Baby Chad Galang anencephaly fund

Life is special and meaningful no matter what the situation. Our upcoming son, Chad, will be born with a neural tube defect called Anencephaly, that will not let him live long after birth. We found this out at our 3 months ultrasound and was devastated by the news. Ryan and I had made a decision to proceed with the pregnancy since he is still our son, who derserves the same amount of love, excitement and attention as any other pregnancy or baby should have. God chose us to be parents to Chad and trusted us to make the right decision and continue his life until God says it's time for him to go home. We are blessed that we will have the chance to meet and hold our little guy even though it will be just for a few hours. Ryan, Spencer and I along with our family will be given each a moment to show him how much love and care he has towards him. Everyone has a beginning and an end, and not everyone's life story will be the same, so do not be saddened by this, but rejoice in God's plan and rejoice in life and death with us, the only difference is his time is meant to be shorter than anyone else. We do ask aside from prayers that in lieu of gifts for a baby shower, that a donation will be made to help us cover funeral costs for our lovely boy, but to primarily be able to donate to Duke University Anencephaly research.  Any amount will help so do not be hesitant to donate.  We would like to shelter other parents from the emotions we have had to go through. We, thank you from the bottom of our hearts and pray for everyone's peace, health and love.
http://dmpi.duke.edu/anencephaly