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Sunday, 26 June 2016

Sunday Spotlight

June is birthday month in our house.

2 little boys in our house, at least 3 cousins, a few aunts, sister in law, grandmothers - every time we turn around from June 1st until July 1st there is another set of congratulations to send along. Birthdays are a happy thing, a time of celebration and reflection . . . unless you're an orphan.


Depending on where you're from, if you're an orphan birthdays mean you're that much closer to aging out and either left to fend for yourself or destined to remain in a lonely adult mental institution that has probably been your home for a few years already.

For some kids on Reece's Rainbow the birthdays left are getting far too few for comfort.


Clara


Morris pic

Soleil June 2013


Scottie

Shirley



For some of these kids there are no birthdays left. This is there last year to find a family before that door closes forever. It's a sad, simple fact and after celebrating with my own babies this past week, one that my Mama's heart finds harder and harder to understand. Every child deserves a parent to love them and celebrate with them. One that won't bypass their hurts and griefs of which these kids have had more than their share. Please share one this week, or hop over to the aging out page at RR and find a child to share so that their last birthday might just be their last one alone.

Sunday, 19 June 2016

Sunday Spotlight

Have you stopped by Reece's Rainbow lately?

In honour of the tenth anniversary the website has undergone a massive overhaul. It's definitely worth going over and taking a look. As with any major reno it takes some time to work out all the kinks in the system so it may take a few extra minutes to spot the page you're looking for or the page may be down for a few more days.

But while you're looking you may just find



Hana (2)

This little sweetheart will be 9 this year. She's noted for her amazing laughter, agreeable nature, intelligence, and hard work. She loves piano and colouring. She also has spina bifida and loads of potential.


emma1


Emma turns 7 this year. She's reported to be friendly and calm although she does struggle with delays. Emma's orphange can only keep her through the summer at which point she will be transferred to a school orphanage for mentally delayed children.



Lucie is 7 and lives in an adult mental institution. This is never the best option for a child this young and yet Lucie still has her smile.


Lexi

Lexi is almost 12 (children age out at 14 in her part of the world) This sweet lady has lower spine issues and an issue with her right knee. At her last update she was reported to love singing, was smart, and had formed close friendships with other children.


These are just four of the reasons why Reece's is overhauling their website and gearing up for another busy decade. No child should be forgotten, every child deserves to be loved and wanted. So celebrate with me by checking out the new website, finding a few new faces, and helping spread the word.

Sunday, 12 June 2016

Sunday Spotlight

It's hard to believe but Reece's Rainbow turned 10 this week!

It's been a crazy ten years and almost 1600 children have be united with their families since those early days.

While there have been some changes over the years, the focus remains the same bringing orphans home. One of the more recent changes involves the oldest children on RR, the aging out who's window for rescue is starting to narrow.

Thanks to a pooling of resources all older children are eligible for a 10 000 grant (until the fund runs down which i'm told is many, many adoptions from now). This 10 000 goes a long way to helping families combat the high cost of international adoption and the lower fund raising time which can accompany these older kids.


Kids like

Already listed for over 6 years and still waiting :(

Listed for over 5 years


20715035453-1-237x300
Maddie
Each listed for 4 years

And Tara my first Angel and so close to aging out who's been listed almost 6 years :(
Tara (2)


Each of these beautiful young ladies have been listed for years, a quarter of their lives waiting on a site that advocates getting these kids seen. Sometime change is hard but in this case I'm so grateful that the older children are now eligible for this amazing grant and hopefully these girls will celebrate 11 years of Reece's with families of their own.

Sunday, 5 June 2016

Sunday Spoptlight

It's always hard to post these pictures.
How to choose a handful of faces from a list that is constantly growing.
To be honest, I get overwhelmed and disappear for a bit to regroup, returning when time or a familiar face like Mandy and Victoria make their way over to the my family found me page.

So I'm back with a new little group to shout for this week and today's post will be different because each of these children are summed up by a single line. Please see them, see the potential behind the name and diagnosis and help get these kids seen and home!



Chelsea - born 2009, mild intellectual delays



Christina - born 2010, blind.


Harlowe- born 2008, Cerebral palsy, focal symptomatic epileptic syndrome, complex local convulsions; rough delay of psychological and speech development


MaryAnn- born 2008, Cerebral Palsy, hydrocephalus


Skyler - born 2003 - Cerebral Palsy, eligible for 10 000 older child grant

See past the line and shout for these kiddo's who deserve so much more.

Sunday, 29 May 2016

I love you

Three little words.

They mean so many things to so many people.

Our oldest turns 3 in a week and a half.

This week he said I love you.

It's the second time he's said it to me.

It's funny the things that go through your mind when your child receives a diagnosis. What will this mean? How do I help my child? If your nerdy like me - Where's the nearest literature? The questions keep coming as you navigate  raising your child in a world that has charts, averages, and progression lines and your child's taken the box and is spinning in the kitchen with it on his head.

