Monday, November 19, 2012

4 or 5 years old.

What do you think it means to be 4 years old. Does it mean laughing and playing with your friends. Well let me give you a new thought on being 4 years old. 4 years old means being sent to an adult mental institution for most kids with special needs. A 4 year old have the mildest delay can be transferred to an adult mental institution. I will soon have a 4 year old in my home. Precious Prince will be turning 4 in December and he has a diagnosis of being developmentally delayed. At the end of this month my Precious Prince will be getting ready to celebrate his 4th birthday.  This is such a wonderful time in his life.  1 year ago this November he started preschool. Precious Prince goes to a developmental preschool where he gets physical therapy and occupational therapy and he was getting speech therapy. Precious Prince just had a annual review where we learned the he no longer qualified for speech. Precious Prince made a 19 month gain in 12 months that is an amazing feat for him.  Precious Prince knows that his mommy and daddy love him and are so proud of the progress that he has made. On Precious Prince’s 4th birthday he would become at risk for transfer or even be transferred on around his birthday. That reality makes this mommy sob big huge tears. I could never imagine my Precious Prince going to such an awful place like an adult mental institution. There he would be locked away forever never be hugged and told that is beyond special. Never be told that he is loved just the way he is. An adult mental institution would bring out the worst in Precious Prince because he would have to learn to fight for his life.
Do you see this face it is a face of a child with the same diagnosis as Precious Prince.  Carlton is FACING TRANSFER an adult mental institution. Carlton Boy, born October 2007 Brown eyes, Nature calm. Carlton is a very bright, charming, and very good looking little boy. He loves to read and recite poetry – and his love for learning has him doing school work at the seven-eight year level, though he’s almost only five years old.  Clearly, he’s an intelligent boy!  He’s also a sensitive boy, who often asks when he will have parents.  He dreams of the day when his forever family will come for him and wants nothing more than to be part of a family. Carlton needs his parents to find him now and act quickly to spare him any time spent in an institution.  He has a lot to offer to a family and will make your hearts glow as he progresses and continues to learn and love.  Are you Carlton’s family?


This face is the face of a Princess. Kalina was in born August 2011. Developmental delays is the only reason that she is not accepted. Kalina is just a little girl, who has already had to fight for her life.  After the birth of Kalina, she required much care; now the girl’s condition is more or less returned to normal – she likes to communicate with adults, showing emotions, respond to affection and attention (and requires them), learning to crawl and pronounce certain syllables.  She really needs loving caring adults.

These faces are faces of brothers who need a mommy to love them for who they are and to help find their way in life. William and Tommy are just cutest little boys ever. William (DOB 11/17/06) Special Needs: developmental delays, autism symptoms, mild thoracic scoliosis, strabismus Tommy (DOB 08/07/08) Special Needs: Developmental delays, congenital thalassemia. William is considered to be a sweet and considerate boy, he helps other children clear up their toys and is “the teacher’s wonderful little helper”. William’s foster mother has been working with him on his emotional control and stability, he is becoming more stable through her guidance and comfort. His schooling is helping him to progress in his learning though he continues to receive speech training through a Speech Language Pathologist. Tommy has adapted very well to his foster family as well. He has developed a close relationship with his foster mother and seeks her attention. His emotions have also stabilized and he gets along well with his foster sister as well. He is very independent and can follow directions and warnings well. He also loves to go to school though he is about one year behind children of his age – it has been recommended that he needs more social stimulations and his therapy seems to be helping him catch up.William and Tommy are looking for a forever home where they can be cared for and loved together!


William has developmental delays, autism symptoms, mild thoracic scoliosis, strabismus and Tommy has Developmental delays, congenital thalassemia
William is considered to be a sweet and considerate boy, he helps other children clear up their toys and is “the teacher’s wonderful little helper”. William’s foster mother has been working with him on his emotional control and stability, he is becoming more stable through her guidance and comfort. His schooling is helping him to progress in his learning though he continues to receive speech training through a Speech Language Pathologist.
Tommy has adapted very well to his foster family as well. He has developed a close relationship with his foster mother and seeks her attention. His emotions have also stabilized and he gets along well with his foster sister as well. He is very independent and can follow directions and warnings well. He also loves to go to school though he is about one year behind children of his age – it has been recommended that he needs more social stimulations and his therapy seems to be helping him catch up. William and Tommy are looking for a forever home where they can be cared for and loved together! William (DOB 11/17/06) Tommy (DOB 08/07/08)


Will YOU please consider helping one of these precious children. I could never imagine what it would be like for my precious prince if he was institutionalized . I love my baby boy so much and he has so much potential and so do these children. What can you do? You can pray, donate, or you could even adopt one of these precious little ones.

