Charity Beds for the poor

Charitybeds.com is an initiative by a group of young individuals who are disturbed by the discrimination faced by the under privileged at private hospitals in the city. We are a team of young professionals across various industries who feel there is a lack of accurate information and awareness about what the law stipulates and the ground reality. Our aim is to also provide information to other charitable institutions and organisations working with the underprivileged, on where they can go for free medical care.

Private hospitals in Delhi have been allotted prime land for Rs 1 an acre as against a market value of 20 – 80 crores an acre, in return for this, the government made it compulsory for them to offer 10 % beds with ALL MEDICINES & TESTS INCLUDED and 25% of all OPD- consultation with doctors to be free. Charitybeds, helps all under privileged people achieve healthcare even when they have no money. A lot of private hospitals have joined hands with us and are actually working with us to fulfil their social responsibility. We do not charge anything, our only role is to facilitate and save lives, wherever we can.

We help patients when someone calls us, we go to government hospitals and pick up patients from there, we help people reaching private hospitals directly. We help people who have BPL ( Below the poverty line) cards and people who do not have any card as they are not aware because they are so poor.

Charitybeds.com works along with Ritinjali, a volunteer-based organization that is firmly rooted in its philosophy of providing a helping hand wherever needed, to anticipate social and community issues and to promote responsible citizenship. Mr. Arun Kapur, Founder,Ritinjali, is a key partner with Charitybeds.com. His team includes Mr. Naveen Pabla and Mr. Ashish Alex have supported us in creating Charitybeds.com. Charitybeds.com was born out of the vision of Mr Kapil Chopra, President,The Oberoi Group. His leadership has brought the initiative together and it is his passion and commitment to the cause that is the key driving force behind this initiative.

Mr. Lalit Bhatia one of the key people heading the initiative has been a social worker for over 25 years and offers his expertise and knowledge in multiple social welfare domains.He works closely with senior citizen welfare schemes and works full time with Charitybeds.com. They visit hospitals daily, creating awareness and till date have distributed over 30,000 flyers and run a poster campaign along with awareness camps in every major hospitals. Gagan works along with Mr Bhatia to ensure that we can even help more people, Gagan is an aspiring filmmaker and a photographer who is passionate about social causes and you can also check out his patient testimonial videos on the website. In addition to this,we have volunteers who come and work with us on a daily basis.You will find our people in all hospitals across Delhi everyday from 10 AM to 5 PM.

We need your help,call us and volunteer a day with us, spread the word, tell friends, tell journalists, post on Facebook, let us get the message out. Everyday, inspite of all our efforts, only 400 out of 653 free beds get utilised, everyday,someone dies because they did not have money to buy medicines or get medical care. We are racing against time, help us to reach more people. It is the least we can do for this country. As of now, we operate only in Delhi but patients can come for any part of India and seek our assistance. We soon plan to be in Mumbai where most of the trusts which run hospitals actually do not support any free healthcare inspire of sitting on government land worth crores.

If you would like to contribute for the cause, please call Lalit Bhatia 99990 71842 or Gagan Bharti 7838348237 we need posters and flyers all the time.

http://www.charitybeds.com

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Body & Cell Regeneration- Removing Negativity From Life

This video is a talk by Ms. Zenobia Khodaiji 13 Feb 2016. Topic “Body & Cell Regeneration- Removing Negativity From Life”. This is part of the HELP Talk series at HELP,Health Education Library for People, the worlds largest free patient education library www.healthlibrary.com

Drug-Induced Dementia IS NOT Alzheimer’s Disease

“The desire to take medicine is perhaps  the greatest feature which distinguishes man from animals.” –– Sir William Osler 

“More than 50 conditions can cause or mimic the symptoms of dementia.” and “Alzheimer’s (can only be) distinguished from other dementias at autopsy.” — from a Harvard University Health Publication entitled What’s Causing Your Memory Loss? It Isn’t Necessarily Alzheimer’s

