“Preach the Gospel at all times and when necessary use words.” -― St. Francis of Assisi

Showing posts with label the kids. Show all posts
Showing posts with label the kids. Show all posts

Wednesday, October 2, 2013

Brenton, and now NOAH..

Okay guys.. you all saw it.. the miracle that happened with Brenton in the post below.  He had untill the 7'th of October to have a family commit to him; and one did.  :)  Amazing, right?

 Want to see it happen again for a boy called Noah?  He wrote a letter talking about how he wants a family.  Click here to read it and to learn about him?  Lets get Noah a family!  Pass this on?  Shout about him.  Let people know he's out there.  Thanks everyone.

Friday, October 12, 2012

All of Us...

Hi there...
 

Did you know that all of us...

Are Looking for Our Mommies and Daddies?

Did you know?

[my family found me]

That all of us

Are are also on a page of kids that are said to be adoptable by single women?

That's right!

If you are only a Mommy...

...but still want to adopt...

That's Great!

 
Come and Get us!  We are waiting!  

All of us and more kids available for adoption by single mom's can be found: 



Wednesday, September 19, 2012

Check this out!!!

You may have to scroll down a little bit when you get there but click HERE and you will find....


Mabel's family has found her!  Omg, omg.. I am so happy [near tears here even, happy tears]  I have no idea who they are yet but thank you God.  Thank you...

Saturday, September 15, 2012

Why is she still waiting??

Update 12.15.2012:  Megan's Family has found her!  Thank you God!

Oh my goodness, why??

This is "Megan" she is nearly fully funded.  And when I say nearly I mean: $24055.50 is said to be available for her adoption.  

I am thinking it is because people just don't know.  Those of you wanting to adopt but don't have the money? This is a good thing. Is she yours? 

Megan was born in 2005. She does have special needs but then in some way or another don't we all.  Click here for her Reece's Rainbow profile.  Contact Reece's Rainbow for more information.  

 If she isn't yours can you post about her own your blogs or put her on your twitter.  Tell everyone you can about her please?  Her family is somewhere out there.  The only reason she is waiting is because they just haven't found her yet.  Let's help them.  Thanks everyone.  ^_^

Sunday, July 15, 2012

Another Year has Gone. He has a New Picture...

Who is he?  My sweet Owen.

I found his new picture with a bunch of other kiddos when I read this post here.  Scroll down, it's there.  Be sure and look at all those other little faces as you do. They need a family too.  Thank you Julia for posting him!  Hopefully someone will get him home, and the rest of them, soon.

Saturday, May 26, 2012

He's 11...

...and he's turning 12 this year.

He looks so sad.  I saw his picture and was like, "Oh Brayden..."  so so sad.  It says he has siblings but they are not available for adoption. 

Almost twelve years without a family.  I'd be sad too.  Someone, pick him up and take him hope.  Does it feel like a part of your heart is missing?  Does he fit it?  Is he your son?



From his Reece's Rainbow Profile:

"Boy, born September 2001
has siblings (not available for adoption)
Open oval window; allergic contact disorder;           
developmental delays 

Brayden was born during the 39th week of pregnancy weighing 3020g. Amniotic fluid was discolored. History of anemia, and obstructive bronchitis in infancy. At age 2 a speech delay was diagnosed. in 2009 an open oval hole in the heart was diagnosed. His main diagnosis’ include congenital diseases of heart’s wall development, disorder of specific motor function development, allergic contact disorder, and the disorder of language and communication. Psychical and physical delays are indicated. He has a moderate level of language delay. The consultation of cardiologist and the help of speech therapist are recommend.

Brayden is a friendly boy, but it has been noticed that he often chooses to ignore the younger children. During games he follows the rules, but is motivation to participate in activities is poor. He has considerable special educational needs. He is currently studying at a speech therapeutical school. He still confuses colors and figures, it is difficult for him to memorize and write. Bradyen likes playing with Legos, he enjoys outdoor activities, but is not interested in arts and crafts. His hygiene skills are good. He is physically developing at an age appropriate level. In new surroundings he behaves adequately, he is quiet and polite. He bashfully communicates with strange people. Bradyen likes affection and compliments very much.

He has a very strong bond with his grandparent, he often talks about him, and eagerly anticipates his visits."

If you think you might be Brayden's family or would like a little more information about how to adopt him please contact Andrea at www.reecesrainbow.com.


Friday, February 24, 2012

Please, give just a few minutes...

...and go read what Adeye has to say, and visit the links she posts in the entry? A few minutes to help these kids? I have posted this before, yes, just a few entries below. Like I said in that entry, they need everyone that visits this page. A few minutes might change lives. Thank you.

Great News...

