Jesy Nelson Says Rare Disorder May Prevent Her Twin Daughters From Walking

ugh i feel so bad for jesy nelson and her little ones 😩 she must be going through the worst pain right now thinking about her babies having to deal with this condition 🤕 i mean we can't even imagine how hard it is as parents already, adding a genetic disorder on top of that is just devastating 💔 at least she's being so open and honest about it though, raising awareness is key 🙏 let's all send our love and support to her and her family 🌟
 
😩 this is literally heartbreaking... i cant even imagine having to deal with this kind of news on top of everything else as a single mom... sma type 1 sounds like such a nightmare, no cure or anything... my heart goes out to jesy nelson and her girls 🤗💕 it's so important for parents to know about sma and seek help ASAP, time really is of the essence here 💯 hopefully with all the treatments and therapies available, ocean jade and story monroe can live full lives despite this diagnosis 💖
 
🤔 I'm not sure how reliable the info on this SMA diagnosis is 🤕. I mean, 60% of cases being accounted for by Type 1 is a pretty big claim. Can we get some credible sources to back this up? And what's the likelihood of her daughters actually never being able to walk? That sounds like a pretty harsh prognosis 💔. Maybe they'll make a miracle recovery or find a treatment that works? We shouldn't be counting out hope just yet 🌟.
 
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