Sunday, November 29, 2009

Showing our support for our families of the week..

This is Ana for the Nemes family:

This is Milos for the Stolz family:



A little About The Stolz Family:
Jim & Mary have been married for 25 years & have 8 great kiddo's so far. On Dec. 3rd they have thier appointment for their adoption of #9, handsome young Milos.
The Stolz family is no stranger to DS children with their oldest bio. son being 19 with DS & a little one named Joey who they adopted from Ukraine in 2007. Milos is going to be a great fit in his new family & has alot of siblings who can't wait for him to be home. Please be prayerful in your giving to this great family.

A Little About The Nemes Family:
Tom & Amberlyn are in Ukraine right now!! They'll be meeting thier little angel, Ana in a couple of days :) Even though their in country right now they can still use our help~ after all, they have a second trip to plan with an extra ticket to buy so their Ana can come home with them. I know when we were in Ukraine, our funds were low & the help we got from RR was a HUGE blessing! With out it, our Isaac would be in an institution now instead of here with us :( What a tear jerking thought! This family can really, really use our help to bring Ana home now! Please be praying for them while their away from their 2 children at home and for their meeting of their newest little girl :) What a blessing!!!
Amberlyn has made their blog private during thier time in Ukraine, but you can alway request an invite..she's asked that you do if you want to follow along on thier journey.

You can give your gifts of support & read more about the families here :
Many blessings to you all! Alysha~one blessed mama :)









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Saturday, November 28, 2009

Fetal Alcohol Syndrome, aka ARND

I am sorry this is late. With it being Thanksgiving, the week got away from me. :)


A common concern of parents adopting internationally is adopting a child with FAS [Fetal Alcohol syndrome], also known as Alcohol-related neuro development disorder.

Facts about Fetal Alcohol Syndrome

Fetal alcohol syndrome (FAS) is a set of physical and mental birth defects that can result when a woman drinks alcohol during her pregnancy. When a pregnant woman drinks alcohol, such as beer, wine, or mixed drinks, so does her baby. Alcohol passes through the placenta right into the developing baby. The baby may suffer lifelong damage as a result. Read more here.

Contrary to popular belief there is no SAFE amount of alcohol consumption during pregnancy. Though the effects of alcohol on a developing fetus are still being studied, and there is much that is not known, there is a lot of good information out there. One of the best resources I have found is the book," Damaged Angels", by Bonnie Buxton. She talks of her daughter with FAS and what her journey has been like.

Another good resource is FASlink. There are so many resources out there. An important thing to remember is that FAS is NOT a death sentence. There are all kinds of degrees of struggles with FAS, and there IS help!

Many children are listed on Reeces Rainbow with FAS. Please take the time to pray for them and if you feel a familiar tug that often happens in teh heart of adoptive parents, consider them becoming a part of your family!

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Friday, November 27, 2009

Friday Focus on Down Syndrome - Darya's Hope



Eight Days.

Eleven year old Lydia saw this photo of Darya on the Reece's Rainbow Christmas Angel Tree. She asked her Mum if she was able to raise the $20,000 it would cost for the international adoption, would they adopt her.
"Being a sensible 41 year old, I told Lydia she would never be able to raise $20,000.00 in 8 days.....she is only eleven. She didn't hear me. Instead, she asked again, "But if I do raise the money, will you adopt her?" I responded yes, if she raised that much money in 8 days, we would know God is in it and would travel to adopt Darya!"
Darya's Hope was born. Eight days before Thanksgiving. Eight days to help God send a miracle. Eight days to raise $20,000.

Lydia got her community involved. She leafleted all the homes in her neighbourhood, she babysat and her friends babysat and gave her the money for Darya. For eight days Lydia and her community and friends and family held bake sales, car washes, photo shoots, dress sales, hair cuts, all with the proceeds being donated to Darya's Hope.

You may have read about Lydia and Darya on some of the blogs you read.

