Categories
Ailmemts & Remedies

Listeriosis

Definition:
Listeriosis is a bacterial infection caused by a Gram-positive, motile bacterium, Listeria monocytogenes,which is often found in soil and is present in most animals. It’s transmitted to humans through contaminated food.

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Healthy people rarely become ill from listeria infection, but the disease can be fatal to unborn babies and newborns. People who have weakened immune systems are also at higher risk of life-threatening complications. Prompt antibiotic treatment can help curb the effects of listeria infection.

Listeria bacteria can survive refrigeration and even freezing. That’s why people who are at higher risk for serious infections should avoid eating the types of food most likely to contain listeria bacteria.

The symptoms of listeriosis usually last 7–10 days. The most common symptoms are fever and muscle aches and vomiting. Nausea and diarrhea are less common symptoms. If the infection spreads to the nervous system it can cause meningitis, an infection of the covering of the brain and spinal cord. Symptoms of meningitis are headache, stiff neck, confusion, loss of balance, and convulsions

Symptoms:
If you develop a listeria infection, you may experience:

*Fever
*Muscle aches
*Nausea
*Diarrhea
*Loss of appetite
*Lethargy
*Jaundice
*Vomiting
*Respiratory distress (usually pneumonia)
*Shock
*Skin rash
*Increased pressure inside the skull (due to meningitis) possibly causing suture separation

Symptoms may begin a few days after you’ve eaten contaminated food, but it may take as long as two months before the first signs and symptoms of infection begin.

If the listeria infection spreads to your nervous system, signs and symptoms may include:

*Headache
*Stiff neck
*Confusion or changes in alertness
*Loss of balance
*Convulsions

Symptoms during pregnancy and for newborns ;

During pregnancy, a listeria infection is likely to cause only mild signs and symptoms in the mother. The consequences for the baby, however, may be devastating. The baby may die unexpectedly before birth or experience a life-threatening infection within the first few days after birth.

As in adults, the signs and symptoms of a listeria infection in a newborn can be subtle, but may include:

*Little interest in feeding
*Irritability
*Fever
*Vomiting

Causes:
Listeria bacteria can be found in soil, water and animal feces. Humans typically are infected by consuming:

*Raw vegetables that have been contaminated from the soil or from contaminated manure used as fertilizer

*Infected meat

*Unpasteurized milk or foods made with unpasteurized milk

*Certain processed foods — such as soft cheeses, hot dogs and deli meats that have been contaminated after processing

*Prepacked salads (unless they’re thoroughly washed)

*Pâté made from meat, fish or vegetables

*Blue-veined or mould-ripened cheeses

*Soft-whip ice cream from ice-cream machines

*Precooked poultry and cook-chill meals (unless thoroughly reheated)

*Poor food hygiene and storage practices also increase the risk of someone developing listeriosis

Unborn babies can contract a listeria infection from the mother via the placenta. Breast-feeding is not considered a potential cause of infection.

Risk Factors:
Pregnant women and people who have weak immune systems are at highest risk of contracting a listeria infection.

Pregnant women and their babies
Pregnant women are significantly more susceptible to listeria infections than are other healthy adults. Although a listeria infection may cause only a mild illness in the mother, consequences for the baby may include:


*Miscarriage
*Stillbirth
*Premature birth
*A potentially fatal infection after birth

People who have weak immune systems
This category includes people who:

*Are over 60
*Have AIDS
*Are undergoing chemotherapy
*Have diabetes or kidney disease
*Take high-dose prednisone or certain rheumatoid arthritis drugs
*Take medications to block rejection of a transplanted organ

Complications:
Most listeria infections are so mild they may go unnoticed. However, in some cases, a listeria infection can lead to life-threatening complications — including:

*A generalized blood infection (septicemia)

*Inflammation of the membranes and fluid surrounding the brain (meningitis)

Complications of a listeria infection may be most severe for an unborn baby. Early in pregnancy, a listeria infection may lead to miscarriage. Later in pregnancy, a listeria infection may lead to stillbirth, premature birth or a potentially fatal infection in the baby after birth — even if the mother becomes only mildly ill.

Diagnosis;
In CNS infection cases, L. monocytogenes can often be cultured from the blood, and always cultured from the CSF. There are no reliable serological or stool tests.

Treatment:
Bacteremia should be treated for 2 weeks, meningitis for 3 weeks, and brain abscess for at least 6 weeks. Ampicillin generally is considered antibiotic of choice; gentamicin is added frequently for its synergistic effects.

