Friday, August 17, 2012

Happy birthday

One month ago today our sweet little girl Avery Joy was born.  6 wonderful and tiring days with her, 25 without her.  We miss her so much.  Everyday.  The first time we felt Avery in our arms, we knew life would never be the same.  It isn't. 

Most of the time we do pretty well.  But then there are times, perhaps moreso lately, when the unescapable reality of the void she left washes over us with a force and speed difficult to predict or to handle.  In a way, I suppose it is comforting.  After all, the place she holds in our hearts and our family is secure.  But at night, when we want only to hold her and lay her down to sleep, comforting thoughts aren't enough...no matter how optimism tries to spin them.  In these times, we run out of pictures to look at, we wear out Melissa's video, and still we want more.  We want Avery.

Perhaps I have learned something of my own grief and God's involvement.  For months I have been searching and searching for God in the midst of this and more specifically what meaningful lesson I can take from this wonderful and awful last year. And when I have prayed on the matter, I have heard...nothing.  No words at all.  There is no lesson?  Allowing myself to grieve though over the last few weeks, I have begun to know in a new way that God has been with me this whole time.  He is with me. Maybe that is the answer to my question, "What is the lesson?"  Perhaps his presence is it, and maybe right now words would only distract.  Lessons can come later.  His presence in the midst of pain is what matters most in these moments. 

That statement means something much different to me now than it used to.  For the first time in my life, "His presence in the midst of pain" hasn't transformed the pain to joy or at least into something digestable or more tolerable.  This situation is still deeply painful and doesn't yet seem to be getting any better.  But verses of the Bible that speak of God's steadfast love now have much greater depth than they used to.

Sunday, August 5, 2012

A week later

Thanks for continued prayers, calls, texts, emails, visits, meals, etc.  (A little overwhelmed with our inability to keep up with thank you's).  We have felt your collective support.  Back to work for me this week; great to see people from work, challenging to be away from home.

We have now had more than twice as many days without Avery as we had with her.  Yet, her absence remains palpable to us. We are grateful everyday and emotional most days.  In the last 24 hours, I am so grateful to have met for the first time three beatiful baby girls of friends, all of whom are NICU graduates!  Thank God for these kids.

Thanks to Steve Walters this week for pointing out that "Grieving is hard work." For someone prone to just putting my nose down and plowing through, I appreciate the wisdom of making sure I don't run from the process.

Some pictures:
1. An awesome picture of wide-eyed Avery being held by Em after receiving an edible arrangement from friends Steven and Aubrey. Avery is so beautiful; it makes me miss her terribly.


2. Em, Liv and I made cookies (with pre-cut cookies from Shannon Gower) this week to take neighbors. I used it as an opportunity to tell them about Avery's passing.  You be the judge: more sprinkles on the cookies or on the sheet?  Either way, I wasn't going to eat them. (We made some for ourselves later.)


3. Thanks to Shae Dalke and family for bringing rotisserie chicken.  We all enjoyed it, but Emily in particular LOVED it.  So much so in fact that she ate every last bit of her chicken leg that was edible...and then some parts that aren't really edible. It was actually a little gross to watch (and hear).

Sunday, July 29, 2012

Many thanks

We are grateful to so many people, it is difficult to know where to begin. We are doing our best to send out thank you cards, but let me say here one enormous thank you to all of you who have consistently given us your love and support.  It humbles us to be surrounded by such wonderful people.

Jessica captured our shared feeling perfectly when she said, "I feel like I had so much more to give Avery as a mom, so it was very important to me that her service go well."  We had, as I mentioned, given most of our time to that end from the time Avery passed until we arrived to church Friday morning. While the service was emotional, it was every bit the celebration we had hoped it would be.  And we had no idea the outpouring of support that would come with everyone that attended.
For those who took the time out of your day to come and support us by your presence at Avery's service, thank you ever so much.  Many we had the chance to speak with at the cemetary and the lunch that followed back at church.  But we also recognize there were many more we did not have the chance to thank personally.  To all of you, thank you.  Lastly, to those near and far who were unable to attend but sent cards, phone messages, texts, emails, facebook posts, blog comments, and spoken and unspoken prayers, thank you.

Yesterday morning, Emily drew a picture of the graveside service from Friday. She included the flowers with surrounding graves, the tree near Avery's grave, the green roof of the shelter the cemetary set out for the service, Avery's pink casket, her own beautiful blond hair, and the tiny bodies of Olivia and her father (whose hair is always spiked).


I have appreciated reading the many cards we have received in the mail. My cousin Debb sent one that says, "We're given many gifts as we go through life.  Some we're allowed to enjoy for a long time, others only briefly.  But each gift has the power to change us, enrich us, to make us better people." Jessica and I believe that is true, but we recognize that we still have a tough road ahead with the grieving process.  This morning, we will go to church with the dull ache of loss and the sense of a void in our earthly family. What we most want is God's presence with us through that process.

Lastly this morning, I want to say thank you for the stories you have told us of God's presence and movement among you.  Some of the remarks have even been related to indirect or direct effects of Avery's life.  Regardless of what circumstances precipitated it, we give God the credit.  One of the biggest highlights of this week and maybe of this year was receiving an email from a dear friend who contacted me a week or two ago to let us know he was praying for us.  In a subsequent email he told me of his earnestness about praying for us because Jesus had stirred in his life within the last year. He is now committed to living a life of faith in God and Jesus.  Nothing brings Jessica and I greater joy than we hear this (literally) life-giving story from our friends and loved ones. 