“Medications have now emerged as a major cause of mitochondrial damage, which may explain many adverse effects. All classes of psychotropic drugs have been documented to damage mitochondria, as have statin medications, analgesics such as acetaminophen, and many others…Damage to mitochondria is now understood to play a role in the pathogenesis of a wide range of seemingly unrelated disorders such as schizophrenia, bipolar disease, dementia, Alzheimer’s disease, epilepsy, migraine headaches, strokes, neuropathic pain, Parkinson’s disease, ataxia, transient ischemic attack, cardiomyopathy, coronary artery disease, chronic fatigue syndrome, fibromyalgia, retinitis pigmentosa, diabetes, hepatitis C, and primary biliary cirrhosis. Medications have now emerged as a major cause of mitochondrial damage, which may explain many adverse effects” —  Neustadt and  Pieczenik  authors of Medication-induced Mitochondrial Damage and Disease

“Establishing mitochondrial toxicity is not an FDA requirement for drug approval, so there is no real way of knowing which agents are truly toxic.”  – Dr. Katherine Sims, Mass General Hospital – http://www.mitoaction.org

“It is difficult to get a man to understand something, when his salary depends upon his not understanding it!” – Upton Sinclair, anti-fascist, anti-imperialist American author who wrote in the early 20th century.

“No vaccine manufacturer shall be liable…for damages arising from a vaccine-related injury or death.”– President Ronald Reagan, as he signed The National Childhood Vaccine Injury Act (NCVIA) of 1986, absolving drug companies from all medico-legal liability when children die or are disabled from vaccine injuries.

Over the past several decades there have been a number of well-financed campaigns, promoted by well-meaning laypersons, to raise public awareness to the plight of patients with dementia. Suspiciously, most of these campaigns come from “patient support” groups lead the public to believe that every dementia patient has Alzheimer’s dementia (AD).

Not so curiously, it turns out that many – perhaps all – of these campaigns have been funded – usually secretly – by the very pharmaceutical companies that benefit economically by indirectly promoting the sale of so-called Alzheimer’s drugs.

Such corporate-generated public relations “campaigns” are standard operating procedure for all of Big Pharma’s drugs, especially its psycho-pharmaceutical drugs. Big Pharma has found that the promotion and de-stigmatization of so-called “mental illnesses of unknown etiology” is a great tool for marketing their drugs.

(http://www.propublica.org/blog/item/health-advocacy-groups-take-drug-company-cashoften-without-full-disclosures)

Recently Alzheimer’s support groups all around the nation have been marketing a documentary about country singer Glen Campbell who has recently been diagnosed with Alzheimer’s disease (of unknown etiology) despite the obvious fact that Campbell was infamous for his chronic heavy use of brain-damaging, dementia-inducing, addictive, and very neurotoxic drugs like cocaine and alcohol. And, just like so many other hard-living celebrities like the (now cured) dementia victim Kris Kristofferson and the suicidal and early dementia victim Robin Williams. All three celebrities were known to have received prescriptions for legal neurotoxic brain-altering drugs, adding to the burdens that their failing brains, livers and psyches had to endure. It is highly likely that all three of them were also on statins and were up-to-date on their mercury and aluminum-containing vaccinations.

It is an established fact that Alzheimer’s disease can only be definitively diagnosed at a post-mortem examination of the cerebral cortex, something that dementia patients are almost never subjected to. Because of the rarity of coroners doing autopsies on dementia patients, we have to question the accuracy of the diagnoses of, for example, the still living Glen Campbell, Kris Kristofferson and our own memory-impaired spouses, aunts, uncles, grandmas and grandpas, especially since so many of them have been on neurotoxic substances such as those mentioned in this article.

And we also have to question the motivations of the Big Pharma corporations that financially underwrite patient support groups like the Alzheimer’s Association. AND, equally importantly, given the total lack of recognition of the reality of drug-induced dementia, we have to question to oft-cited assertion that 2/3 of all dementia cases are because of Alzheimer’s disease (of unknown cause).

Are the Alzheimer’s, Autism and Autoimmune Epidemics Actually Iatrogenic, Drug-Induced Epidemics?

Synchronous with the recent large increases in 1) childhood and adult neurotoxic aluminum-adjuvanted vaccinations, 2) the use of neurotoxic psychotropic drugs, 3) the use of statin drugs (cholesterol-lowering drugs)  known to cause memory-impairment, and 4) the  ingestion of a variety of neurotoxic food additives, there has been a large parallel increase in A) the incidence of chronic autoimmune disorders, especially in childhood, B)the incidence of autistic spectrum disorders, C) “mental illnesses of unknown origin” and D) dementia.

For more go tohttp://www.huffingtonpost.com/david-kirby/new-study—mitochondrial_b_147030.html.

