While it’s true that every Thanksgiving brings with it much to be thankful for, this year’s Thanksgiving (our son’s first) was perhaps our families most thankful Thanksgiving yet. (Whew….try trying that 7 times real fast!)
This year our family has something to be thankful for that less than a year ago we would have never imagined it even being a part of our life, much less saying we were thankful for it. But we are.
This thanksgiving we’re thankful to have a son with Down syndrome.
Our son almost came with an extra, extra bonus….
A few days after our son surprised us by being born with Down syndrome we were called to our pediatrician’s office to discuss something that came back on his newborn screen. This something ended up being the possibility that our son could have Glutaric Acidemia, type 1 (GA-1), in addition to Down syndrome.
Noah's first Thanksgiving day parade!
Now if you’ve never heard of GA-1, you’re not alone. Neither had I until this doctor visit, but I’ll give you the long and short of it: It could kill you. We were told that it was likely a false positive, not to worry (yah, right.), and to go home and enjoy Christmas with our new baby (after taking him to the lab to have some blood drawn.)
I’ll never forget walking in the front door of our apartment after that doctor visit. I was still trying to wrap my mind around the fact that our son was unexpectedly born with Down syndrome just a few days earlier. I was still trying to sort through what that meant for him and for our family. I was still hurt, confused, heavy hearted, and worried about our little baby boy. I mean come on, he was only a few days old, and it takes time for a new parent to sort through all of the emotions of a Down syndrome diagnosis.
Now not only does my son have Down syndrome, but he may also have a very rare metabolic disorder that could kill him. Wow! Talk about kicking a guy when he’s down. I”m getting teary eyed just reflecting on that day as I draft this post.
You can read more about what I call the scariest week of my life if you’d like, but after about a month and a half of testing, which included taking our few weeks old son to a geneticist to have his DNS sequenced, he ended up not having Glutaric Acidemia. Thank God!
The 6 weeks that changed my life…forever.
Our family has much to be thankful for!
Waiting on the test results to come back (about 6 weeks) really changed my life in more ways than anyone will ever know. When Noah was born I had to think about how our life was going to change as a result of his being born with Down syndrome
Our little man had a virus on Thanksgiving. ;(
When I found out Noah may have GA-1 I had to think about how our life was going to change if Noah had Down syndrome and Glutaric Acidemia, including the possibility of loosing our son. That was a whole different animal.
Down syndrome I was ok with, GA-1 (and the reality that our son could die) I was not. I had to have a lot of heart to heart conversations with God during those 6 weeks. I remember pleading with God that our son would just have Down syndrome. When all the dusted settled (and before we received the results) I came to grips with the fact that our children are not are own. They are God’s. They belong to them. We are their parents, their stewards.
One day they will leave us. They get married, they move out, they get a roommate and at some point our children die. Sometimes they die after us, and sometimes, sadly, they die before us. I say that not to be morbid, but just to remind you (and me) that our children aren’t forever. We never know what any day may hold. Our children (and us) are only one Doctor’s appointment away from having their lives changed forever.
Yes, that’s scary, but you have a choice…
You can either allow fear to paralyze you and keep you from enjoying the joy of today, or you can move forward choosing to trust that God truly does have the whole world in His hands, including you and your family. It doesn’t mean that what your facing isn’t scary. But it does means coming to a very real place in your life where you truly trust that God is bigger than your fear, and He is able to see you through it. Your fear doesn’t control you.
When fear comes knocking at your family’s door you tell it to go somewhere else, because fear doesn’t win in your house, God does.
Noah's grandmother feeding him his first Thanksgiving meal.
Noah's first thanksgiving meal. (Can you guess which is Turkey and which is mashed potatoes?)
All of that to say that on the other side of that 6 week waiting period, I came out a different person. God used those 6 weeks to help me deal with my fear and anxiety issues. (Yes, my name’s Rick Smith and I’m worrier!) 🙂 He wanted to show me that He is able to give us joy even in one of the scariest moments of our life. Up until that point in my life I had only heard stories about God giving people this kind of joy, but now I know first hand those stories are true. God really can meet our needs when nothing else on this planet can. How amazing is that!
I think he likes it! 🙂
So on this thanksgiving (our son’s first) I am extremely thankful that I’m not faced with the reality of raising a child born with Down syndrome and GA-1. Don’t get me wrong, our God is a big God. If Noah would have had GA-1, He would have certainly enabled us to get through it. However I’m speaking honest and from my heart when I say I am thankful that we don’t have to go down that road.
