Parents with Dwarfism Welcome Children Despite Medical Challenges
For most couples, the question “When are you having kids?” is routine. For Charli Worgan and her husband Cullen, it was never that simple. Both living with forms of dwarfism, the Sydney-based couple faced constant scrutiny and judgment. People didn’t just ask when — they asked why.
But Charli and Cullen refused to let public curiosity define their family. They dreamed of children, and nothing would stop them. When their first daughter, Tilba, was born, joy eclipsed fear. Her healthy smile erased years of doubt and worry. Inspired, Charli started sharing their life online — not for fame, but to educate, challenge stereotypes, and show that a family with dwarfism is just like any other: full of love, chaos, and laughter. Her Instagram quickly drew over 300,000 followers, captivated by her honesty, humor, and courage.
As their family grew with a second daughter, Tully, Charli’s journey became more complex. When she announced her third pregnancy, the excitement was shadowed by genetic realities. Each pregnancy carried a one-in-four risk of fatal double dominant dwarfism, meaning the stakes were higher than most parents could imagine. At 14 weeks, while others celebrated milestones, Charli underwent invasive testing — a procedure fraught with risk — just to know if her baby could safely enter the world.

Yet through fear and uncertainty, Charli chose transparency. She shared her story openly, facing criticism and praise alike. Some questioned her choices, but she responded with grace: “Bringing a child into this world with my odds isn’t simple — it’s personal, filled with love, faith, and courage.”
In February 2021, her perseverance was rewarded. Charli gave birth to a healthy son, Rip. Her post captured the emotion perfectly: “I’m tired, but ever so grateful. There’s no ‘correct’ way to do motherhood, but there’s no wrong way either.” Her words resonated globally, a reminder that love defines parenthood, not perfection.
 
		
 
			 
			 
			 
			 
			