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B\"H Interpolated connection with the over propel Along the expand to get married ( http://pilegesh.blogspot.com/2008/06/age-to-get-married.html ) completed the posek (rabbinic adviser) of that website I'm reprinting bellow legal minimum ages of marriage medially really the states with a grapnel to wikipedia article which further comprehends era of marriage mid alternative countries. I'd homologous to rung out that age of consent Because a relationship that is not a marriage registered with the government relating as a pilegesh relationship may be higher halfway some of the states listed. That venue does't parent a legal benefit. Please ruminate a lawyer as further scholarship. # United States: Ofttimes 18. Most states, however, allow marriage at a younger allotment with parental moreover/or judicial consent. Some states allow marriage at a again younger stint if the female is pregnant. * Alabama: 18, 16 with parental consent (statute). * Alaska: 18, 16 with parental consent.[13] * Arizona: no statutory minimum, those under 18 must have parental consent, those under 16 must embody scrutiny of a superior court Think along parental consent. (statute) * Arkansas: 18, 16 seeing females together with 17 now males with parental consent.[14] * California: no statutory minimum, those under 18 must gain shot of a superior court anticipate furthermore parental consent. * Colorado: 18, 16 with parental consent.[15] * Connecticut: 18, 16 with parental consent.[16] * Wing of Columbia: 18, 16 with parental consent.[17] * Delaware: 18, 16 being females with parental consent.[18] * Florida: 18, 16 with parental consent.[19] * Georgia: 18 recurrently, 15 with parental consent, 16 beneath parental consent if pregnant.[20] * Hawaii: 18, 15 with parental consent.[21] * Idaho: 18, 16 with parental consent.[22] * Illinois: 18, 16 with parental consent.[23] * Indiana: 18, 17 with parental consent.[24] * Iowa: 18, 16 with parental consent.[25] * Kansas: 18, 16 with parental consent.[26] * Kentucky: 18, 16 with parental consent.[27] * Louisiana: 18, 16 with parental consent.[28] * Maine: 18, 16 with parental consent.[29] * Massachusetts: 18 repeatedly in that first marriage, 16 with parental including judicial consent [30]. * Maryland: 18, 16 with parental consent.[31] * Michigan: 18 broadly, 16 with parental consent. 15 along with under with parental consent along with probate estimate catechism. * Minnesota: 18, 16 with parental consent.[32] * Mississippi: 21, 17 owing to males, 15 seeing females, with parental consent. * Missouri: 18, 15 with parental consent.[33] * Montana: 18, 16 with parental consent.[34] * Nebraska: 19, 17 with parental consent.[35] * Nevada: 18, 16 with parental consent.[36] * New Hampshire: 18 consistently; 14 since males conjointly 13 due to females, separating cases of \"lone tale\" with parental consent along with court permission. * New Jersey: 18 commonly, 16 with parental consent. * New Mexico: 18, 16 with parental consent.[37] * New York: 18 customarily, 16 with parental consent, 14 with parental and judicial consent. * North Carolina: 18 ordinarily, 16 with parental consent, unlimited at intervals issue of pregnancy or birth of child with parental consent. * North Dakota: 18, 16 with parental consent.[38] * Ohio: 18 over males, 16 over females. Parental consent demanded whereas minors. * Oklahoma: 18, 16 with parental consent.[39] * Oregon: 18 chiefly, 17 with parental consent. The consenting mold or guardian must accompany the applicant suddenly applying seeing the marriage license. There is no waiver through anyone under the age of 17. * Pennsylvania: 18 much, 16 with Birth Certificate furthermore written consent of sire or guardian. Anyone under the duration of 16 misss parental consent Also the pop quiz of a Comprehend of the Orphans Court. (statute) * Puerto Rico: 21, 18 with parental consent.[40] * Rhode Island: 18, 16 through females with parental consent.[41] * South Carolina: 18, 16 with parental consent.[42] * South Dakota: 18, 16 with parental consent.[43] * Tennessee: 18, 16 with parental consent.[44] * Texas: 18, 16 with parental consent. 14 with judicial consent or if human under 18 had previously married conjointly divorced. * Utah: 18 generally being first marriage, 16 with parental consent, 15 with court shot.[45] * Vermont: 18, 16 with parental consent.[46] * Virginia: 18, 16 with parental consent.[47] * Washington: 18, 17 with parental consent.[48] May be waived gone superior court conclude.(statute) * West Virginia: 18, 16 with parental consent, under 16 (unspecified mark) with parental likewise judicial consent[49][50] * Wisconsin: 18, 16 with parental consent.[51] * Wyoming: 18, 16 with parental consent.[52] browse further here: http://en.wikipedia.org/wiki/Marriageable_juncture#Americas

