So the CMV Action Family Day, is nearly upon us! Continue reading
I first contacted, my MP John Leech, about Mike’s feeding therapy back in August 2013. It was after five months of hearing nothing back, not even an acknowledgment, from the Clinical Commissioning Group, about the treatment I so desperately wanted for my boy. There began a relationship, that changed the course of my family’s future. Especially Mike’s. Continue reading
Tuesday, 3rd April 2012, around half four in the afternoon my life was turned upside down. Continue reading
So almost half way through Mike’s first year at pre school.
In our area, we have nurseries connected to our primary schools and Mike has joined his big brother there, in a mainstream school. Continue reading
Mike’s birth was nothing but dramatic, the moment my waters broke they were thick with meconium. I was allowed to labour but the doctors struggled to keep a good trace on Mike’s heart and so he was born by emergency caesarean section. Continue reading