Florida teenager

Florida teenager facing 30 felony charges over Twitter hack | TheHill – The Hill

A Florida teenager and two others have been arrested for allegedly being behind a major Twitter hack earlier this month that resulted in several prominent accounts posting messages for a bitcoin scam.

The Department of Justice announced that U.K. resident Mason Shepard, 19, and Orlando resident Nima Fazeli, 22, who go by the hacking aliases “Chaewon” and “Rolex” respectively, were charged with helping carry out the hack. A third person, a 17-year-old who lives in Tampa, has also been charged.

The 17-year-old is facing 30 felony charges including organized fraud, communications fraud, identity theft and hacking, carrying potential penalties of more than $100,000. Those charges have been filed by Hillsborough State Attorney Andrew Warren in Florida, who described the teenager as the “mastermind” of the hack.

Shepard and Fazeli, meanwhile, have been charged in federal court in California. Shepard was charged with computer intrusion, wire fraud conspiracy and money laundering conspiracy, with the most serious charge bringing 20 years in prison and a $250,000 fine. Fazeli was charged with one count of computer intrusion, which carries a max sentence of five years and a $250,000 fine.

The hack, which took place July 15, affected a number of prominent Twitter accounts, including those of former President Obama, former Vice President Joe BidenJoe BidenTrump campaign cancels ad buys to review messaging strategy: report Nunes declines to answer if he received information from Ukraine lawmaker meant to damage Biden Poll: Plurality of ‘Gen Z’ voters say they see more political ads from Trump than Biden MORE, Microsoft co-founder Bill Gates and Tesla CEO Elon MuskElon Reeve MuskReforming environmental review to build a cleaner and brighter future Is it time to designate social media as ‘critical infrastructure’? Hillicon Valley: Senior intelligence official warns Russia, Iran and China targeting elections | Trump says he ‘often’ regrets his tweets | Tech CEO hearing postponed for John Lewis services MORE, among others.

Authorities say the defendants were able to reap more than $100,000 in bitcoin by posting messages on the hacked accounts asking followers to send funds.

Twitter later said that the hackers obtained employee credentials, allowing them to target 130 accounts, tweeting from 45, accessing direct message inboxes of 36 and downloading data from seven. Twitter temporarily prevented verified accounts from tweeting on the day of the incident, and announced an immediate investigation into what occurred.

“There is a false belief within the criminal hacker community that attacks like the Twitter hack can be perpetrated anonymously and without consequence,” U.S. Attorney David Anderson said in a statement Friday. “Today’s charging announcement demonstrates that the elation of nefarious hacking into a secure environment for fun or profit will be short-lived. Criminal conduct over the Internet may feel stealthy to the people who perpetrate it, but there is nothing stealthy about it.”

“In particular, I want to say to would-be offenders, break the law, and we will find you,” Anderson said.

The FBI announced earlier this month that it was launching an investigation into the hack. Special Agent in Charge John Bennett on Friday highlighted the unusual speed of the charges being brought against the defendants.

“While investigations into cyber breaches can sometimes take years, our investigators were able to bring these hackers into custody in a matter of weeks,” Bennett said. “Regardless of how long it takes us to identify hackers, we will follow the evidence to where it leads us and ultimately hold those responsible for cyber intrusions accountable for their actions. Cyber criminals will not find sanctuary behind their keyboards.”

The state attorney told local NBC affiliate WFLA that the 17-year-old in Florida was arrested by federal authorities on Friday and turned over to state officials, who have filed charges against him.

“Working together, we will hold this defendant accountable,” Warren said in a statement. “Scamming people out of their hard-earned money is always wrong. Whether you’re taking advantage of someone in person or on the internet, trying to steal their cash or their cryptocurrency—it’s fraud, it’s illegal, and you won’t get away with it.” 

The Internal Revenue Service and the Secret Service were also involved in the investigation into the hack.

Twitter has posted consistent updates on its investigation into the hacking incident, tweeting Thursday night that the hackers gained access to the accounts through a mobile phone spear phishing attack. This attack allowed the individuals to obtain the credentials of Twitter employees with access to the compromised accounts.

Twitter said it had “significantly limited access to internal tools and systems” as it continued to make improvements stemming from the hacking incident.

