The Katherine Elizabeth Foundation
exists to provide Hope, Support, and Healing
to the families that have encountered a negative or fatal prenatal diagnosis through the term of their pregnancy, after birth, or in the event of a pregnancy loss through a miscarriage, stillbirth, or newborn death

When you find out that your having a baby, in that split second you are filled with dreams, hopes and the future of your baby to be, “is it a girl or boy”, “who will the baby look like”, “what color will we choose for the nursery”, and so on…

Then, in one of your routine monthly check up’s, your doctor gives you devastating news that your precious baby has a birth defect. As you sit there listening to the doctor as to what complications your baby is facing, your dreams, hopes, and future of your infant child are shattered, and emotions of disbelief, shock, denial, grief, and even anger set in. You have so many questions, you feel overwhelmed, and uncertain. You ask yourself, “will I know how to care for my baby when she/he comes home”, “will my baby die before or shortly after birth”, “and how can I deal with all of this”?

Here, at the Katherine Elizabeth Foundation, we completely understand all of those emotions, as we too have been on the journey you find yourself right now. We are parents, families, and friends who have lived through a negative or fatal prenatal diagnosis, and who decided to continue their pregnancy, bring our babies into this world, and some of us have suffered the loss of our infant child.

We invite you to go through our website, resources & links and to e-mail us or call us so we can provide you with our one to one support, and help you find the hope, support, and healing you are seeking at this time. 

YOU ARE OUR