Archive for November, 2009

Lumbrokinase Dissolves Excess Fibrinogen, Increases Prothrombin Time and Plasminogen

The following abstracts indicate Lumbrokinase enzymes dissolve excess clotting by increasing Plasminogen and dissolving Fibrinogen.

Florida Detox and Wellness Institute fibromyalgia, chronic fatigue, phlebitis, Lyme Disease, Babesia and migraine patients report  Lumbrokinase is reducing their excess clotting and pain more effectively, than Nattokinase enzymes.  Nattokinase appears safer to use by uninsured sufferers who might not receive as much followup testing of their clotting system.

Mycoplasma, Lyme Disease, Babesia, Herpes Simplex, Epstein Barr Virus, Cytomegalous Virus,  and HHV6 can all cause excess clotting, fatigue, “brain fog,” and chronic pain.

Steven Sponaugle, Research Director, Florida Detox and Wellness Institute

www.floridadetox.com

1: Int J Biol Macromol. 2003 Sep;32(3-5):165-71. Links

Hydrolysis of fibrinogen and plasminogen by immobilized earthworm fibrinolytic enzyme II from Eisenia fetida.

Zhao J, Li L, Wu C, He RQ.

Lab of Visual Information Processing, Institute of Biophysics, Center for Brain and Cognitive Sciences, Baiao Pharmaceuticals Beijing C.L., Beijing, China.

Earthworm fibrinolytic enzyme II (EFE-II) from Eisenia fetida has a broad hydrolytic specificity for peptide bonds. Our experiments show that EFE-II can hydrolyze the specific chromogenic substrates of thrombin (Chromozym TH), trypsin (Chromozym TRY) and elastase (Chromozym ELA). The Michaelis-Menten constant (K(m)) for Chromozym ELA (approximately 245 microM) is much higher than those for the thrombin (approximately 90 microM) and trypsin (approximately 60 microM) substrates. On the other hand, EFE-II is inhibited most strongly by soybean trypsin inhibitor (SBTI), and weakly inhibited by elastinal, suggesting that EFE-II has a trypsin-like activity. Degradation of plasminogen (PLg) and fibrinogen by EFE-II was investigated after EFE-II had been immobilized onto 1,1′-carboryl-diimidazole (CDI)-activated Sepharose CL-6B. The immobilized EFE-II has 55-60% activity of the native enzyme with a higher thermal and pH resistance. EFE-II cleaves PLg at four hydrolytic sites: Lys(77)-Arg(78), Arg(342)-Met(343), Ala(444)-Ala(445) and Arg(557)-Ile(558). The site Arg(557)-Ile(558) is also recognized and cleaved by tissue plasminogen activator (t-PA) and urokinase (UK), producing active plasmin. Cleaving Ala(444)-Ala(445) released mini-plasmin with secondary activity to hydrolyze fibrin. Immobilized EFE-II degrades not only the Aalpha chain of fibrinogen in the C-terminal region (like human neutrophil elastase, HNE), but also in the N-terminal region at the Val(21)-Glu(22) site.

1: Clin Hemorheol Microcirc. 2000;23(2-4):213-8. Links

Changes in coagulation and tissue plasminogen activator after the treatment of cerebral infarction with lumbrokinase.

Jin L, Jin H, Zhang G, Xu G.

Department of Neurology, Zhongshan Hospital, Shanghai Medical University, China.

This paper aimed to investigate the effect of lumbrokinase on the anticoagulation and fibrinolysis in treating cerebral infarction. Lumbrokinase was used in patients with cerebral infarction. Patients were randomly divided into treatment group (n = 31) and control group (n = 20). Single blind method was used in this investigation. The Chinese stroke score was used to evaluate the results of treatment before and after administration of lumbrokinase. Kaolin partial thromboplastin time (KPTT), prothrombin time (PT), fibrinogen content, vWF content were analyzed, and tissue plasminogen activator (t-PA) activity, plasminogen activator inhibitor (PAI) activity, D-dimer level were assayed. In both groups, the stroke score decreased after administration, but in the treatment group, it was more obvious. In the treatment group, KPTT was prolonged, t-PA activity and D-dimer level increased, while the content of fibrinogen decreased significantly. There were no significant changes of PT and PAI activity in both groups. It is concluded that lumbrokinase is beneficial to the treatment of cerebral infarction. The effect of lumbrokinase is related to the inhibition of intrinsic coagulation pathway and the activation of fibrinolysis via an increase of t-PA activity.

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Corydalis and Stephania herbals reduced cocaine use in rats

Corydalis is a mushroom used for over a thousand years in Chinese medicine.  Stephania herbal has also been used for over a thousand years in China and is recommended by master herbalist, Stephen Buhner, in Healing Lymes, to treat neurological symptoms of Lymes Disease.

Steven Sponaugle, Research Director, Florida Detox and Wellness Institute

www.floridadetox.com

 

Psychopharmacology (Berl). 2007 Jul;192(4):581-91. Epub 2007 Mar 15.

Levo-tetrahydropalmatine attenuates cocaine self-administration and cocaine-induced reinstatement in rats.

Mantsch JR, Li SJ, Risinger R, Awad S, Katz E, Baker DA, Yang Z.

Department of Biomedical Sciences, Marquette University, Schroeder Health Complex, P.O. Box 1881, Milwaukee, WI 53201-1881, USA. john.mantsch@marquette.edu

RATIONALE: Levo-tetrahydropalmatine (l-THP) is an alkaloid constituent of plants from the botanical genera Corydalis and Stephania and is contained in many traditional Chinese herbal preparations. In addition to its low-affinity antagonism of D2 dopamine (DA) receptors, we report that l-THP functions as a higher-affinity antagonist at D1 DA receptors and interacts with D3 DA receptors, suggesting that it may be effective for the treatment of drug addiction. Accordingly, l-THP has been reported to reduce heroin craving and relapse in recovering addicts. OBJECTIVE: This study investigated the effects of l-THP (3.75, 7.5, and 15.0 mg/kg, i.p.) on cocaine self-administration (SA) and cocaine-induced reinstatement. MATERIALS AND METHODS: Rats were trained to self-administer cocaine and food by pressing separate response levers during sessions consisting of a multiple schedule of alternating 30-min FR4 cocaine and 15-min FR4 food reinforcement. During the cocaine components of each session, the available cocaine dose varied such that rats had access to low and high dose ranges in varying sequence on alternating days. After SA, cocaine-reinforced responding was extinguished, and effects of l-THP on cocaine-induced reinstatement (10 mg/kg, i.p.) were examined. RESULTS: l-THP produced a rightward and downward shift in the dose-response curve for cocaine SA and attenuated cocaine-induced reinstatement. l-THP also reduced food-reinforced responding and locomotor activity. However, reductions in cocaine SA were found at doses that failed to alter food-reinforced responding, and significant effects were not observed on food responding during reinstatement. CONCLUSIONS: These findings suggest that l-THP is potentially useful for treating cocaine addiction.

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Low Dose Lithium Increased Brain Gray Matter

Regular use of lithium has been found to protect brain neurons from cell death and to stimulate the growth of new brain cells (Moore et al; 2000 Gray et al; 2003). Recent studies have found that lithium binds to and inhibits the activity of brain enzymes such as glycogen synthase kinase-3 (Pilcher, 2003) and protein kinase C (PKC) isozymes  (Manji et al; 2001) that may be involved in processes leading to brain cell death. In addition lithium administration increases the production of a brain cell protecting protein (Manji et al 2000). In summary, use of lithium as a trace mineral supplement may serve an important role in safeguarding the health of the brain.

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Herpes flare intensity reduced with Low Dose Lithium

AMSTERDAM J. D. (1 2) ; MAISLIN G. (1) ; HOOPER M. B. (1)

Suppression of herpes simplex virus infections with oral lithium carbonate : A possible antiviral activity Pharmacotherapy. 1996 Nov-Dec;16(6):1070-5.

;

(1) Depression Research Unit, Department of Psychiatry, University of Pennsylvania Medical Center, ETATS-UNIS
(2) Wistar Institute of Anatomy, Philadelphia, Pennsylvania, ETATS-UNIS

 

Abstract

In vitro studies have shown an inhibitory effect of lithium salts on herpes simplex virus (HSV) replication by mechanisms that interfere with viral DNA synthesis. Moreover, clinical studies have shown that oral lithium carbonate and topical lithium succinate can suppress genital HSV infections in humans. We conducted a randomized, double-blind, placebo-controlled trial of oral lithium carbonate in 11 healthy subjects age 28-65 years (mean ± SD age 38 ± 11 years) who had at least four recurrent HSV infections in the year preceding the study. Six patients completed at least 5 months of lithium therapy at a mean (± SD) average daily lithium dose of 437 ± 185 mg (range, 150-900mg) and an average serum lithium level of 0.56 ± 0.20 mmol/L. Overall, lithium treatment resulted in a consistent reduction in the mean number of episodes/month, the average duration of each episode, the total number of infection days/month, and the maximum symptom severity. In contrast, treatment with placebo resulted in an increase in three out of the four severity measures. Although the comparisons between the treatment groups did not achieve statistical significance due to the limited sample size, there was a clear trend for a reduction in the total monthly duration of all HSV infections with lithium (p=0.08). Lithium treatment was well tolerated and produced no deleterious effects on renal or thyroid function. These observations lend support to prior observations of an antiviral activity of lithium, and suggest the possibility that oral lithium may represent a safe prophylactic agent in patients with recurrent HSV infections.

 

 

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Medical Marijuana Use Increasing

from Fortune magazine

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How marijuana became legal

Medical marijuana is giving activists a chance to show how a legitimized pot business can work. Is the end of prohibition upon us?