Prognosis:
Listeriosis in a fetus or infant results in a poor outcome with a high death rate. Healthy older children and adults have a lower death rate.Overall mortality rate is 20–30%; of all pregnancy-related cases, 22% resulted in fetal loss or neonatal death, but mothers usually survive

Prevention:
The main means of prevention is through the promotion of safe handling, cooking and consumption of food. This includes washing raw vegetables and cooking raw food thoroughly, as well as reheating leftover or ready-to-eat foods like hot dogs until steaming hot.

Another aspect of prevention is advising high-risk groups such as pregnant women and immunocompromised patients to avoid unpasteurized pâtés and foods such as soft cheeses like feta, Brie, Camembert cheese, and bleu. Cream cheeses, yogurt, and cottage cheese are considered safe. In the United Kingdom, advice along these lines from the Chief Medical Officer posted in maternity clinics led to a sharp decline in cases of listeriosis in pregnancy in the late 1980s

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose

Resources:
http://www.bbc.co.uk/health/physical_health/conditions/listeriosis.shtml
http://www.nlm.nih.gov/medlineplus/ency/article/001380.htm
http://www.mayoclinic.com/health/listeria-infection/DS00963/DSECTION
http://en.wikipedia.org/wiki/Listeriosis

http://abbybatchelder.com/blog/2009/03/02/is-it-safe-to-eat-deli-meats-and-hot-dogs-during-pregnancy/

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Ailmemts & Remedies

Kidney transplant

Introduction:
A kidney transplant is an operation that places a healthy kidney in your body. The transplanted kidney takes over the work of the two kidneys that failed, and you no longer need dialysis.

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During a transplant, the surgeon places the new kidney in your lower abdomen and connects the artery and vein of the new kidney to your artery and vein. Often, the new kidney will start making urine as soon as your blood starts flowing through it. But sometimes it takes a few weeks to start working.

If you have advanced and permanent kidney failure, kidney transplantation may be the treatment option that allows you to live much like you lived before your kidneys failed. Since the 1950s, when the first kidney transplants were performed, much has been learned about how to prevent rejection and minimize the side effects of medicines.

But transplantation is not a cure; it’s an ongoing treatment that requires you to take medicines for the rest of your life. And the wait for a donated kidney can be years long.

Many transplanted kidneys come from donors who have died. Some come from a living family member. The wait for a new kidney can be long. People who have transplants must take drugs to keep their body from rejecting the new kidney for the rest of their lives.

A successful transplant takes a coordinated effort from your whole health care team, including your nephrologist, transplant surgeon, transplant coordinator, pharmacist, dietitian, and social worker. But the most important members of your health care team are you and your family. By learning about your treatment, you can work with your health care team to give yourself the best possible results, and you can lead a full, active life.

Around 40 per cent of patients with end-stage renal failure (ESRF) need a transplant which frees people from the need for dialysis treatments.

A successful kidney transplant has ten times the function of dialysis (for example ten times the ability to remove toxins and extra water from the blood). It means that transplant patients have a better quality of life, with more energy than they did on dialysis.

How transplants work:-
An assessment is necessary to determine whether your body will accept an available kidney. This may require several visits over four to six months, and all potential recipients must be healthy enough for surgery.

Although there is no age limit, few units will transplant patients over 70 years – unless very fit.

If a family member, partner or friend wants to donate a kidney, they will need to be evaluated for general health too.

If there is no potential living donor, you will need to register with hospital and be put on a national waiting list to receive a kidney from a deceased donor. but this varies considerably around the country. Kidneys can also be donated by strangers.

If there is a suitable living donor, the operation can be scheduled in advance, when it suits both sides. If you’re on a waiting list for a deceased donor kidney, as soon as it becomes available, you must go to the hospital quickly – where a test is carried out to check the kidney won’t be rejected. If it’s suitable, the transplant can proceed. The operation usually takes three to four hours.

A surgeon places the new kidney inside your lower abdomen and connects the artery and vein of the new kidney to your artery and vein. Your blood flows through the new kidney, which makes urine, just like your own kidneys did when they were healthy. Unless they are causing infection or high blood pressure, your own kidneys are left in place.

During the operation, the transplant kidney is inserted into the lower abdomen and connected to an artery and vein (to the leg). The blood flows through the new kidney, which makes urine, just like the old kidneys did when they were healthy. The old kidneys are usually left in place.

