Nic’s Adoption Story **Part 8

On January 12, 2017 we walked out the doors of that orphanage where Nic spent almost the first year of his life. Not a single person was there to say goodbye, but he arrived home to be greeted with the hugs, kisses and love of cousins, grandparents, aunts, uncles and siblings!

We celebrated his 1st birthday one week later. The first year of his life was spent alone in an orphanage crib, but he celebrated his 1st birthday surrounded by a mom, dad and six siblings! What a beautiful day!

All six of his siblings, including Colt, were in love with him immediately. They have all learned more about God's love and faithfulness and giving of ourselves for others through this process than any lesson book could ever teach them.

Day by day Nic’s smiles and giggles started coming easier .

He learned to cry because someone loved him and would answer his cries. One of the most eerie aspects of the orphanage is the silence. Rooms full of children but hallways so silent you could hear a pin drop as children have learned that their cries will not be comforted. .

His head shaking completely stopped within weeks of being home.

One of the hardest parts was his trauma in regards to food.  He would not stop eating when he was fed and became upset EVERY time the food was pulled away. His blood tests showed malnourishment when we arrived home and we knew that this would take time and healing. Today he has minimal food issues, but they are still lingering and we remain aware and sensitive to this trauma.

. We know that there might always be scars that we will be sensitive to, but by God’s grace, 19 Months later, Nic has been transformed by unconditional love.

What a beautiful picture we have been given of our adoption into God’s family. Chosen while we were still sinners, broken, hurting, with nothing to offer...Ransom paid by the precious blood of Christ...Made a child of God’s and transformed by His love. The scars of our old self might remain in this life, but we are forgiven and made new by our Father who loves us and hears our cries and nothing we can do will ever separate us from that love.

See what kind of love the Father has given to us, that we should be called children of God; and so we are...

1 John 3:1

ID Bracelets and Safety for Our Children with Down syndrome


Nic got his new ID bracelet and Colt is wearing two because his new one also arrived and he doesn’t want to take his old one off. He loves his bracelets.

 

I get asked about his bracelet a lot. So, here's the reason for the Medical ID bracelet and why I recommend getting one for your little ones.

Wandering, running off, or the clinical term, elopement, can be a frightening and fairly common behavior seen in children with Down syndrome. We have had some scary moments with Colt.

The fact that he loves to meet others, has very little fear and can open locks, buckles, climb gates and every other safety feature, does not put our mind at ease. We are always looking for ways to keep him safe.

After one scary incident we decided to order him an ID Bracelet as added protection should his propensity to wander and run off ever lead to one of our biggest fears, losing him.

Now that Nic is walking we decided it was time for him to have a bracelet of his own. I am still looking into GPS trackers as well, but a Medical ID bracelet is such a simple step we can take to help our boys in a moment of crisis.

Their new bracelets are from American Medical ID who have generously offered to  give 10% back on every purchase (5% on Gold) to Reece's Rainbow Down syndrome adoptions, as well as offered 10% off your purchase(5% off gold) when you enter the code “DWONDERFUL”. (Code will be valid for 2 weeks).

Here are a few more tips to help with the  frightening issue of running off:

According to "Supporting Positive Behavior in Children and Teens with Down Syndrome; The Respond but Don't React Method" by David S. Stein, children with Down syndrome do not process a lot of words in a moment of disciplining.   They process strong emotions, eye contact and facial expressions and seek attention in that way.  Bolting can become an attention seeking behavior.

"When you get upset, make lots of eye contact, raise your voice, and make strong facial expressions, your child is likely to experience your reaction as fun... for people with DS who are highly attuned to other people, this is like winning a slot machine- all the lights are flashing and it's entertaining!" (Stein p. 83)

Things to do: 1) Keep your reaction in check. Run after the child to keep him safe, but do not react.  Do not use a lot of words or yell or make eye contact.  Remain calm.

2) As discussed earlier, ID Bracelets and GPS trackers are an important safety tool for anywhere that you are at, home and away.

3) We have discussed Colt's propensity to wander with our neighbors so that they can be aware of the situation should the boys ever get out.  Nic is not a fast enough walker yet, but I am preparing for the possibility of him joining Colt too.