An eleven year old girl set out an impossible task. And with child like faith, she told everyone she met about Reece's Rainbow and Darya and the other orphans needing families. Lydia is an advocate.


"Once our eyes are opened, we can't pretend we don't know what to do. God, who weighs our hearts and keeps our souls, knows that we know, and holds us responsible to act." Proverbs 24.12

Lydia has a brother and sister who both have Down Syndrome. Lydia loves her brother and sister so much. It broke her heart to learn that these precious children in other countries were being discarded solely because they have Down Syndrome. She knew they were wrong, she knew these children have worth, great worth. What is more, she knew that God knew she knew and she wanted to do something about it.

Another adopting family who had been to the orphanage where Darya lives mentioned that no one holds Darya, no one gives her any attention at all. She was literally being left to die. Lydia was not willing to allow that to happen.

Her local television station had arranged an interview with Lydia for Thanksgiving morning to find out how close to her goal she had come when they heard of her fund raising for Darya. That interview is below.

So, how much did she raise in eight days? Did she make her goal? Well, yes. Yes, she did! Not only did she raise $20,000 so they can bring Darya home, she raised another $6,000+ by Thanksgiving morning. All the donations over the $20,000 they needed are being given to another family who was unable to afford to adopt and so Darya's Hope is bringing TWO Angels home to their forever families!

As of today, Friday, donations are still coming in. In fact, as the following blog post from Melanie's Blog says, it would appear Lydia may be heading up her own ministry as a result!

$28,000 And Still Counting!

You would think once Lydia announced she had raised OVER her $20,000.00 goal, people would stop giving and just celebrate. At least, in my human nature, that's what I thought.

WRONG!!!

Since yesterday, $2,000.00 more dollars have come in. I am blown away by the generosity. When families learned that Lydia is now raising money to help another family adopt a little one who has Down Syndrome in Eastern Europe, they jumped in and have joined her. Amazing. Well, it is just a miracle, don't you think?

Can you believe it has been suggested several times that Lydia start a ministry called:

"100 FOR 200"

WHAT? An eleven year old leading a ministry effort? I am hesitant to say I doubt anything anymore, so I'll be careful not to voice my doubts and fears.

The ministry would be to gather 200 believers who will commit to donating $100.00 each month through 2010 in order to fund 12 special needs adoptions and save 12 orphans. Lydia would provide a picture of the child each month, details that are known about the child, and fund the adoption. Sounds simple? Yes, unless you are the mother of the daughter who is on a path to save the world. I keep thinking to myself: "she is only eleven."

So, stay tuned and let's see what God is going to do. Lydia keeps saying: "With God, nothing is impossible". All smiles....continuing to skip through the house with Hope in tow right behind her.









To read more about Lydia's family, please visit their blog. You can also read about their adoption of Hope, also with Down Syndrome, in Melanie's book, The Journey for Hope. As well, when you purchase her book, 60% of the proceeds will be donated to the Reece's Rainbow Voice of Hope Fund.

a testimony that bi...
By Melanie Hollis

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Christmas Shopping?

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Wednesday, November 25, 2009

New buttons!

Praise God!! so many angels have commited families

They are beginning their journey to bring their kids home, please grab their buttons, share their stories, lets join them through prayer and if you could help them with donations Im sure they will be thankfull!








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Tuesday, November 24, 2009

A Voice of Hope at Thanksgiving

Reece's Rainbow Down Syndrome Adoption Ministry - Lest we forget....








Dear Parents and Down Syndrome Advocates,

Let us give thanks for the opportunity to share our own bountiful blessings with an orphaned child.

Let us not forget those children with Down syndrome around the world who don't have a family of their own.


Keep in your hearts those who are hidden away in orphanages and mental institutions out of shame and ignorance. 

Pray for those who are left behind, the hundreds who die alone and never know the loving arms of a family here on Earth.
***PLEASE SHARE this message with others you know *** 
Let us celebrate for those who now have a VOICE OF HOPE and the CHANCE FOR A FAMILY!