“This was a striking reminder of how important each person on our team is in protecting our service,” the company tweeted. “We take that responsibility seriously and everyone at Twitter is committed to keeping your information safe.”

“We appreciate the swift actions of law enforcement in this investigation and will continue to cooperate as the case progresses,” Twitter said in a statement Friday.

We appreciate the swift actions of law enforcement in this investigation and will continue to cooperate as the case progresses. For our part, we are focused on being transparent and providing updates regularly.

For the latest, see here :point_down:

— Twitter Comms (@TwitterComms) July 31, 2020

Updated: 4:58 p.m.

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apparent teenager

A teenager’s apparent clumsiness foreshadowed a shocking diagnosis – The Washington Post

Judy Kalnas remembers thinking that Jessica, the youngest of her six children, resembled the elastic-limbed cartoon character Gumby.

As a child, she said, Jessica would topple off her bike and “get up laughing.” In high school, she fell during field hockey practice. Over the years, her worst injury was a broken toe. She felt embarrassed by her apparent clumsiness, which stuck out in an athletic family whose members include a shot-putter who qualified for the U.S. Olympic trials.

But when Jessica tumbled off the bleachers while preparing to accept a math award at her South Jersey high school graduation, the undeniable reality that something more than mere clumsiness was at work became glaringly apparent.

Three years later, when her daughter received the shocking diagnosis, Judy Kalnas immediately recalled statements her own mother had made decades earlier about another family.

Those remarks would come to have particular resonance after what Kalnas learned about her own children, especially Jessica, now 31.

A diagnosis discarded

The summer Jessica was 14, her large extended family rented a house on North Carolina’s Outer Banks. One afternoon Judy spotted Jessica crawling up the steep steps from the beach on her hands and knees. When she asked her daughter what she was doing, Jessica replied, “It’s just easier.” After one of Judy’s sisters agreed, she gave it little thought.

But over the next year, Jessica seemed to become increasingly uncoordinated. Although she had been cheering for a decade, she did not make the cheerleading squad her sophomore year. Jessica told her parents she thought her failure to land a spot was the result of not smiling enough. Her mother learned later she couldn’t perform the jumps. Jessica joined the field hockey team instead.

Jessica said that at the time she realized “something was very wrong.” She didn’t say anything to her parents for fear of worrying them or having to limit her activities.

“I thought it would eventually just disappear if I did things to strengthen my legs. So I would always act like I was okay when I would fall,” she said.

Her mother, a preschool teacher, was concerned. “I would go to [field hockey] practices and watch and think, ‘Why isn’t she running like everybody else?’ ” Judy recalled. Later she learned that the coach had been alarmed by Jessica’s repeated falls during practice.

The graduation night fall from the bleachers in 2008, when Jessica said her “knee just gave out,” proved to be a catalyst.

Within days, mother and daughter saw their family physician. He referred Jessica to a neurologist in nearby Camden.

The neurologist ruled out Duchenne muscular dystrophy, a genetic disorder characterized by progressive weakness that strikes young children, usually boys. She prescribed medication for myasthenia gravis, a rare autoimmune disease that affects the muscles and often causes droopy eyelids.

Jessica took the drug for a month but showed no improvement. Her family doctor then referred her to a neurologist in Baltimore with expertise in spinal muscular atrophy, a rare genetic disease that destroys nerve cells.

The specialist told Jessica and her parents he was fairly certain she had spinal muscular atrophy; a muscle biopsy seemed to bolster that diagnosis.

But after a year, an MRI scan showed that one part of Jessica’s brain was shrinking. “I remember everybody seemed stumped,” Judy said.

The specialist expressed doubt that she had spinal muscular atrophy and referred her to the National Institutes of Health. Jessica was seen by a specialist in hereditary muscle diseases who ordered genetic testing. The results, which took many months, stunned and bewildered the family. Jessica had Late Onset Tay-Sachs disease (LOTS), a progressive, incurable genetic illness.

‘That can’t be!” Judy remembers blurting out. “We’re not Jewish.”

