
8.10.2020 | 02:39
Fiskarnir 5, sem ţú átt aldrei ađ borđa, og fiskarnir 5 sem ţú ţarft ađ borđa.
Viđ höfum ţetta í huganum, og meltum ţađ.
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Top 5 Best Fish You Should NEVER Eat & 5 Fish You Must To Eat
https://www.youtube.com/watch?v=0hdVpzvLbYo
klikka mynd, ţá stćrri
klikka mynd, ţá stćrri
Fimm bestu fiskarnir, og verstu fiskarnir til átu.
Omega stafurinn kemur sem stafarugl
|
| â¦*3 | Hg | FREQ | GENERAL |
1 |
| 2590 | 22 | ------ | Protein |
2 |
| 2670 | 50 | ------ | Size/Age |
3 |
| 1500 | 13 | ------ | Location |
4 |
| 1890 | 84 | ------ | Tilefish Atl. (144) |
5 |
| 1070 | 71 | ------ | Tilefish Mex. (1450) |
6 |
| 350 | 9 | ------ | Trout Fresh (71) |
7 |
| 250 | 45 | ------ | Trout Ocean (256) |
8 |
| 320 | 65 | ------ |
|
9 |
| 200 | 111 | ------ |
|
10 |
| 160 | 160 | ------ |
|
11 | Orange Roughy |
| 571 | --- --- |
|
12 | Tuna |
| 350 - 689 | --- --- --- | - Unnatural |
13 | King Mackerel |
| 730 | --- --- --- | - Antibiotick |
14 | Shark |
| 979 | --- --- --- | - Red Dye |
15 | Swordfish |
| 995 | --- --- --- | - 1**PCB (16 x) |
16 | Tile Fish (Mexico) |
| 1450 | --- --- --- | - 1** â¦6 1? â¦***3 |
Egilsstađir, 08.10.2020 Jónas Gunnlaugsson * Omega ** Ör upp. *** Omega
Bloggar | Breytt s.d. kl. 12:25 | Slóđ | Facebook | Athugasemdir (0)
Tekiđ úr bloggi:
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3.10.2020 | 21:32
To sum up:
Posted by Meryl Nass, M.D. at 9:17 AM
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Jónas Gunnlaugsson | 5. september 2020
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Egilsstađir, 05.10.2020 Jónas Gunnlaugsson
Bloggar | Breytt s.d. kl. 22:02 | Slóđ | Facebook | Athugasemdir (0)
Google translate.
@Anonymous fyrir ofan fćrslu mína, ţessar rannsóknir (Recovery and Solidarity and REMAP) voru hannađar til ađ drepa sjúklinga til ađ ófrćgja Hydroxychloroquine.
Sumar rannsóknir sem nota hćfilega skammta sýna mjög góđa lćkkun á dánartíđni, jafnvel hjá viđkvćmum sjúklingum.
Ég ćtla ekki ađ endursegja ţetta. Ţađ er of viđkvćmt. Verđur ađ vera rétt.
Reyniđ ađ ţýđa sjálf međ
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Hér er ein commentin, afrituđ ađ neđan úr comments.
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August 22, 2020 at 8:57 AMAnonymous said...
@Anonymous above my post, these trials (Recovery and Solidarity and REMAP) were designed to kill patients to discredit Hydroxychloroquine.
Some studies using reasonable doses show a very good reduction in mortality, even for vulnerable patients.
If HCQ had not be demonized, there would be no need for a vaccine. There are a couple other cheap drugs being discovered with promising results vs Covid-19 as well
The Solidarity Trial is a WHO-led conglomeration of many national trials of treatments for Covid-19. In March alone, the WHO collected $108 million from donors to cover costs of Solidairy clinical trials. Per the WHO:
As of 3 June 2020, more than 3500 patients have been recruited in 35 countries, with over 400 hospitals actively recruiting patients. Overall, over 100 countries have joined or expressed an interest in joining the trial, and WHO is actively supporting 60 of them...
The hydroxychloroquine arm of the Solidarity trials restarted enrolling patients June 3, after being halted May 25 by WHO Director-General Dr. Tedros Adhanom Ghebreyesus and the Executive Group of the Solidarity Trial. The hydroxychloroquine (HCQ) arm of the trials had been stopped after publication of the Lancet Surgisphere study, which claimed that patients who received chloroquine or hydroxychloroquine had 35% higher death rates, but the Lancet study was retracted 13 days after publication, as its data turned out to be fabricated. The HCQ Solidarity trials are currently ongoing.
Below are the drugs being tested in Solidarity:
Initially, the WHO planned to use neither cloroquine in its trials. But multiple countries requested chloroquines, so both chloroquine (CQ) and HCQ were then added to the trial plan. However, HCQ was felt to be a little safer, countries preferred it, so WHO dropped CQ from its trials. Other clinical trials continue to test both CQ and HCQ against Covid-19. The doses were not specified on WHO's list of the drugs to be trialed, nor were they specified, surprisingly, in WHO's April 8 four-person "consultation on chloroquine (CQ) dosing". The Introduction of the Report of that meeting notes,
"The chloroquine or hydroxychloroquine schedule selected for the trial includes two oral loading doses (250 mg per tablet CQ or 200 mg per tablet HCQ), then oral twice-daily maintenance doses for ten days. This meeting convened to discuss the appropriateness of the selected doses for the trial."
Last week, I was alerted to the fact that India's ICMR, its official medical research agency, had written to the WHO, telling WHO that the hydroxychloroquine doses being used in the Solidarity trial were 4 times higher than the doses being used in India. Then I learned that Singapore had been hesitant to participate in the WHO trial due to the hydroxychloroquine dose.
The UK "Recovery" trial was very similar to, but not part of, the international Solidarity conglomeration of clinical trials. The Recovery trial ended its HCQ arm on June 4, reporting no benefit. In-hospital mortality of the 1542 patients receiving hydroxychloroquine was 25.7%, or 396 deaths, about 10% higher than those receiving standard care, a non-significant difference.
The UK Recovery trial Study Protocol notes it is funded in part by the Wellcome Trust and the Bill and Melinda Gates Foundation, and by UK government agencies. The Protocol provides the doses of hydroxychloroquine used, on page 22. Twitter users began to notice a dosing problem, with hashtag #RecoveryGate.
The HCQ dosing regimen used in the Recovery trial was 12 tablets during the first 24 hours (800mg initial dose, 800 mg six hours later, 400 mg 6 hrs later, 400 mg 6 hours later), then 400 mg every 12 hours for 9 more days. This is 2.4 grams during the first 24 hours, and a cumulative dose of 9.2 grams over 10 days.
Even more disturbing than this, babies weighing 5 kg could be given a dose of 300 mg HCQ in the first 24 hours in the UK Recovery trial, which is 233 mg of the base (47 mg/kg), nearly 4 times the recommended maximum. One to two pills (200-400 mg) is "potentially fatal in a toddler". And authors from George Washington University say:
"Ingestion of 1-2 tablets of chloroquine or hydroxychloroquine is thought to predispose children under 6 years of age to serious morbidity and mortality...ingestions of greater than 10 mg/kg of chloroquine base or unknown amounts require triage to the nearest health care facility for 4-6 h of observation. There is very limited data on pediatric hydroxychloroquine overdoses and no reports of toxicity from 1-2 pills, but given its similarity to chloroquine, it also should be considered potentially toxic at small doses. Thus, similar recommendations should be followed for triage after accidental hydroxychloroquine overdose." UPDATE July 21: The American Association of Poison Control Centers said on March 25: "These medications have a narrow therapeutic window, meaning that accidental ingestion of amounts that exceed recommended dosing can be extremely dangerous with toxicity including coma, seizures, cardiac dysrhythmias, low potassium levels, cardiac arrest and death. Even a single pill can be potentially life threatening to a child."
The quote from the WHO report on dosing, provided 9 paragraphs ago, seems to be deliberately vague regarding the dose used in the Solidarity trial, stating the number of milligrams per tablet, but not the number of tablets to be used. The Solidarity trial is registered but the registration fails to specify dosages.
The registration of the Canadian portion of the Solidarity trial informs us of its HCQ dose: ten 200 mg tablets during the first 24 hours (800 mg initial dose, 800 mg 12 hours later then 400 mg every 12 hours for 9 more days). This is 2.0 grams during the first 24 hours, and a cumulative dose of 8.8 grams over 10 days, or only 0.4 grams less than what Recovery used. The Norwegian Solidarity trial uses dosing identical to Canada.
Co-Principal Investigators of the Recovery trial, Drs. Peter Horby and Martin Landray, said they followed the WHO dosing. This is what their trial document says as well, on page 23. Landray also claimed in an interview with Paris Soir that the maximum allowed HCQ dose was "6 or 10 times" the dose used in Recovery, and that he was using the hydroxychloroquine dose that is used for amebic dysentery. However, the accepted use for HCQ in amebiasis is only for a liver abscess and only then in pregnancy, when other drugs cannot be used. That dose is 600 mg per day for 2 days, then 300 mg per day, considerably less than half the Recovery dose. Co-Principal Investigator Peter Horby said that Paris Soir misinterpreted Landray's comments, but Paris Soir said Landray had confirmed what he told them in an email prior to publication. Landray is a very busy man, too busy, apparently, to look up the proper dose of a drug he gave to over 1500 subjects, who were randomized to the treatment and had no say in the matter.
We know that in Brazil, both a high CQ dose and a low CQ dose were trialed, and by April 17 the high dose arm was stopped prematurely due to an excess of deaths, with 39% mortality (16 deaths in 41 subjects). The mean age in the high dose group was 54.7. The high dose arm used 600 mg CQ twice daily for ten days, with cumulative dose of 12 grams. EKG changes typical of toxicity were seen in 25% of high dose subjects. The low dose trial continues in Brazil.
How is the drug hydroxychloroquine normally used? For chronic daily use in systemic lupus erythematosus, rheumatoid arthritis or Lyme disease, patients receive between 200 and 400 mg daily, or a maximum of 5 mg/kg. In acute Q fever, 600 mg daily may be given at the start of treatment. For acute attacks of malaria, 1,500-2,000 mg may be given over 3 days. Professor Didier Raoult's group in Marseille used 600 mg daily for up to ten days in 1061 Covid-19 patients, and reported 8 deaths, a mortality rate of 0.75%, all over 74 years of age. The mortality rate reported by Landray and Horby in the Recovery trial is 34 times higher.
We know from WHO's March 13 Informal consultation on the potential role of chloroquine that the Gates Foundation had been studying the drug's complex pharmacokinetics, and of the 25 participants at this meeting, 5 were from the Gates Foundation.
The only treatment dose mentioned in the March 13 Informal consultation report was in a paragraph about preventive doses. It said, "Higher doses would be considered for treatment, i.e., 10mg/kg base, followed by 5mg/kg twice daily for seven days."
What is the "base"? A 200 mg dose of hydroxychloroquine contains 155 mg "base" drug. Generally, a loading dose refers only to a high first dose, not to several high additional doses. However, the trial protocol used in Solidarity employs the same dose for all, rather than weight-based dosing.
What is a toxic dose? All experts agree on this: "... chloroquine has a small toxic to therapeutic margin," according to Goldfrank's Toxicologic Emergencies. The drug is very safe when used correctly, but not a lot more can potentially kill. Prof. Nicholas White, a Wellcome Trust Principal Research Fellow and expert in malaria treatment, who attended both WHO consultations on the chloroquines, has confirmed this. Careful monitoring of electrolyte levels and an EKG can prevent most problems.
The WHO hired a consultant to explore the toxicity of chloroquine in 1979. The consultant, H. Weniger, looked at 335 episodes of adult poisoning by chloroquine drugs. Weniger on page 5 notes that a single dose of 1.5-2 grams of chloroquine base "may be fatal."
According to Browning and Goldfrank, the pharmacokinetics and potency of chloroquine and hydroxychloroquine are almost identical, while the maximum used chronic dose of chloroquine is 3.5 mg/kg.
The Recovery trial used 1.86 grams hydroxychloroquine base (equal to 2400 mg of hydroxychloroquine) in the first 24 hours for treatment of already very ill, hospitalized Covid-19 patients. The Canadian and Norwegian Solidarity trials used 2,000 mg of HCQ, or 1.55 grams of HCQ base in the first 24 hours. Each trial gave patients a cumulative dose during the first 24 hours that, when given as a single dose, has been documented to be lethal. (The drug's half-life is about a month, so the cumulative amount is important.)