4) We have windows that open from the top and we do not leave them open from the bottom where the boys can reach.  Why do I include this? Colt has pushed a chair to the window, popped the screen out and climbed out the window to our backyard.  Fortunately, we caught him immediately, but it was a good lesson.  No open windows that he can reach or even climb to reach!

5) Add chimes on doors and windows and add locks where they can't be reached.  Now that Colt has grown we will be adding more locks in higher locations.  We have built extra gates as well, but Colt can climb them.

Hope this has given you some ideas to help keep your child safe.  It is constantly a concern of mine, so please share anything that has worked for you!

Have any of you had a scary moment when your child has wandered? Have you found any sort of GPS tracker or safety aids that you like? 

Colt's Birth Story Part 4: Our Announcement Letter

We wanted to share Colt’s diagnosis in a way that let people know that we celebrated our wonderfully made boy with his extra chromosome.

It has been almost 4 years since Jim and I together wrote Colt’s birth announcement, but the emotions still come flooding back every time I read it...

“We wanted to take a minute to share an update with you on our newest member of the family, Colt. Turns out our little guy has been gifted with an extra chromosome, otherwise known as Trisomy 21 or Down syndrome…. This changes nothing for us in our mind. Psalm 139 hasn’t changed. Colt is just as fearfully and wonderfully made by our perfect Creator as our other five children so why should we feel any different? God didn’t make a mistake when Colt was being ‘intricately woven’ and ‘knitted together…’’(Complete letter below.)

I remember crying while writing these words, not in grief, but in the realization of what a special gift we were given and just how much God was going to use our boy to impact our lives and this world.

I could have never begun to imagine just how soon and how greatly this extra special boy would change us though.

***Part 5 in next post on his 4th Birthday!!***

•Our Announcement Letter:

July 29, 2014... Hi Friends, We wanted to take a minute to share an update with you on our newest member of the family Colt. Turns out our little guy has been gifted with an extra chromosome, (otherwise known as Trisomy 21 or Down syndrome).

We sort of knew this soon after Colt was born when we saw his precious face that revealed one characteristic of down syndrome which is the adorable up-slanted almond eyes. He also didn't cry in the first 24 hours aside from a diaper change, which we also knew wasn't "normal". After a quick search on the internet we learned that many babies that have down syndrome do not cry very often. So this also began to confirm our belief that he could possibly have down syndrome.

When the midwife came back the day after the delivery for Colt's 24 hour check-up, she asked us if he looked like our others, we told her, "well yes, his older brother but with down syndrome". She was caught off guard as she didn't think that we had noticed nor did she realize that we would be just as happy with this possible diagnosis. She then confirmed to us that she also thought that he possibly had down syndrome.

We told her that it changed nothing for us in our mind. After all, Psalm 139 hasn't changed. He is just as fearfully and wonderfully made by our perfect creator as our other five children so why should we feel any different? God didn't make a mistake when Colt was being “intricately woven” and “knitted together”.

Last week Colt was seen by a pediatrician and a genetics doctor who both confirmed that Trisomy 21 was an accurate diagnosis. The last step was waiting for the results of his blood test which we received yesterday morning from genetics lab giving the final confirmation of the diagnosis that we felt we had already known since the day he was born.

We are praying that God will be glorified as we get the opportunity to share with our friends and family why we are just as thrilled and have just as much joy with Colt as with our five others (who as you know are not perfect and also come with their own little package of health and behavior issues that just so happens to not be given a packaged title or cute physical traits that might define their issues into a specific group).

As we were watching all of our kids cuddling Colt and doting on him and Luke carrying him around singing to him, Jim said, "well he couldn't have been born into a better family to always have someone loving on him and taking care of him :)"

Even though we know he'll be a greater gift to us than we are to him. Really it's not about him or us but just that it is an opportunity for God to be glorified and we are so grateful for that. We also know that there will be some unique challenges ahead but we have faith in our perfect Father and praise Him for another amazing gift in Colt!

Love, Jim and Kelsi