When I became brave enough to start “googling” for information on our unborn Daughter’s heart condition – there wasn’t much on out there. Yes I could get all the technical information about the procedure and we could get a rough idea of what to expect in the future, but there was nothing for the here and now! There was nothing out there for families like us who just wanted to know we weren’t alone – that another family had been through this and made it to the other side, with a good or a bad outcome. I needed to know we weren’t the only ones out there to ever go through this. I wanted something more personal than a leaflet from the Hospital; I wanted to have the nose in to someone else’s experience.
To this day I still haven’t found what I am looking for.
For this reason “Heart Mammi” was born.
If I can bring some comfort to just one *Mammi like me who may be going this nightmare of not knowing what to expect – then this blog has served its purpose.
*Mammi = Welsh for “Mummy”