Each of those 4 root causes and the 4 neurological disorders that are closely correlated with them are admittedly multifactorial realities. But the important lesson is that they are also preventable. However, due to clever marketing by Big Pharma and the studied ignorance of Big Medicine and the refusal of Big Media to allow scholars to talk about the connections, “walks for the cure” and drug treatment is what is emphasized rather that prevention.

So what we need to ask – and then demand – is an honest answer to the question “could there be a connection between America’s increasingly common over-prescribing of immunotoxic, neurotoxic, synthetic prescription drugs and the equally over-prescribed immunotoxic and neurotoxic vaccines (that often contain either of the heavy metals aluminum and mercury) and some of the neurodegenerative disorders that supposedly “have no known cause”? Could the disabling American epidemic of autoimmune disorders, psychiatric disorders, autism spectrum disorders, etc (all supposedly of unknown origin) be found to have recognizable iatrogenic root causes and therefore be preventable? Psychiatrist and scholar Grace E. Jackson has the answers in her seminal (and black-listed) book

“Drug-Induced Dementia: A Perfect Crime”.

These are extremely important issues, especially in the case of the dementia epidemic, because the Alzheimer’s patient support groups seem to be unaware of the fact that many psychiatric drugs are known to irreversibly damage brain cells (partly by poisoning their mitochondria, the microscopic hearts and lungs of every cell) and therefore would be expected to cause a variety of other neurological and mental health disorders. (See more info on drugs and mitochondria below.

One of the big problems in America’s corporate-controlled culture, corporate-controlled government, corporate-controlled medical industries and corporate-controlled media is that the giant multinational (especially Big Pharma) corporations are in the business of developing and marketing known mitochondrial toxins with no oversight from regulatory agencies. These businesses obscure the fact that there ARE known causes for the disorders and that they are preventable. The unproven claims expressed in the TV commercials and medical journals advertising the newest drug-of-the-month are often later exposed as plain snake oil propaganda.

It should be a concern for everyone that some Alzheimer’s support groups are actually front groups for the pharmaceutical industry that profit handsomely from the handful of virtually useless drugs such as Aricept, Exelon, Namenda, Hexalon, and Razadyne.

Prescription Drug-Induced and Vaccine-Induced Mitochondrial Disorders

Acquired mitochondrial disorders (as opposed to the rare primary mitochondrial disorders like muscular dystrophy) can be caused by commonly prescribed drugs. They are difficult to diagnose and are generally poorly understood by most healthcare practitioners. When I went to medical school, none of my professors knew anything about the lethal effects that many synthetic drugs and vaccines do to the mitochondria of average brain or body cells. The science of the mitochondria was in its infancy.

A lot of mitochondrial research has been done since then, especially starting in the 1990s,and that research has proven the connections between a variety of commonly prescribed medications and mitochondrial disorders. That evidence seems to have been cunningly covered-up by the for-profit pharma groups whose drug are the culprits. Big Pharma has tremendous control  over the medical education of most health care providers, and they spoon-feed pro-drug and pro-vaccine propaganda to undiscerning “healthcare” journalists, which is where many physicians and patients get their health information.

An Honest Patient Guide for Dementia Patients (from Harvard)

I was pleasantly surprised recently to find a reasonably honest guide for dementia patients on a Harvard University website.

The entire guide can be accessed at

http://www.helpguide.org/harvard/whats-causing-your-memory-loss.htm#top.

The information at that site stated that there were over 50 conditions that could cause or mimic early dementia symptoms. What medical practitioner in our double-booked clinic environment has the time to thoroughly rule out the 50 root causes of dementia symptoms when confronted with a patient with memory loss? It’s simpler to just diagnose every case of dementia as another case of Alzheimers! Who will ever dispute such an authoritative-sounding diagnosis? Certainly not those who want to keep dementia from being recognized as a potentially iatrogenic disorder (doctor or treatment-caused disorder).

I have often said to my patients and seminar participants: “it takes only 2 minutes to write a prescription, but it takes 20 minutes to not write a prescription”. In the current for-profit clinic culture, time is money and very few physicians are ever given the “luxury” of spending sufficient time listening carefully to their patients. (In defense of the physicians that I know, they are not happy about these realities but feel powerless to do anything about it.)

