The first thing you need to know about Harry is that despite his difficult start to life, he’s such a happy little soul.
The short version of his story is that Harry suffered severe brain damage and now has spastic quadriplegic cerebral palsy and many other complex needs. He can’t make his arms move to reach for a toy, hold his head up or eat without the aid of a tube. He’s not meeting any of his milestones and sadly, his list of problems is likely to increase as he grows.
We’ll keep you updated on Harry and how your support is helping to give him the best life possible on here. But for now, we asked Harry’s mum, Hayley to tell us a little more about their journey:
Our little smiler, by Harry’s Mum
When my husband Andy and I found out that we were having a little boy we were just overjoyed, it would complete our perfect little family with his sister Lily being just two years older – a perfect age gap for playing, making them lifelong friends. Andy and I had visions of family holidays, strapping the push bikes on the back of the car and carefree family days out.
It wasn’t until Harry’s second day of life that we realised that there was something wrong with our gorgeous little bundle. Harry started to have seizures… from them on our world started to unravel bit, by bit. He was rushed down to neonatal where doctors conducted tests to try and fathom out what was wrong with him. From the outside Harry looked so perfect, it just seemed so surreal that this was happening to us- this is what happens to other people.
Four days later we were called into a waiting room by Harry’s consultant – his brain scan had revealed that Harry had suffered strokes prior to being born which had caused “significant brain damage”. That was the moment our lives changed forever – 18 months on and the memory is still as vivid and heart breaking as ever. The consultant couldn’t give us a prognosis for Harry other than what he may be likely to have, he listed these like he was giving us a list of groceries; cerebral palsy, visual and hearing impairments, trouble with speech, epilepsy, feeding difficulties, learning difficulties and even breathing difficulties.
19 months on and Harry has been diagnosed with spastic quadriplegic cerebral palsy, this basically means that he has stiffness in all four limbs because his brain isn’t sending the correct messages to his muscles. He also is extremely delayed in his development, has trouble with his eyesight, feeding problems (resulting in him being tube fed) and suspected epilepsy. For Harry this means that he is unable to reach for a toy, or roll over to get himself out of harms way. He is unable to hold his head up properly and the poor tone in his stomach means that he is unable to keep his food down. Despite all of these things though Harry is a little smiler, he loves cuddles and music and giggles like crazy when you put him in his new swing. As a family we are still coming to terms with our new reality and learning to adapt to make sure that we give both of our children the most fulfilling childhood that they can have, it may not be what we imagined but day by day we are growing stronger and more resilient.