Monday, November 5, 2012

The day has come.

The day has come for our Royal Art Auction to finally start. We have some really great stuff that was painted by some very special people. Come check us out. Like the page and you can start bidding away. This is a link to the page https://www.facebook.com/home.php#!/pages/The-Royal-Life-of-Gods-Special-People/218210771584475?notif_t=page_new_likes  THANKS FOR ALL OF YOUR SUPPORT.
This is Prince Pratt himself he is who we are fighting for he has stolen our families heart and we pray for his forever family because we know that they are out there.  Praying that GOD sustains his little body till he can come to receive the medical care he deserves. GOD BLESS YOU ALL

Thursday, November 1, 2012

November 1st what does this mean.

November 1st is the day I have been waiting along time for. November 1st is the official start of Reece's Rainbow's biggest fundraiser of the year. Angel Tree went live today. Today is the first day that you can donate to Pratt and get his ornament with his beautiful picture on it. November 1st also is the the first day of National Adoption Awareness Month. Today will you commit to praying for all those here and abroad that need a forever family. Pratt is one of those children that needs a forever family to call his own. A family would mean so much for this precious Prince. November 1st also means only 5 days till our online auction starts with all donations going to Prince Pratt's adoption grant.

Pray, donate, just do something
Thank You

Tuesday, October 30, 2012

Angel Tree and The Royal Auction

It is 2 days till the offical start of the biggest fundraiser that Reece's Rainbow has each year. Angel Tree starts November 1st and  I can not tell you how excited I am to be doing this for the second year in a row. Now for the Royal Prince himself Meet Pratt.

This will be Pratt's first Christmas and if you didn't see my post from last year your first Christmas is huge in our family. A baby's first Christmas is a big milestone in our family and we do something extra special. This year Pratt will have a little boys my first Christmas stocking hung up and he will have a special baby's first Christmas ornament on the tree along with his official angel tree ornament. Pratt's life will be celebrated in our family and we pray that someone finds it in their heart to open their home to this precious gift from GOD. We love you Pratt.

I am going to give you the run down of Angel Tree. Like I said it starts Nov. 1st and ends Dec. 31st. The goal of this fundraiser is to have every kids grant at least jump 1000 dollars by New Years Eve. All donations are tax duductable and with a 35 dollar or more donation you will get the cutest ornament with this precious prince's photo on it.

The Royal Art Auction starts Nov. 5 and ends on Nov. 26th. The art that is being auctioned off is painted by my sister in love Sandi and some of her special friends. As well as some of our family and our kids. The auction is being held on facebook so come check it out. This is the link to the event https://www.facebook.com/home.php#!/events/453532081352619/

Now for a sneek peek as to what is going to be in the auction.
Painted by Sandi

We love our Kids with the extra 21st chromosome


GO CHECK OUT THE AUCTION MORE WILL BE ADDED IN THE COMING DAYS.


Wednesday, October 10, 2012

Angel Tree Miracles

Well this is take 3 we are starting angel tree November 1 and it runs through December 31. For every 35 dollars donated you can recieve an ornament. We have a new little boy to raise funds for his name is Pratt. Pratt was born in April of this year that means that he is only 7 months old. Pratt has  heart condtion that needs to be addressed. Pratt would benefit very much from early intervention and therapy. Pratt will have his very first christmas by himself with no family to share this milestone. Well Prince Pratt you will have us we will by your baby's first christmas ornament and will celebrate for you. We pray for you that God will sustain you until a family comes for you.

Who wouldn't love a little boy with a paci. My monkey boy just loves his paci and his blanket. We love you baby Pratt.

Tuesday, October 9, 2012

Blessings for Linden

Well its offical Linden has a family. Praise GOD from whom all blessings flow. I am so beyond excited to see who his family is. Thank You GOD for sending families for all of your special kids.
Hold on sweet prince your mommy and daddy are coming for you. Father God I pray for his new family that they can move quickly through this process and that it goes smoothly. Thank you God for their willingness to do what you have called them to do. IN Jesus Name I  PRAY AMEN

Please everyone please pray for linden and his new forvever family.