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Often the new kidney will start making urine as soon as blood starts flowing through it, but about one third of patients will require dialysis for around a week. Most patients leave hospital two weeks after the operation.

To prevent the immune system from seeing the new kidney as foreign and rejecting it, you’ll have to take drugs that turn off (or suppress) your immune response (immunosupressants). It’s important to understand the instructions for taking these medicines before leaving hospital, as missing the tablets for just 24 hours can cause rejection and the loss of the kidney.

Recovery From Surgery:-
As after any major surgery, you’ll probably feel sore and groggy when you wake up. However, many transplant recipients report feeling much better immediately after surgery. Even if you wake up feeling great, you’ll need to stay in the hospital for about a week to recover from surgery, and longer if you have any complications.

Posttransplant Care:-
Your body’s immune system is designed to keep you healthy by sensing “foreign invaders,” such as bacteria, and rejecting them. But your immune system will also sense that your new kidney is foreign. To keep your body from rejecting it, you’ll have to take drugs that turn off, or suppress, your immune response. You may have to take two or more of these immunosuppressant medicines, as well as medications to treat other health problems. Your health care team will help you learn what each pill is for and when to take it. Be sure that you understand the instructions for taking your medicines before you leave the hospital.

If you’ve been on hemodialysis, you’ll find that your posttransplant diet is much less restrictive. You can drink more fluids and eat many of the fruits and vegetables you were previously told to avoid. You may even need to gain a little weight, but be careful not to gain weight too quickly and avoid salty foods that can lead to high blood pressure

Rejection:-
You can help prevent rejection by taking your medicines and following your diet, but watching for signs of rejection—like fever or soreness in the area of the new kidney or a change in the amount of urine you make—is important. Report any such changes to your health care team.

Even if you do everything you’re supposed to do, your body may still reject the new kidney and you may need to go back on dialysis. Unless your health care team determines that you’re no longer a good candidate for transplantation, you can go back on the waiting list for another kidney.

Side Effects of Immunosuppressants:
Immunosuppressants can weaken your immune system, which can lead to infections. Some drugs may also change your appearance. Your face may get fuller; you may gain weight or develop acne or facial hair. Not all patients have these problems, though, and diet and makeup can help.

Immunosuppressants work by diminishing the ability of immune cells to function. In some patients, over long periods of time, this diminished immunity can increase the risk of developing cancer. Some immunosuppressants cause cataracts, diabetes, extra stomach acid, high blood pressure, and bone disease. When used over time, these drugs may also cause liver or kidney damage in a few patients.

Hope through Research:-
The NIDDK, through its Division of Kidney, Urologic, and Hematologic Diseases, supports several programs and studies devoted to improving treatment for patients with progressive kidney disease and permanent kidney failure, including patients who receive a transplanted kidney.

•The End-Stage Renal Disease Program promotes research to reduce medical problems from bone, blood, nervous system, metabolic, gastrointestinal, cardiovascular, and endocrine abnormalities in kidney failure and to improve the effectiveness of dialysis and transplantation. The program seeks to increase kidney graft and patient survival and to maximize quality of life.

•The NIH Organ/Tissue Transplant Center, located at the NIH Clinical Center in Bethesda, MD, is a collaborative project of NIH, the Walter Reed Army Medical Center, the Naval Medical Research Center, and the Diabetes Research Institute at the University of Miami. The site includes a state-of-the-art clinical transplant ward, operating facility, and outpatient clinic designed for the study of new drugs or techniques that may improve the success of organ and tissue transplants.

•The U.S. Renal Data System (USRDS) collects, analyzes, and distributes information about the use of dialysis and transplantation to treat kidney failure in the United States. The USRDS is funded directly by NIDDK in conjunction with the Centers for Medicare & Medicaid Services. The USRDS publishes an Annual Data Report, which characterizes the total population of people being treated for kidney failure; reports on incidence, prevalence, mortality rates, and trends over time; and develops data on the effects of various treatment modalities. The report also helps identify problems and opportunities for more focused special studies of renal research issues.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose

Resources:
http://www.topnews.in/health/kidney-transplant-patients-low-physical-activity-likely-die-early-211177
http://www.nlm.nih.gov/medlineplus/kidneytransplantation.html
http://www.kidney.niddk.nih.gov/kudiseases/pubs/transplant/
http://www.bbc.co.uk/health/physical_health/conditions/in_depth/kidneys/kidneys_transplant.shtml

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Ailmemts & Remedies

Glandular fever

Definition:
Glandular fever is a viral infection associated with a high fever.It’s also known as infectious mononucleosis or kissing disease (long ago it was realised that the infection was passed on through saliva – for example, by kissing).

