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RFK Jr. claims food stamps are fueling diabetes epidemic, wants to block their use for soda, candy

RFK Jr. claims food stamps are fueling diabetes epidemic, wants to block their use for soda, candy

New York Post19 hours ago
Health and Human Services Secretary Robert F. Kennedy Jr. claimed food stamps are fueling diabetes – as he called Sunday to block the taxpayer-funded welfare program for being used to buy soda and candies.
'Taxpayers should not be financing that,' Kennedy said on the 'Cats Roundtable' on WABC 770 AM radio.
He said 18% of federal food stamps to poor families is spent 'on candy and sugared drinks' even as nearly 40% of children now have juvenile diabetes.
Health and Human Services Secretary Robert F. Kennedy Jr. claimed that food stamps are fueling the rise in diabetes.
Photo by SAUL LOEB/AFP via Getty Images
'We are actually paying for people to get diabetes,' RFK told host John Catsimatidis.
Sugary and fatty foods also contribute to obesity.
American taxpayers are paying twice, RFK said — beginning with funding the purchase of food stamps, or the Supplemental Nutrition Assistance Program (SNAP). The program issues electronic benefits that can be used like cash to purchase food.
'We're paying again when they get [treated] through Medicaid and, ultimately, Medicare. We are poisoning them with sugars and ultra-processed food,' RFK said.
Kennedy called on SNAP recipients to be barred from using it to pay for things like soda or candy.
Christopher Sadowski
SNAP helps low-income working people, senior citizens, the disabled and others feed their families. Eligibility and benefit levels are based on household size, income and other factors.
Kennedy said the Trump administration is making headway, noting that 14 states have signed waivers that restrict the purchase of non-nutritious items like soda and candy.
'These waivers are a key step in ensuring that taxpayer dollars provide nutritious options that improve health outcomes within SNAP,' the US Dept. of Agriculture said.
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Ex-Trump surgeon general slams RFK's ‘tepid' response to CDC shooting
Ex-Trump surgeon general slams RFK's ‘tepid' response to CDC shooting

The Hill

time12 minutes ago

  • The Hill

Ex-Trump surgeon general slams RFK's ‘tepid' response to CDC shooting

Former U.S. Surgeon General Jerome Adams blasted Health Secretary Robert F. Kennedy Jr. for his 'delayed and tepid response' to the fatal shooting that occurred at the Centers for Disease Control and Prevention (CDC) in Atlanta on Friday. In an opinion piece published by Stat on Saturday, Adams wrote it was 'clear' that the shooting was a 'a dire reflection of ever-escalating threats public health workers face in a climate increasingly shaped by misinformation, politicization, and inflammatory rhetoric.' Last Friday afternoon, a shooter whom authorities have identified as 30-year-old Patrick Joseph White shot at the Atlanta headquarters of the CDC, killing DeKalb County police officer David Rose. White's father reportedly told police his son had been fixated on the COVID-19 vaccine. In his op-ed, Adams, who served in the first Trump administration, lambasted Kennedy for waiting 18 hours before issuing a statement, writing that he himself heard from staffers at the CDC within that time frame who felt 'already demoralized.' 'Leadership in moments of crisis is critical. Kennedy's delayed and tepid response, coupled with his own record of inflammatory claims, has only deepened the wounds and amplified a dangerous sense of betrayal among America's frontline public health workers,' Adams wrote. He also noted other recent violent incidents, including a shooting at a Pennsylvania hospital and the killing of UnitedHealthcare CEO Brian Thompson. 'What ties these events together is not just the violence — but the context that enables it,' wrote Adams. 'Repeated rhetoric from influential voices, including Kennedy and his supporters, has portrayed health professionals as corrupt, untrustworthy, or outright malicious. They've been labeled 'grifters,' 'enemies of the people,' and worse.' He called on federal leadership to condemn rhetoric that vilifies public health professionals, to stop scapegoating public frustration onto health professionals, protect health care workers and to fund actionable solutions instead of just messaging. Appearing on CBS News's 'Face the Nation,' Adams continued his criticism of Kennedy, noting the secretary's past remarks villainizing the CDC. 'He said no one should be harmed while working to protect the public. There's an out there,' said Adams. 'If you don't believe that people are working to protect the public, then that means it's okay to commit violence, at least in some people's eyes.' Writing on social media following the shooting, Kennedy said, 'We know how shaken our public health colleagues feel today. No one should face violence while working to protect the health of others. We are actively supporting CDC staff on the ground and across the agency. Public health workers show up every day with purpose — even in moments of grief and uncertainty.' 'Secretary Kennedy has unequivocally condemned the horrific attack and remains fully committed to ensuring the safety and well-being of CDC employees,' HHS Communications Director Andrew Nixon said in a statement Monday. 'He extends his deepest condolences to the family and loved ones of Officer David Rose, who was tragically killed. Officer Rose's sacrifice to protect the CDC on its darkest day will never be forgotten. 'This is a time to stand in solidarity with our public health workforce, not a moment for the media to exploit a tragedy for political gain,' Nixon added.

