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Sarah, Duchess of York has paid tribute to Lisa Marie Presley at a memorial to celebrate her life, calling her Sissie and sharing an anecdote about her late mother-in-law, the Queen.

The duchess was one of many paying tribute to the star on the front lawn at Graceland Mansion in Memphis, Tennessee on Sunday.

For years the sprawling estate has been the destination for those paying tribute to Elvis, but following her death on 12 January aged 54, the iconic home has become the venue for those saying a final farewell to his daughter.

FILE PHOTO 1972 - Elvis Presley performs in concert during his "Aloha From Hawaii" 1972 television special. January 8 marks what would have been Elvis's 60th birthday and fans are expected to gather in his home-town of Memphis for the occasion. REUTERS/Stringer
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Elvis Presley in concert in 1972

Lisa Marie suffered a cardiac arrest at her home in Calabasas, California, dying aged 54.

Two days before her death, she had appeared with her mother, Priscilla Presley, at the Golden Globes.

As well as family and friends, members of the public were invited to attend the service, which was also livestreamed.

‘Before Blue Ivy, there was Lisa Marie’

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The event kicked off with a powerful rendition of Amazing Grace performed by Jason Clark and The Tennessee Mass Choir, dressed in black, flanked by a photo of Lisa Marie.

Filmmaker Joel Weinshanker began the service, saying he hoped they could honour Lisa Marie’s wishes “not to be sad”, and was followed to the lectern by Pastor Dwayne Hunt who paid tribute to her “passion, strength, brilliance and tenaciousness”.

In his tribute, former mayor of Memphis, AC Wharton, listed many famous celebrity parents, including Dennis Quaid and Meg Ryan, and Lenny Kravitz and Lisa Bonet, Kurt Russell and Goldie Hawn, he went on: “Before Jay-Z and Beyonce had Blue Ivy, and long before Prince Harry and Meghan had Archie, right here, in this city, our own royal couple, Elvis and Priscilla, had a beautiful bundle of joy, named Lisa Marie…

“Fifty-four years ago there was a star shining over Graceland with the birth of this precious angel.” He said she was inseparably a part of Memphis, calling her “a precious jewel”, and a “sister” to everyone who lived there.

As the only daughter of the King of Rock and Roll, he described her as “the conduit to the throne” and “the keeper of the flame”.

He concluded: “Lisa Marie was all Memphis. She belonged to us and we belonged to her.”

Flowers are seen as music fans pay their respect, in memory of singer Lisa Marie Presley, daughter of the "King of Rock 'n' Roll," Elvis Presley, outside of Graceland, at her birthplace in Memphis, Tennessee, U.S. January 13, 2023. REUTERS/Karen Pulfer Focht
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Tributes left at Graceland ahead of the memorial

Royal friends

Sarah, Duchess of York, then took to the stand, speaking about the Queen in her tribute and offering her support to the late singer’s children.

She said: “We need to stoke our flames within to celebrate extraordinary Lisa Marie. I stand here with great honour, because we called each other Sissie. I’ve been here with you all for all your lives and I stand here with great honour. So Sissie, this is for you with affection.”

She went on to tell an anecdote about the Queen, saying: “My late mother-in-law used to say ‘That nothing can be said, can begin to take away the anguish and the pain of these moments because grief is the price we pay for love’, and how right she was.”

FILE PHOTO: Lisa Marie Presley and her mother Priscilla Presley place their handprints in cement at TCL Chinese theatre in Los Angeles, California, U.S. June 21, 2022. REUTERS/Ringo Chiu/File Photo
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Lisa Marie (L) and Priscilla Presley at the Hollywood Walk Of Fame last summer

‘Our heart is broken’

A tearful Priscilla Presley then read out a poem written by her granddaughter about her mother’s loss, titled The Old Soul. She finished her reading, saying: “Our heart is broken Lisa, we all love you”.

Lisa Marie’s agent, Jerry Schilling, described her as “the only person who could intimidate Jerry Lee Lewis”. He went on: “I was in the hospital with her father when Priscilla was giving birth, I was at the hospital with her mother when she left us. Memphis, I will always love you.”

Rock singer Axl Rose said he was “still in shock” about Lisa Marie’s death, adding, “I feel like I should be texting her right now and telling her how wonderful everyone is”. He went on to perform November Rain on the piano.

Other musical performances included Billy Corgan performing To Sheila by The Smashing Pumpkins, Alanis Morissette singing an emotional rendition of her song Rest and the Blackwood Brothers Quartet singing How Great Thou Art and Sweet Sweet Spirit, both of which were previously performed by Elvis.

