The exact relationship between Favism and G6PD Deficiency is not known. Broad Beans (Fava Beans) contain vicine, divicine, convicine and isouramil, all of which are oxidants.


The condition had been thought to occur only in the Mediterranean variety of G6PD deficiency. However, there have been reports of the condition affecting children in Hong Kong, Thailand and Iran. This reflects common ancestry among populations in different parts of the world due to migration as well as the large number of genetic polymorphisms that constitute the variable alleles causing G6PD deficiency.

G6PD is crucial in maintaining red cell homeostasis and its deficiency leads to increased susceptibility to haemolysis induced by drugs, infections and substances in food. There are a huge number of polymorphisms of the gene with variable effects on the activity of the enzyme and a wide range of phenotypic susceptibility to haemolysis.


The gene for G6PD is located on the X-chromosome hence it is an X-linked inherited disease that primarily affects men. It can have clinical effects in homozygous women and a proportion of female heterozygous carriers.It is thought that the susceptibility to favism is determined by a combination of the particular G6PD polymorphism (predominantly the Mediterranean form), and by variability in other enzymatic mechanisms, particularly in the metabolism of L-DOPA (found in abundance in broad beans), and vicine, convicine and isouramil (the so-called 'anti-nutritional factors' that are present in broad beans)

Epidemiology

· G6PD deficiency is the commonest enzymopathy of man of clinical significance. It is thought to affect more than 400 million people worldwide.
· The highest prevalence of G6PD deficiency is found in tropical Africa, the Middle East, tropical and subtropical Asia, Papua New Guinea and various Mediterranean locations.
· Only a proportion of G6PD sufferers are prone to favism, and this proportion is variable between populations. A study in Sardinia, where there is a high prevalence of G6PD deficiency (7.5% of all males) found 508 cases of favism over a 9-year period. In a Thai study, favism was found in 3.6% of G6PD-deficient children. It therefore appears to be a relatively rare manifestation of a common genetic polymorphism.
Presentation

· There may be a past history of episodes of neonatal or childhood jaundice.
· A dietary history may reveal recent ingestion of broad beans.
· Check for recent medication changes or history consistent with infection.



Favism leads to acute, massive intravascular haemolysis. Its main clinical features are:

· Acute back and/or abdominal pain
· Acute pallor due to anaemia
· Haemoglobinuria causing the passage of dark or orangey-yellow urine
· Jaundice
· Patients with G6PD deficiency are prone to gallstones and splenomegaly due to recurrent, often subclinical, episodes of haemolysis.
Differential diagnosis

· Acute haemolysis caused by an alternative precipitant in G6PD sufferer (e.g. drugs – particularly antimalarials' infection)
· Sickle cell anaemia and crisis
· Exacerbation of other haemolytic anaemias, e.g. hereditary spherocytosis, autoimmune haemolytic anaemia
·
Disseminated intravascular coagulation
·
Systemic lupus erythematosus
Investigations

· Dipstick urine to reveal evidence of haemoglobinuria.
· FBC will show acute haemolytic anaemia picture with low haemoglobin.
· Reticulocyte count may be elevated (although often normal in early acute phase).
· Raised indirect bilirubin (unconjugated) indicating haemolysis.
· LFTs usually normal.
· Serum lactate dehydrogenase may be elevated, indicating haemolysis.
· Serum haptoglobins may be low, indicating haemolysis.
· Abdominal ultrasound may be used to detect gallstones and/or splenomegaly.
· Coombs' test is negative.
· G6PD activity assay in undiagnosed cases – may be normal if there is significant reticulocytosis as reticulocytes are rich in the enzyme; assay may need to be repeated in convalescent phase.


Associated diseases

· Glucose-6-phosphate dehydrogenase deficiency
· Gallstones due to chronic haemolysis
· Splenomegaly due to chronic haemolysis.

Management

· Avoid further ingestion of broad beans
· Folic acid supplementation
· Iron supplementation if ongoing acute severe intravascular haemolysis
· Oxygen therapy
· Bed rest and transfer to a high care/intensive care setting
· Intravenous fluids to reduce chance of acute oliguric renal impairment
· Blood transfusion or exchange transfusion sometimes needed to treat severe anaemia

Complications
· Death due to acute severe haemolytic anaemia (relatively rare)
· Ophthalmological damage due to intra-ocular intravascular haemolysis
· Acute renal failure
· Susceptibility to infection

Prognosis

This is variable depending on the degree of susceptibility to favism, quantity of beans ingested and access to acute medical care. Most cases do well with supportive care but there is significant morbidity and some mortality associated with the disease.

Prevention

· Avoidance of ingestion of broad beans in patients known to be G6PD deficient, or who have suffered previous episodes of favism.
· Genetic counselling and screening may be useful where there is a family history of G6PD deficiency, to allow diagnosis before exposure to haemolytic precipitants.
· Population screening and health education programs in areas of high prevalence of G6PD deficiency have been shown to reduce the incidence of favism in the at-risk population.

Herbs to treat G6PD Deficiency anemia
Chinese herbal doctors have reported some successful applications of using herbal combinations. During observation on patients receiving treatment with herbal remedy, all patients were judged as healing (full recovery and symptom free).