NRx Pharmaceuticals, Inc. (NASDAQ:NRXP) Granted FDA Fast Track Designation for NRX-100 for Suicidal Ideation in Patients with Depression, including Bipolar Depression
NRx Pharmaceuticals, Inc. (NASDAQ:NRXP) Granted FDA Fast Track Designation for NRX-100 for Suicidal Ideation in Patients with Depression, including Bipolar Depression

Yahoo

timean hour ago

  • Yahoo

NRx Pharmaceuticals, Inc. (NASDAQ:NRXP) Granted FDA Fast Track Designation for NRX-100 for Suicidal Ideation in Patients with Depression, including Bipolar Depression

This designation expands the addressable population for NRX-100 to the 13 million Americans who consider suicide each year and represents a 10x expansion of the addressable population compared to the Designation granted in 2017 for bipolar depression alone The Designation includes an FDA determination that NRX-100 has the potential to address an unmet need, based on FDA's assessment of the data submitted Determination of "unmet need" is a requirement for a Commissioner's National Priority Voucher (CNPV) program. Suicide is a public health crisis. Approximately 13 million adults seriously consider suicide each year, according to the CDC, 3.7 million make a plan to commit suicide. An American dies from suicide every 11 minutes. Active-duty personnel, veterans, and first responders have a four-fold higher risk of suicide. WILMINGTON, Del., Aug. 11, 2025 /PRNewswire/ -- NRx Pharmaceuticals, Inc. (Nasdaq:NRXP), a clinical-stage biopharmaceutical company, today announced US Food and Drug Administration (FDA) has granted Fast Track designation to NRX-100 for the treatment of suicidal ideation in patients with depression, including bipolar depression. This designation for NRX-100 as a standalone drug is a 10-fold expansion of the addressable population for NRX-100, compared to the designation granted in 2017 for NRX-100 in combination with NRX-101 (DCS/lurasidone) for treatment of Suicidal Bipolar Depression. In granting the Fast Track designation, FDA made the determination that NRX-100 has the potential to address an unmet medical need, based on an assessment of the preliminary data contained in the Fast Track designation request. This determination of unmet medical need aligns with the eligibility requirements for the Commissioner's National Priority Voucher Program (CNPV)i and for the FDA's Accelerated Approval The Company has applied for a CNPV, which has the potential to substantially shorten the review cycle for NRX-100. Several well-controlled trials submitted to FDA in support of Fast Track Designation demonstrated a clinically meaningful and statistically significant reduction of suicidal ideation. In a Columbia University study licensed by NRx, suicidal patients treated with intravenous ketamine demonstrated a 55% response (i.e. 50% reduction in suicidality) compared to a 30% response to active comparator (P<.02).iii In a trial sponsored by the Government of France and licensed by NRx, 63% of patients achieved full remission from suicidal ideation in three days compared to 31% of those who received placebo (P<.001). This effect has not been proven with intranasal administration of "We thank FDA for its thoughtful review of our Fast Track designation request, and believe this regulatory determination is a significant step forward in our goal to address the national crisis of suicide among soldiers, first responders, veterans, and civilians alike." said Dr. Jonathan Javitt, Chairman and CEO of NRx Pharmaceuticals. "Large-scale government-supported trials have demonstrated a robust and statistically significant reduction in suicidal ideation and depression with administration of ketamine. This drug was also proven to be non-inferior to electroshock therapy in treating depression without the negative side effects of ECT. We look forward to working closely with the FDA in our quest to Bring Hope to Life." Under the terms of the Fast Track program, NRx will be posting an expanded access policy for NRX-100 in the next two weeks and seeking a meeting with FDA leadership to finalize the data to be submitted under the Accelerated Approval / CNPV application. In addition to the benefits above, Fast Track Designation also grants enhanced communication with the FDA, as well as potential Priority Review and Rolling Review. NRX-100 in Suicidal Ideation in Patients with Depression, Including Bipolar Depression According to the CDC, approximately 13 million adults seriously consider suicide each year, 1.5 million attempt suicide, and an American dies from suicide every 11 minutes. NRX-100 – IV ketamine for suicidality in patients with depression, including bipolar depression – is designed to help address this national crisis. NRx will be submitting patient-level data from controlled clinical trials that demonstrate ketamine to be superior to both a placebo and an active comparator, as well as either non-inferior or superior to electroshock therapy in treating various forms of depression, including patients with active suicidal ideation. Although ketamine in various forms is increasingly used to treat depression and related disorders, it is currently only approved by FDA only for use as an anesthetic and, therefore, not reimbursed by most insurance carriers for treatment of suicidality or depression. Intravenous ketamine is reimbursed by the Department of Veterans Affairs and the Department of Defense for its beneficiaries. By applying for FDA labeling for NRX-100 to treat suicidal depression, the Company hopes to make this potentially life-saving therapy available to all Americans, not just those who are able to pay out of pocket. The Company has previously