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Queen Margrethe of Denmark, 85, Discharged After Being Hospitalized for a Cold

Queen Margrethe of Denmark, 85, Discharged After Being Hospitalized for a Cold

Yahoo12-05-2025
Queen Margrethe of Denmark was discharged from the hospital on May 10 after being admitted days before for observation after contracting a cold
The 85-year-old former Queen of Denmark has returned to her residence at Fredensborg Palace, according to the Danish Royal House
The Queen's most recent public appearance ahead of the hospitalization was a May 4 peace service at the Church of Our Lady in CopenhagenQueen Margrethe of Denmark was discharged from the hospital on the morning of Saturday, May 10, after being admitted days before as a precaution for a cold.
The Danish Royal House announced the recovery of the former Queen of Denmark, 85, over the weekend.
'Her Majesty is well and is now back in her residence at Fredensborg Palace,' the court said in a statement. She was initially admitted for observation on Thursday, May 8.
The former Queen's hospitalization forced her to cancel a scheduled outing on May 8, a visit to the Sankt Lukas Foundation's 125th anniversary celebration. Queen Margrethe's latest public appearance ahead of the hospitalization was at a May 4 peace service at the Church of Our Lady in Copenhagen to mark the 80th anniversary of Denmark's liberation.
The Queen abdicated her position in January 2024 on the 52nd anniversary of her rise to the throne, becoming the first Danish royal to voluntarily do so in almost 900 years.
Her eldest son, now known as King Frederik, acceded to the throne later that month, and his Australian-born wife became Queen Mary.
Can't get enough of PEOPLE's Royals coverage? to get the latest updates on Kate Middleton, Meghan Markle and more!
The Queen cited her health during a New Year's Eve 2023 speech announcing her abdication.
"In February this year, I underwent extensive back surgery. Everything went well, thanks to the competent health personnel, who took care of me," she said in part then. "Inevitably, the operation gave cause to thoughts about the future – whether now would be an appropriate time to pass on the responsibility to the next generation. I have decided that now is the right time."
In 2023, the Queen made history as Denmark's longest-reigning monarch after decades of service.
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Medical journal rejects RFK Jr.'s call for retraction of vaccine study
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Medical journal rejects RFK Jr.'s call for retraction of vaccine study

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RFK Jr.'s cancellation of mRNA vaccine research is even worse than it first seemed
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That includes myocarditis, an inflammation of the heart muscle that is often cited by anti-vaccine agitators as a dangerous side effect of the mRNA vaccines. That condition was most commonly seen among young men, particularly if they had received two shots within a short time span. But for the most part it was mild and short-term; once the booster was reformulated after 2022, the effect appeared to disappear. No deaths from the condition were known to have occurred, and myocarditis effects were more common and serious among unvaccinated people infected with COVID. Nor did the agency's data packet include an estimate of lives saved by the COVID vaccines, led by Stanford epidemiologist John P.A. Ioannidis and published July 25. That study calculated that from the beginning of the global vaccination campaign in 2020 through September 2024 as many as 4 million lives were saved by the vaccines. Ioannidis acknowledged that his estimate is 'conservative.' Indeed, in 2022 the Commonwealth Fund estimated that in just the first two years the vaccines were available, the shots prevented more than 18 million hospitalizations and more than 3 million COVID-related deaths in the U.S. alone. A 2022 study in The Lancet, a British medical journal, estimated as many as 20 million COVID-related lives saved around the world in just the first year of vaccination. Weigh those figures against Kennedy's assertion that the mRNA vaccines pose 'more risks than benefits,' and it becomes evident that decision-making has gone seriously awry at the Department of Health and Human Services under Kennedy's leadership. To Jake Scott, an infectious disease expert at Stanford Medical School who painstakingly examined the agency's data citations, they point to 'textbook confirmation bias'—the quest for information that confirms someone's preexisting beliefs. In this case, that someone is Kennedy, whose record of anti-vaccine advocacy is indisputable. The mismatch between the data packet cited by Kennedy and the established facts of the vaccines' safety and efficacy explain why Kennedy's cancellation of 22 contracts supporting mRNA vaccine research has been greeted by experts as a senseless and devastating blow against science and public health. 'I have have been in this business for over 50 years on the front lines of public health,...and I can say unequivocally that this was the most dangerous public health decision I have ever seen made by a government body,' Michael Osterholm, an expert in infectious diseases at the University of Minnesota, told PBS. At the very least, if Kennedy is so convinced that the effects mRNA vaccines are not sufficiently well-understood, the solution is more research, not less. I asked Kennedy's department to respond to criticism of his decision, but received no response. A few words about the mRNA technology. 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The compilation originated as material for a book titled 'TOXIC SHOT: Facing the Dangers of the COVID 'Vaccines',' an anthology of essays by prominent anti-vaxxers. The compilation doesn't make the case for canceling the research. A paper listed as support for the myocarditis threat, for example, states, 'no causality can be assumed or established' linking the condition to the vaccine because of the lack of a control group for comparison. 'There is no direct evidence of a vaccine-induced inflammatory response' to the vaccine. Kennedy's action is almost certain to hamstring American science for years, possibly decades, to come. It's the antithesis of Trump's claim to put 'America First,' for it cedes the development of a life-saving medical technology to Europe and China. And it's not limited to the development of vaccines for respiratory diseases. During a recent appearance on a podcast hosted by the right-wing influencer Steve Bannon, the newly-appointed commissioner of the National Institutes of Health, Jay Bhattacharya, declared, 'As far as public health goes for vaccines, the mRNA platform is no longer viable.' Bhattacharya justified this statement by noting a rise in public skepticism about mRNA technology. What he didn't say was that the skepticism was promoted by Kennedy and other anti-vaxxers denigrating the technology; a competent and responsible NIH chief would be defending a technological innovation, not magnifying disinformation about it. The truth is that the mRNA platform is likely to be seen in retrospect as a historic advance in healthcare ... everywhere but in the United States.