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By Roger Parloff, senior editor
Last Updated: September 18, 2009: 3:30 PM ET

 

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Irv Rosenfeld is one of four U.S. citizens who get their medical marijuana from the federal government.
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Medical marijuana's high society
A pictorial essay on the growers, sellers and users of legal pot. Photographs by Robyn Twomey

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Stephen DeAngelo founded Harborside to show that a marijuana dispensary could make a positive contribution to a community.
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//

(Fortune Magazine) — When Irvin Rosenfeld, 56, picks me up at the Fort Lauderdale airport, his SUV reeks of marijuana. The vice president for sales at a local brokerage firm, Rosenfeld has been smoking 10 to 12 marijuana cigarettes a day for 38 years, he says.

That’s probably unusual in itself, but what makes Rosenfeld exceptional is that for the past 27 years, he has been copping his weed directly from the United States government.

Every 25 days Rosenfeld goes to a pharmacy and picks up a tin of 300 federally grown and rolled cigarettes that have been sent there for him by the National Institute of Drug Abuse (NIDA), acting with approval from the U.S. Food and Drug Administration.

Rosenfeld smokes the marijuana to relieve chronic pain and muscle spasms caused by a rare bone disease. When he was 10, doctors discovered that his skeleton was riddled with more than 200 tumors, due to a condition known as multiple congenital cartilaginous exostosis. Despite seven operations, he still lives with scores of tumors in his bones.

Rosenfeld is one of four people in the United States whom the federal government supplies with medical marijuana. Each is a living anomaly because, officially, the U.S. Drug Enforcement Administration, NIDA, and the FDA all take the position that marijuana has “no currently accepted medical use.”

That’s the only way federal law can continue to classify marijuana, like heroin, as a “Schedule I controlled substance,” forbidden from being prescribed by doctors. (Numerous dangerous, psychoactive, and addictive opium derivatives, by contrast, are more leniently classified as Schedule II drugs, allowing prescription use.)

Over the years the government’s position has become progressively more embattled, if not untenable.

Thirteen states now have laws that let residents use marijuana medicinally, typically to alleviate chronic pain (particularly nerve pain caused by diabetes, AIDS, and hepatitis); manage movement disorders and muscle spasticity (especially for multiple sclerosis patients); as an anti-nausea and anti-vomiting agent (for those, say, undergoing chemotherapy); and as an appetite stimulant (yes, as in “the munchies”) for those with wasting diseases like AIDS and cancer.

Another 15 states are weighing legislation or ballot initiatives that could turn them into medical marijuana states by next year.

The acceptance of medical marijuana has implications that extend far beyond helping those suffering from life-threatening diseases. It is one of several factors — including demographic changes, the financial crisis, and the widely perceived failure of the war on drugs — reopening the country’s 40-year-old on-again, off-again shouting match over whether marijuana should be legalized.

This article is not another polemic about why it should or shouldn’t be. Today, in any case, the pertinent question is whether it already has been — at least on a local-option basis. We’re referring to a cultural phenomenon that has been evolving for the past 15 years, topped off by a crucial policy reversal that was quietly instituted by President Barack Obama in February.

First, some necessary background. Under President George W. Bush (and under President Bill Clinton before him, for that matter), the U.S. Justice Department treated state medical marijuana laws as nullities. Such laws were contradicted and therefore preempted by federal drug laws, the Justice Department reasoned, and the U.S. Supreme Court upheld that position in 2005.

Accordingly, the federal government has periodically raided and prosecuted defendants who at least claimed to be complying with state medical marijuana laws, and when it did, defendants were forbidden from telling juries about the existence of those laws.

In late February, President Obama signaled a new approach. His attorney general, Eric Holder, confirmed at a press conference that he would no longer subject individuals who were complying with state medical marijuana laws to federal drug raids and prosecutions.

0:00 /3:38Pot from Uncle Sam//

This understated act — a simple pledge not to act, really — could have enormous consequences. It potentially leads to exactly the same endpoint as the Twenty-First Amendment, which repealed the federal prohibition on alcoholic beverage sales.

Here’s how. When states make a legal loophole allowing medical use of marijuana, they must grapple with the messy question of what precisely constitutes medical use. After all, doctors regularly prescribe powerful drugs like Valium, Viagra, Prozac, and — give us a break — Botox to patients who are hardly at death’s door.

If a state doesn’t tightly limit what “medical use” means, the camel can get its nose under the tent.

That’s what happened in California. Like most medical marijuana states, California permits doctors to “recommend” marijuana use for patients who suffer from specific serious diseases. (Drafters of the law avoided the word “prescribe” in an attempt to sidestep conflict with federal law.)

California’s law then adds a catchall provision that lets doctors also approve marijuana use for “any other illness for which marijuana provides relief.” In practice, doctors — largely protected from second-guessing by confidentiality privileges — have been free to make the final call as to which conditions those might be.

This is, after all, the norm vis-à-vis medicines. Once a pharmaceutical has been FDA-approved for one use, doctors can lawfully prescribe it for other, so-called off-label purposes, even though the drug has not yet been certified as safe or effective for them.

Accordingly, California doctors are authorizing patients to take marijuana to relieve such ailments as anxiety, headache, premenstrual syndrome, and trouble sleeping. “You could get it for writer’s block,” comments Allen St. Pierre, the executive director of the National Organization for the Reform of Marijuana Laws.

Some California doctors voluntarily report the breakdown of patient medical conditions for which they have approved marijuana use in the Alameda, Calif., medical newsletter O’Shaughnessy’s.

They commonly report that more than a quarter of their marijuana authorizations have been prompted by patients suffering from conditions like “anxiety” or “insomnia.” (The most common complaint is “chronic pain.”)

As a result, in most of California’s coastal metropolitan areas, marijuana is effectively legal today. Any resident older than 18 who gets a note from a doctor can lawfully buy the stuff, and doctors seemingly eager to write such notes, typically in exchange for a $200 consultation fee, advertise in newspapers and on websites.

There are an estimated 300,000 to 400,000 medical marijuana patients in the state now, and the figure is rapidly growing.

More astonishingly, there are about 700 medical marijuana dispensaries now operating in California openly distributing the drug.

These dispensaries — called “compassionate-care clinics” by the solemn and “pot shops” by the skeptical — are decidedly outpatient facilities, with not a few patients arriving on bicycles, roller skates, or skateboards. (They often get discounts for doing so, because it’s greener than using a fossil-fuel-powered car.)

The dispensaries sell marijuana and its concentrated resin forms, hashish and kif, sometimes alongside a range of enticing, non-inhaled alternatives, including marijuana-imbued brownies, cookies, gelati, honeys, butters, cooking oils (“Not So Virgin” olive oil), bottled cold drinks (“enhanced” lemonade is the most popular), capsules, lozenges, spray-under-the-tongue tinctures, and even topically applied salves.

In Los Angeles a high-end three-store chain called the Farmacy employs a pastry chef to oversee production of all its baked goods. Most dispensaries also sell potted plants and seeds for patients who are either thrifty or entrepreneurial.

All these establishments are engaged in what federal penal statutes still humorlessly define as narcotics trafficking. The dispensaries’ affiliated marijuana farms and plant nurseries are sometimes of sufficient size to subject operators to mandatory-minimum five-year federal prison terms.

And this, mind you, is a situation that evolved almost entirely during the Bush administration, when the U.S. Drug Enforcement Administration was still routinely threatening dispensary landlords with forfeiture of their premises, periodically raiding clinics and seizing inventories, and criminally prosecuting the most brazenly abusive operators.

Luke Scarmazzo, who aired a rap video on YouTube two years ago boasting of all the money and great sex he was getting from running the California Healthcare Collective in Modesto, Calif. — “Fuck the feds!” was one ill-advised lyric — was sentenced in federal court this past December to almost 22 years of imprisonment on a continuing criminal enterprise conviction. (He has appealed.)

While the situation in California is unusual, it’s becoming less so. There are now 15 dispensaries in Colorado, according to weedmaps.com, one of many online marijuana dispensary and physician (“pot-doc”) locator services. In Oregon nearly one in four active physicians has authorized at least one of his patients to grow marijuana for medical use.

New Mexico hopes to have the nation’s first state-licensed medical marijuana farm and distributorship up and running by the time this article is published. New Mexico’s law was enacted two years ago, but state officials hadn’t dared implement it until Attorney General Holder blew the all clear in February.

This is the sense in which President Obama’s understated pledge not to interfere with state medical marijuana laws potentially achieves for that intoxicant what the Twenty-First Amendment accomplished for beer, wine, and booze during the Great Depression.

Repeal, remember, simply returned to the states the right to decide whether to permit alcoholic beverage sales, and, if so, when and how. If a state permitted sales, it could also enforce minimum- age requirements, limit store hours, set zoning restrictions, and levy taxes. If it prohibited sales, it could bask in righteousness but exercise no control over the traffic that would occur anyway.

Over time nearly every state fell in line behind the tax-and-regulate model. (During Prohibition, federal law did contain an exception allowing alcoholic beverage sales for medical purposes. Nevertheless the case for medical booze was never compelling, and after repeal no state chose to condition the legality of alcohol sales upon a showing of medical need.)

“I think we’re going to have exactly that kind of local option with marijuana [that we now have with alcohol],” says Keith Stroup, 65, NORML’s founder, two-time past executive director, and current legal counsel. “Once that happens it will be like gambling.”

Initially only Nevada permitted gambling, and then it was just Nevada and New Jersey. “But over a period of time,” Stroup says, “the morality part of the issue kind of dissipated, and there were more and more needs for new revenue, and today almost every state in the country allows legalized gambling.”

Marijuana activists thought they were close to legalization once before. From 1973 to 1978 activists won decriminalization in 11 states. (“Decriminalization” is a grab-bag term but usually refers to schemes under which first-time possession of small quantities of marijuana becomes a noncriminal violation, akin to a parking ticket. Decriminalization falls short of legalization, in that sale and distribution remain serious felonies.)

In 1977, President Jimmy Carter endorsed a federal decriminalization bill. But the bill went nowhere, and soon the movement was all but obliterated by the return swing of the cultural pendulum, now known as the Reagan Revolution. There would be no new state or federal marijuana reforms for the next 16 years.

“Here’s what’s different now,” asserts Ethan Nadelmann, the head of the Drug Policy Alliance, which favors marijuana legalization on a tax-and-regulate model. “First, in the late 1970s no more than 30% of the American public supported making marijuana legal. Now it’s breaking 40%.”