Your gifts of sponsorship for the waiting orphans of the Reece's Rainbow Down Syndrome Adoption Ministry
SAVE LIVES


REJOICE for those who have found their "forever family"!

  • Home in 2006  (2)
  • Home in 2007  (18)
  • Home in 2008  (36)
  • Coming home in 2010  (74+ and counting!)

*** MONEY is the only thing that stands between each of our waiting children and the loving families who are hoping to adopt them ***

Donate for the adoption of a child with Down syndrome through our Christmas Angel Tree Project and throughout the year. 
Watch your gift, no matter how small, change the course of an orphan's life!

"A father of the fatherless, and a defender of the widows, is God in his holy habitation.  
God sets the lonely in families." 
(Psalms 68:5-6)







This email was sent to The Poppies' Blog by Andrea Roberts, Executive Director (. To ensure that you continue receiving our emails, please add us to your address book or safe list. Click here to remove yourself from this mailing list.
Reece's Rainbow Down Syndrome Adoption Ministry | PO Box 4024 | Gaithersburg | MD | 20885
  

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New buttons!

Grab button here


Grab button here

Grab button here

Grab button here

To see this buttons and others go to http://rrbuttons.blogspot.com

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Angel of the week

Meet Artyom!

Boy, Born November 19, 2005

He just turned 5 years!

Artyom is HEALTHY, with a smile that can light up a room. He is an orphanage favorite, and is described as very friendly, affectionate, active, and happy. He has very little time left before being sent to the institution, so someone PLEASE SAVE HIM.

From one of our adoptive families who visited with him in August 2009: "I saw Artyom today, he is such a doll!! He is chunky and walks perfect. We were waiting in the hallway and he came out of the baby room like a little man... walked up to each one of us as if he was saying hello. He pointed at a few pictures they had hanging on the wall, then the nurses noticed he was out of the room and started telling him to come back in the room to the group. He looked at them and shook his hand as if to say "leave me alone!" and we all started laughing. He has got to be adopted! He would bring such joy to any family and looks extremely healthy and very smart."


Please give Artyom the chance to have a family of his own!
Contact Andrea directly for more information

I have $4000in my grant fund towards the cost of my adoption!

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Monday, November 23, 2009

As One We Can..Thankful For These Families

What a blessing it is to have family!! What an honor God's given us to be able to extend our hearts and add to our families. I'm ever so thankful for my Isaac & I can't wait to see where God will take our family next & who He may add to it :) These 2 families are getting ready to multiply :) May we be able to be a blessing to them with our gifts of love.

Paul & Jean Briggs have been one of our families in the past, but I wanted to extend the invite to help them out again. They've been waiting along time for these two angels to come home! With 22 siblings all waiting for them to come home money has got to be really tight this time of year :)


Donovan & Diana for the Briggs family:







The Beasley family is getting ready to go! They'll be heading out soon for their Dec. 9th appointment. This family is a blessing and has accepted God's call to bring home not 1, not 2, but 3 beautiful blessings!! What an awesome thing to be thankful for this Thanksgiving and what a great Christmas they'll be having too!!

Elisa, Vanessa & Arthur for the Beasley family:















You can find both families here : http://reecesrainbow.com/familysponsershipalmostthere.htm


MAY GOD BLESS YOUR THANKSGIVING AND MAY HE STRETCH OUR GIFTS IN A MIGHTY WAY FOR THESE FAMILIES!
Blessing to you all! Alysha~one blessed mama





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Sunday, November 22, 2009

So...about that Buddy Cruise!