It is a viral infection caused by the Epstein-Barr virus. Glandular Fever is often spread through oral acts such as kissing, which is why it is sometimes called “The Kissing Disease“. However, Glandular Fever can also be spread by airborne saliva droplets.

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Infectious Mononucleosis (IM) is an infectious, widespread viral disease caused by the Epstein-Barr virus (EBV), one type of herpes virus, to which more than 90% of adults have been exposed. Occasionally, the symptoms can reoccur at a later period. Most people are exposed to the virus as children, when the disease produces no noticeable symptoms or only flu-like symptoms. In developing countries, people are exposed to the virus in early childhood more often than in developed countries. As a result, the disease in its observable form is more common in developed countries. It is most common among adolescents and young adults.

Especially in adolescents and young adults, the disease is characterized by fever, sore throat and fatigue, along with several other possible signs and symptoms. It is primarily diagnosed by observation of symptoms, but suspicion can be confirmed by several diagnostic tests.

The syndrome was described as an infectious process by Nil Filatov in 1887 and independently by Emil Pfeiffer in 1889.
Symptoms:-
The following are mainly the symptoms of Glandular Fever:
*Headache
*Fever
*Sore throat/hard to swallow
*Tiredness, fatigue and malaise
*Enlarged lymph nodes
*Loss of appetite
*Muscle aches
*Tender enlargement of the glands (lymph glands or lymph nodes)
*Skin rash
*Sweating
*Stomach pain and enlarged spleen
*Enlarged liver
*Jaundice
*Depression
*Joint pain
*Swelling around eyes
*Orange urine (or discolored
*High blood pressure

Causes:
Glandular fever is caused by the Epstein-Barr virus. This can attack only two types of cell in the body: those in the salivary glands and white blood cells known as B lymphocytes (B-cells).

The most common way of spreading the virus is through the transmission of saliva from one person to another. Coughing, sneezing, and sharing drink bottles, eating utensils and other personal items can also spread the virus. In addition, the virus can also be spread through blood transfusion and organ transplantation.

Infection begins in the salivary glands, which release large amounts of the virus into the saliva. The infection spreads to the B lymphocytes, causing them to multiply, and causing the lymph glands to swell and become painful.

Once infected, the virus remains dormant in the body’s cells for the rest of a person’s life.

Diagnosis:
The diagnosis of glandular fever or infectious mononucleosis is based on your physical symptoms, and will include a blood test and a throat swab. Your doctor will perform a blood test to determine abnormalities in the white blood cells. A throat swab will help determine if you have glandular fever.

The most commonly used diagnostic criterion is the presence of 50% lymphocytes with at least 10% atypical lymphocytes (large, irregular nuclei), while the person also has fever, pharyngitis and adenopathy. Furthermore, it should be confirmed by a serological test.  The atypical lymphocytes resembled monocytes when they were first discovered, thus the moniker “mononucleosis” was coined. Diagnostic tests are used to confirm infectious mononucleosis but the disease should be suspected from symptoms prior to the results from hematology. These criteria are specific; however, they are not particularly sensitive and are more useful for research than for clinical use. Only half the patients presenting with the symptoms held by mononucleosis and a positive heterophile antibody test (monospot test) meet the entire criteria. One key procedure is to differentiate between infectious mononucleosis and mononucleosis-like symptoms.

There have been few studies on infectious mononucleosis in a primary care environment, the best of which studied 700 patients, of which 15 were found to have mononucleosis upon a heterophile antibody test. More useful in a diagnostic sense are the signs and symptoms themselves. The presence of splenomegaly, posterior cervical adenopathy, axillary adenopathy, and inguinal adenopathy are the most useful to suspect a diagnosis of infectious mononucleosis. On the other hand, the absence of cervical adenopathy and fatigue are the most useful to dismiss the idea of infectious mononucleosis as the correct diagnosis. The insensitivity of the physical examination in detecting splenomegaly means that it should not be used as evidence against infectious mononucleosis.

