Tuesday, July 3, 2012

Not Just A Coincidence

This story back in 1995. My husband's baby sister Kristin DeAnna Michelle Byler was born on January 12, 1995.  The Byler Family had there princess. Kristen was about 6 weeks old when they noticed something was not right. Kristen's mouth would turn blue when she drank her bottle.  Concerned, the family took her to the doctor. The doctor immediately sent them to Arkansas Children's Hospital, in Little Rock, where they discovered that Princess Kristen had Hypoplastic left heart syndrome (HLHS for short). It was then she underwent surgery to repair her heart. Kristen never fully recovered from her surgery, and on March 4, 2012 she went home to be with Jesus. This was not a coincidence.  The family didn't need to know of Kristen's heart condition. They needed to love her in spite of it. Then the next big event the Byler Family was going to have another blessing; her name was to be Sandi Karynne Byler.  The family was so excited.  After months of so much tragedy, they were finally going to have a princess in their home. The day came, July 17, 1996, Sandi Byler was born, and this was, again, what they thought was a normal birth. The family was in awe and filled with joy.  They would soon fine out that their Princess Sandi had Down Syndrome. Sandi was immediately taken to children's, like Kristen,  for surgeries. One of those surgeries would be an open heart like surgury, again very much like Kristen's. The Byler family was shocked and sad. They had numerous ultrasounds but the diagnoses of Down Syndrome was never detected. This was not a coincidence. God new that they didn't need to know what Princess Sandi was going to endure, but God was faithful to prepare them for it. While the family was shocked; God was never surprised. Life went on, and Sandi began to grow. Sandi did everything the doctors told the family she would never be able to do. Sandi walked, learned to feed herself, talk and even read.  This was far more than what the doctors ever expected out of Sandi, but it was not a coincidence. God knew Sandi would do all of these things. Years past and then Sandi's big brother Michael got married to Kendra in July of 2006. Then in July of 2007 Sandi's oldest brother Robby (my husband) married Amber (ME). Later on in 2007 Robby and I started attending a church in De Queen, AR  It was there that we met the Lynch Family. Then we found out about Michael and Kendra's pregnancy. We prayed for a healthy baby boy or girl. Then in early 2008 my husband and I found out that we were pregnant, and so did the Lynch family. They already had two adorable children, and God was blessing them with a third. Then on June 16, 2008 the Byler Family welcomed a baby girl into our family. Princess Isabelle DeAnna Byler was born, perfectly healthy. Belle's birth was not by coincidence. God had seen fit to bless the Byler family again, this time with a healthy baby girl. "The Lord giveth and the Lord taketh away blessed be the name of the Lord." The Lynch Family would soon find out they were also expecting a girl, but this was not be a normal pregnancy. The Lynch Family blessing was going to be born with Down Syndrome and HLHS. The Lynch Family was making descions and praying for God's Peace. The Byler family was right there in the middle of this. It was no coincidence that God placed us in that church for this season, for this reason. The Byler Family reached out to them, and we were able to minister to their family in their time of need. Then the day came in October of 2008. The Lynch Family's blessing arrived and was whisked away to Children's Hospitol, just as Princess Sandi was, Just as Princess Kristen was on the days of their birth. The Lynch Family blessing was now in the same hospital the Byler Family had been in on numerous occasions. The Byler Family prayed for the Lynch Blessing and the family. Time went on.  Then came the day on December 11, 2008.  Jackson Robertson Byler was born, happy and healthy. Jackson's birth was not just a coincidence. God knew that we needed this beautiful baby boy in our family. Jackson began to grow into a healthy big boy.  He was a few months late on some of his major milestones and didn't crawl until 10 months, but we never gave it a second thought.Then life was going to be getting a little bit busier right before Jackson's 1st birthday we were thrilled to find out, the Byler Family was going to having another blessing. Then on June 28, 2010 Peyton Michael Byler was born perfectly happy and healthy. This was also a big day for Jackson this is the day he learned to walk by himself. It was an eventful day, but it was not a coincidence. Life went on and the Byler boys began to grow into little toddlers. Mean while the Lynch Family blessing continued to make progress and after several heart surgeries, GOD had made her a new heart. GOD healed the LYNCH BLESSING. Then Jackson's 2nd birthday rolled around and became concerned because he was not talking like the other kids his age. It was then we talked the doctors and went to First Step in Glenwood for testing. The staff there determined that Jackson was very far behind and needed speech therapy and other servides he would qualify for. First Step had been in the Byler Family for several years. This is where Princess Sandi had therapy for so many years. Then in November of 2010 God used the Lynch Blessing to imapact the Byler family again, in other ways. God led them to Reece's Rainbow this an adoptive ministry for children around the world who have special needs and need a forever family. God opened the Lynch family's heart to adopt a little girl with Down Syndrome in Russia. The Byler Family prayed right along side of them as the Lynch Family brought their New Adoptive blessing home in September of 2011. The Lynch Family adopted a blessing and this event is what God used to open the Byler Family's eyes to the orphan crisis. We began to relize that the children that we hold so dear to our hearts, Princess Sandi and Precious Prince Jackson, would be total outcasts. We were devestated at the fact that there were so many kids being mistreated and neglected because of their disablitly. That is when I knew God was calling the Byler Family to adopt a princess with special needs. Then in 2011 the Byler Family was once again changed as God showed us another princess in need of love. This little girl is being adopted through the Foster Care System we never thougt about the need for forever parents right here in our backyard. This liitle princess coming into our lives was never a coincidence. God had a plan. Now the Byler Family is waiting on God to move so that we can be obedient to all He has called us to, whatever or wherever He may lead.
These events are not at all coinciedence. God says,  "I know the plans I have for you” —this is the Lord’s declaration—“plans for your welfare, not for disaster, to give you a future and a hope." Jeremiah 29:11
God know the plans HE has for us, and sometimes He know long before we do. God's word is the light to our path. He will show us the next step, but this picture took over 17 years to unfold. And it is not over yet. God is still moving and still working. Our steps are still ordered and we still want to follow in obedience. If we would all pause to look back at the road we have traveled, if we have traveled it with our Savior, He has used all things to work out His good. Not what what we see as good, but what He know is good for us. "All things work together for the good of those who love the Lord and are called according to His purpose." Romans 8:28. 
If you are His you are called!
If you are not His; why not?
He loves You.
Be HIS and follow His leading.
He will do gret things.