So it has been a whole MONTH since I returned from 2009 Buddy Cruise. This was my first trip, and I have to say it was amazing! Not only was it a relaxing and enjoyable cruise, but I had an opportunity to share Reece's Rainbow in person for the first time. I debated long and hard about bringing Reece with me, but in the end, was concerned that he would be overwhelmed and unhappy the whole trip. So I took my younger, typical son Owen...should have made him a t-shirt that said "NO, I am not Reece!"...because everyone who saw us said "it's Reece!" lol This was a wonderful time of fellowship, education, and making new friends in the Down syndrome community. There were families from all over the country and the world on board, even several adoptive families. I got to meet several well-known folks, like Emily Perl Kinglsey (writer for Seseame Street and author of "Welcome to Holland"). Sujeet Desai, the amazing musician and self advocate was also there with his family. All of the presenters were wonderful, relevant, and HUMAN :) They are all just moms and dads of children with Down syndrome who are passionate about advocacy, improving the world for their children and others like them, and focused on changing the way the world sees and includes our children. We talked about hearing problems, speech and language education, medical complications, estate planning and future trusts for our kids with special needs, adults with down syndrome, and of course the adoption and rescue part!....just about everything, it was very educational!

What I liked most about the Buddy Cruise was the length of time it gave all of us (5 days of sun and fun!) to meet and spend time with each other in an extended, casual, social setting. It wasn't just a warehouse full of thousands of people milling booths and picking up brochures. We had many scheduled presentations and events, but plenty of individual time on board, time to get off the ship and do your own excursions, and time to have some coffee with a new friend on deck 4 ;) It was a special time to come together with other folks you didn't know and enjoy yourself. Great opportunityt o make life-ling friends and network with each other. I highly recommend this cruise for any other families, no matter how many kids you have. All of us on the cruise...we're all aware of each other's behavioral struggles. We don't have to worry about what others think when my child goes tearing down the hallway ;) I was worried Reece might try to climb the rail while I wasn't looking, but now I know there were so many experienced DS parents there, I would have had about 30 built-in babysitters ;) All of the kids who attended, regardless of age, bonded with each other and really seemed to appreciate the opportunity to share in a trip like this! And even my Owen, who does noth ave Down syndrome, found himself bonding with several others (Anthony Murphy and Pierce and Joshua Hays, to name a few!), to whom he would proudly say "my brother has Down syndrome too!"

We will definitely be going again in 2010, ALL of us, Reece included! It is going to be held in conjunction with the NDSC Convention in Orlando, Fl July 16-18. www.buddycruise.org The cruise leaves Monday the 19th, and returns the 23rd. It promises to be another awesome trip, so I hope all of you who are hoping to come to the convention will save up your duckets and book a room on board the Buddy Cruise too! There are tons of supervised, curriculum-based activities for the children, INCLUDING OURS, so don't hesitate!

The Buddy Cruise is also a registered 501c3 organization, and just like Reece's Rainbow, relies heavily on donations to provide quality educational programs and a special yearly cruise event! Reece's Rainbow was deeemd not eligible for the new Chase $5 Million Giveaway on Facebook because our focus is international. But the Buddy Cruise IS eligible, so you can still support the adoptive families of RR by voting for the Buddy Cruise in this online project.

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Saturday, November 21, 2009

The Older Child

Adopting an older child presents some unique challenges, but can also have unique rewards. One family has found joy in the adoption of older children. Read some of their story here.

"Families who are willing to adopt any child, particularly an older child, need to accept the child for who they are, helping them grow into successful competent adults," says Collins. "They need to accept and understand that child's sense of loss and need to heal. They need to be persistent and strong advocates for those children."


Here is a blog that seeks to share information about adopting the "older child".

On a personal note: When our son, James, came to live with us 2 years ago at the age of 7, we did not expect him to stay. It was a temporary situation. Now his adoption will be final on Dec. 1st.

I still remember the first week he was here. He slept on one couch and I slept on the other. He was scared to sleep in his room. I never dreamed that those nights of talking for a few minutes before he fell asleep would be the equivalent, in my mind, of the time spent with my newborn in the hospital. But that is exactly what they are. Treasured moments of bonding, and being just what MY child needed.

