Jury Selection Underway in Sam Bankman-Fried’s FTX Fraud Trial

Jury selection is currently underway in Sam Bankman-Fried’s trail on fraud and conspiracy charges, nearly one year after his now-bankrupt cryptocurrency exchange, FTX, collapsed.

According to prosecutors, Bankman-Fried, who has been detained since August, is responsible for embezzling money from FTX for the benefit of his hedge fund, Alameda Research, as well as to purchase luxury properties and donate over $100 million to U.S. political candidates. 

The former billionaire is alleged to have committed this embezzlement from FTX’s founding in 2019 until its bankruptcy in 2022. 

Prosecutors and defense lawyers confirmed that there was never any discussion of a plea deal. Bankman-Fried has pleaded not guilty to seven counts of fraud and conspiracy.

The trial could last up to six weeks. The prosecution is intending to bring three people who were part of Bankman-Fried’s inner circle to testify against him. They are cooperating with Manhattan’s U.S. Attorney’s Office and have already pleaded guilty to fraud charges themselves. 

The defense intends to challenge these witnesses by denouncing their credibility and claiming that they are only cooperating to secure lesser sentences.

The defense’s arguments will primarily revolve around their idea that FTX was not able to meet customer’s withdrawal requests because of a series of poor business decisions rather than deliberate fraud. 

Bankman-Fried, 31, was indicted last December. His trial is the highest-profile case that U.S. prosecutors have brought against a former cryptocurrency manager.

Some information for this report came from Reuters.

LogOn: Bionic Hand Gives Users Touch Feedback

New technologies are giving bionic hands some of the more complex features of human hands. Genia Dulot reports on a California company that is using touch feedback to give users a sense of the objects they are holding or interacting with

3 Scientists Win Nobel Prize in Physics for Looking at Electrons in Atoms During Split Seconds

The Nobel Prize in physics was awarded Tuesday to three scientists who look at electrons in atoms during the tiniest of split seconds.

Pierre Agostini of The Ohio State University in the U.S.; Ferenc Krausz of the Max Planck Institute of Quantum Optics and Ludwig Maximilian University of Munich in Germany; and Anne L’Huillier of Lund University in Sweden won the award.

Their experiments “have given humanity new tools for exploring the world of electrons inside atoms and molecules,” according to the Royal Swedish Academy of Sciences, which announced the prize in Stockholm. They “have demonstrated a way to create extremely short pulses of light that can be used to measure the rapid processes in which electrons move or change energy.”

At the moment, this science is about understanding our universe rather than practical applications, but the hope is that it will eventually lead to better electronics and disease diagnosis.

“Attosecond science allows us to address fundamental questions such as the time scale of the photoelectric effect for which Einstein, Albert Einstein, received the Nobel Prize in physics in 1921,” according to Eva Olsson, chair of the Nobel Committee for Physics.

The Nobel Prizes carry a cash award of 11 million Swedish kronor ($1 million). The money comes from a bequest left by the prize’s creator, Swedish inventor Alfred Nobel, who died in 1896.

Last year, three scientists jointly won the physics prize for proving that tiny particles could retain a connection with each other even when separated. The phenomenon was once doubted but is now being explored for potential real-world applications such as encrypting information.

The physics prize comes a day after Hungarian-American Katalin Karikó and American Drew Weissman won the Nobel Prize in medicine for discoveries that enabled the creation of mRNA vaccines against COVID-19.

Nobel announcements will continue with the chemistry prize on Wednesday and the literature prize on Thursday. The Nobel Peace Prize will be announced on Friday and the economics award on Oct. 9.

The laureates are invited to receive their awards at ceremonies on Dec. 10, the anniversary of Nobel’s death. The prestigious peace prize is handed out in Oslo, according to his wishes, while the other award ceremony is held in Stockholm.

WHO Announces 2nd Malaria Vaccine Recommendation

The World Health Organization on Monday announced the recommendation of a second malaria vaccine, with the aim of giving countries a cheaper and more readily available option to tackle the deadly disease.

