My Son was Dead, and is Alive Again

I remember equating our first time meeting William to how God must feel the first time we ask Him to come into our lives and make us new. The joy mixed with the grief of loving someone so much that you would do anything for them was tangible and it left me in awe of God and His plan for us. The first eight months of William’s life was pretty smooth sailing. We thought it was a bit difficult, but we had no idea what was coming.

When Will was diagnosed with his seizure disorder, my personal grief and depression was intense to say the least. William basically disappeared. We were left with a baby we didn’t know and memories and photos of the old Will that, although they should have been happy, increased my grief all the more. I was conflicted with the loss of my son coupled with the fact that I still had this stranger to care for. His care was so much harder, and I found myself slipping further and further away into my grief. At the time, I was so angry with God that I refused to talk to Him. I turned away. How could He love us and let us go through this? How could I love Him after He didn’t save my son?

William has been seizure free for two glorious months. This week, he began to roll over again and hold his own head up. His beautiful smile lights up our day. William is back. Just as God taught me about salvation when William was born, today He is teaching me about faith. About 18 months ago, I prayed that God would increase my faith no matter what it took, but I had no idea what that meant. I must be difficult to teach, because God had to take me through the deepest, darkest year of my life in order for me to learn to trust Him. I don’t believe for one minute that God makes bad things happen to us, but I do see that through the bad, He brings understanding and makes things new.
I have been pondering the story of the Prodigal Son for the last few weeks, equating it to losing who William was for a while and now getting him back from the brink. But something felt off. We didn’t actually lose him. We felt like it for a while, but William was always there. He was just too sick to reveal himself. Why did God keep bringing this story to the front of my mind?

I realized today that this wayward son story was mine, not William’s. When I asked God to increase my faith no matter what it took, He knew that I needed radical change in my life. The only way to increase my faith was to shatter it and to rebuild it from the ground up. I have been the prodigal child for the last four months. My anger with God was enough to make me turn my back on Him. But He was in relentless pursuit. As I grew angrier, more people told me that they were praying. As I tried to skip church on Sundays, my kids asked to go and I couldn’t say no. As William got better when the doctors said that he wouldn’t, God’s healing was the only answer that made sense.

As Will continues to get better and stronger every day, we are blessed and delighted by seeing his “firsts.” The first time he smiled, the first time he rolled over, the first time his beautiful almond-shaped eyes followed me across the room. The funny thing is, he did all of these things months ago. But God has been gracious to give them to us again. And after being told that they are unattainable, the second first time is even more amazing than the first first time. Does that even make sense? Not to me, but to God, absolutely! Seeing impossible healing right in front of you, in the most precious person in your life makes disbelief in God a ridiculous notion. Through God giving us this amazing time of healing in Will’s life, especially after all that we have been through, He proves Himself over and over.

It took a year of this special needs adoption journey, with all of its ups and downs to find my faith. I thought that after asking God to increase my faith, He had instead destroyed it completely. But looking back, He was there all along. I was the one who had left. The hellish months of worry and grief are over for now, but we don’t know if they are gone for good. What I do know however, is that if they come again, God is in the midst of them. Not only that, He is there now, preparing a way for us to make it through them if we must.

I am unshakable in my faith. I’ve seen so much proof that nothing can convince me otherwise. God granted my naïve yet sincere request to be changed, just not in the way that I expected or would have chosen. Will turns one next week. I don’t even know how to put into words how I feel about that. I have spent the last year trying to save his life in any way that I can, but he ended up saving mine. Thank you God that you give us what we need and not what we think we need. Hallelujah and amen.


The First Advent

I have been so frustrated this holiday season by the fact that I haven’t been at church for Advent services. Christmas is definitely my favorite time of the year and I love being able to sing all the Christmas songs, see the lights and anticipate spending Christmas day with my family. It is just a lot of fun. This year, one kid after another has been sick, and it just keeps happening on Sunday mornings and Wednesday nights during service times.

This past Wednesday our little William was really struggling to breathe from a bad cough. We made the decision to take him in to the Mott Children’s Hospital ER. The day before that, Tuesday, I saw that Will was making a strange movement with his arms and I took a short video of it on my phone. As we were doing a breathing treatment and being diagnosed with RSV at the ER, I happened to mention this video and showed it to the doctor. Then, Will began to do it again and the doctor saw it firsthand. She said that it probably wasn’t a big deal, but that she would show Neurology just in case.

To make a long story short, on Saturday, only three days later, I was sitting in a quarantine hospital room with Will as he recovered from RSV, deeply grieving the new diagnosis of West syndrome that had blindsided me. Our world had changed so quickly, I felt like my head was spinning. Words like catastrophic, debilitating and major loss that the doctors had told me kept racing through my brain. They said that William will probably stop progressing in his development at least until he outgrows his seizures (around age 3 to 5). He may lose milestones that he has already gained and the fact that it is all happening during the most crucial developmental stage of his life will leave him permanently disabled.

I turned on the TV to try and distract myself since I couldn’t leave the room and a commercial with a Christmas song came on. I had completely forgotten about Christmas! This is my favorite day of the year. How did I miss it completely? I began to feel sorry for myself. I was mad that I was stuck in isolation, mad that I was not home to see my other kids, mad that I had missed basically the entire Christmas season and mad that God would let yet another thing happen to my baby.

I was in the midst of intense, angry prayer, basically telling God off for what was wrong in my world. Will was not experiencing his first Advent season the way he should and neither was I. Why would God allow all of these things to keep happening to him?

Then a new thought hit me, or God hit me, or realization hit me, or maybe a combination of all three. I was observing Advent the same way that the world experienced the first Advent. I was in deep mourning and waiting, wondering if God was really going to reveal himself in the midst of our despair. This overwhelming sense of understanding flooded me and Advent became so much more real in my life. We experience Advent by grieving with one another the wrong in this world with the hope and anticipation that somehow God will make it all right.

I hope that people grieve with us. But, and this is a big BUT, I don’t want anyone grieving for us. Although I can already see that my little William is subtly different than a week ago before our world changed, he is still William. He is still the amazing gift that God gave us and he will still change this world for the better. He will just do it with more challenges. Grief and pity for him will not help him become the person that God wants him to be.

But please grieve with us during what’s left of this Advent season. Grieve that the world is not how God intended it to be. Grieve that people are hungry, hurting, lonely, sick and oppressed just as they were during the first Advent. Then, on Christmas day, celebrate with us too! Unlike the first Advent, we already know that Jesus did come, that He did die for us, that He did redeem us and that He is coming back again to finish what He started, making all things new.

I was wondering how I would possibly be able to celebrate Christmas this year with all of the new heavy burdens in my heart. Maybe that is the whole point of Advent on our side of the cross. I can celebrate because I know that the deep grief, mourning and waiting is only the first half of the story.

So on Christmas morning, I will choose to celebrate the gift of my son, the beautiful albeit complicated life that he has led so far, and the fact that doctors told us he may never make it to Christmas to begin with and here he is. All of these things are beautiful miracles in our lives that are made sweeter by the knowledge that my God gave his son for my son. Even though I don’t know what will happen to my son in the future, I know what happened to His son in the past. I choose to see this Christmas for what it is; the promise that no matter what lies ahead, Jesus came in the flesh as a baby as helpless as my own, suffered and died so that we all can live eternally. It all really happened, and it happened for each of us, especially my little William. Amen and Merry Christmas!