https://www.naturalnews.com/2019-11-19-trump-smashes-hospital-bill-secrecy-sham.html

Trump smashes hospital bill secrecy sham, forces hospitals to publicly publish secret prices so that consumers can make informed choices

Image: Trump smashes hospital bill secrecy sham, forces hospitals to publicly publish secret prices so that consumers can make informed choices

(Natural News) The Trump administration is currently in the process of finalizing a new price transparency rule that, once it comes into effect in January 2021, will force all hospitals to publish their service prices publicly for the benefit of consumers.

Currently, hospitals are allowed to charge whatever prices they want to for services, typically in secret, burdening patients with exorbitant bills after they’ve already received medical care. But Trump’s new rule will ensure that customers know right upfront what the charges will be before they opt for oftentimes very expensive hospital services.

“For decades, hospitals, insurance companies, lobbyists, and special interests have hidden prices from consumers so they could drive up costs for you,” the president stated in an announcement to the nation. “And you had no idea what was happening. You’d get bills that were unbelievable and you have no idea why.”

President Trump cited several examples, including hospital patients who have been charged obscene prices for MRI (magnetic resonance imaging) tests and pregnancy services. Even simple blood tests are often billed at absurd rates by hospitals, which have gotten used to bilking consumers by charging insurance companies unrealistically high prices for medical services.

“We’re stopping American patients from just getting, pure and simple – two words, very simple words: ripped off,” Trump is quoted as saying. “Because they’ve been ripped off for years.”

Trump also wants insurance companies to discloses expected costs to policyholders before they receive treatment

Hospitals aren’t the only bad players in the American medical paradigm, as insurance companies themselves are notorious for withholding price information from policyholders until after the medical bills come. This places an enormous burden on patients who oftentimes don’t know what they’re getting themselves into until it is already too late.

“This is the biggest revolution I’ve seen in generations,” stated Dr. Art Laffer, who was recently invited by President Trump to the White House to discuss the significance of the new hospital rule, and its associated proposed insurance rule.

“As opposed to most revolutions, this revolution saves lives; it doesn’t cost lives,” Dr. Laffer went on to explain.

According to Dr. Laffer, the health care industry is in desperate need of transparency reform. Not only do patients deserve to know precisely how much they will be expected to pay before receiving medical care, but they also deserve improved medical care, which simply can’t happen unless the medical industry is forced to be transparent.

Even though President Trump was unsuccessful in fully repealing and replacing Obamacare as he promised to do while on the campaign trail, POTUS has been able to work within this corrupt system to implement important regulatory reforms like this that will at least help to make the process smoother and more pleasant for consumers.

“The changes you described, what we’re doing at HHS (Department of Health and Human Services), will be revolutionary to our health care system – perhaps the biggest single change that President Trump has made to Americans’ health care experience,” added Alex Azar, Secretary of HHS.

Azar, as you may recall, isn’t exactly a revolutionary when it comes to fighting the health care status quo, seeing as how he’s the former president of drug giant Lilly USA, a division of Eli Lilly and Company. Azar has other ties to the drug industry as well, having worked as general counsel and then-deputy secretary of the HHS during the George W. Bush administration.

Still, Azar seems to be cooperating with the agenda of President Trump, which in this case appears to be for the benefit of consumers rather than special interests.

For more related news about President Trump that the mainstream media isn’t telling you, be sure to check out Trump.news.

Sources for this article include:

Breitbart.com

NaturalNews.com

https://www.psychologytoday.com/us/blog/turning-straw-gold/201411/surviving-the-holidays-when-you-re-chronically-ill

Surviving the Holidays when You’re Chronically Ill

Four suggestions for making the holidays as stress-free as possible

Posted Nov 23, 2014

Toni Bernhard J.D.

Turning Straw Into Gold

freeimages.com
Source: freeimages.com

For the chronically ill—which includes those who suffer from chronic pain—the holidays can feel like a no-win situation. If we participate at all, there’s likely to be payback later. On the other hand, if we don’t participate, we’ll feel isolated and risk other people not understanding why we haven’t joined in the festivities….(See link for full article)

 

https://sporteluxe.com/science-and-alternative-medicine-say-its-probably-time-you-try-acupuncture/  Full Article Here

Science And Alternative Medicine Agree: It’s Probably Time You Try Acupuncture

October, 29 2019
image
Image: Antonika Chanel

https://www.prnewswire.com/news-releases/new-york-state-grants-approval-for-igenexs-newly-developed-tick-borne-relapsing-fever-tbrf-immunoblot-tests-300933720.html

New York State Grants Approval for IGeneX’s Newly Developed Tick-Borne Relapsing Fever (TBRF) ImmunoBlot Tests

TBRF ImmunoBlots (IgM and IgG) represent a quantum leap in testing for tick-borne diseases, particularly for patients with Lyme-like symptoms

NEWS PROVIDED BY

IGeneX


MILPITAS, Calif., Oct. 8, 2019 /PRNewswire/ — The Division of Laboratories of the Department of Health of the State of New York has approved IGeneX’s newly developed Tick-Borne Relapsing Fever (TBRF) ImmunoBlots (IgM and IgG), making them immediately available to New Yorkpractitioners.

