on the 23rd march 2016 at a normal 3 month scan we were told it wasnt good news that are baby had a cystic hygroma and further tests would need to be done in the royal belfast the survial rate was very low i had to have serval tests done what seemed like forever and travellin up and down to royal it was confirmed my baby had downsydrome and possibly a heart condition after 6 months of a long list of app and alot of heartache of being told my baby wouldnt survive i had little olivia hope on the 13th sep 2016 after birth her down syndrome and heart condition was confirmed and we were told she would need open heart surgery in the next few months olivia has been on all her heart medcines from birth and a special milk to gain weight she also has endless app for her downs development after a long 11months i got the heartbreakin news this week that our baby girl will fly to london in sep to have open heart surgery a thousand things are going threw my heart and loads of fear as i just cant imagin what is ahead of us and little olivia 💔a few family have suggested we set up this page to help financially over the hard few weeks ahead in london and when she comes back to the royal again as a mumny to 3 kids this has to be the hardest thing i have ever had to go threw and i just hope and pray in my heart that everything will work out and it will help olivia so this is why i have chosen this fundraiser any money that wont be used we will transfer to childrens heartbeat which will be a big part of olivias future many thanks laura and David xxxx