Connect with us

Latest

Parents unsure of key online phrases making it harder to protect their children

The survey found digital safety tops the poll of skills where parents feel most ill-equipped to help their children,

New research reveals almost half of parents and carers feel their children know more than them when it comes to digital technology, with 60% claiming they wish they were more digitally savvy. The study, conducted by Vodafone, reveals a digital knowledge gap between the generations, citing 12 as the age at which parents feel their child’s digital knowledge overtakes their own.

Only one in ten parents are familiar with trending social media platform BeReal and just 35% are familiar with Twitch, despite the soaring popularity of the gaming platform. What’s more, 71% of parents claim their children use technological terms they don’t understand – with digital slang such as ‘GRWM’ (get ready with me) and with OOMF (one of my friends) among the phrases 66% of parents are unfamiliar with. Similarly, ‘smishing’, ‘NFT’ and ‘Digital Activism’ are among the online terms parents wouldn’t be able to explain to their children.

The findings are released in line with the launch of Vodafone’s interactive Digital Parenting Pro, one of the biggest parental controls and safety settings resources in the UK.

Digital Parenting Pro has been created in collaboration with Digital Awareness UK to equip parents and carers with all the information and tools they need to keep their children safe online. The content rich hub will be a place for parents, carers (and kids) to get information and help about staying safe online, including tips from NSPCC experts, so adults can feel confident about what their kids are up to online, what social media they use, games they play and threats they might come across.

The survey found digital safety tops the poll of skills where parents feel most ill-equipped to help their children, with more than a quarter of parents claiming they would feel more at ease with their child using the internet if they had a better understanding of how to keep them safe. Social media proves the biggest area of concern for parents, with apps such as Facebook, TikTok and Instagram coming out top of the list of digital worries for more than half of British mums and dads.

Nicki Lyons, Chief Corporate Affairs and Sustainability Officer at Vodafone UK, said: “When it comes to tech any parent or carer knows what it’s like to feel like your kids know more than you, which is why we’ve created one the UK’s biggest parental controls resources – Digital Parenting Pro. It’s designed to help people easily understand more about the latest games or social platforms, what age they are recommended for and what safety features exist. We’ve been working in this space for over a decade, so we understand just how fast things move and our latest resource will give parents and carers confidence when navigating the digital world.”

Each year SID aims to raise awareness of emerging online issues and help make the internet a safer and better place for everyone. Vodafone’s aim is that Digital Parenting Pro can be part of the solution by providing clear safety advice and support on what to do if things do go wrong – all through its freely accessible and easy-to-use online safety resource.

Will Gardner, Director of the UK Safer Internet Centre, said:“Safer Internet Day 2023 is about encouraging children and young people to talk about their lives online as well as providing parents and carers with the information and tools to facilitate these important conversations that go beyond a single day. Activities supporting the Safer Internet Day are taking place right around the country and being led by thousands of organisations, and this huge collaboration is where the success of the Day lies. It is great to see Vodafone actively supporting the Day, as resources like their Digital Parenting Pro help equip parents with the information they need to help support their children online.”

The launch of the Digital Parenting Pro resource is part of Vodafone’s everyone.connected campaign which is committed to tackling digital exclusion by helping four million people cross the digital divide by 2025. A key part of this programme is providing free support and skills to digitally transform and upskill businesses and communities.

Continue Reading

Latest

A drug company abandoned a treatment for  ‘bubble boy disease.’ After a 5-year fight, this little girl is about to get it

Later this spring, a little girl in California who essentially has no immune system will receive a lifesaving treatment for “bubble boy disease” thanks to the persistence of a dogged group of parents, a pediatrician, a veteran newsman and a few episodes of “Grey’s Anatomy.”

Five-year-old Seersha Sulack has the same rare disease portrayed in the 1976 John Travolta movie, “The Boy in the Plastic Bubble.” A germ – even a common cold – could kill her, and so she stays away from anyone outside her immediate family.

The treatment she’s been waiting for had stunning, near-perfect results in a clinical trial, but it’s been sitting on the shelf for years in the US because the pharmaceutical company that once owned the license abandoned it when it decided not to not to pursue approval from the US Food and Drug Administration.

“It’s a pretty tough situation,” said Dr. P.J. Brooks, acting director of the Division of Rare Diseases Research Innovation at the National Institute of Health’s National Center for Advancing Translational Sciences. “You have an effective therapy like (this one) and people can’t get access to it.”