Thursday, July 26, 2012

Sentimentality versus Reality

It has been so good to be grounded in reality about Avery's passing by people who love us.  Friends and mentors have showered us with text straight out of the Bible that speaks to our situation, and we are so grateful. In the last 24 hours, Jessica has shared a couple times that she does not like the way it feels "easy" having four of us at home again.  She doesn't want our family simply to able to go back to the way it was.  The underlying fear is how this would (in our hearts) threaten Avery's significance.  We really do still want her here...for our sake.  Accepting that we will eventually go to her but that she will not return to us, we at very least want to remember her forever and hold her in our family in our hearts and minds. 

That is so easy to do right now.  We woke up thinking about her and haven't stopped.  Our activities today included meeting with Steve Walters and Sandy Carroll at church to plan out the service, going over music with Margie Alford and Micah Yost, driving all over creation to find an outfit for Avery's body for the funeral (it turns out the market for 5 lb baby funeral outfits either doesn't exist or is incredibly elusive), taking the outfit to the funeral home before driving by the cemetary plots we purchased for Allie, Avery, and us (yep, you heard me right), then coming home and working on getting things ready for the funeral after we put the girls to bed.  In between we talked about her constantly, cried frequently, laughed occasionally, held hands and hugged each other.

But what about next week? What about six months from now?

Sentimentality says to us, "She lives on forever as long as she lives in your heart." Unfortunately, the converse of that assertion is that the moment we stop thinking about her, she ceases to exist.  As we wept over the fear I mentioned above that results from the influence of this sentamentality, tonight I had to stop us and again thank God for the truth and for the people who keep sharing it with us. 

Reality says: it doesn't matter where Avery is in our minds or hearts.  Avery's existence never depended on our thoughts or feelings.  While we will love her forever and miss her forever, we at some point may no longer be able to remember the feel of my cheek against hers, the sweet voice that cooed so often, her little hands and feet that were special and unique to her, those eyes that would seem to stare right at us...before spontaneously going crossed. Someday I may not recall exactly how little of my hand her beatiful head occupied as I held her in the moments before she passed.  Even Jessica, who held her and talked to her and spent more time with her than anyone, will probably at some point cease to remember some of the interaction she had with Avery Joy.  It pains me to say that--especially because of my increased susceptibility to amnesia and eventually dementia that results from a history of recurrent blunt force head trauma.  And it makes us again wish we had more than six and a half days with her outside the womb.

But the reality is, she will be in heaven waiting for us whether we think of her every moment of every day (such as today) or whether she remains an essential part of our family but comes to our mind only every so often (as we have been fearing may eventually happen).  Thank you to wise friends who have reminded us that the only true measure of the value of her life is in knowing reality and the price it cost.  And that is reason to celebrate. 

I have been unable to avoid thinking about abortion through this process.  I am going to share some thoughts but will put it at the bottom for any who wish to avoid reading it.

Jessica and I are pouring our hearts into Friday and are approaching it with four parts dread, one part excitement.  We want to thank God, honor Avery, and have an opportunity for us and those who know and love us to come and grieve, laugh, cry, celebrate, ask questions, and at the end of it, eat barbeque sandwiches.  Thank you so much to those continuing to reach out to us and to those who are working diligently on Friday.  Special thanks to those for whom our family has been a full-time (our parents, Melissa Cheatham) or part-time (our journey group, Connections team, Thrive, MOPS, Steve and Terry Walters) job.
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With due respect to my many friends whom I love that are adamantly in favor of the rights of a woman trumping the rights of a fetus, I would say this:

Though I have long been unequivacobly pro-life, I have never wanted to participate in the vitriolic war of words that seems to result from two sides differing on one fundamental belief on when in fact a human becomes a human.  It has never struck me as complicated, and I have had very pleasant and civil discussions with several friends who believe the weight of the evidence does not convincingly support life beginning at conception. These friends who fall into the category of "Pro-choice" are virtually never anti-life as they are sometimes made out to be. My friends value the life of the mother over what they believe to be either a non-life or a life whose value is less than that of the mother.

Recent events have strengthened my belief in the Bible.  I believe the value of every single fetus will one day be shown and that we will all answer for what we did for those lives. So I am inclined to think I feel inside the very same urgency of those "Pro-life" advocates whose tone may be more biting on the outside.  I hope it isn't lost on my dear friends who see this issue differently that the urgency comes from different beliefs not only about when life begins but about the importance of getting it right. Those of us who see the issue the way we do believe that the one who imagined these children is the same one to whom we will answer.  And just because we may forget or never have known about an aborted fetus doesn't make the life any less real or any less important.

In mixed company this is not appropriate conversation to initiate, is it? But I want you to know if you have read this far that Avery's life cries out to me and says, "Speak.  Do not be silent." Her life matters.  Six days on earth, it matters.  What Avery taught Jessica, me, Emily, Olivia, and what she brought to our family baffles my mind and brings tears to my eyes. Thank you so much to all who have written and called and texted and facebooked and whatever-elsed social media may allow to tell us of the impact of Avery's life.  We cherish every single one one of those messages.

But in the end for those who believe in the God of the Bible, if Avery had died in utero, her life matters no less. Our friends with recent loss in utero--we are so sorry for your loss. And your child matters no less!

