twin

One-eyed cat and Long Beach celebrity Likho celebrates 15th birthday

p]:text-cms-story-body-color-text”>

Elizabeth Kobliha knows her one-eyed cat Likho has more friends than she does. So much so that on his 15th birthday last Saturday, the sidewalk outside her downtown Long Beach store where he spends most of his time transformed into a makeshift fair.

There were vendors selling peach cobbler, watches, hot dogs and offering tattoos and face paint. A DJ spun records in celebration.

“He’s a very good businessman. We’ve got stickers, T-shirts, keychains, and buttons [of him], and it all goes under his account, his name,” Kobliha said of the cat.

  • Share via

Before Likho roamed the 7,000-square-foot Long Beach Vintage Etc, there was Apollo. The “big rag doll” came in with health problems but was the perfect shop cat. Apollo, a Maine coon who died at 13 following a seizure a year after his arrival in 2015, had curbed the shop’s mouse problem and brought “so much love and energy.”

Similarly, Likho, a one-eyed Russian Blue, also was ailing when Kobilha took him in at 8 years old, but she wanted him anyhow.

“I always wanted to open my own shop so I can have a shop cat,” Kobliha says, adding she was inspired by bookstores with cats “just chilling.”

A man in a black shirt and brown pants and woman in a white tank top and blue jeans walk by a vendor selling patches.

Vendors line the sidewalk for Likho’s birthday party. The cat is a local celebrity.

(Jason Armond / Los Angeles Times)

In 2016, Kobliha was swiping through Facebook when a video stopped her scroll. In it, a woman inside of a hoarder’s garage bobbed a feather toy in front of Likho, who jumped up to catch it.

The post was made by Sia Barbi in collaboration with animal rescue group Stray Cat Alliance after the cat had been abandoned at the Hancock Park home. During the early ‘90s, Sia and identical twin sister, Shane, made waves in the fashion and pop culture worlds, often modeling for Chanel, Thierry Mugler and Jean Paul Gaultier. Their rise to fame began after the Los Angeles Times covered a Sunset Boulevard billboard featuring the twins wearing little clothing that had been causing car accidents.

“Guys of a certain generation would get very hot and bothered over them,” Kobliha said of the Barbi twins. As they exited the modeling industry, they pivoted into animal activism and volunteering for rescue groups and trap, neuter and return programs for cats.

A woman with a blonde mullet hairsyle and a yellow, red, white, and blue blazer holds a one-eyed grey cat.

Elizabeth Kobliha holds her cat Likho. When she opened her vintage store, she knew she wanted a shop cat just like chill bookstore cats.

(Jason Armond / Los Angeles Times)

Kobliha wanted to adopt Likho, but first he’d need a $3,000 operation to remove an infected eye, paid for by the Stray Cat Alliance.

“They took care of everything, then we had to wait because he had to recuperate,” she recalls. “The whole time I’m thinking, ‘Oh my God, what if it doesn’t work out? What if the cat gets here and is just absolutely bonkers?’”

That fear was for nothing. Likho, who lives at the shop full-time, acclimated within a day. “He has been a beautiful addition ever since then,” Kobliha says.

He’s since become the face of the shop, with a mural dedicated to him outside to welcome customers. That was done by local muralist LaJon Miller, who worked on another on the sidewalk during Likho’s party.

“I got adopted into it,” he says of the Likho fandom. “He’s been my muse on this street for a while. … He just roams around the store, chills, does his little nap thing, and hangs out with everybody, so he’s very social.”

Likho has never harmed the centuries-old objects in her shop, Kobliha says, but he has spooked suspected ghosts.

A man wearing a black and white shirt and grey pants works on a mural featuring a weightlifting grey cat in a pink singlet.

LaJon Miller, who calls Likho his muse, paints a portrait of the cat on the sidewalk outside of Long Beach Vintage Etc.

(Jason Armond / Los Angeles Times)

Kobliha believes ghosts once connected to shops at the 1922 building — a former patron of a grocery store shamed for his obesity and a former furniture shop owner who died by suicide — still roam her store’s stalls.

“We see shadow figures … there’s a certain area where they pass back and forth. They don’t do anything, but they’re scary as hell,” Kobliha says of unusual sightings. “Likho is very protective, and we do feel really safe when he’s around.”