Developed by Oxford University with the help of the Serum Institute of India, the new vaccine, known as R-21, will be rolled out in some African countries early next year, and expand into other countries later in 2024, according to WHO chief Tedros Adhanom Ghebreyesus.

Research that has not yet undergone the usual process of scientific review suggests the three-dose vaccine to be around 75% effective. Boosters would be available for continued protection.

“Almost exactly two years ago, WHO recommended the broad use of the world’s first malaria vaccine called RTS,S” also known as Mosquirix, Tedros told a briefing in Geneva.

Developed by British pharmaceutical GSK, Mosquirix requires four doses, is only about 30% effective, and fades within months. The WHO says there is not enough data available to confirm whether the newly developed Oxford vaccine will be more effective.

The Serum Institute has said it could produce 200 million doses of the R-21 vaccine per year, while GSK is able to produce only 15 million doses of Mosquirix annually.

The aim of widespread rollout of the vaccine would be to significantly curb infection rates and spread of the disease. However, experts have urged the public not to see vaccines as a replacement for other preventative measures, such as bed nets and the spraying of insecticides.

The WHO also issued a recommendation on a Takeda Pharmaceuticals-produced vaccine against dengue, a disease prevalent in subtropical climates which, like malaria, is spread by mosquitoes.

Takeda Pharmaceuticals’ vaccine was shown to be effective in all four stereotypes of the virus in previously infected individuals, but it showed a lower performance in some stereotypes of people not previously infected.

Some information for this report was provided by The Associated Press and Reuters. 

Nobel Prize Awarded to mRNA COVID-19 Vaccine Scientists

Two scientists who jointly worked on the ground-breaking technology behind some of the most effective COVID-19 vaccines have been awarded the 2023 Nobel Prize for medicine, one of the most prestigious accolades in the field.

Hungarian American scientist Katalin Kariko and her American colleague, Drew Weissman, began working on so-called “mRNA” technology in the early 1990s at the University of Pennsylvania. Their breakthrough was crucial in developing the Moderna and Pfizer-BioNtech coronavirus vaccines, which have proved among the most effective in tackling COVID-19.

Lifesaving vaccines

The Nobel Prize in Medicine Committee in Sweden said the discovery had helped defeat one of the greatest threats to human health in modern times.

“mRNA vaccines, together with other COVID-19 vaccines, have been administered over 13 billion times. Together, they have saved millions of lives, prevented severe COVID-19, reduced the overall disease burden, and enabled societies to open up again,” Nobel committee member Rickard Sandberg told reporters following the announcement Monday.

“mRNA technologies are now being used to develop vaccines against other infections. The technology may also be used for therapeutic protein delivery and cancer treatment in the hope of further improving human health,” Sandberg said.

World Health Organization Director-General Tedros Adhanom Ghebreyesus congratulated the Nobel Prize winners Monday. “Today is a great day for health, a great day for science and a great day for vaccines,” he told reporters in Geneva.

mRNA Technology

mRNA — or messenger RNA — instructs cells to make proteins that match those found on the surface of pathogens, like the coronavirus. The body sees these as invaders and makes antibodies and T-cells to attack them; thus, training it to deal with a real virus in the future.

Kariko and Weissman first met while lining up to use a photocopier machine at the University of Pennsylvania in the early 1990s.

By 2005, the pair had worked out a way to stop the immune system from attacking RNA made in the laboratory, previously seen as a major hurdle against its use.

Kariko said Monday they made a good team.

“I was the RNA person and Drew was [the] immunologist, and we educated each other. And together we learned [from] each other and developed mRNA,” she told The Associated Press.

Future applications

Weissman said the future potential for mRNA was incredible.

“We’ve been thinking for years about everything that we could do with RNA, and now it’s here,” he told AP.

The coronavirus pandemic accelerated the development of mRNA technology, said Paul Hunter, a professor of medicine at Britain’s University of East Anglia.

