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Stories of the lives of infants with anencephaly

 

"Hope is not the expectation that things will turn out well,
but the conviction that something is worth working for,
however it turns out."

Vaclav Havel

 

As anencephaly is usually detected during a pre-natal scan, parents are confronted with a choice between life and death. A choice often made with very little information of what is in store for them. It is with this in mind that we have made the choice to share the stories of the brief, but wonderful lives of babies with anencephaly. We hope that it will be of help to you and impart courage.

 

Anouk Amanda Marie Ava Grace Camdyn Courtney Denise Gabriel John
Gracie Lynn Hope Marie Ira Isabel Eve Jaden Thien James
Jenna Grace Jerry Elijah Jesse Alexander Jonathan Joseph Jerome Joyann
Julie Kyle Benjamin Loren Joseph Lucas Adam Luke Daniel Malachi Samuel
Maryann Elizabeth McCoy Michael Andrew Michael David Pedro Jose Robert William
Rose Dale Sarah Timothy Paul Tyler Damon Zakary Evan Sandra Maritza
Austin John Noah Alexander Isaac Ayden Zion-Grace Grayson Abbott Gianna Faith-Dawn
Taylor Wayne Faith Elizabeth Ajani Josiah Kylie Marie Samuel David Carmen Arviansyah
Peter Eoin Anthony Zak Nathan Emmett

 

Twins

Anna and Logan Anna and Tess David and Jonathan Faith and Sarah Matthew and Emily
Clara and Caleb

 

The site does not necessarily agree with the personal beliefs / faith of the the families and the medical advice they got. However, we have chosen to allow the stories to read as written so that parents could feel safe in sharing their unique experiences of giving birth to their children with anencephaly.

 

I sometimes wonder when things will get back to “normal” again (I think what I’m really asking is “When will this not hurt anymore?”), but I can’t help but think this experience will redefine “normal” for us. And, if normal means going back to being the person I was, even two weeks ago, and tossing out the beautiful lessons the Lord has shown me, then I don’t want “normal.”

Ryan and Laura, parents to Emily Jean

 

Don't waste your child's life
Jon and Jenni are the parents of Chase who had anencephaly. On their blog, Jon shares a few journal entries he wrote during the pregnancy and after Chase's birth and death. Their wish is that others may be comforted with the comfort they received.
We are very grateful that they allowed us to publish their inspiring and helpful texts.

 

It's quite hard to find fathers expressing their feelings about their child with anencephaly. That's why I choose to link to some texts written by fathers:

What it means to be a father to a baby with anencephaly by Kyle Cupp, father to Vivian

From the heart of a daddy by Jason Young, father to Adelle

Hello Good-bye - A Dads journey with anencephaly by Phillip Barnes, father to Noah

 

"What can be gained through heartache?"
Have you ever wondered about God's purpose in allowing you to suffer? The morning Anna died Lynnette wondered why God would ask her to endure heartache a third time. In her candid approach, Lynnette shares her personal story. Her second son Samuel had anencephaly.

 

If you have carried a baby with anencephaly to term and want to share your story with us, just e-mail us, we would be more than happy to add a page for your baby.

 

Stories of parents who carried their baby to term despite a poor prenatal diagnosis

 

 

Last updated January 20, 2010