“It is a little weird, though, when he’s sleeping, and then suddenly he will jump up and look around,” she adds.

Likho’s biggest fan may be a man named Dom Gomez. He lives within walking distance of the shop, and tends to visit after long shifts at a restaurant aboard the Queen Mary. He stopped by the birthday party wearing his work uniform: a white, button-down shirt and black slacks. His hair slicked; his hands behind his back.

A customer wearing a beige shirt and brown rimmed glasses holds a fan depicting a one-eyed gray cat with his mouth open.

Likho’s face graces merchandise at Long Beach Vintage Etc like this fan.

(Jason Armond / Los Angeles Times)

When he speaks of Likho, he speaks with a tender cadence and dignified countenance, as if he were his own.

“Time flies, you know?” he says, smiling, of visiting Likho over the years. “He gets a lot of love from all the ladies that work here and myself … he has a lot of fans. I don’t know who’s more famous, Muhammad Ali or Likho the Cat.”

On a previous birthday, Gomez wanted to get Likho a gift. He settled on a kid’s denim jacket he modified for a cat with a patch for the Cure on the back but, regrettably, it was a “little too big.” Next year, he’ll give it another shot with a sweater.

“That’s my little buddy right there,” he says. “Today is a special day. I didn’t know a cat could live that long, but I think he’s still got a lot of energy to live … maybe another 100 years, I hope.”

Source link

Emotional Jesy Nelson’s fresh heartache as twin daughters suffer health setback after ‘bittersweet’ SMA campaign victory

JESY Nelson says she “can’t stop crying” over her “bittersweet” victory to test all babies in England with SMA – knowing it came too late for her twin daughters.

The groundbreaking rule change comes as the former Little Mix star faces fresh heartache over her one-year-old kids, Ocean Jade and Story Monroe, whose latest test results sparked concern following treatment for the muscle-wasting disease.

Little Mix star Jesy Nelson faces fresh heartache over her one-year-old kids Credit: Shutterstock Editorial
Jesy’s twins Ocean and Story have Spinal Muscular Atrophy Type 1 Credit: Instagram/Jesynelson

It’s feared the girls will never be able to walk after a late diagnosis of the life-threatening condition Spinal Muscular Atrophy Type 1.

In her new Prime Video show, Jesy Nelson: Life Changing, the singer breaks down in tears over the guilt she carries and worries her children will blame her, when they’re older, for not spotting the signs sooner.

Jesy told The Sun: “I know it’s not my fault, but when I watch back videos of when I brought them home and they were kicking their legs, I realise now that over the course of a month, they just stopped.

“That’s the part where the guilt kicks in because I don’t understand how I didn’t see that. Why didn’t I spot that?

HELL & BACK

I had first look at Jesy Nelson’s new doc… watching her break apart stunned me


TEST WIN

Victory for Jesy Nelson as all babies to get free tests for muscle wasting disease

“But when I left the neonatal ward, I was constantly told to check their temperature, make sure you’re monitoring their breathing and there was so much other stuff that I was looking out for because they were premature babies.

“I just honestly didn’t focus on the movement of their legs.

“Thank God for my mum, because God knows what position I would have been in if she hadn’t spotted it.

“That will probably never leave me. I’ll be honest, I don’t think it ever will. But I really hope as they get older, they understand how flipping amazing they are because they are the most resilient little girls I’ve ever known.

It is feared Jesy’s girls will never be able to walk Credit: Instagram/JesyNelson
Jesy Nelson: Life Changing documentary features the singer revealing her guilt over her twins’ health issues Credit: Amazon

“I’m literally in awe of them. Even with what they have to endure every day, they are the happiest babies.”

At Ocean and Story’s most recent three-month review at St Ormond Street’s Children’s Hospital, doctors warned Jesy the girls were not responding to treatment the way they had hoped.

She said: “Unfortunately, some of the numbers have gone down. We had a long discussion and there’s a possibility they may have to go back on treatment, which is just heartbreaking.

“I constantly battle between manifesting they’re going to defy the odds and trying to come to accept that that may not happen.

“It’s a really weird position to be in because you you think ‘well, if that doesn’t happen, am I just going to feel heartbroken for the rest of my life?’

“Then you worry, if I accept it, am I also manifesting that?”

She added: “I don’t ever want them to feel any less than or feel like it defines them. I really want them to know how special they are.

