In early 2011 my son Connor, was diagnosed as Autistic and Mosaic Fragile X, he was not quite 2. It was both shocking news and an explanation of the incredibly hard few years that had led to that point. But I knew, that was just the beginning for us, we still have Connor's whole life ahead of us and since then his baby sister Merryn has also been diagnosed FXS.
We were featured in a story in the September edition of MiNDFOOD along with two other families who also have inherited genetic conditions. The stories of the other two families made me cry. As always I'm just so relieved that we get to keep our kids and don't run the risk of them dying of this condition. Just click below if you'd like to have a read.
posted by ConnorsMum @ 11:21 am
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These days I'm a stay at home mum looking after Connor, 2 and Merryn, 8 months (as at Christmas 2011). In my previous life I worked in the Computer industry mostly with websites and databases. I've lived and worked across a number of cities in Australia like Brisbane, Sydney and Melbourne, as well as in the USA and Canada. I'm now based in Brisbane and haven't had the chance to travel much since starting to have children a few years ago. I started blogging as a way to cope with the ongoing stresses created by Connor or more specifically his diagnosis. Connor has Autism and Fragile X, and while that has massive implications for his future it also has implications for my health too as I am a carrier. I plan to write about our ongoing journey with the syndrome as well as fill in what has happened up to this point on my blog MyFragileXBoy. Update: Merryn has now been confirmed as having Full FXS too.
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