Link April 2018 Volume 27 Issue 2 | Page 54

contributions By Rebecca Perkins MY SPECIAL CHILD F or the first few years of my son Lachlan’s life, I didn’t see received a diagnosis of ADHD and an that he was struggling, that intellectual disability. But there was he was so far behind. Or, I refused to see. Then at three-years-old, his When you’re pregnant with still very little support available to us. I became more and more kindergarten teacher turned to me frustrated with the lack of information one day and said she would like to and support out there for parents. get Lachlan seen by a Special In 2014, I moved from England to Needs Coordinator. Australia, hoping that here there What?! Special Needs??? I was would be more, and there was, but your first child, you have a furious. How dare she try and say think their life will be like, my son. I used to teach children that if there wasn’t enough easily with additional needs and I had accessible information and support qualifications in the field; I’d know, for parents, then I would make it and I told her so. accessible. In February 2015, after perception about what you how clever they will be, how many friends they will have. You look forward to watching them play sports and having parties, and you already can’t there was something ‘wrong’ with still nowhere near enough. So, I made a decision. I decided Children develop at different finally getting my law degree, I gave rates, I thought to myself. So, my son up on a career in law and started My is developing a bit slower than the Special Child. wait for their first parent- other kids … so what, he’ll get there. how well they’re doing. began to see it. I finally began to website. It wasn’t very good, or realise that she may have been right. pretty. And I spent months try to fill it And from there our journey through with articles and information. teacher interview to hear But for some of us, this doesn’t become reality. It was 12 months later that I finally the special needs maze began. Lachlan was four-years-old first version of the My Special Child Then slowly I built up more and more readers, and I realised there was more of a need for good support, fighting for services, fighting quality information and support than for information and fighting for a I had realised. of these things were available. contributions I set to work building the very when I began fighting. Fighting for diagnosis. But sadly, very little of any 54 Lachlan was eight when we finally In January 2017, I set to work building My Special Child linkonline.com.au