“I want this to be their little superpower.”

Speaking candidly, Jesy admits the success of her campaign for a breakthrough rule change – adding screening for spinal muscular atrophy to the NHS‘s newborn blood spot test – was a tough pill to swallow.

Every year 50 babies born with the condition will now find out they carry the genetic condition at birth. It means they can be given treatment before nerves and muscles are damaged beyond repair.

Jesy said: “I’ve not stopped crying, I don’t know what’s wrong with me. I just keep going through waves of emotions. I’ve had an outpouring of messages from families within the SMA community.

“It’s just a real weird one because obviously there’s a lot of mixed emotions. I think for people dealing with children that have got SMA, who got diagnosed too late, feel it’s almost a bit bittersweet.

Jesy with Little Mix’s Leigh-Anne Pinnock (far left), Jade Thirlwall (left) and Perrie Edwards (far right) Credit: Getty
Jesy’s new Prime Video documentary is released on Friday July 17 Credit: Shutterstock Editorial

“It’s a tough pill to swallow to know that, yes, this change is amazing and I really don’t want to take anything away from it, but if only this had been here for our children.

“It’s just sad because so many families have campaigned about this for years.

“So yeah I’ve going through a real mix of emotions, but ultimately I am super proud. I’m ridiculously proud and cannot wait until our children are old enough to tell them they’ve played a massive part in change.”

Her new Prime Video doc is released on Friday, July 17.

The 60-minute episode shows the moment Jesy finds out her daughters’ diagnosis and her grit and determination to launch her campaign.

While a phased rollout will begin in October 2026, Jesy’s fight continues to raise awareness of the condition because the screening won’t be available in other parts of the UK.

“I hope as many people as possible see the documentary because I wanted to raise as much awareness as I could about it and the signs to look out for.

“As amazing as the rollout is, Northern Ireland and Wales are still not part of the heel-prick test, meaning many babies will still be undiagnosed and not treated in time.

“I’m just praying that if they watch this documentary, they will spot the signs early enough, take them to the doctor and get them treatment.”

  • Jesy Nelson: Life Changing will be available exclusively on Prime Video on July 17.

Spinal Muscular Atrophy: Signs and symptoms

Spinal muscular atrophy is a disease which takes away a persons strength and it causes problems by disrupting the motor nerve cells in the spinal cord.

This causes an individual to lose the ability to walk, eat and breathe.

There are four types of SMA – which are based on age.

  • Type 1 is diagnosed within the first six months of life and is usually fatal.
  • Type 2 is diagnosed after six months of age.
  • Type 3 is diagnosed after 18 months of age and may require the individual to use a wheelchair.
  • Type 4 is the rarest form of SMA and usually only surfaces in adulthood.

What are the symptoms?

The symptoms of SMA will depend on which type of condition you have.

But the following are the most common symptoms:

• Floppy or weak arms and legs

• Movement problems – such as difficulty sitting up, crawling or walking

• Twitching or shaking muscles

• Bone and joint problems – such as an unusually curved spine

• Swallowing problems

• Breathing difficulties

However, SMA does not affect a person’s intelligence and it does not cause learning disabilities.

How common is it?

The majority of the time a child can only be born with the condition if both of their parents have a fault gene which causes SMA.

Usually, the parent would not have the condition themselves – they would only act as a carrier.

Statistics show around 1 in every 40 to 60 people is a carrier of the gene which can cause SMA.

If two parents carry the faulty gene there is a 1 in 4 (25 per cent) chance their child will get Spinal muscular atrophy.

It affects around 1 in 11,000 babies.

Source link

Heartbroken reason Jesy Nelson’s twin daughters’ treatment for SMA was delayed

JESY Nelson has revealed the tragic reason her twin daughters’ treatment for SMA was delayed – despite the increased risk of permanent nerve and muscle damage.

The former Little Mix star details the heartbreaking moment Ocean Jade and Story Monroe, who have have Spinal Muscular Atrophy Type 1, are forced to miss out on the gene-therapy infusion earlier this year.

Jesy Nelson opens up about the twins’ health battle in her new Life Changing documentary Credit: Amazon
Story and Ocean were rushed to hospital with pneumonia when they were ready for treatment Credit: Instagram

In her new Prime Video documentary, Jesy Nelson: Life Changing, Jesy says Story was rushed to hospital with pneumonia – just days before Ocean was struck down by another illness.

