Juliet's thriving 15 years later
Juliets story, as told by her mother Marian.
I am the mother of a recently turned 15 year old daughter whose name is Juliet. She was born at Wellington Hospital at a gestation of 24.5 weeks and weighing 725gm. Following 98 days in the Neonatal Unit Juliet, weighing 2.2kg, was discharged to begin her life adventure. Whilst in the unit I spent each day tending to her needs, kangaroo cuddling her, expressing milk and agonising over her health and progress. Each evening it was so difficult leaving her behind in the unit.
15 years later I am finding it difficult to keep up with her – she is 8cm taller than me, rides in her school cycling team, plays saxophone for both the school jazz group and the orchestra; is learning and excelling at Japanese, French, Latin and English as well as all her other core subjects. She does wear glasses as do many full-term students.
Amazingly she does not have asthma or any other health issues at all. For her first 3 years we had to be careful with chesty colds and she did have pneumonia a few times. Our biggest health moment came 2 months after her discharge from the Neonatal Unit with Juliet being airlifted to Starship Hospital suffering from Bronchiolitis and collapsed lungs as a result.
When I think back to our time in the Neonatal Unit I had difficulty imagining her becoming such a normal well-adjusted wonderful kid, able and wanting to participate in life to the extent she does. She has played soccer, rugby, netball, hockey, she swims, can play tennis and has learned to sail.
Juliet has always been a very happy contented child. Being breastfed for over 4 years I believe has helped her overall, both physically and emotionally. She is now a picture of health and happiness.
*** Thanks for sharing your story Marian and Juliet ***
If you would like to discuss sharing the story of your neonatal journey, we’d love to hear from you. Please email info@littlemiraclestrust.org.nz
Interested in how we support families going through the stress and anxiety of a neonatal journey?
Here’s a gallery of support examples.
Thanks so much for sharing your personal story!
We get a lot of positive feedback from families in a neonatal unit who read these stories and feel strength, hope and positivity knowing that they are not alone going through these experiences and feeling certain emotions.
If you would like to discuss sharing the story of your neonatal journey, we’d love to hear from you.
Support Us
If you want to help our support of families going through the stress and anxiety of a neonatal journey, you can donate via the link below.
- The Little Miracles Trust provides support to families of premature or sick full-term babies as they make their journey through Neonatal Intensive Care, the transition home, and onwards. We do not receive any Government funding and are entirely reliant on the generosity of individuals, companies and organisations in the form of donations, value-in-kind donations, grants, sponsorship and fundraising events to supplement operating costs and fund our services and initiatives.
- As we are a registered charity (CC56619) with Charities Services New Zealand we will send you an IRD compliant tax receipt – this will happen automatically by return email.