It is so tempting for us physicians to use the popularized, but rather squishy label of Alzheimer’s dementia rather than to educate ourselves about the possibility of drug-induced, vaccine-induced or malnutrition-related dementia. But what is so important is that many of the 50+ conditions are preventable or reversible, which will be therapeutic only if the real root causes are identified before permanent brain damage occurs. Just one example was the subject of the book “Lipitor: Thief of Memory” written by former astronaut and flight surgeon Duane Graveline, M.D., M.P.H

(for more information go to https://www.spacedoc.com/articles/lipitor-thief-of-memory.)

The Harvard guide actually said that “medications are common culprits in mental decline. With aging, the liver becomes less efficient at metabolizing drugs, and the kidneys eliminate them from the body more slowly. As a result, drugs tend to accumulate in the body. Elderly people in poor health and those taking several different medications are especially vulnerable.”

The guide continued with a list of the possible classes of prescription drugs that number in the hundreds:

“The list of drugs that can cause dementia-like symptoms is long. It includes antidepressants, antihistamines, anti-Parkinson drugs, anti-anxiety medications, cardiovascular drugs, anticonvulsants, corticosteroids, narcotics, sedatives.”

The Harvard guide went on to emphasize that Alzheimer’s can only be accurately diagnosed on a post-mortem examination. The guide states that “Alzheimer’s is distinguished from other dementias at autopsy by the presence of sticky beta-amyloid plaques outside brain cells (neurons) and fibrillary tangles within neurons (all indicative of cellular death). Although such lesions may be present in any aging brain, in people with Alzheimer’s these lesions tend to be more numerous and accumulate in areas of the brain involved in learning and memory.”

“The leading theory is that the damage to the brain results from inflammation and other biological changes that cause synaptic loss and malfunction, disrupting communication between brain cells. Eventually the brain cells die, causing tissue loss and cell carcasses or scars.  In imaging scans, brain shrinkage is usually first noticeable in the hippocampus, which plays a central role in memory function.”

The FDA Does Not Require Big Pharma to Test its New Drugs or Vaccines for Mitochondrial Toxicity

But even the Harvard guide inexplicably fails to mention known mitochondrial toxins such as statins, metformin, Depakote, general anesthetics, fluoroquinolone antibiotics (like Cipro), fluorinated psychotropic drugs (like many of the SSRIs and the so-called antipsychotics).

And Big Food corporations are guilty of feeding us neurotoxins also.

For example, when the ubiquitous synthetic food, soft drink and chewing gum sweetener NutraSweet (aspartame) reaches 86 degrees (whether in our 98.6 degree bodies or in some MidEast desert (as was true for many American soldiers who developed Gulf War Syndrome) every molecule releases a molecule of the excitotoxic amino acids phenylalanine and aspartic acid and one molecule of the cellular toxin methanol (wood alcohol). Methanol then rapidly metabolizes into the known mitochondrial poison formaldehyde (embalming fluid), which is a serious cellular and mitochondrial toxin.

The chlorinated artificial sweetener Splenda, which was initially developed as a neurotoxic pesticide, is in an uncountable variety of foods as well.

These examples are only some of the synthetic chemicals in medicines, vaccines and processed foods that are capable of causing mitochondrial damage in brain and body cells – with memory loss, confusion and cognitive dysfunction, all early symptoms of dementia.

It is a tragedy for reversible and preventable drug- or vaccine-induced dementias (or any of the many neurodegenerative disorders) to be mis-diagnosed as Alzheimer’s disease (or neurological disorder) “of unknown cause” because if the root causes are not recognized preventive care will not be offered. And then, what may be worse, those patients might be placed on costly, potentially toxic and often useless medications that have not been tested for their own potential mitochondrial toxicities. (Tragically, the American pharmaceutical industry is not required by the FDA to test its drugs for mitochondrial toxicity, thus leaving physicians and their drug-consuming patients in the dark as far as safety of those medications is concerned.)

There is much more in the basic neuroscience literature proving the connections between drugs and vaccines and neurodevelopmental disorders. Those basic neuroscience researchers that do not have conflicts of interest with Big Pharma and Big Medicine should be listened to. Those authors with monetary or professional conflicts of interest should be regarded with suspicion.

Don’t expect Big Pharma to respond to such unwelcome revelations as mentioned above. Don’t expect Big Medicine to acknowledge the existence of iatrogenic illnesses or to offer apologies.

