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JFK assassination files released, sending history buffs hunting for new clues

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By JAMIE STENGLE, Associated Press

DALLAS (AP) — More than 63,000 pages of records related to the 1963 assassination of President John F. Kennedy were released Tuesday following an order by President Donald Trump, many without the redactions that had confounded historians for years and helped fuel conspiracy theories.

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The U.S. National Archives and Records Administration posted to its website roughly 2,200 files containing the documents. The vast majority of the National Archives’ collection of over 6 million pages of records, photographs, motion pictures, sound recordings and artifacts related to the assassination have previously been released.

Larry J. Sabato, director of the University of Virginia Center for Politics and author of “The Kennedy Half-Century,” said it will take time to fully review the records.

“We have a lot of work to do for a long time to come, and people just have to accept that,” he said.

Trump announced the release Monday while visiting the John F. Kennedy Center for the Performing Arts in Washington, saying his administration would be releasing about 80,000 pages.

“We have a tremendous amount of paper. You’ve got a lot of reading,” Trump said.

Before Tuesday, researchers had estimated that 3,000 to 3,500 files were still unreleased, either wholly or partially. And just last month the FBI said it had discovered about 2,400 new records related to the assassination.

Jefferson Morley, vice president of the Mary Ferrell Foundation, a repository for files related to the assassination, said in a statement posted on the social platform X that the release is “an encouraging start.” He said much of the “rampant overclassification of trivial information has been eliminated” from the documents.

The National Archives said on its website that in accordance with the president’s directive, the release would encompass “all records previously withheld for classification.” But Morley said what was released Tuesday did not include two-thirds of the promised files, any of the recently discovered FBI files or 500 Internal Revenue Service records.

“Nonetheless, this is the most positive news on the release of JFK files since the 1990s,” Morley said.

 

Interest in details related to Kennedy’s assassination has been intense over the decades, with countless conspiracy theories spawned about multiple shooters and involvement by the Soviet Union and mafia.

He was killed Nov. 22, 1963, on a visit to Dallas, when his motorcade was finishing its parade route downtown and shots rang out from the Texas School Book Depository building. Police arrested 24-year-old Lee Harvey Oswald, who had positioned himself from a sniper’s perch on the sixth floor. Two days later nightclub owner Jack Ruby fatally shot Oswald during a jail transfer.

A year after the assassination, the Warren Commission, which President Lyndon B. Johnson established to investigate, concluded that Oswald acted alone and that there was no evidence of a conspiracy. But that didn’t quell a web of alternative theories over the decades.

Oswald was a former Marine who defected to the Soviet Union before returning home to Texas.

Files in the new release included a memo from the CIA’s St. Petersburg station from November 1991 saying that earlier that month, a CIA official befriended a U.S. professor there who told the official about a friend who worked for the KGB. The memo said the KGB official had reviewed “five thick volumes” of files on Oswald and was “confident that Oswald was at no time an agent controlled by the KGB.”

The memo added that as Oswald was described in the files, the KGB official doubted “that anyone could control Oswald, but noted that the KGB watched him closely and constantly while he was in the USSR.” It also noted that the file reflected that Oswald was a poor shot when he tried target firing in the Soviet Union.

In the early 1990s, the federal government mandated that all assassination-related documents be housed in a single collection in the National Archives and Records Administration. The collection was required to be opened by 2017, barring any exemptions designated by the president.

Trump, who took office for his first term in 2017, had said that he would allow the release of all of the remaining records but ended up holding some back because of what he called the potential harm to national security. And while files continued to be released during President Joe Biden’s administration, some remained unseen.

Sabato said that his team has a “long, long list” of sensitive documents it is looking for that previously had large redactions.

“There must be something really, really sensitive for them to redact a paragraph or a page or multiple pages in a document like that,” he said. “Some of it’s about Cuba, some of it’s about what the CIA did or didn’t do relevant to Lee Harvey Oswald.”

Some of the previously released documents have offered details on the way intelligence services operated at the time, including CIA cables and memos discussing visits by Oswald to the Soviet and Cuban embassies during a trip to Mexico City just weeks before the assassination.

Associated Press writer John Hanna contributed from Topeka, Kansas.

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Robert Pearl: GenAI will save lives — If properly applied

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In medicine, rare moments arise when technological breakthroughs and shifts in leadership create an opportunity for sweeping change. The United States now stands at that crossroad.

A major advance in artificial intelligence, combined with a shake-up at the highest levels of federal healthcare leadership, has the potential to save hundreds of thousands of lives, make medical care affordable and ease the burnout crisis among doctors and nurses.

But there’s a risk this potential will go unrealized. The newly appointed Secretary of Health and Human Services (HHS) Robert F. Kennedy Jr. and Dr. Marty Makary, the incoming head of the Food and Drug Administration (FDA), must move swiftly to capitalize on what U.S. Vice President JD Vance recently called, “One of the most promising technologies we have seen in generations.”