The doses used in these trials are not recommended for therapy of any medical condition, which I confirmed with Goodman and Gilman's Pharmacology textbook, the drug's US label, and the online subscription medical encyclopedia UptoDate.
Excessive, dangerous HCQ dosing continues to be used in WHO's Solidarity trials. While the Solidarity trials have an "adaptive" design which allows midstream protocol changes, no lessons were learned from the Brazil or Recovery trials' experience with excessive dosages. Solidarity has not reduced its HCQ dosing, although it can do so at any time. The Solidarity trials are not, in fact, testing the benefits of HCQ on Covid-19, but rather are testing whether patients survive toxic, non-therapeutic doses.
The WHO Solidarity trials, in order to rapidly enroll patients and spare clinicians a lot of paperwork, collect only limited information on side effects. No information has yet been provided regarding causes of death in the completed hydroxychloroquine arm of the Recovery trial, in which 396 patients died, and may never be.
The Solidarity trial design being employed by WHO obscures whether mortality is due to drug toxicity (in which case, one would expect death to be due to an arrhythmia, neuropsychiatric effects, or hypoglycemia) as opposed to death due to Covid-19.
In fact, the lack of safety data being collected is downright scary. Here is a description of the data obtained on patients enrolled in Solidarity, as reported in Science magazine:
The participant has to sign an informed consent form that is scanned and sent to WHO electronically. After the physician states which drugs are available at his or her hospital, the website will randomize the patient to one of the drugs available or to the local standard care for COVID-19. After that, no more measurements or documentation are required, says Ana Maria Henao Restrepo, a medical officer at WHOs Emergencies Programme. Physicians will record the day the patient left the hospital or died, the duration of the hospital stay, and whether the patient required oxygen or ventilation, she says. Thats all.
The WHO report of its meeting on chloroquine dosing states,
Although the preponderance of opinion tilted towards a reasonable benefit risk profile for the intervention, there was some scepticism about what was considered a minimalistic safety data collection currently included in the protocol.
The high dose regimen being used in these trials has no medical justification. The trial design, with its limited collection of safety data, makes it difficult or impossible to identify toxic drug effects, compared to a standard drug trial. This is completely unethical.
Excessive dosing makes it impossible to assess therapeutic benefit, if any, of HCQ. Furthermore, because there are over 400 trial sites, and relatively few subjects in each, unexpectedly high trends in mortality are likely to be missed at individual trial sites.
Finally, testing the drug only in hospitalized patients means that the window of time during which HCQ would be expected to provide the most benefit, early in the illness when viral titers are rising, has passed.
Didier Raoult's group has recently published on the major differences in treatment and outcomes patients receive when placed in "big data" studies vs. receiving individualized care for Covid-19.
As I was completing this article, the FDA announced it was withdrawing its Emergency Use Authorization for hydroxychloroquine in Covid-19, because the "known and potential benefits" no longer outweigh the risks of the drug. The FDA cited data from the Recovery trial in its announcement. I discuss the implications here.
To sum up:
Posted by Meryl Nass, M.D. at 9:17 AM
John said...
Mind boggling to think Anne Frank if alive could be in these high dose HCQ WHO studies.
Doctors here earned deserving mistrust on level that defies comprehension.
Dr Mengeles School of Medicine in many ways has won the day, and honest physicians could not disregard how high the mountain piles in nearly ever direction of MD Mengele facts!!!
Physicians themselves report dont know what to do about the corruption coming from those in charge!!
Reading about another pile in Bitten on Lyme Disease Kris Newby on Biological Weapons for citizens, the thrill of it all.
Mr. Hilter election Pls Monty Pythons Flying Circus https://m.youtube.com/watch?v=hWIyVRNAxCg&feature=emb_title
Caution Killers https://www.youtube.com/watch?v=vLL5igJOsXo
Human Race Matters?
June 18, 2020 at 12:05 AMUnknown said...
This is an article of exceptional quality. We quickly came to the conclusion that the RECOVERY trials were an act of sabotage. We, however, did not look at the dosage to infants and children. The RECOVERY trials recommend a toxic dose of hydroxychloroquine to infants. Neither infants nor breastfeeding mothers should be administered hydroxychloroquine according to the insert of the manufacturer for the US. It is shocking that the RECOVERY protocol contains such a gross and potentially deadly error. Thank you for your excellent work. The New Neander's Medical.
June 18, 2020 at 9:07 AMDrew458 said...
I hope that President Trump keeps his mouth shut about the news of Dexamethasone. That too will become instant anathema if he so much as nods his head in it's direction.
June 18, 2020 at 12:22 PMAnonymous said...
A very scary and well researched article of evidence to show Cov-19 was made in the USA Not a quick read, so you may want to skip the history of viruses and scroll to: Man-Made SARS-CoV-2 https://www.sott.net/article/437083-Compelling-Evidence-That-SARS-CoV-2-Was-Man-Made
June 28, 2020 at 12:01 PMAnonymous said...
The Elephant in the room is what boys and girls
.?
http://www.rigorousintuition.ca/board2/viewtopic.php?f=8&t=41979
Breadcrumbs.
Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag
Prashant Pradhan, Ashutosh Kumar Pandey, Akhilesh Mishra, Parul Gupta, Praveen Kumar Tripathi, Manoj Balakrishnan Menon, James Gomes, Perumal Vivekanandan, Bishwajit Kundu
This article is a preprint and has not been certified by peer review [what does this mean?]. AbstractFull TextInfo/HistoryMetrics Preview PDF Abstract
We are currently witnessing a major epidemic caused by the 2019 novel coronavirus (2019-nCoV). The evolution of 2019-nCoV remains elusive. We found 4 insertions in the spike glycoprotein (S) which are unique to the 2019-nCoV and are not present in other coronaviruses. Importantly, amino acid residues in all the 4 inserts have identity or similarity to those in the HIV-1 gp120 or HIV-1 Gag. Interestingly, despite the inserts being discontinuous on the primary amino acid sequence, 3D-modelling of the 2019-nCoV suggests that they converge to constitute the receptor binding site. The finding of 4 unique inserts in the 2019-nCoV, all of which have identity /similarity to amino acid residues in key structural proteins of HIV-1 is unlikely to be fortuitous in nature. This work provides yet unknown insights on 2019-nCoV and sheds light on the evolution and pathogenicity of this virus with important implications for diagnosis of this virus.
Breadcrumbs.
https://www.biorxiv.org/content/10.1101/2020.01.30.927871v1
July 3, 2020 at 10:41 AMUnknown said...
in reply to Anonymous: "The Elephant in the room is what boys and girls
.?" and "Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag"
***PAPER WITHDRAWN***
read the comments on it at https://www.biorxiv.org/content/10.1101/2020.01.30.927871v1
it's total rubbish, basically.
July 13, 2020 at 8:48 AMAnonymous said...
I think the same trials should not be continued because they are too risky to human health. Do you think a vaccine is more practical, at least it has no effect on health? Remember to visit my blog if you have some time: สลŕąŕ¸ŕ¸
August 22, 2020 at 8:57 AMAnonymous said...
@Anonymous above my post, these trials (Recovery and Solidarity and REMAP) were designed to kill patients to discredit Hydroxychloroquine.
Some studies using reasonable doses show a very good reduction in mortality, even for vulnerable patients.
If HCQ had not be demonized, there would be no need for a vaccine. There are a couple other cheap drugs being discovered with promising results vs Covid-19 as well
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Bloggar | Breytt 4.10.2020 kl. 12:40 | Slóđ | Facebook | Athugasemdir (0)
Arutz Sheva
Hydroxychloroquine (í Ísrael)
https://www.israelnationalnews.com/News/News.aspx/287773
Ţađ má byrja ađ lesa í litađa letrinu neđar í greininni.
Ísrael fagnađi ţegar ţađ virtist vera ađ komast í gegnum Wuhan-vírusfaraldurinn međ glćsibrag. Í júnílok, međ ađeins rétt rúmlega 300 dauđsföll, ţá vorum viđ heimsmeistarar. Okkur var leyft ađ snúa aftur til daglegs lífs. Síđan dundi ógćfan á okkur aftur. Af fullum ţunga. Dánartölur ruku upp og yfir 1200 manns létust.
Hvers vegna? Hvađ gerđum viđ sem var ólíkt ţví sem áđur var?
Okkur var sagt ađ viđ vćrum ađ halda partí, ađ gifta okkur, ađ safnast saman til bćnafunda, ađ fara á ströndina. En viđ vorum líka ađ gera allt ţetta áđur. Í hverju er ţá munurinn fólginn?
Viđ fengum aldrei nein svör viđ ţví. Í stađinn var ákveđiđ ađ útnefna heilsueinvald, kalla hann Ráđabruggarann, gefa honum lyklavöldin ađ kastalanum, ţ.m.t. ađ fjárhagnum, ráđuneytum, rannsóknarstofum, sjúkrahúsum, heilsugćslum, meira ađ segja hernum, til ađ fletja út seinni bylgjuna. Stjórnmálamennirnir lofuđu ađ halda sig til hlés.
Í fyrsta lagi breytti Ráđabruggarinn landinu í umferđarljósasvćđi. Ţau međ hćstu smitatölurnar voru merkt rauđ og sett í sóttkví. Hljómađi vel ţar til ađ í ljós kom ađ mikill meirihluti rauđu svćđanna, 80%, voru annađhvort arabahverfi eđa strangtrúarhverfi og ţađ olli mótspyrnu ađ ekki sé minnst á háar dánartölur á ţessum svćđum.
Ráđabruggarinn sagđi ađ ţessum svćđum yrđi ađ loka alveg. Og ţá varđ allt vitlaust. Stjórnmálamenn komu fram úr fylgsnum sínum. Ţingfundir urđu ađ uppţotum. Flokksbrot hlynnt forsćtisráđherranum kröfđust stuđnings hans og ţau sem voru gegn honum fóru ađ berja ađ dyrum. Hann sá enga útleiđ ţannig ađ hann gerđi ţađ sem allir stjórnmálamenn hefđu gert. Hann henti áćtlun Ráđabruggarans út um gluggann og fyrirskipađi allsherjar útgöngubann í ţrjár vikur, sem féllu á helstu hátíđir gyđinga, ţ.á m. nýárshátíđina, friđţćgingardaginn og laufskálahátíđina.
Útgöngubanniđ hófst síđdegis á föstudegi fyrir hina hefđbundnu nýárshátíđ til ađ koma í veg fyrir fjölmennar fjölskyldusamkomur. En hugmyndaríkir Ísraelsmenn fluttu hátíđahöldin um einn dag og héldu sínar fjölskylduveislur á fimmtudegi í stađinn fyrir á föstudegi. Bráđsnjallt.
Ţúsundir gyđinga drifu sig á sýnatökustöđvar áđur en ţeir mćttu á Ben Gurion-flugvöllinn og flugu frá rauđum svćđum Ísraels til grćnna grunda frekar en ađ sitja innilokađir svo vikum skipti. Sumir bókuđu bara miđa ađra leiđ.
Mikiđ spjallađ í sjónvarpi. Miklu bleki eytt á síđum dagblađanna.
Ţögn ríkti um stćrstu ráđgátuna.
Hvers vegna var fleira fólk ađ veikjast alvarlega og deyja en áđur?
Hvers vegna erum viđ nú međ yfir 1300 dauđsföll ţegar, í fyrstu bylgjunni, ţau voru ađeins rétt rúmlega 300 talsins? Hvers vegna er ţessi munur upp á 400%?
Ţetta er ekki vegna meiri sýnatöku ţví ađ fólk veiktist, jafnvel án ţess ađ sýni vćru tekin, í fyrstu bylgjunni. Embćttismenn og spekingar tala endalaust um sýnatökur, samskiptafjarlćgđ og útgöngubann en lítiđ annađ. Ţeir hafa áhyggjur af ađ spítalar og rannsóknarstofur kikni undan álagi viđ ađ sinna alvarlega veikum sjúklingum.
En enginn er ađ tala um hvernig á ađ forđa nýlega veiku fólki frá ţví ađ hraka og lenda á spítala eđa ţađan af verra.
Mega heimilislćknar okkar og heilsugćslur gera allt sem í ţeirra valdi stendur til ađ forđa nýveiku fólki frá ţví ađ lenda á sjúkrahúsi og deyja?
Svariđ er nei. Ţau mega ţađ ekki.
Reyndar eru ţessir fyrsta flokks lćknar, sem hafa náiđ faglegt samband viđ sjúklinga sína, hindrađir í ađ nota ţađ sem gćti hjálpađ ţeim ađ međhöndla ţá á árangursríkan hátt.