Do, however, expect denials, dismissals, distractions, delays and ad hominem attacks against the whistle-blowers rather than honest mea culpas.

So it must be up to the consumers of potentially toxic substances to do the research themselves, for those substances may not show symptoms until a tipping point is reached when their livers can no longer detoxify the cocktail of poisons that are presented to it).

Professor of Medicine Oliver Wendell Holmes once said: “If all the medicine in the world were thrown into the sea, it would be bad for the fish, but good for humanity.”

Enough said.

Dr Kohls has spent many years researching the powerful, obscenely profitable and therefore easily corrupted pharmaceutical industry and the many false claims that their lobbyists, think tanks and co-opted opinion leaders in the media have been making. He knows many families whose lives have been devastated by psychiatric drug and vaccine injuries, including the post-vaccination regressive autism that unequivocally began following routine well-baby or well-child vaccinations. He takes seriously the precepts of the Hippocratic Oath that he took when he received his medical degree. That oath says that physicians should above all do no harm to their patients and thus, when there is evidence of potential harm from a prescription drug, vaccine or procedure, physicians should hesitate in doing that harmful treatment until a thorough, unbiased re-evaluation is done. 

Tragically, there has been a proliferation of big medical corporations (for-profit health insurance companies, for-profit clinics, for-profit hospitals, etc) and the secretive, often above-the-law multinational pharmaceutical corporations that regularly use corrupted science to “prove” the safety and efficacy of their obscenely profitable drugs. They employ thousands of workers but mainly work for the economic benefit of their shareholders and not vulnerable patients. 

Dr Kohls practiced holistic mental health care for the last decade of his family practice career. He now writes a weekly column for the Reader Weekly, an alternative newsweekly published in Duluth, Minnesota, USA. Many of his Duty to Warn columns have been archived at

http://duluthreader.com/articles/categories/200_Duty_to_Warn,

http://www.globalresearch.ca/authors?query=Gary+Kohls+articles&by=&p=&page_id= or at

https://www.transcend.org/tms/search/?q=gary+kohls+articles

https://www.globalresearch.ca/drug-induced-dementia-is-not-alzheimers-disease/5545492


What goes into these fragrances? We may never know

AIR WICK ESSENTIAL OILS

 You might think that 80 times the aroma of a particular plant, even a pleasant-smelling one, would overwhelm the senses. But no one’s wincing or dry heaving (thankfully) in the above TV commercial for Air Wick’s essential oils, specifically its lavender scent, which the company claims is “infused with over 80 lavender flowers” per bottle. In fact, two of the three subjects in the ad appear pleasantly surprised when they find out that what they thought was real lavender was actually Air Wick’s product.

But how is this scent really achieved?

A TINA.org reader wrote in:

It is very unlikely that there is any real lavender in this product, as they have supposed customers choose between its scent and “real lavender.” Even if it did contain real lavender, it is highly doubtful that they would be counting the number of flowers in every bottle.

TINA.org asked Air Wick how it arrived at over 80 lavender flowers per bottle. We have yet to get a response.

But what we found when we looked up a lavender-scented essential oil on Air Wick’s website is that the first ingredient in the product (and thus the most predominant) is not “over 80 lavender flowers” but fragrance. The Environmental Working Group, a nonprofit that examines ingredients in consumer goods, has referred to the ingredient fragrance as “a black box for hundreds of chemicals in thousands of everyday products.” This is because fragrance is one of two ingredients on a product label that itself can be comprised of hundreds of natural and synthetic ingredients. The other is “flavor.” Under U.S. regulations, companies are allowed to simply list “fragrance” or “flavor” to protect trade secrets.

But we did some digging and, according to a “safety data sheet” for the lavender-scented essential oil, here’s some of what appears to go into Air Wick’s fragrance formula (in descending order of predominance):

  • Dipropylene glycol monomethyl ether (aka dipropylene glycol methyl ether), a chemical that a federal database describes as “a colorless liquid with a weak odor.” (Perfect for an air freshener, right?)
  • 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one
  • Linalyl acetate, which the database says is “isolated from numerous plants and essential oils, e.g. clary sage, lavender, lemon etc.” (Apparently, this is where Air Wick’s product gets its lavender smell.)
  • Terpineol
  • 1,1-Dimethyl-2-phenylethyl acetate
  • Hexyl salicylate

Perhaps not what you would expect from a product advertised in the commercial as “infused with 100% natural essential oils.”

