Showing posts with label cerebral palsy. Show all posts
Showing posts with label cerebral palsy. Show all posts

Saturday, September 21, 2013

Hope

This post is part two of our adoption story in country. You can read part one HERE


"And then...they brought us our son."

I will refer to our boy as "N" for the time being.

As we sat waiting in an entrance way, with our luggage stacked by the door, a nanny appeared with a little, 3 year old, grinning, blue-eyed, ball of energy! It is difficult to describe the thoughts and emotions swirling through me at that moment. There were other people there as it is the waiting area for the treatment side of the facility as well. The adults in the room were all smiles, and they were perfectly happy to let their children interact with N. 

N's caretakers kept trying to introduce us as "Mama" and "Papa," but N was too busy exploring to care. We had very few things accessible from our luggage, but I pulled out a container of bubbles. I was sure he'd be fascinated with them, but N just thought I was crazy. Why would he sit still and look at soap bubbles when there was a suitcase there? He didn't much care what was *IN* the suitcase as much as he enjoyed playing with the zippers. I just watched and chuckled as he would unzip and zip the suitcase and the outside pocket, over and over again. We grabbed a ball from the ball pit, and he discovered the hilariously fun game of, "throw the ball and watch Daddy go get it!" 

It wasn't long before they had to take him away for lunch. He didn't want to leave, but we promised to be back. We dropped off our luggage at our apartment, ate lunch and bought some bananas, cookies and juice to bring to the afternoon visit. When we got back to the orphanage (after only getting slightly lost), we were able to take N outside to play. That was where we discovered the slide. I wasn't entirely sure he could climb the stairs with his cp, so I helped him up. Each time he got settled on a step, I would say, "step" and he would step again. Then, he started repeating after me, "step! step!" and taking steps each time. I loved it. Daddy was catching him at the end. It was a pretty fast little slide and I worried that he would be scared, but he loved it and kept coming back to do it over and over again. 

We fed him the banana, and a couple little cookies, and gave him a juice box. He knew was juice was, but has clearly never had it in a box with a straw. Because N has a type of cerebral palsy, it was hard for him to drink the juice, but he sure gave it his best effort. We enjoyed our visit with him, and I began to feel an enormous calm about the situation. 

Now, for the way this all came about. 

Little N was born in a certain country that has recently banned adoptions by Americans. His parents, however, were not citizens of that country. When he was refused at the hospital, he entered a baby house there. In Eastern Europe, a person's citizenship is not so much based on where they are born, but on the parents' citizenship. There is also a law that states that citizens of other countries cannot be kept in the orphanages of other countries. And so, last year, all the paperwork was completed and little N was brought to this country and this orphanage. I do not know if his parents were from this region, or if he simply went where there was room. But either way, little N was given a chance. Had he remained in the other country, it would have been impossible for him to be adopted. In the year since he has been here, one domestic family came to see him, but could not accept his cp. And then, we came, specifically looking for a child with cp, and through the most excruciating, round-about process, ended up here. No advocacy groups come here. Most kids with special needs get foster families here...but certain disabilities are still very hard to place. The ones people can see with their eyes are the hardest. And so, little N waited. I never could have imagined how this process would unfold, but God knew. 

We attend a small branch of our church here, with English speaking missionaries. Last Sunday, a woman introduced herself, and told us that years ago, she placed her grandson for adoption because she could not care for him properly. He was adopted by an American family of our faith. He is now an adult, and is coming back here to serve a two year mission. She was so very proud, and so thankful for his family. She said the same family also adopted another boy who had problems with his legs. His future was pretty grim in this country, but after being adopted, he received two surgeries and is now an impressive hockey player! It's stories like this, and more importantly, the people sharing them, that have stirred my heart and strengthened my faith beyond what I could have imagined. 

Where I once felt anguish, I now feel hope....and joy. I cannot publicly show N's face until after court, but this one sums it all up. This was the first time I held out my arms and said, "N, hug Mama?" He thought about it a second, smiled, and ran into my arms. I am so thankful that my husband took this picture. It is my favorite. 












Saturday, April 27, 2013

Bittersweet...New Hope For The Ones Who Wait

Last week, it became clear that the ban on American adoptions from Russia would remain in place for the foreseeable future. So many families are hurting over this decision and even more children will never know the love of a family. It is a very hard time for the families who had committed to children, and in many cases met them, before being told they would never get to bring them home. My heart and prayers go out to these grieving families and children.