 






Monday, July 2, 2012

Freedom

What does freedom mean. It means the power or right to act, speak, or think as one wants without hindrance or restraint.  
This week is a week of celebration in America. On the July 4, 2012 we celebrate our FREEDOM.Today marks 236 years since our government signed the Declaration Of Independence. On this day we celebrate that momentous day and all that it means to us. Freedom . This is also a day of sadness for so many. Today there are 146 million orphans across the world who don't have those same freedoms. Today there are children lying in beds who only know the walls of their cribs. Children who should be running and playing with friends are confined to beds and have only human touch to be fed or changed. Today I am so thankful that I got to take my Precious Prince to school where he gets therapy. Today we got to walk outside of the walls our house and my precious prince was not considered a outcast. The most horrible thing is that there are so many children who don't get this chance. They are given up at birth and from that moment on their freedom is no more . Today I am so thankful for my freedom and the freedom that my family has that we can provide what our precious prince and princess what they need. 


Below are the faces of some of the newly listed children on Reece's Rainbow. These children deserve freedom and happiness. As you Pray ask GOD what he would have you do to help them.









Tuesday, April 10, 2012

Autism Awareness

April marks Autism Awareness month and I am going to be sharing about several different things on this subject. First off did you know that 1 and 88 children have autism. Boys are four times more likely than girls to have autism there are 1 and 54 boys diagnosed.There will be more children will be diagnosed with autism this year than with AIDS, diabetes & cancer combined. These statistics are not to scare you but to inform you. Each individual with autism is unique just like each child with Down Syndrome is unique. Each child or adult with autism in unique and, so, each autism intervention plan should be tailored to address specific needs. Early intervention is the key just like for any child with a special need of any kind. There are so many therapy options for kids that have autism speech therapy, occupational therapy, behavior therapy and physical therapy. This link will take to the page that talks about 10 things every child with autism wished you knew. Autism is just a diagnoses just like Down Syndrome or CP    http://www.autismspeaks.org/family-services/tool-kits/100-day-kit/ten-things-every-child-autism-wishes-you-knew 


