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Monday, April 6, 2026

Mamdani ‘emergency’ order to block concerts, food festivals at NYC parks during FIFA World Cup

 Soccer mega-fan Mayor Zohran Mamdani signed an emergency order that will block events including some concerts and food festivals from city parkland during the FIFA World Cup.

The city Parks Department adopted the rule at the request of the NYPD, denying new permits for special events on park property during the tournament, which runs from June 11 to July 19.

NYC Mayor Zohran Mamdani made an infrastructure improvement announcement inside Sunset Park in Brooklyn on March 31, 2026.Paul Martinka for New York Post

The directive could block any events with 20 or more people that require the special permits which could even include birthday celebrations at the Big Apple’s 100 featured parks.

However, critics contend it wouldn’t be necessary if City Hall did a better job hiring officers to fill the NYPD’s depleted ranks — and worked on keeping cops from fleeing the force.

“Police officers are already burned out by the short-staffing they experience on a daily basis,” Hendry said. “When this summer’s massive workload hits, it’s going to push even more of them out the door.”

City Councilman Frank Morano (R-Staten Island) agreed.

“New York used to be the city that never sleeps,” said Morano, who sits on the council’s parks committee. “Now it’s the city that cancels. If we had the police staffing we should have, families wouldn’t be paying the price for City Hall’s mismanagement.”

The New York City Parks Department adopted an emergency rule denying permits for events on park property during the FIFA World Cup tournament, which runs from June 11 to July 19.REUTERS
The USTA Billie Jean King National Tennis Center at Flushing Meadows-Corona Park in Queens, New York, is pictured on Jan. 4, 2024.Domingo Sáez – stock.adobe.com

NYC Parks said it adopted the rule denying or restricting “special events” at the request of the police force because manpower will be stretched patrolling events tied to the soccer tournament as well as events commemorating America’s 250th anniversary.

“To more effectively deploy resources and control overtime costs, the NYPD has recommended that the department deny certain permit applications for new events between June 11, 2026 and July 19, 2026,” the parks agency said.

Applications for events not held last year could be rejected.

About 1.2 million visitors are expected to converge on the New York metro region for eight World Cup games at MetLife Stadium at the Meadowlands in New Jersey.NYPCS for the New York Post

But permits for demonstrations will be exempt from the rule, the agency said.

“The events associated with the FIFA World Cup and United States 250th anniversary will require significant realignment and deployment of NYPD personnel, which will further divert resources from regular assignments and from crime-fighting, public safety, and counter-terrorism duties,” according to the rule, which was signed by Mamdani and Parks Commissioner Tricia Shimamura.

Before NYC Parks decides on special permit applications, they will consult the NYPD to determine if resources are available to patrol the events.

“This is outrageous — besides making no sense,” one Big Apple event planner told The Post on Monday. “Normally, during the summer months, there would be over 1,000 new events where the city takes in millions of dollars. 

“That money could’ve been used for [Mamdani’s] budget deficit,” the planner said. “Maybe he should hire an accountant.”

About 1.2 million visitors are expected to converge on the New York metro region for eight World Cup games at MetLife Stadium at the Meadowlands in New Jersey. Many fans will stay at Big Apple hotels.

Another 6 million visitors are expected for events around the 250th anniversary of the country, with which Fleet Week will coincide this year.

There are already a number of related gatherings planned locally.

The NYNJ World Cup 26 Fan Zone Queens will take place at the USTA Billie Jean King National Tennis Center’s Louis Armstrong Stadium from June 17–28. In addition to live match broadcasts, the Fan Zone will include entertainment, games, local food vendors, official merchandise, VIP hospitality experiences and more.

FIFA Fan Festival NYNJ will be held at Liberty State Park in New Jersey throughout the tournament, with live match screenings, music, celebrity appearances and other family-friendly programming.

https://nypost.com/2026/04/06/us-news/mamdani-signs-emergency-order-to-block-concerts-food-festivals-at-nyc-parks-during-fifa-world-cup/

' Kennedy rewrites rules for membership on US vaccine advisory panel'

 U.S. Health ​Secretary Robert ​F. Kennedy Jr. is rewriting the rules of membership for a key vaccine advisory panel, according to a document published by his department on Monday, after a judge last month declared ‌most of his prior selections unqualified and put their decisions on hold.