Monday, October 8, 2012

Adoption and Walking On Water

You are are probably wondering what these two things have to with each other. In Matthew 14:22-36 22 Immediately Jesus made the disciples get into the boat and go on ahead of him to the other side, while he dismissed the crowd. 23 After he had dismissed them, he went up on a mountainside by himself to pray. Later that night, he was there alone, 24 and the boat was already a considerable distance from land, buffeted by the waves because the wind was against it. 25 Shortly before dawn Jesus went out to them, walking on the lake. 26 When the disciples saw him walking on the lake, they were terrified. “It’s a ghost,” they said, and cried out in fear.27 But Jesus immediately said to them: “Take courage! It is I. Don’t be afraid.” 28 “Lord, if it’s you,” Peter replied, “tell me to come to you on the water.”29 “Come,” he said. Then Peter got down out of the boat, walked on the water and came toward Jesus. 30 But when he saw the wind, he was afraid and, beginning to sink, cried out, “Lord, save me!” 31 Immediately Jesus reached out his hand and caught him. “You of little faith,” he said, “why did you doubt?” 32 And when they climbed into the boat, the wind died down. 33 Then those who were in the boat worshiped him, saying, “Truly you are the Son of God.” 34 When they had crossed over, they landed at Gennesaret. 35 And when the men of that place recognized Jesus, they sent word to all the surrounding country. People brought all their sick to him 36 and begged him to let the sick just touch the edge of his cloak, and all who touched it were healed.Why do we doubt GOD. Why do we think that is so far removed from our daily life. Christians are so scared to commit to helping orphans or even adopting because it is scary. Well I have news for you Peter was scared but yet he steped out in faith. Jesus was right there to calm his fear. Why don't you step up and do what GOD is calling us all to do.
"Speak up for those who cannot speak for themselves…defend the rights of the needy." (Proverbs 31:8,9)
"You are the helpers of the fatherless." (Psalm 10:14) He says in Isaiah 43:5-6 "Do not be afraid, for I am with you; I will bring your children from the east and gather you from the west. I will say to the north, "Give them up!" and to the south, "Do not hold them back." Bring my sons from afar and my daughters from the ends of the earth" 

Please consider stepping out in faith and do something for the fatherless. Adopt, donate, or pray just do something because every life matters.
Linden
Mara and Alice
Sandi


Precious Prince
EVERY LIFE MATTERS

Thursday, October 4, 2012

Today is a day of Blessings

Today Princess Melody moved to new commitments that means that her family sponsorship is done and that you can make donations straight to her new family. The McCracken family is amazing and GOD has used them in some pretty awesome ways. I know that she is going to be a blessing to them and they will be a blessing for her. Will you be in pray with our family that God will sustain her until her Mommy and Daddy can wrap their loving arms around her. I hope to have her FSP button on my page soon.

Now I would like to introduce you to our new Angel Tree Baby. Linden is a precious prince. Linden was born in 2010 same year as our Monkey Boy. Linden is described as “a very happy little guy”. You can just see the potential in his face. Linden has Down syndrome and hypothyroidism. He does not have a heart condition or any other medical conditions. His development is considered delayed. Please don't shy away from this little guy because he has medical issues. They can certainly be managed with proper care and love. All children want is to be loved. Do you have a place in your home for this little guy.  
Linden you have a place in my heart and this holiday season you will have a family even though we can't physically hold you we will hold you up in prayer. We love you Prince Linden. Linden you are fearfully and wonderfully made. I am so humbled at the fact that God has chosen us to warrior for this child.
Angel Tree 2012 starts November 1st and runs through
December 31st. This christmas our families goal is to raise 1,000 dollars for this little mans adoption grant. People have said that money has been the key factor in the reason they don't adopt please help me raise this money so that we can help Linden's find his forever family.

Tuesday, October 2, 2012

Name Change

I am changing the name of this blog because I think that all of these kids are Royaltly and we need to give them the royal treatmeant just a King david did to Mephibosheth in 2 Samuel chapter 9. King David wanted to do right by Johnathan which was Sauls son. David's servant Ziba was called and he told David that there was one living relitave of Saul. That mans name was Mephibosheth. Mephibosheth was crippled in both feet. David gave Saul's grandson all of of his grandfathers land. Then King David called Saul’s servant Ziba and said, “I have given Saul’s family and everything he owns to your master’s grandson, Mephibosheth. You will farm the land for Mephibosheth. Your sons and servants will do this for him. You will harvest the crops. Then your master’s grandson will have plenty of food to eat, but Mephibosheth will always be allowed to eat at my table.”



