{"id":2231404,"date":"2026-01-12T10:14:12","date_gmt":"2026-01-12T10:14:12","guid":{"rendered":"https:\/\/celebrity.land\/en\/?p=2231404"},"modified":"2026-01-12T10:14:12","modified_gmt":"2026-01-12T10:14:12","slug":"heres-heartbreaking-reason-why-a-singers-twin-infant-daughters-might-not-ever-walk","status":"publish","type":"post","link":"https:\/\/celebrity.land\/en\/heres-heartbreaking-reason-why-a-singers-twin-infant-daughters-might-not-ever-walk\/","title":{"rendered":"Here\u2019s heartbreaking reason why a singer\u2019s twin infant daughters might not ever walk"},"content":{"rendered":"<p><\/p>\n<div>\n<p class=\"article__paragraph article__paragraph--left\" id=\"DPLZFYXDCZBYLMIWZXDAETOMHU\">Jesy Nelson is staring down a situation that no parent would want to face. <\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"3NA24HZAWZFNXGZJMR73TQ4WTM\">The former Little Mix member turned to Instagram recently to share some devastating news.<\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"JX6FQX3JVVDWTI2GEZB6BHEEXI\">In a <a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/www.instagram.com\/reel\/DTFcIARCLE1\/?utm_source=ig_embed&amp;ig_rid=b1d37478-575a-4c92-8437-acf7dd619947\" target=\"_blank\" rel=\"\" title=\"https:\/\/www.instagram.com\/reel\/DTFcIARCLE1\/?utm_source=ig_embed&amp;ig_rid=b1d37478-575a-4c92-8437-acf7dd619947\">video<\/a>, Nelson provided a health update about her 8-month-old twin daughters, Ocean Jade and Story Monroe, revealing that they have been diagnosed with a rare genetic condition called Spinal Muscular Atrophy (SMA) Type 1.<\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"WQRRTTMXVRDODEJ45SD3NU3GFI\">\u201cWe were told that they\u2019re probably never going to be able to walk,\u201d the 34-year-old tearfully explained in the clip. \u201cThey probably will never regain their neck strength, so they will be disabled. And so the best thing we can do right now is to get them treatment, and then just hope for the best.\u201d<\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"7ALXQV6PNJF47PQYRCFC5B23PY\">\u201cThankfully, the girls have had their treatment, which you know, I\u2019m so grateful for because if they don\u2019t have it, they will die,\u201d she added. <\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"S7SGIS3K2ZHA7BEKUIRJXDH6VQ\">Also heartbreaking was the fact that the singer admitted to feeling \u201clike a nurse\u201d for her daughters since she\u2019s had to put them on breathing machines and see about \u201clots of stuff that no mother should have to do.\u201d <\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"W2EFEKVAMFHU3LESSLPCLNHVNI\">The condition is an inherited neuromuscular disorder that causes muscle weakness to the point that they can waste away, according to the <a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/my.clevelandclinic.org\/health\/diseases\/14505-spinal-muscular-atrophy-sma\" target=\"_blank\" rel=\"\" title=\"https:\/\/my.clevelandclinic.org\/health\/diseases\/14505-spinal-muscular-atrophy-sma\">Cleveland Clinic<\/a>. There are five subtypes, which range in severity to age of onset. <\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"LN7LDLPFSVHSXH7A7YKBKU5QAM\">SMA Type 1 makes up about 60% of cases, with symptoms usually showing up in the first six months of life. Since there is no cure, certain therapies and medications are able to help manage symptoms.<\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"EB7EFC2N6VAMXOCB5SRZPXYQXQ\">The identical twin girls were born to Nelson and her fianc\u00e9, Zion Foster, on May 15, 2025. They were born prematurely at 31 weeks after the singer experienced complications from carrying monochorionic\/diamniotic twins. <\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"3YQEQWPTYNGVZDTJM7YGQVGJFY\">These are twins that share a placenta but have separate amniotic sacs.<\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"NYAPHMW6FND2LCFKLG3LDJJNOY\">To Nelson, sharing her bad news on social media will hopefully reach women who are also facing the same, anguishing diagnosis and pinpointing similar symptoms in their child. <\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"SSXLTIUDCNGYPPTGWSP2HF5IDI\">\u201cI just think that I can raise as much awareness about this as possible, and the signs, then, you know, something good has to come out of this,\u201d she said. <\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"UGN7RQG5HVHKDB4JHBSMZHO33E\">Nelson also described tell-tale symptoms such as the inability to hold themselves up without support, a \u201cfrog-like\u201d leg position, and rapid tummy breathing.<\/p>\n<p class=\"article__paragraph article__paragraph--left\" id=\"X2PTLLEUZZFC5GYQXUQE6PBPPE\">\u201cIf anyone is watching this video and they think they see these signs in their child, then please, please take your child to the doctor, to the hospital, because time is of the essence, and your child will need treatment. And the quicker you get this, the better their life will be.\u201d<\/p>\n<\/div>\n<p><script async src=\"\/\/www.instagram.com\/embed.js\"><\/script><\/p>\n<p><em> \u2018 The preceding article may include information circulated by third parties \u2019 <\/em><\/p>\n<p><em> \u2018 Some details of this article were extracted from the following source www.pennlive.com \u2019 <\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Jesy Nelson is staring down a situation that no parent would want to face. The former Little Mix member turned to Instagram recently to share some devastating news. In a video, Nelson provided a health update about her 8-month-old twin daughters, Ocean Jade and Story Monroe, revealing that they have been diagnosed with a rare [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"_jetpack_memberships_contains_paid_content":false,"jnews-multi-image_gallery":[],"jnews_single_post":[],"jnews_primary_category":[],"jnews_social_meta":[],"footnotes":""},"categories":[25172],"tags":[],"class_list":["post-2231404","post","type-post","status-publish","format-standard","hentry","category-entertainment"],"jetpack_featured_media_url":"","jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/posts\/2231404","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/comments?post=2231404"}],"version-history":[{"count":1,"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/posts\/2231404\/revisions"}],"predecessor-version":[{"id":2231405,"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/posts\/2231404\/revisions\/2231405"}],"wp:attachment":[{"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/media?parent=2231404"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/categories?post=2231404"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/celebrity.land\/en\/wp-json\/wp\/v2\/tags?post=2231404"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}