Lisa Lee, 25, was sleeping next to her husband Lewis Little when she thought she heard him snoring. “I shoved him out of bed to stop what I believed was snoring,” Lisa explained. But as she touched the moist sheet, she knew something wasn’t right. Lewis wasn’t breathing. “I turned on the light and stared at his battered face,” she added.
Panicked, Lisa called for an ambulance, but the wait felt endless. When medics arrived, they broke the heartbreaking news: Lewis had passed away hours earlier. The sound Lisa had mistaken for snoring was, in fact, air escaping his body and passing through his vocal cords.
Lewis had been diagnosed with Brugada syndrome, a rare heart condition, just a year earlier. Doctors had assured him that his life wasn’t in danger and that he could live a long life despite the condition. Tragically, just a year later, Lewis died unexpectedly in his sleep.
Lisa was left in shock. “I couldn’t believe it. The doctors told us he was going to be fine,” she said, still processing the sudden loss of her husband.
Brugada syndrome is a genetic condition that affects the heart’s rhythm and can lead to sudden death. In Lewis’s case, it proved fatal despite earlier reassurances.
Despite the danger: a woman with dwarfism boldly poses with her baby belly on the beach.
Most married couples get asked “when,” but Charli Worgan and her husband Cullen frequently received “why” questions.
The parents, who live in Sydney, are frequently in the spotlight due to their unique forms of dwarfism, most notably when Charli got pregnant with their first child.
After giving birth to their first child, the content Australian mother created a social media account to share updates on their family life with others. Little did she know how well-liked her account would become.
With two stunning daughters under their belt, Charli has amassed over 300,000 Instagram followers.
Charli recently revealed that she was fourteen weeks pregnant with her third child, but the announcement was bittersweet.
Charli has had to undergo thorough genetic testing during each pregnancy. Experts warn that if Charli and Cullen’s offspring inherit just one type of dwarfism, inherit both forms, or are of average height due to their genetic problems, the results might be fatal.
Charli expressed her disappointment at not being able to celebrate her pregnancy’s 12-week mark with her family, as most mothers do.
But at 12 weeks, I was preparing for a procedure called Chorionic Villus Sampling (CVS), which is similar to an amniocentesis, whereas most individuals are pleased to be able to announce their pregnancy. To check the embryo’s genetic composition, a big needle is placed into my abdomen to extract a sample of the placenta, which has a 2% miscarriage rate.
Their two daughters, Tilba, 4, and Tully, 2, each have one of the two varieties of dwarfism, so they waited to find out which of the four possible dwarfisms Charli’s third child would have.
In an Instagram post, Charli explained, saying, “Our child would be of ordinary height.”
Our child would have achondroplasia and be dwarfed similarly to me.
Our child would have geleophysic dysplasia, the same type of dwarfism that Cullen has.
As a result of inheriting both genetic defects, our child would be born with “double dominant dwarfism,” which is fatal according to every expert medical assessment. In the event that this had occurred, I could have decided to terminate the pregnancy or to go on and see how things turned out.
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