That jump reflects an important demographic change, Nadelmann notes. “Back then there was a whole older generation of Americans who didn’t know the difference between marijuana and heroin,” he says. “Now that generation is mostly gone. The people in power are baby boomers, a majority of whom actually smoked marijuana.”

The past three Presidents have all more or less admitted trying the drug, Nadelmann continues, and the current one, when asked if he inhaled, famously retorted, “I thought that was the point.”

Beyond the demographic change, there is a perception that after 40 years of blood, sweat, and tears, the war on drugs — formally declared by President Richard Nixon in 1969, a month before the Woodstock festival — has failed to reduce the availability of illegal drugs, has enriched and empowered organized-crime gangs, and has subjected millions of people to arrest who pose little threat to anyone but themselves.

On top of that, we’re now mired in the worst economic environment since the Great Depression, which makes the prospect of collecting taxes on marijuana sales as alluring to contemporary politicians as beer, wine, and liquor taxes looked to President Franklin Delano Roosevelt and his party when they took office in 1933, the year Prohibition was repealed.

Assuming a national consumer market for marijuana of about $13 billion annually, Harvard economist Jeffrey Miron has estimated that legalization could be expected to bring state and federal governments about $7 billion annually in additional tax revenue, while saving them $13.5 billion in prohibition-related law enforcement costs.

In California, where the fiscal crisis is so grave that the state has had to issue vendors more than $1 billion in IOUs, a Field Poll published in April showed that 56% of the state’s population favored legalizing marijuana, prompting Gov. Arnold Schwarzenegger to call for an “open debate” on the question. A legalization bill has been introduced in the state legislature, and the state board of equalization has estimated that if passed, it would bring in $1.4 billion in new revenue, a seemingly conservative estimate.

It’s even possible that legalization would reduce national health-care costs, by easing demand for costly pharmaceuticals.

In the most recent issue of O’Shaughnessy’s, one doctor reported that his cannabis patients had either stopped or cut back their use of “analgesics of all kinds [including] Tylenol, aspirin, and opioids; psychotherapeutic agents including anti-anxiety medications, anti-depressants, anti-panic, obsessive-compulsive, anti-psychotic, and bipolar agents; gastrointestiminal agents including anti-spasmodics and anti-inflammatory medications; migraine preparations; anticonvulsants; appetite stimulants; immuno-modulators and immunosuppressives; muscle relaxants; multiple sclerosis management medications; ophthalmic preparations; sedative and hypnotic agents; and Tourette’s syndrome agents.”

“Medical marijuana is God’s little joke on the [marijuana] prohibitionists,” says Richard Cowan, 69, a longtime legalization activist who claims he’s smoked almost every day since 1967. “There is clearly a medical need, and it ranges from minor to life-saving…. From my perspective, the dividing line between medical and nonmedical should not be decided by the police.”

Medical marijuana is clearly the crowning factor making things different this time. Not only is it changing perceptions of the drug, but it has also given legalization advocates in California a first-ever opportunity to devise and showcase a business prototype.

They’ve been afforded the chance to show a skeptical public that a safe, seemly, and responsible system for distributing marijuana is possible. If they succeed, they’ll convince the fence sitters and lead the way to a nationwide metamorphosis.

If they fail, the backlash will be savage. If communities cannot adequately regulate the dispensaries, they’ll descend into unsightly, youth-seducing, crime-ridden playgrounds for gang-bangers, and this flirtation with legalization will conclude the way the last one did: with a swift and merciless swing of the pendulum.

Pot’s medical history

Marijuana, whose botanical name is cannabis, has been used medicinally — and as an intoxicant, of course — for thousands of years in Eastern cultures. It is believed to have been introduced to Western medicine in the early 19th century by a British doctor, W.B. O’Shaughnessy, who learned about it while stationed in India (and for whom the medical cannabis newsletter is named).

Several well-known pharmaceutical companies, including Eli Lilly (LLY, Fortune 500), sold cannabis in powdered or tincture forms in the early 20th century as a painkiller, antispasmodic, sedative, and “exhilarant.” (For this article Fortune asked Eli Lilly for historical details on its cannabis sales, but a spokeswoman responded, “Due to competing priorities, we … are unable to facilitate your query.”)

Though cannabis remained listed in the U.S. Pharmacopeia — a standard desk reference for drugs — until 1942, its use in Western medicine began declining in the late 1800s, according to a history of cannabis written by Harvard psychiatrist Lester Grinspoon titled “Marijuana: The Forbidden Medicine.”

The decline, Grinspoon writes, was due in part to the rise of more stable and effective pharmaceuticals — though many of them later proved to have grave potential side effects — and because modern hypodermic syringes could deliver faster pain relief using opiates. (Opiates were soluble; cannabis wasn’t.)

Then, in the early 1900s, states began outlawing cannabis, which had become associated in legislators’ minds with violent crime and psychosis. The drug was then being used in the U.S. mainly by Mexican migrant workers in the West and African Americans in the South, so apprehensions about it may have been intertwined with racial and ethnic fears. In 1937 the federal government, over the objections of the American Medical Association, effectively outlawed cannabis.

Modern-day medical assessments of marijuana’s properties have not corroborated the outsize dangers that lawmakers had attributed to the plant. While it is a “powerful drug,” concluded an Institute of Medicine report conducted in 1997 at the behest of the White House Office of National Drug Control Policy, its “adverse effects … are within the range of effects tolerated for other medications.”

Yes, someone who is high on marijuana shouldn’t drive — his motor skills and mental powers are impaired — but that’s true of alcohol and many prescription drugs too.

The long-term risks to chronic users appear to center mainly on the generic dangers of smoking (respiratory disease and possibly lung cancer) and upon the “mild and short-lived” withdrawal symptoms that a minority of marijuana users experience, according to the IOM experts. They considered marijuana less addictive than tobacco, codeine, or Valium.

Still, many doctors are squeamish about recommending marijuana to patients — putting aside issues of legal liability. To begin with, most pharmaceuticals consist of a single, purified chemical compound. Such drugs are susceptible to double-blind, placebo-controlled testing, and once they are approved, doctors can prescribe known dosages.

Marijuana, in contrast, consists of the dried, ground-up flowers of a highly variable plant. It is made up of at least 400 compounds, including more than 60 that are unique to cannabis, known as cannabinoids, several of which are believed to have therapeutic effects. The proportions of these compounds vary greatly from plant to plant. A plant may attract harmful molds.

Lighting a match to the mix then introduces a whole new set of variables. Finally, smoking — even putting aside its health risks — is an idiosyncratic delivery system. Everyone smokes differently, so one never knows how much of which compounds the patient is receiving. These factors all make marijuana hard for researchers to test meaningfully and hard for doctors to prescribe confidently.

Accordingly, even those doctors who recognize the therapeutic powers of marijuana often prefer the notion of looking for one or two key active ingredients in it, isolating them, and then devising a delivery system that would not involve smoking.

And that’s been done. In 1986 the FDA approved a synthetic version of what has long been recognized to be the main psychoactive ingredient of marijuana — delta-9-tetrahydrocannabinol, or THC. After rigorous testing, the FDA found THC to be safe and effective for the treatment of nausea, vomiting, and wasting diseases. This lawful, Schedule II drug, trade-named Marinol, is taken orally, by capsule.

The trouble is, for many patients Marinol turns out to be inferior to good old-fashioned pot. Smoked marijuana is much faster acting and, as a consequence, easier for patients to control in terms of dosage. The patient inhales as much as he needs and then stops. In contrast, with a THC pill the patient can easily ingest more than he can handle.

“Oral THC is slow in onset of action but produces more pronounced, and often unfavorable, psychoactive effects that last much longer than those experienced with smoking,” according to a 2008 report published by the American College of Physicians. (Incidentally, the FDA-approved warnings for Marinol — pure THC — do not flatly forbid patients from driving under its influence. Rather, they simply caution patients not to do so “until it is established that they are able to tolerate the drug and to perform such tasks safely.”)

Still, despite the disappointing performance of oral THC, many doctors want to continue exploring faster-acting THC delivery systems, including a skin patch or a suppository.

Meanwhile we’re still awaiting hard proof that smoking marijuana can actually cause lung cancer. That evidence has proved surprisingly elusive, maybe in part because typical marijuana users smoke so much less than typical tobacco smokers.

In any case, marijuana users are increasingly turning to a means of inhalation that does not involve smoking known as vaporization. With a vaporizer — the Volcano brand is the best known — users heat marijuana to a temperature sufficient to vaporize the cannabinoids but insufficient to spark combustion and most of its associated noxious gases. The vapors are captured in a balloon and then inhaled.

The government’s compassionate-use program

As a teenager Irv Rosenfeld was a strong opponent of marijuana use. He would sometimes give talks against marijuana at local schools. “I’d hold up bags of my prescription drugs and say, ‘Be thankful you’re healthy,’” he recounts. He was then taking prescription muscle relaxants, sleeping pills, anti-inflammatories, and a range of addictive, debilitating, opioid painkillers, including codeine, Demerol, and Darvon.

Shortly after Rosenfeld started college at the University of Miami, he caved in to peer pressure and tried pot. “Nothing happened,” he says. (To this day Rosenfeld maintains that he never has been able to get high from marijuana. In my six or so hours with him, during which he drove me from Fort Lauderdale to Miami and back, all the while chain-smoking joints, I never noticed any apparent impact on him, other than an occasional cough.)

Rosenfeld continued smoking socially when others did. “About the 10th time,” he continues, “I was playing chess when I realized that I’d been sitting still for 30 minutes.” Normally he couldn’t do that because his muscles would begin to ache and he’d have to change position. “I hadn’t taken a pill in six hours. Just then someone handed me the joint, and it hit me. The only thing I’d done different was smoke pot.”

Rosenfeld ran repeated experiments, and both he and his surgeon became convinced that marijuana helped him more than his prescription drugs, with fewer side effects. In 1971, with the blessing of his doctors and the indulgence of sympathetic police officials, he began smoking marijuana to treat his pain.