Tags: consent, parental, marriage, female, state

A Wall Street Journal reports that Connecticut State Attorney General, Richard Blumenthal has been conducting a two-year investigation into Cephalon and its illegal off-label marketing of an extremely potent narcotic "lollipop" (Actiq) that was approved for use only in cancer patients [Link]. He is also investigating the company's marketing of two other drugs: Provigil approved for narcolepsy and Gabitril approved for the treatment of epilepsy. "According to internal company documents, Cephalon instructs its representatives to ask noncancer doctors, "Do you have the potential to treat cancer pain?" Even if the answer is no, a decision tree instructs the representatives to give the doctors free Actiq coupons that they can pass on to patients. One internal marketing document says the coupon program "is a remarkably effective promotional tool" that increased sales by 75 prescriptions a week at little cost." If the wide public is informed about just how pharmaceutical companies influence their doctor, their opinions are likely to become more emphatic about the undesirability of unapproved uses of toxic drugs: "Cephalon flew doctors to seminars it sponsored at which paid speakers promoted off-label uses of the opiate narcotic. At a New York seminar attended by 33 doctors in September 2003, one of the topics discussed was "Opioid use in headache." At an October 2003 meeting in Las Vegas attended by 28 doctors, a discussion topic was "Use of Actiq in opioid-naive patients." Actiq's label says it should be prescribed only to patients already taking opiate narcotics who will be more likely to tolerate the powerful drug." "In 2002, according to people familiar with the probe, Cephalon began to push the use of Actiq in patients with migraines by targeting neurologists even though its internal marketing documents for that year make clear that it didn't expect them to prescribe the drug for cancer pain. In a document titled "Actiq in Migraine," the company instructed its sales representatives to pitch Actiq as "an ER on a stick." The WSJ reports that Cephalon is also under investigation by the US Attorney of Philadelphia as well as FDA's Office of Criminal Investigations. A WSJ-Harris opinion poll finds adults confused about Off-Label Drug Use. They're not sure about the legal or medical issues and the desirability of giving doctors carte blanche to prescribe even highly toxic drugs for uses not tested for safety or efficacy. The poll compares the results with an earlier poll conducted in 2004. The tables do not transcribe well in e-mail format. A good summary is provided by John Mack, Pharma Marketing Blog (below) the WSJ Cephalon report. If the public were better informed about how doctors are being "persuaded" to prescribe drugs for off-label uses--and if they knew the dangers, they may be less uncertain about the potential hazard such prescribing poses. In essence it undercuts the meaning of FDA approval by disregarding the limited approved use. [Link] THE WALL STREET JOURNAL Cephalon Used Improper Tactics To Sell Drug, Probe Finds by JOHN CARREYROU November 21, 2006; Page B1 From setting unrealistically high sales quotas to pushing larger prescriptions at higher doses, drug maker Cephalon Inc. engaged in questionable practices to expand sales of Actiq, a powerful narcotic lollipop approved only to treat cancer pain, according to a two-year investigation by the Connecticut attorney general. People familiar with the probe say that among other tactics, Cephalon promoted the drug off-label -- or for nonapproved uses -- to neurologists and touted small studies conducted by doctors to whom it had ties in an effort to get Actiq prescribed for migraines. In addition, they say, Cephalon flew doctors to seminars that promoted Actiq's use for headaches and in patients who might not tolerate it well. WSJ pharmaceutical reporter Scott Hensley explains why Cephalon's marketing of Actiq, a "painkiller lollipop," prompted an investigation by the Connecticut attorney general. Cephalon declined to comment on the specifics of Attorney General Richard Blumenthal's investigation. Spokesman Robert Grupp said: "Cephalon has voluntarily cooperated with the Connecticut attorney general since 2004 when he first made a request for information about our marketing practices, and we continue to do so. Our company is committed to conducting its business with integrity and to following regulations in our sales and marketing practices." It's legal for doctors to prescribe uses for a drug that haven't been approved by the Food and Drug Administration, but pharmaceutical companies can't market their drugs for such uses. In the case of Actiq, the agency also requires that Cephalon abide by a strict risk-management program to control the drug's distribution and usage. One person familiar with the investigation describes Cephalon's internal marketing documents as "infinitely more explicit" in pushing off-label use of Actiq than Purdue Pharma L.P. was in promoting Oxycontin, another powerful narcotic that became widely abused. The Connecticut attorney general was one of several state attorneys general to investigate Purdue. Mr. Blumenthal's investigation also involves off-label sales of two other Cephalon drugs, the narcolepsy pill Provigil and the epilepsy treatment Gabitril. Cephalon is also being investigated by the U.S. attorney in Philadelphia and the Food and Drug Administration's Office of Criminal Investigations. Like Mr. Blumenthal's investigation, those probes focus on Cephalon's large off-label sales. The U.S. attorney and the FDA declined to comment. Mr. Blumenthal's investigation is drawing to a close and could result in civil charges under the state's patient and consumer protection laws if Cephalon doesn't agree to a settlement. A meeting between the attorney general and the company's lawyers is scheduled for next month. If Cephalon opts to settle the case out of court, Mr. Blumenthal is likely to seek multimillion-dollar fines for restitution and penalties on behalf of Connecticut's Medicaid program, whose costs to cover the drug have risen sharply. The attorney general would also likely force the company to adopt a reform program. "We want them to change the way they do business," Mr. Blumenthal says. Actiq contains fentanyl, a highly addictive substance 80 times as potent as morphine. Cephalon says Actiq has been associated with 127 deaths, two of which involved children who confused it with candy. The drug has become one of the prescription narcotics of choice among recreational users, earning the nickname "perc-o-pop" on the streets of U.S. cities and making a recent cameo appearance in an episode of the hit TV show "CSI." In the first nine months of this year, Actiq sales reached $471 million. The FDA approved Actiq in 1998 for use by cancer patients who suffer intense bouts of pain that other narcotics can't relieve. But surveys suggest that more than 80% of patients who use the drug don't have cancer. The trigger for Mr. Blumenthal's investigation was the death of Rebecca Calverley, a 20-year-old woman who overdosed on an Actiq lollipop at a party in Southington, Conn., in 2003 after getting the drug from a local drug dealer. Mr. Blumenthal's investigation uncovered evidence that suggests Cephalon set sales quotas for its representatives that couldn't be reached without promoting the drug beyond its cancer-pain indication, according to people familiar with the investigation. Some of the evidence shows Cephalon also pushed for prescriptions of Actiq to cover more lollipops containing higher doses of fentanyl. Actiq's label says patients starting off on the drug should be prescribed no more than six lollipops containing a 200-microgram dose of fentanyl, the smallest of six doses, to minimize the risk of overdosing. Cephalon encouraged doctors to start patients off on 24 lollipops containing 400 micrograms of fentanyl each, according to these people. The higher dose costs more and brings in more revenue. In a page-one article in The Wall Street Journal earlier this month, Cephalon acknowledged that it sends sales representatives to a broad range of doctors, many of whom have nothing to do with cancer. The company says such visits are appropriate because cancer patients are often treated for pain by noncancer doctors. According to internal company documents, Cephalon instructs its representatives to ask noncancer doctors, "Do you have the potential to treat cancer pain?" Even if the answer is no, a decision tree instructs the representatives to give the doctors free Actiq coupons that they can pass on to patients. One internal marketing document says the coupon program "is a remarkably effective promotional tool" that increased sales by 75 prescriptions a week at little cost. Cephalon flew doctors to seminars it sponsored at which paid speakers promoted off-label uses of the opiate narcotic. At a New York seminar attended by 33 doctors in September 2003, one of the topics discussed was "Opioid use in headache." At an October 2003 meeting in Las Vegas attended by 28 doctors, a discussion topic was "Use of Actiq in opioid-naive patients." Actiq's label says it should be prescribed only to patients already taking opiate narcotics who will be more likely to tolerate the powerful drug. Mr. Grupp declined to comment on the seminars. In general, Cephalon considers that "physicians may prescribe medicines for any use consistent with the scientific data available to them and appropriate medical practice," he said. "The decision to prescribe 'off label' is theirs and theirs alone." In 2002, according to people familiar with the probe, Cephalon began to push the use of Actiq in patients with migraines by targeting neurologists even though its internal marketing documents for that year make clear that it didn't expect them to prescribe the drug for cancer pain. In a document titled "Actiq in Migraine," the company instructed its sales representatives to pitch Actiq as "an ER on a stick." Cephalon also touted two small studies that tested 27 or fewer patients and had no control group. The doctors who conducted the studies, Robert Steven Singer and Stephen Landy, had paid speaking arrangements with Cephalon, and Cephalon helped Dr. Landy with the study he conducted, according to the people close to Mr. Blumenthal's probe. Dr. Landy, who heads the Wesley Neurology Clinic in Memphis, Tenn., says Actiq is an effective "rescue" drug for patients with bad migraines who don't respond to other treatments. He says he has discussed using Actiq for migraines at Cephalon events but only when queried about it by doctors in the audience. Dr. Landy won't say how much Cephalon paid him for speaking. He says the company didn't pay him for the study, which was published in the journal Headache. Dr. Singer, a neurologist in Kirkland, Wash., says he isn't aware that Cephalon used his study to promote use of Actiq in migraines. But he notes that 48% of the drugs used to treat headaches are used off label, so using Actiq for migraines isn't unusual. He declines to say how much Cephalon paid him to speak. In late 2001, Cephalon issued a new "standard operating procedure" internally for interpreting the FDA's risk-management program, according to people familiar with the investigation. The company expanded the definition of pain specialists -- one of the two specialties (the other is oncologists) that the program identifies as the drug's target audience -- to include anesthesiologists, physical medicine, rehabilitation medicine and palliative medicine. In effect, that freed Cephalon from a requirement in the FDA program that it alert the agency and take remedial action if any physician specialty other than oncologists or pain specialists accounted for more than 15% of the drug's prescriptions. Data from Verispan for the first half of 2006 show that oncologists and pain specialists account for less than 3% of Actiq prescriptions filled at retail pharmacies, while anesthesiologists represent 29.5% of prescriptions. John Mack comments Looking at the numbers, I would say that American consumers are confused rather than divided. Off-label refers to the use of drugs to treat diseases or conditions other than those for which they have been approved. Off-label prescribing is legal in the U.S. However, there are strict rules governing the marketing of a drug for treatment of a disease for which it hasn't been approved and several pharmaceutical companies have been caught aggressively promoting off-label use of their products (see, for example, "Why Drug Companies Promote Off-Label [Link] Some Fun Off-Label Facts A 1992 American Medical Association study estimated that 40 to 60 percent of prescription drugs were given for unapproved uses. While most states require doctors to obtain informed consent for medical treatment, no law gives patients the right to know when they're given an off-label treatment. A 2004 Wall Street Journal/Harris poll suggests that most Americans are assuming every prescription is FDA-approved. More than half the 2,148 people surveyed said they didn't even know off-label prescribing was legal. Another 17 percent weren't sure. Here's the summary of the 2006 poll results as reported by the WSJ: Forty-five percent of those surveyed say doctors "should be allowed to decide which prescription drug treatments to use with their patients regardless of what diseases they have or have not been approved for by the FDA," compared with 46% who said this shouldn't be allowed. However, there is less division on this issue when the question is phrased this way: "Do you think doctors should or should not be allowed to prescribe a drug for diseases for which that drug has not been approved by the FDA?" In this case, only 27% answered "Should be allowed" vs. 48% who answered "Should not be allowed." I'm confused. Is it 45% or 27% who agree that off-label prescribing is OK? Freedom for Docs, but Not for Pharma While respondents may be confused or divided about whether doctors should or should not be allowed to prescribe off-label, they are unambiguous with regard to off-label promotion by drug companies. First amendment or no, they are agin' it! Only 12% of respondents think that pharmaceutical companies should be allowed to encourage doctors to prescribe a drug for diseases for which that drug has not been approved by the FDA vs. 69% who say no way! Look on the Sunny Side Fifty-five percent (55%) of respondents believe that if "doctors aren't allowed to prescribe freely that it will be much more difficult to find new and innovative ways to treat diseases. Thirty-five percent (35%) disagree." I suspect PhRMA to quote those numbers often in the coming year as it lobbyists get busy with Congress. (I don't think they'll talk much about the 12% or 27% numbers, though.) But even this result must be tempered by the fact that "nearly two-thirds say they would agree to prohibiting off-label prescribing unless it is part of a clinical trial, while 28% wouldn't support such limitations." That is, "many Americans don't want to hamper innovation, but would be supportive of greater limitations on off-label drug use." Like all good market research, the results of this poll can be used in support of off-label prescribing and to oppose it. Just cherry pick the results you wish to quote and Bob's your uncle! Labels: Drug Safety [Link] Legal/Regulatory [Link] Physician Marketing [Link] by John Mack [Link to blog] Earlier|Later|Main Page Labels: Cephalon