The most powerful feature of Traditional Chinese Medicine is that it allows you to easily combine multiple ingredients to form a recipe to suit the specific need of individual. The list below are to give you an idea of why you can get the herbal remedy best for you.

When you choose a herbal remedy there are two important things among your concerns: a good recipe and a correct way to cook it. A good recipe is half the good results.

Some Herbs are good for G6PD Deficiency anemia

Rhizoma Ligustici Chuanxiong
Radix Salviae Miltiorrhizae
Radix Angelicae Sinensis
Radix Codonopsis Pilosulae
How Is Anemia Diagnosed?
Anemia can be detected by a simple blood test. Most causes can be diagnosed by analysis of blood samples and by examination of the blood cells under a microscope.
A complete blood count test is always performed. The red blood cells and their iron-bearing protein, hemoglobin, are measured. The percentage of red blood cells in the blood is called a hematocrit.

A blood smear will determine the size, shape, and color of the blood cells. The shape of the red blood cells can be distorted in many blood disorders, such as sickle cell anemia.

Normal red blood cells (1) and abnormal sickle shape red blood cells (2)

Iron deficiency anemia is suspected when the red cells are low in number and unusually small. Measuring the amount of iron and its associated proteins in the blood can confirm this diagnosis.
Those with vitamin deficiency anemias have larger-than-normal red blood cells.

In some cases, a bone marrow biopsy may be necessary to confirm a diagnosis. A sample of bone marrow is removed from the back of the pelvic bone or from the breastbone. This sample allows physicians to determine the overall activity of the marrow and whether abnormal cells, such as cancer cells, are interfering with its function.

Other tests that may be needed include chemical examination of the stool for traces of blood, x-rays of the bowel to detect the presence of internal bleeding and examination of the small bowel lining to access its ability to absorb food normally.

How Is Anemia Treated?
The treatment for anemia depends on the type and cause.Iron deficiency anemia is treated with iron (ferrous sulphate) supplements, initially taken three times a day. If nausea, stomach cramps, diarrhea or constipation occur, the medication may be taken with a little bit of food.

Treatment should be continued for three to six months in order for the body to fully replenish its iron supply. As long as excessive bleeding is not present and there are no other complicating factors, the anemia will be corrected within a few weeks. However, if the iron deficiency is caused by blood loss that is not due to menstruation, the source of bleeding must be found and stopped. This may require surgery


ferrous sulphate

Pernicious anemia, or vitamin B-12 deficiency, is treated by a life-long course of intramuscular injections of B-12. Persons with this type of anemia receive a shot of B-12 several times a week when first diagnosed. The treatment may continue for life, with one shot about four times a year.
Folic acid deficiency anemia can be corrected by taking folic acid supplements once a day.


Hereditary hemolytic anemias, such as thalassemia is treated by first eliminating any existing infections and avoiding medications that suppress the body's immune system. These medications may attack red blood cells. In addition, persons with these types of anemia may require regular blood transfusions.

Sickle cell anemia patients may be given oxygen, oral and intravenous fluids and pain-killing drugs to reduce pain and prevent complications. Antibiotics are commonly prescribed as well. Sufferers will need blood transfusions when the anemia becomes severe or if misshapen hemoglobin needs to be replaced. In some cases, a bone marrow transplant may be effective. Adult patients may be treated with the cancer drug hydroxyurea (brand names Droxia, Hydrea).


Sometimes rare aplastic anemias and autoimmune hemolytic anemias will respond to steroids. Failure to respond to steroids may require removal of the spleen which can become enlarged with defective red blood cells. Aplastic anemias may require blood transfusions and medications to fight infections.

Most common symptoms of anemia

Other treatment options may be appropriate based on the cause of the anemia.
For instance, if the bone marrow has failed because of leukemia, intensive chemotherapy may be required. Bone marrow transplantation may be contemplated if a suitable donor exists.
With proper treatment, many types of anemia can be eliminated, especially those caused by iron deficiency and vitamin deficiency.


Good food for anemia

Need To Know:
Most cases of anemia are mild. Without treatment, however, serious problems can occur, since the reduction in red blood cells decreases the ability to absorb oxygen from the lungs.
Certain inherited forms of anemia, including thalassemia major, pernicious anemia, and sickle cell anemia can be life threatening.
You should never self-diagnose yourself with anemia. The symptoms of fatigue and weakness can be the result of many other diseases. If you suspect you have anemia, contact your doctor.

Typical tongue in case of vitamin B12 deficiency anemia

Putting It All Together
Here is a summary of the important facts and information related to anemia.

. Anemia affects about 400 millions around the world and making it the most common blood disorder in the U.S. where 3.5 million American already affected
. Anemia is the result of below-normal levels of hemoglobin in the red blood cells.
. There are many different kinds of anemia ranging from mild and easily treatable iron and, vitamin deficiency anemias to serious, and sometimes life-threatening aplastic and sickle cell anemias.
. Fatigue is the main symptom of most anemias.
. Anemia can be usually be detected with a simple blood test.
. Treatment of anemia is based on the cause of the disorder. Treatments range from folic acid or vitamin supplements in mild cases to bone marrow transplants in severe cases.
. You should never self-diagnose anemia. Symptoms of fatigue and weakness can be the result of many other diseases. If you suspect you have anemia, consult your doctor.

Medical laboratory is the place you can diagnose the anemia