GALL-STONES

FACTS

There is no such thing as stone in the gall bladder. In fact, the bile normally produced in the liver is stored in the gall bladder; and due to changes in the physio-chemical composition of bile, cholestrol etc is precipitated giving appearance of gallstones.

Gall stones may be :

Solitary - size can be measured accurately.
Few (countable) - Number and size of stones is measurable.
Multiple - Number of stones may vary upto 200 or more, filling the gall bladder completely. Size of the stones is generally difficult to measure but the size of the few larger stones can be monitored.
Gallstones can be seen initially by Ultrasonography and their size and number can be monitored by subsequent Ultrasonograms at regular intervals, while the homeopathic treatment is continued.

Generally patients of gallstones can present as :

Without any overt symptoms - gallstones discovered accidentally on routine ultrasonography.
Severe colicky pain in epigastric area and right-sided below chest pain, with nausea, vomiting.
Recurrent indigestion and acidity, in which ultrasonogram reveals gallstones.
HOMEOPATHIC APPROACH

Aim of homeopathic treatment is :

To relieve the immediate sufferings - pain, vomiting.
To relieve recurrent problem of acidity and indigestion.
Dissolution of stones: which can be monitored by subsequent ultrasonogram done at 6 months interval. Size and number (when few) of stones should be compared. The reduction in size and number is though slow but is sure to follow if the symptomatic improvement is there and treatment is continued.
The general medical opinion about gallstones is that there is no treatment available, only surgery is the answer. And in the name of surgery, gallbladder is removed fully instead of gallstones. But even after surgery, at times the indigestion and acidity, phantom pains and discomfort continue to bother the patient as the basic physio-chemical change in the bile remains uncorrected.

Fully cured cases of gallstones, in which stones have dissolved completely and partially improved cases in which gallstones have reduced in size on subsequent ultrasonograms, negate the general belief. Thus, gallstones can be cured with homeopathy, provided treatment is continued and size of the stones is monitored by ultrasonography at regular intervals.

The stimuli come from external or internal environment. If these are troublesome; then these are called VYADHI in Sanskrit. In Ayurveda these are classified holistically into ADHYATMIK, ADI DAIVIK and ADI BHAUUTIK. Thus physiological and pathological are ADHYATMIK, the psychological (para psychological) are ADI DAIVIK and the physical stimuli such as heat, cold, accidents, physical assaults, war wounds etc are called ADI BHAUUTIK.

Their impact on brain, autonomic and somatic nerves, endocrine secretions, metabolism and the other cellular activities (both at unconscious and conscious levels); and produces physical, metabolic, endocrine and neuro psychiatric disorders and/or lust, craving, petty pleasures, guilt, fear, suffocation, pride, repentance, misery etc!

Together this is called STRESS and embodies individual and global degeneration, disease and destruction; if our sensations, feelings and responses; to these stimuli (DEHABUDDHI); are NOT evolved appropriately through TOTAL STRESS MANAGEMENT (the core of which is NAMASMARAN)!

Reading, analysis, imagination, discussions, explanations, experimentations with various techniques and procedures can only build our convictions. Alternatively; practice of different rites and rituals can give us some satisfaction and solace.

But TOTAL STRESS MANAGEMENT (the core of which is NAMASMARAN) is the solution and involves riding over the floods of extremely rapid tornados of above mentioned stimuli; and their invisible, deceptive harmful; metabolic, endocrine and neuro-physiological (and pathological) effects! This is victory over DEHABUDDHI!

This upward impetus, evolutionary transformation, conscious sublimation, or freedom of self; obviously involves enormous inner empowerment through connection with the true self or cosmic self!

Isn’t the awareness of ‘past’ and ‘future’; the function of neuro-physiological (and pathological) effects of physiological stimuli? Doesn’t the “living in present”; actually imply living beyond ‘time’ by actually being (cognition, affect and conation); beyond the impacts of physiological sensations? Isn’t this a supra-physiological plane of existence? Isn’t such living equivalent to being in ‘causal’ plane; by going beyond the level of ‘effects’? Isn’t this the same as STHITAPRAJNA? Isn’t this associated with the blissful cosmic romance; benevolent to the universe? Is this not the conquest of DEHABUDDHI and the dawn of HOLISTIC RENAISSANCE?