To the parents of a child facing a posable Glutaric Acidemia diagnosis…
If you ended up on this page somehow because your child is facing the possibility of a GA-1 diagnosis I’m sure I’ve only added to your fear. But I want you to know that I’m speaking to you from the heart, and yes as a parent that is scary, very scary. Your child really can die as a result of it. That’s perhaps one of the scariest things I can think of. Now let me try to give you some encouragement.
Now this is one happy (and full) baby!
First, there are a lot of false positives on the newborn screen. and it’s very likely that will be the case with your child. If that’s not the case, GA-1 is like most everything medically related in that there is a wide range of how it affects a person. Your medical team will help you develop a plan for your child that helps keep them from having a metabolic crisis. Furthermore, as stressful as newborn screens (and false positives) can be, it’s all worth it if it helps just one child catch a genetic condition as early as possible.
This is his "I'm getting stuffed" face...!
As with almost everything medically related, the earlier a person is diagnosed with a condition, the better. I tell you all of this in an attempt to encourage you. I’m sure you are very scared, but know that we live in a time like no other time in history, and our medical community has become very good at helping children with all sorts of conditions (including GA-1) live long and healthy lives.
Noah’s first Thanksgiving
As I’ve mentioned we have a lot to be thankful for this Thanksgiving. I can honestly say that I’m thankful to be the parent of a child with Down syndrome. This child has changed our family’s life in more ways than I could even begin count. I’m thankful that my son is healthy. That he is growing, learning, and developing. I’m thankful for how joyous and fun this little boy is. It’s awesome being his daddy.
Noah loves his uncle!
Will there be bumps in the road? Sure. Will there be lots of scary times in our future? Sure, what child doesn’t scare his parents from time to time? But for today, for this first Thanksgiving with our new little baby boy, things are ok. The rush of emotions we dealt with the few months of Noah’s birth has subsided. I don’t freak out as much every time we have to take Noah to see his pediatrician (although waiting for the results every time Noah gets a CBC still causes my heart to beat faster than normal.) I don’t get (as) worried every time Noah gets a little cough.
More uncle love!
Other than Noah having a little virus (as you can see in some of the pictures) today is a great day of enjoying life, eating lots of yummy food (thanks Abbie!) and enjoying time with family…and being very, very thankful that my son just has Down syndrome!
I'm so in love, and thankful, for this family!
I know it’s not Thanksgiving right now, but it’s always good to reflect on things you’re thankful for. So please take a second to leave a comment below and let me know one or two things that your especially thankful for right now.
About Rick Smith
Thanks so much for this post. I can really relate to you. With my husband’s parents both passed away and my side of the family cutting off contact with us, I was apprehensive enough just having a third child. We planned our vacation time around it and worked out babysitters for our other 2 kids. It wasn’t until 10 days after Elias birth that we knew he had Down Syndrome. At that time we were in the hospital for phototherapy. That was overwhelming enough let alone the echocardiogram that showed there might be a problem with his heart. In the end it was okay, but I can say i saw God’s hand in everything. He let me know that Elias might have DS before we got the result, He inspired me to remember a friend who’s son has DS and gave her the opportunity to share with me many feelings and thoughts that helped to quell some of the fear. Friends and adopted family have gathered around us, extentions of His hands that let us know we are not alone. When I remind myself of these things, faith takes the place of fear. Undoubtedly there will still be storms and waves as life goes on, but peace buoys our little family up as work on things, one day at a time. Gratitude helps to keep our perspective
Flo,
Thanks for sharing your story with us. You guys sound like great parents! I’m sorry to hear about your husbands side of the family cutting you off. It sounds like you have a great group of friends and other family supporting you, that’s great!
How old is your son now, and how old are your other children?
Elias is now nearly 3 months and he is adored by Isaac who is 5 and Keila who is about to turn 3. Actually it was my parent who cut us off the moment we were engaged. The Lord works in mysterious ways though. We kept a family blog (an iinformal way to allowing them to choose when they wanted to know what was up with us anonymously) and worked on forgiving. Over the last 10 years little things occured to enable us to see each other at my brother’s wedding. They wanted minimal contact with us and our kids but when they heard Elias was born with DS they were devastated and worried for us. (love shows in funny ways…) and have since initiated contact through skype in the last 4 weeks. I think Elias is our bridge and an answer to our prayer.
