Thursday, June 30, 2011

"The Day I Will Never Forget" :: written by Genesis House

Genesis is 11 years old and her family just adopted two precious little ones, Gabe and Levi
Post reprinted by permission from The House Family Blog
Photos by Lindy House Photography

"The Day I Will Never Forget"

written by Genesis House

This morning we drove to the orphanage where Gabe and Levi have spent their 5-6 years of life. We're allowed to visit them twice a day. So first we went to Gabe's building and brought him outside, then my mom and I walked over to Levi's building/room... One of the nannies opened the door, we walked in and saw all of Levi's groupa sitting in what I call "the waiting room". As soon as they noticed us, the kids got so excited! Waving, smiling and laughing... The next thing I see is our little monkey walking out :) My mom and I got down on his level with arms wide open. Guess what he did? Hugged ME. (have I told you how much I love that kid??).

But the best part is still to come.

All of the nannies were taking the children outside... I wanted so badly to go with them! After we brought Levi outside to see his daddy and brother, we took him over to his groupa. Right when I set Levi down he ran to the other lil' ones... We had bubbles and of course a camera in our hands. They absolutely LOVED the bubbles and a couple of them got so hyper that we decided to put it away. We didnt want the nannies getting mad at us. Man were they upset! But after, I played with them and gave lots of hugs =) I wanted to take them all home!!





This little sweetie loved when I would take a picture and show it to her on the screen. She would point out who was in the photo smiling proudly



This little guy was craving attention





Levi's buddies



I especially wanted the little boy with down syndrome that Levi sat by most of the time.



I'm not sure what his name is but I would go tickle him, sit with him and he wanted to hold my hand. So sweet!






All of those special angels are just dying for love and attention! Levi's nannies are really nice. They let us take pictures and in fact, they were telling the kids to look and smile at the camera!





And that was the day I will never forget. The hugging, playing, and making those lonely children all smile and laugh was the best feeling.

147 MILLION

Genesis wristband says "147 million" which is how many orphans there are that are waiting for a HOME

Genesis Holding Gabe

MINUS ONE

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Wednesday, June 29, 2011

Believe it or not!

As the US celebrates Independence day, these beautiful children are celebrating their freedom for the first time. 

Just in case there is any question that children with Down syndrome are WANTED...

Please enjoy and share our new 3 minute 4th of July video with your friends, family, colleagues, and other forums!







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Tuesday, June 28, 2011

Meet the Families of Reece's Rainbow - The Stewart Family


I want to introduce you to the Stewart family. They are adopting from Eastern Europe! You can follow their adoption journey on their blog!








I've asked some questions to help you get to know Craig and Gretchen Stewart.


Tell me about yourself and your family. We are the Stewart Family, from Atlanta, Georgia! I am mom, Gretchen, 40, there is Dad, Craig, also 40, and our son Ari, who is 4 years old. I am a special education administrator and Craig works in IT. Ari attends preschool through a special program for children with special needs. Ari loves to swim, ride horses, and drive his John Deer power wheels! Ari is an amazing kid and he is really ready for his big brother to come home. Our schedules are busy with therapy and family fun! We love to travel on day trips to the lake or just relax at home. We can’t wait to have another little boy running around our home and keeping us busy! We are a Christian family who relies on faith and prayer, as well as study, to guide us in how to live. We support others through provision of special needs equipment for children whose families have no financial resources, and we sponsor child in Haiti through Compassion International, whom we committed to sponsor until she is 18 years old (she is now 5). We can’t wait until our boys are older and we can all go on mission trips together! Craig and I love to take photographs, and we have enjoyed doing free photo sessions for families with children with the debilitating disease Epidermolysis Bullosa (EB). We have made many dear friends this year through Reece’s Rainbow who are also adopting and we have been able to meet a number of families from the Atlanta area who are in the process of brining children home! We are ready for Ian to come home and we are excited and nervous for the next few weeks are we prepare for court and to bring him home.
What can you tell me about the children you are adopting?
We first saw Ian on Reece’s Rainbow in May of 2010. A month later, after Gretchen began to have sleepless nights over what might happen to Ian if he was not adopted, she went to Craig and asked him if they could bring him home! Craig said yes, and so the journey began. Ian was 4 years old when we first saw his photo. He turned 5 years old 3 days before we made our first trip to his country to meet him. Ian is an energetic and happy child! During our visits with him, we all had plenty of fun laughing and playing. We were told that Ian does not speak, but when we met him, he did! He only said one word, but to us, it was confirmation that he can speak and that with love, attention, and the right interventions, he are confident he will be talking so much we’ll be wishing for some silence every now and then! When we committed to Ian, we were told he was healthy, with no heart condition. However, he has developed the symptoms of a heart condition that will require medical attention, medication, and likely surgery. He were shocked by this news but it never changed our minds on bringing Ian home, we love him to the ends of the earth and beyond and we will seek out the best medical care and attention that is available for his needs. Ian has two other conditions that for privacy reasons, I won’t go into here, but we already know he will need two surgeries for those, which will be just a few days hospital stay each.