Voru ísraelskir lćknar ađ gefa sjúklingum sínum eitthvađ í fyrstu bylgjunni sem kom í veg fyrir háar dánartölur, eitthvađ sem ţeir eru ekki ađ gefa sjúklingum sínum núna?
Svariđ er já.
Lćknar og heilsugćslustöđvar mega ekki ávísa lyfi sem virkađi áđur en er núna bannađ. Lyfiđ sem ekki má nefna heitir Hydroxychloroquine (hér eftir skammstafađ HCQ).
Lyfjafrćđingum er bannađ ađ minnast á ţetta efni í fjölmiđlum. Sumir hafa veriđ reknir fyrir ađ voga sér ađ nefna ađ ţetta lyf, í bland viđ önnur, hafi bjargađ óteljandi lífum.
Núna er búiđ ađ setja ţetta bann á heilsugćslulćkna í Ísrael og fleira fólk deyr.
HCQ er lyf sem hefur fengiđ alţjóđlegan opinberan stađal sem međal viđ margskonar veikindum og sjúkdómum. Ţađ er međ ótrúlegt öryggismet til sextíu ára.
En í einni andrá varđ ţađ ađ djöfladrykk.
Mörg hundruđ lćkna og ţúsundir sjúklinga sem fullyrđa um gagn ţess ţegar ţađ er notađ á fyrstu stigum sjúkdómsins, í réttu magni og međ öđrum lyfjum eins og t.d. sinki og azithromycin, hafa veriđ settir í gapastokk og ţeim bannađ ađ sýna gögn sín eđa segja frá reynslu sinni.
Fariđ er međ lćkna, sem eru í nánu sambandi viđ sjúklinga sína, eins og villutrúarmenn.
Yfirvöld segja ađ HCQ hafi ekki stađist seinni stig klínískra prófana. Ţau fullyrđa ađ nokkrir sjúklingar hafi upplifađ hjartaóreglu, fullyrđing sem margir hafa hrakiđ, ţ.á m. dr. Harvey Risch, prófessor í farsjúkdómafrćđi viđ Yale-lćknadeildina, sem er mjög gagnrýninn á hversu lélegar ţessar klínísku prófanir voru.
Eftir ađ hafa kynnt sér ţćr ţá komst hann m.a. ađ ţeirri niđurstöđu ađ lyfiđ hefđi veriđ gefiđ á rangan hátt, jafnvel í banvćnum skömmtum, oft ekki međ öđrum lyfjum, til sjúklinga sem ekki áttu miklar lífslíkur, hvađ sem öllum lyfjum leiđ.
Risch prófessor er ákafur talsmađur fyrir notkun HCQ í bland viđ önnur lyf á fyrstu stigum sjúkdómsins, sem og dr. Vladimir Zelenko, grísk-kaţólsk-trúađur amerískur lćknir, sem fann upp Zelenko-reglurnar ţar sem lýst er í smáatriđum, fyrir heimilislćkna og heilsugćslustöđvar sem eru ađ međhöndla sjúklinga á fyrstu stigum Covid, hvernig á ađ skammta lyf og fylgjast međ sjúklingum fyrstu fimm dagana eftir ađ hafa greinst međ kórónuveiruna.
Prófessor Risch skráir niđur og sundurgreinir velgengni og mistök í međhöndlun snemmstigs Covid-sjúklinga og er sannfćrđur um ađ HCQ, í bland viđ önnur lyf, sé örugg og árangursrík ađferđ til ađ koma í veg fyrir lamandi áhrif kórónuveirunnar.
Ţessari snemmstigsmeđhöndlun var hleypt af stokkunum í Frakklandi af veirufrćđingnum Didier Raoult, sem međhöndlađi hundruđ Covid-sjúklinga, áđur en Big Pharma útmálađi hann sem skottulćkni.
Alţjóđaheilbrigđismálastofnunin (WHO) bannađi HCQ fyrir Covid-sjúklinga á grunni ţessarar löku útkomu í seinni stigs prófunum.
En WHO mćlir međ parasetamóli, lyfi sem hefur ekki veriđ sett í klínískar prófanir fyrir Covid-sjúklinga, og er ţekkt fyrir alvarlegar aukaverkanir.
Ţetta er ekki ađeins hrćsnisfullt heldur líka mjög grunsamlegt. Og WHO er grunsamleg stofnun eins og Donald Trump sagđi í rćđu sinni hjá Sameinuđu Ţjóđunum.
Sem kallar á spurninguna: Hvers vegna ţessi mismunun?
Athygli mín á ţessu hrópandi ósamrćmi var vakin ţegar ég tók viđtal viđ dr. Rob Elens, heimilislćkni međ heilsugćslu í suđurhluta Hollands.
Dr. Elens hafđi upphaflega tuttugu og fimm sjúklinga sem veiktust af Covid. Ţeir fengu međhöndlun skv. reglum frá hollenskum heilbrigđisyfirvöldum, semsagt parasetamól og einangrun.
Ţeim versnađi öllum. Ţeir lentu allir á sjúkrahúsi. Tólf ţeirra dóu.
Dr. Elens, sem er samúđarfullur lćknir, lá ţađ mjög á hjarta ađ eitthvađ betra hefđi getađ bjargađ sjúklingum hans.
Ţannig ađ hann gerđi ţađ sem allir ábyrgđarfullir lćknar myndu gera. Hann sökkti sér í vísindin og fann Zelenko-reglurnar, reynda og prófađa afleiđu af rannsóknum nokkurra lćkna viđ ađ hjálpa sjúklingum á fyrstu stigum Covid-veirusýkingar ađ komast yfir veikindin.
Ţannig ađ ţegar nćsti sjúklingur kom til hans ţá bauđ hann honum upp á opinberu leiđina eđa lyfjablönduma međ sinki, HCQ og azithromycin. Dr. Elens fylgdist međ sjúklingnum á klukkustundarfresti og var hćstánćgđur međ ađ sjá ađ sjúklingurinn svarađi međferđ vel og var búinn ađ ná sér ađ fullu innan ţriggja daga.
Lćknirinn endurtók sömu međferđ í ráđlögđum skömmtum á nćstu níu snemmstigs-sjúklingum. Allir náđu sér fljótt.
En ţegar hann tilkynnti hollenskum heilbrigđisyfirvöldum um vel heppnađa međferđ sína ţá var honum sagt ađ hćtta.
Í myndbandi mínu, Covid, og lyfiđ sem ekki ná nefna, (e. Covid, and the drug that dare not speak its name), svarar hinn, nú óhlýđni, dr. Elens um sjúklinga sína: Ţađ er betra ađ vera ólöglega á lífi en löglega dauđur.
Í samanburđarrannsókn sem gerđ var í júní á Covid-19-sjúklingum á saudi-arabísku covid-sjúkrahúsunum, var komist ađ ţeirri niđurstöđu ađ snemmtćk íhlutun međ međferđ byggđ á HCQ á lítiđ til međalveikum Covid-sjúklingum tengdist lćgri sjúkrahúsinnlögn, gjörgćsluinnlögn og/eđa dauđa.
Hvers vegna, ef ţađ er svona mikilvćgt ađ koma í veg fyrir ađ sjúkrahúsin okkar yfirfyllist, erum viđ ekki ađ tala opinberlega um tálmun á notkun á lyfi sem ekki má nefna ţegar svo margir lćknar og nafntogađir sérfrćđingar ábyrgjast áhrif ţess?
Ţetta er spurning sem á rétt á sér og krefst svara á svo viđsjárverđum tímum.
Barry Shaw, Senior Associate, Israel Institute for Strategic Studies
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Israels Covid mystery
HCQ was banned for Covid patients by the WHO on the basis of late stage trials. But doctors claim it worked in early stage usage. Opinion.
Tags: hydroxychloroquine Coronavirus Barry Shaw lockdown
Barry Shaw , 23/09/20 10:27
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Hydroxychloroquine
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Israel congratulated itself on coming through the Wuhan virus pandemic with flying colors. By the end of June, with only 300 plus deaths, we were king of the world. We were allowed to go about our normal daily lives. And then we were hit again. Big time. The death rate rocketed to over 1200.
Why? What did we do differently?
They said we were partying, getting married, gathering to pray, going to the beach. But we were doing all that before. So why the difference?
We were never given the answer. Instead, they decided to appoint a health czar, called him the Projector, gave him the keys to the castle, including budget, ministries, laboratories, hospitals, the health clinics, even the army, to flatten the second curve. The politicians promised to stay in the background.
First, The Projector turned the country into traffic light zones. Those with the highest infection rate were zoned red and required to be quarantined. Made sense, until it was discovered that the vast majority of the red zones, fully 80%, were either Arab or Orthodox towns, and that caused resistance - never mind the high morbidity in those sectors.
These places, The Projector said, must be placed in immediate lockdown. Then all hell let loose. Politics reared its inevitable head. Knesset meetings became riots. Factions which the Prime Minister depended for his support, and those that opposed him, began banging on his door. He could not win so he did what any politician would do. He threw The Projectors plan out the window and decreed a national lockdown of three weeks coinciding with the Jewish High Holidays encompassing Rosh Hashanah, Yom Kippur and Sukkot.
It began on the Friday afternoon before the traditional New Years eve to prevent mass family gatherings. But innovative defiant Israelis moved Rosh Hashanah festivities a day earlier and held their family gatherings on Thursday night instead of Friday. Brilliant.
Thousands of Jews rushed to test centers before heading to Ben Gurion Airport and flying from red Israel to green pastures rather than remain in lockdown for weeks. Some booked indefinite one way tickets.
Lots of TV chatter. Lots of ink splashed in pages of news media.
Silence about the biggest mystery of all.
Why are more people becoming seriously ill and dying than before?
Why do we now have over 1,300 deaths when, in the peak of the first curve, our mortality rate was just over 300? Why the over 400% difference?
It isnt due to greater testing because people got sick, even without testing, in the first wave.
Officials and pundits talk endlessly about testing, social distancing, lockdown, but little else. They are worried about hospitals and laboratories becoming overloaded with seriously infected patients.
But no one is talking about how to stop early stage sufferers from deteriorating into hospitalization and worse.
Are our local doctors and clinics being allowed to do everything possible to stop early stage patients from becoming hospitalized and dying?
The answer is no. They are not. In fact, these first-line physicians, who have intimate professional contact with their patients, are being prevented from what might lead to treating them successfully.
Were Israeli doctors prescribing something in the first wave that prevented massive mortality figures they are not prescribing now?
The answer is yes.
Local doctors and clinics are being prevented from prescribing a drug that worked before, but is banned now. The drug that dare not speak its name is hydroxychloroquine. Medical experts are forbidden on social media to mention its name. Some have been fired from their professional for daring to suggest that this drug, in combination with others, has saved countless lives.
Now that ban has been placed on Israeli local physicians, and more people are dying.
HCQ is a drug that received global official status use for a number of illnesses and diseases. It has a remarkable sixty-year safety record. But overnight, it became the devils potion.
Many hundreds of doctors and thousands of patients who swear to its efficacy when used on early stage sufferers in the right dose and in combination with other medications such as zinc and azithromycin, have been pilloried and banned from expressing their data and from sharing their experiences.
Professional physicians, in intimate contact with their private patients, are treated like heretics.
The authorities say HCQ failed late stage clinical trials. They claim it left a few patients with heart irregularities, a claim refuted by many experts, including Dr. Harvey Risch, Professor of Epidemiology at the Yale School of Medicine, who is highly critical about how badly the clinical trials were conducted.
After studying the clinical trials, he concluded, among the things, that they applied the drug incorrectly, even in dangerously high dosages, often not in combination with other drugs, to patients who had little chance of surviving with any drug.
Professor Risch is an ardent advocate for the application of HCQ in combination with other medications to early stage patients, as is Dr. Vladimir Zelenko, an Orthodox American physician, who came up with the Zelenko Protocol which details, for local doctors and clinics dealing with early stage Covid patients, how to prescribe and monitor patients starting in the first five days of contracting the coronavirus.
Professor Risch records and analyses the successes and failures of treating early stage Covid patients and is convinced in his judgment that HCQ, in combination with other drugs, is a safe and efficient method of preventing the debilitating effect of the coronavirus.
This early stage treatment was pioneered successfully in France by virologist Didier Raoult, who successfully treated hundreds of Covid patients, before he was pilloried as being a quack by Big Pharma.