Speaking in the docu-series, which is released on Friday, July 17, Jesy said: “Not long after we got the diagnosis, they were booked in to have their treatment.

“Then Story got pneumonia and was really struggling to breathe.

“She started choking so we had to rush her into hospital. It breaks my heart because she’s so vulnerable.

JESY’S HURT

Jesy Nelson breaks down in tears as she reveals mum guilt over twins’ struggle


PROUD MUM

Jesy Nelson shares her daughter’s milestone moment amid heartbreaking SMA battle

“That’s when we were told that she can’t have the treatment.”

Any delay in treatment increases the chance of permanent nerve and muscle damage

After close monitoring, it was decided that Story and Ocen were not well enough to receive the gene therapy.

Jesy added: “That was when she got given her breathing machine.

“She came home and then Ocean got ill.”

During the episode, which began filming straight after the cameras stopped rolling on her first series, Life After Little Mix.

Zion Foster celebrates his twin daughters’ 1st birthday Credit: Instagram
Jesy has been documenting the twins’ SMA battle Credit: Amazon

Her partner Zion Foster – who has since split from Jesy – said: “I’m not equipped to deal with this. I’m out of my depth; emotionally, physically and mentally.”

The documentary covers their split, which was revealed by The Sun earlier this year.

Jesy has since thrown herself into work – tirelessly campaigning to raise awareness of SMA and pressure the government to add the condition onto the NHS newborn heel-prick test, which currently screens for ten other conditions.

On Wednesday, April 1, the Department of Health and Social Care announced that England will bring forward the newborn screening of SMA.

A phased rollout will begin in October 2026. However, screening will not be available in all parts of England.

Spinal Muscular Atrophy: Signs and symptoms

Spinal muscular atrophy is a disease which takes away a persons strength and it causes problems by disrupting the motor nerve cells in the spinal cord.

This causes an individual to lose the ability to walk, eat and breathe.

There are four types of SMA – which are based on age.

  • Type 1 is diagnosed within the first six months of life and is usually fatal.
  • Type 2 is diagnosed after six months of age.
  • Type 3 is diagnosed after 18 months of age and may require the individual to use a wheelchair.
  • Type 4 is the rarest form of SMA and usually only surfaces in adulthood.

What are the symptoms?

The symptoms of SMA will depend on which type of condition you have.

But the following are the most common symptoms:

• Floppy or weak arms and legs

• Movement problems – such as difficulty sitting up, crawling or walking

• Twitching or shaking muscles

• Bone and joint problems – such as an unusually curved spine

• Swallowing problems

• Breathing difficulties

However, SMA does not affect a person’s intelligence and it does not cause learning disabilities.

How common is it?

The majority of the time a child can only be born with the condition if both of their parents have a fault gene which causes SMA.

Usually, the parent would not have the condition themselves – they would only act as a carrier.

Statistics show around 1 in every 40 to 60 people is a carrier of the gene which can cause SMA.

If two parents carry the faulty gene there is a 1 in 4 (25 per cent) chance their child will get Spinal muscular atrophy.

It affects around 1 in 11,000 babies.

Source link

Survivors and bodies still being pulled from rubble days after twin quakes | Earthquakes

NewsFeed

International aid teams have played a key part in Venezuela’s ‘miracle rescues’, days after twin earthquakes struck, but now they’re preparing to leave. Thousands of people are still searching for their relatives amid the rubble, as frustration continues to build towards the government response.

Source link

Venezuela struggles to respond to devastating twin earthquakes | Earthquakes

NewsFeed

Reporting from Caracas for Al Jazeera, Noris Soto says authorities appear to lack a clear response plan in the aftermath of two powerful earthquakes. The recovery is being hampered by severe damage to communication systems, as displaced residents are housed in hotels.

Source link

Jesy Nelson shares her twin daughters’ spinal braces with emotional message ahead of Parliament debate

JESY Nelson has shared her twin daughters’ spinal braces with an emotional message ahead of the upcoming Parliament debate.

The mum-of-two made a candid post explaining her daughters now have to wear them every day.

