I am 8 years old.
I am Colombian American.
I am adopted.
I have four older sisters, two older brothers and one slightly younger brother.
I am, nonetheless, the baby of this family.
I am stunningly beautiful.
I am the most-photographed member of our family, I think.
I am silly.
I am able to correctly dance along with all musical numbers in High School Musical and HSM 2.
I am not able to speak much.
I am an excellent communicator.
I am Mommy's sweetheart.
I am a hugger.
I am the sweetest kisser because I have the most beautiful lips (mommy is slightly jealous).
I am known as Jealous Ella when I won't let the other kids have access to My Mommy.
I am gorgeous in just about any color.
I am not a fan of baths but I LOVE to swim.
I am funny.
I am observant and have a great memory.
I am the only girl in this family to like dolls.
I am into squeezing our very patient dogs.
I am my oldest sister's roommate.
I am not a fan of transitions and change, but I try.
I am a sensory-seeker.
I am giggly.
I am blessed with the most beautiful tan skin.
I am a cheerleader and a flyer on the team.
I am charming with men.
I am still blossoming.
I am still learning.
I am a "surprise" adoption...the best kind of surprise!
I am the daughter my parents adore.
I am wanted, cherished, loved...and I know it!
I am a tremendous blessing to my family.
I am perfect.
Showing posts with label Down Syndrome. Show all posts
Showing posts with label Down Syndrome. Show all posts
Wednesday, March 20, 2013
I am...Emma
I am 12 years old.
I am a Canadian American.
I am the one who started it all, whose infectious joy helped my parents understand that more children with Down syndrome would be best for our family.
I am in a family with three older sisters and one younger sister, two older brothers and one younger brother.
I am a stinker of a little sister sometimes.
I am the girliest of girls in my family.
I am involved in a long term, on again/off again relationship with Nick Jonas...it's complicated.
I am a dancer.
I am a huge Taylor Swift fan.
I am swift to tell my parents not to sing or dance....it's embarrassing!
I am cute and sassy and giggly.
I am the baby who slept through the night when I was 2 weeks old, making me Mommy's favorite forever!
I am a stutterer, but I really don't even notice it or let it bother me at all.
I am smart.
I am motivated to learn.
I am often unwilling to do my chores.
I am often willing to bend the truth about whether or not I've done them, hoping Mom won't check this time!
I am deeply apologetic and downright tearful when I'm found out.
I am a loyal fan of our dearly departed dog, Holly.
I am completely apathetic toward our two remaining dogs.
I am funny.
I am charming and friendly in group settings.
I am emotional.
I am a lover of pink and purple.
I am so lovely.
I am so loving.
I am helpful...on my own terms.
I am plucky.
I am supremely self-confident...I'm pretty darn fabulous and I know it!
I am The Love Geyser...it just builds up in me and explodes all over my family from time to time.
I am not a kisser at ALL.
I am a hugger, but sparingly.
I am a fan of Shake It Up.
I am sometimes mad, but I forgive very easily.
I am a huge iPod fan.
I am healthy, with just celiac disease to keep things interesting.
I am very easygoing about not being able to eat certain foods. I don't want my tummy to hurt!
I am the child my parents didn't know they wanted but could not for one second imagine living without.
I am a gift straight from God.
I am Emma Lane Spicer, and I am a person.
I am a Canadian American.
I am the one who started it all, whose infectious joy helped my parents understand that more children with Down syndrome would be best for our family.
I am in a family with three older sisters and one younger sister, two older brothers and one younger brother.
I am a stinker of a little sister sometimes.
I am the girliest of girls in my family.
I am involved in a long term, on again/off again relationship with Nick Jonas...it's complicated.
I am a dancer.
I am a huge Taylor Swift fan.
I am swift to tell my parents not to sing or dance....it's embarrassing!
I am cute and sassy and giggly.
I am the baby who slept through the night when I was 2 weeks old, making me Mommy's favorite forever!
I am a stutterer, but I really don't even notice it or let it bother me at all.
I am smart.