My son Jackson has not been diagnosed with Autism but has all the classic signs of Autism. Jackson is a delight although we may have challenges he is a blessing. We love Jackson just the way he is some things are more difficult for him than for his baby brother Peyton but that's OK. We take each day know that GOD will help us through any struggle we have and that GOD made Jackson just the way he wanted him to be. We are thankful for our spunky little man. Jackson goes to school 5 days a week 8 hours a day. Jackson has speech and occupational therapy and we have seen a big difference in him. We know that therapy is a big part of that. Well here comes the other part of this post did you know that there are kids in the world who don't get the chance to have therapy. This may come as a shocker to some since we live in the US even if your in foster care you get therapy services but in other countries its not like that. Children with autism are treated like the scum of the earth as are children with Down Syndrome and other special needs. I know many have heard that children learn self soothing behaviors and with the right therapies they are good things. Well kids in other countries bite themselves, claw themselves and rock themselves so much that they hit their heads on walls and cribs. At the age of 5 most children are sent to an adult mental institution and this is a death sentence for them. They have little to no chance to be rescued and receive the services that they need. Now to introduce you to some sweet precious childern.

 This is Denver he is 6 years old he was born in 2006. Denver is physically healthy, with no medical concerns. He has been diagnosed with childhood Autism. We do not have a lot of information on his current skill level. He is listed as having delays in every aspect of his development. He participates in therapy and has a 1:1 caregiver that spends time with him each day. He is very attached to this caregiver and has a good relationship with her.
Additional photos and a video are available of Denver


Meet Roger he is also 6 years old he was born in 2006. This dear boy is listed as having "childhood autism" — if it is truly autism or autistic behaviors due to orphanage life and his other special needs, we really don't know. He is said to have encephalopathy (unspecified disease of the brain) Childhood autism, and moderate mental delays. He also has vision problems: Convergent concomitant strabismus (crossing eyes) and hypermetropia (far-sighted); and is said to be anemic. Look at Roger's sweet smile he is smiling for his mommy and daddy.


Finally meet Justine she is 11 years old her birthday is June 11, 2001. Yes it is a fact that there are more boys that have autism than girls but girls can have this disablity. Justine is a pretty girl with dark hair and eyes. She is fully mobile and active. Her face bears features of FAS, but this is not documented and is only a cautionary disclosure. From her medical records: congenital microcephaly, autism
 
As with all children living in these difficult conditions, this child's cognitive development has regressed significantly since he/she was younger. It is of crucial importance that any family considering the adoption of an older child from the mental institution setting be well prepared for what to expect with regards to how the neglect and lack of adequate medical care and nourishment has affected this child. These children all have TREMENDOUS potential for improvement, and deserve to have a life outside these four walls.
 These children are truly living on borrowed time, and families should be home study approved before an official commitment can be made for this child.
 
All three of these childern have autism and would greatly bennifit from therapy and a loving home. If your child has autism or you know someone that has autism you know how much therapy is important. Will you please consider making a donation to there grant funds and spreading the word about them. Maybe you are there mommy or daddy.
 
Be Blessed
Amber Byler
P:S in honor of my son Jackson who is the light of my life and I can't imagine life without him we are truely blessed

Tuesday, March 6, 2012

Bulgeria Medical Fund

Good Morning to all. The sky is bright and full of sunshine. I have a question for you do you ever take the sunshine for granted? I know that seems quite crazy but in Pleven, Bulgaria there are children that should be playing outside on swings and slides. They should be climbing on monkey bars and spinning on merry go rounds. Yet these children wither away in a cold bare building without any hope. The physical conditions of this place are horrid and are just unsantory. It is not fit for any human to live in but yet there are hundreds of cribs everywhere. I ask you to close your eyes and picture a 15 year old girl weighing only 18 pounds. You say this isn't really happening she couldn't live like this. Well here is proof.

 Now close your eyes again and imagine a 11 year old weighing 12 pounds.