Jesy Nelson has shared her twin daughters’ spinal braces with an emotional message ahead of the upcoming Parliament debate Credit: Tiktok/Jesynelson
The mum-of-two appeared on social media in an emotional post explaining her daughters now have to wear them every day Credit: Instagram/Jesynelson

Jesy shared a snap of her twin daughters Ocean and Story’s spinal braces as she urged fans to attend the Parliament debate on SMA screening.

She captioned the image: “Just a reminder that future SMA babies’ lives don’t need to look like this!

“These are Ocean and Story’s spinal braces that [they] now have to wear every day.”

Jesy also shared a snap of the Parliament debate poster and wrote: “I hope to see as many of you there tomorrow. It’s going to be a big day.”

SO BRAND NEW

What Jesy Nelson really thinks of Perrie’s brutal put-down after ‘glow-up’ hol


KATIE’S RAGE

Katie Price slams ‘beggy’ women after Lee Andrews gets saucy snap from fan

Jesy also shared a snap of the Parliament debate poster Credit: Instagram/Jesynelson
Ocean Jade and Story Monroe were born prematurely in May last year and were diagnosed with Spinal Muscular Atrophy (SMA) Type 1 Credit: Instagram/Jesynelson
Jesy recently spoke out about the unjust and “nsane” SMA “postcode lottery” – which “decides if children will be disabled or not” Credit: Instagram
Jesy has fought hard to get SMA heel prick testing on the map Credit: Instagram/Jesynelson

It comes after Jesy spoke out about the unjust and “nsane” SMA “postcode lottery” – which “decides if children will be disabled or not.”

The loving mum appeared on social media in a candid video expressing her deep frustrations over ‘unfair’ Spinal Muscular Atrophy (SMA) heel prick testing.

The X Factor star – who has racked up over 150k signatures – is calling for SMA to be tested for at birth regardless of where you live.

The debate is set to take place tomorrow, June 22, and, if granted, SMA screenings will be added for newborns.

Jesy is calling for SMA screenings to be added for newborns all over England Credit: Instagram
The singer shared the areas currently missing out on screening Credit: Tiktok/Jesynelson

The singer’s daughters Ocean Jade and Story Monroe were born prematurely in May last year and were diagnosed with Spinal Muscular Atrophy (SMA) Type 1.

In the emotional video, the singer said: “I just wanted to come on here to basically chat about a few things that are just so incredibly important to me and I know so many other people.

“Some of you may be aware of the fact that I’ve been trying to get SMA as part of the heel prick test here in England, and thank God for you guys, the signatures got over 150,000 and because of that, it is now going to get debated in parliament this Monday coming up, which is just crazy to me to know that we did that and I just need you guys to know that this has never been debated in parliament before.

“There has been a whole community of people that have been screaming and shouting about this for years and years and years, and it’s never been able to get this far, because it’s been ignored every single time.

“But you guys did it, because you made enough noise and you supported this and you got it there and I cannot thank you guys enough…

“So many thoughts have been going through my mind over this week, because every time I think about it, I’m like, how am I going to Parliament on Monday to debate whether children, future children, are going to be disabled or not?

“That’s how deep it is, because if your child gets this treatment from birth with a simple heel prick test and they get this treatment, you would not even know that they have SMA. 

“That’s how deep it is, right? That is how life-changing this treatment is. You would not even know that your child has SMA, but if they don’t get this treatment and they don’t get the heel prick test, they will go on to be disabled…

“And not only be disabled, but they will go on to have breathing machines, coughing machines, constant operations. It never ever ends.

“And I still can’t believe that in this day and age, when we’ve had three life-changing treatments now for nearly six years, it’s still a thing. It’s still not here in England.

“It is being rolled out in October, but only in certain parts of England.

“How does that make sense? How are we playing postcode lottery with children’s lives? How is that okay? I cannot stress you how important this is.

“This is our future, future children we are deciding on. Mums now that are currently pregnant and maybe about to have a baby that could potentially have this disease. We’re basically going to decide whether they’re going to be disabled or not, like it blows my mind.

“And I just seem to stress this so much, because that’s how deep it is. We are playing with children’s lives and it is not okay.

“It’s not okay to be like, if you live in this area, your child won’t be disabled, but if you live in this area, yeah, they’ll be disabled.

“We’re not doing this anymore. We’ve made too much noise now for this to be ignored.