Fatal regression

For roughly a century Tay-Sachs disease, named after two physicians who pioneered the description of the neurodegenerative disease, was believed to almost exclusively affect Ashkenazi Jews from central or Eastern Europe. One in 27 people of Ashkenazi Jewish ancestry carry the genetic mutation that causes Tay-Sachs, a rate ten times higher than the general population.

Tay-Sachs, which typically affects infants, results from the absence of an enzyme called hexosaminidase A, which prevents the harmful accumulation of a fat in the brain and spinal cord. Babies, who are typically affected in utero, appear normal until about 6 months when they begin to regress, eventually becoming blind, demented and paralyzed. The disease is nearly always fatal by age 5.

Since the discovery of the gene that causes Tay-Sachs in the late 1980s, screening programs and genetic counseling in Jewish communities have become routine and the number of infants with Tay-Sachs has plummeted.

Scientists now know that anyone can carry a disease-causing mutation, of which there are more than 100. Concentrations of Tay-Sachs cases have been discovered in often isolated non-Jewish populations including the Irish, French Canadians from Quebec and Cajuns in Louisiana, NIH specialists informed the Kalnas family. Late-onset Tay-Sachs, a recently discovered, less-severe variant of the disease resulting from a deficient level of HexA, surfaces in adolescence or adulthood.

“It was an eye opener,” said Judy, who has Irish ancestry. “All I could hear was my mother’s voice talking about a family we knew whose child had Tay-Sachs” and how terrible it was. “I remember thinking as a child, ‘Why is she bringing this up?’ I’ve wished so many times I could ask her.”

Judy Kalnas has since often wondered whether the disease had struck her own family decades before Jessica was born. Was that why her mother kept mentioning it?

Unlike babies with Tay-Sachs, who have a telltale cherry red spot in their retinas, late onset cases can be very difficult to diagnose. Symptoms and severity vary greatly and decline is more gradual. Diagnosis of the disease is made through enzyme and genetic testing.

“Not only does the average person not know about this,” said neurogeneticist Heather A. Lau, associate director of the division of neurogenetics at NYU Langone, “but my colleagues in neurology aren’t aware of LOTS.” Some people with late onset disease have been told they have multiple sclerosis or ALS, said Lau, who treats about a dozen LOTS patients, several of whom were diagnosed in their 50s.

Diagnosis is further complicated because in about 40 percent of cases initial symptoms include a manic episode or other psychiatric symptom, according to the National Tay-Sachs & Allied Diseases Association, a Boston-based support and advocacy group.

All forms of the disease result from the inheritance of a mutated gene, one from each parent who are both carriers. For each such pregnancy, there is a 25 percent chance the child will be affected by inheriting two abnormal genes, a 25 percent chance the child will be neither affected nor a carrier, and a 50 percent chance the child will be a carrier who typically shows no symptoms.

After Jessica was diagnosed, testing revealed that two of her brothers are carriers, while her sister is unaffected. Two brothers have not been tested.

‘An eye opener’

Doctors at NIH referred the family to Edwin H. Kolodny, a pioneering Tay-Sachs researcher who is currently a research professor of neurology at NYU School of Medicine. Judy said Kolodny, one of the first scientists to describe late onset disease, was encouraging and realistic as he prepared them for what lay ahead.

Treatment for LOTS is largely supportive. Jessica is enrolled in a long-term study at NIH and has participated in a research trial run by Lau at NYU of a drug not approved in the United States that may lessen Tay-Sachs symptoms.

“Jessica is very thoughtful,” Lau said. “She has good organizational skills and is quite independent and eloquent.” Lau added that she does not show signs of impaired judgment that can accompany the disease.

Jessica can no longer walk without the use of leg braces and two canes; if she doesn’t use them, her legs buckle. Her arms are weak and she does exercises daily and rides a stationary bike. Speech therapy has been helpful for slurred speech, which is common among late onset patients.

For her mother, the diagnosis of Tay-Sachs has been “an eye opener.” Jessica’s siblings, who include two nurses and an emergency medical technician, have been supportive and helpful.

“My biggest fear was: ‘How am I going to live with this? How am I going to watch this happen?’” Judy said. “The main thing is that we weren’t going to lose her.”

From Jessica’s perspective, one of the hardest things about living with her disease is the inability to drive. “The most important thing is not to give up,” she said. “Keep going.”

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