In the past the most common test for diagnosing infectious mononucleosis was the heterophile antibody test which involves testing heterophile antibodies by agglutination of guinea pig, sheep and horse red blood cells. As with the aforementioned criteria, this test is specific but not particularly sensitive (with a false-negative rate of as high as 25% in the first week, 5–10% in the second and 5% in the third). 90% of patients have heterophile antibodies by week 3, disappearing in under a year. The antibodies involved in the test do not interact with the Epstein-Barr virus or any of its antigens. More recently, tests that are more sensitive have been developed such as the Immunoglobulin G (IgG) and Immunoglobulin M (IgM) tests. IgG, when positive, reflects a past infection, whereas IgM reflects a current infection. When negative, these tests are more accurate in ruling out infectious mononucleosis. However, when positive, they feature similar sensitivities to the heterophile antibody test. Therefore, these tests are useful for diagnosing infectious mononucleosis in people with highly suggestive symptoms and a negative heterophile antibody test. Another test searches for the Epstein-Barr nuclear antigen, while it is not normally recognizable until several weeks into the disease, and is useful for distinguishing between a recent-onset of infectious mononucleosis and symptoms caused by a previous infection. Elevated hepatic transaminase levels is highly suggestive of infectious mononucleosis, occurring in up to 50% of patients.

A fibrin ring granuloma may be present.

Diagnosis of acute infectious mononucleosis should also take into consideration acute cytomegalovirus infection and Toxoplasma gondii infections. These diseases are clinically very similar by their signs and symptoms. Because their management is much the same it is not always helpful, or possible, to distinguish between EBV mononucleosis and cytomegalovirus infection. However, in pregnant women, differentiation of mononucleosis from toxoplasmosis is associated with significant consequences for the fetus.

Acute HIV infection can mimic signs similar to those of infectious mononucleosis and tests should be performed for pregnant women for the same reason as toxoplasmosis.

Other conditions from which to distinguish infectious mononucleosis include leukemia, tonsillitis, diphtheria, common cold and influenza

Treatment:
Self care:
Infectious mononucleosis is generally self-limiting and only symptomatic and/or supportive treatments are used.  Rest is recommended during the acute phase of the infection, but activity should be resumed once acute symptoms have resolved. Nevertheless heavy physical activity and contact sports should be avoided to mitigate the risk of splenic rupture, for at least one month following initial infection or splenomegaly has resolved, as determined by a treating physician.

MedicationsIn terms of pharmacotherapies, non-steroidal anti-inflammatory drugs (NSAIDs) like ibuprofen may be used to reduce fever and pain. Prednisone, a corticosteroid, is commonly used as an anti-inflammatory to reduce symptoms of pharyngeal pain, odynophagia, or enlarged tonsils, although its use remains controversial due to the rather limited benefit and the potential of side effects. Intravenous corticosteroids, usually hydrocortisone or dexamethasone, are not recommended for routine use but may be useful if there is a risk of airway obstruction, severe thrombocytopenia, or hemolytic anemia. There is little evidence to support the use of aciclovir, although it may reduce initial viral shedding. However, the antiviral drug valacyclovir has recently been shown to lower or eliminate the presence of the Epstein-Barr virus in subjects afflicted with acute mononucleosis, leading to a significant decrease in the severity of symptoms. Although antivirals are not recommended for patients presenting with simple infectious mononuscleosis, they may be useful (in conjunction with steroids) in the management of patients with severe EBV manifestations, such as EBV meningitis, peripheral neuritis, hepatitis, or hematologic complications. Antibiotics are not used as they are ineffective against viral infections. The antibiotics ampicillin and later the related amoxicillin   are relatively contraindicated in the case of any coinciding bacterial infections during mononucleosis because their use precipitates a non-allergic rash close to 99% of the time.

In a small percentage of cases, mononucleosis infection is complicated by co-infection with streptococcal infection in the throat and tonsils (strep throat). Penicillin or other antibiotics (with the exception of the two mentioned above) should be administered to treat the strep throat. Opioid analgesics are also relatively contraindicated due to risk of respiratory depression.
Prognosis:
Serious complications are uncommon, occurring in less than 5% of cases:

*CNS: Meningitis, encephalitis, hemiplegia, Guillain-Barré syndrome, and transverse myelitis. EBV infection has also been proposed as a risk factor for the development of multiple sclerosis (MS), but this has not been confirmed.