I am motivated to learn.
I am often unwilling to do my chores.
I am often willing to bend the truth about whether or not I've done them, hoping Mom won't check this time!
I am deeply apologetic and downright tearful when I'm found out.
I am a loyal fan of our dearly departed dog, Holly.
I am completely apathetic toward our two remaining dogs.
I am funny.
I am charming and friendly in group settings.
I am emotional.
I am a lover of pink and purple.
I am so lovely.
I am so loving.
I am helpful...on my own terms.
I am plucky.
I am supremely self-confident...I'm pretty darn fabulous and I know it!
I am The Love Geyser...it just builds up in me and explodes all over my family from time to time.
I am not a kisser at ALL.
I am a hugger, but sparingly.
I am a fan of Shake It Up.
I am sometimes mad, but I forgive very easily.
I am a huge iPod fan.
I am healthy, with just celiac disease to keep things interesting.
I am very easygoing about not being able to eat certain foods. I don't want my tummy to hurt!
I am the child my parents didn't know they wanted but could not for one second imagine living without.
I am a gift straight from God.
I am Emma Lane Spicer, and I am a person.
Tuesday, March 19, 2013
I am...Vera
I am a 14 year old girl.
I am a sister to three brothers and four sisters.
I am a daughter.
I am an adoptee.
I am a Russian American.
I am an athlete.
I am full of sass.
I am full of spirit.
I am 100% teenager with the attitude to prove it.
I am the best big sister to Ella, who has an extra chromosome, too.
I am loyal.
I am stubborn.
I am beautiful.
I am very into movies.
I am competent.
I am a hugger.
I am a kisser...of Mommy.
I am a ray of sunshine.
I am fascinating to talk to.
I am the kid who knows what's what around our house, even if I can't always explain it.
I am quite adventurous in my clothing choices.
I am a pack rat.
I am a hoarder of pens and composition notebooks.
I am an artist.
I am endlessly amusing.
I am Mommy's girl but not a momma's girl.
I am scared of lightning storms.
I am always ready to go...anywhere.
I am a salsa aficionado.
I am my brother Luke's little buddy.
I am a wii player.
I am a music lover...Come Thou Fount is my favorite hymn.
I am a person, fully and completely.
I am calm, usually.
I am happy, often.
I am mad, rarely.
I am impatient and determined and strong and energetic.
I am my sister Emma's very best friend and roommate.
I am loved and valued beyond measure.
In honor of World Down Syndrome Day, March 21. Thanks to the IDSC for the idea to write the "I am" posts. My girls with Down syndrome are so different from each other, from other people with Down syndrome, yet they share so many common features, attitudes, abilities, interests and relationships. They are, in a word...people.
I am a sister to three brothers and four sisters.
I am a daughter.
I am an adoptee.
I am a Russian American.
I am an athlete.
I am full of sass.
I am full of spirit.
I am 100% teenager with the attitude to prove it.
I am the best big sister to Ella, who has an extra chromosome, too.
I am loyal.
I am stubborn.
I am beautiful.
I am very into movies.
I am competent.
I am a hugger.
I am a kisser...of Mommy.
I am a ray of sunshine.
I am fascinating to talk to.
I am the kid who knows what's what around our house, even if I can't always explain it.
I am quite adventurous in my clothing choices.
I am a pack rat.
I am a hoarder of pens and composition notebooks.
I am an artist.
I am endlessly amusing.
I am Mommy's girl but not a momma's girl.
I am scared of lightning storms.
I am always ready to go...anywhere.
I am a salsa aficionado.
I am my brother Luke's little buddy.
I am a wii player.
I am a music lover...Come Thou Fount is my favorite hymn.
I am a person, fully and completely.
I am calm, usually.
I am happy, often.
I am mad, rarely.
I am impatient and determined and strong and energetic.
I am my sister Emma's very best friend and roommate.
I am loved and valued beyond measure.
