Have you ever wondered why any mother would voluntarily choose to get her heart broken?
I’m sure every mother knows what it’s like to check on a sleeping baby, just to make sure they’re still breathing.
I’m also pretty sure every mother knows what it’s like to have her heart skip a beat when she wonders for just an instant what life would be like if she lost that precious child.
Some mothers – far too many of them – DO know the devastating grief of burying a child. They have lived through long, anguished nights wondering “Why me?!” and “If only….” Only those mothers who have walked that path know the soul-crushing pain that leaves you breathless and drained – as if you had run a marathon uphill, in the rain, with no preparation.
So why would any mother voluntarily choose to adopt a child she knows will die? Why would she put herself through that kind of pain? Is she crazy? Is she a saint? Would you believe me if I told you the answer was neither craziness nor sainthood but simply love?
At least it was for me.
In the early summer of 2007, my husband and I had a full house – 13 kids at home, to be exact. With 4 by birth and then 19 by adoption, you could say we had our hands full. Not all 23 lived with us – 3 were stuck in Africa waiting for US visas that have never come, several were grown and gone and 2 of our daughters had passed away.
In the middle of June, I got an email forwarded from a forward, desperately seeking a family for a little girl who had just been born. This baby was missing most of her brain and would be severely disabled all of her short life – and she needed a family.
My heart leapt at that email and I knew that sweet baby was meant to be my daughter. Every child deserves to be loved and cherished and I knew we could offer this baby a lifetime of love.
As a family, we decided we wanted her to join us and when she was 9 days old, she came home from the hospital, straight into our hearts.. Because of her diagnosis of hydranencephaly – meaning she had fluid where most of her brain was supposed to be – and her prognosis of a very short life, where 50% of the kids with hydranencephaly never even see their first birthday, we made a conscious effort to treasure every moment we had with her.
We named her Angelia for the sweet angel that she was. She couldn’t sit up or roll over – or even hold her head up, but she could be held and loved and – so she was! That sweet baby was held almost every second she was awake. I typed many a blog post with her on my lap and when all the other kids were at school, the two of us would laugh and giggle and sing – and even twirl around the living room. And pink – there was lots and lots of pink – pink ruffles, pink bows, pink fingernails, pink toes….
I knew there would be a coming day of sorrow, but I did not guard my heart or hold back in loving her. In fact, I opened my heart as wide as I could. I poured myself into her. I cherished her. I adored her – and I wanted her to know it. She was blind and could never see my face, but she felt it every day as I held her close to me. I touched her and talked to her, held her and even sang to her for hours – even though that’s not something I’m particularly talented in.
When she was 3 ½, she left us on a cold February morning. My heart broke into a million pieces, as I knew it would.

It remains one of the hardest losses I have ever experienced. The tenderness has lingered longer and the tears still come regularly – and yet I have never, ever, regretted adopting our sweet Angelia.
We all do hard things because the trade-offs are worth it.
Some people train for – and complete – marathons, trading sore muscles, blisters, fatigue, running in bad weather and hours of precious time because it’s worth it. Virtuosos trade years of their lives to become experts in their craft. Young married couples sacrifice time and money now as they work 2 jobs to pay for school so that later, their family is provided for in a comfortable manner. For me, loving Angelia was worth the trade-off in grief.
Every long, lonely night, every tear-stained pillow, every bout of empty, aching arms that long to hold her, EVERY MOMENT of sorrow is STILL worth the trade-off in the joy and love she brought to our home, the joy and love that came to me as her mama and the joy and love I believe she felt during her life with us.
I would do it all again – in a heartbeat. Not because I’m crazy or a Saint or have some special talent.
Simply because LOVE is worth it.


I have no doubt that love got you those extra years my friend.
Hugs to you.
LL
Holly you made me cry
I loved this little girl plus lizzy
I don’t know how you do it to lose three children
You are a loving mom with a heart that is as strong as
Ever
Sending love to you and your family
Charlotte
Thank you, Charlotte, for sharing so many special times with our girls. We love you.
I count myself very fortunate to have been able to meet her and hold her. Her smiles were precious. What I most remember is the gentle, loving way the rest of your children treated her. I loved seeing how each child took turns holding and caring for her and I know that the experience will enrich their lives and make them all better, more compassionate people. I’m so happy for your love (rather than saying “so sorry for your loss”).
Thank you, Cynthia. We cherished every day we had. Perhaps that is the lesson – cherish every day, for we never really know when the end will be here…..
Love you my dear friend but I do beg to differ one point: the makings of, not so much Sainthood, but rather, acting as a Disciple of Christ IS simply love. You are one of the finest examples of choosing love and light that I’ve ever known.
Ah, you are so sweet, Krista! Thank you!
LOVE!
You did an amazing job explaining a very complex situation. Accepting that love is worth it. Wish you had spoken in conference!
Beautiful post, Holly! I am the founder of a nonprofit called Global Hydranencephaly Foundation, which was founded in honor of my own son Brayden in 2011. I would love to share your story with our supporters via our blog Journey of the Bees: Believe in the Impossible (http://braydenalexanderfoundation.blogspot.com) and make you aware that we also have an online support & resource network of families who have been given a diagnosis of hydranencephaly for their little loved ones, as well as a separate one for those who have faced loss of their sweet angels. If you’re interested in our mission, contact me directly at my email address or simply send me a friend request via Facebook: (http://www.facebook.com/AliNichole0619). While you’re there, you can check out our foundation’s page (http://www.facebook.com/globalHYDRANENCEPHALYfoundation.org)