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Our baby's journey with Hypoplastic Left Heart Syndrome | 
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Our baby's journey with Hypoplastic Left Heart Syndrome Diagnosed in utero at 20 weeks with HLHS, our son, Mason Stephen Terrazas, has been one tough cookie. Join us for a glimpse of Mason's journey, including photos of his Norwood and Glenn surgeries. HLHS, initial paralysis of left vocal cord, reflux, g-tube.
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.
Monthly updates on my grandson who was born with HLHS. Daily life of a child with HLHS{;}
* 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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