How could you not love this sweet face?

Eline at 6 weeks

  • Holding up her head – from tummy – for quite a few seconds at a time
  • Has rolled from stomach to back seven or eight times
  • Making eye contact more frequently, noticing objects, turning to look for the source of noises
  • On the verge of full smiles
  • Loves, loves, loves to be held and cuddled
  • Taking 3 1/2 to 4 oz. of pumped breast milk or part-breast milk/part-formula by bottle 7 times/day
  • Weighs a little over 8 lbs.

Ode to a Breast Pump

A Halloween Offering of Bad Poetry to Purge My Demons

Oh Medela Pump-in-Style, how I hate to love thee.
Thy motor’s whine is my ever constant melody.
Thy suction leaves me sore and humorless;
My counter’s cluttered with thy apparatus.
Oh, the time I while like a dairy cow,
Whilst my toddler cries, “Mommy, please come now!”
But my lazy babies do not nurse,
And so, like that bad penny curse,
Again you haunt these many days
And horrify in all thy many ways.
But fie, the milk my baby needs,
The gift of thy ungentle deeds.
So again we’ll meet in an another hour or two,
And thou shalt do that hateful, needful thing you do.

Downpours of blessings

It’s a truth I have known but am experiencing in a whole new way that as big as any challenge is, God is bigger. It has dawned on me that perhaps it is through the enormous, threaten-to-swallow-you-whole challenges that we experience how BIG God truly is. What I know for sure is He has poured out blessings on us over the last few weeks that have left us in awe, even as we have struggled to find our footing in a changed landscape. As I count out those blessings, I can’t help but feel grateful.

1. The unwavering love of family – I am certain the news of Lina’s diagnosis was as great a shock to our family as it has been to us. But there has never been a moment of hesitation in the acceptance and love they have shown to our daughter. Grandparents, great-grandparents, uncles and aunts have cuddled, cooed and swooned over our newborn, exactly as we imagined they would. From the moment of her birth, Lina’s familial fan club has proclaimed her beautiful and remarkable with a genuineness that has helped heal our hearts. Our little girl will not lack for doting relatives. She is unquestionably loved.

My dad and Lina nap together on her second day at home

Jon’s dad and Lina, second day at home

Great-grandma Ginnie meets Lina, 1 month old

Great-grandpa Bill

Jon’s mom, a proud Mimi

2. An amazing network of friends – I mentioned earlier that friends have organized an entire month of meals for us. Many of them drive quite a ways to get to us, many of them have their own little ones demanding their time and attention, and all of them lead busy lives we know make the meals they bring a true act of love. It has been such a gift to us. And as these friends come bearing food or meet us at church, they, too, cuddle and admire Lina with a genuine acceptance that bolsters our hopes for her future. This past Saturday night, I attended my rescheduled baby shower (which had been planned for the weekend after Lina was born), and I again was overwhelmed by the love and support of some amazing people. Friends from all over the country have reached out to us with support and encouragement that has touched and strengthened us when we have needed it most. Neighbors have offered support and love. People we barely know have contacted us to offer encouragement through their own personal stories and experiences. God is using so many people to meet our needs.

3. The circumstances of Lina’s birth – I have had many occasions over the last several weeks to be so thankful that even with all the unexpected that came our way on September 13, I was able to have the home VBAC I hoped for. At 5 weeks post-partum, I feel pretty much normal. Even with the D&C, recovery has been easier than post-cesarean with Corin. The peaceful, spiritual atmosphere here at home as we welcomed Eline is a memory I treasure, and I am so grateful I was not facing a more extended hospitalization myself as we dealt with those first few days of Lina’s NICU stay.

4. Our remarkable donor family – Some of my first thoughts as I began to process Lina’s diagnosis were for our donor family. I put myself in their place and thought about all the ways this new development would be hard for them. I knew they were waiting on pins and needles for news of our baby’s arrival. It took me several days to work up to writing that email. I wanted to make sure they knew that a diagnosis of Down syndrome did not change the gratitude we felt to them. I wanted them to know we still believed we had been led to them and to our Lina, and that she was our miraculous gift. I wanted them to know that she would be loved and accepted, and that they would not have to worry for her. I sent the email to our donor mom a few days into our NICU stay and waited anxiously for her response. It came quickly, and when I read it, I felt again how much I loved this amazing family. Lauren* wrote first about how beautiful Lina was and about how she looked like their daughter. She offered congratulations and such genuine sympathy for what we were facing. She said their hearts were with us. She expressed an interest in learning about Down syndrome along with us. I just now went back and re-read her message, and it made me tear up again. I know it has been a lot for their family to process, and I imagine they have wrestled with their own difficult emotions. We’ve talked since about how it was certainly not what any of us imagined and how it has already changed all of us. But I also know Lauren* and her family love our little Lina, and I am so grateful that with the long list of things we will have to worry about in the coming months and years, how her biological family responds to her will not be a concern.