When we met Ian, while our hearts sang to finally be with the child we have worked so hard to finally be in the company of, we were broken a bit by the facts. Ian was given up at birth, left at the hospital, and has never had a single visitor, never a single inquiry, nothing – ever – before us. We found out he has a grandmother that lives in the same city as him, which again, broke our hearts. Ian is rare in his country because he is half African. In the adoption world, Ian’s chances for adoption were very slim because he is a male, has Down Syndrome, a heart condition, and has mixed racial heritage. We were told early on that we were Ian’s only “hope,” but I must tell you that we feel like Ian is our hope and that he and this journey to him has changed all of us so much for the better – we like it is Ian saving us rather than us saving him!

Ian is such a smart little boy! He learned to operate our iPod in just a few moments! He knows his left from his right shoes too! Ian is not used to human touch and affection so we know that he needs to get home soon, so that he can learn to find safety and love in our arms. We know that Ian will be an awesome addition to our family and he is already much loved and adored and much anticipated by many people in our family all over the country!
Tell me why you decided to adopt a child with special needs? Many people who choose to adopt children with special needs feel that they have been called by their individual faith to do so. We too, feel that God called us to the miracle of adoption, as we are Christian. We saw Ian’s face and we loved him from that moment on, for all that he is and all that he comes with, because we feel he was created just as he was intended to be. We have little fear of special needs because our biological child has special needs and so we are very familiar with all that will need to be done for Ian to be able to live a very full and rich life. My 15-year career in special education too, allows us to be realistic and to know that while Ian may never live away from our home, he might! Children with Down Syndrome grow up into young people that are Homecoming Kings and Queens, who work, who work as teachers, and who even go away for a year at a time to college on big state school campuses in inclusive settings! For almost 5 years we have had the very great honor and blessing to be parents to a child with special needs. We feel that our son Ari has shown us how to love to a whole new depth that we had not known before. We know that Ian will double our blessings because he is very special too!
What would be your advice to anyone wanting to adopt?  Pray and ask God to answer the question in your mind that may be keeping you from taking the step to commit to a child to adopt. The children who are waiting need families very quickly and very desperately. It is a matter of life or death. The money is a big deal but many, and most on Reece’s Rainbow, raise the funds they need throughout the adoption process. We are no different, and we are blessed that we could have the experience of fund raising more than $20,000 so far. Adoption is a miracle to which I don’t know if I can do it justice with words. If you are thinking of adopting, read blogs, follow some children, go to local playgroups to meet children with the same needs as the child you are thinking of adopting, talk to adoptive parents, and read books and do research too. All of these things will help you prepare for the homecoming of your new addition. We are so, so grateful for this experience, it is tough and will push you out over your what you thought were your limits to many things (patience, faith, relationships), but the rewards are never ending and so magical!