In honor of World Down Syndrome Day, March 21. Thanks to the IDSC for the idea to write the "I am" posts. My girls with Down syndrome are so different from each other, from other people with Down syndrome, yet they share so many common features, attitudes, abilities, interests and relationships. They are, in a word...people.
Tuesday, March 29, 2011
Who's the winner now?
Yep, that's me. A winner of the lovely bracelet in the picture, above. I also 'won' a pie in the face of the sweet friend who had the giveaway. I know she's very grateful for my help in that regard. Right, Renee?
I also won something from the very start...the satisfaction of knowing I was helping a little beauty, Paisley Tam, find her way home. That's no small thing.
Just ask my mom. Yes, my mom.
From my soul sistah, Ashley of The Chaos Diaries, my mom learned that a little girl in Eastern Europe had been transferred to a mental institution despite having a family who was working hard to bring her home. A little girl Mom had seen countless times here on this very blog. A little girl who reminded us all of our precious Vera, of the fate that could have befallen her, of the potential we see blossoming in her.
My mom was heartbroken. Absolutely heartbroken. She was waking up at night, worrying and praying for Lera. Worse still, my mom found out that the adoption agency had demanded Lera's parents-to-be have all the money they needed for their adoption raised by the end of March. It was the middle of March. Things were looking a bit desperate, as they hadn't had huge success in raising their funds.
So, one fine day my mom up and wrote a letter. Here it is, in part:
Dear friends,
Of necessity, this is a long email. Please bear with me.
As most of you know, my daughter Jill has adopted two daughters with Down syndrome internationally. It is a very expensive process without even counting the money for international travel. As a result of these adoptions, Jill has become an advocate for adoption of Ds children and their new parents. I am constantly amazed by all of the wonderful people who are willing and enthusiastic about sharing their lives with these children. By experience, these are some of the most wonderful persons in our lives. We are thrilled to have three beautiful granddaughters with Down syndrome.
Now, the reason for my email:
In eastern Europe and Russia, once Ds children reach the age of five, they are taken from the baby house orphanage and placed in an institution for the mentally ill/insane. They are tied to their cribs and neglected, with no nourishing, and usually die within the first year. This situation is deplorable, as bad as the asylums of years ago in the United States.
A couple that Jill knows has been trying to adopt a beautiful little girl named Lera. I have seen pictures of her and she is precious. They have about $21,000 of the $30,000 they must have in hand before the adoption can move forward. They are desperately trying to raise the funds. However, Lera has already been moved to an institution, and I cannot get her out of my heart.
Reese's Rainbow is a non-profit that helps identify Ds children and helps with grants for the adoption. Jill has worked with them and the founder, Andrea Roberts. Right now, I am asking any of you who can afford $100, or really anything, to consider helping this family. All you will get from this is their, and my, eternal gratitude. And also, a charitable tax deduction.
She mailed it to friends, family, her Sunday School class. In less than a week, she had collected over $2,000 and a guarantee from a longtime family friend to cover the remainder, whatever the family needed to get Lera home. Some people had to wait until payday to give. Some people had the wife write a check for one amount, the husband for another and then agree to give both checks. Last I heard, the total she collected was over $7,000. It would have been higher had it needed to be but the family had lots of other support, too.
So who's the winner now? Paisley and Lera, of course. My mom. Those who gave, though perhaps not in the way they expected.
Some of those people have grandchildren who have yet to be born. If one of those babies is found to have Down syndrome I will just bet that they will be excited to welcome their grandbaby into the family, knowing that there are families willing to go for broke (literally) in their adoption of a child with Ds.
Some of those people may not be used to giving outside of church, or to adoptions. Perhaps their hearts have been opened to helping the least of the least around the world because that's what God told us to do. Perhaps they took a peek at Reece's Rainbow and opened their hearts to praying for those precious, precious faces who don't yet have a family fighting to bring them home.
I really enjoy winning things in giveaways, I do. Moreso, I really enjoy being a part of miracles. I would bet my mom would say she does now, too! It's an amazing place to be, watching God move mountains. It's amazing to know you were a part of it, whether it's by writing letters, donating, praying, encouraging.
