twins

When the horn sounded to end Friday night’s City Section Open Division boys’ basketball final, the first person OJ and EJ Popoola wanted to hug was their father, Chris.

Thirty years ago, he transferred from Westchester to Palisades to help the Dolphins reach the 4A semifinals. In June, his twin sons transferred to his alma mater from a Detroit prep school with hopes of making their papa proud and lifting the town’s spirit.

Mission accomplished.

OJ scored 19 and EJ added 17 as the Dolphins used tenacious defense, a three-point barrage and a relentless transition attack to overwhelm Cleveland, 75-56, at L.A. Southwest College.

Jack Levey made five three-pointers, raising his season total to 108, and Phil Reed had 13 points.

“This means everything,” OJ Popoola said. “Since the first day we came here this is what we wanted to do, bring joy back to the community.”

“We’re coming back next year to defend the title,” EJ Popoola added. “My dad’s team came up short but we finished the job.”

Playing the final at a neutral site was nothing new for a squad that did not play in its own gym for 42 straight games — a span of 388 days — in the aftermath of the Palisades fire last year.

“We accomplished two goals, winning league and City,” second-year coach Jeff Bryant said. “Now state is the third goal.”

Palisades (20-11) was in command from the start. OJ Popoola swished a three-pointer from the corner, Reed got a steal and scored on a layup, and Levey passed to OJ Popoola for a dunk, making it 7-0 after only 55 seconds. The Dolphins stretched the lead to 25-8 by the end of the first quarter and the margin was 19 by halftime.

Both teams lost in the Open Division semifinals last winter and were the preseason favorites to play for the title. They were awarded the top seeds in the eight-team bracket after each finished first in its league.

The Dolphins staked their claim as the best team in the City for the first time since 1969, when Palisades routed Reseda 85-57 in the final at Pauley Pavilion under the program’s first coach, Jerry Marvin, to finish the season 21-1 when there was only one playoff division. Leading that team was forward Chris Marlowe, who was named MVP after netting 29 points in the title game. He went on to captain the U.S. Olympic volleyball team that won the gold medal at the 1984 Summer Olympics.

Since it opened in 1961, Palisades has been the crown jewel of the City Section, claiming more than 260 titles across all sports (more than twice as many as the next-closest school), but this is only the third in boys’ basketball.

Palisades captured the Division I crown six years ago under former coach Donzell Hayes, who was a teammate of Chris Popoola on the Dolphins’ 1995-96 team that fell in overtime to Crenshaw (coached by the legendary Willie West) in the 4A semifinals.

“My team was one game away but these kids completed the circle,” Chris Popoola said, then referenced a famous Dolphins alum. “I hope Steve Kerr was watching.”

Sophomore guard Charlie Adams, who scored 24 points in the Cavaliers’ 68-64 overtime win against Fairfax in the semifinals, was limited to 13 — part of Bryant’s pregame plan.

Sergine Deme scored 19 points and had five dunks, and TJ Wansa added 11 points for No. 2 Cleveland (20-10), which was seeking its first championship since back-to-back 3A titles under Greg Herrick in 1981 and 1982.

No City opponent came closer than 15 points against Palisades, which now waits to see what division it will play in for the state playoffs.

“We’re not done,” OJ Popoola said.

“We can compete with anyone,” EJ added.

JESY Nelson has shared an adorable new video of her giggling twin girls.

The pop star’s mum Janice can be seen holding one of the twins who erupts into laughter as her nan nuzzles her face into her neck.

In another clip, Jesy, 34, can’t help but chuckle about her daughter’s little mullet hairstyle, while she likens the other to a Cabbage Patch doll as she runs her fingers through her hair.

Nine-month-old sisters Ocean Jade and Story Monroe look happy and well-loved in the sweet footage on Instagram.

The singer gave birth to her little girls prematurely at 31 weeks and is no longer with their music producer dad Zion Foster.

Last month, Jesy bravely revealed the tots have been diagnosed with Spinal Muscular Atrophy Type 1 (SMA1).

brave mum

Jesy Nelson reveals new video of twins holding hands after breaking down in tears

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Jesy Nelson bursts into tears over struggle her twins are facing

The incurable condition causes muscles to waste away, but early detection and treatment can significantly improve prognosis. The girls have had gene therapy infusion to prevent their muscles from deteriorating, but damage already suffered cannot be reversed.

If untreated, the life expectancy of a baby with SMA Type 1 is two years.

Jesy and Zion have been told it is unlikely the girls will ever walk and may face serious breathing and swallowing difficulties.

Only around 50 children in the UK are born with the condition a year.

The former Little Mix star and mum-of-two has seen her Amazon documentary on her parenthood journey hit number one spot while continuing her fight for life-saving SMA tests.

Recently, she became emotional about the struggles her twins will face growing up.

Jesy revealed she “burst into tears” after receiving the special feeding chairs her daughters will need.

She admitted the arrival of the equipment brought home the reality of their condition.

She posted a photo of one of the special feeding chairs to her Instagram story.

Spinal Muscular Atrophy: Signs and symptoms

Spinal muscular atrophy is a disease which takes away a person’s 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 faulty 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.

It showed a pink cushioned chair with straps, a headrest, a tray, a foot stand, handlebars, and wheels.

She wrote: “So the girls need special feeding chairs that came yesterday, and I couldn’t help but burst into tears yesterday when I saw them.

“It just made me feel so sad as it’s just another reminder of another obstacle we have to tackle. Do any other SMA mummies feel this way?”

In her first TV interview since revealing the twins had SMA, Jesy tearfully told This Morning hosts Cat Deeley and Ben Shephard: “I just want to be their mum. I don’t want to be a nurse. It’s hard.

“They’ve had their treatment, thank God. A one-off infusion. That puts the gene back in their body that they don’t have. It stops the muscles still working from dying. Any that have gone, you can’t regain them back.

“Now it’s down to constant physio. We’ve been told they’ll probably never walk or regain their neck strength. They’ll probably be in wheelchairs.”

Jesy revealed how the twins were going to Great Ormond Street Hospital twice a week.

“They’re still smiling, they’re still happy, and have each other. That’s the main thing I’m so grateful for because they could be doing this by themselves,” she continued. “All I can do is try my best to be there for them and give them positive energy, keep doing physio.

“My whole life has completely changed. If you came to my house, it looks like a hospital. My whole hallway is filled with medical stuff. It’s crazy how you can go from one extreme to the next.”

Since revealing her twins’ diagnosis, Jesy has called on the NHS to expand the standard heel prick test to screen for SMA1.

Large-scale trials are currently taking place, though Jesy is pushing Health Secretary Wes Streeting to speed up the process.