Jesy Nelson has split from her fiancé, Zion Foster, after recently revealing a heartbreaking update regarding her twin daughters, Ocean Jade and Story Monroe Nelson-Foster.
The Sun reports that Nelson was spotted no longer wearing her ring, with a source telling the outlet that, “she and Zion remain friends and are fully focused on their daughters.”
“They are fully united in co-parenting,” the source added. “Their priority continues to be the well-being of their daughters.”
Nelson and Foster got engaged in September 2025, which was four months after they welcomed their daughters.
Jesy Nelson Shares Her Daughters Were Diagnosed With Spinal Muscular Atrophy
In an Instagram video on January 4, Nelson revealed that her daughters were diagnosed with a rare and serious genetic condition called spinal muscular atrophy.
“A few months ago, my mum noticed that the girls were not showing as much movement in their legs as they should be,” she said in the video. “[It] wasn’t really a concern to me at the time because from the minute I left the NICU, I was told, ‘Your babies are premature, so do not compare your babies to other babies. They won’t reach the same milestones. Take them as they are.’”
“When the healthcare visit came, we were told, ‘They look great, they’re healthy and everything is fine,’” she added. “A few signs then started to show a bit later on that they were struggling to feed properly. It was getting gradually less and less and less.”
“Long story short, after the most grueling three [or] four months and endless appointments, the girls have now been diagnosed with a severe muscle disease called SMA type 1,” the singer continued. “Type 1 is the most severe type that a baby can get. It stands for spinal muscular atrophy, which can affect every muscle in the body down to legs, arms, breathing, swallowing and … over time it kills the muscles in the body. If it’s not treated in time, your baby’s life expectancy will not make it past the age of 2.”
Jesy Nelson Reveals Her Daughters May Never Walk Again
Due to the diagnosis, Nelson explained in the video that doctors told her that her daughters are “probably never going to be able to walk,” adding that they will be “disabled.”
“I’m so grateful because if they don’t have it, they will die,” Nelson said. “It has just been endless, endless amounts of hospital appointments. I practically feel like the hospital has become my second home.”