I feel like I'm dancing around my point, so here it is: be a part! Don't just sit on the sidelines and let everyone get blessed.
Luke 6:38 ~~ Give, and it will be given to you. A good measure, pressed down, shaken together and running over, will be poured into your lap. For with the measure you use, it will be measured to you.
Here's your chance to be Jesus's hands and feet in the life of another family chasing hard after God and His command to care for the orphan: GO! BE A WINNER!
I also won something from the very start...the satisfaction of knowing I was helping a little beauty, Paisley Tam, find her way home. That's no small thing.
Gorgeous Paisley!
From my soul sistah, Ashley of The Chaos Diaries, my mom learned that a little girl in Eastern Europe had been transferred to a mental institution despite having a family who was working hard to bring her home. A little girl Mom had seen countless times here on this very blog. A little girl who reminded us all of our precious Vera, of the fate that could have befallen her, of the potential we see blossoming in her.
Beautiful Lera
So, one fine day my mom up and wrote a letter. Here it is, in part:
Dear friends,
Of necessity, this is a long email. Please bear with me.
As most of you know, my daughter Jill has adopted two daughters with Down syndrome internationally. It is a very expensive process without even counting the money for international travel. As a result of these adoptions, Jill has become an advocate for adoption of Ds children and their new parents. I am constantly amazed by all of the wonderful people who are willing and enthusiastic about sharing their lives with these children. By experience, these are some of the most wonderful persons in our lives. We are thrilled to have three beautiful granddaughters with Down syndrome.
Now, the reason for my email:
In eastern Europe and Russia, once Ds children reach the age of five, they are taken from the baby house orphanage and placed in an institution for the mentally ill/insane. They are tied to their cribs and neglected, with no nourishing, and usually die within the first year. This situation is deplorable, as bad as the asylums of years ago in the United States.
A couple that Jill knows has been trying to adopt a beautiful little girl named Lera. I have seen pictures of her and she is precious. They have about $21,000 of the $30,000 they must have in hand before the adoption can move forward. They are desperately trying to raise the funds. However, Lera has already been moved to an institution, and I cannot get her out of my heart.
Reese's Rainbow is a non-profit that helps identify Ds children and helps with grants for the adoption. Jill has worked with them and the founder, Andrea Roberts. Right now, I am asking any of you who can afford $100, or really anything, to consider helping this family. All you will get from this is their, and my, eternal gratitude. And also, a charitable tax deduction.
She mailed it to friends, family, her Sunday School class. In less than a week, she had collected over $2,000 and a guarantee from a longtime family friend to cover the remainder, whatever the family needed to get Lera home. Some people had to wait until payday to give. Some people had the wife write a check for one amount, the husband for another and then agree to give both checks. Last I heard, the total she collected was over $7,000. It would have been higher had it needed to be but the family had lots of other support, too.
So who's the winner now? Paisley and Lera, of course. My mom. Those who gave, though perhaps not in the way they expected.
Some of those people have grandchildren who have yet to be born. If one of those babies is found to have Down syndrome I will just bet that they will be excited to welcome their grandbaby into the family, knowing that there are families willing to go for broke (literally) in their adoption of a child with Ds.
Some of those people may not be used to giving outside of church, or to adoptions. Perhaps their hearts have been opened to helping the least of the least around the world because that's what God told us to do. Perhaps they took a peek at Reece's Rainbow and opened their hearts to praying for those precious, precious faces who don't yet have a family fighting to bring them home.
I really enjoy winning things in giveaways, I do. Moreso, I really enjoy being a part of miracles. I would bet my mom would say she does now, too! It's an amazing place to be, watching God move mountains. It's amazing to know you were a part of it, whether it's by writing letters, donating, praying, encouraging.
I feel like I'm dancing around my point, so here it is: be a part! Don't just sit on the sidelines and let everyone get blessed.
Luke 6:38 ~~ Give, and it will be given to you. A good measure, pressed down, shaken together and running over, will be poured into your lap. For with the measure you use, it will be measured to you.