It has taken a while, but he inhabits the place in my heart that my biological children do. It took prayer. It took discipline [for me, not him], and it took conviction of my belief that "Every child deserves to hold a place in someones heart where if need be, that person would walk through a fire to get to them!"

I weep for the baby he was, the one I will never know. I love babies, everything about them! But....

A child is only a baby for a short while, but they are a human being in need of a family forever!

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Friday, November 20, 2009

Friday Focus on Down Syndrome - She Can. She Did!


Sarah Sherman is no more special than any of the 141 other students inducted Thursday night into Blue Valley North High School’s chapter of the National Honor Society.

Her 3.75 grade-point average is high, yes, but they all have at least the required 3.5. Every one of the students worked hard to pull the grades while participating in school activities and logging at least 40 hours of community service.

She is, however, the only one who has Down syndrome.


Rising to the occasion again: Student with Down syndrome inducted into National Honor Society at Blue Valley North 

As she was called to walk across the Blue Valley North stage at Thursday night’s ceremony, her achievement was not singled out. Her name carried no extra weight on the program. She blended in

She belonged.

“That’s the part of it that’s the greatest achievement,” said Nancy Pence, the faculty co-sponsor of the National Honor Society. “That she’s a part of this group.”

The society’s national headquarters doesn’t keep statistics on how many students with Down syndrome have been inducted into the elite honor society. But Sarah’s achievement is unusual enough that she is the first in Pence’s seven years as a sponsor, and the only inductee with Down syndrome that Carter Burns has known in more than 30 years of being a principal.

Unusual but not surprising to Sarah’s teachers. Or her parents.

They’ve watched their little girl surpass expectations all her life. She’s so social, she runs into friends wherever she goes. So good at memorizing facts, she’s a “Jeopardy” whiz. She’s been in three school musicals. She taught herself sign language.

“People would look at us like, ‘She can’t be doing that,’ ” said her mother, Pam Sherman. “She can. She did.”

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Tuesday, November 17, 2009

Angel of the week

Meet Ashleigh!






Girl, Born January 31, 2007

From a missionary video, they mention how she didnt do much but to lay down in a crib,and with the missionary group, love, care, they could give her while they where there, she soon was rolling, and even sitting!

Ashleigh is completely healthy, with soft brown hair and big brown eyes! She has a smile that can light up a room, and will blossom in a family setting!

Contact Andrea directly for more information
and to see her and other Eastern Europe kids click here

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Sunday, November 15, 2009

Angel Tree ornament shipment has begun!

The assembly and shipment of the Angel Tree ornaments is in full swing!
Anyone who donates $35 or more to the grant fund of a waiting child on the Angel Tree will receive a porcelain ornament with the Angel Tree logo and the sponsored child's photo on it. These ornaments are beautiful and also make great gifts.
Here's the result of the first 12 days of donations. Over 70 ornaments were assembled and shipped this weekend.
The goal of the Angel Tree is to raise $1,000 for each of the waiting angels on the tree.
A few children have already reached this goal, but many others are still waiting on sponsors.

THERE IS NO SHORTAGE OF FAMILIES WISHING TO ADOPT CHILDREN WITH DOWN SYNDROME, only a shortage of funds to do so!

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Saturday, November 14, 2009

BLESSINGS raining down!

In just 13 days, ELEVEN children on the Angel Tree have found families and Timosha is going HOME to his birth family!