  She was in this same orphange and was adopted three months ago by some amazing people. Katie was 9 years and 7 months and weighed 10lbs 9oz. Here she is below when her mommy first met her.
 Now Mrs. Katie has been home for three months and after a quick stay in the hospital in Sofia, Bulgaria just to get her stable enough to come home to the states. Then weeks of care in the hospital in America she now weighs 22lbs 13oz see picture below.

Now that you have seen these pictures now two simple questions come to mind how and why?  Well I am not sure why they do this but this post from Katie's Mommy might help.
March 5, 2012 at 8:58 AM by Susanna
[Disclaimer: The conditions in the Pleven orphanage are the exception in Bulgaria. The orphanages usually do their best to provide for the children and they are not like the one in Pleven. The care is good compared to other Eastern European countries, as far as care in an orphanage can be good. The Bulgarian governmental institutions not only do not defend the personnel at the Pleven orphanage, but they are taking steps to change things. The following post, and this disclaimer, has been approved by our attorney.]
There have been three major turning-points in the past two years of our family’s journey…
Halfway through my pregnancy with Verity, the news of her Down syndrome began to open our eyes to the world of special needs.
That was the first turning point.
Four months after Verity was born, our hearts broke when we learned what was happening to thousands of Eastern European children with special needs. Vulnerable children just like Verity.
Second turning point.
Then one year ago this week…
We had officially committed to adopt Katerina just a few weeks earlier. We knew that she was in a poor orphanage, and wanted to send help.
God set up the perfect contact for us, a Bulgarian Christian missionary named Sasha Bliss.
She was allowed up to Katie’s floor, the top floor.
Yes, Sasha sent photos and videos of Katie, but unexpectedly, that’s not what made my heart squeeze in pain and cry out to the Lord.
Our tiny Katerina’s photos may as well have been stamped with the words “SAFE,” and “SAVED.” She had a family who loved her and would come for her.
But the other children…
All those small, lonely faces…nobody was coming to take them home.
O Lord…please…all these little people…please…
I called Stephanie Carpenter and could hardly choke the words out. ”The other children! How will I ever be able to turn and walk away from the other children?”
That was the third turning point
That was the day our family began to pray in earnest, “Please show us a way to help the other children in Katerina’s orphanage!”
A fire was lit in my heart for the rest of the children with special needs, the children that Bulgarians would never adopt.
You may know some of what was discovered when our attorney and I reached the orphanage last August, and were taken to the top floor.
After that trip, and the hope that was ignited for all the other children there who had special needs, the fire in my heart burned hotter.
You may know some of what happened at the orphanage between my first trip in August and our second trip in November.
But I could not tell you the whole story, until now.
With our attorney’s permission, I’d like you to read the story in her own words, as she recently reported it to many high governmental officials in Bulgaria.
“From the first second that we stepped our feet on the sixth floor, a long and tormenting journey began. Terrifying smell of musty air, rotting flesh, vomit, urine mixed with feces, filth, acid fumes, and who knows what else, hit us in the face. The sixth floor, also called “malformations”, is a hallway, to the left of which there are only windows (never opened!) and to the right of which are the so called “kitchenettes”, each of them having six to eight children stuffed in the small room, lying each in a separate small bed. The distance between the “cages” was literally as much as an adult could stand sideways. The sheets on which the children were lying were soaked with their urine and vomit.
The first thing the adoptive mom Susanna Musser did was to change Veronika’s diaper. The horror of what we saw was indescribable – the faint with hunger, emaciated skeleton of a nine year old child who was the size of a four to five month old baby; terrifying rash in the private parts.”
“A lot could be written about the five days spent in the baby house in Pleven.”
“A lot could be written about the five days spent in the baby house in Pleven.”
“But for the purposes of compact presentation, I will note that the children, regardless of their age, are fed with old beer bottles with a nipple with a huge opening; no one even tries to spoon-feed children who are three years old and older; the children are fed with liquid resembling in look, smell and taste fried flour mixed with water; the children are fed in lying position, on their backs, with the nipple thrust in their mouths and the liquid starts flowing with the speed reminding one of the speed of light.”
“The diapers are changed once or twice in twenty-four hours; the children spend all of their time lying in their cages and no one tries to move them, to play with them, to communicate with them, to teach them simple, age-appropriate skills and knowledge…
The list can go on.
After my first collision with the reality at Pleven on August 15, 2011, it became my mission, nightmare and way of life.
You may be asking yourselves what I have been doing and how I have been keeping quiet half a year already…why don’t I name the culprits. I will give you one name – [the former director]. But she is not alone. Her team is with her because the horror triumphing in this institution cannot be one woman’s doing.