Here's your chance to be Jesus's hands and feet in the life of another family chasing hard after God and His command to care for the orphan: GO! BE A WINNER!
Labels:
adoption,
Down Syndrome,
Nini,
Reece's Rainbow
Thursday, March 10, 2011
My friends are CrAzY!!!
But one stands head and shoulders above the rest:
Renee.
She is one CrAzY CaJuN!
Renee.
She is one CrAzY CaJuN!
Right now, my CrAzY CaJuN friend is having a crazy fun chance to win some jewelry and humiliate some gals and guys who may or may not deserve it.
Why is my CrAzY CaJuN friend doing this? Why are those gals agreeing to help her?

Grab This!
You probably could have guessed why.
Renee is CrAzY in LoVe with PaIsLeY!!
Renee has been working so hard to bring Paisley home, cooking up a storm, saving pennies (and a whole lot more) but those international adoptions don't come cheap so she and her husband and some ZaNy FrIeNdS came up with this lovely giveaway.
Wanna see what you might win for the low, low donation of a mere $5? $5 that gets Renee that much closer to Paisley, that is.
Well, here ya go:
Aren't those gorgeous?
Now that I've tempted you with goodies, go over and read about the ways your $5 (or more...much more) could go toward humiliating some deserving (or not) people. That may be better than jewelry, but maybe that's just me.
Now that I've tempted you with goodies, go over and read about the ways your $5 (or more...much more) could go toward humiliating some deserving (or not) people. That may be better than jewelry, but maybe that's just me.
Why are you still reading?
Labels:
adoption,
Down Syndrome,
friends,
giveaway,
Reece's Rainbow
Friday, February 25, 2011
Angelina
Meet Angelina. Angelina is Elizabeth's best friend.
Elizabeth is being adopted by a precious family. They are so sad to think that Elizabeth's best friend does not have a family coming for her. They are trying to start a very important fundraiser for Angelina. You can read about it here. If you'd like to participate, let me know.
Not only is Elizabeth's soon-to-be family concerned about Angelina, so is a 14 year old girl who is trying to raise funds and awareness of Angelina's plight. Angelina has just a few months before she will be transferred to a mental institution. This is the same type of fate our Vera would have been subjected to had she remained in the orphanage when she turned 7.
Angelina is just a few weeks older than Ella. A few weeks. Ella will be 7 on August 19th. Ella happens to be standing right beside me. I'm looking at her tiny self and wondering how in the world I could drive her to an adult mental institution and leave her there. How could I leave her in such hard surroundings. Yet here I am, standing by as Angelina staggers toward that very same journey.
I want to help her. How about you?

These are older pictures of Angelina in the awful glasses. See the little girl in the background, below? Her new mommy took a couple of new pictures of Angelina during their first adoption trip a few months ago. You can see one picture at the bottom of this post. She looks great without the outdated, too-big glasses they stuck on her.
Look at Elizabeth and Angelina playing mommy with their dolls together! I think Angelina would LOVE to be mothered, too!!

Grab This!
You can read all about Angelina here. She has a long list of medical issues, but mostly they sound like minor issues or eye-related issues. Honestly, she seems very healthy and fairly typical for a little girl with Down syndrome. That's not a medical opinion so please don't take it as such!
I know that many people were very moved to find out that Elizabeth had been transferred to a mental institution and they were spurred to action to find a family and get her out of there. I would so love for God to find a family for Angelina BEFORE she has to be moved from the orphanage. It's really not a bad orphanage at all and it seems she is doing well there. Let's don't make her take a trip to a scary new place.
Please share the blogs that I've shared. Share the pictures. Share her story. Let's get this sweet girl home while we still can. Thanks!
Remember Elizabeth, below?
Not only is Elizabeth's soon-to-be family concerned about Angelina, so is a 14 year old girl who is trying to raise funds and awareness of Angelina's plight. Angelina has just a few months before she will be transferred to a mental institution. This is the same type of fate our Vera would have been subjected to had she remained in the orphanage when she turned 7.