In addition to that great news, several children now have large grants:

TONYA has a $4,239 grant
(includes waiting child grant and angel tree grant)

ARTYOM has a $4000 grant
(includes waiting child grant and angel tree grant)

ANNA has a $5000 grant
(includes waiting child grant and angel tree grant)
TANNER has a $5000 grant
(includes waiting child grant and angel tree grant)

ANNA and TANNER can be adopted together, and with their combined grants of $10,000, the facilitation fee is nearly completely paid for! (only shy by $500)

All of these children are in the same country, requirements listed below:

Married couples only may apply
No more than 45 years between at least one parent and child
(one older parent OK)
No stated family size restrictions
Total with travel approx $24k
Both parents for 2 1/2 weeks to attend court
Both parents return home for 3 weeks, and only one must return to complete the adoption for approx 10 days
No history of mental health conditions or infectious diseases
May adopt multiple unrelated children

Interested families should read carefully through http://www.reecesrainbow.org/newfamily.html to determine their eligibility and financial preparedness to adopt internationally.

Serious inquiries and commitments for any of these children can be directed to Andrea.

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Blindness....

I have always had a desire to adopt a blind child. Admittedly, when we took that first step and committed to adopting a little girl who is blind we knew very little. I have found this site to be most helpful.

It is full of great articles not only on blind children, but ideas for other disabilities as well. I have been reading a lot about orientation and mobility, something that the little girl we are adopting has not had any focus or help on. Here is a good article to start with.

Orientation and Mobility

Did you know that it's never too early to begin teaching your blind baby orientation and mobility skills? Even if your blind infant is barely holding up her own head, let alone moving anywhere on her own, orientation and mobility is still a key factor to future independence and many of the basic teachings can begin as early as infancy.


Reeces Rainbow has many children with vision impairments waiting for their forever family to find them. Could you be the one God is calling?

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Friday, November 13, 2009

Friday the 13th


Usually, we all get silly nervous about Friday the 13th. But so far, THIS Friday the 13th has turned out to be an incredible day. So I had to blog about it!

First, we got confirmation of a committed family for Lera in Russia.

Then TATYA in Ukraine finds her family.
Then LILYA in Ukraine finds her family.
And the most amazing thing...little Timosha's (in Russia) birth family, who I have built a lovely personal relationship with, has decided to take their most loved son home with them.

Every child Reece's Rainbow has had the honor of serving, every child saved has beena reason to rejoice! But for a birth family to be so moved, to see new light and have renewed hope and faith in their Savior and His plans for their family through His gift of their child with Down syndrome...that is a true VICTORY! That is when I am the most moved, and I wanted to share this most joyous news with the world ;)

The message from Timosha's mother, who has also committed to serve the other children with down syndrome in his orphanage, and to help us get new photos and find families for them!:

"Andrea, I thank you for your prayers. Yesterday my husband has told that we will take away Timosha home!!!!!!! Since Monday we will start to make all papers. Also I hope that Christmas we will meet all together. I yet don't know, what will be our life, but I trust the Lord and I believe that with the Divine help at all of us it will turn out. All not casually also can children from our region can find family. I will do the utmost to update photos of other children. This smallest that I can make for them. I thank you, Andrea and if the help which I in forces to render is necessary to you, I will make it with pleasure."

This is why we do what we do!

Andrea Roberts, Executive Director
Reece's Rainbow
bamaroberts@comcast.net

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We Were ALL Orphans Before that First Christmas...

Well this is perhaps one of the best posts I could be so privileged to make.

This past week has seen a flurry of blogs and emails posting about a little girl named Lera! As you can see by her photos, she is a gorgeous little girl full of LIFE! She lives in an orphanage in Russia, presently.

But her time was literally drawing to a close THIS WEEK. Without a family committing to her able to move forward quickly with an adoption in Russia her fate would be sealed. Life in a Russian mental institution that does NOT allow adoptions.

Andrea asked people to help and within a couple of days her grant grew from $1000 to $5000 but still she needed a family. The people able to donate the money to her adoption grant were not able to adopt her but thankfully because of that grant another family is!


So, the wonderful news is that Lera has a family! Now that she has that official commitment she will be spared from the transfer to the institution. Her new family were not the ones to bring her into this world, but indeed they are the ones who will be giving her LIFE!