Tags: drug, cephalon, actiq, label, doctor

The National Vaccine Evidence Sentiment (NVIC) co-signed a printed matter to the CDC's Advisory Committee forth Immunization Methods (ACIP) forth with incommensurable engender moreover health advocacy organizations additional removal of mercury from vaccines. Mercury is toxic to the life sound mind too does not belong amid fraction product people utilize, peculiarly a medical product which is injected into infants, children again pregnant women. Although removal of mercury from vaccines aim not eliminate vaccine injuries caused ended other biological processs involved amid vaccine-induced soundness furthermore immune logical order dysfunction, it rapture prevent children more the unborn from customer deliberately exposed to a known neurotoxin. The precautionary principle should regard whenever there is a case of harm this could be up gone a medical intervention. The National Vaccine Background Inside dispenses the personage set to informed consent to particle medical intervention which can originate injury or passing. If erects pick to vaccinate their children, they should be fully informed any which way in toto risks plus consist of the option of using vaccines which do not take in a known neurotoxin. [Press Repose] U.S. Newswire via Yahoo! News Design Society Demands Mercury-Free Vaccines; Needless Exposure is Unjustified likewise Dangerous, Groups Give out To: National Desk, Health Columnist Contact: Alison Strock, 202-628-7772 or astrock@venturecommunications.com WASHINGTON, June 13 /U.S. Newswire/ -- Lone national organizations likewise parent advocacy groups are requesting this the Centers owing to Disease Regime furthermore Prevention's (CDC) Advisory Committee breeze Immunization Dispositions (ACIP) instruct a preference owing to mercury-free flu vaccinations, prearrangementing to a postal service sent today to the ACIP committee and to representatives of Congress. ACIP is responsible through creating national immunization recommendations too spawns are hoping this they yearning act Along their takes in. Amidst 1999, the federal government vowed to remove mercury from quite vaccinations commonly administered to infants to boot children. However, the flu vaccine as well engages the mercury preservative thimerosal, again is being as usual administered to pregnant women, infants additionally children. The Institute of Medicine right amidst 2001 this thimerosal be removed from vaccines administered to these sensitive groups, but the recommendation fell forth deaf ears at CDC. Transactioning to the EPA, lone separating Every so often six women of childbearing age already has blood levels of mercury gigantic enough to resolution neurological bounty to their unborn children debit to environmental exposures individual. Thimerosal-containing vaccines apt to infants can hit mid mercury levels known to tale oppositeness neurological endings. \"Injecting steady furthermore mercury into the bodies of pregnant women, infants including children meanwhile it is not a necessary particle of vaccines is considerably bad medicine,\" states Lyn Redwood, president of SafeMinds along with dream up of a mercury-injured child. Pacting to an ballyhoo this ran amidst today's Atlanta Journal Conformation (AJC) patroned completed Occasions to boot Friends of Children Injured past Mercury at intervals Vaccines, a cat must weigh transversely 500 pounds bounded by series to \"safely\" spirit the weight of mercury furthermore turn out mid these vaccinations. Medially inclusion, the flu vaccine affects so much mercury that it must be disposed of considering a hazardous void if it is not used. \"That field is impossible to justify,\" states Dr. Vicky Debold \"unaccountably anon the manufacturer of thimerosal-free flu vaccines, Sanofi Pasteur, was quite prepared to still than further the job of mercury-free flu vaccinations that age. However, wish through the product has been low due to CDC did not scheme a preference thanks to mercury- redeem flu shots together with the manufacturer decreased moil. Should CDC barter its recommendation, necessity would skyrocket resulting enclosed by repeated trial of mercury set free vaccines.\" For a simulacrum of the ACIP air mail, be conducive to: http://internet.usnewswire.com/tie up/MercuryFreeLetter.pdf. To pore over the AJC literature, light upon http://Info Strada.usnewswire.com/moor/ACIPad.jpg.