“Prior to COVID, people knew that work was being done on mRNA vaccines,” he told VOA. “But I don’t think we were ever close to getting real-world use of the technology. Now that it’s been shown to work — to work probably better than many if not most other vaccine types — I think is a big boost to it, and there are a substantial number of potential uses of this technology.

“Then there is the speed of the development of this technology,” he added. “It’s a lot easier now and a lot quicker to develop new vaccines.”

Cancer hope

The chair of the Nobel Committee for Medicine, Gunilla Karlsson-Hedestam, expressed hope that mRNA technology could one day be used to fight cancer.

“Vaccines that are targeted towards specific kinds of tumors, maybe even to specific individuals or personalized cancers. That will become an area that this platform is really ideally suited for, because of the flexibility,” she told Reuters.

Kariko and Weissman share the prize of $1 million and will receive their medals at a ceremony in Stockholm in December.

Kenya Panel Urges Shutdown of Worldcoin’s Crypto Project Within Country

A Kenyan parliamentary panel called on the country’s information technology regulator on Monday to shut down the operations of cryptocurrency project Worldcoin within the country until more stringent regulations are put in place.

The government suspended the project in early August following privacy objections over its scanning of users’ irises in exchange for a digital ID to create a new “identity and financial network.”

Worldcoin was rolled out in various countries around the world by Tools for Humanity, a company co-founded by OpenAI CEO Sam Altman. It has also come under scrutiny in Britain, Germany and France.

The project still has a virtual presence in Kenya and can be accessed via the internet, even after the August suspension.

The regulatory Communications Authority of Kenya should “disable the virtual platforms of Tools for Humanity Corp and Tools for Humanity GmbH Germany [Worldcoin] including blacklisting the IP addresses of related websites,” the ad hoc panel of 18 lawmakers said in a report.

It also called for the suspension of the companies’ “physical presence in Kenya until there is a legal framework for regulation of virtual assets and virtual services providers.”

Worldcoin’s press office said it had “not seen anything official announced by the Committee directly.”

The panel’s report will be tabled at the National Assembly for consideration and adoption at a later date.

During the suspension of data collection in August, authorities said the project’s method of obtaining consumer consent in return for a monetary award of just over $50 at the time bordered on inducement.

Registering to use the platform involved long lines of people queuing to get their irises scanned. The parliamentary panel’s investigation found that Worldcoin may have scanned the eyes of minors as there was no age-verification mechanism during the exercise, its report said.

The panel also asked government ministries to develop regulations for crypto assets and firms that provide crypto services and called on the police to investigate Tools for Humanity and take any necessary legal action.

Endangered Sumatran Rhino Born in Indonesia

An endangered Sumatran rhinoceros, the smallest and hairiest of the five extant rhino species, was born in Indonesia last week in a conservation area, the government said Monday. 

Weighing about 27 kilograms (59.52 lbs.), the yet-to-be named female calf, was born Saturday at the Sumatran Rhino Sanctuary (SRS) facility in Way Kambas National Park, Lampung province in the tropical Southeast Asian country. 

Covered in black hair, the newborn stood about 45 minutes after her birth. On the next day, she began to walk around the jungle, the environment ministry said in a statement. 

The mother, 22-year-old Ratu, was in a healthy condition, the ministry said. 

Ratu is a native of Lampung, while her mate, Andalas, aged 23, was born at the Cincinnati Zoo, in the midwestern U.S. state of Ohio, but has since moved to the same park as Ratu. 

The pair previously had Delilah in 2016 and Andatu in 2021. 

“This is a happy news, not only for Indonesia but for the world,” Indonesia’s environment minister, Siti Nurbaya, said in the statement. 

There were just 80 Sumatran rhinos left in the world, based on a 2019 assessment of threatened species by the Indonesian government. 

The mammal, also known by the scientific name, Dicerorhinus sumatrensis, is the only Asian rhino with two horns and can grow up to 1.5 meters-tall, weighing between 500 kg to 960 kg (1,102 lbs. to 2,116 lbs.). 