Angelina is just a few weeks older than Ella. A few weeks. Ella will be 7 on August 19th. Ella happens to be standing right beside me. I'm looking at her tiny self and wondering how in the world I could drive her to an adult mental institution and leave her there. How could I leave her in such hard surroundings. Yet here I am, standing by as Angelina staggers toward that very same journey.
I want to help her. How about you?

These are older pictures of Angelina in the awful glasses. See the little girl in the background, below? Her new mommy took a couple of new pictures of Angelina during their first adoption trip a few months ago. You can see one picture at the bottom of this post. She looks great without the outdated, too-big glasses they stuck on her.
Look at Elizabeth and Angelina playing mommy with their dolls together! I think Angelina would LOVE to be mothered, too!!
This button is another link to the blog of the 14 year old girl who is advocating for Angelina.
Isn't that just the best?

Grab This!
You can read all about Angelina here. She has a long list of medical issues, but mostly they sound like minor issues or eye-related issues. Honestly, she seems very healthy and fairly typical for a little girl with Down syndrome. That's not a medical opinion so please don't take it as such!
I know that many people were very moved to find out that Elizabeth had been transferred to a mental institution and they were spurred to action to find a family and get her out of there. I would so love for God to find a family for Angelina BEFORE she has to be moved from the orphanage. It's really not a bad orphanage at all and it seems she is doing well there. Let's don't make her take a trip to a scary new place.
Please share the blogs that I've shared. Share the pictures. Share her story. Let's get this sweet girl home while we still can. Thanks!
Wednesday, January 12, 2011
A Decade of Delights
All pictures by Alyssa Maisano Photography
Wow! Ten years ago we welcomed our tiny little bundle of joy into the world around 1 a.m. on a cold Canadian night. Miss Emma Lane is our sweet sunshine, our sassy, spunky sister, our sugar-coated Spicer. No one in our family can quite believe that she is ten years old. It seems only yesterday we started our journey with Emma and with Down syndrome. How the years have flown!!
Wow! Ten years ago we welcomed our tiny little bundle of joy into the world around 1 a.m. on a cold Canadian night. Miss Emma Lane is our sweet sunshine, our sassy, spunky sister, our sugar-coated Spicer. No one in our family can quite believe that she is ten years old. It seems only yesterday we started our journey with Emma and with Down syndrome. How the years have flown!!
I couldn't possibly list all the wonderfulness of Emma Lane. She is such a sheer joy to have around. One thing we all like is the way she says her name: Emma Wayne. So do we, now. While she is quite capable of saying it correctly, I think she keeps saying Emma Wayne because she knows we (especially her beloved cousin Andrea) love it.
I love the way Emma has been carrying around a bedraggled, lined notebook for her homework. She pretends to write lines and lines of cursive in it, or perhaps practices some letters, or writes her name over and over again. I love it when she comes up and asks for her homework. "Mommy, homework please."
I love her confidence. She thinks nothing of walking into a room and announcing herself. She thinks nothing of sticking up for herself in a large family: No way, Luke! Stop it, Vera!
I love her confidence in herself as a valuable person. She is quite sure that everyone wants to listen to her sing (at top volume) or watch her dance (she has some MOVES). If you were to ask her why we should listen or watch she would clearly answer: I'm Emma! (And she'd probably roll her eyes...just a bit)
I love her hope for the future. She is going to marry Nick Jonas. She is 100% sure of that. One time, her daddy actually met the Jonas brothers and called home to tell her about it. She decided that meant her daddy was bringing Nick home as a present to her. She put down the phone and immediately started setting the dining room table for four: Mommy, Daddy, Emma and Nick, of course. While I loved that she wanted to double date with us, I was devastated to have to tell her Nick wasn't coming. It's a terrible thing to disappoint that loving, trusting, smiling girl.
I love the way Emma poses for pictures, just like the pictures here. She LOVES to have her picture made. Of course, if I were such a beauty I would like it, too.