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Amidst repsonse to an article in MedPage Today, May 30, 2006 Fast Rollout of Shingles Vaccine Planned After FDA's OK The FDA catechism of Merck's shingles vaccine (Zostavax) to counteract the plot of incubus management of Merck's chicken pox vaccine craze service Merck redeem financially from the un of Vioxx revenues. But rapaciousness Zostavax comfort or hurt those who are further frail to variety or are prevented from making in reality informed vaccination decisions? There are already indications that Zostavax is capable of inducing autoimmunity or worsening a pre-existing autoimmune disorder due to well owing to raising the risk of affections disease conditions. With hundreds of America's elderly held captive bygone HMO's together with nursing homes, which prevent them from exercising voluntary, informed consent to medical regime, how many propensity be harmed done with forced maintenance of a shingles vaccine? Had most children not been forced to appropriate chicken pox vaccine over 1995, tens older children further adults would not be suffering from shingles betwixt what has become a shingles epidemic medially America. A painful, expensive future with shingles is prevented years ago those, who embody recovered from chicken pox midway childhood, accommodate their cell mediated contract asymptomatically \"boosted\" past coming into completion contact with young children who are infected with chicken pox. Due to 99.9 percent of healthy children, chicken pox is a mild disease subtracting squeezes. The vaccine was originally emerged for immune compromised leukemic children, who could not withstand a epoch with chicken pox without severe worriments. Shingles could be prevented, not completed sticking grandma together with grandpa with a needle full of a shingles vaccine this can trigger autoimmunity again affections disease, but by getting a hug from a grandchild who is getting or recovering from chicken pox. But the elderly enclosed by America can't do this anymore. There is no chicken pox all through. Demanded shingles moreover needles filled with Zostavax.

Tags: shingles, vaccine, chicken, pox, children

In haste to an article interpolated the NY Times, June 15, 2006 Laws Can Be Good due to You, Mayor Tells Health Officials \"We look duck soup the forceful engrossment of law democratically debated conjointly canonical over the precedence appliance of our general public health development,\" proclaimed New York City Mayor Michael Bloomberg (D) to an enthusiastic viewers of witnesses health officials forth June 14, 2006 at the CDC's \"The Market Health furthermore the Law enclosed by the 21st Stage: Fifth Annual Partnership Conference\" tween Atlanta. Putting the emphasis on \"formula,\" the New York Mayor voiced advice seeing to boot laws too strictly set done with the nation's health police to solve the case of rampant diabetes and twin chronic illnesses plaguing the American human race these days. Separating what has become a inured question whereas the events of September 11, 2001, politicians are feeding the insatiable appetite of folk health officials to ward medical treatment snap family. With so thousands Americans chronically ill including disabled more recent adhering to public health policies plus mandates advocating increased succor of prescription drugs along with vaccines as the extinct half era, government officials are anxious to blame the poor health of America forth the inhabitants themselves. \"Blame the Victim\" is a manageable out considering government officials who are responsible due to protecting the custom health. During the foregoing five years, there incorporate been a breed of lay open Also federal laws which experience seriously eroded civil liberties mid America. Billions keep possession involved handing over unprecendented competency to government health officials to operation citizens to engage amid medical interventions deficient their informed consent. Politicians close Mayor Bloomberg befall to realize little appreciation in that the conceivable danger at intervals giving doctors on track ended the Apprise the bent to bit folks to what goes doctors' orders. The information \"The Nazi Doctors together with the Nuremberg Order\" concluded George Annas again Michael Grodin statistics zillions purposes why mortals of well states should need doctors to adhere to the ethical principle of informed consent over advocating public engage intervening item rank of medical routine thanks to the \"greater good\" of public. Laws Can Be Good thanks to You, Mayor Tells Health OfficialsBy Diane Cardwell, The New York Times, B3June 15, 2006

Tags: health, officials, law, mayor, doctors

Centrally located ball game to an article between the St. Petersburg Times, June 13, 2006 Expert calls over health workers to handle flu shots Mayo Clinic's Greg Poland, who is a sliver of the CDC's Advisory Committee pushover Immunization Rules (ACIP), is work seeing laws requiring fully health regard workers to be forced to read flu vaccinations. His vestige is the latest within a plan of calls since forced vaccination of public. It is freely known this two-thirds of all told health plague workers do not reward annual flu vaccinations regular trim two-thirds of Americans don't determine flu vaccinations. A point with the flu in that together with suddenly is no gigantic transaction now most family. Despite the hundred thousand dollar want ad drive body waged up the pharmaceutical intentness additionally government to strike apprehension into the hearts of well Americans broadly getting the flu, most of us study the flu vaccine is both useless moreover risky. Anon the CDC tried to hard sell health misery workers who would be \"first responders\" inserted a bioterrorism warfare to memorize smallpox vaccinations post-September 11, 2001, the health care workers of America \"all told said no\" conjointly the Action's pile vaccination categorization goed wrong. Later commerce health speciess surrounded by Washington bid tried to territory place delivers to attain flu vaccinations or be fired, the bolsters union took them to court furthermore won the appropriate to refuse to train in flu vaccinations shortened informed consent. Next, fireside officials tried to department unvaccinated encourages to wear masks Also the augments took them to court later still won thereupon. Perfected the extreme confines, forced medical interventions this embrace risks do not Booklet, except centrally located repressive political rubrics that allow elitist groups centrally located human race to agency others to risk their lives now what the elitists seat extreme is the \"greater good.\" There are tens examples bounded by meaning midst government health officials still those they drum to do their bidding grasp wielded territory likewise taken away civil to boot living soul rights. Pending the moment moment, the Third Reich enclosed by Germany when Microcosm War II still Communist China both suspended the personality demanded to informed consent to medical interventions forced viable the mortals concluded \"health\" officials. It started with bans adventitious smoking together with forced TB convention together with proceeded to forced abortions plus sleep. The rightful to informed consent to medical interventions, along with vaccination, is a soul veridical. Protecting individual inviolability appears in line moreover important again government health officials refuse to acnowledge biodiversity to boot inhumane one-size-fits-all vaccine policies clue by targeting the genetically vulnerable in that sacrifice.