“Anyway, sorry for getting irate about this, but it makes me so sad to think that my children’s lives could look so different and not only my children’s lives, but so many other families and children are dealing with this across the whole of England.”

Alongside the tear-jerking post, she added: “We have had some amazing news that screening is due to start in October this year, which is a huge step forward!

“But there’s still a big problem… it will only cover 72% of England. That means some babies won’t be screened simply because of where they live.

“A postcode lottery like that just isn’t fair. Every baby deserves the same chance, everybaby’ss life matters!

“On Monday 22nd June, the petition will be debated by MPs in Parliament. I’ll be there alongside @gileslomax from SMA UK and we’re hoping this debate will help push for screening to be available for every newborn across England.

“We’ll be arriving at 5pm on Monday, and it would mean so much to see as many of you there as possible. We’d love to get a photo together outside Parliament before we head inside.

“Please if you can, tag your MP in the comments and ask them to attend the debate and support universal newborn screening for SMA.

“The areas currently missing out on screening are: Bristol, CambridgePortsmouth, Leeds, LiverpoolOxford.

“No baby should miss out because of their postcode. Let’s keep fighting until every newborn has the same opportunity. Thank you for standing with us every step of the way!”

Source link

Twin Peaks actor Owain Rhys Davies dies suddenly aged 44 as his heartbroken brother pays tribute

TWIN Peaks star Owain Rhys Davies has died aged 44.

Owain’s heartbroken family confirmed the news of his sudden death on social media, hailing him as “a brother to many” in a touching tribute.

Owain Rhys Davies arriving at the 2017 AMD British Academy Britannia Awards.
Owain Rhys Davies’ heartbroken family confirmed the news of his death on social media Credit: Getty
Owain Rhys Davies on the red carpet, wearing a blue suit and a tie with a tropical leaf pattern.
The Twin Peaks star was hailed as “a brother to many” in a touching tribute from his brother Credit: Alamy

The Welsh actor was best known for his role as Agent Wilson on Twin Peaks: The Return.

He also starred in Disney’s Alice Through The Looking Glass and A Serial Killer’s Guide To Life.

And his talents took him to the West End too, with appearances in London productions such as The Wizard of Oz and Mamma Mia!.

Owain’s brother Rhodri wrote: “It is with profound sadness that my father and I share the news that my brother, Owain, has passed away.

NO SHAME

I was first to interview Lee Andrews — his reaction proves he’s out for himself


CAREER STALLED

Shamed Stephen Bear selling £2 SMOOTHIES on street market with teen wife

“This news will come as a great shock to many. The reach of Owain’s love, friendship, and generosity was vast.

“While there are still questions that remain unanswered regarding the circumstances of his death, our understanding at this stage is that Owain passed suddenly, naturally, and peacefully.

“The outpouring of messages we have received over the past few days has been deeply moving and a testament to the impact he had on so many lives.

“Owain was fortunate enough to have more than one family.

“Alongside his biological one, he built extraordinary, family-like bonds with many of his closest friends, colleagues, and loved ones.

“I am incredibly proud that, while he was my brother, he was also a brother to so many others.

“We know that this loss will be felt by a great many people, and we take comfort in knowing how loved he was.”

Tributes have flooded in from celebs across the acting world, including Coronation Star Hayley Tamaddon.

The devastated actress, 49, described Owain as a “beautiful friend” in a heartbreaking tribute.

It read: “Heartbreaking to hear that my beautiful friend has passed away. Owain was loved by so many. He lit up Every room he went into.

“I have some wonderful memories of us together, we go back so many years.. but our time together in LA will always make me smile.

“Sleep well my love. My heart goes out to his friends, and family Rhodri and Conway.”

Downton Abbey star Joanne Froggatt said: “No words seem to convey my emotions. I am so sorry for your loss and the grief you must be feeling.

“I am devastated to lose our beautiful friend, he was more than a friend, he was joy and life and talent and kindness and fun and intelligence.

“He was everything and my brain can’t compute that we don’t get to hug him again.

“What I would give for one more hug. You’re forever in our hearts cariad.”

More to follow… For the latest news on this story keep checking back at The Sun Online

Thesun.co.uk is your go-to destination for the best celebrity news, real-life stories, jaw-dropping pictures and must-see video.

Like us on Facebook at www.facebook.com/thesun and follow us on TikTok @TheSun.



Source link