Until recently, diagnostic tests for TBRF have been grossly insensitive and have not been able to detect many of the ever-growing list of species and strains of TBRF Borrelia carried by hard and soft ticks. The new IGeneX ImmunoBlots overcome these obstacles with the ability to detect antibodies to TBRF Borrelia species including, but not limited to, B. hermsii, B. miyamotoi, and B. turicatae.

TBRF is often considered a Lyme disease imitator because both TBRF and Lyme sufferers display many similar symptoms, such as high fever, chills, and headache, often leading to misdiagnosis. Moreover, some of the Borrelia that cause TBRF are transmitted by the same ticks that transmit B. burgdorferi, the causative agent of Lyme disease. Therefore, it is important for physicians to test for both TBRF and Lyme.

“We are very excited to be able to offer the TBRF ImmunoBlots to physicians in New York State,” said Dr. Jyotsna Shah, President of IGeneX. “Doctors use to call me and say ‘my patients have Lyme-like symptoms. Why are your tests negative?’ We now know that their symptoms might have been due to TBRF Borrelia infection. These new TBRF ImmunoBlot tests will help patients in this group, as well as patients with Lyme and TBRF Borrelia mixed infections.”

The accuracy of the TBRF ImmunoBlot has been established. The specificity is 98.5% for IgM and IgG based on a study performed on 212 well characterized samples, of which 50 were provided by the CDC. Additionally, the TBRF ImmunoBlots can detect the full spectrum of disease: early, active and late-stage disease.

For more information on IGeneX and the TBRF ImmunoBlot tests, please visit http://igenex.com.

About IGeneX
For over 25 years, IGeneX has been at the forefront of research and development of diagnostic testing for Lyme disease, TBRF, Bartonella, and other tick-borne diseases. IGeneX arms its talented scientists with the most cutting-edge technology available to enable them to find new solutions that challenge the status quo of testing for Lyme and associated tick-borne diseases. The mission of IGeneX is to aid practitioners in their diagnosis of tick-borne illnesses by providing the most comprehensive testing possible. Learn more at: www.igenex.com

Media Contact:
Joseph Sullivan
225913@email4pr.com 
408-504-7691

SOURCE IGeneX

Related Links

http://www.igenex.com

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More on Relapsing Fever:  https://madisonarealymesupportgroup.com/2018/12/28/relapsing-fever-spirochete-uniquely-adapted-to-highly-oxidative-salivary-glands-of-soft-bodied-tick/

https://madisonarealymesupportgroup.com/2019/03/22/tick-borne-relapsing-fever-in-arizona/

https://madisonarealymesupportgroup.com/2017/12/22/tbrf-in-texan-dogs-yep-despite-poor-tests-its-there/

https://madisonarealymesupportgroup.com/2019/01/10/relapsing-fever-found-at-popular-recreation-site-in-ca-ticks/

https://madisonarealymesupportgroup.com/2018/12/20/tick-borne-relapsing-fever-as-a-potential-veterinary-medical-problem/

https://madisonarealymesupportgroup.com/2017/05/04/us-soldier-aquires-tickborne-relapsing-fever-caused-by-b-turicatae-from-a-ornithodoros-turicata-tick/

https://madisonarealymesupportgroup.com/2019/03/17/first-case-of-b-corocidurae-in-native-european-presenting-as-meningitis-with-cranial-polyneuritis-cavernous-sinus-thrombosis/

https://neurosciencenews.com/ketamine-side-effects-depression-15222/

Side effects mild and brief with single antidepressant dose of intravenous ketamine

Summary: The side effects of administering ketamine to treat major depressive disorder are mild and persist for no longer than four hours, researchers report. Most of the side effects peaked within an hour of treatment, and many patients reported the effects as being significantly reduced two hours post ketamine administration.Source: NIH/NIMH

National Institutes of Health researchers found that a single, low-dose ketamine infusion was relatively free of side effects for patients with treatment-resistant depression. Elia Acevedo-Diaz, M.D., Carlos Zarate, M.D., and colleagues at the NIH’s National Institute of Mental Health (NIMH) report their findings in the Journal of Affective Disorders.

Studies have shown that a single, subanesthetic-dose (a lower dose than would cause anesthesia) ketamine infusion can often rapidly relieve depressive symptoms within hours in people who have not responded to conventional antidepressants, which typically take weeks or months to work. However, widespread off-label use of intravenous subanesthetic-dose ketamine for treatment-resistant depression has raised concerns about side effects, especially given its history as a drug of abuse.

