Im Back !!💙💛

As im sure some of you have seen my post announcing my unborn has a condition called 'Lumbosacral SpinaBifida' I am sure that someone in the world might want an update on how my little one is doing as they could be going threw it or simply just want to know. His fluid on the brain has stayed the same which we had hoped. The chairi malformation is Mild which is amazing and they have named his case in our hospital as the most unique. My little boy has severe Club foot but with spina bifida usualy that is caused by severe tugging on the brain WELL.........

my son has suprised them up to now by having MILD tugging which they are so curious to know what is causing the severe club foot. His wound is quite big on his back and my gorgeous little boy might not have the chance to walk. But thats okay because he'll have an amazing set of wheels to help him get around. If he had the chance to walk it probably wouldnt be for long so introducing a wheel chair can benefit him so much when hes born. This little boy of mine has gone from weighing 14 ounces on the 22nd of March to weighing 1 pound 4 oz on monday which means hes growing perfect. I have so much love amd faith in my son that I know what ever he does in life he'll do it with pride and confidence because thats what me and his daddy will teach him. Hes our special little boy and I only have around 15 weeks left to finally meet him which is scary but in a good way. I love him already and can't wait to meet him. But for now here is a beautiful picture of my son at the minute. Thank you everyone on here for your support it truly is AMAZING. We are crossing every bridge as we come to it and know as much as there will be hard times there will also be possitive good times 💛👪🤰😙

Our little boy due around the 4th of August 2018💛🤞😍💋♥️