filed full Chemical Manufacturing and Controls (CMC) information for NRX-100 with FDA and has reported stability and sterility data sufficient to anticipate three-year room temperature shelf life for preservative-free ketamine. Having completed this Fast Track Designation, NRx is now filing draft labeling for NRX-100 to comply with the CNPV requirement. NRX-100 is the first preservative-free presentation of ketamine to be filed with FDA. Currently available product, primarily of foreign manufacture, contains a known toxic preservative, Benzethonium Chloride (BZT) that is not Generally Recognized as Safe (GRAS) and is not allowed by FDA to be used in hand cleaners and topical antiseptics. NRx demonstrated long term stability and sterility with its patented preservative-free formulation of NRX-100. The Company has additionally filed a Citizen Petition seeking to have BZT removed from all intravenous ketamine products. The Company has instituted US-based high-volume manufacture of sterile, preservative-free ketamine. Regarding Fast Track designation, FDA's website states: A drug that receives Fast Track designation is eligible for some or all of the following: More frequent meetings with FDA to discuss the drug's development plan and ensure collection of appropriate data needed to support drug approval. More frequent written communication from FDA about such things as the design of the proposed clinical trials and use of biomarkers Eligibility for Accelerated Approval and Priority Review, if relevant criteria are met. Rolling Review, which means that a drug company can submit completed sections of its Biologic License Application (BLA) or New Drug Application (NDA) for review by FDA, rather than waiting until every section of the NDA is completed before the entire application can be reviewed. BLA or NDA review usually does not begin until the drug company has submitted the entire application to the FDA. NRX-100 is poised to address the >$3 billion Suicidal Depression market in the US. References i Grunebaum, et al. Ketamine for rapid reduction of suicidal thoughts… Am J Psychiatry 2018;175: Abbar, et al. Ketamine for the acute treatment of severe suicidal ideation… BMJ 2021;167:194-203 About NRx Pharmaceuticals, Inc. NRx Pharmaceuticals is a clinical-stage biopharmaceutical company developing therapeutics based on its NMDA platform for the treatment of central nervous system disorders, specifically suicidal depression, chronic pain, and PTSD. The Company is developing NRX-100 (preservative-free intravenous ketamine) and NRX-101, (oral D-cycloserine/lurasidone). NRX-100 has been awarded Fast Track Designation for the treatment of Suicidal ideation in Depression, including Bipolar Depression. NRX-101 has been awarded Breakthrough Therapy Designation for the treatment of suicidal bipolar depression. NRx has recently filed an Abbreviated New Drug Application (ANDA) and initiated a New Drug Application filing for NRX-100 (IV ketamine) with an application for the Commissioner's National Priority Voucher Program for the treatment of suicidal depression. The filing is based on results of well-controlled clinical trials conducted under the auspices of the US National Institutes of Health and the Government of France, licensed under a data sharing agreement. Notice Regarding Forward-Looking StatementsThe information contained herein includes forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended. Forward-looking statements generally include statements that are predictive in nature and depend upon or refer to future events or conditions, and include words such as "may," "will," "should," "would," "expect," "plan," "believe," "intend," "look forward," and other similar expressions among others. These statements relate to future events or to the Company's future financial performance, and involve known and unknown risks, uncertainties and other factors that may cause the Company's actual results to be materially different from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. The Company has reported regulatory milestones as they have been achieved but has not predicted the outcome of any future regulatory determination. You should not place undue reliance on forward-looking statements since they involve known and unknown risks, uncertainties and other factors which are, in some cases, beyond the Company's control and which could, and likely will, materially affect actual results, levels of activity, performance or achievements. Any forward-looking statement reflects the Company's current views with respect to future events and is subject to these and other risks, including uncertainties and assumptions relating to the Company's operations, results of operations, growth strategy, and, among other things, liquidity. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company's most recent Annual Report on Form 10-K and other filings with the Securities and Exchange Commission. Investors and security holders are urged to read these documents free of charge on the SEC's website at Except as may be required by applicable law, the Company assumes no obligation to publicly update or revise these forward-looking statements for any reason, or to update the reasons actual results could differ materially from those anticipated in these forward-looking statements, whether as a result of new information, future events or otherwise. For further information: Matthew Duffy Chief Business Officer, NRx Pharmaceuticals mduffy@ Brian Korb Managing Partner (917) 653-5122 View original content to download multimedia: SOURCE NRx Pharmaceuticals, Inc. Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