Essential oils are appealing to consumers because the source is natural. However, the FDA warns:

Sometimes people think that if an “essential oil” or other ingredient comes from a plant, it must be safe. But many plants contain materials that are toxic, irritating, or likely to cause allergic reactions when applied to the skin.

Find more of our coverage on essential oils, which are prevalent in the MLM industry, here.

https://www.truthinadvertising.org/air-wick-essential-oils/

Popping Calcium Tablets? Think Again

Orthopaedic doctors and general physicians are quick to prescribe calcium supplements as being good for our bones. They are already 10 years behind. A 2008 study in New Zealand found that excess calcium (caused by calcium supplements) in the gut could lead to mal-absorption of fat, reducing saturated fat absorption. With less saturated fat absorbed, your cholesterol might fall. The researchers in New Zealand were expecting to lower heart attack rates by giving women calcium supplements because it showed a lower blood pressure, initially. There appeared to be more heart attacks in the calcium-supplemented group.
Separately, Women’s Health Initiative, the largest and longest randomised, controlled trial of calcium supplementation, reported no adverse effects. However, the participants were already on calcium supplements before the study started. So, the study was just comparing higher versus lower doses of calcium supplementation rather than supplementation versus no supplementation. The researchers then went back and checked about the women who started out not taking supplements and then were randomised to the supplement group. These women suffered more heart attacks or strokes. Thus, calcium supplements seemed to increase cardiovascular disease risk.
What happens when we take calcium tablets? Apparently, we get a spike of calcium in our bloodstream (this does not happen when we take calcium-rich foods) and can stay up for as long as eight hours. This leads to a situation when your blood clots more easily, leading to a risk of clots in the heart or brain. Is this why, in the months after a hip fracture, risk of dying shoots up, with about one in five women passing away within a year. Hip fractures can shorten the lifespan of men by an average of four to five years.
So, don’t pop the calcium pills; get calcium from foods and sunshine. In a 2012 study, one group of women received sunlight exposure and the other took calcium pills. The group taking pills had significantly increased mortality, living shorter lives than those in the sunshine group. Calcium is best taken as part of the diet with the knowledge that our body itself has a way of adjusting to calcium levels. If our calcium intake goes down, our body starts absorbing more and vice-versa. The top calcium foods are raw milk, kale, sardines, yogurt and broccoli.

Dangers of Statin Drugs

Dangers of Statin Drugs: What You Haven’t Been Told About Popular Cholesterol-Lowering Medicines

Hypercholesterolemia is the health issue of the 21st century. It is actually an invented disease, a “problem” that emerged when health professionals learned how to measure cholesterol levels in the blood. High cholesterol exhibits no outward signs–unlike other conditions of the blood, such as diabetes or anemia, diseases that manifest telltale symptoms like thirst or weakness–hypercholesterolemia requires the services of a physician to detect its presence. Many people who feel perfectly healthy suffer from high cholesterol–in fact, feeling good is actually a symptom of high cholesterol!

Doctors who treat this new disease must first convince their patients that they are sick and need to take one or more expensive drugs for the rest of their lives, drugs that require regular checkups and blood tests. But such doctors do not work in a vacuum–their efforts to convert healthy people into patients are bolstered by the full weight of the US government, the media and the medical establishment, agencies that have worked in concert to disseminate the cholesterol dogma and convince the population that high cholesterol is the forerunner of heart disease and possibly other diseases as well.

Who suffers from hypercholesterolemia? Peruse the medical literature of 25 or 30 years ago and you’ll get the following answer: any middle-aged man whose cholesterol is over 240 with other risk factors, such as smoking or overweight. After the Cholesterol Consensus Conference in 1984, the parameters changed; anyone (male or female) with cholesterol over 200 could receive the dreaded diagnosis and a prescription for pills. Recently that number has been moved down to 180. If you have suffered from a heart attack, you get to take cholesterol-lowering medicines even if your cholesterol is already very low–after all, you have committed the sin of having a heart attack so your cholesterol must therefore be too high. The penance is a lifetime of cholesterol-lowering medications along with a boring lowfat diet. But why wait until you have a heart attack? Since we all labor under the stigma of original sin, we are all candidates for treatment. Current dogma stipulates cholesterol testing and treatment for young adults and even children.

