As many know my son, Noah was diagnosed with severe Haemophilia in January. It was and continues to be a life changer for all of us.

Noah is too young to understand the implications of it all just yet, but he will one day. Nevertheless, he’s the happiest lad in the world and faces everything with such determination. Treatment every other day, surgery at 12 months, blood tests and all.

We’re determined that nothing will be off limits for Noah despite the obvious difficulties. This is for him therefore..

The Haemophilia  society offer support for people like us. Days out, advice, advocacy and support. Their ongoing support is invaluable for sufferers and families.