Wow, that is very cool indeed how God used circumstances in your life to help bring your family closer. We’ve found that our son has done the same thing in our family. It’s been great.
Where are you guys from by the way?
While we haven’t had the scare you had, I have met so many children with so many conditions worse than Down syndrome and so many with Down syndrome who have complications that we don’t face with our Wesley, 3 yrs old. I have seen in my life and in others’ lives how that God’s grace is sufficient whether the problem we face is big or small. Some things specifically that I’m thankful for (and some of these are piddly): no need for hearing aides or glasses, being able to wear foot supports that fit inside normal shoes instead of something visible, no heart surgery, no intestinal issues. Some things we need grace for right now: changing schools in the fall, possible speech apraxia. God is good. Thank you for the reminder!
Susanna,
I’m glad to hear things are going well for Wesley. I always am hesitant to write posts like this because the last thing I ever want anyone to do is feel worse if their child isn’t doing well. I also know that at any moment things could take a turn for the worse for Noah, myself, my wife or anyone else, which keeps me very humble.
My heart breaks for children and families going through hard times, and I pray for so many of the families I’m able to connect through our site.
But think it’s ok to speak from the heart as a parent and say I’m thankful for how well my child is doing. Thank you for sharing how your child is doing!
Do you have any other children? What’s Wesley up to now? Is in in school or anything? Just curious since he is just a little older than Noah!) 🙂
I can definitely relate to this. Little Man was a week old when we got the call from the pediatrician’s office that there might be something wrong with his newborn screening. A lot of tests happened over the next few days and weeks and when Little Man was about three and a half months old, we had our definitive answer: Little Man was born with a rare metabolic disorder, acronymed VLCAD. It, too, was something that could kill him…..but it’s totally manageable.
Now he’s 19 months old and things are fine. He’s pretty much “normal” except when he gets sick…then we have to visit the hospital and we have to put the metabolic doctor on alert. It’s not fun.
As long as he takes care of himself, he can live a long, and relatively normal life.
But I can remember what I went through after that first phone call and your story relates so much (minus the religion part – we’re not overly religious in our house).
@Renee,
Thanks for sharing. There is no fear like the fear of something happening to your child and you not having the power to do anything about it, huh?
I’m so glad to hear that your son is doing well now! By the way, do you guys have any other children?
Today I’m thankful for the excellent information and contacts we were given when Daniel was born. He turned 3 months on Monday and we’re already done our Early Intervention evaluation plus two visits with the occupational therapist. Plus we’re scheduled to go to the Sie Center (a Down syndrome specific clinic associated with Children’s Hospital in Denver) next week and meet with a team of doctors and talk to a geneticist. I never would have managed all that without people pointing us in the right direction!
Also, Daniel rolled over for the first time last week, so I’m thankful for meeting milestones 🙂
Wow…rolling over for the first time…!!! That’s a huge milestone indeed! Congrats! You guys must be so proud. We’re proud as well. Thanks for sharing that with us.
I’m thankful for all the info that we have at our fingertips as well (sometimes a little to much it seems.)
That place in Denver sounds very cool, please be sure to keep us posted on how everything goes after your visit. We have family in Denver and visit a few times a year (I think we may even go there this summer.) Maybe we can meet you guys one of these trips! 🙂
Rick, I can totally relate to your feelings and thankfulness. At week 15 of my pregnancy, the nuchal translucency test showed a 1in 5 chance of our Leo having Trisomy 13 or 18, both of which are fatal either during the pregnancy or soon after birth. Trisomy 21 was far from our minds since the test showed little additional risk. We showed up for an amnio to basically find out if our baby would survive! Needless to say, the positive result for trisomy 21 was a shock. But at least it was the good news we had prayed for! I never imagined in the midst of my shock, fear and sadness, that someday I would be happy Down Syndrome is all that Leo has. Like you, I am thankful!!
It sounds like you know JUST how I feel. 🙂 I’m so glad that Leo is doing well.
How old is he now by the way, and do you guys have any other children?
I am thankful for your for your post. I am a big worrier about everything and even though my boys 2 1/2 and 6 1/2 are healthy for the most part, your post is a reminder to let go of some of my anxiety and worry and let God. Thank you.