Click Here to continue reading this interesting article

Sanofi under fire over its Dengue vaccine

French drugmaker Sanofi has come under fire as Philippines has suspended the company’s Dengvaxia vaccine — the first promising vaccine for dengue— amid widespread fears about its safety and growing public anger over its use in 830,000 schoolchildren, reports The New York Times. Dengue is a disease spread by mosquitoes that infects about 400 million people worldwide. It puts 500,000 people in the hospital each year and kills 25,000, mostly in Latin America and South Asia.

“The newly revealed evidence, confirmed recently by Sanofi’s review of study data, found that in rare cases, Dengvaxia can backfire: If people who never had dengue are vaccinated and later become infected, the vaccine may provoke a much more severe form of the illness,” the report says.
The World Health Organisation (WHO) is reviewing the situation and has issued an interim recommendation that only people who have had a prior dengue infection be vaccinated.
Sanofi too has said that the vaccine should only be given to people who have been previously sickened with dengue. Jack Cox, head of global media relations at Sanofi, told STAT , that “We propose that health care professionals would need to assess the likelihood of prior dengue infection in these individuals before vaccinating and for individuals who have not been previously infected by dengue virus, vaccination should not be recommended.”
However, the issue is most people do not know if they have been infected or no. Dengue could be a serious disease with severe complications. However, in many cases there are no or mild symptoms. In addition, there is no ‘readymade’ test available to determine is someone was infected in the past and now can be vaccinated.
The Philippines health secretary, Francisco T Duque III, had reportedly stated that the government is demanding a refund from Sanofi for the 3.5 billion Philippine pesos, or about $69 million, it spent on the vaccine. It is also asking the company to set up a fund to cover the treatment of any children who develop severe dengue.
According to a report from the New York Times, the Philippines government has begun investigations into the rollout of the immunisation program by Sanofi, which allegedly discounted early warnings that its vaccine could put some people at heightened risk of a severe form of the disease.
Death rates are highest among children, and just last week a 7-year-old girl who had not been vaccinated died from dengue in the Philippines, says the NYT report, quoting agencies.
Dengvaxia, the world’s first dengue vaccine, had been developed by Sanofi over decades of research and is approved in 19 countries.
Meanwhile, the Indian government is working on such vaccines and Phase 1 clinical trials of this vaccine is likely to be held in 2020. Minister of State for Health, Ashwini Kumar Choubey told the Rajya Sabha that DSV4, the vaccine developed by International Centre for Genetic Biotechnology (ICGEB)-Sun Pharma collaborative venture, is a recombinant vaccine on the Virus-Like Particles (VLP) platform with a tetravalent four-in-one VLP design; expressed in yeast, it elicits antibodies to all four DENV serotypes in a shorter schedule of 0, 1 and 2 months.
The other experiment involves the Panacea Dengue Vaccine, which is a cell culture-derived live attenuated, recombinant, freeze- dried, lyophilized tetravalent vaccine with the seed strain borrowed from the US-based National Institute of Health (NIH) and the Drug Controller General India had granted permission to conduct clinical Phase I/II studies, the Minister said.
Triggering public outrage, politicians in the Philippines are demanding information about Sanofi’s advertising campaign and their government’s aggressive push, against the advice of some experts, to vaccinate a million children. The backlash has alarmed researchers who worry that Sanofi’s stumble could stoke mistrust in vaccines around the globe.
Dr William Schaffner, an infectious disease expert at Vanderbilt University, said, “It’s hard to think of another circumstance when a major public health program was introduced with this much controversy.”
The episode could prove to be a cautionary tale for pharmaceutical companies, who have already been reluctant to invest in vaccines and drugs that are used mainly in the developing world.
Sanofi saw the Philippines as a key market. In the fall of 2016, the company initiated a “disease awareness” campaign that did not name Dengvaxia but directed people to a Facebook page where Sanofi was mentioned.
The company has told investors that it expects to lose 100 million euros, or about $117 million, as a result of diminished sales. Sanofi is one of the world’s biggest pharmaceutical companies, reporting sales of nearly 34 billion euros in 2016, or nearly $40 billion. Two other dengue vaccines are in late-stage development and could threaten future sales of Dengvaxia if they show better results.
You may also wish to read…

 

 http://www.moneylife.in/article/sanofi-under-fire-over-its-dengue-vaccine/52535.html