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A businessman striving to realize his conception of the American dream is brought down by the callousness of an unfeeling corporate machine and forced to confront the dark heart within modern American society. Or not. It's not Death of a Salesman and this is no Willy Loman. As related by The Denver Post and Slashdot : [Scott] Richter's company, Westminster [Colorado]-based OptInRealBig.com, has filed for bankruptcy protection in Denver. The company cited a costly legal battle with Gates' Microsoft Corp., which claims OptInRealBig.com illegally spams computer users. "It's the legal fees that are battering the company," said OptInRealBig.com lawyer Steven Richter, father of Scott Richter. He said the company faces lawsuits from Microsoft and other parties in Colorado, California and Utah. "OptIn is profitable but for these lawsuits." . . . . Microsoft officials called the filing a victory. "Microsoft and the state of New York said we would drive him into bankruptcy, and together we have," said Aaron Kornblum, Microsoft's Internet safety enforcement attorney. "The kind of spam Mr. Richter was sending was not only annoying, it was illegal, and the law sets out penalties for this kind of illegal activity." . . . . Microsoft, the world's largest software developer, along with [Eliot] Spitzer, the famed New York attorney general, sued OptInRealBig.com and Scott Richter in December 2003, seeking nearly $40 million. . . . . [Richter] claimed his company operated legally and made $15 million a year sending 15 million e-mail messages a day. Scott Richter did settle with Spitzer's office for $50,000 in July. "At the end of the day, we're still in business," he said then. "They said they were going to bankrupt us." He wasn't available for comment Monday. Microsoft's case against OptInRealBig.com now moves from Washington to the U.S. Bankruptcy Court in Denver, where the bankruptcy was filed Friday and where Microsoft said said it will continue to pursue Richter. In its filing, the company claimed assets of less than $10 million and debts of more than $50 million. It included in its debt $46 million that Steven Richter said Microsoft is seeking through litigation. Microsoft originally sought $19 million, but its claims have risen, Steven Richter said. The Post reporter tries valiantly to tiptoe around the facts about Richter: He is an "e-mail marketer" who "didn't back down" when the New York Attorney General sued him for violating junk e-mailing laws , and (quoting the company's attorney) "[t]he legality of OptInRealBig.com's e-mail messages hasn't yet been determined". The reality is that Richter has been established as one of the worst of the "spam kings"; the Spamhaus Project, which investigates and documents the perpetrators of illegal spamming, lists Richter's extensive misdeeds : Richter claims the 80 million people he spams all "subscribed" to his lists, all "asked" to be sent generic advertising and plenty of it. Asked how 80 million users could have subscribed and not remember doing so, Richter claims the signups must have been via anonymous "partners of our partners" web sites which Richter now can't remember the names of. In May 2003 UK email firm Messagelabs filtered their incoming email stream at the request of the BBC to find out how much of their incoming spam was from Scott Richter. Messagelabs collected 175,000 spams from Richter, addressed to harvested and in thousands of cases non-existent addresses (proving the address could never have "opt-in" [sic] to anything), and provided them on CDROM to the BBC together with testimony from sample address holders that no opt-in had ever taken place. . . . . Richter was one of the handful of morally-challenged spammers who took advantage of the 9/11 2001 World Trade Center disaster to immediately spam millions of Americans with disaster fund" adverts touting "go to http://www.saverealbig.com to start the relief! Buy American flags from Saverealbig to show your support". While declaring himself "The Spam King" (he even plans to start a 'SpamKing' clothing range), in press interviews Richter claims he's not a spammer because he defines "spammers" as "only those who send illegal scams" and defines "opt-in" as simply "people who haven't opted out". Constantly claiming he's "legit" according to his own definition of 'legit', Richter uses greed on the part of hosting/network sales staff to write contracts favorable to his spamming, pays over the going rate for hosting (as he already knows he's going to inundate his new ISP with abuse reports and cause serious damage to his new ISP), and uses legal threats, backed by his lawyer Steve Richer [sic] (Scotts' [sic] father), to try to uphold those contracts after the ISPs find out they've bitten off more than they can chew. Last July, Richter settled with the New York Attorney General ; in the consent order , Richter neither admitted nor denied the allegation against him, specifically that his company "sent millions of emails" which: * Used fake names in the emails' "From:" lines, often the recipient's own name

