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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”

I would welcome a guest post from a Family in a similar situation, being a Heart Condition, difficult pregnancy or anything you want support for.

You can reach me:-
E-mail -

Twitter - @HeartMammi

Instagram - HeartMammi

If you are a Children's and/or Heart Charity looking to promote a fundraising event I would love to hear from you. Equally if you have some helpful information regarding any type of Heart Condition I would be delighted to chat with you.

Thanks again for your support - believe me, just the thought that someone
 has stopped by for a read is making a world of difference.