During my first visit to Pleven I sent a signal to the Bulgaria Helsinki Committee. Unfortunately, the procedure for initiating a sudden check-up of the institution was slow and trying. At the end, it finished with the disciplinary firing of the director at the end of last year.
The investigation of Pleven, initiated by the Bulgaria Helsinki Committee, finished with a long report where endless shocking facts were described. Fifteen children died there in the year 2011. Even while I was typing this presentation, information reached me that one more child from Pleven has died. She was almost thirteen years old. Her diagnoses were not terminal. I do not doubt that, again, the necessary medical and human care had not been provided to this child.
From the day we picked up Katie, the fire in my heart for the children with special needs she had left behind her burned all the hotter. Now I was living with a daily reminder of their need. Now we knew what a tremendous difference love and food and care could make for the others!
From the day we first heard the fabulous news that the former director had been fired, I was overjoyed that perhaps now some roadblocks would be removed, and the rest of the children with special needs could be listed for adoption! This was the roadblock we’d been praying about for months! Now there was hope!
At the same time, there was cause for serious concern for the other very malnourished children in Pleven. They were so close to receiving the care they needed! However, what if well-meaning but ignorant people began giving them more nutrition than their bodies could handle, throwing them into fatal re-feeding syndrome?
Beseeching emails were sent to Dr. Lilova. Dr. Lilova had seen Katie and would know I was not a random spamming crackpot, talking about nonsensical concepts such as teenagers the size of babies and toddlers. She responded kindly by saying that a team from the hospital would arrange a visit with the orphanage.
But did you wonder…
Why did our attorney need to write a report to many high governmental officials in Bulgaria now?
Because in the middle of January, some unspeakably shocking news came to us
The director was still in Pleven.
She had never left.
Over the next weeks, we Pleven moms slowly pieced together what had happened.
This person is not at all done defending her bastion. Even now she is employed at Pleven as Director of Human Resources. Her daughter is the head social worker of the whole institution. None of the personnel, directly responsible for the condition of the children, has been fired or replaced. And the director has stated that she is going to defend her rights in court and would plead for revocation of the (according to her, unlawful) disciplinary firing.
We were back to secrecy and silence.
But underneath the surface, God continued to work.
Several Pleven adoptive parents took their first trip to see their children. None of them had children on the top floor. But even on the floors below, the atmosphere was entirely different than when our attorney and I had been there last August. Back then, we rarely saw a caregiver. It seemed as if we could walk out unnoticed with armfuls of children if we wanted to. Six months later, the atmosphere was tense and the parents were under constant surveillance.
While several parents were still there in Pleven, we received word from an unlikely source that Liliana, up on the top floor, was in dangerously poor condition. We heard that she was unresponsive, had lost the will to live, and was refusing to eat or drink.
Again emails flew to Dr. Lilova. Again Sasha Bliss was an invaluable help, this time by making direct telephone calls. ”We have heard such-and-such a report. We need your help. But be warned, because we have learned that the former director is still in power.”
Dr. Lilova arranged the hospitalization of three children with the help of the MOJ, the Child Protection Agency, and our attorney. The orphanage resisted this plan in various low and shabby ways, including an attempt to blackmail our attorney into dropping the whole idea. As you know they were not successful! The children spent more than two weeks in Tokuda Hospital, and each of them was stabilized and gained weight.
Their hospital stay would have a far-reaching effect on more than just their physical lives, however. As they were being released, one of the orphanage caregivers who accompanied them told Sasha Bliss that she would do all in her power to take better care of the children.
It was also inevitable that the children’s medical treatment by the world-class professionals at the Tokuda Hospital would force the orphanage situation to come to a head.
Again, our attorney~
“Prof. Lilova’s initiative brought a time-bomb to explosion. Since Susanna’s blog is public, I took the liberty to provide the MOJ with its link. EVERYONE at the MOJ was shocked with and appalled at what they saw and read. They took the initiative themselves to [decide to] totally remove the former director from the orphanage, to change the personnel, to bring CHANGE to this terror. They don’t have the power to do it all themselves as they have no direct authority over orphanages. It is the Ministry of Health (MOH) and the CPA who could bring to fruition the efforts of so many to bring change to the 240 children in Pleven.
So today, the MOJ called me and asked me if I would submit a document with them so that they can start the process with MOH and CPA. They also said they’d understand if I felt uncomfortable or afraid. I didn’t think twice. I am fed up with all this evil.”
All this while, more disturbing information continued to trickle in, helping to explain the poor condition of the children.