5. An awesome big brother – Corin has certainly had his adjustments to life with Baby Sister, but he has been so very sweet with Lina. His parents have no shortage of meltdowns and battles of the will to navigate, but none of his angst has thus far been directed baby-ward. He clearly loves her and is proud of her, and it reminds me of what Jon said in the NICU, when I was thinking about Corin and how he would relate to Lina. Jon said, “At this point, Corin is the one person who won’t look at her as being different. To him, she will just be Baby Sister.” He was right. This is what unconditional love looks like. I pray this is the beginning of a very special relationship.

He announced to strangers at the greenway, “I am pushing Baby Sister’s stroller all by myself.”

There are more blessings to count, but given it has already taken me two weeks to write this post, I figure it’s time to wrap this up. There is always more to say, but I have a date with my old friend, the breast pump. (That really is a post for another day.)

*Name has been changed for privacy reasons. 

The road before us

I have followed the blog Enjoying the Small Things for probably the past couple years, and it has been consistently among my favorite internet reads. It’s written by Kelle Hampton, mother of two beautiful girls, the youngest of whom has Down syndrome. It has a huge readership, so many of you may already be familiar with it. In fact, a lot of people have recommended it to me in the last couple weeks. Kelle also recently published a book, which I just received as a gift and can’t wait to read. I’ve always strongly identified with her perspective on finding joy in the unexpected.

In the earliest moments of coming to terms with Lina’s diagnosis, I thought a great deal about that blog. It seemed so STRANGE that after so long reading about the Hampton family, I was now on such a similar journey. There have been moments when I have almost felt as if I somehow wished this upon myself. But aside from the uncanniness of the whole thing, it was so encouraging to be able to think about the beautiful photos of Kelle’s family. It helped me begin to picture our own family’s future. It seemed as if the time I had spent reading that blog had in some small way been preparation for Lina’s arrival.

In fact, there are a lot of things that, looking back, have probably helped prepare me for the experience of being Lina’s mommy. My dad was in an accident when I was 18 months old that left him legally blind. “Different is okay” was a theme of my upbringing, not just in what my parents said to us but in the whole way our family lived. I spent many, many hours at disability awareness seminars my parents helped conduct at churches all over the region. I had a childhood friend with a chromosome disorder similar to Down syndrome.

But it’s also been a bit jolting for me to realize how different it is now that it’s MY baby. I have smiled at children with Down syndrome in the stores or at the park and thought, “He is adorable,” or “She is just precious.” But suddenly I was thinking about the closet full of gorgeous clothes for my little girl and having a very hard time picturing those clothes on a child with Down syndrome. This is me being brutally honest. I was so accepting of everyone else’s children with Downs, but coming to terms with it being my child was a whole new ball game.

Those first couple days were complicated. I was initially in shock, just trying to wrap my head around this new reality. How I felt varied from minute to minute. Jon wanted to be sure we were able to celebrate the arrival of our sweet baby. I agreed, but I was surprised by what a relief it was when I called our embryo adoption counselor to tell her about the situation and her first response was, “Oh, Jolene, I am so sorry.” At that moment, I was hungry to have my feelings of grief and loss validated. I cried and cried on the counselor’s virtual shoulder.

Jon seemed to have an easier time coming to terms with Lina’s diagnosis than I did in those first few days. He was immediately on the internet, reading wikipedia entries and finding blogs by parents of children with Down syndrome. He found it encouraging to read stories of people with Downs leading successful lives. I wasn’t there yet. I did think and talk about the positives, but I was also grieving. During our NICU stay, I picked up a book about Down syndrome that had been given to us by our contact at Vandy’s Downs clinic. I started reading through the list of common health and developmental problems, and suddenly I felt very angry. It wasn’t so much for myself, but I was angry that my precious baby was going to have to face so many extra challenges. I resented that so many children would breeze through their milestones while my Lina had to work so much harder for every achievement. I felt envy for parents with “normal” babies. I thought about all the children in our circle of friends who will be so close to Lina’s age, and I grieved for the type of friendships I had imagined for my daughter. I thought about the family of the future I had imagined so many times: big, loud holiday gatherings with lots of grandchildren to fill our golden years. I thought, “Corin better marry someone who wants a lot of kids,” and then I thought, “Goodness, I hope I don’t actually put that kind of pressure on him.” Jon and I talked about how he had fallen in love with the name Eline because he pictured how elegant it would look on a wedding invitation. I felt keenly the loss of that future I had imagined for my daughter.