Deadly Dengue Outbreak in Bangladesh 

More than 1,000 people have died from dengue fever in Bangladesh this year, making 2023 the deadliest year due to dengue, since the disease was first detected in the country, according to government figures.

The Directorate General of Health Services said that more than 200,000 dengue cases were recorded this year.

In a recent 24-hour period, nearly 3,000 were admitted to hospitals because of dengue, the Daily Star newspaper said.

The Mayo Clinic says dengue fever is “a mosquito-borne illness that occurs in tropical and subtropical areas of the world. Mild dengue fever causes a high fever and flu-like symptoms. The severe form of dengue fever, also called dengue hemorrhagic fever, can cause serious bleeding, a sudden drop in blood pressure [shock] and death.”

“All our efforts to control the mosquito population have been ineffective,” Mushtaq Hussain, a consultant at Bangladesh’s Institute of Epidemiology, Disease Control and Research, told The Daily Star. He said the extended monsoon season is another contributing factor to the high case load.

Some information for this report came from AFP.

Nobel in Medicine Goes to 2 Scientists Whose Work Enabled Creation of COVID-19 Vaccines

Two scientists won the Nobel Prize in medicine on Monday for discoveries that enabled the development of mRNA vaccines against COVID-19.

The award was given to Katalin Karikó, a professor at Sagan’s University in Hungary and an adjunct professor at the University of Pennsylvania, and Drew Weissman, who performed his prizewinning research together with Karikó at the University of Pennsylvania.

“Through their groundbreaking findings, which have fundamentally changed our understanding of how mRNA interacts with our immune system, the laureates contributed to the unprecedented rate of vaccine development during one of the greatest threats to human health in modern times,” the panel that awarded the prize said.

Thomas Perlmann, secretary of the Nobel Assembly, announced the prize and said both scientists were “overwhelmed” by news of the prize when he contacted them shortly before the announcement.

Gunilla Karlsson Hedestam, part of the panel that chose the winners, said of their work that “in terms of saving lives, especially in the early phase of the pandemic, it was very important.”

The Nobel Prize in physiology or medicine was won last year by Swedish scientist Svante Paabo for discoveries in human evolution that unlocked secrets of Neanderthal DNA which provided key insights into our immune system, including our vulnerability to severe COVID-19.

The award was the second in the family. Paabo’s father, Sune Bergstrom, won the Nobel Prize in medicine in 1982.

Nobel announcements continue with the physics prize on Tuesday, chemistry on Wednesday and literature on Thursday. The Nobel Peace Prize will be announced Friday and the economics award on Oct. 9.

The prizes carry a cash award of 11 million Swedish kronor ($1 million). The money comes from a bequest left by the prize’s creator, Swedish inventor Alfred Nobel, who died in 1896.

The prize money was raised by 1 million kronor this year because of the plunging value of the Swedish currency.

The laureates are invited to receive their awards at ceremonies on Dec. 10, the anniversary of Nobel’s death. The prestigious peace prize is handed out in Oslo, according to his wishes, while the other award ceremony is held in Stockholm.

Swiss-Led Team Drives Electric Vans From Geneva to Doha, Qatar

A Swiss-led team has driven electric vans across Europe and the Arabian Peninsula to Qatar to showcase zero-emission battery powered vehicles, organizers said Sunday.

The five-strong Swiss and German team set out from Geneva on August 28 in two electric Volkswagen vans on a 6,500 kilometer (4,000 mile) journey that ended in Doha on Saturday.

“The motivation was really to do something unusual,” the group’s leader Frank Rinderknecht told AFP. “Certainly we did have the risk of not arriving — technical issues, health issues or an accident.”

The journey aimed to raise awareness about the environmental benefits of electric vehicles, he said. “If our trip put just a little bit of rethinking, of initiative, into people’s minds then I am not unhappy.”

The journey started with a crossing of the Swiss Alps and included what organizers believe was the first west-to-east crossing of Saudi Arabia with electric vehicles.