Specific testing for Trisomy 18 exists.  We are thankful it does because it allowed us to starting preparing for Avery's arrival.  But many times getting the diagnosis becomes the basis for elective termination of a pregnancy. To my wonderful friends who believe in neither God nor heaven, I would just ask you to look closely at the life of our baby girl.  Even if you measure the value of her life in its impact (rather than believing it has inherent value), you will never convince me or my family that her life was in any way expendable. 

And this is why this huge tangent is in here.  I am not staying up late to sway people's politics.  I am writing to help get over the heartbreak of losing my youngest daughter to a disease that diminished the duration but not the importance of her life.

Wednesday, July 25, 2012

Avery's Memorial Service

Avery's service will be at Christ Community Church this Friday, July 27th, at 10:00am.

We continue to be so thankful for all of your love and prayers.

Tuesday, July 24, 2012

Empty

Not sure I have ever erupted into tears the moment I woke up.  I can't leave our room without passing the empty Pack and Play, her hat and blanket neatly folded. Still smells like her.


As quickly as she came into our home, she left. Holding her as she gasped final agonal breaths late last night, I just kept telling her I loved her and that it was ok to let go. The struggle to live and breathe was over.

I  have heard it said that the universal love language of infants is physical touch.  From the beginning, my favorite thing to do with her was rub my cheek to hers.  Not only did she have that amazingly soft baby skin, but it was the most tangible way to tell her "I love you, I am here with you."

It was so hard to watch them take that sweet delicate little body from her mommy's arms.  Now today--5 days after we were elated to celebrate so many firsts with Avery in our home--we confront the day of firsts without her. And much as it seems an imposition to continue to ask for prayer, would you pray for us to have God's tangible presence in our home today? We need to hear those words from him that we fought so desperately to convey to Avery for the last six and a half days.

I meet with the funeral home at 4:30.  There should be a post later today with date and time of service.
Thank you for honoring God and the dignity of Avery's life by your prayers.

Avery Joy Reade - We will love her forever.

Chad and Jessica asked me to blog this.  Avery Joy Reade went to be with our Lord at 11:30 Monday night, 7/23/12--six days after her birth.  Their family, and we, both sets of grandparents, were able to be with Avery as she went into the presence of God.  Emily was the BEST big sister, right up until Avery left us.  Emily has taught us all so many lessons about honesty with God and total, unconditional love.

They and we are so grateful for the time God allowed us to spend with this precious little girl.  It is an awesome love that God instilled in our hearts in the short time we were allowed to spend with her.  Actually, we have loved her from the moment we have known about her.

In closing for now, Avery is healed.  She was a fighter, but now is totally, completely and gloriously healed! 

Howevery, hearts are broken here.  Please lift Chad, Jessica, Emily, Olivia in particular...and, the rest of the family up in prayer for comfort and healing that only God can provide.  I'm sure they will blog here eventually, but, as you might understand it could be some time.

For all the family,
John and Terri Steyer, and Bob and Carolyn Reade-Avery's proud grandparents.

Monday, July 23, 2012

Not a great day

Tough day today.  Avery has been uncomfortable most of the day and hasn't slept. Everything we have tried has at best been a temporary fix, from feeding to diaper changes to rocking--and we even tried the oxygen without effect.  Just tried tylenol.  Still jaundiced but making plenty of dirty and wet diapers.  Don't think the jaundice has anything to do with the discomfort.  She appears a little duskier today with some cyanosis around her nose and mouth. Certainly we are not hitting the panic button, but at the same time it is hard to feel great about what has transpired today.

As you read this, we appreciate your prayer not only for Avery but also for those whose hearts ache from having watched loved ones die and in particular for those who have experienced the pain of loss of a child.  We grieve with you.

On a brighter note, Liv really wanted to hold Avery today, creating photo op:

Sunday, July 22, 2012

More pics

More pictures taken by Melissa...favorite is smiling Avery.


Sunday update

Good 48 hours since last post.  Avery seems to be doing well.  Gets blue when she has a diaper, and last night appeared to go apneic and severely blue.  Scary few moments of trying to stimulate her before return to breathing.  Thanks to friends and family for visits but also for being sensitive to our needs with sleep.  Jessica sleeping right now (she has not been sleeping nearly enough, so it makes me feel good everytime she sleeps).

Highlights from last couple days:
Avery's eyes being more open and her more alert more often
Funeral morning passed yesterday without a funeral
Family Bible story time.
Getting to play the piano (quietly) with Avery in my lap
Some time I have had with Emily and Olivia, especially bath time last night in mommy and daddy's tub using the jets and bubbles, followed by dancing.
Avery is crying with more fervor when she cries
This morning, getting to overhear Olivia playing Candy Land with Grammie (my mom) and hearing her say "That's your house, Grammie." She was pointing to the house for "Grandma Nutt." No comment.
Eating more (Avery and us)
Olivia again pointing out the family resemblance between her and Avery
Timely delivery of diapers--thanks Courtney!
Jessica letting me work out yesterday morning with Ryan Horner
Meeting a new friend Karl at that workout yesterday, who left me in the dust despite being 12 years my elder...then prayed for Avery and our family when we were done.  What a stud!
Answered prayers for the protection of Emily's delicate heart and for Olivia's transition to having a baby in the home

Mostly, we are grateful for a fresh perspective.  We now understand in a way we never could have (had we not met Avery) just how much God loves her and what a treasure she is to him.  Jessica and I feel so privileged to have had nearly five days with her now. 