The Royal Life Of God's Special People

Rejocing( Miracle in our Midst)

I have recently reveled who our Angel Tree Princess was for this year. Her name is Melody she won my heart over with her adorable chubby little baby face. Melody reminded me so much of my little Monkey boy. Over the weekend my family moved into a new house and I woke up Monday morning feeling blessed beyond measure but then I found out that this Princess was on Reece's Rainbows My Family Found Me Page. If you ask the question what does this mean well here it is this means that this precious Princess is being adopted. Melody is blessed and highly favored. The fundraiser that I started will continue but it will go to her family sponsorship account that will go to help with her adoption.


So now we have chosen another child to be our Angel Tree Baby. I will not stop shouting for Princess Melody till she is safe at home with her family wherever they maybe. We love you Princess and pray for you and your family. May God Bless them and their journey.

Wednesday, September 19, 2012

HER SHE IS!!!!!!!!!!!!


Melody
 Well here she is our I would like to introduce you to our Angel Tree Princess for this Christmas. God placed this Princess on my heart sometime ago. When the Angel Tree sign up finally started I sent in my request to be her warrior and then I just stared at her picture. I knew she look familiar then it hit me she looks like our Monkey Boy. I know what you are saying how can you say that well if you look at their faces they just resemble each other. We love her this is going to be her second Christmas. I remember how much fun the boys second Christmas' was they just let loose and tore into their gifts. Well this year we are going to honor our Princess and by gifts for the heart babies at the Children's Hospital. Why the heart babies well Melody just recently had heart surgery to fix Congenital heart defect. My prayer for our Angel Tree Princess is that God would sustain her while she waits for her forever family and that where ever her forever family is that they would hear God's call on their lives to go bring her home. This Christmas though she will not know it she will have a family for Christmas. The boys always get new ornaments for Christmas so this year Princess Melody will have a ornament on our tree with all of our family ornaments. We will have a stocking for her and just celebrate her life. We love you so much Melody you are a Princess and I pray that someone in your temporary home shows you love.

Angel Tree officially starts Nov. 1 and runs through Dec. 31 our goal is to raise 1.000 dollars for her grant fund. We will be doing some fundraisers and we hope you will consider making a donation to this precious Princess.

Tuesday, August 28, 2012

A Cry For Help!!! for two Princess'

I am writing this in hopes that you will find in your heart to give. If you have read my blog I posted something titled Not A Coincidence. Well I have to tell you another part of this story. Alice 2h and Mara 2h are being adopted together they will be sisters forever. June of 2011 my family walked in a race called One Less 5k that our church done for there 5/5/5 warrior child Alice 2h. This is when we started to learn more about Reece's Rainbow and all they have done for kids across the globe.


We walked the race to raise money for Alice 2h adoption grant it was a huge success and thousands of dollars was added to her grant. Then in October of 2011 we got to be apart of Reece's Rainbows Angel Tree project for the first time and my husband an I prayed for which child to raise money for that is when GOD showed me Mara 2h.

We prayed for her daily and so did our boys. We spread the word and prayed that people would donate to her grant. We bought her ornament and it hung on our tree. Christmas of 2011 was this sweet Princess' first Christmas so we bought her a baby's first Christmas ornament that also hung on our tree with all of our family ornaments. I prayed everyday that our Angel Tree Princess would have a family. One day I was searching the website for Alice 2h because we also prayed for her everyday also. I finally found her she was listed under MY FAMILY FOUND ME!!!!!! OH the joy that we all had. We waited and waited to see who her new family would be. Christmas came and instead of stocking stuffers we donated money in honor of each of them to our Angel Tree Princess Mara 2h and continued to pray for her and for her to have a family. Then the day came I woke up on December 26, 2011 to all the messages and notification that our Angel Tree Princess was listed on MY FAMILY FOUND ME PAGE. Along with our family we shed tears of joy that our Princess would be saved and she would know the love of a mommy and daddy. Then a couple of weeks later after stocking the RR for updates on both Mara 2h and Alice 2h it was in front of my eyes nothing but a miracle. Mara 2h and Alice 2h were going to be sisters we were so overjoyed both us and our church family in De Queen. In June of 2011 we didn't know that the sweet Princess that we were walking for and our soon to be Angel Tree Princess would be sisters but they are. Now their family is working so hard to bring them home. They have had numerous fundraisers, auctions, yard sales and even cut back on all their expenses but they are 1.000 short of being fully funded. 1.000 dollars is all is it to much to ask for you to help this family out and donate to these two very adorable Princess' and help them get home to their new family. Mara 2h is in need of medical attention immediately and Alice has been in institution for several months the Groves family needs your help. The Groves family sponsorship button is on the right side of my blog and all donations are tax detectable.

