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The face of Facebook – Debbie Sinclair

Debbie Sinclair.JPGWe thought it would be useful to introduce you to Debbie Sinclair – our Facebook page administrator. Many of you will have read Debbie’s updates on Facebook.

My name is Debbie Sinclair, I am married to David, together we have three children Mark aged 21 years, Kelly aged 10 years and Andrew aged 9 years. 

In April 2005 I was phoned at work by my specialist following a routine weekly scan at 27 weeks gestation saying I needed to pack up and come to hospital as my third child needed to be delivered as he had stopped growing and there were issues. I was shocked and thought she was having me on.  I was admitted to Dunedin Hospital where I remained an inpatient until 31 weeks and our son Andrew was eventually born by GA emergency c-section, weighing 2lb 10z (1.215kg).

The first four days following Andrew’s birth were a blur.  I lay in delivery suite for this time as the medical team worked hard to stabilise me as I was so sick and unaware of what was going on around me but soon reality sunk in and we were the proud parents of this small little boy who had a big fight on his hands and we were about to take a life changing journey.  Andrew remained in NICU for nine weeks, was discharged and then spent the first four years in and out of  hospital with ongoing chronic lung disease and respiratory illness. 

In 2009 I was notified that The Little Miracles Trust were coming to Dunedin with a view to setting up a regional branch and I decided that I wanted to be a part of  this and felt the need to give back to others. I arrived at the meeting with other families but never did I imagine when I left the meeting that I would be the first Chairperson for The Little Miracles Trust (Otago). I will never forget that  day because it was a double celebration of my daughter’s fifth birthday and the beginning of an amazing journey where I could give back to other families and the staff who gave so much to us.

I was very proactive for The  Neonatal Trust (Otago) and spent a lot of time building relationships with the Dunedin Unit, public figures and addressing media requirements. We hosted an annual charity ball and did many other events to help raise funds for our families. I remained on the Otago Board until I moved to Greymouth 3 years ago and at that time was approached to take over the role as the Facebook administrator for The Little Miracles Trust page. I thought long and hard about this and still wanted to keep giving to the Trust so I accepted this opportunity.

I get a sense of peace and goodwill hearing other people’s stories and the realisation we are a very special group of people who have all walked the same path and whether you are in the Unit for one day or one hundred days, whether your child is born premature or is full term but sick. We have a bond and an understanding that many people will never really understand. 

Giving back is my way of saying thanks to the medical team that saved our son’s life and if I can make the smallest amount of difference to other families then I will be there. A lot of tax payer’s money goes into saving our precious bundles of joy and I will always feel indebted to society, the people who have cared for Andrew and those who have supported us. Every day when I wake up and watch Andrew in his daily activities I thank God for the  blessing and smile knowing that, even though he still lags behind, he will get to where he needs to be in his own time… after all he is our million dollar miracle!

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.

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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.
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