And yet, even as I grieved, God was working on my heart. Truthfully, I wasn’t doing a whole lot of praying. I just didn’t have the words, or the heart, to try to piece together what I needed to say to Him. Our first night in the NICU, I stood in the middle of the room after a midnight feeding, tears pouring down my face, and told God, “I don’t know what to say, but you know what’s in my heart. I need you more than ever before.” My faith was weak, and I was facing that question without an answer: “Why?” Why, after all the lengths we went to to give us the best odds of a healthy baby, after all the prayers we prayed, specifically asking God to bless our child with intelligence and to guide her development in the womb, why this outcome? Why, when it came to building our family, could nothing just be simple? I knew there was no answer, but asking the questions was a part of trying to process an outcome that was so very different from the expectations we held so closely for all those months.

Slowly, over those days in the NICU and in the following days since we’ve been home, my perspective has begun to shift. The second night in the NICU was much better than the first, and I found myself beginning to really bond with Lina. Over those late-night feedings, I looked into her face and began to recognize my daughter. The wheels of those deep instincts of motherhood began to turn, and I realized that already, I would go to the ends of the earth to give this child the best odds of happiness and success.

I began to see more clearly that my child’s extra chromosome will not prevent her from finding that happiness and success. Jon and I talked about how many “normal” people lead lives of dysfunction and unhappiness. It somehow brought me comfort to remember that having a child without development challenges does not guarantee freedom from parental disappointment or heartache. I began to remember the truths of those disability seminars: We all have our own difficulties. Some may be more visible than others, but they are there. Lina will have more challenges than some, but it was sinking in that she will find her own path to achievement and fulfillment. It is our job to help her. She will have her own interests and passions, her own talents and skills. They might not look like those we had imagined, but they will bring her happiness. I began to value the innocence she will likely carry with her through life.

As I have gotten to know this tiny new person over the past three weeks, I have fallen more and more in love. She is my precious daughter. I have stood over her cradle, watching her sleep, and breathed the prayer of every God-fearing parent: “You have entrusted her to me. Teach me. Help me be the mother she deserves.” I have looked down at her tiny form in the stroller as we walked at the greenway and felt joy that she is mine. I am more certain every day that her diagnosis does not change the fact that God chose this child for our family. I believed all along that He led us to embryo adoption, to our donor family, and to this baby. Yes, there is disappointment, confusion and pain, but I know Lina is a priceless gift, and I believe deep down in my soul that she will be a blessing in ways we can’t yet imagine.

Our day-to-day reality right now is really just your normal newborn stuff: round-the-clock feedings, sleep deprivation, lots and lots of tiny diapers, soaking burp cloths, the struggle to balance the needs of a toddler and a newborn while maintaining a semblance of normal routine. But truthfully, most of the time I’m finding it to be easier than I feared. I reserve the right to change my mind at any time, but for now, I am able to enjoy the tiny newborn stage with much less stress than I experienced with Corin. Lina’s feedings are complicated (nursing, pumping and supplementing by bottle), but she’s actually a better eater than Corin was at this age. Lina is a snuggler, and as much as I want her to sleep in her cradle peacefully all night, I kind of enjoy that she likes to be held close. I remember feeling in those first weeks with Corin as if someone had dropped me off on an alien planet; I recognized nothing of my life. This time, I have been pleasantly surprised by how much of our family life feels normal, even as so much has changed.

As we mark three weeks of Eline’s life, I am finding joy in picturing her as she grows. I think she’s going to be beautiful. And those clothes hanging in her closet? They are perfect for her. I know it won’t all be smooth sailing from here. There are still times when my heart hurts, and there will be many more of those as we walk the road in front of us. But this is our road, and as different as it is from where we thought we would be, it is beautiful in its own right. Here’s to the journey ahead.