The Stewarts are leaving for Ian’s country on July 9, 2011. This is their court trip. Then, on or about August 1st, one of them will return to bring Ian home (in order to save on costs). They are still $7,000 short of being fully funded for what they needed to raise to bring Ian home. They have contributed thousands themselves but the costs in Ian’s country are the most expensive worldwide with three required trips.

They are prayerful that people will continue to share Ian’s story and donate to their FSP on Reece’s Rainbow so that they can finally bring Ian home! Please keep their family in your prayers and if you have a blog will you put their button on it? If you can help in any way, thank you!




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For other ways to help the children from Reece's Rainbow, please read the How You Can Help page on the Reece's Rainbow site!  Are you adopting? If you'd like to be featured on the 'Meet the Families' segment, please CLICK HERE. We'd love to feature your family!

If you have a blog, we'd love for you to put our Meet the Families Button on it!




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Monday, June 27, 2011

The ABC's of learning...

This is one of those toys that is perfect for hours of educational enjoyment.   Before  you know it...your child will be an alphabet expert! 

What is it: The Melissa and Doug Alphabet Puzzle Book combines the fun of a puzzle while challenging a child to identify letters and objects that begin with each letter.

What does it do:  The Melissa and Doug Alphabet Puzzle Book is a magnetic, wooden, bound book with removable letter and picture pieces.  It promotes fine motors skills and reasoning skills by encouraging your child to match each letter with it's corresponding picture that begins with that same letter.  It's very durable and the magnetic pieces ensure that all the puzzle parts will remain securely in the book until your child is ready to play.

Where do I get one:  You can find this toy and the entire line of Melissa and Doug educational toys at Toys R Us.

How much does it cost:  $16.99


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Sunday, June 26, 2011

The Lucas family & their Liam...













Amy is working hard to be able to raise the funds still needed to bring home her Liam. Liam, listed as Ivan on RR has been waiting so long to know the joys of a family. He's already 6 years old and God is placing him in the perfect home for him! He'll be coming home to a great family full of love.
 
Amy is a hard working Special Ed teacher and loving single mom to 4 wonderful boys. Three who've blessed her life with that wonderful 21st chromosome. Her oldest son Jimmy was her first introduction into the world of Down syndrome 24 years ago. When Jimmy turned 18 God started blossoming the seed of adoption He had planted and she willingly obeyed. She brought home her first Russian prince, Caleb, in 2005 and her second Russian prince, Elijah, in 2009.  God has called her again and she's faithfully following the path He's set before her. She's working hard at raising the funds still needed to be able to bring her third Russian prince home.
 
Amy has gathered all her paper work & her dossier is complete. She's just awaiting her USCIS approval & then she'll be ready to submit. Please won't you consider blessing this beautiful family?

You can follow the Lucas family on their journey to Liam by going to their blog found here: http://amyandsons.blogspot.com/

And you can give your gifts of love to help bring Liam home by clicking here: http://reecesrainbow.org/sponsorlucas

You'll also find a chip-in on her blog that you can use to donate through as well. 
 
Please also grab our As One We Can button to place on your blogs! Thank you!


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Saturday, June 25, 2011

Angel of the Week

Meet Reese!




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Reese needs a 5/5/5 Warrior!


We normally feature our children who have little or no money in their grant funds but for the next weeks througout the 5/5/5 Warrior Project, we will be featuring our 5 year olds. 

We still have some of our 5/5/5 children who need a warrior so please sign up if you haven't already! 

Will you be her 5/5/5 Warrior and help her find her family? Are YOU her family?
 
If you would like more information on Reese or any of the other children, please contact us

Please help Reese find her forever family by sharing her on facebook, twitter, your blogs and any social media you use! Thank you so much!

She can be found here: http://reecesrainbow.org/reese3902

Reese


Girl, Born March 2006
Reese is a sweet little dumpling with brown hair and brown eyes.  She has CP and is not able to walk on her own.  She uses a wheelchair.
Reese is said to be a very friendly and communicative girl who has expressed a desire to be adopted and have a family of her own.   She is blessed to be in an institution where the children are loved and have outside aid support from other organizations.
More photos available, married couples only.