FILE -Elvis Presley poses with wife Priscilla and daughter Lisa Marie, in a room at Baptist hospital in Memphis, Tenn., on Feb. 5, 1968.  Lisa Marie Presley, a singer, Elvis... only daughter and a dedicated keeper of her father...s legacy, died Thursday, Jan. 12, 2023 after being hospitalized for a medical emergency. (AP Photo/File)
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Elvis with wife Priscilla and daughter Lisa Marie in 1968

Riley’s tribute to her mum, and first mention of her daughter

Actor and stuntman Ben Smith-Petersen, the husband of Lisa Marie’s daughter Riley, read an emotional tribute, written by Riley and titled To My Momma.

Part of the letter read: “I hope I can love my daughter the way you loved me, the way you loved my brother and my sisters. Thank you for giving me strength, my heart, my empathy, my courage, my sense of humour, my manners, my temper, my wildness, my tenacity. I’m a product of your heart, my sisters are a product of your heart, my brother is a product of your heart.”

Smith-Petersen and Riley have been married since 2015, but haven’t previously revealed they had a daughter together.

Lisa Marie Presley (C), with her children Riley and Benjamin Keough (R), attend the 75th birthday celebration for Elvis Presley in Memphis, Tennessee January 8, 2010. Presley, who died in August 1977 aged 42, is one of the top earning dead celebrities, bringing in $55 million in 2009 according to Forbes.com and marketed by Elvis Presley Enterprises which entertainment mogul Robert Sillerman revitalized in 2005. REUTERS/Nikki Boertman (UNITED STATES - Tags: ENTERTAINMENT ANNIVERSARY OBITUARY) FOR
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Lisa Marie with her children Riley and Benjamin Keough in 2010

‘Her father’s protector’

Joel Weinshanker closed the ceremony, saying: “Lisa’s voice will only be amplified with time, and never be silenced or diminished. She was and will always be her father’s protector, and we will continue to be hers”.

He asked everyone present to respect the family’s wishes not to be photographed or videoed.

Those present were then invited to come in groups to view Lisa Marie’s headstone in Meditation Garden.

Elvis is also buried at Graceland, as are Elvis’s parents, his paternal grandmother, and his grandson Benjamin Keough – Lisa Marie’s son – who took his own life in 2020, aged 27.

Lisa Marie’s final resting place is next to her son and near to her father.

Elvis died from heart failure aged 42 when Lisa Marie was aged just nine. She was four when Elvis and Priscilla Presley were divorced in 1972.

Read more: The tragic life of Lisa Marie Presley

Lisa Marie was married four times, including to pop star Michael Jackson and actor Nicolas Cage.

She had struggled with opioid addiction following the birth of her twin daughters in 2008.

Just months before her death she wrote in an essay for People magazine: “I’ve dealt with death, grief and loss since the age of nine years old.

“I’ve had more than anyone’s fair share of it in my lifetime and somehow, I’ve made it this far.”

She went on: “Death is part of life whether we like it or not – and so is grieving.”

Lisa Marie is survived by her three daughters, actress and model Riley Keough, and teenage twins Finley Lockwood and Harper Lockwood.

Her children will inherit the Graceland estate, as she inherited it from Elvis following his death.

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California mocked over ‘billion-dollar’ bridge to nowhere

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California mocked over 'billion-dollar' bridge to nowhere

Authorities in California have been mocked over a “billion-dollar” bridge to nowhere.

The state government of California has long planned for a Los Angeles to San Francisco high-speed rail project.

Despite initial funding being approved back in 2008, the line is still a long way off and expected to cost over $100bn in total.

So far, construction has only begun on the earliest phase and further funding has been used on environmental planning ahead in the Phase I System.

However, the California High-Speed Rail Authority recently publicised one of the completed sections of construction – finished back in 2018 and reported to cost $1bn on its own.

This is a 0.3-mile stretch of bridge, called The Fresno River Viaduct in Madera County, and it has attracted ridicule for going from nowhere to nowhere.

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Pictures shared by the authority of the bridge show it connected to nothing at either end with some claiming it is indicative of the wider project.

It runs above a road and close to a number of houses – parallel to another rail track – but currently serves no purpose.

Elon Musk poked fun at the recent X post of the construction, with the billionaire posting a crying emoji in response to news of the project.

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Others waded in as well on social media.

However, a number of those criticising it made false claims of the viaduct, its cost and time it took to complete it.

Since it was finished six years ago, after three years of construction, dozens more structures have been completed and there are over a hundred miles in active construction across the project.

Due to the vast scale of high-speed rails, they are often complex, expensive and lengthy projects – with the California High Speed Rail being no different.

The rail would come into use some time in the early 2030s but scrapping it reportedly remains a possibility.

California High Speed Rail has been approached for comment.