Please pray and Donate to these two girls they need you. Pray that GOD will sustain them till they can come home. Please Pray for Mara pray that she will healthy to make it to the states for her treatment and that Alice will be protected from all of what the institution means for kids with special needs. Pray for protection for them both and that their caregivers will be loving toward them. Pray for their new family will have peace while apart of their family is on the other side of the world and that when they go to get them they have a safe journey with a smooth adoption process.

Tuesday, August 21, 2012

Church Rise Up. Children do matter!

In James he says "27 Religion that God our Father accepts as pure and faultless is this: to look after orphans and widows in their distress and to keep oneself from being polluted by the world" In Deuteronomy it says that He defends the cause of the fatherless and the widow, and loves the foreigner residing among you, giving them food and clothing. In Psalms it says "Speak up for those who cannot speak for themselves…defend the rights of the needy." (Proverbs 31:8,9) In Hosea it says "In you the fatherless find mercy." (Hosea 14:4). In Luke Jesus says "Let the little children come to me, and do not hinder them, for the kingdom of God belongs to such as these." (Luke 18:16).

Church why is that you think that just because you don't see orphans in your backyard that this gives you the excuse not to act. You were given the commandment to act on the behalf of the orphaned and the widowed. Today another child past away not knowing the love of a earthly mommy and daddy. Walden was 9 days away from meeting his forever family but his heavenly father called him home. Jaxon not very long ago passed away he also had a loving family in the process of adopting him. In this year alone there have been so many lives lost. Margaret, Lynette,and Mali all died without knowing the love of a earthly daddy. Jaxon and Walden's families were working so hard to get them home. Church there are 143 million orphans in the world. There are 400,540 children in the U. S foster care systems this does not include the children who are in church run homes. Church what is it going to take for you to stand up for these children and provide for them. You might not all be called to adopted but that doesn't give you the excuse to do nothing. Church sponser kids or orphanges. Church you could provide respit care for foster families or you could even foster yourself.

THERE IS NO EXCUSE
DO SOMETHING!!!
PRINCESS LYNETTE
PRINCESS MALI
PRINCESS MARGERET

PRINCE JAXON
PRINCE WALDEN

These are some websites that can point you in the right direction.
http://reecesrainbow.org/
http://www.thecallinarkansas.org/
http://www.adoptuskids.org/

Tuesday, July 17, 2012

Happy Birthdays

Birthday: The annual anniversary of the day on which a person was born. This what Webster says the meaning of birthday is. Well today is a very special birthday. Think back with me what did you do for your Sweet 16 birthday. How did you celebrate such a momentous occasion?


Today is my sister in love Sandi Byler's 16 birthday. On this day we celebrate her life, her accomplishments, her ups and her DOWNS. Sandi didn't want a big hug party all she wanted is cake and ice cream with her
family.

We all love Sandi but life has not been easy for her. Sandi has had several surgeries in her life. On the bright side there are lot more good things that have happened than bad. Doctors said Sandi would never learn to walk, feed herself, talk or even read but yet she did. Sandi did learn to walk, talk, feed herself, and she has even learned to read. Sandi has overcome a lot in her life. Sandi Byler is a true picture of GOD's amazing love for us all. Happy Sweet 16 Sandi we love you so much you are such a blessing.

Now here is why I am telling you this there are 146 million orphans in the world( big understatement there are more now) and they each have a birthday that goes uncelebrated every year. This little girl will turn 16 this year she should get have a party to celebrate the first 16 years of her life but it is likely that without a family to call her own she will not get that. Her birthday will just be another day on the calender nothing special. She will not have any cake, ice cream and deferentially no presents. This precious angel will continue her life bedridden in a crib with bars.
http://reecesrainbow.org/35821/trina-9ha
This handsome young man also turn 16 this year. His birthday will not be celebrated either. He will most likely continue his life in an institution confined to a bed.

As for so many orphans these kids will probably not live much longer in an institution. Statistics show that most die within the first year of being placed in the institution due to lack of care and love. Please I beg of you to pray for what GOD would have you to do to save a precious life.

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/