Yes! This all means the same; and is true! This is the same as; ‘living in present’, “going to one’s own core”, “going to the center of universe”, “going beyond time”, “going beyond MAYA”; and ensures individual and universal blossoming!

We keep fast on certain days or on certain occasions; as a part of our devotion to God, a part of rituals or for improving health.

Sometimes we refuse to eat or drink water; because we are angry or excited.

But these days we come across; people going on fast to protest against certain issues and/or insist on certain maters.

While no one can be; judgmental and/or object to the right of an individual to go on fast; fasting for pressing one’s subjective opinions and/or feelings towards certain issues (how much ever noble they may appear to be) has to be reviewed and reassessed.

Such fasting or self infliction does not emancipate us; from our slumber, lethargy, indolence, pettiness, superficiality, meekness and our over all weakness and helplessness. It does not release us; from sectarian and piecemeal activities and conflicts.

Rather than fasting; we better be holistic and evolve a consensus; on holistic solutions and their practice; at individual, local, national and global levels; and conquer of the stress (as well as participate in holistic renaissance) at all the levels!

Super Toxic Bug” of Escheritia Coli strain- H4 0104 is a new threat to India and whole world as it causes first a bloody diarrhoea due to infection of gut and platelets leading to loss of water and blood causing Anaemia and setting a kidney failure and later failure of Liver,Lung,Brain and Heart or Multi Systemic Organ Failure and Death. Its toxicity is more alarming as no good vaccine or medicine is available to check its infection as this BUG OR TOXIN is resistant to most widely used Antibiotics like NDM-1 BACTERIA.Name of toxin of this E.COLI STRAIN (STEC 0104:H4) IS SHIGA TOXIN.but nothing is of very serious concernas it affects mainly children in summer season and it is also very dangerous in few cases only and as mode of transmission is mainly contact contamination in form of water or polluted food so a hygenic check up at personal or comunity level will control it completely but in country like us once infected will have to suffer a lot due to our style of living and hugh population and will cost us very high due to unavailability of any medicine or vaccine resulting our dependance only merely supportive treatment.
India,A FASTLY GROWING ECONOMY LIKE WHOLE WORLD is on high alert against the deadly strain of Shiga toxin-producing E coli (STEC 0104: H4) as this strain has infected over 1823 cases across 12 European nations (Austria, Czech Republic, Denmark, France, Netherlands, Norway, Spain, Sweden, Switzerland, Britain and the United States) including 520 cases of hemolytic uremic syndrome (HUS). Twelve HUS cases were fatal, and 6 deaths were reported among non-HUS cases. (17 deaths in Germany and 1 in Sweden).
The Food Safety and Standards Authority of India has informed its officials to watch out for all food items, especially fruits and vegetables, coming in from Europe.The FOOD source is organic Spanish cucumbers. Cucumbers, tomatoes, and lettuce are top suspects.E coli is a common bacteria in the GI tract and part of the normal bacterial flora. However, some E coli strains produce a toxin that could produce serious infection. The infection is acquired by consuming contaminated food or water.The incubation period is 3-4 days in conventional strain but in the STEC 0104: H4 strain it is 7-12 days. Most patients' symptoms resolve within 5 to 7 days. However, HUS STEC 0104: H4 can develop a week after diarrhea begins.
Symptoms range from mild to severe bloody diarrhea, mostly without fever. The strain STEC 0104: H4 is causing severe symptoms, including stomach cramps, bloody diarrhea, vomiting, and fever. However, fever is not usually high.
As per WHO, this STEC 0104:H4 strain of E coli "is a unique strain that has never been isolated from patients before" and there may be "various characteristics that make it more virulent and toxin-producing".The hemolytic-uremic syndrome (HUS) is characterized by the simultaneous occurrence of a triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute renal injury.Microangiopathic hemolytic anemia: Hemoglobin levels are usually less than 8 g/dL. The Coomb's test is negative and the peripheral blood smear is characterized by the large number of schistocytes and helmet cells. There is no correlation between the severity of the anemia and the severity of the renal disease.Thrombocytopenia: Platelet counts are generally around 40,000/mm3. There is no correlation between the degree of thrombocytopenia and the severity of the renal disease.Acute renal injury: The severity of renal involvement ranges from hematuria and proteinuria to severe renal failure and oligoanuria, which occur in one-half of cases. Hypertension is also frequently observed. Although as many as 50 percent of those with HUS require dialysis during the acute phase, the prognosis for recovery of renal function is generally favorable.Up to 10% of patients with this latest infection with STEC 0104: H4 strain may develop HUS, with a case-fatality rate ranging from 3% to 5%.
