I am proud mum to 2 gorgeous kids with additional support needs. Both are undiagnosed and affectionately termed SWANS as they have syndromes without a name.

Our lives are anything but straightforward and by the time I started this blog in January 2014 we had come quite a journey…

The live of hopes and dreams for your children was grieved for a few years ago, expectations reset and every small step celebrated and every challenge faced head on with a newfound strength…

Fighting for support is now part of life….

This blog seeks to take you on the journey of our angel and solider, laugh with us, cry with us, share our joy and our challenges….enjoy the ride (you’ll need a tissue every now and again!)

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