“The most common short-term side effect was feeling strange or loopy,” said Acevedo-Diaz, of the Section on the Neurobiology and Treatment of Mood Disorders, part of the NIMH Intramural Research Program (IRP) in Bethesda, Maryland. “Most side effects peaked within an hour of ketamine administration and were gone within two hours. We did not see any serious, drug-related adverse events or increased ketamine cravings with a single-administration.”

This shows two brain diagrams

The researchers compiled data on side effects from 163 patients with major depressive disorder or bipolar disorder and 25 healthy controls who participated in one of five placebo-controlled clinical trials conducted at the NIH Clinical Center over 13 years. While past studies have been based mostly on passive monitoring, the NIMH IRP assessment involved active and structured surveillance of emerging side effects in an inpatient setting and used both a standard rating scale and clinician interviews. In addition to dissociative (disconnected, unreal) symptoms, the NIMH IRP assessment examined other potential side effects – including headaches, dizziness, and sleepiness. The study did not address the side effects associated with repeated infusions or long-term use.

Out of 120 possible side effects evaluated, 34 were found to be significantly associated with the treatment. Eight occurred in at least half of the participants: feeling strange, weird, or bizarre; feeling spacey; feeling woozy/loopy; dissociation; floating; visual distortions; difficulty speaking; and numbness. None persisted for more than four hours. No drug-related serious adverse events, cravings, propensity for recreational use, or significant cognitive or memory deficits were seen during a three-month follow-up.

Credit: NIMH.To overcome the limitations associated with side effects and intravenous delivery, ongoing research efforts seek to develop a more practical rapid-acting antidepressant that works in the brain similarly to ketamine. These NIMH researchers, in collaboration with the National Institute on Aging, and the National Center for Advancing Translational Science, are planning a clinical trial of a ketamine metabolite that showed promise as a potentially more specific-acting treatment in pre-clinical studies. Meanwhile, the U.S. Food and Drug Administration earlier this year approved an intranasal form of ketamine called esketamine, which can be administered to adults with treatment-resistant depression in a certified doctor’s office or clinic.

ABOUT THIS NEUROSCIENCE RESEARCH ARTICLE

Source:
NIH/NIMH
Media Contacts:
Jules Asher – NIH/NIMH
Image Source:
The image is credited to NIMH.

Original Research: Closed access
“Comprehensive assessment of side effects associated with a single dose of ketamine in treatment-resistant depression.”. Acevedo-Diaz EE, Cavanaugh GW, Greenstein D, Kraus C, Kadriu B, Zarate CA Jr, Park LT.
Journal of Affective Disorders doi:10.1016/j.jad.2019.11.028.

Abstract

Comprehensive assessment of side effects associated with a single dose of ketamine in treatment-resistant depression.

Background
Concerns about ketamine for treating depression include abuse potential and the occurrence of psychotomimetic effects. This study sought to comprehensively assess side effects (SEs) associated with a single subanesthetic-dose intravenous ketamine infusion. A secondary aim was to examine the relationship between Clinician-Administered Dissociative States Scale (CADSS) scores and dissociative symptoms reported on a comprehensive, clinician-administered SE questionnaire.

Methods
Data from 188 participants were pooled from four placebo-controlled, crossover ketamine trials and one open-label study (n=163 with either treatment-resistant major depressive disorder or bipolar disorder and 25 healthy controls). SEs were actively solicited in a standardized fashion and monitored over the time-course of each study. Statistical analyses assessed the effect of drug (ketamine, placebo) on SEs and measured the relationship between CADSS total score and SEs contemporaneously endorsed during structured interviews.

Results
Forty-four of 120 SEs occurred in at least 5% of participants over all trials. Thirty-three of these 44 SEs were significantly associated with active drug administration (versus placebo). The most common SE was feeling strange/weird/loopy. Most SEs peaked within an hour of ketamine administration and resolved completely by two hours post-infusion. No serious drug-related adverse events or increased ketamine craving/abuse post-administration were observed. A positive correlation was found between dissociative SEs and total CADSS score.

Limitations
The post-hoc nature of the analysis; the limited generalizability of a single subanesthetic-dose ketamine infusion; and the lack of formal measures to assess ketamine’s cognitive, urological, or addictive potential.

Conclusions
No long-lasting significant SEs occurred over the approximately three-month follow-up period.

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For more:  https://madisonarealymesupportgroup.com/2019/04/18/ketamine-reduces-depression-related-behaviors-in-mice-limits-bb-in-vivo-relieves-chronic-pain/

It’s also been shown to limit borrelia in vitro:  https://madisonarealymesupportgroup.com/2018/03/10/ketamine-limits-bb-in-vitro/

And its’s been shown to relieve chronic pain, improve quality of life, reduce depression and suicidal ideation, and reduce opioid consumption:  https://madisonarealymesupportgroup.com/2017/09/14/iv-ketamine-in-ptls/

https://madisonarealymesupportgroup.com/2019/04/26/fda-approves-ketamine-nasal-spray-for-depression/

https://madisonarealymesupportgroup.com/2019/09/20/the-chemical-imbalance-myth-and-antidepressant-harm/