Blessings in Unexpected Places

Welcome to the March 2012 Carnival of Natural Parenting: Parenting With Special Needs
This post was written for inclusion in the monthly Carnival of Natural Parenting hosted by Hobo Mama and Code Name: Mama. This month our participants have shared how we parent despite and because of challenges thrown our way. Please read to the end to find a list of links to the other carnival participants.

For this month’s carnival I am thrilled to introduce you to my amazing college roommate, Callie! She is an inspiration is so many avenues of life, but most recently as she has entered the parenting stage with her two children, Mia and Liam. Read on and you’ll see exactly what I mean!

We welcomed our first child, Mia Grace, into our family in September of 2009. We went into labor full of nothing but excitement and anticipation, without a clue that we would be welcoming anything other than a healthy baby. We did everything possible to make sure that our baby would have a safe and healthy arrival to this world. We attended birth classes, followed a strict high protein diet and took all the right vitamins.
Upon Mia’s arrival, she was quickly taken away because there was excess fluid in her lungs and she needed breathing support. While our daughter was out getting the medical attention she needed, our midwife came to our room and told us that she was pretty sure that our daughter had Down syndrome. While my husband has always desired to adopt a child with special needs, it was still a far off idea that we expected to happen on our terms much later in life. At that moment, there were so many emotions, questions and fears that rushed through our minds. We had no idea what our future as a family was going to look like. We questioned why this was all happening and wondered what the diagnosis of Down syndrome even meant in its entirety.
Before we were able to fully process that diagnosis, another diagnosis came to the immediate forefront. A common attribute of children with Down syndrome is congenital heart defects. At one week old, we found out that Mia had a large hole between the two ventricles in her heart and that she needed surgery as soon as she was strong enough. At one month old, she wasn’t getting any stronger, began losing a lot of weight, was struggling to eat and got a bad cold. We found out that the hole began causing her a lot more trouble and she began to show signs of heart failure. She needed surgery as soon as possible, but she needed to gain weight first (which was nearly impossible with how inefficiently her heart was working). The next 4 weeks were the longest of our life. Mia was working extremely hard to breathe and eat, so all she could do was sleep. Our nights were sleepless, but not because of a crying infant, but because crying was too much work for her, so we had to watch her carefully and constantly. Finally, Mia was able to undergo open-heart surgery at just 8 weeks old to repair the hole in her heart. Handing her over for surgery with tear stained cheeks was the hardest thing we have ever had to do. But we knew she needed the surgery to live, thrive and grow.
Through that journey, Mia showed us how much of a fighter she could be. She overcame all odds, blew everyone away and recovered from surgery like an absolute champion, allowing us to leave the hospital only after five days. This moment is at the top of my list as the proudest & best moment of my life, so we made a video to help us remember the immense gravity of that journey and how to be grateful for each day as a gift of grace. You can watch it here (disclaimer: not for the faint of heart):
The joys and blessings are so rich after jumping countless hurdles, trials and medical struggles. Triumphs and milestones around here remind us that we have so much to celebrate and be thankful for. The perspective that is gained on this journey is constant and life changing and I am so grateful for that. We (those with special needs children AND those without) ought to see each day, each moment, each triumph and each trial as an opportunity to learn something and experience God’s immense grace in our life. It is there. Sometimes it is really hard to see. It takes practice and perspective to see it, give thanks for it, trust and be changed by it (trust me, this is something I have far from perfected and am continually learning)!
So much joy and beauty emerged from those times of great trial and brokenness (don’t they always?). One of the greatest gifts that we have received through Mia’s life has been the gift of faith. That gift is priceless. God used a helpless baby, struggling to breathe and eat to show us His power, love and grace. In my heart, it so closely parallels how Jesus came to Earth as a vulnerable baby and turned the world upside down, bringing His grace and love into the most unexpected people and situations. God is all about transfiguring the messy into beautiful and using the weak to teach the strong. He is without a doubt doing that through Mia and He is changing many hearts to value and love what He values and loves. He is continually showing up and teaching us more about himself and His kingdom through Mia. What a gift.
Despite everything that happened in those first 3 months of Mia’s life, from the first moment we learned of her having Down syndrome, we felt honored and blessed that God would entrust such a treasure and a gift into our hands. We didn’t know a lot, but we knew that He was doing something incredible in our life and through our baby. And we haven’t been the same since. God has used Mia in more ways than we can count to share His deep love, grace, mercy, hope, joy and beauty with us. He gives incredible blessings through these precious children, if we are able and willing to open our eyes and hearts to receive them. Even if those blessings are different from the ones we always thought we would receive, they are no less. In spite of all that she has been through, this child (who doesn’t even speak) has taught us more than a few things by just being her:
To love unconditionally and freely, without judgment. 
To offer a sincere and full grin at every opportunity. 
To persevere with joy in spite of setbacks. 
To rejoice in all things. 
Her joy of life is humbling. 
Her spunk & humor are hilarious. 
Her laughter is frequent & contagious.  
Her personality is adorable & sweet.  
Her kindness & love runs true and deep.  
Her wonder & appreciation for life is beautiful.  
Her fight & strength in the face of all odds is incredible. 
She takes what some call a disability and shows so much ability.
    She has taught us more in her short life than a lifetime of study could ever yield and we are forever changed for the better because of her. Ultimately our desire for our children (special needs or not), is that they would experience the love of Christ, love others and lead purposeful, meaningful lives. In many ways, Mia has already done these things in her very short, but incredibly powerful 2.5 years of life. What more could we ask for? We are surely blessed.
    Thank you for the opportunity to share! If you are interested in the full version of our story & journey, you can take some time to read it here on my blog: Those Crazy Kackleys.
    If you or someone you know is facing a diagnosis or is already on this journey with a child with special needs, know that there is so much hope and love to look forward to! I’d be happy to touch base and get you connected to some incredible resources that have guided and blessed us tremendously!

    Thank you so much for welcoming Callie! Don’t you agree that she and Mia are inspiring? I can’t wait to see all Mia grows to become. With her sweet spirit, family support, and perseverance she is bound to move many mountains … she already has!

    … Oh so many ways to follow along …
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    Carnival of Natural Parenting -- Hobo Mama and Code Name: MamaVisit Hobo Mama and Code Name: Mama to find out how you can participate in the next Carnival of Natural Parenting!

    Please take time to read the submissions by the other carnival participants:

    (This list will be live and updated by afternoon March 13 with all the carnival links.)

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