Hydroxychloroquine was banned for Covid patients by the World Health Organization on the basis of these failed late stage trials. But the WHO recommends paracetamol, a drug that has not undergone clinical trials for Covid patients, and is known to have serious side effects. This is not only hypocritical, but highly suspect. And the WHO itself is suspect - as Donald Trump said in his UN speech.
Which begs the question. Why the difference?
This troubling discrepancy was brought home to me when I interviewed Dr. Rob Elens, a local physician with a busy clinic in the south of Holland.
Dr. Elens had an initial twenty-five patients who came down with Covid. They were prescribed with the Dutch health authorities recommendation, namely paracetamol and isolation.
The condition of all twenty-five worsened. All were hospitalized. Twelve of his patients died.
Dr. Elens, a compassionate doctor, was gravely concerned that something better could have saved his patients lives. So he did what any self-respecting doctor would do. He went in search of the science and came across the Zelenko Protocol, a tried and tested derivative of several doctors experiences in helping their early stage patients get over Covid.
So, when his next infected patient came along he offered him the choice of the official track or the drug combination of zinc, HCQ and azithromycin. Dr. Elens monitored the patient hourly and was pleased to discover that his patient responded well to the treatment and recovered completely within three days.
The doctor repeated the same medication in the required doses with his next nine early stage patients. All recovered quickly. But when he reported his successful cases to the Dutch medical authorities he received a warning to desist.
In my video Covid, and the drug that dare not speak its name, the now defiant Dr. Elens responded by saying of his patients, Better illegally alive, than legally dead.
A June comparative study, carried out into Covid-19 patients by the Saudi national fever clinics, concluded that early intervention of a HCQ-based therapy in mild to moderate COVID-19 patients was associated with lower odds of hospitalization, ICU admission and/or death.
And why, if it is so important to prevent our hospital system from being overwhelmed, are we not having a public conversation on the prevention of the use of a drug that dare not speak its name, but about which so many physicians and renowned specialists swear to its efficacy?
This is a legitimate questions that demands answers at such a critical time.
Barry Shaw, Senior Associate, Israel Institute for Strategic Studies.
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Egilsstađir, 02.10.2020 Jónas Gunnlaugsson
Bloggar | Breytt s.d. kl. 23:14 | Slóđ | Facebook | Athugasemdir (0)
Endursögn.
Núna er til ódýr, örugg. og skilvirk međferđ fyrir ţá sem eru međ greinileg einkenni veikinnar.
Međferđin er ađ nota HCQ (hydroxychloroquine), zinc og azithromycin.
Ef ţessi međferđ, er gerđ strax, kemur bati og oft ţarf ekki sjúkrahús vist.
Nćstum engin ţarf ađ deyja.
(severe ţýđi ég hér sem greinileg, vegna ţess, ađ best er ađ gefa HCQ strax til ađ stöva svokallađa vírusa, svo ađ ţeir nái ekki ađ veikja varnarkerfi líkamans og opna fyrir ađ sýklarnir komist í hin ýmsu líffćri.
HCQ virkar á vírusa en ţegar sýklarnir hafa komist í líffćrin, verđur ađ nota sýkla lyf.
HCQ, hydroxychloroquine er sagt virka sem bóluefni.
Ţessvegna er elítan, sögđ taka HCQ til ađ verjast veikinni.)
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Meanwhile, there is an affordable,
safe and efficient therapy available
for those who do show severe symptoms of disease
in the form of HCQ (hydroxychloroquine), zinc and azithromycin.
Rapidly applied this therapy leads to recovery and often prevents hospitalisation. Hardly anyone has to die now.
slóđ
Slóđ
24.9.2020 | 21:06
Lćrum viđ af Ríkistjórunum, Governorunum og lćđum lausninni til fólksins.
Kannt ţú betra ráđ?
slóđ
13.8.2020 | 16:00
Egilsstađir, 01.10.2020 Jónas Gunnlaugsson
Bloggar | Breytt s.d. kl. 13:33 | Slóđ | Facebook | Athugasemdir (0)
29.9.2020 | 21:34
https://davidicke.com/wp-content/uploads/2020/03/CORONA-SCAM-IMAGE.jpg
Er ađ athuga ţetta. Klikka á ţessa slóđ, sérđ + á bendli, og klikkar aftur, mynd stćrri.
https://external-preview.redd.it/jNaaN3my2JZDqQql727KL2e9Y2FvE0EfzsafSn2xmXc.jpg?auto=webp&s=abd9e4da3b3688f5c83c87aa830974bdca21d32dborder="0" width="427" height="632" />
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Egilsstađir, 29.09.2020 Jónas Gunnlaugsson
Bloggar | Breytt 1.10.2020 kl. 03:59 | Slóđ | Facebook | Athugasemdir (0)
Bloggar | Breytt s.d. kl. 21:33 | Slóđ | Facebook | Athugasemdir (0)
(Hvađ má setja á blog? Má segja frá lyfinu sem sagt er ađ byrji ađ lćkna eftir ţrjá klukkutíma? Ţađ er sagt ađ ţađ virki eins og bólusetning ef ţú ert ekki veikur. Er snjallt ađ bjóđa ţađ farţegum sem koma til landsins, annars sóttkví? jg)
"We know that hydroxychloroquine helps Zinc enter the cell," wrote Dr. Zelenko.
"We know that Zinc slows viral replication within the cell.
Regarding the use of azithromycin, I postulate it prevents secondary bacterial infections.
These three drugs are well known and usually well-tolerated; hence the risk to the patient is low."
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'Zelenko Protocol' discoverer 'still in the fight'.
"Zelenko Protocol" discoverer Dr. Vladimir Zelenko today announced he has ended a seven-day Twitter suspension he was subjected to for having reported on the efficacy of his treatment with his patients.
'Zelenko Protocol' discoverer 'still in the fight'.
Zelenko reports he has been saving his patients' lives with his Zelenko Protocol since March.
Dr. Zelenko wrote: "Twitter suspended me for 7 days for saying that xxxx works for Covid," with "xxxx" understood to refer to hydroxychloroquine.
"Thank G-d Im surviving and still in the fight. Ty so much for your positive blessings and support. It really helps; keep up [morale]."
Dr. Zelenko's outpatient treatment regimen consists of
hydroxychloroquine, 200mg twice a day for five days;
azithromycin, 500mg once a day for five days;
and zinc sulfate, 220mg once a day for five days.
"We know that hydroxychloroquine helps Zinc enter the cell," wrote Dr. Zelenko.
"We know that Zinc slows viral replication within the cell.
Regarding the use of azithromycin, I postulate it prevents secondary bacterial infections.
These three drugs are well known and usually well-tolerated; hence the risk to the patient is low."
000
"Zelenko Protocol" discoverer Dr. Vladimir Zelenko today announced he has ended a seven-day Twitter suspension he was subjected to for having reported on the efficacy of his treatment with his patients.
As COVID-19 treatment by hydroxychloroquine, azithromycin, and zinc sulfate continues to be suppressed by mainstream media and social media networks, Zelenko reports he has been saving his patients' lives with his Zelenko Protocol since March.
Dr. Zelenko wrote: "Twitter suspended me for 7 days for saying that xxxx works for Covid," with "xxxx" understood to refer to hydroxychloroquine. "Thank G-d Im surviving and still in the fight. Ty so much for your positive blessings and support. It really helps; keep up [morale]."
Dr. Zelenko's outpatient treatment regimen consists of hydroxychloroquine, 200mg twice a day for five days; azithromycin, 500mg once a day for five days; and zinc sulfate, 220mg once a day for five days. "We know that hydroxychloroquine helps Zinc enter the cell," wrote Dr. Zelenko. "We know that Zinc slows viral replication within the cell. Regarding the use of azithromycin, I postulate it prevents secondary bacterial infections. These three drugs are well known and usually well-tolerated; hence the risk to the patient is low."
Egilsstađir, 27.09.2020 Jónas Gunnlaugsson
Bloggar | Breytt 28.9.2020 kl. 00:13 | Slóđ | Facebook | Athugasemdir (0)
Sannleikurinn er sá, ađ framleiđslufyrirtćki ţjóđanna geta ekki veriđ ađ hanga međ vandamála pakka, sem ađeins baka vandrćđi.
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Blog: Bjarni Jónsson
Nú sjást merki ţess, ađ olíurisar á borđ viđ BP og Shell hafi áttađ sig á vatnaskilunum og séu ađ selja óhagstćđari olíulindir sínar og lćkka verđmćti óunnins olíuforđa síns í bókhaldi.
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Ţetta er umhugsunarverđ setning.
Er hćgt ađ selja tapiđ?
Já, ég myndi halda ţađ.
Selja einhverjum sem vantar tap.
Ég sel auđvitađ sjálfum mér tapiđ.
Ţá leiđ ţarf ađ skođa betur, til dćmis til ađ lćkka skatta tilsvarandi, auđvitađ engin vandi.
Önnur leiđ?
Stórfyrirtćkin eiga auđvitađ marga banka.
Ég er auđvitađ fyrir löng búinn ađ stofna mörg fyrirtćki, til ađ grípa til ţegar svona stendur á.
Ég kaupi fyrirtćkin tímanlega yfir í annađ fyrirtćki sem ég á, á matinu frá í gćr, tek lán í hinum ýmsu bönkum, fyrir öllum kaupunum.
Auđvelt vćri ađ láta hćkka matiđ um 20 %, ef ađeins má lána 80% af matsverđi.
Sannleikurinn er sá, ađ framleiđslufyrirtćki ţjóđanna geta ekki veriđ ađ hanga međ vandamála pakka, sem ađeins baka vandrćđi.
Ţađ sem er úrelt, ţađ verđur ađ víkja, en viđ finnum nýjar lausnir til ađ nýta eignirnar.
Bankinn lćtur lániđ fyrir kaupunum á úreltu eignunum, koma viđ á reikningi í bankanum, og má ţá skrifa 10 sinnum ţá upphćđ, verđur 10 sinnum ríkari, viđ ađ lána fyrir kaupunum á gömlu úreltu, órekstrarhćfu eignunum.
Svona losnum viđ okkur viđ vandamálin.
Vandamálin eiga ekki ađ vera haft á starfsgetu ţjóđarinnar.
Svona á hugsunin ađ vera, ţegar viđ leysum vandamál Jóns og Gunnu.
Heimska okkar, hefur veriđ og er mikil.
Egilsstađir, 12.09.2020 Jónas Gunnlaugsson
Bloggar | Breytt s.d. kl. 21:18 | Slóđ | Facebook | Athugasemdir (0)
Lćrum viđ af Ríkistjórunum, Governorunum og lćđum lausninni til fólksins.
Kannt ţú betra ráđ?
Endursagt
Nevada er sjöunda ríkiđ í Bandaríkjunum, sem dregur til baka svo ađ lítiđ beri á, banniđ viđ ađ ávísa lyfinu HCQ, hydroxychloroquine vegna Covid-19.
Lćknar í Nevada geta nú aftur ávísađ HCQ eins og ţeir telja nauđsynlegt.
US - Ríkisstjórar sögđu ósatt, og takmörkuđu ađgang ađ lyfi sem gćti hafa bjargađ mannslífum.
Ţeir ćttu ađ vera gerđir ábyrgir fyrir gerđina.
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Nevada is now the 7th state to quietly reverse their decision to block HCQ prescriptions for COVID-19. Physicians in Nevada can now once again prescribe HCQ as they deem necessary. Governors lied & restricted medicine that could have saved lives. They should be held accountable.
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Ţetta er sýnishorn frá Twitter
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Dr. Simone Gold
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Nevada is now the 7th state to quietly reverse their decision to block HCQ prescriptions for COVID-19. Physicians in Nevada can now once again prescribe HCQ as they deem necessary. Governors lied & restricted medicine that could have saved lives. They should be held accountable.
Egilsstađir, 24.09.2020 Jónas Gunnlaugsson
Bloggar | Breytt s.d. kl. 21:25 | Slóđ | Facebook | Athugasemdir (0)
Smá tölvuţýđing og endursögn.
Covid ráđgáta Ísraels
HCQ var bannađ fyrir Covid sjúklinga af WHO á grundvelli rannsókna á seina stigi. En lćknar halda ţví fram ađ ţađ hafi virkađ á byrjunarstigi.
https://jonasg-egi.blog.is/blog/jonasg-egi/entry/2254978/
Ţögn um stćrstu ráđgátuna.
Af hverju verđa fleiri alvarlega veikir og deyja en áđur?