The Advisory Committee ⁠on Immunization Practices, which advises the Centers for Disease Control and Prevention on the use of vaccines, had been a major tool in ‌Kennedy's efforts to reshape U.S. vaccine ‌policy.

In a March 16 decision, Boston-based U.S. District Judge Brian Murphy concluded that ACIP had been unlawfully reconstituted after Kennedy, a longtime anti-vaccine activist, last year removed and replaced all 17 independent experts who previously ​served on the panel, adding several members who share his controversial vaccine views.

In his decision, Murphy concluded that Kennedy's ACIP panel violated the Federal Advisory Committee Act and repeatedly pointed to the panel's charter, which ⁠required that its members have expertise in the use and research of vaccines and immunization practices.

On Monday, the Department of Health and Human Services led ​by Kennedy published a renewal of the charter that broadens the list of expertise for individuals who could serve on that panel, which makes recommendations impacting the use ​of vaccines, including the U.S. childhood immunization schedule.

A previous version ‌of the charter signed by Kennedy in December stipulated that panel members should be knowledgeable about immunization practices and public health, and have expertise using vaccines in clinical practice ⁠or preventive medicine or have expertise in vaccine research, or in vaccine efficacy and safety.

Two former ACIP members appointed by previous administrations said the new charter appears to broaden the requirements for membership, listing examples of specialists in biostatistics and toxicology.

In his ⁠decision, Murphy said the members Kennedy appointed were "distinctly unqualified," with only six of the 15 members having any meaningful experience in ​vaccines.

HHS spokesman Andrew Nixon downplayed the significance of the changes, saying the ACIP charter renewal and publication "are routine statutory requirements and do not signal any broader policy shift."

The revamped charter followed a letter sent to Kennedy on March 25 by attorney Aaron ‌Siri representing Informed Consent Action Network, a group critical of vaccine safety and mandates, recommending changes to the ACIP charter.

According to a press release on the ICAN website ‌promoting the letter, the group called on Kennedy to "clarify committee member criteria" and argued that all 13 of the ACIP ⁠members whose qualifications were challenged in Murphy's decision "do ‌have the requisite experience."

So far, ​the Trump administration has not appealed Murphy's ruling, but still has time to do so under a 60-day window.

https://www.streetinsider.com/Reuters/Kennedy+rewrites+rules+for+membership+on+US+vaccine+advisory+panel/26277698.html

Iran: 'Most extensive attacks' tonight, tomorrow

 A spokesperson for Iran's Khatam al-Anbiya Central Headquarters Ebrahim Zolfaghari said on Monday that Iran will launch its largest attacks since the start of the war.

"Tonight and tomorrow night, Iran will carry out its most extensive attacks since the beginning of the war against the United States, the Israeli regime, and their regional allies," Zolfaghari wrote on X.

The warning comes after US President Donald Trump threatened that "the entire country [Iran] can be taken out in one night," adding that "that night might be tomorrow night," and described Tuesday's deadline as "final." He also warned Iran's infrastructure could be destroyed "over a period of four hours" if no deal is reached.

https://breakingthenews.net/Article/Iran:-'Most-extensive-attacks'-tonight-tomorrow/66016538

Federal Appeals Court Reinstates $656 Million Judgment Against Palestinian Authorities

 by Joseph Lord via The Epoch Times,

A federal appellate court has agreed to reinstate a $656 million judgment against Palestinian authorities for Americans killed or wounded in attacks by the Palestinian Liberation Organization (PLO) and the Palestinian Authority while in Israel.

The ruling from the 2nd U.S. Circuit Court of Appeals was issued in the wake of a Supreme Court decision authorizing such suits for victims of international terrorism in a legal saga that’s been ongoing since the mid-2010s.

“We conclude that the original judgment for the plaintiffs should be reinstated. That conclusion is consistent with the plain import of the Supreme Court’s decision,” the judges said in a decision dated March 30.

