Jul 10 2009
Molly Rose … A Miracle Premmie Baby
Molly-Rose,
our true little miracle
(story by Shus, Mollys mum)
Molly-Rose was born on the 5th February 2003 at 25 weeks (3 months early).
We started IVF in August 2002, keeping a very positive and open mind as we knew it could possibly be a long road. We took the normal course of drugs and then came the big day, they put two little embryos back and we all prayed hard for a positive result. What happened next caught everyone off guard. For some unknown reason I had a rare reaction to the drugs and ended up in ICU at Epworth hospital, with severe hyper-stimulation, my right lung had collapsed then my left lung partially collapsed. My stomach had also started retaining fluid. Throughout the next 8 weeks in hospital I underwent numerous procedures to drain litres of fluid from my lungs and stomach and had grown so big. I was told I had a high chance of not keeping the pregnancy.
Finally after 2 mths I was released from hospital and had a wonderful few months, with continuous scans and tests and at every one, bub was still there, growing bigger every day, proving them wrong. I willed her on with all my strength. Then at 20 weeks the haemorrhaging started and I ended up in hospital for the remainder of the pregnancy. Five weeks later at 25 weeks Molly-Rose decided she would join us and at 8.20pm on Wednesday 5th Feb 2003 she was born weighing 880grams (less then a pound of butter), no bigger then my hand, amidst quite a commotion at Cabrini hospital. The NETS ambulance arrived very shortly after and she was whisked away to the Royal Women’s Hospital. My lasting memory of that was seeing this tiny little face peering out from a mass of bubble wrap tucked up inside an incubator. I followed with my Hubbie driving the car, I don’t think either of us really understood what had just happened, we were in a sort of limbo. Did I just give birth?
When we arrived at the RWH they took us to the Neonatal Intensive Care ward (NICU), and so began our fast track introduction to a whole different world. A world of beeps and humming machines, good days and bad. You soon learnt a good beep from a bad beep. The NICU became a new home for us, the nursing staff our new family. It took me 15 mins before I could approach Molly-Rose’s incubator, all I could see at first was a lot of tubes and wires, then somewhere under them all I made out the tiny form of our little baby girl. My heart broke, what had I done, how could I let this happen, I kept saying sorry over and over again. It was late and the blue glow from the lights on the baby next to us lit the area we were in. The next 24hrs were critical for her and we sat by her all night, praying god would let our little girl live and give her the strength to battle this.
Molly-Rose was in hospital for a total of 117 days (4 months), it was a mixed bag of ups and downs, good days and bad days, days when you couldn’t see that light at the end of the tunnel and days when it was quite clear. In those fours months we went forward a few steps then back a few steps, then forward again. She had chronic lung disease, which was making it a little difficult for her to get off her breathing machine (CPAP), we had a few attempts then after 43 days it happened. A wonderful day for us, then came the count down to her coming off oxygen, she’d become an “oxygen junkie”!!. She caught golden staph twice, the first time she was very ill and we had her christened in the Incubator, the second time it was caught early. The usual blood transfusions, heel pricks and IVs. She had ROP stage 3(eye disaese) and then developed haemorrhaging behind the right eye, which lasted for weeks, at one stage we were told she might lose her sight in it. She was a terrible feeder, we would get so far and then end up back on a continuous feed drip, but finally after lots of perseverance from the staff we got the mls up, this meant she was very slow to put on weight, though to this day food is definitely not the centre of Molly-Rose’s world. I will never forget the first time I got to hold her when she was 2 weeks old, an amazing feeling of love and admiration for this little person filled me. Every little feature so tiny, except for two big blue eyes that spoke volumes to me. People asked how we coped, I told them that we drew our strength from her each day, as we watched with such admiration as she battled the odds, if she could do this we certainly could. She was one month corrected when we finally took her home on the 4th June 2003 weighing 2656 grams. The day we left was one filled with absolute joy, excitement and nerves, we’d always had someone around to guide us, from now on it was just the three of us, a family at last. We stood at the entrance of the hospital door as we left, took one deep breath of fresh air and walked on into our new life together.
Since leaving we have spent a lot of time back and forth to the Royal Childerns Hospital, she has been back in hospital twice for respiratory issues and ended up back on oxygen for a while at home when she was younger but we did our best to get over each hurdle and move on. We can never thank enough the staff from the Royal Womens Hospital and the staff at Frances Perry House where she spent time in the special care nursery, without their fantastic work and marvellous support I don’t know how we would have got through. They are all our angels and we can never thank them enough. The other prem mums I have made good friends with since leaving have been a great source of strength for me and I thank them all, they are a wonderful group of strong women, who all have amazing stories of their own to tell. It was these great friendships and encouragement from the RWH that spurred us on to start Lifes Little Treasures (www.lifeslittletreasures.org.au) for parents like us, along with our online support partner
L’il Aussie Prems, we aim to assist as many families as we can. We don’t want any parent to have to go through this experience alone.

Molly-Rose has grown into a most wonderful little human being, she is very active and social, always eager to discover her surroundings and meet new people, and she is now 6 years old and weighs 14 kilos. She has just started school & loves it. To watch her walk around as she busily gets on with her day is a constant source of enjoyment to me; I’m never far from a tear of Joy.
Shusannah
Vice President
Lifes Little Treasures Inc
“Supporting families of premature babies”
Web: http:// www.lifeslittletreasures.org.au
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Thank you so much for sharing your amazing story. What a rollercoaster ride for you and those around you. Your website is full of great support and news and a must for family and friends looking for ways to support those around them through the journey of the birth of a premature baby.
Warmly
Elizabeth xx
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April 2009 
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