Hvers vegna eru nú yfir 1.300 dauđsföll ţegar hápunktur fyrstu ferilsins var dánartíđni okkar rúmlega 300?
Af hverju er yfir 400% munurinn?
Embćttismenn og sérfrćđingar tala endalaust um próf, félagslega fjarlćgđ, lokun, en lítiđ annađ. Ţeir hafa áhyggjur af ţví ađ sjúkrahús og rannsóknarstofur verđi ofhlađnar af alvarlega veikum sjúklingum. En enginn er ađ tala um hvernig eigi ađ koma í veg fyrir ađ ţjást á byrjunarstigi frá ţví ađ versna sem kallar á sjúkrahúsvist og ţađ sem verra er (dauđa?).
Er stađbundnum lćknum (hérađslćknum) og heilsugćslustöđvum heimilt ađ gera allt sem unnt er til ađ koma í veg fyrir ađ sjúklingar á byrjunarstigi leggist á sjúkrahús og deyi?
Svariđ er nei.
Reyndar er komiđ í veg fyrir ađ ţessir fyrstu lćknar, sem hafa náiđ faglegt samband viđ sjúklinga sína, geti hafiđ međferđ fyrir ţá.
Voru ísraelskir lćknar ađ ávísa einhverju í fyrstu bylgjunni sem kom í veg fyrir stórfelldar dánartölur sem ţeir eru ekki ađ ávísa núna?
Svariđ er já.
Ţađ er veriđ ađ koma í veg fyrir ađ lćknar og heilsugćslustöđvar á stađnum ávísi lyfi sem virkađi áđur, en er bannađ núna.
Sumir hafa veriđ reknir frá fagađila sínum fyrir ađ ţora ađ gefa í skyn ađ ţetta lyf, ásamt öđrum, hafi bjargađ óteljandi mannslífum.
Nú hefur ţađ bann veriđ sett á ísraelska lćkna á stađnum og fleiri deyja.
HCQ er lyf sem fékk alţjóđlegtsamţykki og notast fyrir fjölda sjúkdóma. Lyfiđ hefur reynst vel í 60 ár.
En á einni nóttu varđ ţađ djöfulsins drykkur.
Mörg hundruđ lćknr og ţúsundir sjúklinga sverja ađ lyfiđ virki vel ef ţađ er notađ strax og mađurinn veikist, í réttum skammti og í samsettri međferđ međ öđrum lyfjum eins og sinki og azitrómýsíni.
Ţá hafa ţeir veriđ settir í straff og bannađ ađ sýna gögn sín og deila reynslu sinni.
Faglćknar, í nánu sambandi viđ einkasjúklinga sína, eru međhöndlađir eins og sakamenn, (villutrúarmenn).
Jónas Gunnlaugsson, 25.9.2020 kl. 23:15
ţá spyrum viđ, er baráttan á milli Efnistrúarinnar og Sköpunar trúarinnar?
Hér athugist, mađurinn skapađi robot, Guđ skapađi manninn.
Ath. string theory , multi verse jg
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HCQ was banned for Covid patients by the WHO on the basis of late stage trials. But doctors claim it worked in early stage usage. Opinion.
Why? What did we do differently?
They said we were partying, getting married, gathering to pray, going to the beach. But we were doing all that before. So why the difference?
We were never given the answer. Instead, they decided to appoint a health czar, called him the Projector, gave him the keys to the castle, including budget, ministries, laboratories, hospitals, the health clinics, even the army, to flatten the second curve. The politicians promised to stay in the background.
First, The Projector turned the country into traffic light zones. Those with the highest infection rate were zoned red and required to be quarantined.
Made sense, until it was discovered that the vast majority of the red zones, fully 80%, were either Arab or Orthodox towns, and that caused resistance - never mind the high morbidity in those sectors.
These places, The Projector said, must be placed in immediate lockdown.
Then all hell let loose. Politics reared its inevitable head. Knesset meetings became riots. Factions which the Prime Minister depended for his support, and those that opposed him, began banging on his door. He could not win so he did what any politician would do. He threw The Projectors plan out the window and decreed a national lockdown of three weeks coinciding with the Jewish High Holidays encompassing Rosh Hashanah, Yom Kippur and Sukkot.
It began on the Friday afternoon before the traditional New Years eve to prevent mass family gatherings. But innovative defiant Israelis moved Rosh Hashanah festivities a day earlier and held their family gatherings on Thursday night instead of Friday. Brilliant.
Thousands of Jews rushed to test centers before heading to Ben Gurion Airport and flying from red Israel to green pastures rather than remain in lockdown for weeks. Some booked indefinite one way tickets.
Lots of TV chatter. Lots of ink splashed in pages of news media.
Silence about the biggest mystery of all.
Why are more people becoming seriously ill and dying than before?
Why do we now have over 1,300 deaths when, in the peak of the first curve, our mortality rate was just over 300?
Why the over 400% difference?
It isnt due to greater testing because people got sick, even without testing, in the first wave.
Officials and pundits talk endlessly about testing, social distancing, lockdown, but little else. They are worried about hospitals and laboratories becoming overloaded with seriously infected patients.
But no one is talking about how to stop early stage sufferers from deteriorating into hospitalization and worse.
Are our local doctors and clinics being allowed to do everything possible to stop early stage patients from becoming hospitalized and dying?
The answer is no.
They are not.
In fact, these first-line physicians, who have intimate professional contact with their patients, are being prevented from what might lead to treating them successfully.
Were Israeli doctors prescribing something in the first wave that prevented massive mortality figures they are not prescribing now?
The answer is yes.
Local doctors and clinics are being prevented from prescribing a drug that worked before, but is banned now.
The drug that dare not speak its name is hydroxychloroquine. Medical experts are forbidden on social media to mention its name.
Some have been fired from their professional for daring to suggest that this drug, in combination with others, has saved countless lives.
Now that ban has been placed on Israeli local physicians, and more people are dying.
HCQ is a drug that received global official status use for a number of illnesses and diseases.
It has a remarkable sixty-year safety record.
But overnight, it became the devils potion.
Many hundreds of doctors and thousands of patients who swear to its efficacy when used on early stage sufferers in the right dose and in combination with other medications such as zinc and azithromycin, have been pilloried and banned from expressing their data and from sharing their experiences.
Professional physicians, in intimate contact with their private patients, are treated like heretics.
The authorities say HCQ failed late stage clinical trials.
They claim it left a few patients with heart irregularities, a claim refuted by many experts, including Dr. Harvey Risch, Professor of Epidemiology at the Yale School of Medicine, who is highly critical about how badly the clinical trials were conducted.
After studying the clinical trials, he concluded, among the things, that they applied the drug incorrectly, even in dangerously high dosages, often not in combination with other drugs, to patients who had little chance of surviving with any drug.
Professor Risch is an ardent advocate for the application of HCQ in combination with other medications to early stage patients, as is Dr. Vladimir Zelenko, an Orthodox American physician, who came up with the Zelenko Protocol which details, for local doctors and clinics dealing with early stage Covid patients, how to prescribe and monitor patients starting in the first five days of contracting the coronavirus.
Professor Risch records and analyses the successes and failures of treating early stage Covid patients and is convinced in his judgment that HCQ, in combination with other drugs, is a safe and efficient method of preventing the debilitating effect of the coronavirus.
This early stage treatment was pioneered successfully in France by virologist Didier Raoult, who successfully treated hundreds of Covid patients, before he was pilloried as being a quack by Big Pharma.
Hydroxychloroquine was banned for Covid patients by the World Health Organization on the basis of these failed late stage trials.
But the WHO recommends paracetamol, a drug that has not undergone clinical trials for Covid patients, and is known to have serious side effects. This is not only hypocritical, but highly suspect.
And the WHO itself is suspect - as Donald Trump said in his UN speech.
Which begs the question. Why the difference?
This troubling discrepancy was brought home to me when I interviewed Dr. Rob Elens, a local physician with a busy clinic in the south of Holland.
Dr. Elens had an initial twenty-five patients who came down with Covid. They were prescribed with the Dutch health authorities recommendation, namely paracetamol and isolation.
The condition of all twenty-five worsened. All were hospitalized. Twelve of his patients died.
Dr. Elens, a compassionate doctor, was gravely concerned that something better could have saved his patients lives. So he did what any self-respecting doctor would do.
He went in search of the science and came across the Zelenko Protocol, a tried and tested derivative of several doctors experiences in helping their early stage patients get over Covid.
So, when his next infected patient came along he offered him the choice of the official track or the drug combination of zinc, HCQ and azithromycin.
Dr. Elens monitored the patient hourly and was pleased to discover that his patient responded well to the treatment and recovered completely within three days.
The doctor repeated the same medication in the required doses with his next nine early stage patients. All recovered quickly. But when he reported his successful cases to the Dutch medical authorities he received a warning to desist.
In my video Covid, and the drug that dare not speak its name, the now defiant Dr. Elens responded by saying of his patients,
Better illegally alive, than legally dead.
A June comparative study, carried out into Covid-19 patients by the Saudi national fever clinics, concluded that early intervention of a HCQ-based therapy in mild to moderate COVID-19 patients was associated with lower odds of hospitalization, ICU admission and/or death.
And why, if it is so important to prevent our hospital system from being overwhelmed, are we not having a public conversation on the prevention of the use of a drug that dare not speak its name, but about which so many physicians and renowned specialists swear to its efficacy?
This is a legitimate questions that demands answers at such a critical time.
Barry Shaw, Senior Associate, Israel Institute for Strategic Studies.
Bloggar | Breytt 26.9.2020 kl. 00:49 | Slóđ | Facebook | Athugasemdir (0)
Hver ber ábyrgđ á, spurning, ţúsunda milljarđa tapi fólks og fyrirtćkja?
Hver ber ábyrgđ á dauđa, fjölda manna?
Hefnnndin, (erum viđ sjálf međ stíflađa hugun, innsći) (bera út börnnnin), nefnnndin, dillar sér.
Fólkiđ klappar fyrir hefnnndinni, nefnnndinni, heimskunni.
Heimskan heldur ađ hún geti faliđ drápin á milljón manns.
Sagt er ađ 73 % fćrri dauđsföll séu í löndunum sem nota HCQ.
Slóđ
Jónas Gunnlaugsson | 6. september 2020
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Hver bannar lćknunum ađ nota lyfiđ Hýdroxýklórókín
Ríkisstjórnin?
Ţađ voru aldrei deilur um hýdroxýklórókín, alveg fram til 20. mars 2020.
Trump hćldi lyfinu, eftir ađ hann heyrđi frá rannsóknum í Kína og Frakklandi.
Ţá sáu efnistrúarmenn ađ pestin myndi ekki nćgja til ađ fella Trump, og hófu ófrćingar herferđ gegn lyfinu HCQ.
Ţessir efnistrúarmenn ţurfa ađ lesa sér til í efna og eđlisfrćđi.
Látum skólana kenna nýjustu vísindi strax í dag.
Reyndu ađ skilja hvernig Guđ bjó manninn til og hliđstćđuna, hvernig mađurinn bjó róbott til.
Ţarna er sköpunarandinn, ađ verki.
Fylla kirkjurnar og taka ţátt í bćnunum og opna fyrir innsćiđ, hugunina, ţá opnast fyrir leiđbeininguna frá miđjunni, kjarnanum, Guđlegu ástúđinni, Heilögum anda og Guđi.
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Ţađ ţurfti ađ setja herforingja sem heilbrigđis ráđherra í Brasilíu til ađ heilbrigđisráđuneytiđ hvetti lćkna til ađ nota HCQ , hydroxychloroquine.
https://www.ruv.is/frett/2020/09/17/hershofdingi-heilbrigdisradherra-brasiliu
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Endursögn.
Ég vil alltaf minna fólk á, ţetta er FDA-samţykkt lyf í 65 ár.
Ţađ er ekki verndađ međ einkaleyfi.
Ţađ er ódýrt.
Ţađ er víđa fáanlegt. (fćst í Lyfju, (og einnig lyfiđ Budesonide sem er andađ ađ sér.))
Viđ gefum ţunguđum konum ţađ. (HCQ)
Viđ gefum konum sem hafa barn á brjósti ţađ.(HCQ)
Viđ gefum öldruđum sjúklingum ţađ.(HCQ)
Viđ gefum sjúklingum sem eru í ónćmiskerfi. (skert?)(HCQ)
Flestir ţessara sjúklinga eru á ţví í áratugi! (HCQ)
Ţađ voru aldrei deilur um hýdroxýklórókín, alveg fram til 20. mars 2020.