Medical debt can still appear on credit reports, judge rules
Medical debt can still appear on credit reports, judge rules

Yahoo

timean hour ago

  • Yahoo

Medical debt can still appear on credit reports, judge rules

A federal judge blocked a rule from the Biden-era Consumer Financial Protection Bureau that would have kept medical debt from appearing on credit reports. Mind Your Money host Julie Hyman reports on the latest. To watch more expert insights and analysis on the latest market action, check out more Mind Your Money. A judge has blocked a Biden era ban on medical debt in credit reports. Now, technically, the rule from the Consumer Financial Protection Bureau never took effect, but if it had, it would have stopped medical bills from appearing on credit reports and barred lenders from using that data to make lending decisions. The CFPB says removing medical bill information could have wiped $49 billion off credit reports of about 15 million Americans and increased their credit scores by an average of 20 points. But a judge ruled in favor of two trade associations that argued the CFPB overstepped its authority in issuing that rule. This comes at a precarious time in health care, with millions of Americans expected to lose health insurance by 2034 due to changes in Medicaid under President Trump's new tax bill. So how does medical debt and your credit report work without this rule? Say you get medical care. The provider will send your bill to insurance, and you're responsible for whatever your insurance does not cover. If you don't pay that balance, the provider will likely send you reminders. If you still don't pay, they may send that debt to a collection agency. Once it's with the agency, they own that debt. They'll start calling and sending you letters, and they may report it to credit bureaus. Once reported, it can appear on your credit report. Now, it may not hurt your credit score right away. Medical debt must be one year old before it shows up on your credit report. Debt under $500 is not reported. And 14 states have provisions in place to remove medical collection debt from credit reports. But still, consumers are left with the responsibility to stay on top of changes to their credit as they face mounting bills.

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