As many of you are aware, Reece's Rainbow provides grant funds for orphans with special needs. Many of the waiting children in Russia had sizable grants, but no committed family. This week, staff of Reece's Rainbow has started the tedious and time consuming process of reallocating the money from the Russian waiting children, to waiting children in other countries. Out of the ashes of a terrible loss, comes New Hope. Many children are now receiving significant grants that will hopefully help families to feel confident in stepping out to claim them as sons and daughters. 

Here is one of my very favorite New Hope recipients. Please allow me to introduce you to Frank.

Frank wants a family. He is very tiny, but he is almost 13 years old. He has a mild mental delay and was living in a boarding house when, for reasons unknown, he was transferred to a level IV adult mental institution. This boy is smart, kind, has very good language skills and just needs out of there. Frank received a New Hope grant from Reece's Rainbow and now has nearly $12,000 in his adoption grant. Please, if you are considering a son...or maybe adding one...please consider Frank. There are many photos and videos of him available and I can even put you in touch with someone who saw him for 7 weeks last year while adopting their boy. Please share Frank far and wide so his family can find him.
http://reecesrainbow.org/?s=frank

If a family is already headed to his country for an adoption, Frank's grant would more than cover the fees for adding him. If a family is starting from scratch, his adoption is around 2/3 covered and he as several advocates (myself included) who will happily help out with the remaining funds. Please help us find a family for Frank.


Next we have sweet little Vytas

Vytas is a darling boy who turned 5 this month. He is very small due to having Down Syndrome and being in an orphanage, but he would thrive in a family where he can get therapies and interventions. Vytas also has a couple great advocates pulling for him over at Hope for Vytas
Vytas' grant currently has over $10,600! What a blessing to his future family!
http://reecesrainbow.org/40627/vytas

And Brandi

Look at that happy smile and sweet pigtails! Brandi is 5 years old and has Cerebral Palsy and microcephaly (smaller head size). She is described as "physically active" and her profile even has a picture of her enjoying time on the piano. Such a gorgeous little girl!
Brandi should be getting ready for kindergarten, not a mental institution. 
Brandi received New Hope funds and her adoption grant now has over $10,600! 

There are more to come later, but for now, I would love it if my followers would consider praying for these children to find families. Please share them on your own blogs and social media sites. It was through a Reece's Rainbow posting on Facebook that I first started scrolling through pictures of orphans. It was there that I saw our sweet Carolina's face. It was reading the blogs of other adoptive parents and advocates that my heart was completely broken and changed for these kids. It was people sharing their experiences and their fundraising ideas that we finally gained the confidence to step out and BE one of those families. 


Our little one will soon know that she has a Mama and Daddy who love her. 2 years ago, I never would have thought we would be doing this now. You just never know who will see one of your advocacy posts and realize they are seeing their child. So many people loved Carolina before I ever saw her. Take it from me, there is a special place in a Mama's heart for those who helped advocate for her child. 









Monday, August 13, 2012

Teamwork Tuesday...Kurt

Welcome to my first Teamwork Tuesday post. This is where bloggers from all over the web come together to spread the word on one waiting child. Today, that child is sweet little Kurt.
Kurt is an adorable little boy who has spent his entire life in an Eastern European orphanage with no mother or father to read to him, tuck him in at night, take him to the park or to the zoo.


Why has this sweet boy been dealt this fate? Quite simply because he is labelled as "defective." In his home country, children with disabilities are viewed as burdens. Perhaps his birth mother simply felt she could not afford to care for him? Whatever the reason, this adorable boy with big, brown, puppy dog eyes and dark brown hair is running out of time. You see, Kurt is still residing in what is known as a "baby house." But sometime in the next year, Kurt will be transferred to an older child "internat" at best or at worst, a mental institution. Kurt has mild cerebral palsy. Despite this, he can walk. You can see full-length pictures of Kurt standing and even running here on Daneille's blog.
Sweet little Kurt will blossom in a family where he can receive the therapy needed for his cerebral palsy. This boy has stolen my heart. Please consider donating to his grant fund, sharing his profile on your blog or social networking site, and of course, please consider if Kurt is your son. 
Let's plaster the internet with this boy's photo and help his Mama and Papa find him!