Svo ég myndi skođa rannsóknirnar fyrir ţann tíma.
Fyrstu rannsóknirnar, frá Kína og frá Frakklandi, áđur en Trump sagđi ađ hann vćri hrifinn af lyfinu, voru óumdeildar, hćldu lyfinu.
Ţađ virtist lofa góđu.
Ég veit ekki hvađ endanleg gögn munu sýna, ég finn hins vegar ađ gögnin eftir ađ Trump hélt ađ ţau vćru mögulega gagnleg eru grunsamleg ...
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JAMA rannsóknin var í Brasilíu. Ţeir notuđu klórókín.
Banvćnn skammtur af klórókíni hefur veriđ vel stađfestur í meira en 30 ár, áriđ 1988, New England Journal Medicine.
Aftur, eitt af helstu frćđiritunum og allir sćtta sig viđ ađ banvćnn skammtur af klórókíni er 5 grömm.
Jćja, Jama rannsóknin var međ tvo hópa.
Í háskammta klórókín hópnum gáfu ţeir ţeim 1,2 grömm á dag sem ţýđir ađ á fjórđa degi voru ţeir međ nćstum 5 grömm ...
Hýdroxýklórókín og klórókín sitja mjög lengi í líkama ţínum, ađ minnsta kosti mánuđ, kannski 2 mánuđi; einhvers stađar á milli 30 og 60 daga er helmingunartími ţess.
Svo ađ gefa einhverjum 4,8 grömm á fjórum dögum er mjög stór skammtur; fólk kallađi ţađ hugsanlega banvćnan skammt.
Rannsóknin stóđ yfir í 10 daga, sem ţýddi ađ fólkiđ í ţeim hópi fékk 12 grömm. Aftur, New England Journal of Medicine áriđ 1988 stofnađi 5 grömm sem banvćnan skammt ... Hafđu í huga, ţetta eru aldrađir, alvarlega veikir sjúklingar sem eru intubated eđa eru í miklum öndunarerfiđleikum ...
Ţađ eru ekki bara vangaveltur mínar eđa vísindagögnin sem segja ađ ţađ sé mjög hár, eiturskammtur. Svo margir sjúklingar létust í háskammta hópnum ađ ţeir stöđvuđu rannsóknina snemma. Ţeir hćttu í stóra skammtahópnum vegna ţess ađ svo margir sjúklingar dóu. Ţađ er ákaflega dramatískt fyrir vísindalega rannsókn.
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I always want to remind people, this is an FDA-approved drug for 65 years. Its generic. Its cheap. Its widely available. We give it to pregnant women. We give it to breastfeeding women. We give it to elderly patients. We give it to patients who are immune-compromised.
Most of those patients are on it for decades! There was never controversy about hydroxychloroquine, right up until March 20th, 2020. So, I would look at the studies before then. The early studies, before Trump said he kind of liked the drug were uncontroversial, from China and from France. It looked promising.
I dont know what the final data will show, however, I do find that the data after Trump thought it was possibly helpful is suspect
The JAMA study was in Brazil. They used chloroquine.
The lethal dose of chloroquine has been well-established for more than 30 years in 1988 a New England Journal Medicine.
Again, one of the world premier journals established and everyone accepts that the lethal dose of chloroquine is 5 grams.
Well, the Jama study had two groups.
In the high-dose chloroquine group, they gave them 1.2 grams a day which means by the fourth day, they had almost 5 grams
Hydroxychloroquine and chloroquine sit in your body for very long time, at least a month, perhaps 2 months; somewhere between 30 and 60 days is its half-life.
So, to give someone 4.8 grams in four days is a very large dose; people would often possibly call that a lethal dose.
The study went on for 10 days, which meant that the people in that group got 12 grams. Again, New England Journal of Medicine in 1988 established 5 grams as a lethal dose Mind you, these are elderly, critically-ill patients that are intubated or in severe respiratory distress
Its not just my speculation or the science data that says its a very high, toxic dose. So many patients died in the high-dose group that they halted that study early. They quit the high dose group because so many patients died. Thats extremely dramatic for a scientific study.
https://jonasg-egi.blog.is/blog/jonasg-egi/entry/2254276/
Egilsstađir, 22.09.2020 Jónas Gunnlaugsson
Bloggar | Breytt 27.9.2020 kl. 09:45 | Slóđ | Facebook | Athugasemdir (0)
Hver ćtlar ađ bjarga Íslandi, atvinnuvegunum og fólkinu?
Ein pilla viđ komuna til Íslands, ef veikur ţá finnst bati eftir ţrjár klukkustundir.
Ef ekki veikur ţá virkar pillan sem bólusetning.
Ţarna virđist sem herinn í löndunum, sé ađ berjast viđ stjórnkerfiđ, og vilji ađ fólkiđ fái ađ nota, HCQ, Hydroxychloroquine,
slóđ
12.9.2020 | 22:02
slóđ
21.8.2020 | 13:09
Endursagt frá RÚV. Hershöfđingi sem hefur enga reynslu af heilbrigđismálum var skipađur heilbrigđisráđherra Brasilíu í gćr.- ellefti herforinginn í tuttugu og ţriggja manna ríkistjórn Brasilíu.
Hann og ţá herinn, hugsum viđ, vill ađ fólkiđ fái ađ nota HCQ, hydroxychloroquine, sem ţúsundir lćkna nota í óţökk stjórnsýslunar, og ţá stóru lyfjarisanna.
Endursagt, frá RÚV. - Ţar á međal má nefna ađ ţeir hvetja báđir lćkna til ađ ávísa gigtarlyfinu hydroxychloroquine án ţess ađ fyrir liggi óyggjandi sönnun á virkni ţess gegn Covid-19.
Ég er međ nokkur blog, ţar sem lćknar útskýra hvađ lyfiđ virki vel á vírusinn.
slóđ
12.9.2020 | 22:02
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RÚV fćrslan.
Hershöfđingi heilbrigđisráđherra Brasilíu
17.09.2020 - 02:28
https://www.ruv.is/frett/2020/09/17/hershofdingi-heilbrigdisradherra-brasiliu
Erlent · Hydroxychloroquine · Brasilía · COVID-19 · heilbrigđismál · Jair Bolsonaro · Kórónuveiran · Kórónuveirufaraldurinn · Stjórnmál · Suđur-Ameríka · útgöngubann
Mynd: EPA-EFE - EFE
Hershöfđingi sem hefur enga reynslu af heilbrigđismálum var skipađur heilbrigđisráđherra Brasilíu í gćr. Hann er ţriđji ráđherra heilbrigđismála í landinu frá ţví kórónuveirufaraldurinn skall á.
Jair Bolsonaro forseti tilnefndi hershöfđingjann Eduardo Pazuello tímabundiđ í maí síđastliđnum. Hann er ellefti hermađurinn í 23 manna ráđuneyti Bolsonaros.
Hann, ólíkt forverum sínum, er sammála forsetanum um hvernig bregđast eigi viđ útbreiđslu faraldursins. Ţar á međal má nefna ađ ţeir hvetja báđir lćkna til ađ ávísa gigtarlyfinu hydroxychloroquine án ţess ađ fyrir liggi óyggjandi sönnun á virkni ţess gegn Covid-19.
Viđ innsetningarathöfnina sagđi forsetinn rannsóknir sýna ađ koma hefđi mátt í veg fyrir 30% dauđsfalla af völdum Covid-19 hefđi lyfiđ veriđ gefiđ í tíma. Hann tiltók ţó ekki hvađa rannsóknir hann ćtti viđ.
Ţeir eru sömuleiđis mjög gagnrýnir á landstjóra ţeirra sambandsríkja Brasilíu sem beitt hafa útgöngubanni til ađ hafa hemil á útbreiđslu veirunnar. Opinberar tölur sýna ađ nú hafa 134 ţúsund látist af völdum Covid-19 í Brasilíu sem telur 212 milljónir íbúa.
Bloggar | Breytt 19.9.2020 kl. 09:34 | Slóđ | Facebook | Athugasemdir (0)
Sett á blog: Magnús Sigurđsson
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Mér heyrist ţiđ vera farnir ađ sjá samhengiđ.
slóđ
12.9.2020 | 22:02
Ţađ er búiđ ađ gera hershöfđingja ađ heilbrigđisráđherra í Brasilíu, og ţá eru 11 ráđherrar herforingjar en 23 eru ráđherrar í ríkisstjórninni.
Ríkistjórnirnar reyna ađ koma lyfunum sem virka til fólksins, en lyfjaiđnađurinn vill nota tćkifćriđ til ađ fella Trump međ ţví ađ koma öllu í ólag.
Hluti hersins vill taka völdin af Djúpríkinu og fékk Trump í liđ međ sér.
Ţađ virđist sem Brasilía sé á sömu leiđ.
Ţađ var í Brasilíu, sem svikarannsóknin á chloroquine var gerđ og var fólkinu gefin allt ađ tvöfalldur dauđaskammtur og ţađ fór ađ deyja.
Sagt er ađ herinn í Bandaríkjunum setji brotlega, svo sem ţá sem drápu Kennedy fyrir herdómstóla.
Venjulegir dómstólar virka ekki.
Ef herir landana taka völdin hvađa afl verđur látiđ hreinsa til á Ísland?
Ţetta sést betur í slóđinni hér fyrir ofan.
Egilsstađir, 17.09.2020 Jónas Gunnlaugsson
Bloggar | Breytt s.d. kl. 13:55 | Slóđ | Facebook | Athugasemdir (0)
DOCUMENTING EARTH CHANGES DURING THE NEXT GSM AND POLE SHIFT
https://electroverse.net/noaa-confirms-a-full-blown-grand-solar-minimum/
Hér eru breytingar yfir nćstu GSM og pólskipti.
klikka, mynd stćrri
The COLD TIMES are returning, the mid-latitudes are REFREEZING,
in line with historically low solar activity, cloud-nucleating Cosmic Rays,
and a meridional jet stream flow.
Both NOAA and NASA appear to agree, if you read between the lines, with NOAA saying
were entering a full-blown Grand Solar Minimum in the late-2020s,
and NASA seeing this upcoming solar cycle (25) as the weakest of the past 200 years,
with the agency correlating previous solar shutdowns to prolonged periods of global cooling Slóđ here.
Egilsstađir, 15.09.2020 Jónas Gunnlaugsson
Bloggar | Breytt 16.9.2020 kl. 19:08 | Slóđ | Facebook | Athugasemdir (0)
Svona á hugsunin ađ vera, ţegar viđ leysum vandamál Jóns og Gunnu.
Heimska okkar, hefur veriđ og er mikil.
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Blog: Bjarni Jónsson
Nú sjást merki ţess, ađ olíurisar á borđ viđ BP og Shell hafi áttađ sig á vatnaskilunum og séu ađ selja óhagstćđari olíulindir sínar og lćkka verđmćti óunnins olíuforđa síns í bókhaldi.
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Ţetta er umhugsunarverđ setning.
Er hćgt ađ selja tapiđ?
Já, ég myndi halda ţađ.
Selja einhverjum sem vantar tap.
Ég sel auđvitađ sjálfum mér tapiđ.
Ţá leiđ ţarf ađ skođa betur, til dćmis til ađ lćkka skatta tilsvarandi, auđvitađ engin vandi.
Önnur leiđ?
Stórfyrirtćkin eiga auđvitađ marga banka.
Ég er auđvitađ fyrir löng búinn ađ stofna mörg fyrirtćki, til ađ grípa til ţegar svona stendur á.
Ég kaupi fyrirtćkin tímanlega yfir í annađ fyrirtćki sem ég á, á matinu frá í gćr, tek lán í hinum ýmsu bönkum, fyrir öllum kaupunum.
Auđvelt vćri ađ láta hćkka matiđ um 20 %, ef ađeins má lána 80% af matsverđi.
Sannleikurinn er sá, ađ framleiđslufyrirtćki ţjóđanna geta ekki veriđ ađ hanga međ vandamála pakka, sem ađeins baka vandrćđi.
Ţađ sem er úrelt, ţađ verđur ađ víkja, en viđ finnum nýjar lausnir til ađ nýta eignirnar.
Bankinn lćtur lániđ fyrir kaupunum á úreltu eignunum, koma viđ á reikningi í bankanum, og má ţá skrifa 10 sinnum ţá upphćđ, verđur 10 sinnum ríkari, viđ ađ lána fyrir kaupunum á gömlu úreltu, órekstrarhćfu eignunum.