The team’s ID. Buzz VW vans — modelled on the German manufacturer’s Combi campervan — travelled across 12 countries, reaching Aqaba in Jordan from Turkey by ship.

However, the trip highlighted shortcomings of the charging infrastructure, Rinderknecht said, comparing the mismatch of technologies to the “early days of telecommunication.”

In Europe, the team had to use numerous apps to pay for charging points across different regions. In Jordan, they had to adapt their European systems to the Chinese hardware they found.

The journey to Doha was completed in partnership with the Geneva International Motor Show, which is being held outside the Swiss city for the first time since its inception in 1905.

The 10-day motor show to be held in Qatar from October 5 will feature 31 automotive brands and overlap with the October 8 Qatar Grand Prix at the Lusail International Circuit on Doha’s northern outskirts.

Saad Ali Al Kharji, deputy chairman of Qatar Tourism, said holding events like the motor show was part the gas-rich Gulf state’s “strategic vision of becoming the fastest-growing destination in the Middle East by 2030.”

South Sudan Faces Growing Health and Hunger Crisis   

The World Health Organization warns that soaring rates of severe malnutrition, acute hunger, and deteriorating health conditions are threatening the lives and well-being of millions of people in South Sudan with the situation set to worsen as the climate crisis kicks in.

“South Sudan is a country where you see the overlap and compounding impact of conflict, climate crisis, hunger crisis, and disease outbreaks that have been going on for several years,” said Liesbeth Aelbrecht, WHO incident manager for the Horn of Africa. “Three in four South Sudanese need humanitarian assistance this year; two in three are facing crisis levels of hunger,” she said. “And these numbers are only getting worse.”

The United Nations reports 6.3 million South Sudanese are suffering from acute hunger and more than 9 million of the country’s population of 12 million people depend on humanitarian assistance.

As conditions continue to deteriorate, the World Health Organization reports 500,000 more people this year will need international aid. Among the most vulnerable are the children.

Aelbrecht said, “The numbers of children with severe malnutrition needing medical intervention have been higher this year than at any point in the last four years,” adding that almost 150,000 children had been treated for severe acute malnutrition so far this year.

She warned the humanitarian crisis facing South Sudan will worsen with the onset of El Niño, a climate phenomenon that can cause temperatures to rise and excess rains.

“Flooding and hunger and drought will increase hunger even further. But it is also very likely to increase the risk of mosquito-borne diseases, especially malaria and dengue and water-borne diseases,” she said, adding that malaria is one of the five main causes of death in South Sudan.

Aelbrecht recently returned from a mission to South Sudan, where she visited so-called stabilization centers for severely malnourished children in the capital, Juba, and in Bentiu, the capital of Unity State.

Speaking Friday from the Kenyan capital, Nairobi, to journalists in Geneva, Aelbrecht said she watched doctors trying to resuscitate babies on life support. In one of these centers, she said she saw a baby pass away in her mother’s arms.

“I quote figures. I give you percentages, but behind those figures there are just faces. I am standing there as a bystander and watching this child die of hunger and of preventable diseases,” she said. “Even after doing humanitarian work for 25 years now, it does remain one of the most difficult things to do.”

She said the international community must not act as a bystander but help South Sudan during this time of immense need. Since conflict in Sudan erupted in April, she said there has been a large inflow of refugees and returnees from Sudan, putting an even greater strain on South Sudan’s overstretched health system.

“In fact, one out of four of all the people who had fled Sudan, 1.2 million people who fled Sudan are being hosted now in South Sudan,” she said.

The Office for the Coordination of Humanitarian Affairs, OCHA, reports humanitarian operations in both Sudan and South Sudan are severely underfunded. It says lack of security in these countries is also a huge hindrance to the delivery of aid to the millions in need.

“South Sudan and Sudan are the world’s most dangerous countries for aid workers,” said Jens Laerke, OCHA spokesman.

Of 71 aid worker deaths recorded so far this year, he said 22 were in South Sudan and 19 in Sudan.

“The victims are overwhelming local humanitarians working on the front lines of the response,” he said.