The Supreme Court’s decision directly overturned a prior ruling made by the 2nd Circuit Court of Appeals on the matter.

The case has its earliest origins in a law passed by Congress in 1992, the Anti-Terrorism Act, which permitted victims of international terror to sue the offender.

In 2014, in the case Sokolow v. PLO, the PLO was successfully sued under that law in the U.S. District Court for the Southern District of New York. In the case, victims were awarded $218.5 million in damages by a jury—tripled to $655.5 million under the Anti-Terrorism Act.

The victims and their families have stated that Palestinian agents were either directly involved in the attacks or helped incite them.

The Palestinians have consistently argued that the cases shouldn’t be allowed in American courts.

In 2016, the case was brought before the 2nd Circuit Court of Appeals. In their decision, circuit judges tossed out the verdict from the lower court, and ruled that U.S. courts had no jurisdiction over international actors in non-U.S. countries.

Frustrated by the ruling, Congress in 2019 passed the Promoting Security and Justice for Victims of Terrorism Act (PSJVTA), which sought to create a legislative carve-out to ensure that lawsuits against the PLO and Palestinian Authority could move forward.

The legislation stated that the PLO and Palestinian Authority had “consented” to the jurisdiction of U.S. courts if they either paid martyr benefits to terrorists or their families or if they maintained any non-United Nations offices in the United States.

In 2023, the matter came again before the 2nd Circuit Court of Appeals, and the court held that the PSJVTA was unconstitutional. Its ruling stated that Congress could not simply “deem” an action to constitute consent to U.S. jurisdiction without running afoul of the Due Process Clause of the Fifth Amendment.

In a unanimous decision in June 2025, the Supreme Court ruled in favor of victims, overturning the 2nd Circuit Court of Appeal’s ruling that the Fifth Amendment was violated by the PSJVTA.

With the vacation overturned, the courts will now move toward enforcement of the lower court ruling in favor of the plaintiffs, although collecting the funds from the PLO may meet with practical obstacles.

https://www.zerohedge.com/geopolitical/federal-appeals-court-reinstates-656-million-judgment-against-palestinian-authorities

CMS Finalizes 2027 Medicare Advantage and Part D Payment Policies

 The Centers for Medicare & Medicaid Services released the Calendar Year (CY) 2027 Medicare Advantage (MA) and Part D Rate Announcement today to improve payment accuracy across both programs. The finalized policies also advance CMS’ vision of a sustainable and stable MA program that offers choice to Medicare beneficiaries and is a responsible steward to taxpayers. 

The policies in this Rate Announcement are projected to result in a net average increase of 2.48%, or over $13 billion in additional MA payments to plans in CY 2027. This expected increase includes consideration of the various elements that impact MA payments, such as growth rates of underlying costs, 2026 Star Ratings for 2027 quality bonus payments, and risk adjustment updates.

“Medicare Advantage and Part D should work for the people who rely on them,” said CMS Administrator Dr. Mehmet Oz. “These updates keep coverage affordable and ensure patients get real value from their plans.” 

CMS is committed to ensuring Medicare beneficiaries are free to choose the health coverage that best meets their needs, and that such coverage maximizes value. Establishing accurate payments in MA and Part D is foundational to this objective and will enable the agency to maintain affordable Medicare coverage while acting as good stewards of a more sustainable and credible program over the long term.

“CMS’ vision for Medicare Advantage and Part D is clear: a great choice for seniors and a smart deal for taxpayers,” said Chris Klomp, Director of Medicare and Chief Counselor of the U.S. Department of Health and Human Services. “The Rate Announcement improves payment accuracy and strengthens competition based on quality—not on coding practices—helping put the program on a more sustainable path for the long term.”

