Heart Mission

Our Heart Mission

Have you ever tried explaining what CHD your child has to someone and they look at you clueless? I have been there.

Why is it that most people are aware of cancer, AIDS, and diabetes even if they were never affected by it or know someone

who was affected by it? The truth is, there is not information, awareness, or research about CHD. This has to change.

I hope this site will be a start. We may not be able to prevent these CHD's, but how will we know if we don't try? We may not

be able to make all understand, but how will we know if we do not open our mouths? We may not even be able to find a cure,

but how will we know if we do not do the research?

My mission is to get the word out about CHD's. I want all that I come in contact with to not only know what it is,

but to understand it and how it will affects them. No one should ever have to go through what these babies go through,

but right now, the truth is more and more children are diagnosed with some sort of CHD. I pray that this site

will bring an increase in awareness, hope, and support for all who have been dealt this horrible defect. I pray that we will all

find courage to stand up and speak about what we have been through, what we will go through, and what we all can do.

If you do not know someone with a CHD, give it time, you will.

I ask that every one who reads this will be moved to join this mission!

By spreading CHD Awareness, we will heighten the public's understanding of the need for research

and we will enhance people's opportunities to receive the help they so desperately need.