Inside Jesy’s heartbreaking split as she ditches ring after twins’ heartbreaking diagnosis

Inside Jesy’s heartbreaking split as she ditches ring after twins’ heartbreaking diagnosis

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Following the heartbreaking news that their daughters have been diagnosed with type 1 spinal muscular atrophy, Jesy Nelson has decided to break off her engagement to Zion Foster.

After four years, Little Mix star Jesy Nelson is rumored to have broken up with her ex-boyfriend Zion Foster. Jessica, who announced her engagement in September, was last seen on ITV This Morning without her ring.

After dating rapper Zion for years through mutual friends, Jesy and Zion first started dating in 2022. The pair “remain friends,” according to a source, and Ocean Jade and Story Monroe, their daughters, continue to be their top priority after being diagnosed with type 1 spinal muscular atrophy. Jesy revealed her heartache earlier this month after doctors warned the actress that the two girls might never walk.

READ MORE: Jesy Nelson and Zion Foster’s love story as they ‘split’ after three yearsREAD MORE: Jesy Nelson’s fiancé pens heartbreaking letter to ‘warrior’ twins after devastating diagnosis

She and Zion are still friends and focused on their daughters, according to a source close to The Sun. They are completely at peace with co-parenting. The well-being of their daughters is still top of their list of priorities.

Just days before the split news, Zion posted an eyebrow-raising post on Instagram claiming Jesy to be a “superwoman” and telling fans, “we are one.”

He cited an “Ocean &amp, Story” poem. We are one in all. The definition of a superwoman is Jesy addressing a serious issue with our healthcare system. It needs to be changed because reality is so inconvenient. With the development of novel treatments, in the UK, how can children be tested for SMA at birth?

Thank you for accepting, supporting, and fighting with us, SMA and the wider community of those living with more unique challenges.

Zion’s self-written poem, which he wrote, focused on accepting the daily reality of seeing his eight-month-old daughters cope with the condition.

He said, “They said it’s unlikely you’ll walk, you might not be able to talk, you might not be able to hold your head up,” which is what Jesy and I heard. SMA Type 1. What’s certain, then, since it became so obvious that doctors only measure what they can determine?

“I watch your smiles as sunsets, real as they are, not promised.” When I listen to you babble the sweetest melodies, I wonder if I’m loving you or loving my fear if I keep telling you who I want you to be, what I want you to do, what I expect from you. Am I loving you if I accept you for what God gave you, exactly as He knitted you, with no modification? Is that okay with me?

He continued, “Story, is your heart okay? ” How are you, Ocean? Two young warrior girls who already know how to fight, you always seem to have strength in your lungs when you cry. Sincerely, my concern isn’t the milestones; it’s just that life is being forced to go through a different trajectory. My concern is more profound and quiet. It’s about being open to and loving you without conditions for who you are now.

Ocean Jade and Story Monroe, both of whom were born prematurely and after Jesy spent weeks in the hospital as a result of a serious condition known as Twin-to-Twin Transfusion Syndrome (TTTS), were born on May 15, 2013.

The chart-topping actress documented the two babies’ early years for a documentary special by documenting their first few weeks in intensive care before they were finally allowed home.

The couple revealed on social media that Zion had asked the question and Jesy had accepted it in September of last year. Jesy proposed to my best friend in a hurry.

But on January 7, Jesy appeared on ITV This Morning to discuss their daughters’ diagnosis – and her diamond sparkler was clearly missing. She also didn’t mention her relationship with Zion.

Jesy explained in a video earlier this month that her daughters had been diagnosed with SMA, a genetic condition that eventually destroys body parts. The singer cried out as she grieved a life she believed she would lead with her children.

SMA causes limb floppiness, breathing difficulties, swallowing, and motor skills that are delayed. Jessica claims that by “putting them on breathing machines and engaging in activities that no mother should have to do with their child,” her life has been turned around.

After her mother noticed the twins weren’t moving as much as they should, the star first visited her GP. Jesy claimed she told herself not to “compare” the babies to other babies of the same age because she had been warned that they would develop more slowly as they were premature. Jesy pushed for answers while the twins were battling with SMA Type 1 and her daughters were given the keys to feeding.

Jesy said in an Instagram update that she was unsure where to begin with the video. My mother noticed a few months ago that the girls’ legs weren’t moving as much as they should.

I didn’t really care about it at the time, I thought. Your babies are premature, so don’t compare your babies to other babies, I was told right away when I left the NICU. They simply accept them as they are, and they won’t achieve the same goals.

She said, “I didn’t really hear the alarm bells.” I was instructed not to compare them to my first set of children because they are my first. The girls’ health care providers reaffirmed that everything was alright and that the girls were healthy.

Later, there were some indications that the girls were having trouble consuming enough food. Our babies are not consuming as much food as they should, we would tell the doctor. They said it was fine and that they were careful and frequently, she said.

The girls have been given the diagnosis of a severe disease called SMA type one after the most exhausting three to four months and endless appointments, Jesy continued. Every muscle in the body, from the legs to the arms, is affected by spinal muscular atrophy, which affects swallowing as well. It eventually causes the body’s muscles to become dead. Your baby’s life expectancy won’t exceed two if it isn’t treated in time.

And last week, protective father Zion described the lack of testing at birth for SMA as “indefensible” in a poem that he posted on Instagram. He wrote: “They said it’s unlikely you’ll walk, you may not be able to talk, probably won’t be able to hold your head up.

“That’s what Jesy and I heard,” Doctors only measure what they can measure, and it became so obvious as a result. What’s the matter then?

Continue reading the article.

Two young warrior girls who already know how to fight, “I hear strength in your lungs every time you cry.” Sincerely, the milestones are not my concern. doesn’t make life look different. My concern is more profound and quiet. No matter what the outcome of tomorrow or what yesterday was, it’s about accepting you and loving you for who you are right now, without conditions.

Source: Mirror

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