The policies in the Rate Announcement address coding differentials between MA and Original Medicare for CY 2027. CMS is working towards a MA risk adjustment system guided by three principles: (1) simplicity to reduce day-to-day administrative burden for both plans and providers; (2) competition for all plans irrespective of size or resources,  creating greater value for patients; and (3) achieving payments that accurately reflect beneficiary health risk and facilitate the efficient use of healthcare resources, enhanced program integrity, and greater accountability. Working towards a risk adjustment system guided by these principles will promote a more stable and sustainable MA program in the long run by giving beneficiaries and taxpayers confidence that CMS is mitigating unnecessary cost growth from coding practices that do not lead to better quality coverage.

In consideration of the impact that the 2024 MA risk adjustment model had between CY 2024 and CY 2026, CMS will continue using the 2024 MA risk adjustment model for CY 2027. The agency will evaluate the public feedback received as it considers future updates to the MA risk adjustment model. 

CMS is excluding diagnosis information from unlinked chart review records, which is diagnosis information not associated with a specific beneficiary encounter, from risk score calculation starting in CY 2027, with an exception for beneficiaries who switch from one MA organization to another. As a result, aside from the exception, diagnoses that are not associated with a service will not be considered for risk adjustment. CMS expects the payment impact to be greater for MA organizations that heavily rely on unlinked chart review records to report risk-adjustment eligible diagnoses for their enrollee population.

CMS is finalizing updates to the Part D risk adjustment model that include accounting for Inflation Reduction Act changes to the Part D benefit for CY 2027, reflecting more current costs, and separately accounting for MA prescription drug plan and standalone prescription drug plan costs in order to improve the accuracy of Part D payments for these two segments of the Part D market. Additionally, CMS is aligning sources of diagnoses for use in risk adjustment to be consistent with similar policies finalized for MA (e.g., excluding diagnoses from unlinked chart review records, with an exception for beneficiaries who switch from one MA organization to another). These updates will bring additional stability to prescription drug benefits for all Medicare beneficiaries.

The CY 2027 MA and Part D Rate Announcement may be viewed at: https://www.cms.gov/files/document/2027-announcement.pdf.

https://www.cms.gov/newsroom/press-releases/cms-finalizes-2027-medicare-advantage-part-d-payment-policies-strengthen-accountability-long-term

At-Home Gel Nails Pose Underrecognized Risks

 Users of at-home gel nail kits are at an increased risk for adverse skin reactions, according to new data presented at the annual meeting of the American Contact Dermatitis Society.

Dermatitis associated with gel nail products has been documented in nail technicians, but the COVID pandemic accelerated the use of at-home gel nail kits, many of which contain 2-hydroxyethyl methacrylate, according to Samantha K. Ong, MD, a dermatology resident at Saint Louis University School of Medicine, St. Louis, and colleagues.

Previous studies of gel nail products have focused on professionals, and the risk for allergic contact dermatitis from these products remains underrecognized in nonoccupational users, Ong told Medscape Medical News.

“By focusing on at-home users rather than salon professionals, this study addresses a gap in the literature and highlights a growing public health issue that affects real-world consumer behavior,” she said.

Ong and colleagues posted a survey about at-home gel nail use on six Reddit subgroups focused on gel nails or contact dermatitis. The 163 respondents answered questions about demographics, manicure habits, dermatitis symptoms, allergen knowledge, help-seeking behavior, and financial impact.

Overall, 88 respondents (54%) reported adverse skin reactions associated with the use of at-home gel nail products; most were young women, and 98% were not nail technicians. The rates of skin reactions increased the more the products were used, with 80% of weekly users reporting some adverse reaction. Itching was the most common reaction, reported by approximately 75% of the participants. Redness and swelling occurred in approximately 70% and 60%, respectively.

Although the cost of an at-home gel nail kit is less than a salon manicure, users of the at-home kits faced additional expenses from seeking treatment for their reactions or from changing products, the researchers noted. A total of 20 respondents reported using prescription treatments to manage the adverse reactions.

Notably, users of the at-home kits who reported prior allergen awareness were significantly less likely to have adverse reactions than those who were unaware of possible problems (36% vs 88%; P < .0001).

“I was most surprised that knowledge of allergenicity was protective, regardless of knowledge of proper application, since most of our users were not professional technicians,” Ong told Medscape Medical News.