Alexander has a family! Someone has come forward for him. If they create a public blog I will try and post it here. Thank you, God. Thank you.

Friday, February 10, 2012

Sad...

...out of all the people whom visited today, it doesn't look like even one bothered to go look at the link to blog posted in the entry below.

Normally I don't write blog posts like this. But really, that's amazingly sad that no one even gave a few minutes of time to just go look. A few minutes that may change kids lives, and maybe their own life too.

Thursday, February 9, 2012

Please ...these kids need you...

..not the next person to visit this page -- they need every person who visits page. They need you. No matter how you found this blog, no matter what you do. You may not be able to adopt but you can do something. Please these kids need you today. Please go to the post and read what Adeye has to say - she can say it much better than I can. Which is why this entry on my blog -while desperately important- is so short. Please go read hers and follow the links she placed in it --- or come back here and look at the faces of these kids in another entry on that same blog. And after, don't just move on to another page. Ask yourself what you can do today. Thank you everyone.

Friday, January 20, 2012

Krysten

Just moving Krysten back up to the top. :)

Tuesday, January 17, 2012

Meet Krysten:

Hi everyone. Today, I would like to introduce you to the little girl in the picture to the left - Krysten. I have never met this child, probably I never will. I realised today that it has been a very long time since I posted a child needing adoption on this blog, and friends, little Krysten really, really needs a family to love her and I am beyond honored to include her today.

Let me back up a little here to say that I don't know why I was browsing "AdoptUsKids.Org" hopeful I guess, that some of the kids I posted before might have been adopted by now. But I know I felt led there. And soon, after seeing this sweet little girl's face, I knew why.

Little Krysten is only 7, and she lives with a disease/condition called metachromatic leukodystrophy. Folks, my heart broke into a million pieces, this is a life-shortening disease. Let's get her a family to live it with for every blessed second she has got? Is she your daughter? If you can't adopt her can you please pass word of her along; on your facebook, your blog, the next time you are out with a neighbor? It doesn't matter where. Her family is out there. These kids deserve love and a family too. Like little Julia who had previously been diagnosed with Cockane Syndrome, who came home last year after an outpouring of love brought her to her family's attention?

The following is from Krysten's profile at adoptuskids.org:


Krysten is a sweet little girl who loves being in the midst of family activities. While she can contentedly watch TV, her favorite activities are having regular time with favorite adults, including visits by her birth mom, and being around children who interact and play with her.

A medically fragile child, Krysten's overall development is much like that of a non verbal baby who communicates primarily by facial expressions, such as smiling, or pointing and gesturing. While her care needs are extensive, Krysten seems to be content and accepting of what life has to offer without much complaining.

Krysten has an inherited condition called metachromatic leukodystrophy (or sulfatide lipidosis) caused by the lack of an essential enzyme, which results over time in an accumulation of metachromatic lipids in tissues of the central nervous system, kidney, spleen, and other organs that impact her health and her life expectancy.

In addition, Krysten has global (overall) developmental delays, a neuromuscular disorder, and seizures. Her special needs require that she be fed through a G-tube.

Krysten's routine care and treatment include daily medication and feeding regimens, frequent medical appointments, and attendance at a specialized school program for children who have significant developmental delays. Her adoptive parent(s) will need the interpersonal skills to interact effectively and cooperatively with doctors, therapists, and special education teachers on a regular basis, and will need to be proactive and creative in advocating for Krysten's needs.

Krysten is doing well in her school setting. Her IEP includes physical, occupational, and speech/language therapies, and incorporates goals for increasing her developmental growth and acquiring life skills.

Her physical and occupational therapies are helping her to increase her strength and range of movement in her limbs. Currently, Krysten's right arm appears to be stronger than the left arm and she is using it more than the other, but she moves both of them and is able to point and grasp a hold of toys and other objects. Although she has a wheelchair, she also crawls and walks about. When out of her wheelchair, Krysten really must have a caring adult nearby to provide highly attentive supervision as she has a propensity for getting into whatever is within her reach.

Her adoptive folks will need to have experience caring for medically fragile and/or significantly developmentally delayed children or, at the very least, be able and willing to learn a new specialized skill set.

It will be important for her adoptive family's well being to be able to strike an emotional balance between investing wholly in Krysten's growth and development while knowing that they may lose her prematurely; many children born with metachromatic leukodystrophy do not live into their teens. Given the circumstances of her special needs, Krysten deserves to experience life to her fullest capacity and to belong to a family and know that she is wanted. Patience, kindness, and the capacity to love and nurture will be parental traits that Krysten and Krysten's family recruitment team will value highly.


Ok everyone, let's past this on? Let's find her family. For more information visit her profile. Information for "the next step" is there. Thank you very much and have a wonderful day.

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