Areas for prayer:
Jessica's rest
For our hearts to find a balance between trying to enjoy every moment and not exhausting ourselves with overdoing it (in terms of sleep deprivation, visitors, etc.)
For me: attention to the needs of Jessica first and protecting her, loving and spending time with Emily and Olivia, and perhaps making time for Jessica to have some special time carved out with each of them as well
Spiritual disciplines
Emily starting school in a few weeks
Me going back to work on Tuesday (1/2 days this next week)
Our parents: rest for them (they have been SO helpful; we are trying to find the balance of letting them be with Avery as much as possible but not asking too much of them)

That is all I have.  Maybe more pics with the next post.

Friday, July 20, 2012

Friday Update

Update: No alarming of the monitor overnight!  Good visit with hospice nurse today.  Thanks to our brother Adam for mowing our yard in this beastly heat.

Here is a picture that Jessica took with Avery AT HOME! I think it captures the situation with the sisters: Emily's unbridled joy, Olivia's distractibility.
However, Olivia did make this comment about Avery at the hospital: "Oh, she's so cute! She looks just like me!"

Avery Joy Reade


Hard to believe I am writing on this blog again.  I thought I left it behind after Olivia’s twin sister Allie died during the last pregnancy.  And when we learned of Avery’s diagnosis 19 weeks ago, I had no intention of writing on this. Even a few weeks ago when Jessica told me she had written here, I had no intention of even looking at the blog…much less writing on it. But here we are.  I am going to tell my version here, more for my own processing of these events than anything else.  Read if you want.  Skip what you want.

I.                    THE EXTENDED BACK STORY (IN AGONIZING DETAIL)

Jessica first told me of the pregnancy when I was in Houston teaching for our dear friends’ (Kyle and Melissa) Optometry Board Prep Course. Kyle was with me, while or wives and children hung out together back in Nebraska. Somehow Melissa knew Jessica was (less than 4 weeks) pregnant and encouraged her to take a test. I think that is the day I became a true believer in women’s intuition…although Jessica had no idea she was pregnant until the test was positive.  She cried about having to tell me over the phone.  For women who want to avoid this, I would suggest not taking a pregnancy test while your husband is out of town.  Nonetheless, we were ecstatic. 

When I got home, of course we were all thrilled…though perhaps no one more than Emily. She was jumping up and down with excitement.  As I have told many people, I told Emily that Jessica and I would need to make sure she was strong enough before she would be able to hold the baby.  The next day when she awoke, she immediately told me she wanted to go down to the unfinished basement (aberrant behavior for a child who loves her breakfast first thing).  She told me we both needed to work out.  Picking up Jessica’s 5 lb. weights, she curled them to shoulder level, then pressed them over her head.  Then she was done.
The event was joyous for me and Jessica as well.  We had long discussions about whether or not to even try to get pregnant or to pursue adoption after the twin-twin pregnancy last time.  Seeing the toll it took on Jessica, me, and us, I was reticent to take the proverbial leap.  After much prayer and talking with Jessica though, we had made the decision to try.  We had no rational reason for being anxious in November, but I was guarded.  When we learned of the twin pregnancy last time at 14 weeks, I had serious misgivings that also had no rational basis.  One of the lessons to me after it was said and done was that things usually turn out right…but that I shouldn’t ignore misgivings.  In November I had no specific misgivings but still noticed my enthusiasm was dampened relative to the last two pregnancies.

The weekend of January 7 I was in Columbus Ohio and Jessica didn’t tell me when we spoke on the phone that she felt something abnormal that made her worry she might have a problem with her pregnancy.  When I arrived home from the trip, she shared her feelings and it was clear she would have no peace of mind until we got in for an appointment.  They set her up for an ultrasound and appointment the morning of Tuesday, January 10.  Frankly, Jessica was concerned that the problem might be with her cervix; I had little concern anything was wrong because I thought there was no way that kind of problem would show up this early. An hour after her appointment time there, my MA at work pulled me out of a room.  Her OB, Dr. Jacobi, was on the phone telling me I needed to come over to her clinic.  Sensing my confusion, she explained that there were concerning ultrasound findings and Jessica was beside herself.  My clinic canceled my appointments for the rest of the morning and I got over to the Women’s Hospital clinic as quickly as I could.   From then on, all appointments were scheduled on Tuesday afternoons (my afternoon off).

Jessica remembers that morning how she appreciated my calm demeanor and reassuring her that we would get through this.  I remember saying that we didn't have a diagnosis and that until we did not to panic.  However, I also remember frantically calling friends on the way to and away from the hospital.  And I remember Jessica apologizing again and again, saying that we never should have tried to get pregnant again.  Of course, how could she know this would happen?  (The statistics of this were terrifically unlikely.  Eventually I would learn that the likelihood of a twin to twin pregnancy followed by Trisomy 18 is somewhere in the neighborhood of 1:5,000,000.) I was glad that she and I had discussed it as much as we had; we went in with our eyes open.  Admittedly, neither of us knew what was ahead.