Then, in 1976, Rosenfeld learned of the extraordinary case of Bob Randall (now deceased). Randall, who had severe glaucoma, had been prosecuted that year for marijuana possession in the District of Columbia but won acquittal after advancing a “medical necessity” defense. Randall’s doctors had testified that he risked going blind without marijuana to relieve the pressure within his eyeballs.

Randall then brought a civil suit against the government. In 1978 a mind-boggling settlement was reached: The government agreed to supply Randall with marijuana for the rest of his life.

The government had the capacity to strike such a deal because since 1968, NIDA had been growing a small quantity of marijuana for research purposes under contract with the University of Mississippi’s pharmacy school. FDA and NIDA officials theorized that the U.S. government could lawfully become Randall’s supplier if they observed the pretense that he was part of a clinical study to investigate a potential new drug. A research “protocol” was drawn up, though the study design called for just one patient: Randall.

Rosenfeld drew up a similar protocol for a clinical study of himself. With the help of supportive doctors and threatening lawyers, Rosenfeld became the second patient to pry his way into what became known as the compassionate-use investigative new drug program.

By 1991 the compassionate-use program had grown to include 13 patients. That year, after Randall counseled AIDS advocacy groups on how to seek admission to the program, it suddenly found itself deluged with 40 new applications. In early 1992, seeing the unworkable direction in which matters were headed, the government shut the program down, though the 13 existing patients were grandfathered in. Today just four are left, including Rosenfeld.

For them, federal marijuana grown at the University of Mississippi is sent to a contractor in Research Triangle Park, N.C., where it is rolled into cigarettes on an old machine obtained from the local tobacco industry. About every five months the contractor sends six tins of the cigarettes to the pharmacy where Rosenfeld picks them up.

Rosenfeld’s weed is hardly connoisseur quality by contemporary California dispensary standards. The government grows its crops only sporadically, so it dries the harvested flowers and places them in cold storage. When I visited him in June, Rosenfeld was smoking marijuana harvested nine years earlier. Because Rosenfeld finds the government’s cigarettes too dry, he unwraps them, rehydrates the marijuana by placing it in a container with lettuce, and then re-rolls his own joints, he says.

Rosenfeld’s cigarettes are also not very potent by contemporary standards. They contain around 3.5% THC, which was about the average strength of dope seized in domestic street busts in 1996, according to NIDA data.

By contrast, marijuana seized from such busts in 2007 had an average potency of about 4.8%, while the fresh “manicured bud” available at today’s best California dispensaries boast THC content ranging from about 6% to 22%.

It’s as if Rosenfeld were receiving vanilla ice cream joylessly made in the Soviet Union and stored for decades, when there’s fresh Ben & Jerry’s Chocolate Chip Cookie Dough for sale just around the corner.

Still, Rosenfeld’s not complaining. The government charges him nothing, so his only costs are medical consultations and pharmacists’ fees — about $50 a month. Subpar or not, the 8.3 ounces he receives every 25 days would cost him more than $2,000 on the street.

The battle to legalize marijuana

After the compassionate-use program was shut down, medical marijuana activists had one last hope for changing federal policies. Back in 1972, NORML and other groups had sued the predecessor of the DEA to force the rescheduling of marijuana as a prescribable drug, and incredibly, two decades later, the litigation was still raging.

During 14 days of hearings in 1986 the plaintiffs had presented many anecdotal accounts of nearly miraculous experiences patients had had with marijuana. Rosenfeld testified, as did the psychiatrist and medical historian Grinspoon, who related not only the evidence his research had unearthed but also a personal anecdote.

In 1972, Grinspoon’s own teenage son, who had leukemia, began undergoing chemotherapy. “He would start to vomit shortly after treatment and continue retching for up to eight hours,” as Grinspoon later described the ordeal in his book. “He vomited in the car as we drove home, and on arriving he would lie in bed with his head over a bucket on the floor.”

Having heard that marijuana could help, Grinspoon’s wife proposed that the couple let their son try it, but Grinspoon refused because it was illegal. His wife then defied him, secretly smoking marijuana with the teenager before one of his treatments. This time there was no vomiting, and in fact, on the way home the child asked to stop for a submarine sandwich. “From then on he used marijuana before every treatment, and we were all much more comfortable during the remaining year of his life,” according to Grinspoon’s account.

In 1988 the administrative law judge hearing the case ruled in NORML’s favor. “Marijuana, in its natural form, is one of the safest therapeutically active substances known to man,” Judge Francis Young concluded. Young was referring to the fact that it is almost impossible to overdose fatally on marijuana, a circumstance that distinguishes it from virtually any other drug. “By any measure of rational analysis,” Young concluded, “marijuana can be safely used within a supervised routine of medical care.”

In one of those maddening circularities of federal administrative law, however, the DEA’s appeal from Judge Young’s ruling was heard by John C. Lawn, then administrator of the DEA itself. Not surprisingly, in 1989, Lawn overturned all of Young’s findings.

Lawn gave short shrift to anecdotes like Grinspoon’s and Rosenfeld’s. “These stories of individuals who treat themselves with a mind-altering drug … must be viewed with great skepticism,” he wrote. “Many of these individuals had been recreational users of marijuana prior to becoming ill. These individuals’ desire for the drug to relieve their symptoms, as well as a desire to rationalize their marijuana use, removes any scientific value from their accounts.”

Lawn also stressed the absence of any controlled clinical studies proving marijuana’s safety or efficacy. He was right; such studies didn’t exist (at that time), both because of the inherent difficulties of performing them on a whole plant and the unique difficulties of performing them on an illegal plant. To even obtain marijuana for such tests, researchers would have had to first win approval from three federal bureaucracies – the DEA, the FDA, and NIDA — a daunting task even assuming the best of good will on everyone’s part.

As for the controlled studies showing that marijuana’s chief psychoactive ingredient — THC, in the form of Marinol — was safe and effective for treating certain medical conditions, Lawn saw them as simply proving conclusively that there could be no conceivable excuse for smoking marijuana. To whatever extent THC might be helpful, patients could use Marinol.

In 1994 the federal court of appeals for the District of Columbia upheld Lawn’s decision, and the activists’ last hope for achieving reform at the federal level died.

So they turned to state government. In 1996 a group of marijuana activists in California got enough signatures to put a legislative initiative on the ballot known as Proposition 215. It called for permitting medical marijuana patients or their “primary caregivers” to possess marijuana on the “recommendation or approval” of a physician.

The measure passed with a 56% majority, and California became the first medical marijuana state. Precisely what that meant, though, remained totally unclear. Prop. 215 did not specify how much pot patients could possess, and it said nothing about the way patients would obtain it. Nothing in the initiative explicitly legalized sales or distribution of any kind.

Nevertheless, a few intrepid souls opened dispensaries.

Dispensaries – A legal gray area

“In the immediate wake of passage of Prop. 215 in 1996,” recalls Stephen DeAngelo, who would later open what is now Oakland’s largest dispensary, “local governments tended to take a hands-off attitude toward medical cannabis.” They wouldn’t explicitly license dispensaries to open, he says, but they also didn’t instruct the police to go shut them down. “Dispensaries were tolerated but not sanctioned.”

Even those local politicians who supported the goals of Prop. 215 were reluctant to regulate in the area, because any such effort would have had to begin with dispensary operators filling out forms providing incriminating information about themselves. Any such documents could then have been subpoenaed by federal prosecutors and used to shut the operators down or put them in prison.

DeAngelo, now 51, was then a longtime marijuana activist but also a businessman. From 1990 to 2000 he founded and headed the industrial hemp company known as Ecolution. (Hemp, from which rope and other products are made, is a non-psychoactive strain of cannabis. Hemp products are legal in this country, but growing hemp is not.) Excited by the medical cannabis phenomenon in California, DeAngelo moved there in 2001, when the legal environment was still extremely gray.

He found two main types of dispensary managers operating at that time, he recalls. “The best of them were the well-motivated activists who brought really good intentions … but had, for the most part, no business experience whatsoever and no capital to invest. Despite that, they managed to thrive, simply because they were the only game in town.

“This engendered a second wave of operators, who were attracted by the money, as opposed to the cause,” DeAngelo continues. “A whole new wave of dispensaries got thrown up, which I refer to as ‘thug dispensaries.’ These were operations run by people who had a background in illicit activities, whether it was selling cannabis or other drugs on the street, or trading in illegal firearms, or in the porn industry or gambling industry — people comfortable operating in the gray zone. Very rapidly you began to see some big problems. Several armed robberies. You had a spate of stories about operators being arrested.

“As a patient,” says DeAngelo — he uses marijuana to relieve pain from a degenerative disk disease — “I was profoundly unhappy about it. As an activist I became concerned because these types were really hurting the public image of medical cannabis.”

In an effort to improve the Wild West atmosphere, the California legislature then passed Senate Bill 420 (“420″ is a slang term for pot), which took effect in 2004. This law fleshed out a bit more about the way Prop. 215 would work, requiring counties to issue identification cards to patients who sought them (to help them in their interactions with the police) and setting up minimum guidelines for how much marijuana patients could possess: eight ounces of dried marijuana plus either six mature plants or 12 immature plants. (Counties could allow higher amounts.)

Though SB 420 was still silent on the issue of dispensaries, it did contain a provision that protected patients or caregivers who “associate … in order collectively or cooperatively to cultivate marijuana for medical purposes.” Accordingly, nearly all the dispensaries in California now claim to be patient “collectives” or “cooperatives,” protected under this provision.

At the same time another provision of SB 420 seemed to cut against the idea that dispensaries were legal — at least as many of them were (and still are) being run. It said that nothing in the law should be construed to “authorize any individual or group to cultivate or distribute marijuana for profit.”

“In my opinion,” says Bill Panzer, a criminal-defense lawyer and marijuana legalization advocate who helped draft Prop. 215, “the vast, overwhelming majority [of dispensaries] are not legal, because they’re not collectives or cooperatives. If somebody owns the store, sells marijuana, and at end of day takes the extra money and puts it in his pocket and goes home, that’s not a collective.”