*Hematologic: Hemolytic anemia (direct Coombs test is positive) and various cytopenias; Bleeding (caused by thrombocytopenia).[

*Mild jaundice

*Hepatitis (rare)

*Upper airway obstruction (tonsillar hypertrophy) (rare)

*Fulminant disease course (immunocompromised patients) (rare)

*Splenic rupture (rare)

*Myocarditis and pericarditis (rare)

Once the acute symptoms of an initial infection disappear, they often do not return. But once infected, the patient carries the virus for the rest of his or her life. The virus typically lives dormantly in B lymphocytes. Independent infections of mononucleosis may be contracted multiple times, regardless of whether the patient is already carrying the virus dormantly. Periodically, the virus can reactivate, during which time the patient is again infectious, but usually without any symptoms of illness.  Usually, a patient has few if any further symptoms or problems from the latent B lymphocyte infection. However, in susceptible hosts under the appropriate environmental stressors the virus can reactivate and cause vague physical complaints (or may be subclinical), and during this phase the virus can spread to others. Similar reactivation or chronic subclinical viral activity in susceptible hosts may trigger multiple host autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis, Sjogren’s syndrome, antiphospholipid antibody syndrome, and multiple sclerosis. Such chronic immunologic stimulation may also trigger multiple type of cancers, particularly lymphoma—strongest cancer associations with EBV are nasopharyngeal carcinomas, Burkitt’s lymphoma, and Hodgkin’s lymphoma. EBV’s potential to trigger such a wide range of autoimmune diseases and cancers probably relates to its primary infection of B lymphocytes (the primary antibody-producing cell of the immune system) and ability to alter both lymphocyte proliferation and lymphocyte antibody production.

Prevention:
A vaccine against the Epstein-Barr virus is under development. The infection is most contagious during the feverish stage, when contact with others should be avoided.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

Resources:
http://www.nativeremedies.com/ailment/glandular-fever-symptoms-info.html
http://simple.wikipedia.org/wiki/Glandular_fever
http://simple.wikipedia.org/wiki/Glandular_fever
http://www.bbc.co.uk/health/physical_health/conditions/glandularfever2.shtml

http://www.treatfast.com/mononucleosis-xidc18255.html

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Herbs & Plants

Indian chickweed

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Botanical Name :
Stellaria media
Family:
Caryophyllaceae
Genus:    
Stellaria
Species:    
S. media
Kingdom:  
 Plantae
Order:
Caryophyllales

Other Names: Addre’s mouth, Chickweed, Indian chickweed, tongue grass, satin flower, star chickweed, starwort, starweed, stitchwort, winterweed, tongue-grass

Parts Used:dried herb

Habitat : Chickweed grows  in many areas across the globe, especially in fields, at the side of the road, in waste areas and so on. The scape has the average length of 7 inches and is covered with round-shaped leaves. The plant is characterized by white flowers of compact size.In both Europe and North America this plant is common in gardens, fields, and disturbed grounds. Control is difficult due to the heavy seed sets. Common Chickweed is very competitive with small grains, and can produce up to 80% yield losses among barley

Description:
Chickweed is an annual or biennial weed found in abundance all over the world in gardens, fields, lawns, waste places, and along roadsides. The usually creeping, brittle stems grow from 4 to 12 inches long and bear opposite, entire, ovate leaves. The small white flowers can be found blooming all year long in terminal, leafy cymes or solitary in the leaf axils.Chickweed is a plant with a lifespan of 1-2 years.

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Chemical Constituents:
The active constituents are largely unknown. Chickweed contains relatively high amounts of vitamins and flavonoids, which may explain some of its effect. Although some older information suggests a possible benefit for chickweed in rheumatic conditions, this has not been validated in clinical practice.

Edible Uses:
There is some data on the fact that chickweed was used as a food supplement.Chickweed is still used today as a salad herb or may be cooked as a vegetable. It is one of the ingredients of the symbolic dish consumed in the Japanese spring-time festival, Nanakusa-no-sekku.

Medicinal Uses:
Chickweed is reputed to treat a wide spectrum of conditions in folk medicine, ranging from asthma and indigestion to skin disorders. Traditional Chinese herbalists use chickweed internally as a tea to treat nosebleeds.

Being a widely-used medication in herbal medicine, this herb is known for its ability to have a positive impact on the digestive system, respiratory system and even skin. In China this plant was applied in form of a hot drink to cure nose bleeding. The plant was extensively used to treat stomachaches, digestion problems, coughs, bronchitis, various inflammations and so on. Until recently it has been considered a universal remedy for almost every disease.