New Report Gives Mexicans Hope for Long-Awaited Mine Cleanup

Nine years after a massive waste spill from a copper mine in the northern Mexican border state of Sonora, locals are still suffering from “alarming” levels of soil, air and water pollution, Mexico’s Environment Department said Thursday.

Summarizing a 239-page report, officials also confirmed, using satellite images, that the spill was not solely caused by dramatic rainfall, as was initially reported, but by the “inadequate design” of a dam at Buenavista del Cobre mine, owned by the country’s largest copper producer, Grupo México.

Locals and environmental advocates say the report offers the clearest view yet of the catastrophic scale of the accident and, with it, new hope that Grupo México may finally be held financially accountable after almost a decade of legal battles and broken promises.

“We expect that, with this new document, we’ll have an easy path for getting the money,” said Luis Franco, a community coordinator with regional advocacy group PODER. “At the moment, I’m happy but at the same time I know this is just the beginning for the people of Sonora,” he said. “We have to keep fighting.”

On Aug. 6, 2014, after heavy rainfall, 40 million liters of acidified copper sulfate flooded from a waste reservoir at Buenavista mine into the Sonora and Bacanuchi rivers, just under 100 kilometers from the border city of Nogales, Sonora.

After the spill, Grupo México first agreed to give 1.2 billion pesos (about $68 million) to a recovery fund, but in 2017 that trust was closed and the remaining funds returned to the mining company, PODER claims. After a legal battle, the trust was reopened three years later but, said Franco, without any new funding.

Mexico’s environmental secretary María Luisa Albores González insisted Thursday during a news briefing that the report was solely “technical,” not “ideological,” but added that the trust would remain open until 2026.

“We in this institution do not accept said trust is closed,” said Albores González.

In another report earlier this year Mexico’s National Institute of Ecology and Climate Change calculated the total cost of the spill at over 20 billion pesos ($1.1 billion), more than 16 times the size of the original support fund.

“Under no circumstances” have locals been given enough money to recover, according to the report. “Neither the amount paid for the fine, nor the compensation given to the Sonora River Trust cover the direct, indirect or cumulative effects on the population, the ecosystem or the economy.”

The initial fund promised to open 36 water treatment stations and a toxicology clinic. But according to the Sonora River Basin Committees, a group of locals from the eight polluted townships, only one water station is open and the clinic has long been abandoned.

Unsafe levels of arsenic, lead and mercury have been recorded across over 250 square kilometers around the spill. Across the Sonoran townships of Ures, Arizpe, Baviácora, Aconchi, Banamichi, Cananea, Huépac and San Felipe de Jesús, locals have complained of health risks and decreased productivity in their farms and ranches.

In what officials described as one of their most “alarming” findings, 93% of soil samples from the city of Cananea did not meet international requirements for arsenic levels.

Adrián Pedrozo Acuña, director general for the Mexican Institute for Water Technology, said the pollution had also impacted the region’s drinking water. “The results presented here show very clearly that there is a safety or health problem in the water the population consumes,” he said.

Franco, who lives in the nearby city of Hermosillo, said this brings the most urgency for communities in which many cannot afford to buy bottled water.

Since the spill, Buenavista del Cobre has continued to operate — and grown in size. In the years immediately before the accident production increased threefold, according to Pedrozo. By 2020 it had grown half as big again, in what he described as “chronic overexploitation” of the area’s water supplies.

New Zealand PM Tests Positive for COVID 2 Weeks Before Election

New Zealand Prime Minister Chris Hipkins has tested positive for COVID-19 and will work remotely while isolating, his office said Sunday, just two weeks before a general election in which his Labour party is struggling.

The positive test will temporarily sideline Hipkins in the campaign for the Oct. 14 election. Labour has been sliding in the opinion polls, with the center-right National party leading by 31.9% to 26.5% in a recent survey.

Hipkins has cold and flu symptoms that began Saturday and will isolate for five days or until he returned a negative test, the prime minister’s office said in a statement.