The proof-of-concept challenge

DeAngelo opened the Harborside Health Center dispensary in Oakland in October 2006 as a proof-of-concept that might show the rest of the nation how such an establishment could provide top-flight patient services, adhere to the letter of the law, and interact with the surrounding community beneficially.

His clinic, across from a scenic stretch of Oakland harbor, is identified only by its address — a large, block-letter “1840″ painted on the façade of an inconspicuous, gray-blue one-story building on Embarcadero Drive.

On the inside it’s a spacious, wood-trimmed, tastefully appointed room that blends clean, contemporary lines with sparingly employed Eastern medicinal themes: a laughing Buddha here, a dancing goddess statuette there.

The mood is broken only by the metal detector at the door and the multiple casino-style cameras embedded in the ceiling. Oakland has a high crime rate, and precautions must be taken. There are at least three security guards inside the facility at all times, as well as two more outside, patrolling Harborside’s 100-car parking lot.

“Whenever a patient comes into the clinic for the first time,” explains DeAngelo, “they sign a collective cultivation agreement. They authorize all the other patients in the collective to grow medical cannabis on their behalf. That sets up a 100% closed-loop distribution system that isolates my patients from any contact with the illicit market.”

But that doesn’t mean that every member of the collective actually knows what a hoe looks like. “For a variety of very valid reasons,” DeAngelo continues, “most patients are unable to grow their own medicine. We act as a clearinghouse between patients who are able to grow and patients who aren’t able to grow.”

Harborside now has 30,000 patients registered in its database, and their purchases of medicine bring in about $20 million annually in revenue, according to DeAngelo. “I’d rather not discuss my specific salary,” he says. “I can tell you if I was working in any other industry and showed the kind of financial returns that this business has shown, I’d be paid three or four times as much as I’m making at Harborside.”

First-time patients, upon stepping through the metal detector at Harborside, immediately undergo a thorough paperwork check. The patient produces his doctor recommendation, the clinic verifies its authenticity with the doctor, and then the clinic also verifies the doctor’s credentials with the state medical board.

About 600 patients come to Harborside each day, according to DeAngelo, most to buy marijuana, a few to supply it. Suppliers can bring in as much as three pounds at a time. (Bay Area police generally allow patients to transport this much, DeAngelo says.) The patient-grown marijuana is inspected for quality, examined for molds and fungi, and tested with a gas chromatograph mass spectrometer to determine its THC content.

At Harborside, there are eight selling stations along a long counter, each near a glass case displaying the wide array of medicines available, labeled as to strain and THC content. “Our most popular strains are our purple strains,” says DeAngelo, “like Purple Urkle or Granddaddy Purple. The purples tend to be heavy indicas” — one of the two main varieties of psychoactive cannabis — “with a very strong, relaxing effect. They have a characteristically sweet, almost candy-like flavor.

“Another popular family of strains is the Kush family,” he continues. “That would include OG Kush, Baba Kush, and Pure Kush. The Kushes tend to be more sativa-dominant,” referring to the other main variety of cannabis, which is said to produce a more cerebral, “daytime appropriate” high, with less body impact. “They have a pungent flavor as opposed to a sweet flavor.”

At Harborside, I experienced a mild personal epiphany: I realized that I never really knew before what fresh marijuana smelled like. Though I had easily recognized, from East Coast college days 30 years back, the smell of smoked marijuana inside Rosenfeld’s SUV, I had never before smelled the sweet, herbal fragrance suffusing Harborside. At first I incorrectly assumed it was some sort of incense being artificially introduced to mask the odor I was familiar with.

As I further inspected Harborside’s medicines, I also realized that I had never really known before what fresh, high-quality marijuana looked like. I remembered baggies half-filled with crushed brown twigs, leaves, stems, and even seeds. But the dispensaries sell only fresh “bud,” which looks like cute, plump, fuzzy caterpillars curled in a ball.

After my education at Harborside I went on to explore some of the other approaches that marijuana entrepreneurs and activists are experimenting with as they try to rise to the proof-of-concept challenge.

Pioneering canna-businessman Richard Lee, also in Oakland, has opened his Blue Sky Café dispensary as a coffee shop, taking his cue from Amsterdam. Lee acknowledges that he runs the Blue Sky as a for-profit business, a situation that the City of Oakland authorities have at least tacitly endorsed, notwithstanding SB 420’s apparent prohibition of “for profit” distribution.

In 2004 the city, seeking to avoid being overrun by dispensaries, passed municipal regulations limiting the permissible number to four. Those regs required that dispensary operators not earn “excessive” profits, which has been understood to imply that some profit must be permissible. Lee was granted one of the city’s four permits.

Lee has also opened an array of affiliated businesses in the immediate neighborhood of the Blue Sky, several of the few bustling businesses in Oakland’s otherwise depressed downtown. The best-known is Oaksterdam University, which trains medical cannabis entrepreneurs to navigate the business and legal challenges.

It also teaches trades to those who seek jobs as, say, a medical cannabis cultivator or “bud-tender,” i.e., the quasi-pharmacist sales clerk who helps customers choose their medicine. Oaksterdam has now opened branches in Los Angeles and Sebastopol, Calif., about an hour north of Oakland, and stages conferences in Ann Arbor.

The most open dispensaries I saw were two branches of the Farmacy chain in Los Angeles. They are full-service herbal medicine stores under the management of registered pharmacist JoAnna LaForce, with marijuana being sold inconspicuously alongside scores of uncontroversial, legal plant products with putative healing powers. At these stores all members of the public, of any age, are welcome to enter, and only those who ask about marijuana are required to produce paperwork. “That way, a young mother with children can come into a store and not feel like a criminal,” LaForce explains.

For my aesthetic taste, the most inviting dispensary I toured was the immaculate Peace in Medicine facility in Sebastopol. Here, patients enter a handsome, freshly painted house — the former sales office for a Ford dealership — and come to what looks like a cheery doctor’s waiting room.

After taking care of the paperwork, patients are summoned into the dispensary. There, I mention to Robert Jacobs, 32, Peace in Medicine’s idealistic young executive director, how enticing the fresh medicine smells. “If it smells good, the body probably wants it,” he responds, smiling a bit and sounding like Eve in the Garden of Eden.

I then notice a journalistic hole opening up in my reporting. Until now I had assumed that my haphazard, stale, youthful experiences with marijuana would need no refreshing in order for me to write a thorough article about medical cannabis. Now I’m not so sure.

Unfortunately, most dispensaries are intransigent about serving only California residents, and I am not one. I explain my quandary to Jacobs. Listening back upon my words as they hang in the air, I realize that it sounds as if I’ve just asked him to break the law. He very politely declines.

Taxing and regulating dispensaries

In the early days of dispensaries the California Board of Equalization, which collects state and local sales tax, refused to issue seller’s permits to dispensaries that sought them — the necessary prelude to paying sales tax in the state. The board viewed such establishments as certainly illegal under federal law, and possibly illegal under state law.

In October 2005 the board changed tack and began allowing dispensaries to pay sales taxes if they wanted, and in 2007 it completed the reversal by requiring them to pay sales taxes and demanding that they do so retroactively to October 2005.

The board assured the dispensaries in a February 2007 letter that it would now issue seller’s permits even if the dispensary refused to answer portions of the standard application — identifying the product sold, for instance, or listing suppliers — due to “concerns about confidentiality or self-incrimination.”

Since sellers’ permits do not require establishments to identify themselves as medical marijuana dispensaries, the board has no hard records on sales taxes collected from them. Unless there is extremely poor compliance by dispensaries, however, the numbers should be robust.

Harborside alone reported about $15 million in sales in 2008, for instance, and DeAngelo estimates that the average revenue for each of California’s 700 dispensaries probably ranges from $3 million to $4 million annually. If so, gross statewide medical cannabis sales are approaching $2.5 billion, generating taxes of around $220 million. That does not include the state and federal income taxes that dispensaries and their employees also pay, and employee payroll taxes.

In addition some localities, like Oakland, have begun imposing their own taxes. Each of Oakland’s four dispensaries pays the city $30,000 annually for its license, plus a business tax on gross sales (over and above state or local sales tax).

This past July, Oakland increased that business tax 15 times over, from $1.20 to $18 for every $1,000 in sales. Tellingly, the increase had been sought by the dispensary owners themselves, who well understand the importance of being seen as good citizens and becoming indispensable to the city’s revenue supply.

Has medical cannabis been a good thing for Oakland? “I think so,” says Ignacio De La Fuente, Oakland’s current deputy mayor and, from 1998 to 2008, president of its city council. “I was not one of the initial supporters,” he concedes, and he still doesn’t favor legalizing marijuana for recreational purposes. “But I became educated about the medicinal value of cannabis” over the years of debate, De La Fuente explains. “You kind of make a decision of, Is this measure worth the risk to help the people that really need it?”

On balance he believes it was, though he urges other localities considering legalizing medical marijuana to “do their homework about how they want to regulate establishments, so they don’t become a problem or a nuisance.”

“It’s not working,” says Councilman Dennis Zine of Los Angeles, a city that began regulating its dispensaries late, and is now overrun. “Too many of these places have become distribution places for recreational purposes under the guise of medical,” he says.

In 2007 the city set a deadline after which no new dispensaries would be permitted. A staggering 186 establishments met the cutoff, yet another 736 filed late applications, citing a “hardship” exception, and many of those opened too. Zine estimates that there are about 600 dispensaries in his city. He seeks tougher regulations, plus assistance from city, state, and federal authorities to help shut down any operator whose intent is “profit-making” as opposed to “compassionate” distribution for “medical purposes.”

“I think the next five or six years are going to be incredibly exciting for this issue,” says Stroup, who founded the National Organization to Reform Marijuana Laws 39 years ago. “I honestly believe we’ll stop arresting individual smokers in almost all states and start to see the first one or two states experiment with a legalization bill.”