After awhile things start to even out. You learn terms like OT, PT, Speech path. You start your own experiential master class in sensory needs, therapy techniques, and how to feed a child who's brain literally makes most common food textures public enemy number 1.
You even start learning to ignore the stares and glares when your child melts down because the lights and to bright and the noise echoing hurts in the stores but you go because life goes on.

You find the joys as the grow, like any child, like every child, just on their own pace.

In our house:
We've cuddled over trains, laughed over tickles, and blown bubbles til our cheeks hurt.
We've painted pictures to give away because even in his own world he likes to share smiles and boy do his grandparents smile when they get a picture. We've bakes cupcakes because he loves to pour and sprinkle sprinkles. We snuggle every day and get lost in books because that's who our little guy is and so much more.

But there are still challenges and even though the big ones remain in varying forms, we're far enough in that new variations have come to light.

Like speaking.

Autism and speech delay seem to go hand in hand. A terrible twosome that helps keep kiddo's in their own world. Those first words come with such work and for some never come.

We took our techniques and lessons, our speech path and OT's, our self regulation and started small: bubbles, Dada, Mama.
Slowly jabbering came and turned into words.
We've moved to jabbering and small sentences. He just learned No :) For us each emphatic "No" is a slightly exasperating victory. We also have entered the realm of echolalia, a world that makes me wish all those autism books I uncovered months ago had a chapter on cryptography.

It's two steps forward and 1 step back (with a few spins, flips, and a little breakdance thrown in for good measure).

This week we snuggled and like every other day I told him I loved him and in his little voice he parroted right back.

Somedays you make your victories out of the scraps, others they're given to you on a silver platter if you have your eyes open to see them.

Sunday, 6 March 2016

Sunday Spotlight

Another week has passed and that means it's time for some more faces.

It can be hard to choose so few when the number to draw from is so large. So many children and each needing and deserving their own home.

If you manage to stumble across this blog, I beg you take 5 minutes and look at these children, go to Reece's and look at the faces. If you want to see the power of sharing a single story I urge you to go and check out Micah 6:8's post from this week. The power of sharing and sacrificial love is amazing.

Now onto this week's faces.

First up is Penny


Penny will be 5 years old this year and look at this sweetheart! Penny has been diagnosed with CP and crossed eyes, but is also listed as being able to walk independently. Some therapy and a family would do this little girlie wonders.


Annie's a face that has become all too familiar on RR due to the amount of time she's been listed


Annie just celebrated her 10th birthday and was transferred to an institution over a year ago which coincides with her last update :(
She was noted as having delays at that time but also noted for being an affectionate girl who sought attention and had a willingness to learn. 

Merida


is another sweetheart who's been listed too long and dear to my heart as we featured her at our wedding (another sign of how long she's been listed.)
This little sweetie breaks my heart every time I check in on her. Her grant hasn't grown since July of 2012 and her profile hasn't been update since before that. If you only have time to share one this week, please, share this girlie for me.


Finally we have Tracy and Bart


These older siblings NEED to be adopted together.
Tracy is reported to be healthy and a top student in her class. Bart has a cleft lip (in the picture it appears corrected?) and like so many is reported to love soccer.
Siblings are so much harder to place and are even considered special placements in domestic adoptions due to the added difficulty. Do you know someone ready to take a leap for these two?

Sunday, 28 February 2016

Sunday Spotlight

Another week has come and gone and I'm sleepy.

It's the time of year that brings a lot of illness which translates to late nights for moms, dads, and kiddos alike. The good thing is that everyone seems to be on the mend as I write this and lots of hugs and snuggles were doled out alongside good food and some good old cough syrup and vicks depending on the day and person who was down.

Everyone once in awhile it hits me that for each face on Reece's in a child who doesn't have someone to sit up with them until the wee hours of the morning when they're sick or scared. There just isn't the resources in some places despite the amount of care and in others there isn't even that. So we keep sharing, and shouting, and praying, and hoping that one day each of these precious kiddos will find a family.


First up is Mila


So young to be listed which is such a blessing. Mila has been diagnosed with Arthrogryposis a condition affecting the joints. Both A White River and Micah 6:8 talk about their amazing kiddos who live with this condition for those who are unfamiliar with it.

Next is Byron
Byron is a  sweet little guy who is facing transfer soon as his current facility is transitioning roles. This is sad as the staff sound very involved and pro-adoption where he was not to mention his home and friends. It would be wonderful for him to find a forever home.


Look at the life in those eyes. Stacey has some delays but is also in a space where therapy is available and she is quite determined in her efforts. Stacey is reported to be a friendly little girl who loves playing with her friends.

Finally we have Sophia


Sophia goes to school and can communicate. However she does struggle with more in depth communicating. She is listed as having scoliosis and mental delay.