“He will continue with engagements he can undertake via Zoom,” the statement said.

Deputy Prime Minister Carmel Sepuloni would stand in for Hipkins at a Samoan church service in Auckland on Sunday, a spokesperson said.

“Thanks to all of Labour’s great volunteers and supporters who I know will keep our campaign going in my absence,” Hipkins said on his official Facebook page. “There’s a lot at stake this election, and I’ll be working doubly hard when I can get back out there to make sure Labour is reelected.”

The prime minister’s office said further updates on his schedule “will be provided in due course.”

The government removed its last COVID restrictions in August, but health authorities still recommend that people stay home for five days if feeling unwell or if they have tested positive.

Biden Signs Bill to Fund US Government, Avoid Shutdown

President Joe Biden has signed a bill to fund the U.S. government through mid-November and avoid a shutdown, less than an hour before money for federal agencies was set to run out.

Biden posted a picture of himself signing the bill on X, the social media platform previously known as Twitter, late Saturday night. In the message, he urged Congress to get to work immediately to pass funding bills for the full fiscal year.

The U.S. Senate, in a rare weekend meeting, approved a funding bill Saturday night, sending it to President Joe Biden for his signature and averting a widely dreaded shutdown of the federal government.

The bill, which passed the Senate 88-9 after winning approval in the House of Representatives, would fund the federal government through Nov. 17. The bill contains $16 billion in disaster aid sought by Biden but did not include money to help Ukraine in its war against Russia’s invasion.

After the vote, Biden released a statement saying the bill’s passage prevented “an unnecessary crisis that would have inflicted needless pain on millions of hardworking Americans.”

“We will have avoided a shutdown,” Senate Majority Leader Chuck Schumer said in a statement after the vote. “Bipartisanship, which has been the trademark of the Senate, has prevailed. And the American people can breathe a sigh of relief.”

Had the bill not been approved by Congress and signed by the president by midnight Saturday, the federal government would have shut down.

More than 4 million U.S. military service personnel and government workers would not be paid, although essential services, such as air traffic control and official border entry points would still be staffed. Pensioners might not get their monthly government payments in time to pay bills and buy groceries, and national parks could be closed.

For days all of that seemed inevitable.

The abrupt turn of events began Saturday when Speaker of the House Kevin McCarthy changed tactics and put forward the funding bill that hard-line members of his Republican caucus opposed.

The House passed the bill, 335-91. More Democrats supported it than Republicans, even though it does not contain aid for Ukraine, a priority for Biden, Democrats and many Senate Republicans.

“Extreme MAGA Republicans have lost, the American people have won,” top House Democrat Hakeem Jeffries told reporters ahead of the vote.

Republican Representative Lauren Boebert criticized the passage of the short-term stopgap bill.

“We should have forced the Senate to take up the four appropriations bills that the House has passed. That should have been our play,” she told CNN. “We should have forced them to come to the negotiating table, to come to conference, to hash out our differences.”

McCarthy is likely to face a motion from the right-wing members of his party to remove him as speaker.

“If somebody wants to remove me because I want to be the adult in the room, go ahead and try,” McCarthy said of the threat to oust him. “But I think this country is too important.”

Ukraine aid still likely

In his statement, Biden noted the lack of funding for Ukraine in the bill and said, “We cannot under any circumstances allow American support for Ukraine to be interrupted.”

Support for Ukraine remains strong in Congress and late Saturday night, a bipartisan group of Senate leadership members, led by Schumer and Minority Leader Mitch McConnell, released a statement vowing to ensure the United States continues “to provide critical and sustained security and economic support for Ukraine.”

NBC News quoted an unnamed U.S. official as saying Biden and the Defense Department have funds to meet Ukraine’s battlefield needs “for a bit longer,” but it is “imperative” that Congress pass a Ukraine funding bill soon.

In the House, the lone Democrat to vote against the funding bill was Representative Mike Quigley of Illinois, the co-chair of the Congressional Ukraine Caucus. “Protecting Ukraine is in our national interest,” he said.