It’s applications have traditionally included: bronchitis, pleurisy, coughs, colds, hoarseness, rheumatism, inflammation, or weakness of the bowels and stomach, lungs, bronchial tubes.

Chickweed had been used for externallly for: skin diseases, boils, scalds, burns, inflamed or sore eyes, erysipelas, tumors, piles, cancer, swollen testes, ulcerated throat and mouth, and all kinds of wounds.

External application of chickweed is known to produce healing effect on skin sores of different types, as well as reduce inflammations locally (especially those related to throat diseases). Chickweed was even used to treat cancer.

Chickweed is used for boosting metabolism, healing inflammations, producing an expectorative effect and giving a relief from cough and respiratory diseases.

Severe skin problems like eczema and minor sores like insect bites are also regarded as cases of chickweed application. Stomach and bowel dysfunction, swollen testes, sore-throat, and various types of wounds are effectively treated by applying chickweed.

Chickweed may be useful for:
Used externally for:
Cuts, Wounds, itching and skin irritation; Skin diseases, boils, scalds, burns, inflamed or sore eyes.

Internally:
Rheumatism

Other indications include:
* Eczema
*Insect stings and bites
*Traditionally used for all cases of bronchitis, pleurisy, coughs, colds, hoarseness, rheumatism, inflammation, weakness of the bowels and stomach, lungs, bronchial tubes, and any other forms of internal inflammation.

*Crushed, fresh leaves many be used as a poultice for inflammation and indolent ulcers with most beneficial results. A poultice of Chickweed enclosed in muslin is a sure remedy for a carbuncle or an external abscess. The water in which the Chickweed is boiled should also be used to bathe the affected part.

Also said to regulate the thyroid gland.

Dosage:
Although formerly used as a tea, chickweed’s main use today is as a cream applied liberally several times each day to rashes and inflammatory skin conditions (e.g., eczema) to ease itching and inflammation. As a tincture, 1-5 ml per day can be taken.

Known Hazards:  S. media contains plant chemicals known as saponins, which can be toxic when consumed in large quantities. Chickweed has been known to cause saponin poisoning in cattle. However, as the animal must consume several kilos of chickweed in order to reach a toxic level, such deaths are rare.

Disclaimer : The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplement, it is always advisable to consult with your own health care provider.

Resources:
http://www.wildcrafted.com.au/Botanicals/Chickweed.html
http://www.holisticonline.com/herbal-med/_Herbs/h45.htm
http://www.oshims.com/herb-directory/c/chickweed

http://en.wikipedia.org/wiki/Stellaria_media

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Ailmemts & Remedies Pediatric

Cytomegalovirus

Definition
Cytomegalovirus (say: si-toe-meg-ah-low-vi-russ), or CMV, is a very common virus. It  is a viral genus of the viral group known as Herpesviridae or herpesviruses. It is typically abbreviated as CMV: The species that infects humans it is commonly known as human CMV (HCMV) or human herpesvirus-5 (HHV-5), and is the best studied of all cytomegoloviruses. Within Herpesviridae, CMV belongs to the Betaherpesvirinae subfamily, which also includes the genera Muromegalovirus and Roseolovirus. It is related to other herpesviruses within the subfamilies of Alphaherpesvirinae that includes herpes simplex viruses (HSV)-1 and -2 and varicella-zoster virus (VZV), and the Gammaherpesvirinae subfamily that includes Epstein-Barr virus. All herpesviruses share a characteristic ability to remain latent within the body over long periods. Although they may be found throughout the body, CMV infections are frequently associated with the salivary glands in humans and other mammals. Other CMV viruses are found in several mammal species, but species isolated from animals differ from HCMV in terms of genomic structure, and have not been reported to cause human disease.

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People are usually infected by the time they are 2 years old or during their teenage years and carry the virus for life (usually in a dormant or inactive state). The majority of adults carry the virus by the time they are 40 years of age.

Many people are infected with CMV and don’t even know it because the virus rarely causes symptoms and usually does not cause long-term problems.

However, CMV can cause problems in people who have weak immune systems and in a newborn if the mother gets the infection during pregnancy.