Two days later we sat with the perinatologist who explained that the abnormalities required surveillance but were by no means diagnostic.  In the two weeks that passed before we saw him again, we enlisted the prayers of family and friends.  To our amazement, on January 26, the size of the abnormality seen on the first ultrasound had returned to being within normal limits!  We left overjoyed that the chance of our baby having a chromosomal abnormality (the most likely of which was Down’s) had returned to average for the population.
In the days from the first ultrasound to the repeat, I felt a kind of callous resignation.  When on January 26 we learned we were back to average risk and just needed to return in another four and a half weeks to recheck the 18 week ultrasound, I was happy.  Still, in the back of my mind, I wouldn’t let myself rule out the possibility of something still going wrong.  No point dwelling on it until I had more reason to dwell on it.
And that brings us to the 18 week ultrasound, where substantial cardiac defects, brain and skeletal abnormalities were strongly suggestive of chromosomal problem.  In a matter of 60 seconds, we went from normal to the need for amniocentesis. As the doctor was getting his materials for the procedure, the clinic manager came in to tell us the more than $1000 procedure would not be covered by our insurance.  Methodist’s insurance.  At the clinic attached to the hospital for women and children.  Rrrrrrrrright.
Jessica learned of the Trisomy 18 diagnosis at 3 p.m. on a Friday a week and a half later…two and a half hours before I got home from work.  I have little recollection of the events that followed.  Steve and Terry Walters (family friend and mentors, and Steve officiated our wedding) spent much of that weekend comforting us and our family, and we are forever grateful for their availability at a moment’s notice, their wisdom, and their genuine care.

The weeks that followed were marked by a deep hurt that was easy to repress amidst the needs of my family.  Jessica’s tender heart was wounded, and I love being her protector.  We struggled to find the balance of honoring her wish not to be out in public and be asked by well-meaning people about her pregnancy with the need to avoid isolating ourselves from our support network.  Much prayer, time spent with her family, friends, bible study and mentors has done amazing things for Jessica.  I was able to avoid confronting my own fears, pain, and doubts for the most part.  While so many men around me offered their time and counsel, for the most part I have chosen to focus on the needs of Jessica and the girls.  It has been good to be reading through the bible in one year with our church, and until the last month or so, I have continued singing with our worship team at church.  Still, I was consciously making a decision not to deal with this pregnancy emotionally or spiritually until I had to.

From a planning standpoint, Dr. Jacobi has managed Jessica like a normal pregnancy with a couple exceptions:
1.       We have seen her every two weeks since the diagnosis (our request, she has been as   
much counselor as physician)
2.       With Avery’s multiple problems, Dr. Jacobi recommended not monitoring Avery during labor.  As it was, Avery has been at risk for dying in utero and was at high risk during labor.  Dr. Jacobi thought that risks of proceeding to C-section due to fetal distress would outweigh the potential benefit, and we agreed.
3.       We met with the comfort care team to prepare for how to make the hospital experience and the short time we would have with Avery everything it could be.
We set the induction date of this last Tuesday on July 3.  Even then, it didn’t really hit me how close we were getting until a week out from induction.  After all, life had reached a steady state of pseudonormality.  From about 26 weeks on, Jessica felt mentally much better than she had initially.  She was feeling Avery moving frequently and Emily was loving it.  (We chose Avery’s name by around 28 weeks and let people know because we had no idea whether she would ever be born.) Jessica was measuring near normal and felt all the normal symptoms of a normal 3rd trimester pregnancy.

But when July 10 came, suddenly the mental countdown started.  We had read the statistics: 50% of babies with Trisomy 18 are dead by 7 days, 90% by one year.  Most of the 50% who pass within the first week actually die within the first few hours due to heart defects like Avery’s.  So it felt like less than a coin toss’ chance of her surviving a day.  Still, Avery had been a living part of our family for 37.5 weeks, we had felt her moving and had been treasuring it for several months.  She is an important part of our family, and however short the time, we were already used to her.  Anxiety mounted as the veil of pseudonormality evaporated.  We weren’t counting down to her birth; we were counting the days until her death.

Up until last week, Emily had been seemingly unfazed by the gravity of Avery’s condition-- even though she understood that Avery might die before she was born and told her friends the very same blunt facts. Thursday night, Jessica was at a planning meeting for the MOPS (Mothers of Preschoolers) group she helps lead at church.  The girls and I were going through our usual bedtime routine with Bible story from the Jesus Storybook Bible, then prayer and putting Olivia to bed before going in to listen to Emily negotiate her way into reading another book.  After Emily and I finished Fancy Nancy: Posh Puppy, she was talking about Avery and getting ready for her arrival (as she has done almost daily for the last 4 months).  I was again explaining to her the situation with not knowing whether we would meet Avery alive. Picturing Emily’s grief at the moment she would first discover that Avery had already passed, I began to weep knowing how much she had anticipated her baby sister's arrival.

Seeing me cry got to Emily.  She turned away from me, but when I apologized for crying and asked if it made her uncomfortable, she just nodded her head, “No.” She faced away from me for a few more minutes, before rolling on to her stomach with her head buried in the pillow. Her shoulders began to shake seconds before the great sobs came.  For another fifteen or twenty minutes she cried, turning away from me when I tried to hug her or talk to her.  Never having seen her like this, I even asked at one point if she wanted me to leave.  Again I got the head nod.  Eventually, she did turn toward me but kept crying.  And when she was finally able to utter the words, “I just wanted to be a big sister to a baby so bad,” we both began to sob.  She collapsed in my arms.  No longer could either one of us ignore our feelings.