“This does look very chaotic, but this is not the first time it’s happened,” Todd Belt, director of the school of political management at The George Washington University, told VOA. “There is a price that has to be paid here. But that is the price of democracy. It does seem very messy sometimes. But eventually, usually you get some compromise.”

Such shutdowns have occurred four times in the last decade in the U.S., but often have lasted just a day or two until lawmakers reach a compromise to fully restart government operations. However, one shutdown that occurred during the administration of former President Donald Trump lasted 35 days, as he unsuccessfully sought funding to build a wall along the U.S.-Mexican border.

FDA to Regulate Thousands of Lab Tests That Have Long Skirted Oversight

The Food and Drug Administration on Friday laid out a proposal to begin regulating laboratory medical tests, a multibillion-dollar industry that the agency says poses a growing risk to patients because of potentially inaccurate results.

The proposed rule would end decades of regulatory ambiguity and formally bring thousands of tests performed in large laboratories under FDA oversight. FDA Commissioner Robert Califf said the change will help ensure tests used to diagnose cancer, heart disease and many other conditions are safe, accurate and reliable.

“A growing number of clinical diagnostic tests are being offered as laboratory-developed tests without assurance that they work,” Califf said in a statement. He added that the agency has long worried that many tests offered by laboratories are not as accurate or reliable as those that undergo FDA review.

Here’s a look at the history and background of the testing issue:

What are laboratory-developed tests?

Most Americans are familiar with medical tests like those used to screen for COVID-19, strep throat and other health conditions. Those tests are developed by a handful of large manufacturers that undergo FDA review before selling their test kits to hospitals, doctors offices or pharmacies.

The tests targeted by the FDA’s latest action are developed and used by high-tech laboratories, including those at academic medical centers and companies such as Quest Diagnostics. They include tests for complex diseases like cancer, as well as simpler conditions like high cholesterol and sexually transmitted infections.

Over time, laboratory-developed tests have grown into a multibillion-dollar nationwide business, with labs processing thousands of blood, urine and other samples per week from hospitals and clinics. Others advertise directly to consumers — including some claiming to measure the risk of developing ailments like Alzheimer’s and autism.

Laboratory-developed tests have long skirted FDA oversight, though the agency has maintained that it has the authority to step in. The debate over regulating the space stretches back to the 1990s, with several government advisory groups recommending greater FDA oversight.

Why does the FDA want to regulate them now?

Many lab-developed tests are staples of medical care, used to make important decisions about pregnancy, nutrition and many other health issues.

FDA officials have long voiced concerns about the accuracy of some tests, pointing to patients who have received inaccurate results for heart disease, Lyme disease, cancer and other conditions. Inaccurate tests can lead to patients getting an incorrect diagnosis, skipping treatments or receiving unnecessary medication or surgery.

More than a decade ago, the agency drafted tougher guidelines for the industry, but they were never finalized.

The tests attracted new scrutiny with the downfall of Theranos CEO and founder Elizabeth Holmes, who was sentenced to prison last year for misleading investors about the potential of her company’s blood testing technology.

What do test makers say?

The laboratory industry has long argued that FDA regulation would stifle their ability to quickly innovate and develop new tests. They also say that additional federal regulation is unnecessary because it would duplicate existing requirements.

Under a quirk of federal law, testing laboratories are overseen by the same agency that runs Medicare and Medicaid, the government health plans for seniors, the disabled and the poor. Inspectors evaluate the general conditions and procedures at labs, but not specific tests or the claims used to market them.

Lawmakers in Congress drafted a bill last year — backed by FDA officials — that would have given the FDA explicit authority to regulate high-risk tests. But the measure failed to pass the House or the Senate amid opposition by testing industry lobbyists.

What is the FDA proposing?

Under the new proposal, FDA would gradually phase in tighter regulation of lab tests over five years. The agency is considering exempting some existing tests from review but is seeking public input on its approach. At the end of the process, most new tests would be subject to FDA standards and regulatory review before launching.