Causes:
CMV gets into body fluids, such as saliva, blood, urine, semen and breast milk. A person is able to transmit (or “shed”) the virus to others only when it is active in his or her system (not dormant). It can be spread from one person to another through sexual contact and contact with blood and other body fluids. CMV can rarely be transmitted by blood transfusion or organ transplantation. In developed countries, blood supplies are screened for CMV when they’re to be used for those at greatest risk from the infection.

 Symptoms:

Usually, CMV does not cause symptoms or only causes mild symptoms. A few people will have symptoms that are similar to mononucleosis. Symptoms of CMV can include:

•Sore throat
•Swollen lymph nodes (lymph glands)
•Fever
•Headache
•Fatigue
•Weakness
•Muscle aches
•Loss of appetite


People who have weakened immune systems due to conditions like human immunodeficiency virus (HIV) or because they received an organ transplant and are taking immunosuppressant medicines may have severe symptoms. (Immunosuppressant medicines are medicines that lower or suppress the immune system.) Symptoms of severe CMV include:
•Blindness
•Pneumonia
•Diarrhea
•Bleeding ulcers in the esophagus (windpipe) or intestines
•Inflammation of the brain (encephalitis)
•Seizures

If a pregnant woman transmits CMV to her unborn baby, miscarriage, stillbirth or death of the newborn may occur. Newborns who survive are at an increased risk for hearing loss and mental retardation. However, only 1% of newborns who are infected with CMV during pregnancy experience problems from the virus. Most are born healthy, or with only mild CMV symptoms.

Who’s affected?
In most cases, CMV is harmless, but for some people infection can have disastrous consequences.

People with weakened immune systems (because of HIV, for example) can suffer serious illness. They may experience high fever for two or three weeks, accompanied by hepatitis and jaundice.

Other serious complications include pneumonia, inflammation of the brain (encephalitis) and blindness as a result of inflammation of the retina at the back of the eye.

CMV remains in the body for life. For those with strong immune systems, it remains inactive. If the immune system is weakened through illness or medical treatments, CMV may be reactivated, causing further medical problems and distress.

If a pregnant woman becomes infected with CMV for the first time, the virus may pass through the placenta and infect her unborn baby. If this happens early in pregnancy, the risk of miscarriage increases, as does the chance of the baby being born with malformations. For example, CMV infection in the womb is the leading cause of congenital deafness.

If the infection is contracted later in pregnancy, stillbirth and premature labour are more likely. A newborn baby may suffer severe illness shortly after birth – jaundice, enlargement of the liver and blood disorders.

Diagnosis:
CMV is diagnosed with a blood test.

CMV is more likey to cause vision problems in people who have weakened immune systems, so if you have conditions such as HIV or AIDS, your doctor may recommend that you visit an eye doctor to find out whether the virus has infected your eyes. Be sure to let your doctor know if you are having any painless blurring of your vision, “floaters” only in one eye, light flashes or areas of blindness. You should also let your doctor(s) know if you are experiencing frequent shortness of breath with flu-like symptoms, or if you are having problems hearing.

Treatment:
For otherwise healthy people, CMV usually doesn’t require treatment. If your immune system is weakened, your doctor may use one of several different medicines to treat CMV infection. However, because CMV is a virus, regular antibiotics won’t work against it. Antiviral drugs are usually prescribed, which slows the virus down (but cannot cure CMV).

If you are pregnant, your doctor may want to test you for CMV to determine if there is a risk for your unborn baby. If you do carry the virus, your doctor may suggest a test called amniocentesis, which collects a sample of the amniotic fluid for testing. It can help determine whether your unborn baby has CMV.

If you are pregnant and your baby has CMV, you doctor will likely check your baby once he or she is born for any problems or birth defects so they can be treated early. Treatable symptoms in newborns include pneumonia, hearing loss and inflammation of the eye.

Prevention:
In child care centers, as many as 70% of children ages 1 to 3 can shed the virus. Careful, frequent hand washing with soap and water may help prevent the spread of CMV.

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

Resources:
http://www.bbc.co.uk/health/physical_health/conditions/cmv1.shtml
http://familydoctor.org/online/famdocen/home/common/infections/common/viral/743.html
http://en.wikipedia.org/wiki/Cytomegalovirus
http://medippt.files.wordpress.com/2010/10/cytomegalovirus.jpg

http://health.allrefer.com/health/cmv-immunocompromised-host-cmv-cytomegalovirus.html

http://archive.microbelibrary.org/ASMOnly/Details.asp?ID=658

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