Thanks for the kind words. I’m also a huge worrier and in fact even after I wrote that post, I started worrying about some new thing. Not worrying about our children is much easier said than done. But we’re all a work in progress, aren’t we? 🙂
I sounds like you’re a great mom doing a great job, keep it up! Does one of your children have Down syndrome?
No, neither has Down’s Syndrome, but the youngest was hospitalized a couple of times when he was younger for pyloric stenosis, a neck abscess, and severe RSV. Both are facing growth issues and we have a long-awaited appointment with a pediatric endocrinologist in July.
I enjoy your blog; Noah is lucky to have you for a Dad!
I dropped by your site via the WP.org support forum to see how I could help you with the TC widget, and instead was excited to read your amazing blog! Noah is SOOOOOO ADORABLE, I just want to squish his chubby chubby cheek and kiss his perfect round eyesssss!
Yeah. I know the feeling. I thank God every day that my Edry only has Down Syndrome too. He’s just so healthy and is the life of the household right now. His big bro especially spoils him to pieces and Edry can’t get enough of it!
OK, let me get back to looking at your HTML codes and see what I can do….
Wow, it’s a small world! I’m a tech geek, and a dad! 🙂
Are you on our Facebook page? (http://facebook.com/noahsdadcom/), we’d love to see a picture of your Edry! 🙂
My daughter Jovie has just been diagnosed with Rett Syndrome. We’d suspected it for over a year, and finally the DNA results came in last week. If I’m honest, I had hoped her Autism & Developmental Delay diagnosis was it – because this whole Rett Syndrome world is scary HOWEVER I am grateful we live in a world where I can email another Rett mum and she is there. I am grateful for science for giving us this information about our children. And I am grateful for my children for teaching me about this world.
xx
Thanks for sharing that with us. I’m sorry about the Rett Syndrome diagnosis, but like you said, this is a time like no other in history. We can connect with our people that’s “where we are” any time, online.
How old is Jovie? Do you guys have any other children?
Jovie just turned 3 🙂 And we have a beautiful son Jasper who is 4 – busy times!
I wanted to say that I hear you. Once you are faced with the mortality of your child it really puts everything else into perspective. Hearing “Down Syndrome” was hard, I’ll admit. But 4 hours after that, hearing “Heart defect requiring open heart surgery” just didn’t compare. Otto is now 7 months old. I honestly never ever thought we’d get here. He came through surgery, and I thank God for that. We had 860 people attend a Facebook prayer event for the little guy. Represented were all continents (excluding Antarctica, selfish little penguins). God wanted us to have this baby (a surprise) and He wanted us to rely on Him during those trying times. I am glad they are all over. But really, once you hand your baby over to a stranger and you may not see your baby again nothing else can compare to holding him in your arms again. So I’m with you…thank God its ‘just’ Down Syndrome!
Thanks for sharing, and I’m so thankful that his heart surgery went ok. The Facebook prayer event sounds awesome as well! When was that prayer event? (Was it 7 years ago?)
Also what’s Otto up to these days?
When my son Aiden was born 6-30-08 he was in Children’s Mercy Hospital for a month before we could take him home. He had numerous problems. But I’ll never forget one nurse told me, “If you had to have a child born with a disability, Down Syndrome is the best one to have. You are so lucky!” At that time I couldn’t understand. But after making several trips there for appointments with different specialists and therapist, I finally understood and she was right! Thank God my son has Down Syndrome. There are so many sad, scary things that could have so much worse that I saw of children there. I never knew babies could be born with so many things wrong with them (I have 6 healthy boys). Thank you for your blog. I really enjoy it. Ruth
Ruth, thank you for leaving your comment. You have no idea how much we enjoy reading all of these stories that everyone shares with us, so thank you!
And 6 boys, wow…! My mother had 4, and we were way more than a hand full! 🙂 I bet you guys have a lot of fun in your house.
What are the ages of your children?