Normally HUS is the most common cause of acute renal failure in young children but this strain (STEC 0104: H4) is affecting female adults above the age of 20.It can cause neurological complications like seizure, stroke and coma in 25% of HUS patients and chronic renal sequelae, usually mild, in around 50% of survivors.Usually HUS can be typical HUS or atypical HUS. Typical HUS is Shiga-like toxin (Stx)-associated HUS and atypical HUS is non-shiga toxin (NStx)-associated HUS.Typical Stx HUS occurs after a prodromal episode of bloody diarrhea. It normally affects children under the age of five years. On the other hand, atypical non-shiga toxin associated (NStx) HUS is a heterogeneous disorder distinguished clinically by the absence of diarrhea or Shiga toxin-producing E. coli infection, but with microangiopathic hemolytic anemia, thrombocytopenia, and acute renal injury.
Typical HUS primarily follows an infection with Shiga toxin producing strains of E coli. The most common serotype is O157:H7, which is found in 70 percent of cases. The annual incidence is 2 to 3 per 100,000 children less than five years of age. The current strain is different Shiga toxin–producing E coli O104:H4.This disorder is commonly observed during the summer.The differential diagnosis includes: Other enteric infections, Henoch-Schönlein purpura, systemic vasculitis, sepsis and disseminated intravascular coagulation.
There is no known effective therapy to prevent progression from the bloody diarrheal phase (acute infectious phase) to the post diarrheal phase of HUS.Therapy is supportive. One can give antibiotics but NOT anti-motility agents. Some research has shown that administering antibiotics may in fact increase their risk of developing HUS, but the CDC recommends that clinicians ultimately determine treatment according to each individual patient. There may be indications for antibiotics in patients with severe intestinal inflammation if perforation is of concern. Of note, isolates of STEC O104:H4 from patients in Germany have demonstrated resistance to multiple antibiotics.Patients may require red blood cell transfusions when the hemoglobin is below 6 g/dL.
Platelets are transfused when there is active bleeding or prior to a required invasive procedure in patients with platelet counts less than 30,000/mm3.Dehydration is corrected as per requirement.Dialysis is done as per standard indications.
Hypertension is managed by fluid restriction, antihypertensive agents, and dialysis if needed. Nifedipine is the drug of choice in initial phase to be substituted with ACE inhibitors later.
Parenteral diazepam, phenytoin, and fosphenytoin are used for seizures.One can try plasma exchange in cases with significant neurological symptoms.Do not use anti-thrombotic agents or oral Shiga toxin-binding agent.
In general, prognosis is excellent with mortality rates below 5%. Around 5% of patients will have significant long-term sequelae of either stroke or end-stage renal failure. In patients who require renal transplantation, recurrence of HUS is rare.
All stools submitted for testing from patients with acute community-acquired diarrhea should be cultured for STEC O157:H7. These stools should be simultaneously assayed for non-O157 STEC with a test that detects the Shiga toxins or the genes encoding these toxins.It is often difficult to isolate STEC in stool by the time a patient presents with HUS.
WHO does not recommend any trade restrictions related to this outbreak because it is not being spread as airborne infection as was SARS,SWINE FLU etc,so noquarantine checkup or isolation or any cholera type vaccination has been ordered but an immense research is going on world wide to develop vaccine against this toxin as we have got for typhyoid or paratyphoid bacteria or food sensitive Antibiotic to nip in the bud this wildly growing killer bug as called 'SUPER KILLING BUG OF THIS YEAR.-BY DR.D.R.NAKIPURIA,09434143550