Svona losnum viđ okkur viđ vandamálin.
Vandamálin eiga ekki ađ vera haft á starfsgetu ţjóđarinnar.
Svona á hugsunin ađ vera, ţegar viđ leysum vandamál Jóns og Gunnu.
Heimska okkar, hefur veriđ og er mikil.
Egilsstađir, 12.09.2020 Jónas Gunnlaugsson
Bloggar | Breytt s.d. kl. 08:37 | Slóđ | Facebook | Athugasemdir (0)
Sett á blog: Bjarni Jónsson
Ţađ er fullt af greinum á bloginu mínu. https://jonasg-egi.blog.is
Ekki gleyma Forseta Bandaríkjanna, međ bestu fáanlega sérfrćđinga, reynir ađ koma lyfjum til fólksins, sem oft virka 100%, og oft ţarf ekki ađ fara á sjúkrahús.
Mér er orđa vant, ég er hugsi. Hér bollaleggiđ ţiđ um COVID-19, en ţiđ nefniđ ekki ađ til eru lyf sem virđast minnka dánartíđni um 73 % í heilu löndunum.
Slóđ
6.9.2020 | 10:25
Ekki getur ţetta veriđ rétt? Ţetta er varúđar setning.
slóđ
14.8.2020 | 15:53
Slóđ
3.9.2020 | 11:04
Getur ţađ veriđ ađ ţađ sé bannađ ađ leysa vandamáliđ?
slóđ
5.9.2020 | 22:38
Skilabođ mín til vísindamannanna eru: Ég skil ađ ţađ er mikill ţrýstingur ţarna úti, kannski frá stórum lyfjafyrirtćkjum eđa tímaritum um ađ komast ađ ákveđinni niđurstöđu. Ég biđ vísindamenn ađ standa međ sannleikanum. Ef bandarískir vísindamenn standa ekki í lappirnar og segja ekki satt undanbragđa laust, ţá gerir ţađ enginn - vissulega ekki fjölmiđlar, örugglega ekki stjórnmálamenn. ***
"Ţetta var svo átakanlegt fyrir mig," segir Dr. Gold, sem er einnig lögfrćđingur. "Ţađ hafđi aldrei gerst, ađ ríkisstjórnin segđi lćkni hvort ţeir hefđu rétt eđa ekki rétt til ađ ávísa FDA- samţykktri lyfja međferđ.
Og ég hugsađi međ mér: "Ef lćknar láta ţetta yfir sig ganga, ţá töpum viđ allir." **
The JAMA study was in Brazil. They used chloroquine.
The lethal dose of chloroquine has been well-established for more than 30 years in 1988 a New England Journal Medicine.
Again, one of the world premier journals established and everyone accepts that the lethal dose of chloroquine is 5 grams.
Well, the Jama study had two groups.
In the high-dose chloroquine group, they gave them 1.2 grams a day which means by the fourth day, they had almost 5 grams
Hydroxychloroquine and chloroquine sit in your body for very long time, at least a month, perhaps 2 months; somewhere between 30 and 60 days is its half-life.
So, to give someone 4.8 grams in four days is a very large dose; people would often possibly call that a lethal dose.
The study went on for 10 days, which meant that the people in that group got 12 grams. Again, New England Journal of Medicine in 1988 established 5 grams as a lethal dose Mind you, these are elderly, critically-ill patients that are intubated or in severe respiratory distress
Its not just my speculation or the science data that says its a very high, toxic dose. So many patients died in the high-dose group that they halted that study early. They quit the high dose group because so many patients died. Thats extremely dramatic for a scientific study.
Its very unusual for a study to have given such a large dose of a medication, because all the scientific studies that involve human subjects have to be overseen by an ethics board. The scientists that did this study and presented the paper to JAMA are saying that they went through an ethics board however, thats in doubt.
The Brazilian Ministry of Justice is actually investigating. Theres no proof that there actually was an ethics board
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Egilsstađir, 12.09.2020 Jónas Gunnlaugsson
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It sure looks like it
From Europe By Karma Singh
Habeus Corpus Most lawyers will know of this most important legal principle but I wonder how many outside of that profession have heard of it.
I only know about it because I had to study law as part of my degree in international trade way back in the early 1970s.
We had the great good fortune to have a mad Welshman as our law lecturer who loved nothing more than relating anecdotes from judicial history. His enthusiasm almost led to my changing faculty to study law; then he retired and his replacement was such a grey character that he repelled me totally.
Habeas Corpus or, as our Welshman explained it, show us the body stems from 12th century England and was created to prevent wild accusations with no factual basis. So, for example, if someone was accused of murder, he/she could apply for Habeas Corpus, i.e. first prove that a murder has taken place before you can try me for it.
health care and healing I wonder how many of my colleagues have heard of Habeas Corpus and have realised how relevant it is to our present situation?
We are all being punished for potentially harbouring a deadly virus. Further, we are being punished without trial or even a concrete accusation of wrong doing. Surely Habeas Corpus applies here?
A writ of Habeas Corpus would surely succeed because the burden of proof lies with the accuser, not with the punished. To evade a Habeas Corpus ruling that the punishment is not lawful and is immediately to cease, the accuser must, in this case, prove the following absolutely:-
1) That viruses exist.
2) That viruses cause disease.
3) That a virus named Covid-19 exists.
4) That Covid-19 causes severe illness and death.
5) That this disease is highly infectious.
6) That face masks and social distancing prevent infection.
7) That sufficiently large numbers of people have become seriously ill and/or succumbed to it to warrant extreme measures to control it.
They will, inevitably, fail in this as none of the above can be proven to the required standard (or, in most points, at all).
To 1: Germanys highest court has already ruled in December 2016 that the existence of viruses is not proven.
To 2: The preponderance of the evidence shows that the protein particles labelled virus are much more likely to be exosomes which communicate solutions to sickness and other problems.
To 3: The only evidence for the existence of Covid-19 is a computer model based upon guesswork as to what such a virus might look like. The virus itself has never been found or isolated.
To 4: a) Where a purported cause cannot be found, any claims as to its effects are completely spurious. b) All of the purported deaths are with and not of Covid-19, i.e. it did not cause the disease/death.
To 5: There is no reliable evidence of transmission from one human to another. To the contrary, studies which have been carried out show that this does NOT take place!
To 6: a) The necessary porosity of the masks to allow breathing enables the virus particles to pass through unhindered. b) Because these particles are so small, they are essentially weightless and random air currents will carry them for kilometres. Such particles regularly cross the Pacific in 3 days and the Atlantic in a little more than one day. A distance of 1.5 metres is, therefore, seen to be meaningless.
To 7: All serious illness and deaths claimed are in people who were already seriously ill and, basically, in the process of dying. In some countries, there was an upswing in deaths caused by the lockdowns denying people essential treatments. Following their deaths which began two weeks after lockdown started, death figures have returned to normal.
I, therefore, apply for this writ of Habeas Corpus and an order of immediate cessation of all punishments imposed by the respondent.
Blessed be
Karma Singh
www.karmabooks.co.uk
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Ekki getur ţetta veriđ rétt? Ţetta er varúđar setning.
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Dr. Anthony Fauci: His Disastrous Track Record Tells the Real Story →
Hard Scientific Data Confirms HCQ Dramatically Lowers Fatality
Vísindaleg gögn stađfesta ađ HCQ fćkkar dauđsföllum. Ţessi setning endursögđ jg.
Posted on September 3, 2020 by State of the Nation
http://stateofthenation.co/?p=27211
Hér er ţýđing í Google, ég breyti engu.
Lönd sem notuđu hýdroxýklórókín viđ međhöndlun covid-19 sáu 73% lćgri dánartíđni, sem ţýđir ađ Fauci, CDC og FDA hafa lagt á ráđin um ađ DREPA tugi ţúsunda Bandaríkjamanna til ađ vernda ábatasaman bóluefnaiđnađ
Hér er ţýđing í Word, ég breyti engu.
Lönd sem notuđu hydroxychloroquine til ađ međhöndla covid-19 sáust 73% lćgra banamengi, sem ţýđir ađ fauci, CDC og FDA hafa ađ ađ drepa tugi ţúsunda Bandaríkjamanna í ţví skyni ađ vernda ábatasamur bóluefni iđnađur
000
http://stateofthenation.co/?p=27215
000Egilsstađir, 06.09.2020 Jónas gunnlaugsson
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Skilabođ mín til vísindamannanna eru: Ég skil ađ ţađ er mikill ţrýstingur ţarna úti, kannski frá stórum lyfjafyrirtćkjum eđa tímaritum um ađ komast ađ ákveđinni niđurstöđu. Ég biđ vísindamenn ađ standa međ sannleikanum. Ef bandarískir vísindamenn standa ekki í lappirnar og segja ekki satt undanbragđa laust, ţá gerir ţađ enginn - vissulega ekki fjölmiđlar, örugglega ekki stjórnmálamenn. ***
My message to the scientists is, I understand that theres a lot of pressure out there, maybe from big pharmaceutical companies or journal editors to come to a specific result. I implore scientists to stand the line. If US scientists dont stand the line and hold for truth and accuracy, nobody will certainly, not the media, certainly not politicians. ***
Ţessvegna eru skilabođin mín til vísindamanna og ritstjóra, vinsamlega hlustađu ekki á fjölmiđla og hlustađu ekki á stjórnmálamenn, en einbeittu ţér ađ vísindunum.
Mannkyniđ á allt undir ţví, ađ ţú verjir vísindin.*
(Öll mennskan, er í ţínum höndum, stattu stöđugur í sannleikanum, vísindunum. jg)
So my message to the scientists and the editors is, Please ignore the media and please ignore the politicians. Please focus on the science. All of humanity depends on you doing that.
Smá endursagt af leikmanni.
Dr. Gold segir:
"Ég ákvađ ađ tala út vegna ţessa tilviks.
Ég fékk sjúkling, sem var međ smit af covid og ég ávísađ hydroxychloroquine og sink, sem ég hafđi lesiđ um.
Ég fékk kvassa áminning fyrir ţađ.
Ég hafđi líka fengiđ bréf frá ríkissaksóknara, sem hótađi lćknunum ég var bara einn í hópnum, hugsanlegri rannsókn fyrir ófaglega hegđun ef ég vćri ađ ávísa hydroxychloroquine.
"Ţetta var svo átakanlegt fyrir mig," segir Dr. Gold, sem er einnig lögfrćđingur. "Ţađ hafđi aldrei gerst, ađ ríkisstjórnin segđi lćkni hvort ţeir hefđu rétt eđa ekki rétt til ađ ávísa FDA- samţykktri lyfja međferđ. Ég meina, ţađ var bara (rugl) og einstćđur atburđur fyrir mig. (Sui kerfi [Unique]).
Og ég hugsađi međ mér: "Ef lćknar láta ţetta yfir sig ganga, ţá töpum viđ allir." **
Laga.
Ađeins settur litur á valda texte. jg
http://stateofthenation.co/?p=17415
BRAVE DOCTORS BREAK DOWN COVID RESPONSE AND THE DEMONIZATION OF HCQ
Posted on June 20, 2020 by State of the Nation
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FORBIDDEN KNOWLEGE
Emergency Physician, Dr. Simone Gold and Cardiologist, Dr. Dan Wohlgelernter are two brave doctors who join Austen Fletcher of the Fleccas Talks YouTube channel with very important information, countering the breathtaking skullduggery coordinated worldwide across governments and health agencies against the drug, hydroxychloroquine. Furthermore, they say the lockdowns were and are completely unnecessary.
Dr. Wohlgelernter says, Ive decided to speak out, because I think that were dealing with a tragic situation, where the scientific process has been violated. Studies have been published that had not been adequately vetted and should not have been published and those studies were used to terminate further evaluations of hydroxychloroquine.
He says, I have decided to speak out because the political interference in the physician decision-making process is objectionable and should not be allowed to continue. There are lessons to be learned from this pandemic on many levels. Weve spoken about the dangers and the irrationality of the lockdown process. Weve spoken about the violation of the scientific purity of investigation. Weve spoken about media presentations and misrepresentations of data. This is injurious to the health of our population now and I dont want to see this replicated in the future.
I think as physicians, we have a moral responsibility to protect our patients, to protect the science behind our medical decisions and to prevent intrusions into the purity of the scientific process by outside forces that may have bad intent and its important to speak out. Its a moral imperative for us to speak out and to protect our patients and protect our profession.