Although Stroup originally wanted the “R” in NORML to stand for “Repeal,” he was later talked into softening it to “Reform” by cooler, more politically savvy advisers. Now he thinks society might finally be closing in on his original goal.

Could be. Just watch out for those swinging pendulums. To top of page

First Published: September 11, 2009: 4:20 PM ET

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Destruction of Mold Contaminated Products Was First Recommended In Bible

The Envirionmental Protection Agency estimates 30 percent of buildings in the United States are contaminated with mold neurotoxins.  Aspergillus, Fusarium and Stachybotrus molds can all produce fatal neurotoxins.  Deadly peanut allergies are caused by fungal Aflatoxins.

Florida Detox and Wellness Institute offers testing and treatment for mold neurotoxicity, which can cause disability and hundreds of symptoms, including addiction, anxiety, depression,  fatigue, irritibility, fibromyalgia, attention deficit disorders, immune suppression, headaches, including migraines, cancer and many other disorders.

We are excited to be able to offer testing for Ochratoxin, Tricothecene and Aflatoxin mold neurotoxins, in addition to genetic testing for increased sensitivity to Lymes Disease and mold neurotoxins.  Twenty four percent of the population possesses specific HLA DR DQ genetic patterns, which reduce their ability to clear mold neurotoxins over 400 percent, compared to the other seventy six percent of the population, which does not genetically clear mold neurotoxins more slowly.  This explains why only a minority of us are affected by sick building syndromes, caused by mold contamination.

Steven Sponaugle, Research Director, Florida detox and Wellness Institute

www.floridadetox.com

Leviticus, Chapter 13

47 “If any clothing is contaminated with mildew—any woolen or linen clothing, 48 any woven or knitted material of linen or wool, any leather or anything made of leather- 49 and if the contamination in the clothing, or leather, or woven or knitted material, or any leather article, is greenish or reddish, it is a spreading mildew and must be shown to the priest. 50 The priest is to examine the mildew and isolate the affected article for seven days. 51 On the seventh day he is to examine it, and if the mildew has spread in the clothing, or the woven or knitted material, or the leather, whatever its use, it is a destructive mildew; the article is unclean. 52 He must burn up the clothing, or the woven or knitted material of wool or linen, or any leather article that has the contamination in it, because the mildew is destructive; the article must be burned up.

53 “But if, when the priest examines it, the mildew has not spread in the clothing, or the woven or knitted material, or the leather article, 54 he shall order that the contaminated article be washed. Then he is to isolate it for another seven days. 55 After the affected article has been washed, the priest is to examine it, and if the mildew has not changed its appearance, even though it has not spread, it is unclean. Burn it with fire, whether the mildew has affected one side or the other. 56 If, when the priest examines it, the mildew has faded after the article has been washed, he is to tear the contaminated part out of the clothing, or the leather, or the woven or knitted material. 57 But if it reappears in the clothing, or in the woven or knitted material, or in the leather article, it is spreading, and whatever has the mildew must be burned with fire. 58 The clothing, or the woven or knitted material, or any leather article that has been washed and is rid of the mildew, must be washed again, and it will be clean.”

59 These are the regulations concerning contamination by mildew in woolen or linen clothing, woven or knitted material, or any leather article, for pronouncing them clean or unclean.

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Computer Viruses Can Load Child Pornography Onto Computers

 

AP IMPACT: Framed for child porn — by a PC virus

  • By JORDAN ROBERTSON, AP Technology Writer – Sun Nov 8, 2009 12:17PM EST
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  • San Jose Mercury News Monday 02nd November, 04:33:51 PM

Of all the sinister things that Internet viruses do, this might be the worst: They can make you an unsuspecting collector of child pornography.

Heinous pictures and videos can be deposited on computers by viruses — the malicious programs better known for swiping your credit card numbers. In this twist, it’s your reputation that’s stolen.

Pedophiles can exploit virus-infected PCs to remotely store and view their stash without fear they’ll get caught. Pranksters or someone trying to frame you can tap viruses to make it appear that you surf illegal Web sites.

Whatever the motivation, you get child porn on your computer — and might not realize it until police knock at your door.

An Associated Press investigation found cases in which innocent people have been branded as pedophiles after their co-workers or loved ones stumbled upon child porn placed on a PC through a virus. It can cost victims hundreds of thousands of dollars to prove their innocence.

Their situations are complicated by the fact that actual pedophiles often blame viruses — a defense rightfully viewed with skepticism by law enforcement.

“It’s an example of the old `dog ate my homework’ excuse,” says Phil Malone, director of the Cyberlaw Clinic at Harvard’s Berkman Center for Internet & Society. “The problem is, sometimes the dog does eat your homework.”

The AP’s investigation included interviewing people who had been found with child porn on their computers. The AP reviewed court records and spoke to prosecutors, police and computer examiners.

One case involved Michael Fiola, a former investigator with the Massachusetts agency that oversees workers’ compensation.

In 2007, Fiola’s bosses became suspicious after the Internet bill for his state-issued laptop showed that he used 4 1/2 times more data than his colleagues. A technician found child porn in the PC folder that stores images viewed online.

Fiola was fired and charged with possession of child pornography, which carries up to five years in prison. He endured death threats, his car tires were slashed and he was shunned by friends.

Fiola and his wife fought the case, spending $250,000 on legal fees. They liquidated their savings, took a second mortgage and sold their car.

An inspection for his defense revealed the laptop was severely infected. It was programmed to visit as many as 40 child porn sites per minute — an inhuman feat. While Fiola and his wife were out to dinner one night, someone logged on to the computer and porn flowed in for an hour and a half.

Prosecutors performed another test and confirmed the defense findings. The charge was dropped — 11 months after it was filed.

The Fiolas say they have health problems from the stress of the case. They say they’ve talked to dozens of lawyers but can’t get one to sue the state, because of a cap on the amount they can recover.

“It ruined my life, my wife’s life and my family’s life,” he says.

The Massachusetts attorney general’s office, which charged Fiola, declined interview requests.

At any moment, about 20 million of the estimated 1 billion Internet-connected PCs worldwide are infected with viruses that could give hackers full control, according to security software maker F-Secure Corp. Computers often get infected when people open e-mail attachments from unknown sources or visit a malicious Web page.

Pedophiles can tap viruses in several ways. The simplest is to force someone else’s computer to surf child porn sites, collecting images along the way. Or a computer can be made into a warehouse for pictures and videos that can be viewed remotely when the PC is online.

“They’re kind of like locusts that descend on a cornfield: They eat up everything in sight and they move on to the next cornfield,” says Eric Goldman, academic director of the High Tech Law Institute at Santa Clara University. Goldman has represented Web companies that discovered child pornographers were abusing their legitimate services.

But pedophiles need not be involved: Child porn can land on a computer in a sick prank or an attempt to frame the PC’s owner.

In the first publicly known cases of individuals being victimized, two men in the United Kingdom were cleared in 2003 after viruses were shown to have been responsible for the child porn on their PCs.

In one case, an infected e-mail or pop-up ad poisoned a defense contractor’s PC and downloaded the offensive pictures.

In the other, a virus changed the home page on a man’s Web browser to display child porn, a discovery made by his 7-year-old daughter. The man spent more than a week in jail and three months in a halfway house, and lost custody of his daughter.

Chris Watts, a computer examiner in Britain, says he helped clear a hotel manager whose co-workers found child porn on the PC they shared with him.

Watts found that while surfing the Internet for ways to play computer games without paying for them, the manager had visited a site for pirated software. It redirected visitors to child porn sites if they were inactive for a certain period.

In all these cases, the central evidence wasn’t in dispute: Pornography was on a computer. But proving how it got there was difficult.

Tami Loehrs, who inspected Fiola’s computer, recalls a case in Arizona in which a computer was so “extensively infected” that it would be “virtually impossible” to prove what an indictment alleged: that a 16-year-old who used the PC had uploaded child pornography to a Yahoo group.

Prosecutors dropped the charge and let the boy plead guilty to a separate crime that kept him out of jail, though they say they did it only because of his age and lack of a criminal record.

Many prosecutors say blaming a computer virus for child porn is a new version of an old ploy.

“We call it the SODDI defense: Some Other Dude Did It,” says James Anderson, a federal prosecutor in Wyoming.

However, forensic examiners say it would be hard for a pedophile to get away with his crime by using a bogus virus defense.

“I personally would feel more comfortable investing my retirement in the lottery before trying to defend myself with that,” says forensics specialist Jeff Fischbach.

Even careful child porn collectors tend to leave incriminating e-mails, DVDs or other clues. Virus defenses are no match for such evidence, says Damon King, trial attorney for the U.S. Justice Department’s Child Exploitation and Obscenity Section.

But while the virus defense does not appear to be letting real pedophiles out of trouble, there have been cases in which forensic examiners insist that legitimate claims did not get completely aired.

Loehrs points to Ned Solon of Casper, Wyo., who is serving six years for child porn found in a folder used by a file-sharing program on his computer.

Solon admits he used the program to download video games and adult porn — but not child porn. So what could explain that material?

Loehrs testified that Solon’s antivirus software wasn’t working properly and appeared to have shut off for long stretches, a sign of an infection. She found no evidence the five child porn videos on Solon’s computer had been viewed or downloaded fully. The porn was in a folder the file-sharing program labeled as “incomplete” because the downloads were canceled or generated an error.

This defense was curtailed, however, when Loehrs ended her investigation in a dispute with the judge over her fees. Computer exams can cost tens of thousands of dollars. Defendants can ask the courts to pay, but sometimes judges balk at the price. Although Loehrs stopped working for Solon, she argues he is innocent.

“I don’t think it was him, I really don’t,” Loehrs says. “There was too much evidence that it wasn’t him.”

The prosecution’s forensics expert, Randy Huff, maintains that Solon’s antivirus software was working properly. And he says he ran other antivirus programs on the computer and didn’t find an infection — although security experts say antivirus scans frequently miss things.

“He actually had a very clean computer compared to some of the other cases I do,” Huff says.