This is a perfect example of how Reece's Rainbow and all of you work. There are families ready and willing; qualified and able to adopt a child with Down Syndrome. Families that share the passion to bring these children home and give them life. The only thing standing in their way are the costs of the international adoption.

The Christmas Angel Tree Project is the biggest fund raising event of the year for Reece's Rainbow and many families find their children through seeing them on the Waiting Angels page.

Lera is a gorgeous and lovely example of how important your donations to these children are! Without her grant, her new family may not have been able to commit to her adoption but because of it, Lera is going to be given the most amazing Christmas gift any orphan could ever hope for, or even know to hope for!

Please, also watch our Official Ministry Video and feel free to share it on your own blogs.



As well, if you have a blog, have you chosen your Christmas Angel Tree bauble to put on it?





Baubles

We also have the 2010 FREE 'Redemption' Calendar and this button is another way you can help raise awareness for Reece's Rainbow and these precious angels!




Grab This Button

Those of you on twitter can also put this on your blogs or if you don't have a blog, just follow us on twitter!



Reece's Rainbow on twitter




Grab this! Be sure to right click on the box below and then select all.






For those interested, the qualifications again for adopting from Lera's Region (2), Russia are:


  • 2 trips
  • Both parents for first trip, about one week
  • Both parents travel for 2nd trip, approximately 14 days (One parent may leave after the court proceedings are finalized, after about 5 days.)
  • Total program and travel fees under $25k
  • Fee includes a $1000 orphanage donation
  • Only one child can be adopted at a time
  • Married couples and single mothers may apply

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Friday Focus on Down Syndrome - Brought to You by the Letter E

Well, I could hardly do a Friday Focus this week without it being somehow related to Sesame Street could I? If you have been using Google's homepage or reading the Reece's Rainbow blog, you already know what I'm talking about.




10 November 1969 was the very first episode of Sesame Street. One year later a brilliant young woman started her career with Sesame Street. One that would span 39 years and counting!

(Happy 40th Birthday, Sesame Street!)

This woman's name is Emily Perl Kingsley. In 1974 she had a son, she named him Jason. Soon after Jason Kingsley was born, a doctor recommended that his mother institutionalise him and tell her friends that he had died in childbirth. Jason, the doctor predicted, would "never read or write or have a single meaningful thought or idea," he has Down Syndrome, you see. Well, he most certainly is able to walk and talk and he has plenty of meaningful thoughts and ideas AND has also written a book!

Over the years of writing for Sesame Street, she has done much to include children with disabilities on the show. There have been many beautiful children with DS that have been part of the show over the years and many children in wheel chairs (including a character on the show) and other disabilities, as well. She was honoured in October 2008 with a special award from the U.S. Government Department of Health and Human Services in recognition of her ground-breaking work including individuals with disabilities on Sesame Street. She has won 12 Daytime Emmys and 9 nominations through her work with Sesame Street, three EDIs and a Grand EDI from Easter Seals, and an award from the National Theatre of the Deaf.

As well, if you have ever known someone with Down Syndrome you have probably read the very well known 'Welcome to Holland'. It was written in 1987 by none other than Emily Perl Kingsley. This written work has become the face, if you will, of Down Syndrome. 'Holland' has become part of the 'lingo' that parents with a child with Down Syndrome use.

Read 'Welcome to Holland' Here






To know that Jason is also a gifted writer should really come as no surprise and to those with children with Down Syndrome, well, it isn't a surprise. To the doctors that initially told Emily her son had Down Syndrome it may be a surprise.

Jason was on roughly 50 episodes of Sesame Street as he was growing up. He completed High School and he lives in group home and he and his mother have made great strides in changing the perceptions people have of disabilities.

To purchase Jason's book through Good Search so that Reece's Rainbow will be automatically given a donation CLICK HERE

As well, check back for information on how you can see Emily and Jason speaking at the Buddy Cruise in July! As both Meredith and Andrea can tell you, they are absolutely lovely in person and very inspiring speakers!

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