Seersha is expected to get the treatment next month. She’ll become only the second child in the US in the past five years to receive it; the first child received it earlier this month.

The treatment is for a particular type of severe combined immunodeficiency called ADA-SCID that’s extremely rare – in the US, eight babies a year are born with it. Currently, 26 children in the US and Canada are on the waiting list to get the therapy, according to Dr. Donald Kohn, a UCLA scientist who has been working on the treatment for nearly 40 years.

The treatment is a type of gene therapy: Doctors will give Seersha a normal copy of the defective gene that disabled Seersha’s immune system.

Gene therapies hold great hope for all sorts of diseases, but they’re very expensive to develop, and pharmaceutical companies can’t be sure that they’ll make a profit because health insurance companies haven’t always agreed to pay the multi-million dollar price tags.

“It has not escaped our attention at FDA that there have been some clouds on the horizon in gene therapy,” Dr. Peter Marks, head of the US Food and Drug Administration’s Center for Biologics Evaluation and Research, said at a biotech conference in California in October. “We really want to try to see what we can do to move things forward.”

The gene therapy Seersha’s been waiting for was once called OTL-101, for Orchard Therapeutics Limited. Orchard launched in 2016 with OTL-101 as its “lead candidate,” but four years later, the company announced it would “reduce investment” in the therapy and prioritize treatments for more common conditions.

“A lot of us were upset and angry,” said Seersha’s mother, Shayla Sulack, noting that OTL-101 was developed with millions of dollars in state and federal government aid.

“We were always, ‘it’s going to happen, it’s going to happen,’ ” she added. Then, after Orchard decided not to pursue the therapy, “a bunch of us SCID moms were like, ‘Excuse me?’ ”

In a statement to CNN, an Orchard spokesperson wrote that “after encountering technical challenges related to the commercial-grade manufacture of this particular therapy, we made the very difficult decision to limit additional investment in [the SCID gene therapy].” The spokesperson spoke on the condition of anonymity.

A mother’s ‘oh, crap’ moment
Shayla and her husband, Stephen Sulack IV, were high school sweethearts at Tehachapi High School, about 100 miles north of Los Angeles. In 2010, when she was 18 and he was 19, they married at the Little White Wedding Chapel in Las Vegas.

Stephen was in the Army, and over the next few years, the young couple moved to various military bases. Their daughter Skylar was born in 2012 and son Stephen V in 2014.

In 2017, the family moved to Hawaii for Stephen’s new post as a Black Hawk helicopter pilot at Schofield Barracks in Oahu. Two weeks later, Seersha was born at Tripler Army Medical Center in Honolulu.

Weighing 6 pounds and 10 ounces, Seersha appeared perfectly healthy, and her parents took her on family outings, going to Dole Plantation and Waikiki Beach when she was five days old.

Strolling around the shops near the beach that day, the family went into a Tesla dealership just for fun. While sitting in a showroom car, Shayla got a phone call from a number she didn’t recognize.

It was a geneticist at Tripler. He told Shayla that a routine blood test, a prick on a newborn’s heel done in nearly every state, showed Seersha’s level of T cells – a type of white blood cell crucial to fighting off infections – was just five. Normal T cell levels for newborns are around 3,000.

This meant any infection, no matter how small, could kill Seersha. The geneticist said to bring her back to the hospital at Tripler immediately.

Shayla says her first reaction was: “Oh, crap.”

Not only had they been going everywhere with their new baby, but Seersha’s big brother and sister had been affectionately pawing all over her.

Shayla and Stephen left the Tesla dealership and made the 20-minute drive to the hospital while Shayla’s parents took the older two children home in their car.

At Tripler, doctors explained more about SCID, and a psychologist was on hand to help the Sulacks deal with the shocking news.

Only about one baby a year is born with the SCID in Hawaii, according to Sylvia Mann, genetics coordinator at the state’s department of health.

The next day, Shayla and Seersha were on a military medical transport flight to Los Angeles. Seersha was in an incubator in the front of the plane, and the other patients were kept in the back to decrease the chances they could get her sick.

An ambulance drove Shayla and Seersha to UCLA Mattel Children’s Hospital, one of 47 medical centers in the US and Canada that specialize in SCID as members of the Primary Immune Deficiency Treatment Consortium funded by the National Institutes of Health.

Once there, doctors laid out the options for saving Seersha’s life.