The jury took two hours to convict Solon.

“Everybody feels they’re innocent in prison. Nobody believes me because that’s what everybody says,” says Solon, whose case is being appealed. “All I know is I did not do it. I never put the stuff on there. I never saw the stuff on there. I can only hope that someday the truth will come out.”

But can it? It can be impossible to tell with certainty how a file got onto a PC.

“Computers are not to be trusted,” says Jeremiah Grossman, founder of WhiteHat Security Inc. He describes it as “painfully simple” to get a computer to download something the owner doesn’t want — whether it’s a program that displays ads or one that stores illegal pictures.

It’s possible, Grossman says, that more illicit material is waiting to be discovered.

“Just because it’s there doesn’t mean the person intended for it to be there — whatever it is, child porn included.”

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Vitamin D supplementation reduces insulin resistance

British Journal of Nutrition Cambridge University Press
Copyright © The Authors 2009
doi:10.1017/S0007114509992017

Full Papers

 

Human and Clinical Nutrition

Vitamin D supplementation reduces insulin resistance in South Asian women living in New Zealand who are insulin resistant and vitamin D deficient – a randomised, placebo-controlled trial


Pamela R. von Hursta1 c1, Welma Stonehousea1 and Jane Coada2

 

a1 Institute of Food, Nutrition and Human Health, Massey University, Private Bag 102 904, North Shore Mail Centre, Auckland, New Zealand
a2 Institute of Food, Nutrition and Human Health, Massey University, Palmerston North, New Zealand

Abstract

Low serum 25-hydroxyvitamin D (25(OH)D) has been shown to correlate with increased risk of type 2 diabetes. Small, observational studies suggest an action for vitamin D in improving insulin sensitivity and/or insulin secretion. The objective of the present study was to investigate the effect of improved vitamin D status on insulin resistance (IR), utilising randomised, controlled, double-blind intervention administering 100 μg (4000 IU) vitamin D3 (n 42) or placebo (n 39) daily for 6 months to South Asian women, aged 23–68 years, living in Auckland, New Zealand. Subjects were insulin resistant – homeostasis model assessment 1 (HOMA1)>1·93 and had serum 25(OH)D concentration < 50 nmol/l. Exclusion criteria included diabetes medication and vitamin D supplementation >25 μg (1000 IU)/d. The HOMA2 computer model was used to calculate outcomes. Median (25th, 75th percentiles) serum 25(OH)D3 increased significantly from 21 (11, 40) to 75 (55, 84) nmol/l with supplementation. Significant improvements were seen in insulin sensitivity and IR (P = 0·003 and 0·02, respectively), and fasting insulin decreased (P = 0·02) with supplementation compared with placebo. There was no change in C-peptide with supplementation. IR was most improved when endpoint serum 25(OH)D reached ≥ 80 nmol/l. Secondary outcome variables (lipid profile and high sensitivity C-reactive protein) were not affected by supplementation. In conclusion, improving vitamin D status in insulin resistant women resulted in improved IR and sensitivity, but no change in insulin secretion. Optimal vitamin D concentrations for reducing IR were shown to be 80–119 nmol/l, providing further evidence for an increase in the recommended adequate levels. Registered Trial No. ACTRN12607000642482.

(Received June 04 2009)

(Revised August 06 2009)

(Accepted August 11 2009)

Key Words:Vitamin D; Type 2 diabetes; Insulin resistance

Correspondence:

c1 Corresponding author: Pamela R. von Hurst, fax +64 9 443 9640, email p.r.vonhurst@massey.ac.nz

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What To Do if You are Forced to Take Swine Flu Shot

By Dr. Russell Blaylock, M.D. October 2009 “By 1853, Parliament began passing laws to make the untested vaccine compulsory throughout the British Empire. Other countries of Europe followed suit. Once the economic implications of compulsory vaccinations were realized, few dared to disagree. Then, as now, the media were controlled by the vaccine manufacturers and the government, who stood to make huge money from the sale of these spurious vaccines…” Tim O’Shea, D.C. What is in the Regular Flu Shot? Egg proteins, including avian contaminant viruses Gelatin, known to cause allergic reactions and anaphylaxis are usually associated with sensitivity to egg or gelatin Polysorbate 80 (Tween80™), which can cause severe allergic reactions, including anaphylaxis Formaldehyde: a known carcinogen Triton X100: a strong detergent Sucrose (table sugar) Resin, known to cause allergic reactions Gentamycin, an antibiotic Thimerosal: mercury is still in multidose vials Analysis of material by the Centers for Disease Control and Prevention by Dr. Russell Blaylock. (September 5, 2009) Critical Observations: Doctor visits for flu are down from the level in April Total flu hospitalizations are similar or lower than for seasonal flu (yearly flu) The number of death secondary to flu and pneumonia is unchanged from yearly rate Only two states are reporting widespread infections — Georgia and Alaska. Other states report only regional or sporadic activity, meaning it’s not very contagious. There is no evidence that the virus has mutated at all anywhere in the world The virus remains susceptible to the drugs Tamiflu and Relenza. Only 43,771 cases have been reported in the United States. Because of poor reporting the CDC estimates that true numbers indicate that one million have been infected. Many people did not get sick enough to go to a doctor. Likewise, not all people are tested who go to a doctor. Of these 5,011 have been hospitalized and 302 have died. Death Rates From the H1N1 Flu If we use the 43,771 figure and 302 deaths that means the death rate is 0.6 percent, an extremely low death rate for any flu. The percentage of hospitalized patients who died was 6 percent, again a very low incidence of death. Since the CDC estimates that one million have been infected, we must recalculate death rates. Using this more accurate figure, the death rate is in truth 0.03 percent, which means 99.97percent will not die from this flu. Your chances of dying are incredibly low. Age and Death Rates We hear a lot about the unusual age distribution with this virus, especially as regards death rates, with the young being more affected than, as with seasonal flu, the elderly (90% of deaths are usually among those greater than 65 years old). The risks of becoming infected are as follows: Ages 5 to 24 y/o——–26.7 per 100,000 (0.027%) Ages 0 to 4 y/o ———22.9 per 100,000 (0.023%) Ages 25 to 49———–6.97 per 100,000 (0.0069%) Ages 50 to 64 y/o——3.9 per 100,000 (0.0039) Over 65 y/o————-1.3 per 1000,000 (0.00013%) And the risk of needing to be hospitalized are: Ages 0 to 4 y/o———0.0045% Ages 5 to 24 y/o——–0.0021% Ages 25 to 45 y/o——0.0011% Over 65 y/o————-0.0017% This indicates that for all age groups, the risk of being hospitalized are far less than 1 percent and well over 99 percent of people will not need hospitalization. This explains why this infection is being downplayed by the virologists themselves, the ones who know most about the dangers of viruses. The distributions of death also vary considerably by age. Below is the distribution of deaths according to age. Ages 25-49 y/o———41% Ages 50 to 64 y/o—–24% Ages 5 to 24 y/o——16% Over age 65 y/o——- 9% Ages 0 to 4 y/o——– 2% So, we see that the greatest death rates in the extremely small fraction that die are between ages 25 to 49 and 65 percent are between ages 25 to 64. The least likely to die are babies up to age 4 years, yet they are targeted for vaccination and as we see from the above data, children below age 2 years get absolutely no protection from the flu vaccines. Analysis of the New Government Projections to the Media If we analyzed it according to the worst case scenario released by the government we see far lower figures than being projected: They say 150 million Americans will be infected. That is 150 X as many as now infected, and represents a much larger figure than now estimated with a 6 to 6.5 percent of a localized population. For the United States itself with a population slightly over 300 million, their figures indicate a 50 percent infection rate. There is nothing to indicate such a high infectivity rate from the past 7 months of analysis. It should also be appreciated that the infections will not occur all at once, but will slowly evolve, as we have seen thus far, meaning that at any one time a much smaller amount of Americans will be infected — which also reduces the numbers who will require hospitalizations at any one time, and who will need ICU care. As far as the number that will need hospitalization, the government now says there will be 1.8 million people hospitalized, of which 300,000 may need ICU treatment. If we use the existing data we see that the numbers are quite different. At the time the data was taken, 303 people out of one million infected died and 5,011 needed hospitalization. This means a projected hospitalization incidence of 750,000 and a death rate of 45,000 deaths. Remember, this is using their data applied to the outrageously high figure of 50% of the population being infected — that is, 150 million people. If the infection rate is 6 percent, as all the studies have shown thus far, we see much smaller numbers. Instead of 150 million infected we see 18 million infected. Using these more realistic figures we can estimate a hospitalization rate of 90,000 and a projected death incidence of 5436. Again, it is important to keep in mind that the infections will be evolving and not all at once as both sets of figures seem to imply. If we spread this over several months and waves of the infection, we see that at any one time the hospitalizations will be a much smaller number, as will the deaths. Thus far, there have been nationwide 2,000 hospitalizations a month and 99 deaths a month. Certainly the hospitals in the United States can handle the increase. In the United States we have 5,759 hospitals containing 955,000 beds and 70,000 ICU beds. Most hospitalized people will not require intensive care. Most are suffering from dehydration and only required IV fluid infusion. It should also be appreciated that most pediatric deaths and elderly deaths will occur early in the epidemic because the chronically ill and immune suppressed will become infected early. Therefore one would expect the deaths to rise initially and then fall as the infection spreads as we see from this graph: In this chart we see that the hospitalization rates are actually lower for the swine flu than in previous seasons. In this graph we see that the hospitalization rates were either lower or barely above the seasonal flu admissions in the previous two years. We can see from the CDC’s own data that the hospitalization rates and death rates are no higher, in fact they are significantly lower, than the previous two to three flu seasons. It is obvious that the government is using “scare tactics” to promote vaccine use in the United States and that the pharmaceutical makers of vaccines are in bed with these officials. The public should be outraged. Why Do Some Die From Such a Mild Virus? As stated by the virologists, this virus is no more a danger than the seasonal virus that visits each year and actually seems to be much weaker. One may also note from the CDC’s own data, the previous nonsense about 36,000 dying from the seasonal flu every year is pure fiction. We have had a little over 400 deaths nationwide over the past 5 months, nowhere near the 36,000 figure screamed from the airwaves and our TV sets, yet the public is in a state of panic. So, why are some dying from this virus? What is little understood by the general public is that the only reason people die from the flu is that they have either an immune suppressing chronic illness, such as diabetes, direct immune dysfunction, dietary deficiencies of critical immune-supporting nutrients, chronic pulmonary disease, heart disease or cancer. Smoking powerfully suppresses immunity as well as damages lungs, and we know that smokers are much more likely to suffer complications and die than non-smokers. Excess dietary omega-6 fats (corn, safflower, sunflower, soybean, peanut and canola oils) also severely weaken immunity. The EPA component of omega-3 oils also powerfully suppresses immunity. A study by the CDC found that 32 percent of children dying from H1N1 flu had asthma, when the incidence of asthma in the general population was 8 percent. Two thirds of the children who died had neurological disorders, such as seizures and cerebral palsy. So, the vast majority of children who are dying have one of a number of chronic health conditions, yet the media gives us the impression that perfectly healthy children are dying. A recent study of why so many died during the 1918 flu pandemic found that most of the deaths were secondary to bacterial pneumonia and not the flu virus itself. In 1918 hospitals had little to offer a sick patient — there were no antibiotics, other than sulfur drugs, no IV fluids and no respirators — all they could offer was a warm bed and aspirin. It was also disclosed that the number of flu-related deaths among children was lower this year than the previous two years. What are the Virologists Saying? Virologists are scientists who study viruses — their classification, their genetics, methods of spread and their ability to cause disease. No one knows more about this virus than the virologists. The British science magazine, The New Scientist, recently polled 60 virologists to get their opinion. These are the results of specific questions: Will the virulent version of the virus appear? Extremely likely—————–none Likely—————————-5 A 50/50 chance—————– 14 Possible————————– 38 Not at all————————–3 What the virologists are doing personally Stock Tamiflu or Relinza—————–14 Stock above plus antibiotics————- 6 Stock food, water and power source—-5 Get pneumococcal vaccine—————3 Nothing———————————— 30 Hand washing, mask, etc————— 3 Notice there was no mention of taking the swine flu vaccine. Behind the push to vaccinate the entire population are the pharmaceutical makers of the vaccines, who are working in conjunction with the government to make the vaccine mandatory. Homeland security and FEMA are pushing for forced vaccinations and the medical experts, virologists and epidemiologists are calling for calm and resorting to voluntary vaccination only. The former have links with the vaccine manufacturers via political contacts. A great deal of money will be made by the manufacturers, should forced vaccinations be mandated. Will This Vaccine Be Tested? According to Anthony Fauci, director of the National Institutes of Allergy and Infectious Diseases, 5 tests are planned. It is not clear as to the use of the squalene adjuvants, ASO3 and MF-59. Because of concerns raised, the FDA is now hedging. Independent studies of squalene used as a vaccine adjuvant indicates that it is associated with a very high incidence of autoimmune diseases, such as an MS-like neurological syndrome, rheumatoid joint disease and especially Lupus. The developer of MF-59 is Chiron pharmaceuticals, which was purchased by Novartis pharmaceutical company, who will be the main supplier of the swine flu vaccine for the world. According to Dr. Fauci, testing in both children and adults will be without this adjuvant and he admits that we have no data on the safety in children.(See Nature Vol 460/30 July 2009, p 562 for the interview.) There are 5 tests scheduled for safety before mass vaccinations will resume. I looked up on clinicaltrials.gov the actual studies being done. It is instructive to note that the only studies actually being done do not contain any adjuvant (the immune booster) either for babies or adults. Yet, when the mass vaccinations begin, the vaccines will have adjuvant added, possibly squalene. The real irony here is that this is the same bait and switch game they played in the 1976 swine flu vaccine disaster. They tested one vaccine and gave a different one during the mass vaccinations. Here we go again. Over 500 people were paralyzed with Guillain Barre disorder. The incidence was much higher, because it was not a reportable disease. And over 300 people died, which is also a very low figure. Dr. Fauci admits that they have no idea what will happen when they mix the three viruses from the vaccines together or when they are given sequentially. When he was asked if the results of the studies would be reviewed by the health authorities, he answered, “yes, except for those done by the Novartis company.” He justified this secrecy by saying that Norvartis had a very advanced testing system, which was done “in-house” — that is, in secrecy. It is also important to appreciate that this vaccine has been fast-tracked, meaning that many of the usual safety precautions used to prevent contamination of the vaccines will be overlooked by the regulatory agencies. According to a number of studies, vaccine contamination is widespread, with vaccines containing pestivirus, mycoplasma, viral fragments, DNA fragments and bacterial components, all of which can produce chronic systemic disorders, cancer, neurologic diseases and even slow brain degeneration. – - – The Following was composed by Dr. Russell Blaylock as a method to reduce autoimmune reactions to the flu vaccines only. Do not use this if you have the flu itself. These are just general observations and not medical advice. You should work with your doctor for a specific program.