For the first time, generative AI isn’t solely the domain of billion-dollar companies. Instead, entrepreneurial and midsize companies can build tools for patients without having to raise massive amounts of capital.

A new generative AI model, DeepSeek-V3, recently emerged from China, and unlike models built by OpenAI, Google or Anthropic, it wasn’t developed with billions of dollars in funding. DeepSeek used a technique called “knowledge distillation” that allows GenAI applications to learn from existing models faster, cheaper and with greater efficiency.

While DeepSeek is free to use for Americans, there are serious concerns about data retention policies and privacy issues for data stored on servers in China. However, the biggest advance won’t derive from the use of DeepSeek in America but from the rapid advancement of American open-source AI packages. This means any company, researcher or startup will soon be able to access and refine it to build tools for patients. If RFK Jr. and Makary act quickly, they can unlock AI’s full potential before red tape strangles it.

But where will innovative companies find the biggest opportunity to save lives and make medical care affordable?

America is currently mired in an urgent and worsening crisis of chronic disease, which affects 60% of Americans and drives 70% of healthcare costs. Right now, most chronic diseases are poorly managed. Hypertension, diabetes, and heart failure remain uncontrolled in at least 40% of U.S. cases, leading to millions of avoidable strokes, heart attacks, kidney failures and cancers each year. According to CDC estimates, effective control of these conditions would prevent 30%–50% of these life-threatening events.

Rather than spending hundreds of millions to build AI “large language models” from scratch, healthcare startups will be able to create their own generative AI tools at a fraction of the cost. But unlike today’s broad AI applications, which answer general medical questions, this next generation of generative AI will be different. It will be hyper-specialized, trained on massive amounts of existing (but largely unused) patient data to monitor and manage these chronic diseases.

Right now, 97% of hospital bedside monitor data is discarded, never analyzed to improve patient care. Similarly, today’s GenAI models have never been trained on millions of hours of recorded medical-call-center conversations and chronic disease management check-ins that provide medical advice and offer personalized care recommendations.

Here’s how it could work: For a newly diagnosed patient with diabetes or hypertension, GenAI-enabled wearable monitors would continuously track blood sugar or blood pressure, analyzing fluctuations in real time. And for patients, instead of waiting four months for a routine follow-up visit, the new AI system would identify poor chronic disease control months earlier, provide timely medical advice and flag issues for clinicians when medication adjustments are needed — all for an estimated cost of less than $9 per hour.

For heart failure patients, GenAI-driven monitoring tools would assess daily clinical status, detecting subtle signs of deterioration before a full-blown crisis occurs. Instead of being rushed to the hospital two days later when they can’t breathe, patients and their doctors would receive early alerts, allowing for immediate intervention and eliminating the need for hospitalization.

These disease-specific GenAI agents won’t replace doctors. They’ll fill the gaps between office visits, identify patients at risk, and provide continuous and data-driven care, lowering costs and decreasing daily demands on clinicians.

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Despite AI’s potential to save lives and lower healthcare costs, outdated FDA regulations threaten to stall these innovations before they can reach patients.

The agency has long treated AI like a traditional drug or medical device, demanding information on the data sources and expecting years-long clinical trials. This isn’t how GenAI operates. Unlike pharmaceuticals that keep the same chemical structure, GenAI systems continuously learn and improve — a process driven by the application itself.

RFK Jr. and Makary have a rare opportunity to fix the burdensome regulatory process and lower the barriers to implementation. While Kennedy’s stance on vaccines has drawn criticism, his stated commitment to public health and tackling chronic disease aligns with what GenAI can achieve. Meanwhile, Makary has built a reputation for patient safety and challenging outdated medical policies. He is likely to recognize the value GenAI provides for patients.

Rather than forcing GenAI-driven disease management programs to fit into an antiquated approval model, HHS and the FDA should encourage the development of these programs and fast-track implementation by:

— Prioritizing GenAI applications that focus on diabetes, hypertension, heart failure and similarly high-impact chronic diseases.

— Comparing GenAI-driven programs to existing clinician-led models rather than some hypothetically perfect model. When GenAI-powered disease management tools can outperform humans by at least 10% in advice quality, successful disease control and patient satisfaction, they should be given FDA approval.

As U.S. life expectancy remains stagnant, and over half the population can’t afford medical care, the window for action is narrowing. RFK Jr. and Makary must act now to modernize the approach the HHS and FDA take to GenAI. If not, bureaucratic inertia will lock American medicine in the past.

Dr. Robert Pearl is a Stanford University professor, Forbes contributor, bestselling author, and former CEO of The Permanente Medical Group. He wrote this column for The Fulcrum, a nonprofit, nonpartisan news platform covering efforts to fix our governing systems.

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