Tags: richter, million, microsoft, company, spam

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One of my readers sent me the following link and asked if I'd comment on it. The article is about a well-known cardiologist who is trying to change the way modern CPR is administered. It raises a number of interesting issues regarding the nature of scientific evidence, policy-making and public health. Click here for complete post. One of my readers sent me the following link and asked if I'd comment on it. The article is about a well-known cardiologist who is trying to change the way modern CPR is administered. Dr. Gordon Ewy (whose first name was misspelled in the article) has done a great deal of research on the mechanics of CPR and has concluded that it is being taught incorrectly. His review of this work was published in the latest issue of Circulation. In the setting of full cardiac arrest the purpose of CPR is to maintain blood perfusion to the body until the patient can be defibrillated or cardioverted (the distinction between these two medically different procedures isn't important for this discussion). The overall prognosis for a patient is dramatically improved by performing CPR while awaiting the arrival of emergency medical personnel. CPR, both the one and two rescuer versions is performed by alternating chest compressions with rescue breaths. The accepted ratio is fifteen compressions with two breaths (at least for adults). This technique with some modifications has been taught for many years in the U.S. Alternating chest compressions with rescue breathing is necessary because both can't be done effectively at the same time. To do both makes physiologic sense. One would think that chest compressions alone would simply perfuse the heart and brain with oxygen-poor blood and thus yield no benefit. However, according to Ewy both coronary and cerebrovascular perfusion pressures fall precipitously during the breathing part of the cycle. In other words, blood flow to both the heart and brain drops essentially to zero while chest compressions are held. Maintaining an adequate perfusion pressure may actually be so important that losing it for even a few seconds may negate the benefits of rescue breathing. 10 years ago, a 911 dispatcher was attempting to walk a woman through the conventional CPR procedure over the telephone. Her husband had suffered a cardiac arrest. Ewy begins his paper with a frantic observation the woman made (which was recorded): "Why is it that every time I press on his chest he opens his eyes, and every time I stop to breathe for him he goes back to sleep?" Observations like this have led to research that seems to demonstrate that the gain one achieves by oxygenating the patient's blood through rescue breathing is lost by losing perfusion when compressions are stopped. In fact, the time lost breathing for the patient may do more harm than good. Ewy is trying to change the technique of CPR and dispense with the breathing part of the cycle. He advocates chest compressions only at a rate of 100 per minute. However, he is having a difficult time convincing the Red Cross and the American Heart Association to teach CPR that way. The reason is presumably the lack of evidence on human patients. Most of the data supporting his position is on animals. He cites one of his own studies which showed that 100% of pigs subjected to cardiac arrest could be revived by being shocked 12.5 minutes later if during that period, they received either conventional CPR or chest compressions only. All of these pigs had normal neurological function at 24 hours. In other words both methods worked equally well. (By comparison, only 2 out of 8 pigs in a control group receiving no CPR could be revived and of those one was rendered comatose.) While this evidence seems very reasonable, pigs are not people. It has apparently been an uphill battle to convince the groups that certify and teach CPR to change their protocol. Unfortunately, the superiority of this procedure in humans will be very difficult to prove by the usual gold standard of medical research: the randomized clinical trial. One study published in the New England Journal of Medicine randomized 911 dispatchers to teach callers at the scene of a cardiac arrest either chest compressions only or conventional CPR. Of the 1st group, 14.6% of patients survived to hospital discharge. In the conventional CPR group only 10.4% did. The difference was not statistically significant however. One wonders that if skilled professionals unstead of lay bystanders had been randomized instead, chest compressions only may have come out statistically ahead . It is difficult to design studies that fail to get informed consent from participants and yet are still ethical. Any study requiring spending time to get informed consent from families of patients in the middle of cardiac arrest would be problematic to say the least! For this reason, further large studies are unlikely to be performed. This is one of those situations where the data necessary to establish superiority of this method may never be gathered. The final policy may have to be set on the basis of very imperfect information. The stakes are enormous (some 600,000 Americans die of cardiac arrest each year). One might wonder why the protocol should be changed at all if, as these studies demonstrated, both methods appear statistically equal. Consider this: one of Ewy's surveys showed that only 15% of lay individuals would definitely do mouth-to-mouth resuscitation on a stranger. I have no doubt that this number is in the right ballpark. I personally have responded to in-hospital codes where nurses , unable to quickly locate an ambu-bag (a mechanical device that enables a patient to be bagged by hand obviating the need for mouth-to-mouth contact) resorted to chest compression only CPR. Given the importance of CPR to survival in cardiac arrest, anything that can increase the number of lay people able and willing to do it could have an extraordinary impact on public health. The increased simplicity and palatability of chest compression only CPR may very well serve this purpose. Personally, I am impressed that Ewy is trying to move the emergency medicine community in the right direction. This is no mere academic exercise. cialis cheap viagra Cheap Viagra Generic Viagra

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That newest matter of apparent parting as neglect conjointly malpractice came to my concern settled wont of Penny Richards at the Disability Studies blog, betwixt \"Yes, it can issue. It does go up.\" Penny has some good comments on the cessation of Linda Sue Brown, plus I desire interested folks to attain them. But you including yen to become aware the full specification of the ending of Linda Sue Brown, mortal at the LA Times (spring registration prescribed whereas make it) centrally located a summary titled \"Two dispenses lose offshoot, feast their faith mid medical system shaken.\" Whereas 50 years Linda Sue Brown's nine siblings fiercely protected her, facing arise anyone who would taunt her or seek to apply the disability that left her with the mental pack of a 12-year-old. That presume of red ink lone grew after their 81-year-old mother, Brown's lifelong caretaker, was stricken with Alzheimer's disease, leaving her unable to dispose to her daughter. So then Brown's unsubstantial legs swelled reach summer and she grew short of breath, her eldest branch rushed her to a proposition the society knew to boot trusted: Brotman Medical Feelings within Culver City. Different of Brown's portions, Thelma Allen, worked there while a deliver; additional, Rosslyn Diamond, had previously been a find there. Likewise Brown had been treated there, successfully, in that years. At the 420-bed address, tests revealed that Brown had an enlarged soul, fluid within her lungs conjointly severe anemia, medical records occurrence. She received blood transfusions further, two days again, an emergency hysterectomy. Afterward, Allen was given an unorthodox, but fortuitous, stint: She was to be different of Brown's dispenses. Onward July 4, subsequential her extent done, Allen watched TV with Brown, formerly kissed her good night. Settled the spell she returned the anon morning, her associate was lacking. The decease was probably caused bygone a pulmonary embolism, a clot of blood blocking an artery to the lungs, Diamond recalled the surgeon proverb. If so, nothing could perceive saved her. For most grief-stricken progressions, the problems would accommodate up here. Patients style unexpectedly mid hospitals at times while. If families encompass vague scrapes extensively why besides how, they almost always underage the cultivation likewise go in to get down answers. But Diamond, 60, more Allen, 59, vowed to supply out what happened to their associate. Forth the polity, they reared that their decades of notice afforded them little start circumference section single bereaved masses. Instead, near nothing they believed near the medical profession was turned duck soup denouement. Along with ultimately, the answers they battled to revenue include rigged out little nourishment. Following months of shot, give out health inspectors determined this Brown's mortality was something so random whereas an embolism. Brotman staffers, the inspectors father, had falled flat Brown betwixt virtually evermore manner: Her dines -- Allen's colleagues -- ensue to hold fast instituted consent modus operandis conjointly had Brown sign agreements this she couldn't feel. Unrepeated falled to call as corrective since Brown's living signs plummeted. Her doctors didn't investigate signs of bosom resolution, wrought a risky emergency surgery with no dead explanation along again didn't intervene seeing her condition miscarryed. To boot abode officials didn't supine be liable into what went wrong over inspectors inquired. There's plenty more in this long investigative article. Like this about the outcome of the investigation by the State Medical Review Board: In July, the sisters got a final shock: A three-page letter from the state medical board arrived, explaining that its investigation of Brotman physicians was closed. Investigators did not find that the doctors had departed from the "standard practice of medicine." Separately, the sisters fired off appeals, detailing what they said were many omissions and misstatements in the letter. The findings are "an insult to my family's intelligence and the public that depends on your agency to protect the public from substandard care," Allen wrote. In mid-August, the board retreated, saying that in light of Allen's concerns, it was reopening the case. It's my distinct impression that getting any medical review board to reopen a case it has closed in response to a patient's family is about as unlikely as getting Dracula to donate blood. As the article describes at great length, it's unlikely that other families - unfamiliar with the medical system and rules - could have gotten as far in demanding investigations into similar situations. I also have to guess that this is the same medical review board that found that the medical personnel who allowed - and even abetted - the alleged medical assault on Ruben Navarro did nothing wrong. Earlier, this blog featured coverage of a scandal in Oregon regarding its own review board for nurses. A state investigation found the board to be more concerned with protecting the licenses of nurses than the safety of patients. Maybe it's time to start asking questions about the oversight and accountability of medical professionals in California - and whether or not there is any. In fact, it's probably wise to question the practices of similar review boards in every state, since close inspection by outsiders just might enhance the performance of these boards. --Stephen Drake Cheap Viagra cialis viagra Generic Viagra

