Special Babies
Baby Shinzo 
Baby Carlie 
Hypo-plastic Right Heart Syndrome
Baby Miguel  
Total Anomalous Pulmonary Venous Return
Baby Joseph  
Hypo-plastic Right Heart Syndrome, Transposition of the Great Arteries, and Artial Stenosis
Isaiah 40:31
But they that wait upon the Lord shall renew their strength; they shall mount up with wings as eagles; they shall run, and not be weary; and they shall walk, and not be faint.
Baby Aubrey
Shone's Complex
Aubrey is truly an angel.  We had no idea how many people she was going to affect, including those who have not even met her.  Aubrey is such a happy, outgoing child despite or maybe because of her difficult first year.  Her dad and I love her more every day.  She is definitely a special baby to us and everyone that meets her.
Baby Callie
Hypo-plastic Right Heart Syndrome & Tetralogy of Fallot
Callie has impacted our lives in so many ways. She has one of the most complicated heart defects to be repaired. She makes us grateful for everyday and has opened our eyes to how great the Lord is and that anything is possible if you put all your trust in Him. Our hope is she can help other babies by overcoming this and show everyone that this defect is not a death sentence.  We hope that they will be able to learn from her and help others that are born with the same heart defect.
Baby Anthony
TAPVR heart defect
Metapneumo virus
After three weeks the doctors found an abnormality in his heart. They immediatly rushed him to Loma Linda where they diagnosed him and upon arrival  they had a crash team ready and preparedd him for surgery. The doctor spoke with us explaining  what was wrong, what must be done and before surgery prayed with us.  I left my son in Gods hands and God put him in hands of an angel, Dr. Razzouk.  Miguel is one and weighs 23lbs. He is very inteligent.  His cardiologist said he will be a normal child and will be able to play sports. He is my miracle baby!  
My daughter Lauren has taught me so much. Taught me lessons on life, love and having complete trust and faith in in God. I found out at 22 weeks that Lauren would be born with a rare heart defect called Shone's Complex. The medical community calls this condition a condition with half a heart but that is one thing my daughter does not have. She has had three open heart surgeries and a million sticks with a needle but her strength and smile are insurmountable. Her battles with sensory issues and also feeding issues have been difficult but her laughter and kisses melt all the pain and anxiety I have. Her future is in God's hands and I rejoice in knowing that his plans for her are so much greater than my own.
Laurens 1st birthday Party