 Treatment for Toxic Vaccine Exposure

Place a cold compress on the site of the injection immediately after the injection and continue this as often as possible for at least two days. If symptoms of fever, irritability, fatigue or flu-like symptoms reoccur — continue the cold compresses until they abate. A cold shower or bath will also help. Take fish oils — I recommend the Norwegian fish oil made by Carlson Labs — it has the correct balance of EPA and DHA to reduce the cytokine storm. The dose is one tablespoon a day — if severe symptoms develop — two tablespoons a day until well and then switch to one tablespoon a day. Children — one teaspoon a day. Curcumin, quercetin, ferulic acid and ellagic acid as a mixture — the first two must be mixed with extravirgin olive in one teaspoon. Take the mix three times a day (500 mg of each) Vitamin E (natural form) 400 IU a day (high in gamma-E) Vitamin C 1000 mg four times a day Astaxanthin 4 mg a day Zinc 20 mg a day for one week then 5 mg a day Avoid all immune stimulating supplements (mushroom extracts, whey protein) except beta-glucan — it has been shown to reduce inflammation, microglial activation and has a reduced risk of aggravating autoimmunity, while increasing antiviral cellular immunity. Take a multivitamin/mineral daily (one without iron — Extend Core) Magnesium citrate/malate 500 mg of elemental magnesium two capsules three times a day Vitamin D3: All Children — 5000 IU a day for two weeks after vaccine then 2000 IU a day thereafter Adults — 20,000 IU a day after vaccine for two weeks then 10,000 IU a day thereafter Take 500 mg to 1000 mg of calcium citrate a day for adults and 250 mg a day for children under age 12 years. Avoid all mercury-containing seafood Avoid omega-6 oils (corn, safflower, sunflower, soybean, canola and peanut oils) Blenderize parsley and celery and drink 8 ounces twice a day Take Jatoba tea extract (add 20 drops in on cup of tea) one day before the vaccine and the twice a day thereafter. (you can get it at http://www.iherb.com/Amazon-Therapeutics-Jatoba-1-oz-30-ml/14429?at=0) It is inexpensive. Dr. Russell Blaylock (www.russellblaylockmd.com)

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Curcumin Stimulates Immune Cells To Clear Alzheimers Plaque

October 05, 2006
Curcumin Stimulates Immune Cells To Clear Alzheimers PlaqueCurcumin is a compound found in turmeric spice which is used in curries. While only done in cell culture the use of curcumin enhanced the performance of immune system macrophage cells to take up beta amyloid plaques.

UCLA/VA researchers found that curcumin — a chemical found in curry and turmeric — may help the immune system clear the brain of amyloid beta, which form the plaques found in Alzheimer’s disease.

Published in the Oct. 9 issue of the Journal of Alzheimer’s Disease, the early laboratory findings may lead to a new approach in treating Alzheimer’s disease by enhancing the natural function of the immune system using curcumin, known for its anti-inflammatory and anti-oxidant properties.

Using blood samples from six Alzheimer’s disease patients and three healthy control patients, the researchers isolated cells called macrophages, which are the immune system’s PacMen that travel through the brain and body, gobbling up waste products, including amyloid beta.

The team treated the macrophages with a drug derived from curcumin for 24 hours in a cell culture and then introduced amyloid beta. Treated macrophages from three out of six Alzheimer’s disease patients showed improved uptake or ingestion of the waste product compared to the patients’ macrophages not treated with curcumin. Macrophages from the healthy controls, which were already effectively clearing amyloid beta, showed no change when curcumin was added.

It only helped in cells from half the patients.

“Curcumin improved ingestion of amyloid beta by immune cells in 50 percent of patients with Alzheimer’s disease. These initial findings demonstrate that curcumin may help boost the immune system of specific Alzheimer’s disease patients,” said Dr. Milan Fiala, study author and a researcher with the David Geffen School of Medicine at UCLA and the VA Greater Los Angeles Health Care System. “We are hopeful that these positive results in a test tube may translate to clinical use, but more studies need to be done before curcumin can be recommended.”

Older immune systems might be less able to clear the plaque junk that accumulates in the brains of those with Alzheimer’s.

The patients ranged in age from 65 to 84. Fiala noted that the patients whose immune cells responded were younger and had higher scores on a Mini-Mental State Examination suggesting that curcumin may help those with less advanced dementia. Some of the patients may have already had additional curcumin in their systems due to participation in another UCLA study, which may have impacted findings.

Rejuvenation of the immune system will probably lower the incidence of Alzheimer’s and might also reduce the incidence of other diseases caused at least in part by the accumulation of misfolded proteins and other junk. Check out some evidence that immune system aging leads to Alzheimer’s: Immune System Deficiencies May Lead To Alzheimer’s Disease

Also see my post Alzheimers Curable With Insulin Receptor Drug? for another approach that might help. Then there’s the stoner approach to protection from Alzheimer’s: THC Blocks Alzheimer’s Plaque Formation

By Randall Parker at 2006 October 05 09:15 PM  Brain Disorder Repair

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