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Inspicommunity Hearts living with congenital heart disease | 
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Inspicommunity Hearts living with congenital heart disease I thought I would start a blog of adults with Congenital Heart Disease. Instead of talking about their disease, talk more about the stories, and how they see life. I want to ask a series of questions and see what answers I get. Also I want to be able to let some of the first generation of survivors tell their stories. Together I hope to give hope to future generation of survivors, but also inspire each other to live life even in the face of such challenges
Our youngest daughter was born with a serious congenital heart defect called Transposition of the Great Arteries. This site is all about how our family keeps our faith in God ducommunity the good times & the bad (mostly good!)
I'm a stay-at-home-mom / stay-at-home-mum (SAHM) from Australia. On May 1st 2008, I gave birth to a beautiful baby boy who was born with a Congenital Heart Defect (CHD) known as Severe Pulmonary Stenosis, Tricuspic Valve Regurgitation, and enlarged right atrium. I'm a blessed wife of a DH whose love, care and support I could not live without. My goals for this blog are to raise CHD awareness, and to support those familes who are going through the same situations.
* Congenital Heart Disease Community * Personal websites about congenital heart{;}defects. Congenital Heart disease affects one in one hundred babies, it is the most common birth defect. Read our heart warming stories. Watch our children grow up. Most of our children are living and doing well, but many have lost their battle with CHD..
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