Donated toys are put into a bag and henceforth ignored in a toy closet.
The staff all know the routine to impress visitors. An insider described this routine as “making one sick.”
The donated therapy room is hardly used, but it benefited the director–as leverage to get herself a higher pension.
Sometimes the children aren’t fed on Sundays, when there is a skeleton staff.
The children’s diapers aren’t always changed every day.
One child has been kept in isolation for two years for an upper respiratory infection.
The caregivers unashamedly lift the children from the beds and carry them across the room by one arm.
They are deliberately underfeeding the children to keep them small and weak, so that they don’t need much food or attention, and can’t be transferred (along with their government stipend) to the next institution.
One way or another, more photos of other Pleven children manage to make their way out of the orphanage to the Pleven moms’ private yahoo group.
With every new little face, the fire inside me grows hotter.
I hear from families who are waiting to commit to adopt small ones from Pleven as they are made available.
The fire leaps up still hotter.
How, how can we get the message through to the right people so they will list the children for adoption?
This is the dilemma that is burning a hole in my heart.
On the one side, the families who are ready to commit to the children!
On the other side, the officials who need to list the children with the MOJ!
Our attorney has explained that they have been trying for years to get the social services to list all the kids in all the orphanages, to no avail. It looks so hopeless!
I am helpless to do anything but pray to the only One with the power to make it happen! To Him, there is no dilemma!
During the day, every day, I scheme and pray for a way, some way, to get the message through to the right people. If they thought about the children at all, they would think the children are unadoptable! They have no idea that there are families lining up in the United States to snatch them up as they become available! How can we let them know this? How can we tell them that they must give every single child with special needs in the Pleven baby house a chance at a family? They must list the children!
During the night, I dream that I am writing eloquent appeals to officials, begging them to register the children for adoption.
I dream that I am carrying the children one by one from their beds out to groups of waiting parents, pleading with them, “What about this one? Please, see his beauty, see her worth!”
I dream that I am walking through the orphanage at night, leaning down to kiss each one as he sleeps, as she sleeps, too unconscious to object.
I dream that I gaze into their faces, nuzzle their temples, smell their hair, feel the slight weight of their bodies in my arms. As if they are my own little ones.
For many weeks, I have been dreaming of the Pleven children every night.
For many weeks, I have been crying out to the Lord for them every day.
Now you need to know that the battle lines have been drawn.
Things are beginning to happen quickly.
This week, from Monday to Friday, two of my friends are visiting their five children in Pleven for the first time. Jenny is visiting Liliana, Sophia and Butler, and Shelly is visiting Tommy and Steven. Click on those links to follow their visits–both ladies are blogging. Children many of you have prayed for, who were lost and now are found!
This week, on Tuesday and Wednesday, the team from the Tokuda Hospital will be at Pleven.
Next week, a friend of mine, with two other women, will make a visit to Bulgaria. You can help these ladies to help many Bulgarian orphans with special needs. During her visit, my friend will be having a vitally important meeting!
For the first time, it looks like there is a way for the message to get through to the right people.
In addition to this, the closer we get to the showdown, the more intensely the people involved are experiencing spiritual attack. The enemy seems to be doing his best to get people to give up the fight.
Praying friends, you have not been slackers. You have soldiered on beside us for so many months! You have not given in to apathy, cynicism, doubt, or discouragement. You have opened your hearts to the children, given financially, helped to spread the word, and prayed! This week, my friend Julia is gearing up for a huge giveaway to help many of the families who are adopting from Pleven.
It is obvious that this situation is beyond our ability to control. But our true and living God has it well in hand! We can have boundless and endless hope in Him!
I am coming to plead with you to cover the next two weeks in fervent, concentrated prayer.
Please pray that God would finally break down the stubborn walls remaining around the Pleven children! Pray this as if you were one of the children who has been lying in an orphanage cage for years, kept there by the self-interest of those who are being paid to take care of you!
Please pray that the enemy would have no power to harm our attorney, the children, their adoptive parents, my friend who will be meeting with key people, and anyone else who is fighting for the lives of the children!
One full year after God first broke our hearts for the rest of the children…
…the battle lines are drawn.
O Lord, may this be the final battle for the children’s lives, and may you be magnified in your victory!
At the sign of triumph Satan’s host doth flee;
On then, Christian soldiers, on to victory!
Hell’s foundations quiver at the shout of praise;
Brothers, lift your voices, loud your anthems raise.
“…I will build my church, and the gates of hell shall not prevail against it.” ~Jesus40