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In Washington DC and Gaza two very different families are united by one very rare disease

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In Washington DC and Gaza two very different families are united by one very rare disease

It is a paradox that humanity at its very worst so often also brings out its very best too.

This is a story about the kindness of strangers. It’s a story about hope over hopelessness. It’s about the war in Gaza but also about the rarest of diseases.

It is about two families in worlds far apart. It is a story about two little girls, Julia and Annabel.

I don’t yet know how it will end. But this is how it started.

It was two weeks ago when my phone pinged: a message on Instagram from a friend-of-a-friend. Her name is Nina Frost.

Nina and I first met a few years ago at a party in Washington DC where she had told me about her daughter Annabel, a little girl with an ultra-rare genetic disorder called AHC.

I remember Nina explaining how it was a disease like no other.

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‘The human time bomb disease’ she had called it, based on the all-consuming parental nightmare that their little girl could have a fatal seizure at any moment.

Image:
The Frost family

I’ve followed Nina’s Instagram, @HopeForAnnabel since we first met.

The good news is that Annabel is doing well, albeit with that eternal danger hanging over her. She requires constant care, attention and love.

Nina’s message to me wasn’t about her own daughter. It was about another little girl, in Gaza.

Rare diseases like AHC, which stands for Alternating Hemiplegia of Childhood, generate tight networks; the families living with the condition. Only about 1,000 people worldwide have been diagnosed with AHC. It really is rare.

“There is a little girl stuck in Gaza with the disease,” Nina wrote to me.

“Julia is three – after the last few months she has become paralyzed and unable to eat as her symptoms have worsened dramatically. We are desperate to help as she is massively vulnerable – literally on the brink of death.”

Julia Abu Zaiter is from northern Gaza originally. But with her father Amjad, her mother Maha and her older sister Sham, she was forced south by the Israeli military.
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Julia’s mother administers medication

Nina told me how she and her husband, Simon, are trying to organise the impossible: to get specialist drugs into Gaza and, ultimately, to try to get Julia and her family out.

Nina was modest about an endeavour that I now know has been all-consuming and expensive.

To tell this remarkable story of kindness and hope, I asked Nina to share with me Julia’s father’s number. Our local colleagues in Gaza then tracked the family down to a tent in the southern city of Rafah.

Julia Abu Zaiter is from northern Gaza originally. But with her father Amjad, her mother Maha and her older sister Sham, she was forced south by the Israeli military.

“My girl is three and a half years old. I want her to go out and play with the other children. Now, she cannot move at all,” Julia’s mother told our team, cradling her severely disabled little girl.

Rare diseases like AHC, which stands for Alternating Hemiplegia of Childhood, generate tight networks; the families living with the condition. Only about 1000 people worldwide have been diagnosed with AHC. It really is rare.
Image:
Annabel Frost

Rafah is on Gaza’s southern border with Egypt. Safety is so close and yet beyond reach unless the right strings are pulled with different authorities and governments in a labyrinth of wartime bureaucracy.

The images filmed by our team confirm what Nina had feared in her message to me.

Julia and her family are in the toughest of conditions. The house next to the tent was bombed a few days before our team visited.

The Abu Zaiters are now stuck in the city that could be the next battlefield and with a daughter whose condition is compounded by just the slightest stress, a little girl with, as Nina had told me, the ‘time bomb disease’.

“I told myself ‘it’s over, my girl is gone’,” Julia’s mother told our Gaza team, showing them Julia’s semi-paralysed state.

“Then a man named Simon contacted us and told us he will see if he can help, because his daughter’s situation is similar to mine.”

Five thousand miles away, and a world apart, in a leafy northwest suburb of Washington DC, I am now sitting with Simon, Nina and Annabel.

Julia Abu Zaiter
Image:
Julia Abu Zaiter

It is humbling to listen to their words – about their own daughter, but about their fight for a stranger too.

“Annabel lives with the most challenging condition that we can imagine – a neurological degeneration – and she lives with it with a smile on her face,” Simon says. “And we’re imagining the same for Julia in the most dire of circumstances.”

We look at videos of Julia which Amjad has sent to Simon.

“Our kids are all so similar… we feel a sense of connection to so many families and our world of rare disease,” Nina tells me.

“This is like that but on steroids. I mean, we feel so distressed for the situation that they’re facing.”

“Julia’s circumstances are exponentially worse, but I think we’ve always embraced the idea that we can do something to help, we must do something to help and that we should. I mean, I think it’s always been if not us, then who?” Nina adds.

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Amjad’s message highlights concerns he has about his daughter. He is looking for reassurance from Simon.

Julia is experiencing some severe paralysis and via a translated SMS and a few photos, Amjad wants some encouragement which Simon can’t give.