I gave birth to my first child, Matthew on 7 Nov 2011 after a very straight forward pregnancy. The day after Matthew was born we were told that they thought Matthew had DS. It was confirmed a week later, although I already knew in my heart. It was the craziest emotional rollercoaster ever but I just decided to get on with things and not treat Matthew any differently. Although he has a heart defect he is doing brilliantly. He started rolling over at 5 months, saying dada at 6 months and enjoys 3 healthy meals a day now at 7 months. He is the smiliest littke guy ever and brings joy to anyone who meets him! Who knows what the future may hold but for now I just treasure every amazing moment with my gorgeous, funny, babbling boy x x
Thank you so much for your blog. I am a mother of 4. Philip, 8, Isaac, 4, Luke, 3, and Katie, 20mos. i am pregnant with our 5th child, a boy, due in september. we have been told from our quadscreen results, a 1 in 6 chance of DS. Add to that soft markers on the ultrasound now brings us to a 1 in 2 chance. I have chosen not to have an amnio to confirm, so I am just preparing for DS. I love your blog, because I see how much noah is loved, and how much he is more like other children than he is different. i can’t wait to meet our little guy either way. I am scared, but hope it will JUST be down syndrome. The thing I most worry about now is that we are from a small town in Indiana where therapy services are very limited and most people still have a pretty old fashioned view of the capabilities of children with DS. Thanks again for your blog. Rachel
I just wanted to say that your website has really helped me realize that having a baby with DS isn’t the end of the world. My son was born with DS April 27, 2012 & he has totally & undoubtedly changed our lives for the better. He is such a bright light in our world. We love the lil guy so much & our whole family has been so supportive & loving towards him. He is our only boy. He has 4 older sisters who absolutely love & adore him. We thank God for him everyday. We can’t imagine life without him. Thank you for your awesome website!
Congrats on your baby!!!!! One of our goals is to bring encouragement to new families and show them that life is actually pretty awesome 🙂 I am glad that you are discovering that :):) have you seen our Facebook page, there are a lot of families on there sharing their lives and pictures 🙂 do you have a support group in your area?
Hi Rick,
I am so thankful my wonderful wife, and two beautiful boys. I am thankful that all of us are healthy, and for the good Lord’s protection on our life. Thank you for sharing your heartfelt stories here, and I do look forward to reading more about Noah and your family.
Noah is beautiful. God bless him & his family. I do not have words to express what I went through after reading the blog. I think when God sends across a child with DS he sends along loads of extra love and affection too. The families with ds kids Ive seen are the most loving families I’ve known.
Noah is so beautiful and so are you. Thank you for sharing your feelings and personal thoughts. You are a champion and so is Noah. 🙂
Thank you SO SO much for this post. I will be coming back and reading it often over the next few weeks. Got the call from our pediatrician yesterday that our 1 week old tested positive for GA-1. We take him in for the extensive testing next week. Praying for a false positive!!!!!!!!
I feel like I’m in a nightmare! How is this possible?!
Hi Rick, First off I want to tell you how much your boys and you mean to me. I love Noah so much and see God in that little face. There is no DS in our family, but my Grandson Alex was born 3 months early with four holes in his heart, underdeveloped lungs, and something missing out of his right eye so if you take a picture all you will see is white. His mouth was so small at birth they had to use an eye dropper to feed him. When he came home he was in cabbage patch kids clothes. Then the DR told us that by the shape of his ears and hands, he had a weird illness and wouldn’t live much past 2 or 3 days. Of course his parents and grandparents got scared. I told my daughter not to worry until they could prove it. Drs. don’t know everything. Then I noticed that his hands and ears were shaped just like his Mommy. I knew he was going to make it when the Elders from our church came and did the laying of hands on him. We all could feel the peace . To make a long story short, he was kept out of school until he was 7. DR. Faggan was afraid someone would step on him or knock him downstairs. The teachers anad kids were great with him. He was tested and was found to be extremely intelligent. He had open heart surgery when he was 11 and did great there. He has some hearing problems and his speech is still being worked on. Thanks to God he is now in his 3rd year of college and doing great. Later we found out it was the DRS. fault with what happened. He knew my daughter had extra fluid and left it alone. If he had done his job Alex would have been born full term with out the problems he had. He gave her a C section and cut so far in her legs that she didn’t heal right and she had to have mostly bed rest for her last one because her new DR was afraid the baby might fall out. As I said I don’t have a DS child but have worked with them at the school and always felt happy around them. A woman at the store said that all DS babies slobbered all over people and she coulsn’t stand to be around those type of kids. I told her “I feel sorry for you. Those beautiful children add so much to life and she should read up on them and go meet some.” Thank you for sharing your two awesome boys with us and for being such a great Dad,