Well if your saying how can I help the children in Pleven Bulgeria here is how you can make a tax deductable donation to the fund that has been set at the Eli Project or you can donate to the chip in on this mommies blog.
http://www.only1mom.com/
and if you can't donate you can pray for health and the saftey of these kids. There are currently 17 children being adopted out of the orphange and there are a total of 240 children in the baby house.
They are currently getting medical treatment in Sofia but this is not cheap and they need help.
We are raising money for transportian for everyone involved, specialized formula and boarding. The doctors in Sofia are going to give their services free but everything else is not free. Pray about what God would have you do.

P:S this is Katie's mommies blog http://theblessingofverity.com/

Tuesday, February 7, 2012

Our Precious Angels

This story begins on April 30, 2008.  This is the day we had weighted on for a long time. This was extra special day this was the day that we found out that we were pregnant with our first child. Around this time millions of miles away a little boy was conceived his mommy was probably as happy as I was. Then the world wind of doctor visits started. Then ultrasounds came we found out that we were having a boy. Then the visit came that we could be tested for abnormalities. This visit was just like any other visit but we had positive attitudes either way. This test was given to a woman millions of miles away and the outlook was not so positive that child had to be her idea of perfect (normal). That test for us didn’t matter but for her it did. The pregnancy went on to be somewhat normal and then the day came that my blessing would enter the world. At this time we just prayed and laid our son’s life in GOD’s hands. Then Jackson was here perfect in our eyes and true blessing from GOD. At this time another little boy was born his mommy was giving birth to what she thought would be the perfect child (normal child).  When our little boy was born all we could do was kiss him and love him. When this other child was born his mother saw his imperfections. She couldn’t even see his potential.  My little boy is thriving and growing.  He is the light of our world but this other little boy is sitting in a orphanage. He does not know the love of a mommy and does not get kisses just for the sake of giving kisses. This other little boy sits in an orphanage not having the care he deserves. He does not receive therapy and can’t talk to tell you what he wants. He deserves the love of a mommy and daddy. This little boys name is Eric he has so much potential and just needs some love. We are his Guardian Angels for the Reece’s Rainbow Project and we want to find him a family. Please inquire about him he just needs some love and attention. We love you Eric and are praying for your family to find you.
This is what his profile says:
Boy, born Dec 2008
Eric is a smiley little fellow who likes to feel his caretaker’s heartbeat or pulse, because it comforts him. He would be a wonderful little brother in a household of older children.
Eric has arthrogryposis and compensated hydrocephalus. He has had a surgical repair of spina bifada. Overall, he is healthy and would do well in a family without smaller children. His upper body is quite strong and he has full use of his hands, fingers and arms, but he has little control or movement in his lower limbs and they are significantly smaller than his upper body. He can squeeze very tightly with his hands, and reach a full arm’s length with no problems even though his resting position is the one you see in the pictures. He does not talk, according to the caretakers but does make sounds to communicate. Cognitively, he has significant delays due to his history of spina bifida and hydrocephalus. He is very much still an infant in many ways.

The picture in the orange shirt was taken at age 18 months, and the second picture was taken at 3 years old. He may have a sister a few years older in a different region who possibly could also be available for adoption or he could be adopted separately. She also has special needs. Eric has no money in his adoption fund we know that GOD can move mountians and we know that he has a plan for Eric.
We love you sweet boy.