The findings were limited by several factors, including the cross-sectional design and lack of clinical assessment, as well as reliance on self-reports and the potential for selection bias given the recruitment through Reddit, Ong said. “Additional research would be useful in larger, more diverse populations, ideally with confirmatory patch testing and prospective designs to better define causality, risk factors, and long-term outcomes,” she noted.

However, the current study results highlight the underrecognized public health risk allergic contact dermatitis from at-home gel nail products and the need to raise consumer awareness of the possible risks associated with at-home gel nail kits, the researchers concluded.

“Ask specifically about at-home gel nail use when evaluating hand, periungual, or facial dermatitis, especially in younger patients and frequent cosmetic users,” Ong said. The findings also support counseling patients on the risk for acrylate allergy, recommending that they stop using the offending products if dermatitis develops, and considering patch testing when contact allergy is suspected, she said.

Frequent Users Don’t Have Fewer Problems

The new study provides perspective on the potential risk for acrylate allergy in people who use at-home gel nail kits, said Amber Atwater, MD, a past president of the American Contact Dermatitis Society and a dermatologist in private practice in Vienna, Viginia.

“We know the risk may be higher in this population because users are not trained professionals and because they are typically applying the product to themselves,” said Atwater, who was not involved in the study.

Atwater said she was surprised that more than half of the gel nail kit users reported skin reactions. “Also, I would expect weekly users to have more application expertise, and therefore fewer reports of reactions; instead, they had more reactions,” she told Medscape Medical News.

Atwater acknowledged that the findings were limited by the use of a single source for the survey (Reddit) but also said the study provides a heads-up to clinicians that their patients may be using at-home nail kits. “Prior allergen awareness was associated with fewer reactions, so counseling patients on the risk of acrylate allergy from home kits could be of value,” she added.

This study received no outside funding. Ong had no financial conflicts to disclose. Atwater had no relevant financial conflicts of interest to disclose.

https://www.medscape.com/viewarticle/home-gel-nails-pose-underrecognized-risks-2026a1000aco

Physicians, Lawsuit Challenge Medicare’s WISeR Prior Auth Experiment

 When Matthew Crooks, MD, interventional pain specialist in Phoenix, first heard about Medicare’s new prior authorization (PA) program, he was optimistic about its goal of reducing unnecessary care and controlling costs.

But nearly 3 months in, the reality is much different. Medicare has denied payment for any epidural steroid injections since the rollout, even for procedures with valid authorization numbers, Crooks said.

“This system is completely nonfunctional and unsustainable, and we have been given no guidance to navigate it,” Crooks said.

Many physicians and medical societies have reported delays, denials, and communication breakdowns since WISeR — the Wasteful and Inappropriate Service Reduction program — launched on January 1 in select states.

Now, a lawsuit against the Centers for Medicare & Medicaid Services (CMS) is underway.

Last week, the Electronic Frontier Foundation (EFF) filed a lawsuit seeking detailed information from CMS about how the program uses AI and third-party vendors for PA reviews, including financial incentives vendors receive and whether those could influence authorization decisions.

CMS did not respond to Medscape’s request for comment.

PAs for Select Services in Six States

WISeR marks a major change for traditional Medicare, which has historically allowed physicians to provide most covered services without authorization. The program applies to a subset of treatments — including nerve stimulators, epidural steroid injections, and some types of wound care — that CMS says may harm patients or involve fraud, waste, and abuse.

The pilot program, set to run through 2031, is now being tested in Arizona, New Jersey, Ohio, Oklahoma, Texas, and Washington. It’s not clear whether the program will expand to more states or cover more treatments in the future.

Each state has been assigned a single contractor to review PA requests, and those vendors may use AI technology to automate parts of the process.

A spokesperson for Cohere Health, the WISeR vendor for Texas, told Medscape Medical News its technology is “never used to deny care but rather to automate approvals” for faster care decisions. More complex cases are reviewed by board-certified clinicians within 3 days, the spokesperson said.

Participation in WISeR is optional. Physicians can either submit PA requests through the program for the required services or have their claims routed for prepayment medical review. Providers who pursue the former can benefit by confirming coverage and payment upfront, and those with a strong track record of authorization approvals may earn a “gold card,” exempting them from future authorization and prepayment review requirements for some treatments.