$18.00 is available towards the cost of my adoption!
 

Please grab our Child of the Week Button for your blog. Each week this button will change to show the current week's child (you only need to add the button once to your blog). The children that will be featured will be ones with $0 or very low adoption grant funds. By hosting our Child of the Week button we are hoping to not only raise awareness for that particular child but also to hopefully raise the amount in their fund. These funds have proven to help families who would otherwise be qualified and able to adopt them, except for the cost of an international adoption, feel able to commit to bringing home and giving the precious gift of a family to these angels.
Thank you for all you do to support and help Reece's Rainbow!

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Friday, June 24, 2011

Focus on Down Syndrome :: Clemson University Graduates First Class of Disabled Students

This article can be read from its original source, the Anderson, North Carolina IndependentMail.com. Reprinted with permission.

Mary Alice Shartle talks with ClemsonLIFE program director James Collins about her experience in the program at Clemson University.
Mary Alice Shartle talks
with ClemsonLIFE program
director James Collins about
her experience in the
program at Clemson University.
— Mary Alice Shartle, 24, dreams about getting a job someday working with small children.

At the same time, Shartle is clear about the hurdles she faces.
“I have Down syndrome,” she said. “I have trouble thinking sometimes.”

Shartle learned how to speak frankly about her disability during a two-year life skills program at Clemson University. She built on her strengths and can articulate her challenges — both key to a prospective employer, said the program’s director, James Collins.

This spring, Shartle and five other intellectually disabled young adults were among ClemsonLIFE’s first class of six graduates.

“They are adults now,” said Sharon Sanders, the program’s founder and former director. “They were not when they came to me. We treat them like adults. We so often treat them like children, and they grow. All students do that.”

ClemsonLIFE is among five college programs in South Carolina for intellectually disabled adults seeking higher education. The state’s public schools allows these students to remain in high school until they are 21, but there were no further education options for them until three years ago, when the first such program started at the University of South Carolina.

Without opportunities to keep learning, the prospects for independent living are poor for these adults, said Donald Bailey, executive director for College Transition Connection. His non-profit organization coordinates state funding to five colleges, including Clemson, that offer higher education for the intellectually disabled.
South Carolina has about 2,000 intellectually disabled adults who would be eligible.

With 92 percent of this population unemployed, the benefits to the state are obvious, Bailey said. A similar program at Tate College in California has reported that 88 percent of its graduates over the past decade are employed.

“This will ultimately save the state millions of dollars,” Bailey said.

Shartle not only forged friendships with other disabled adults, but also with mainstream Clemson students. She also tried a range of jobs she might someday take on full time.

Her parents live in Greenville. After moving away from home, Shartle learned online banking, sharing chores with roommates, traveling by bus on her own, shopping for groceries and cooking her own meals. She attended Clemson football games and recitals at the Brooks Center.

“I like to cook healthy foods,” Shartle said. “Salmon is my favorite.”

Collins said Shartle shared a normal college experience with other people her age.

Shartle’s mother, Janice Shartle, said her daughter has always wanted to learn.

“As a parent, we found out she can do more than we expected,” she said.

ClemsonLIFE has grown from six students to nearly 20 this coming fall and has acquired dedicated office and classroom space in Godfrey Hall. Created as a two-year program, ClemsonLIFE will add a third-year program in the fall for four students who want to get work internships and try living off campus without a mentor.

Cally Vollmer of Atlanta will be one of those students. She has a summertime job selling jewelry at a store in Delaware, and her parents had to discourage her from taking on too many hours.

“When I first got there, I was completely nervous,” Vollmer said of ClemsonLIFE. “I didn’t know what I was going to do. I didn’t expect to be with so many awesome kids.”

She and her classmates interacted with more than 130 Clemson student volunteers.
Clemson has drawn several out-of-state students because of the relative rarity of the programs.

