Hi all,
I’ve been waiting for a group like this to appear. I was born in New Zealand in 1978 with Gastroschisis. I am not aware of anyone else in NZ that had survived this previous to me. I am turning 29 this year.
When I was born, I was a surprise for all. I was a month premature and ended up in hospital for about a year before I went home. I had various obstructions in my gut and therefore had to have numerous surgeries.
I’ve had various health issues so far - including overall deficiency in absorbing vitamins; B12 deficiency, iron deficiency. I’m now lactose intolarant and also have short bowel syndrome as a result. I also believe I may have had Pica as a child as a result of malnourishment - but hid that from my parents.
I am however very positive about everything. I am very lucky to have survived, and am thankful every day. I have a huge amount of scarring on my stomach due to having so many operations at such an early age.
I would love to hear from anyone else who was born with gastroschisis and see how it has affected them.
Lisa
lisa[at]niche.co.nz (Replace the [at] with @)


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