“They don’t have the medicines they need and the doctors that they need to really treat and properly prevent episodes and to address them when she has them,” Simon says.

“So we’ve been trying to gather a group that can support her. It’s been constant communication and really difficult with the translation issues,” Simon tells me.

Over in Gaza, Julia’s mum is desperate. “Our conditions due to the war are below zero.

“Our situation is horrible. I cannot provide my daughter with any food or drinks. I can get medications through lots of difficulty, and I tell myself that getting these medications is more important than getting food for us.”

Rare diseases like AHC, which stands for Alternating Hemiplegia of Childhood, generate tight networks; the families living with the condition. Only about 1000 people worldwide have been diagnosed with AHC. It really is rare.
Image:
The Frosts speak to Sky’s Mark Stone

Against the odds, Simon has managed to coordinate with the right people to get the right medication into Gaza for Julia.

Through the tight AHC network, one doctor has prompted another who knows another and another. That’s how this works. Threads of kindness stitched together.

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Now the challenge is getting Julia out to Egypt and then on a medical flight to Abu Dhabi. It will be hard, maybe impossible.

“And it seems like she’s really declined,” Nina says looking at the latest videos of Julia.

“I mean, it seems like exactly what we would have predicted has happened. She has gone from being a happy three-year-old with a profoundly difficult disease to being this shell of herself.”

“I feel like I am losing her,” Maha says with Julia in her arms. “She is dying right next to me and I cannot even do anything. The thing I fear the most is losing my daughter.”

There is some chance of an extraction to safety soon. It is not guaranteed but it is some hope for one little girl in a place where uncertainty is all around.

This is a story about two families worlds apart but bound by a disease.

I don’t yet know how it will end. This may feel sometimes like a world of hopelessness, but I have some hope.

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‘Part of the American spirit’: Arrested student denies protests are violent

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'Part of the American spirit': Arrested student denies protests are violent

Much has been said about the students whose protests have gripped America this past week.

Their cause has been framed in polarising ways. A violent Hamas-sympathising mob? Or peace activists striving for equality?

Within a frenzied spectrum of views and noise, one young student sat down with me for a conversation.

Aidan Doyle, 21, is a philosophy and jazz double major at the University of California in Los Angeles (UCLA).

He was arrested early on Thursday morning for being part of an encampment at the university.

He told Sky News he was shocked that the police arrested so many student protesters, despite not intervening in an attack on the protesters by a pro-Israeli group the day before.

Police clash with pro-Palestinian demonstrators on the UCLA campus early on Thursday morning. Pic: AP
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Police clash with pro-Palestinian demonstrators on the UCLA campus on Thursday. Pic: AP

He said his arrest had not deterred him from continuing his protest, which he likened to the Vietnam War demonstrations of the 1960s.

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Mr Doyle rejected the notion, from President Biden, that the protests are not peaceful.

“Graffiti, putting posters up, that’s all peaceful,” he said, commenting on the president’s statement from the White House.

“I also think that President Biden needs to actually take some introspection and realise that maybe the reason so many of these protests are happening is partially due to him.”

Police advance on demonstrators on the UCLA campus Thursday, May 2, 2024, in Los Angeles. (AP Photo/Ryan Sun)
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Police advance on demonstrators on the UCLA campus. Pic: AP/Ryan Sun

Mr Doyle added: “Protests in general are part of the American spirit. They’re part of being an American. And if we were to just stand around in circles and sing and dance, and pretend everything was fine, then nothing would change and nobody would care at all.

“Part of a protest is causing disruption and causing at least a minor level of chaos that is, again, not violent but that actually disrupts things.”

Read more:
Why are university students protesting in the US?
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He denied any accusations of antisemitism, but conceded there is a spectrum of opinion within the movement.

“If you’re going to criticise a movement, I think you have to look at the movement’s goals and their mission, not what fringe members of the group say or do.

“You have to actually look at what we say, what the organisers say, and what is in the mainstream, and what our mission and our goal is: the peace and prosperity of the Palestinian people.”

Asked if he believed in Israel’s right to exist as a country, he said: “I think Jewish sovereignty is incredible. I think it’s an amazing thing.”

Demonstrators are detained on the UCLA campus .
Pic: AP
Image:
Demonstrators are detained on the UCLA campus. Pic: AP

He added: “I think that if there is a country for Jewish people that protects the Jewish people, that is of utmost importance, especially with the vile and rampant antisemitism that exists across the world that I see every day and that I try and combat as much as possible.

“But doing that and then simultaneously repressing another group of people, dehumanising them and brutalising them, then the question of whether your state has the right to exist becomes secondary.”

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