The next night at bedtime, we finished the Bible story and said prayers.  Even though we had prayed for mommy and Avery on countless evenings before that, the events of the previous night no doubt led Emily to ask, “Daddy, when we pray does it work?”  Uh oh.  “If we ask God to make Avery healthy, will it work?”  And again, though more matter of fact this time, “I want to be a big sister to a baby so bad.”  I had no easy answers but felt a kinship to her in hearing her ask that question.  What followed was not rehearsed but felt more like an explanation I was hearing for the first time too.  I told her that our prayers are conversations with God, and that in a relational sense the prayer itself is valuable for us and God.  He most wants us to relate to and rely on him, so that kind of prayer is pleasing to him.  And I said that sometimes it does work in the way we want it to.  In my experience, prayers for this kind of healing for the most part though are not answered in the way we want.  I told her that when Emily asks her earthly parents to do things, we don’t always say yes.  And when we say no, she doesn’t always understand why.  Still, she trusts that we love her.
Far from perfect, it is an explanation that gives some perspective but leaves much to be desired. This isn’t us asking God to do something he cannot do, nor something that is contrary to his will.  And to be honest, the “spiritual” answers that made sense to me when we went through Allie’s death no longer satisfied.  I stayed up Friday night thinking that this was exactly the reason I had avoided dealing with my own feelings about Avery and this pregnancy.  Deep down lies the fear that some part of my faith died the day we learned of Avery’s diagnosis.

Starting Friday night, I sat down at the piano to try to make sense of things.  A very simple chord progression without words felt like it was expressing something inside me. Saturday night at bedtime, we (coincidentally) read the story of Jairus’ daughter from their bible.  Someday I may share more of the exact wording, but sufficed to say for those not familiar with the story that it recounts the miraculous healing by Jesus of a young girl already declared dead. More to the point this time, Emily asked, “Dad, why won’t God do what we want him to?” She just cut right to the core of the issue with the same bottom line question I refused to admit I was asking. Ironic that my five year old was the one with the courage to say it out loud.

As I sat at the piano late Saturday night, words began to come to the simple chord progression.  Slowly it began to don on me that this was a song for Avery’s funeral.  The words came from my heart, from Emily’s question, from the story of Jairus’ daughter.  And in the midst of it, I got the first glimpse that maybe I could do more than just survive through this process.  Oh, and I forgot to mention this was happening while I was on call last weekend.  49 calls and six admissions left me rather tired by Monday, but I fortunately I have this whole week off.

ALRIGHT, IF YOU HAVE BEEN SKIPPING TEXT BECAUSE YOU JUST WANT TO KNOW WHAT HAPPENED SINCE TUESDAY, BEGIN READING NOW!


II.                  THIS WEEK (IN AGONIZNG DETAIL)

Tuesday morning at ~6 a.m. we arrived to the hospital.  The pitocin (to facilitate labor because Avery was so high in Jessica’s pelvis) was running by 6:45, and Dr Jacobi arrived to break Jessica’s water by 8:30.  At 11, Jessica was 5cm and getting closer.  The plan was to check again at noon and if she was 7cm to call Jessica’s parents to bring the girls. Aside from Jessica’s health, my biggest concern for things we could reasonably hope to control was that the girls be at the hospital (not in the room) at the time of delivery to maximize the chance they could meet her before she died.  At noon, Dr. Jacobi said, “You’re going to have a baby.”  I am by no means an OB but felt I already had a grasp of that insight.  She then clarified what she meant in saying, “Avery doesn’t have a lot of hair on top of her head.  I am looking at it right now. It shouldn’t take more than a push or two.”  After frantic calls to our dads, I thought I was going to vomit.  No amount of preparation actually had us ready for that moment.  On top of fear for my ability to remain composed was the fear of Emily and Olivia missing their sister alive.  With Jessica, Dr. Jacobi and our wonderful L+D nurse Abby looking at me, the question was whether I wanted to wait.  It felt like a silly question, and ½ a push later, Avery was out at 12:08.  5 lbs, 2 oz., 17 inches.

She was so blue and was gasping for air but was alive.  After Dr. Jacobi cut the cord, she immediately gave Avery to us and we sobbed as we felt her slipping away from us.  It was a crazy mix of joy, sorrow, and desperation at the fleeting moments.  After I steadied myself, the girls arrived within a couple minutes and I went and got them to bring them in.  Olivia I had to pull and Emily I had to keep from running.  We had a good while with the four of us.  Our friend Melissa (the first one to know of Avery’s existence, even before Jessica) was there capturing every moment.  She took pictures of us, the kids, our parents, and everyone who came into the room.
As I mentioned in an email some of you may have seen, I literally was counting the seconds from the moment Avery was born.  By the time we reached  1p.m., three things had happened:

1.       Avery looked notably more pink than she had at delivery
2.       I was beginning to count our time with Avery in minutes rather than seconds
3.       Melissa had taken almost 1000 pictures (wow)

We stayed in that room enjoying her and letting family enjoy her with us.  At 5p.m., we went upstairs to the 4th floor.  The normal Mom-baby floor is the 5th, but the comfort care team helped arranged for special placement for us.    We got situated there and were loving every second with this little girl.  Everyone left by about 7:30 (so Jessica tells me.) Here is a pic from my phone that night at about 9 p. m.

Jessica had issues with bleeding that night requiring hourly checks and some medication. Dr. Mike (our pediatrician) stopped by at about 9 to check on Avery.  About 1030 that night, she turned more blue.  Her vitals were ok, and we decided not to put oxygen on her then as we expected this.  With some repositioning and time though, she turned more pink again.  Jessica wanted to stay with her as much as possible, but nursing staff and doctors had both recommended we send her up to the nursery.  Around 1 a.m., I dozed off.  At around 2, I awoke to Jessica sobbing that Avery was blue and not moving.  I immediately picked her up off Jessica’s chest and gently bounced.  Her respirations seemed to pick up and she rather quickly turned pink again.  After that, we decided we needed to let the nurses watch her and we get some sleep.  I think we were both dozing at about 2:45, praying we would see her alive when we woke up.