‘Radical Change’ in Documentation

For Crooks, president of the Arizona Society of Interventional Pain Physicians, the program has been far from seamless. He said the authorization vendor and Medicare’s payment systems appear to not communicate well, with each side directing providers back to the other when claims are denied.

The result has been hundreds of delayed claims and a growing administrative burden that, he said, is affecting “every interventional pain practice I’ve spoken with in Arizona.”

“We initially saw wait times of 1-2 weeks to get an authorization decision, and denial rates of up to 30%-40%, even when Medicare Local Coverage Determination guidelines were being followed,” he said. Those rates have gradually improved as his practice adapted to a “radical change in documentation requirements,” which he said were necessary due to “AI being used to deny authorization.”

In some cases, they must now document that a patient’s primary care physician has been informed, as well as the specific type and dosage of medication planned for a future procedure, and “much, much more.” Despite these changes, he said some procedures are still denied for reasons that do not align with Medicare guidelines.

Arizona pain medicine physician William Thompson IV, MD, told Medscape Medical News some denials appear to reflect a “fundamental misunderstanding of the anatomy and technical aspects” of certain procedures.

At Northwest Endovascular Surgery in Richland, Washington, all authorization submissions since the program began have taken more than a week to generate a determination letter, well beyond the stated 3-day turnaround, Yasamin Alazawi, staff member who has been managing WISeR authorizations, told Medscape Medical News.

She said the office has had multiple claims denied, despite closely following CMS guidance and obtaining valid authorization numbers before submitting claims. “Because the claims are coded as ‘unprocessable,’ we have no right to appeal. No one can tell us what the error actually is,” she said.

Like Crooks, she described being caught between the vendor and the Medicare Administrative Contractor (MAC), with “no resolution in sight.” Alazawi estimated the practice’s staff has spent close to 100 hours navigating the portal, guidelines, and follow-up calls.

Concerns Grow Among Physician Groups

Several medical societies and physician groups told Medscape Medical News their members are experiencing similar delays and denials since WISeR’s launch.

Jason Jameson, MD, president of the Arizona Medical Association, said physicians are reporting more denials and longer wait times for peer-to-peer reviews, straining clinic resources and slowing access to care.

He’s also concerned about vendors’ use of AI, saying it should not replace physician judgment. Arizona, like many other states, has passed legislation limiting the role of AI in healthcare decisions, though Jameson said it does not apply to Medicare or Medicaid services.

In a March 26 letter to CMS, the Washington State Medical Association (WSMA) outlined similar issues affecting providers, including claims rejected despite valid authorization numbers, calling the situation “a systemic administrative disconnect…rather than a physician compliance issue.”

The state’s physicians have reported portal access issues, peer-to-peer scheduling delays, and inconsistent communication between vendors and MACs, said Jeb Shepard, WSMA’s director of policy, who noted “a real gulf in communication.”

The Society of Interventional Radiology raised concerns with CMS in September about WISeR’s proposed authorization requirements for vertebral augmentation. The organization said its members have voiced “overwhelmingly negative” since the program began, citing burdensome documentation requirements, vague criteria, unreliable technology, and minimal technical support.

Lawsuit: Calls for Transparency

Victoria Noble, JD, EFF staff attorney, told Medscape Medical News the WISeR model lacks transparency, which “increases the risk that unsafe uses will go unnoticed until it’s too late to protect people from harm.”

Earlier this year, EFF submitted a Freedom of Information Act request seeking records related to vendor payment agreements, algorithms, system testing, and data and privacy safeguards, but CMS has not provided them, according to the complaint.

Back in Arizona, Crooks said his group has begun warning Medicare patients about the delays.

“This is not in line with WISeR’s stated goal,” he said. “We have been trying to work through it, but as of now, our only choice is to inform our patients and ask that they reach out to their representatives.”

https://www.medscape.com/viewarticle/unsustainable-physicians-lawsuit-challenge-medicares-wiser-2026a1000ae8