I love, love, love the way she tells me: Mommy, I miss you. She invariably says it when we've been together all day, not when I've been away. I think it means she loves me and doesn't want me to leave, that she likes it much better when we're together. Me, too, Emmy.
I also love another of her frequent utterances: Mommy, come snug me. She wants me to drop whatever I'm doing and sit with her on the couch, or hold her in my arms, or anything else that involves close contact with Emma and her mommy.
I love to listen to her pray. She's been known to have some long prayers. She always asks God to bring Daddy home safely. Most famously, she was mid-prayer one night at dinner and prayed for Daddy to come home now and at just that moment the door opened and it was Daddy! I think God was showing off for His sweet girl.
I love the way she plays with blocks. Not only does she like to build but she likes to organize by type. She can be very thoughtful in her play.
I love the way we can always bring her back to a smile. She gets mad, she cries, she pouts, she is stubborn, but her default setting is happy and smiling and it usually doesn't take much effort at all to get her reset. After she cried about Nick, for instance, she didn't dwell on it or fall into despair. She went on with her day, happy as a lark. It's a great attribute.
I can't believe ten years have come and gone so quickly with my baby girl. She was the one I thought would stay young forever but she didn't. And that's good. I have loved all her stages and look forward to those we have yet to see. She's an amazing blessing and I love her more than I could ever express.
HAPPY BIRTHDAY EMMA LANE!!!
All pictures by Alyssa Maisano Photography
Labels:
birthdays,
blessings,
Down Syndrome,
Emma,
family
Saturday, January 1, 2011
Elizabeth C. and her NEW FAMILY!
I just realized I hadn't updated my blog with respect to the beautiful Elizabeth C. yet. Her family found her (which I had noted), and what a darling family they are! Click on their blog to meet the Clark family...a family with three brothers for Elizabeth (they're keeping her name!) and two sisters. Both sisters have that extra chromosome, and one of those sisters just came home from China in September. Isn't that incredible?
I hope you will follow their family blog as they move quickly forward to claim their daughter and reclaim her and the abundant life the Lord has for her. I was searching my blog for pictures of Elizabeth that they may not yet have and found my prayer for her. What an amazing blessing to see how God answered that prayer with this fantastic family. My only complaint is that He didn't bring a family that lived a little closer to me, but who can really quibble with God's divine plan?
Give thanks to the Lord for He is good; His love endures forever!!
I hope you will follow their family blog as they move quickly forward to claim their daughter and reclaim her and the abundant life the Lord has for her. I was searching my blog for pictures of Elizabeth that they may not yet have and found my prayer for her. What an amazing blessing to see how God answered that prayer with this fantastic family. My only complaint is that He didn't bring a family that lived a little closer to me, but who can really quibble with God's divine plan?
Give thanks to the Lord for He is good; His love endures forever!!
Labels:
adoption,
Down Syndrome,
Elizabeth,
orphanages,
prayer
Thursday, December 30, 2010
Alexander the Great!
As my facebook friends may have noticed, I am more than just a bit smitten by a certain little boy named Alexander from Reece's Rainbow. I was reading a friend's blog yesterday and found out Reece's Rainbow is about to start a new initiative called the New Year Warriors and I knew just who I would choose to 'warrior' for, having already decided that I would advocate for him this year! I do hope I am out of a job soon, though.
Alexander, as described below, has dual diagnoses of Down syndrome and epilepsy. In the coming days, I will be trying to demystify the idea of having a child with epilepsy by sharing what other moms are sharing with me. The quick answer, though, is that in the big picture it (having epilepsy or some other seizure disorder) just isn't that big of a deal.
Isn't that great to know?
Alexander-2H
Birthdate: February 2007Gender: Male
Eyes: Brown
Hair: brown
Character: Calm, sedentary
Alexander is a sweet boy with brown hair and eyes. He was born with Down syndrome and also struggles with epilepsy. He has strabismus as well. Alexander is described as affectionate and social.
He sounds perfect to me!
Labels:
adoption,
Alexander 2H,
Down Syndrome,
Reece's Rainbow
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