“These kids desperately need them,” said Saralynn Vollmer, Cally’s mom. “We couldn’t have made it any better than it was.”

This past year, 30 students were enrolled in the state’s five new programs, but Bailey predicts that number will quickly grow closer to 100 over the next year.

The College of Charleston and Clemson each had 20 applicants for the fall, he said. Two challenges still facing families are affordability — tuition is comparable to full tuition and board for a regular university — and awareness.

“Families didn’t plan on their intellectually disabled son or daughter going to college,” Bailey said. “Then there are families who flat can’t afford it.”

This past year federal Pell grants became available to such programs for the first time, and South Carolina students can get some tuition assistance though the state’s vocational rehabilitation program. Lottery funds that mainstream college students can access for college tuition, however, is not available to these students.

“We are very, very, very lucky,” Saralynn Vollmer said. “We’ve done well. Usually kids who are learning disabled come from low-income situations.”

Bailey said South Carolina is setting a national standard for its public support of the programs. The state Legislature appropriated about $1 million over the past five years to launch programs at Clemson, USC, College of Charleston, Winthrop and Coastal Carolina.

“The Legislature has stepped up; educators have stepped up,” Bailey said. “And they have made a good name for themselves nationally.”

Bailey said he got involved because he wanted in-state higher education options for his own intellectually disabled son, also named Donald. He has a form of high-functioning autism and was unable to finish high school.

Earlier this month, Donald, 23, walked the stage at the University of South Carolina as the first graduate of that school’s LIFE program. Today, he has a job at a county park near his parent’s home in Mount Pleasant.

“He drives himself back and forth,” Bailey said. “He lives on his own. He’s independent.”

Our thanks to Anna Mitchell for permitting us to share this article. Please visit IndependentMail.com for this and other stories of interest!


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Thursday, June 23, 2011

Focus on Down Syndrome :: Graci's Story

Graci's story is a wonderful new Android app (with an iphone/ipad one coming soon) for any parent of a child with Down syndrome. I shared with you about the Reece's Rainbow Android app and this app is also by our app developer, TeamCaz

I decided I should have a look at it on my phone before sharing it and I'm so glad I did!

I didn't even know the half of what was included in the app before I used it! I'm posting some screen shots of it so you can get an idea of just what a wealth of information it is. As well, you'll notice in the donate section a charity that we all know and love! Such a blessing!

First things first, here is where you can get Graci's Story... CLICK HERE or on the image below.

Here is what the developer has to say about Graci's app:
Graci’s app combines information on Down
Syndrome, resources, ways to volunteer and donate
and best of all it follows the life of two year old
Graci who is living beautifully with Down Syndrome.
 Here are a few screenshots of the app so you can get an idea of some of what you will have at your fingertips with Graci's app.
Download Android Version Now

Coming Soon to iphone!
And here is Graci, who is living beautifully with Down syndrome!

Thank you, again, TeamCaz for your heart for families with children with Down syndrome and Reece's Rainbow!




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Tuesday, June 21, 2011

Going Mobile.... Android Style

Reece's Rainbow has been growing by leaps and bounds. There are so many exciting things coming up but one thing that I'm very happy to share with you, today, is our NEW Android App!

Click Image or search 'Reece's' in The Market

If you have an Android phone you can grab our FREE Reece's Rainbow app right now!

CLICK HERE to install or search 'Reece's' from the Android Market.

There will be more news to come as the iphone and ipad versions are also awaiting approval and we will be announcing them very soon, as well!

We have been so blessed to have a wonderful app developer come alongside us and offer to make these. We are more than impressed with how quickly he set them up, as well!

Our developer also has another iphone/android app for parents with children with Down syndrome that we will be featuring as soon as that is available. Graci's story will include stories and resources for parents who have a child with Down syndrome. As well, they are donating a portion of the proceeds from Graci's Story to Reece's Rainbow!

If you have a business or product and are interested in developing and iphone/ipad or android app, please contact TeamCaz. We can definitely recommend him with confidence.

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