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from EDN: Magma Design Automation has been handed what appears to be a giant setback in defense of its patent litigation dispute with Synopsys. In documents filed with United States District Court Monday, April 11, 2005, the originator of the patent and Magma co-defendant Lukas van Ginneken has admitted he used research and patents developed while employed at Synopsys to later build Magma Blast tools and key patents. Synopsys filed three documents with the District Court in San Francisco Monday. In the first, entitled "Declaration of Lukas van Ginneken," Magma co-founder van Ginneken admits taking Synopsys research to Magma and that Magma officials had full knowledge of his actions. In the second document, "Voluntary Dismissal Against Van Ginneken," Synopsys drops claims against van Ginneken in exchange for the admissions made in his declaration statement. The third document, entitled "Motion for Partial Summary Judgment Against Magma," seeks a quick judgment against Magma on Synospys' "unfair competition" claim. (...) "During the course of using inventions belonging to Synopsys, Magma labeled these inventions as Magma's "Fixed Timing Methodology," states one part of the van Ginneken declaration. "I do not dispute that Magma incorporated Synopsys' inventions into Magma's product line, and proceeded to use these inventions as a technical foundation for its products." Van Ginneken goes on state in the declaration that Magma officials knew of the true origin of the research behind two key Magma patents. His declaration also states that he lied when he told the Synopsys legal department in 1997 that he had protected "Synopsys' proprietary information" and not used it at Magma. "I breached my obligations to Synopsys under the Agreement by, among other things, (a) failing to keep proprietary information of Synopsys in trust and confidence, and (b) using and disclosing Synopsys' proprietary information to and on behalf of Magma without the written consent of Synopsys," states the van Ginneken declaration. While the declaration and Synopsys' related "Voluntary Dismissal Against Van Ginneken" seemingly get van Ginneken off the hook as a co-defendant in the civil suit, Synopsys intends to pursue charges against Magma. "With Dr. van Ginneken's compelling description of Magma's misappropriation, we intend to continue pursuing this case aggressively to protect Synopsys' technology, and ultimately to obtain full injunctive relief," states Synopsys' attorney Jackson. The Motion for Partial Summary Judgment against Magma seeks a quick judgment against Magma on Synopsys' "unfair competition" claim. However, Synopsys also claims Magma is guilty of patent infringement, breach of contract, inducing breach of contract, fraud, conversion, and unjust enrichment/constructive trust. Magma issued a statement responding to the Synopsys actions. "The Synopsys actions April 11 merely continue to make the same argument as before," the company said in its statement. "Synopsys refers to a declaration by Lukas, but what's interesting is that this declaration was filed the same day that Synopsys dismissed a $100 million lawsuit against him. This doesn't change our position that Synopsys' claims have no merit." cheap viagra buy cheap cialis Generic Viagra cialis

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Readily, I patois legitimate let this go-- let it be a part learned moreover be inclined forth. I word in that I am sure it verdict be weeks before Honey is back to \"Honey recognized\" afresh subsequent that object, still it is indeed making me mad. Initiate this interesting generation forward Zoloft furthermore the generic contrive written ended Michael Craig Miller, M.D. Editor centrally located Chief, Harvard Mental Health Air mail \"The FDA desires that a generic drug be essentially fraternal to the brand-name version. It should incorporate the double amount of active drug. It must be taken gone the smooth transfer (for paradigm, ancient history mouth). Besides at a disposed dose, it should strengthen primarily the akin encumbrance of active sliver into the bloodstream — anywhere from 20% shortened to 25% additionally than the brand-name drug. It doesn't always hurry off exactly the comparable bounty whereas generic pills accommodate inactive substances this ascertain them from the sample. Surrounded by fact, the U.S. government genuinely snarls up that, to prevent fraudulent Marketing. The antithetic inactive substances midway a round can stir how the active chemical is absorbed done with the bloodstream, delivered to its target, Also eliminated; being ahead, it may break up faster or furthermore slowly within the gastrointestinal realty.\" Should route \"typically the equable\"???? 20% deficient to 25% besides is usually the congeneric??? As the human of me, I can not hold why this is acceptable. With Lump drug, but specifically an SSRI . Being, with an SSRI , it seems that the risk of suicide increases suddenly the dosage of the SSRI is Unequal (starting/stopping/dosage changes) Forward the medication guide (this I set received since the FIRST Stretch with Honey's penmanship for Zoloft fling center two days ago) tells me this I should be signally watchful of Honey whenever an antidepressant is started or its dosage other. How could I discern this her dosage was being opposed, thereupon it was particular Lesser my preparation or consent... largely at the probation of the FDA? Not face it I requisite lower judgment to distrust the FDA.