**
Dr. Gold says, I decided to speak out for one very specific reason. I was actually presented with a definite COVID-positive patient and I prescribed hydroxychloroquine and zinc, because I was very up on the literature on this and I got severely reprimanded for it. I also had received a letter from the State Board, threatening all doctors I was just one with potential investigation into me for unprofessional conduct if I was to prescribe hydroxychloroquine.
This was so shocking to me, says Gold, who is also an attorney. It had never happened, where the government told a physician if they had a right or not a right to prescribe an FDA-approved medication. I mean, that was just a sui generis [unique] event, that took me by surprise. And I thought to myself, If doctors dont speak up weve really all lost.
Dr. Wohlgelernter says, The cost of the shutdown, in terms of the physical, emotional and psychological health of people is enormous. Weve only seen the tip of the iceberg; of people who have been shut-in, whove lost their businesses, who are facing depression, who are facing issues of mental health because of the consequences.
This should never happen again. If we ever face this kind of situation again, we need to learn the lessons from the mistakes in policy that were implemented
I think that the focus should have been on protecting the high-risk population. And we knew from the data that had come out from China and from Italy and from France, that the people at risk were the elderly and frail; people who are immunocompromised.
As Dr. Gold said, young people had very little risk from this infection; they rarely got ill from it. So, it was not a good decision to shut down schools, to shut down all businesses and it certainly was not a good decision to send actively-infected coronavirus patients to nursing homes.
The strategy was inverted. We should have protected the people in the nursing homes and given those homes more resources to protect the people at risk
Thousands of infected patients were sent to nursing homes, leading to massive death when there were plenty of new beds set up at great expense, between the Javits Center and the USNS Comfort. This was unconscionably negligent.
Dr. Gold says, The question of why Governor Cuomo did this is very unpleasant to speculate but one thing that was absolutely known when he made the decision to let the patients go back to the nursing homes it was 100% known that it was risky to send the nursing home patients back
The Health Commissioner of Pennsylvania really had an egregious situation, where she took her own mother out of an assisted living facility but she told the rest of the state that it was perfectly safe to leave your grandparent in an assisted living facility. Thats just egregious. Theres no question that [the danger] was known, at the time
Dr. Wohlgelernter says, Its estimated that as many as 40%, even 50% of the deaths in New York were nursing home patients. This was preventable.
Austen asks Dr. Wohlgelernter about reports that hydroxychloroquine is dangerous. He replies, Ive prescribed it. Ive also recommended it to people and Ive had conversations with physicians literally around the globe; in Israel and Italy and England and the East Coast of the United States and and Ive read the literature extensively.
Hydroxychloroquine definitely has a role. That role is specific. Its an antiviral agent that is effective in early stages of infection. When used in that context, it is effective and it is safe.
Unfortunately, there have been studies that have looked at hydroxychloroquine but have looked at it in the wrong context; looked at it and severely critically ill people in the hospital setting. At that point, the antiviral isnt effective, because youve gone beyond viral infection to an immune-mediated widespread inflammatory reaction, so that was the wrong population to look at hydroxychloroquine in.
And that kind of study sabotages the whole story about hydroxychloroquine Im not quite certain why they were designed that way, but it was obvious that hydroxychloroquine would fail in that context.
Hydroxychloroquine has been reported to have heart toxicity and as a cardiologist, Im intimately aware of this literature and Im familiar with hydroxychloroquine and the study that was most specific in looking at the cardiac issues; specifically, with rhythm abnormalities.
There was a study done in the East Coast, in the New York area, where they looked at 200 patients and carefully monitored their EKGs and looked for arrhythmias and they found no serious arrhythmias in any of those patients.
Some of the reports about danger to the heart and dangerous effects of hydroxychloroquine are based on misinterpretation of data or on faulty data.
Austen asks, We did see the World Health Organization ordered countries to stop using hydroxychloroquine recently and theyve also stopped trial testing on it, as well. Was this decision based on those studies from Lancet, New England Journal of Medicine and JAMA?
Dr. Gold responds, The World Health Organization stopped the hydroxychloroquine trials based specifically on the faulty studies that were printed in The Lancet and printed in the New England Journal of Medicine. Also, the European Union stopped it and it was headlines all across the world that we should stop using it.
I do want to clarify for the audience that they did restart the trials once The Lancet and New England Journal of Medicine retracted those faulty studies. However, its not so easy to restart a trial. You have all these patients, they were in the trial that had to stop and start and gather new patients and the damage has certainly been done.
And in addition to those studies, theres been so much negative press about hydroxychloroquine, that its actually difficult to even enroll patients in hydroxychloroquine studies. Thats been well-documented. Theres a professor at Columbia who said its hard for me to even get patients in this study, because they hear about hydroxychloroquine, they think its so negative.
I always want to remind people, this is an FDA-approved drug for 65 years. Its generic. Its cheap. Its widely available. We give it to pregnant women. We give it to breastfeeding women. We give it to elderly patients. We give it to patients who are immune-compromised.
Most of those patients are on it for decades! There was never controversy about hydroxychloroquine, right up until March 20th, 2020. So, I would look at the studies before then. The early studies, before Trump said he kind of liked the drug were uncontroversial, from China and from France. It looked promising.
I dont know what the final data will show, however, I do find that the data after Trump thought it was possibly helpful is suspect
To be published in The Lancet and to be published in the New England Journal Medicine is no easy feat to have them do a retraction was a major story, which is why you heard about it in the headlines. The reason their study was retracted is the data that went into those studies could not be independently verified
We asked the company that provided the data, a company called Surgisphere, which has been quite secretive to reveal their data and they have absolutely refused. Because they refused to reveal their data, those studies HAD to be retracted by the journals
In addition, a story that hasnt been discussed really in the media is a third world premier class Medical Journal, the Journal of the American Medical Association, known as JAMA
The first major flaw in the JAMA study is what I would call pseudo randomization. To do an effective medical study, you have to randomize the patients into different groups; groups that have this character and that character and the point being that the group should be generally similar, so that you know if the drug actually made the difference
When you look at the study itself, as its printed right now in JAMA, your listeners I encourage you and viewers to go and look this up, yourself on Page 7 of the study. You can look and see that the groups are not equal. The higher-dose group is seven years older, they have almost 80% heart disease. Those are just two of the differences. The other group is seven years younger and has 0% heart disease and theres a number of these flaws that are different in the two groups.
By itself, thats cherry-picking of patients that would make any data that comes from such a study suspect. So I want to be clear that the JAMA study used not exactly hydroxychloroquine, they used a drug called chloroquine which is really a precursor to hydroxychloroquine. Sometimes, we use those drugs, those names interchangeably but in America, we only use hydroxychloroquine.
The JAMA study was in Brazil. They used chloroquine.
The lethal dose of chloroquine has been well-established for more than 30 years in 1988 a New England Journal Medicine.
Again, one of the world premier journals established and everyone accepts that the lethal dose of chloroquine is 5 grams.
Well, the Jama study had two groups.
In the high-dose chloroquine group, they gave them 1.2 grams a day which means by the fourth day, they had almost 5 grams
Hydroxychloroquine and chloroquine sit in your body for very long time, at least a month, perhaps 2 months; somewhere between 30 and 60 days is its half-life.
So, to give someone 4.8 grams in four days is a very large dose; people would often possibly call that a lethal dose.
The study went on for 10 days, which meant that the people in that group got 12 grams. Again, New England Journal of Medicine in 1988 established 5 grams as a lethal dose Mind you, these are elderly, critically-ill patients that are intubated or in severe respiratory distress
Its not just my speculation or the science data that says its a very high, toxic dose. So many patients died in the high-dose group that they halted that study early. They quit the high dose group because so many patients died. Thats extremely dramatic for a scientific study.
Its very unusual for a study to have given such a large dose of a medication, because all the scientific studies that involve human subjects have to be overseen by an ethics board. The scientists that did this study and presented the paper to JAMA are saying that they went through an ethics board however, thats in doubt.
The Brazilian Ministry of Justice is actually investigating. Theres no proof that there actually was an ethics board
They normally have a certain committee number thats stamped on the paperwork and they dont have that. We have written to them and tried to get it and there has been no response on that. So, the Ministry of Justice is actually investigating the deaths of all those patients who died in the high-dose chloroquine group.
Austen asks Dr. Wohlgelernter why hydroxychloroquine has become so politicized and he responds, I think one of the serious casualties of the COVID pandemic has been scientific truth. We rely on the scientific process to be pure and untainted by political influence.
The fact that, as Dr. Gould said two of the worlds most prestigious journals, Lancet and the New England Journal of Medicine published studies hastily, without adequate peer review and studies that were based on data where there was no transparency, that creates widespread skepticism about the reliability of medical journals to give information that can be trusted and were going to need to look into that whole process and to and to reform the process of publication so that we never see that kind of violation of scientific truth.
Now, why did this become politicized? The fact is that President Trump first mentioned hydroxychloroquine and advocated for its use, as a non-physician in mid-March but we had data from China and from France well before that in February, showing a significant beneficial impact of hydroxychloroquine.
Yet you saw physicians, politicians, journalists saying that hydroxychloroquine is all hype, its all due to the president pushing it and thats revisionist history.
The fact is there was a great deal of excitement in the medical community internationally, a month before President Trump ever mentioned it, because of the data reported from China and from Dr. Raoult in France and its sad that people used whatever political animosity they had towards the President to attack the medication that, in fact had helped many people with coronavirus and could have helped many more, had its reputation not been so sullied by political accusations and by poorly-designed studies and by medical journals allowing publications that were negative, as far as their conclusions publications that never should have reached print, because they hadnt been adequately vetted.
I got asked a lot of questions about the VA study of hydroxychloroquine and my immediate instinct is to wonder why hydroxychloroquine keeps getting studied at the later stages of the disease.
I cant emphasize enough that the mechanism of action of a drug and the pathophysiology of a disease is the number one factor when youre structuring a scientific study. The disease early in the course is all about viral replication; how much virus can be produced and how quickly. Thats the problem in the early setting. In the late setting, the problem is your bodys over-response to trying to cure itself and thats called a cytokine storm and in that setting, that affects all of your organs, including your lungs failing.
In the first group, which is the early group, you would like a drug that is very good at preventing the viral replication. Thats what hydroxychloroquine with zinc is very, very good at. So, I was always a bit confused why we kept doing study after study after study but hydroxychloroquine we studied it in the late-stage disease population. And kind of like it doesnt snow in August, it wasnt working very well.
So, to me, the VA study, The Lancet study, JAMA all of those studies Im not that surprised, because I already know it doesnt snow in August. Im waiting to see the data but hydroxychloroquine and zinc, how well it works early on. Mechanism of action, when indicated would work well and before hydroxychloroquine got politicized, the preliminary data that we have from China and from France, it was very promising.
As Dr. Gold mentioned, hydroxychloroquine and chloroquine had been around since the 1950s. Azithromycin, which is an adjuvant agent used with hydroxychloroquine has been around for 30 years. These agents have been shown to be safe and to be effective. And again, you needed to understand which context it worked in. It wasnt going to work in the critically-ill, hospitalized patients on ventilators with multi-organ system failure. That was not what it should have been used for. It works in early-stage, where the antiviral effect can terminate the infection and prevent people from getting critically ill.
And its sad that many people to this day have been deprived of the potentially beneficial use of an agent that in fact is safe and that is inexpensive and thats widely available.
Dr. Gold says, My message to the media is, I understand that you have a point of view and God bless you and you can say it. Free speech is very important. But dont have an opinion on the science of a medication. Think of your own family and your own loved ones and relegate to the scientists the purity of the scientific result, because one day, you could suffer the harm of having polluted that process.
*** My message to the scientists is, I understand that theres a lot of pressure out there, maybe from big pharmaceutical companies or journal editors to come to a specific result. I implore scientists to stand the line. If US scientists dont stand the line and hold for truth and accuracy, nobody will certainly, not the media, certainly not politicians.
Im very distressed on two levels about the JAMA study. The first level is that the scientists who read that actual study it, doesnt seem as though it was done in the correct scientific manner. The other part Im upset about is the journal, itself, which I dont think vetted it in the manner that a world-class medical journal supposed to vet it.
* So my message to the scientists and the editors is, Please ignore the media and please ignore the politicians. Please focus on the science. All of humanity depends on you doing that.
___ https://forbiddenknowledgetv.net/doctors-break-down-covid-response-and-the-demonization-of-hcq/
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Egilsstađir, 04.09.2020 Jónas Gunnlaugsson
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