At 6:30 that morning, the nurse wheeled her in and we immediately heard her little grunt breathing.  Sweet, sweet sound.  The nurse told us that Avery transiently went a little blue when she got agitated but had overall done very well.  Unfortunately, I was beginning to feel the after effects of having been on call the weekend before and felt like a dump truck ran me over. (Complaints on your wife’s 1st post-partum day don’t ever seem to be well received by onlookers though.)  We were both tired—I am sure Jessica more than me, though she is tougher. With some help from parents, we got a little more sleep before getting up for the day.

By about 9:30, I started to believe Avery was going to make it to 24 hours.  Just after noon, my dad brought up birthday cake, we light a candle and all (all 20 family members who had come up at that time) sang to Avery.  What a joyous celebration!

That afternoon we began to think that we might actually get to bring this beautiful baby home.  Then we realized we were absolutely unprepared to do so.  My parents brought up the car seat we bought 3.5 years ago for Allie but never used.  We talked to the social worker and Dr. Mike about arrangements, but last night began to fear what may happen at home.  The biggest issue looming was her apnea that was responsive to repositioning.  We felt like we might need a monitor but didn’t know if this was possible.  Fortunately it turned to be relatively straightforward with the help of the team at the hospital making arrangements.

Last night we sent Avery to be held and cuddled by the nurses at 12:30, and she came back in at 6 making her sweet little sounds. After a smooth morning making preparations, we came home at 12:45. The hospice team arrived at about 1:15 and stayed until 2:45.  The respiratory therapist arrived at 3:15 and stayed an hour getting us trained in her monitor (monitors Avery while she sleeps for heart rate under 50 or respiratory rate under 15, lets out ear-piercing alarm if need be) and her oxygen tank.  Then we (finally) were able to nap.
What a cool and unexpected evening of firsts.  Our first meal as a family of five (though Avery ate almost none of the dessert); our first Bible story time together (yes, those moments from last week remained fresh in my mind); she even stayed up past Olivia’s bed time and went in with Em to hear a Fancy Nancy story.



III.                Closing thoughts as of today
Monday (the day before Avery's birth), I asked my friend Micah to reserve the chapel of our church for Saturday morning for Avery’s funeral.  We had every expectation she would at best live a couple hours. She may still pass before Saturday morning, but as you read this would you celebrate with us that we are going to have to postpone that funeral?   We are elated but remain very aware that we are living on borrowed time.  To be sure, Avery’s days are numbered.  But so are yours and mine.  And while we think we have a better idea about her number than the rest of ours, someone forgot to tell her she was supposed to die within hours of birth. Far from causing us to fear, we have been given more time with Avery than we ever expected.  This borrowed time is immensely invigorating.  Maybe this is what the hospice social worker meant today when she said, “Avery has a lot to teach us.”

I also want to thank everyone for everything they have done.  To say we are fortunate is an unbelievable understatement.  And the phrase “we are so blessed” misses what I mean to say.  No question we have been blessed, but I don’t intend to use the word as an adjective.  I mean to tell all of you that amazing people have blessed (action verb) us by their thoughtful words, gifts, acts of servce, and absolutely yes, prayers.  The right answer to Emily’s question is that healing will come to Avery’s body. That prayer finds its answer in eternity. Until then, thanks to innumerable friends and family who have knowingly and in some cases unknowingly been agents of healing and comfort to us.

For fear of leaving anyone out and for fear of missing any more time with Avery, will you forgive me if I leave the thanks there and not go into specifics? We hope to thank people individually ASAP.

Below are some of the pictures Melissa took within the first several minutes of Avery's life:





Friday, July 13, 2012

Next Tuesday

Hi friends,

After a lot of prayer, we have decided to go ahead and induce labor next Tuesday. I will be 38.5 weeks, which is about the time I went into labor naturally in my previous pregnancies. We decided it would be best to have a small bit of control in this uncontrollable situation in regards to our doctor requesting particular staff, the comfort care team being ready, and our family having the ability to plan ahead and be at the hospital.

I will admit, I'm scared. We have lived with our little girl's diagnosis of Trisomy 18 for 4 months now, but she has held on and been such an active little baby. It is difficult to accept that the time is finally here for her to arrive and actually deal with the realities of her defect. I am still praying for complete healing of her little body, but if that isn't God's will, I'm asking Him for at least a little bit of time with her.

So this week has been difficult, knowing we are close to the end of the pregnancy and that the really hard stuff is about to begin. But at the same time, we have continued to be blessed by so many around us. Our family, our friends, our bible study, my MOPS group, our worship team...the list goes on. My precious Thrive group has been constantly blessing us since our diagnosis with surprises at our door each week, which this last week included our yard flooded with pink plastic flamingos! The culprit knew I needed a really good laugh...it was awesome!

So thank you for all of the calls, cards, texts, emails, gifts, food...you have been so generous. We have definitely felt so much love and support in this time. I'll say it again: Even in the midst of heartache, we are blessed.

Much love,
Jessica

Friday, June 22, 2012

Baby Girl

It has been a very long time since I touched this blog. After I posted about Olivia's first birthday, I wondered what I might do with it...tell stories about the girls, us, life...I don't know. It seemed the best thing to do was to put it to rest. We had used it to share our story and communicate with so many who graciously thought of and prayed for us during our pregnancy. And while we still miss our Allie, our daughter we never got to know in this lifetime, we have been blessed and have experienced so much joy over the last few years with our darling Emily and precious Olivia.