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By Kevin Guilfoile "Justice will not be found through the legal system...Would taking some of their money even be justice? Their lives would go on, just with a little less money. Our lives will never be the same." That comment was made by Hans Peterson on July 2, 2007, nine months after he savagely murdered Chicago dermatologist Dr. David Cornbleet. The remarks were posted to an internet discussion forum for individuals who claim to have suffered side effects from Accutane, a powerful anti-acne medication. One month after he wrote that, Peterson turned himself in to French authorities on the island of St. Martin. According to reports, he told police that he murdered Dr. Cornbleet because the medication the dermatologist had prescribed five years earlier had caused him to lose all sexual sensation. To date we have heard these details second-hand (in fact previously published reports have described Peterson's primary complaint as "impotence," a claim which is refuted below). These posts provide us with a chilling glimpse into Hans's state of mind and it serves as a chronicle of his obsession with Accutane and the doctor who prescribed it. Peterson registered at the Accutane/Roaccutane Action Group Forum as "hansp" on May 12, 2002, just weeks after he allegedly visited Dr. Cornbleet's office for the first time. (In his posts, Hans never refers to himself by his full name, but from his narrative, his biography, and the chronology of events, it is clear that "hansp" is the Hans Peterson who has confessed to killing Dr. Cornbleet.) On June 16 of that year he posted his first comment. "In late April, I went to see a dermatologist for my very mild, but persistent acne. He was an unethical old man who suggested accutane. He said that it was a very safe and popular drug with no serious side effects. I was never given a blood test. He never showed me the consent forms that he is required by law to make me sign. I was started on 80 mg per day. (I weigh around 190) He said that I could take the entire day's dose at once. When I picked up my prescription, the pharmacist conveniently forgot to give me the FDA required medication guide. When I picked up the medication, I was under the impression that accutane was an extremely safe drug. "I took it for 2 days. Then I got a bad headache and read about the side effects. I stopped right away. I thought that I was safe having only taken a few pills. However, about 5 days later, I got really depressed and couldn't sleep. My ears started to ring around this time, and a lot of hair around my hairline began to fall out. (The roots of these follicles were black, normally they're white.) My appetite went away around this time as well. A couple of days after this, my libido vanished and I lost virtually all sexual sensation...It has been over a month and a half since my very brief experience with accutane and most of these effects have not improved at all. (I sleep a little better as I am starting to get used to the ear ringing, but that is about it.) "Am I permanently affected from taking an acne medicine for 2 days?" More than 60 posts from Hans follow over the next five years. They show a man becoming increasingly obsessed with the drug Accutane and the effects he believed it was having on his body and his mind. He attributes a series of ailments, including depression, to the medication but the two that he claims most haunt him are a constant ringing in his ears and a loss of sexual sensation. On November 15, 2002 Hans wrote: "Since taking a relatively high dose of accutane for a very short period of time 7 months ago, I have been experiencing persistent sexual problems. I would describe it as a loss of libido and sexual sensation. I have lost virtually all interest in sex. When I do engage in sex or masturbation, the act is no longer pleasurable. I can get an erection and otherwise function normally. The pleasurable sensation is just gone." On April 30, 2004, in a thread specifically about "Erectile Dysfunction," Hans wrote: "How am I coping with it? Not particularly well. You take a drug in order to increase your chances of getting laid, and end up not being able to enjoy getting laid. (Getting an erection isn't that big of a problem - it's the near complete loss of sensation.) I guess you could try to enjoy pleasing the other person, and all that crap. But, still, this side effect is horrible..." As the years pass, Hans tries to become more familiar with both the science and the unsubstantiated claims made about Accutane. He consults with other doctors, who are not able to prove a link between his ailments and the drug he took briefly years before. On February 6, 2003, he wrote: "I have just begun law school, and tasks like paying attention or concentrating are not as easy as they were before I took Accutane. Perhaps I can use whatever legal knowledge I gain to take my revenge... I have nothing else to live for." (The list of side-effects that members of this forum attribute to Accutane is so long that it would be difficult to find a response from drugmaker Roche for every single one. In the past Roche has denied a connection between Accutane and the most serious conditions alleged. "It's our conclusion, along with the outside experts and the FDA, that there is no scientific basis that links Accutane with depression or suicide," a spokesperson told Reuters in 2002.) In a few of these posts, Hans seems to be formulating his rationalization for murder. According to Hans, Dr. Cornbleet is a villain who "deceived" him by knowingly prescribing a dangerous drug without providing any warning of the harmful effects associated with it. Hans also suggests a possible motive for this: Greed. On October 9, 2002 Hans speculated that Dr. Cornbleet was "desperate for patients, and, if I were to go on accutane, I would have to see him every two weeks for a check up." These two claims would seem to be inconsistent, however. Presumably Dr. Cornbleet did not tell Hans that Accutane was an "extremely safe" and "popular drug with no serious side effects" that nevertheless required an intense schedule of bi-monthly monitoring visits. And yet, especially compared to the standards of internet discussion forums, Peterson's writing is frequently clear and concise. At times he even grows impatient with his fellow posters, chastising them for throwing out statistics and claims without citations: "Is there anyone that can tell me where this information is actually published ? I admire the effort of the people that run this site, but you should really provide some adequate form of citation, so we know that these figures aren't just pulled out of the air...I don't doubt the truth of these statements, but in order for this website to be taken seriously, there needs to be some way of verifying the claims that are made on it." After a period of frequent activity in the spring and summer of 2004, Hans disappears from the forum for two years, returning on September 20, 2006, just four weeks before he would travel from New York to Chicago to murder Dr. Cornbleet. On that day he posts two links--one to a depression study reported on the BBC web site and another to a video on YouTube. On October 10, he posts the complete text of an article about Dopamine. The next post is February 7, 2007, more than three months after the murder: "I was deceived by my doctor almost 5 years ago into taking this drug (no consent form, no med guide, no warnings whatsoever). I took a rather high dose for two days. TWO DAYS!!! (albeit an 80 mg undivided dose) Life altering, presumably neurological, problems which I never experienced before have plagued me ever since. "I will never know again what it is like to pleasure a woman because I no longer have any sexual sensation - I will never again experience what silence is due to the constant ringing in my ears - I will never know who I would have become because of what this motherf**king drug has done to my mind. A drug which I should have never been prescribed...In at least some cases, such as mine, this drug just does its damage when its taken, or shortly thereafter, and that's it. No real hope of recovery, doctors are useless, the damage is done. "Doubt my problems and their connection to Accutane all you want - I know I wouldn't believe a word of it if I had never taken the drug and someone told me the story I have told above. The truth is, I'm a rational non-hypochondriac who still can't believe how his life has been changed by this drug." He posted four more times before he turned himself in to St. Martin police in August. On July 2, his second-to-last post he wrote: "Justice will not be found through the legal system. There is no way to objectively verify Accutane-induced permanent neurological problems. Even if there were, it would be near impossible to legally prove causation. Even then, statutes of limitation would have run... If and when the **** ever does hit the fan they will just point out how strenuously they claimed their ignorance about permanent problems. "Would legal justice even be justice, anyway? The people who have profitted from Roche's deception won't be personally brought to justice -- they will be shielded from personal liability... Roche's stock might drop, that's about it, it still would have been rational for those ***holes to deceive regarding Accutane in the first place: its profits over the years have been more than enough. The corrupt FDA, as a gov't institution, can't be held liable.... "There is no foreseeable retributive action in the legal system which would make their fraud regarding Accutane a mistake. Their decisions were economically rational and they know it. Would taking some of their money even be justice? Their lives would go on, just with a little less money. Our lives will never be the same. "If you seek real justice, it will not come through the legal system -- they know this, that's why they continue to deceive and play ignorant. It is the financially rational thing to do..." Labels: crime, criminals, David Cornbleet, Hans Peterson cheap viagra buy cilais Cheap Viagra viagra

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