Why Eli Lilly's (LLY) Tasty Q2 Earnings Left a Bitter Aftertaste
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While sentiment around orforglipron has cooled, the sell-off appears overdone. Given Eli Lilly's robust obesity franchise and deep pipeline, the company's long-term growth story remains compelling, making LLY attractive at current levels for patient investors. I remain confidently Bullish on LLY, despite the market beating the stock has taken in recent days. The High-Stakes Obesity Market For some background, the global obesity market is expected to eclipse a staggering $100 billion in the next few years. Eli Lilly, with its popular Zepbound, is a clear leader in this space, alongside Novo Nordisk (NVO), a Danish pharmaceutical company, and its GLP-1 injectable Wegovy. While Eli Lilly and Novo Nordisk act as a duopoly in the obesity market, this isn't expected to last. Innovation happens fast in medicine, and both Zepbound and Wegovy will soon face competition. Fortunately for Eli Lilly, the billions of dollars it generates from treatments like Zepbound and its diabetes medication Mounjaro can be funneled back to R&D efforts, procuring a flywheel of innovative drugs. Orforglipron Versus the Competition Orforglipron is an investigational oral GLP-1 being studied in late-stage trials. Orals would significantly broaden the obesity market, appealing to patients averse to needles and interested in maintenance, 'step down' weight loss therapy. Before Phase 3 data, some analysts expected orforglipron could generate over $15 billion in peak annual revenue. So, expectations were high. Naturally, in the oral obesity market, the two main competitors are Eli Lilly and Novo Nordisk, with their oral GLP-1, high-dose semaglutide. In its pivotal OASIS 4 trial, oral semaglutide demonstrated an average weight loss of between 13.6% to 15%, which is superior to orforglipron's 12.4%. Regarding safety, the GLP-1 class continues to feature gastrointestinal side effects like nausea and vomiting, which can lead to treatment discontinuations and compliance issues in a real-world setting. Novo Nordisk has already submitted all the paperwork required to achieve FDA approval for oral semaglutide, positioning it to be the first oral GLP-1 treatment. Eli Lilly's Ace in the Deck I believe the market is missing some important nuances here. First, the gap between 13.6% and 15% weight loss is likely clinically insignificant. Cross-trial comparisons are fraught with pitfalls—differences in patient populations, study designs, and treatment protocols can skew perceptions. Until orforglipron and its rivals are tested head-to-head (as Wegovy and Zepbound were in SURMOUNT-5), declaring one clearly superior is premature. More importantly, orforglipron holds two decisive advantages: convenience and manufacturing. As a non-peptide small molecule, it imposes no food or water restrictions—unlike oral semaglutide. The simpler chemistry also makes it far cheaper and easier to mass-produce than complex peptides. In a weight-loss market plagued by supply shortages, this could be a game-changer for Eli Lilly. Let's also bring some perspective to the drama. Orforglipron's potential, combined with Zepbound and Lilly's aggressive access strategy, is enormous. High list prices for injectables—often over $1,000 per month—remain a barrier, with many insurers refusing coverage. That leaves a vast patient population unable to pay out-of-pocket. By leveraging orforglipron's low manufacturing costs and LillyDirect's direct-to-consumer reach, Lilly can offer lower cash prices and dramatically expand access—turning a perceived setback into a long-term competitive edge. 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Morgan believes LLY's recent plunge is a 'compelling' entry point, noting that orforglipron's '1-2 percentage points lower weight loss,' compared to oral semaglutide, is unlikely to meaningfully impact its commercial potential. Eli Lilly Transitions from Perfection to Resilience The Eli Lilly story has moved from one of flawless execution to one of strategic resilience. While the orforglipron results fell short of the lofty expectations embedded in its stock price, they still reinforce the strength of Lilly's broader portfolio—and come with notable competitive edges in convenience, manufacturing scalability, and potential for disruptive pricing. Near-term volatility is likely as the market recalibrates, but the core drivers of Lilly's long-term growth remain firmly in place, keeping the bullish case intact.

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