Options for Seersha
It turned out none of them were very good.

ADA-SCID is treated with regular injections to replace a missing enzyme that helps with immune function. They help a great deal, but they don’t give the child a full immune system, and their effectiveness can wane over time.

The UCLA doctors laid out two longer-term options. Seersha could receive a stem cell transplant, which is lifesaving and the standard treatment for SCID. Doctors would test her mother, father, brother, and sister and determine the best genetic match, and then would extract cells that specialize in forming blood cells and give them to Seersha.

Testing showed that any of her family members could donate to her, but none of them was a particularly good match. This was bad news for two reasons: One, the transplant likely wouldn’t be as effective. Two, Seersha would be more likely to suffer complications.

Continue Reading

Latest

Youssef Ramadan earns ACC Men’s Swimmer of the Year

After his historical season, Youssef Ramadan took the ACC Men’s Swimmer of the Year title for the 2022-23 season, the league announced Monday afternoon.

Ramadan became the first-ever national champion in program history, swimming the second-fastest 100 fly time in NCAA history at 43.15. He earned five All-American awards and two honorable mentions at NCAA’s.

Ramadan was named male MVP at ACC’s in February for the second year in a row, on top of two gold medals and two silver medals. He also took ACC Male Swimmer of the Week twice earlier in the season.

Throughout the 2022-23 season, he’s broken four individual school records and two relay records.

Continue Reading

Latest

Changes on tap for Americans who hunt waterfowl in Manitoba

Americans planning to hunt waterfowl this fall in Manitoba will be able to draw a seven-day license but must enter a lottery for a limited number of “foreign resident” licenses in subsequent years if they don’t book their trip through an outfitter, under new waterfowl regulations the province announced earlier this month.

“As part of the initial phase-in strategy for fall of 2023, Manitoba is ensuring that all applicants for the draw will receive a seven-day Foreign Resident Migratory Game Bird License,” Manitoba’s Ministry of Natural Resources and Northern Development said on its website. “In subsequent years the allocations for each license type will be determined based on license sales, hunter questionnaire data from all user groups and stakeholder input. The combination of the seven-day license and associated draw for freelance foreign resident hunters is intended to discourage visiting hunters from creating lasting systems of control that inhibit other hunters.”

The new regulations are a key component of the Waterfowl Hunting Modernization Project, a proposal the Manitoba government unveiled last fall before a 45-day comment period that ended Friday, Oct. 7.

American hunters will now have the opportunity to access the following Manitoba waterfowl and upland game bird licenses, the province said:

Foreign Resident Upland Game Bird License: Required to hunt upland birds and can be purchased online and is subject to the same regulatory framework as resident hunters.
Foreign Resident Migratory Game Bird License: Required to hunt migratory birds and is a seven-day license, which can be accessed either by entering a draw process or booking with a licensed outfitter.
Foreign Resident Legacy Migratory Game Bird License: A grandfathered opportunity for qualifying foreign resident landowners or lessees of Crown land.
To qualify for the special grandfathered provisions, Americans (and other foreign residents) must have owned property in Manitoba before Sept. 1, 2022, and still own that property; be a shareholder of a corporation owning registered property in Manitoba; or be a crown land lessee. Eligible land interest holders must also have hunted waterfowl in Manitoba during the previous five years between 2018 and 2022 to qualify for the legacy license.

Continue Reading

Trending

slot777 slot thailand slot777 https://situsterpercayaslot777.com/ slot gacor hari ini slot gacor maxwin slot deposit pulsa slot deposit pulsa tri http://sia.unidha.ac.id/repository/dosen/riwayat/login/dewajasin/ https://karanganyar.alabidin.sch.id/wp-content/shop/ https://smpabbs.alabidin.sch.id/dewajasin/ https://thehero.alabidin.sch.id/merdeka/ https://abbs.alabidin.sch.id/angkorwd/ https://gemoy99.com/jutsu/ https://alabidin.sch.id/katon/ https://platinum.alabidin.sch.id/gold/ https://stia.alabidin.sch.id/bavet/
pasangan ini menang 200 miliar dengan algoritma starlight terbaru kemudahan head unit mobil listrik bermain no limit city stevia pengganti gula dengan aroma sweet bonanza perpecahan timothy dan raymond chin pola mr fa chai gacor peran ai dalam meningkatkan kualitas mahjong ways pajero vs turbo awd melibas ganesha fortune