But life is never predictable, and we have been thrown another curve ball.

After a lot of prayer over the past couple years, we decided to try for another child. And shortly before Thanksgiving 2011, we found out we were expecting. Although I felt physically rotten most of December, we were excited to share the news with family over Christmas. Fears lingered within me, knowing there were no guarantees that this pregnancy would be "normal," but I continued to pray and trust God with the circumstances.

Shortly after Christmas, I felt like something wasn't quite right. I was primarily concerned that the toll the last pregnancy took on my body was going to cause me to have issues carrying this baby. I went in for an ultrasound again at 11 weeks. My body was fine, but there were concerns with baby.

A large pocket of fluid on the back of baby's neck had developed. All babies have a little bit of fluid there, but our baby's was thicker. We were told that this could be an indicator of a chromosome defect: Down's Syndrom, Trisomy 13, or Trisomy 18. We were referred to the perinatologist to take a closer look and then spoke to a genetics counselor. At that point we were told that our baby had a 30% chance of having a defect, but that left a 70% chance that things were just fine. We were to come back in two weeks to do another ultrasound and examine the fluid.

Two weeks later we returned, and it seemed our prayers had been answered. The pocket of fluid had reduced dramatically to a normal size, and other than baby being a little on the small side, everything else looked great. So we felt safe to begin sharing the news with others beyond our families that we were expecting.

Five weeks later we returned for our 18 week ultrasound with the perinatologist. My hope was the biggest news of the appointment would be baby's gender, and then they would send us merrily on our way.

The ultrasound technician informed us that we were expecting another precious girl. So many people had asked us, "Are you hoping for a boy this time?" But in all honesty, we did not care. We adore our girls, and while having a boy would be fun, the thought of another little sister was just as much fun.

But after the news that baby was a girl, our perinatologist entered the room, and we could tell all was not good. He said that baby had some heart defects, and that there were cysts on her brain. He suggested we do an amniocentisis to get the full picture of what was going on with baby girl, so we would know how best to treat her. I asked what specifically he would be looking for, and he replied that chromosome defects were still a possibility.

I think our hearts hit the floor for a second time. Minutes later we had the amnio done, and we began the 7-10 day waiting process for results.

Okay, heart defect, we could do surgery. Brain cysts, I've had two friends whose children had them in-utero and they went away on their own. Certainly this could all be "fixed."

But ten days later I finally received the call from the genetic counselor. I really thought she would call and say, "Good news! Baby is going to be fine!" Instead she gently delivered the news that our precious baby girl had Trisomy 18.

I was familiar with Down's Syndrome (also called Trisomy 21), and had seen a video about a family who lost their son to Trisomy 13, but I didn't know anything about Trisomy 18. The counselor shared some information with me and gave me some resources, but all in all, it just plain isn't good.

The effects of having three copies (a trisomy) of your 18th chromosome causes not only developmental issues, but multiple issues with your organ systems. So our baby girl's heart defects and brain cysts are very characteristic of Trisomy 18 babies. But there are many other issues that arise from it too, so many that babies with this defect rarely make it a week after birth, and those who do almost never see their first birthday.

So right now I am closing in on 35 weeks, and we are awaiting our sweet girl's arrival. It is truly amazing that she has made it this far...many babies with Trisomy 18 don't make it to term. And if we didn't have the diagnosis, I would never think anything was wrong. She is super active...so roly poly, always flipping and kicking. But things will be different when we deliver. We don't have any idea how much time we will have with her, but we don't anticipate it will be long.

So there is the story, in the factual sense.

I have struggled for the last few months about whether or not to even write about this situation. In some ways I'm ashamed of putting yet another Reade "drama" out there. I know everyone goes through hurts in their lives, and I'm in no way trying to say that our current hurt is worse than anyone else's. There are lots of people for whom I am praying right now, because they too have very difficult things going on in their lives.

In addition, going through this has been very draining, physically, emotionally, and spiritually. For a long time I didn't have the energy to try and write our story. But as time draws near for our baby girl to arrive, I felt this sense of urgency to write. There was something comforting about writing about Allie during our last pregnancy. We didn't get to raise her on earth, no one ever got to meet her in person, but she was here, and I have never questioned the significance of her short little life. And this blog documented the everlasting impact she had on us.

And to say this little girl has had an impact on us is an understatement, and I want it documented too.

I have no idea how much I will write in the next few weeks...I feel there is so much to say in regard to the way people have once again reached out to us and loved on us. I am amazed at people's capacity to bless us. After everything everyone did for us during our last pregnancy, then to come back and bless us again...we just feel, in a way, spoiled.

And there is even more to say about our journey of faith. Like Twin-to-Twin Transfusion Syndrome (the issue Allie and Olivia had), Trisomy 18 just happens. There is no cause, there is no prevention, it is just a mutation. All of our doctors have solemnly said that we have been hit by lightening twice. But I don't really believe this is all just by chance. I believe in the sovereignty of God, and there is purpose behind all of this. Don't get me wrong, if I could change our situation and have both my Allie and this baby girl with me forever, I would. But I take comfort in knowing that this is not a mistake. This precious girl is fearfully and wonderfully made, even with all of her earthly "imperfections." She is perfect in the eyes of God, and her little life has great purpose. God has told me that over and over again through this process: through a mentor, through our pastor, through devotions, through His Word. And I love her more than life itself.

Thank you for reading about our sweet baby girl.

Much love,
Jessica