Orphans with Arthrogryposis

There are kids with Arthrogryposis all over the world who wait for a family to call their own. Every child should have a Mama and Papa to love them. Sadly many kids will never know the love of a family as they will live out their shortened lives in institutions. The children posted here are from Reecesrainbow.com If you can't adopt, you can donate to their grants on reecesrainbow.com Don't leave them to die in institutions.

Friday, March 1, 2013

Meet our focus for March: Caius!

Meet Caius!
 
Caius turns 1 year old next month. We have one month to focus on him and prepare for his birthday celebration. Of course we can't throw a party in person, but we can make some noise across the ocean! What if he got parents for his birthday? My son did. Well we committed to him two months after his first birthday. (I remember crying all through his first birthday because he didn't have a mommy.) And we took our son out of the orphanage forever right before his second birthday. (Average adoption processing time for this country and kids with AMC is around 7 months. Ours got delayed a bit since my husband had a major surgery.) Here's my son, Roland.
 
Roland.
Already adopted! Mine mine mine!
 
Roland and Caius were born in the same country and have the same condition so obviously we want to help Caius get his own family and show you how wonderful having a son with AMC can be! Roland is one of the best things to ever happen to us.
 
We have had our son home for six months. In that time he has almost completely caught up developmentally from the lack of having a mom and dad (attention/stimulus) early on. He enjoys going to preschool six hours a week. He enjoys dancing to music, playing on the iPad my employer gave me and turning the pages of his books. Last week he learned to walk and now walks everywhere independently. He also loves to imitate everything his big sister says and does. It's hilarious.
 
Oh and this boy can give serious hugs and kisses. He's a cuddle pro.
 
And since we *just* went through this journey, let me share what your life may look like if you adopt Caius.
 
Medically you can expect to come home and see a good pediatrician who knows about adoption stuff. Your new boy will need a blood test to determine what immunizations if any he needs. He'll need to see how his little body is doing and what things you may need to give him to get him healthy. (Orphanages are not healthy places with good nutrition.) We started giving our son pediasure, vitamin D gummy vitamins (that are delicious and help his bones and joints) and we even snuck fish oil into his apple sauce. Seriously one day he'll have real apple sauce and it will be like ambrosia. ;) But you don't need to do those things, or you may want to do different things. (Although I do recommend the vitamin D suppliment for AMCers.) They also checked him for parasites and that involved waiting for him to have a poopy diaper and getting out the little kit they send you home with that has the little shovels. Yes the glamorous life of the adopting parent. ;)
 
Then when you feel your son is bonded to you and he reacts to you as his parents (giving you eye contact and crying for you when he gets a booboo) then you can start dealing with his orthopedic issues. Some do this sooner and others do this later. We started three weeks after adopting him and felt that was a bit soon, but not by much. But it all worked out. Caius will need a pediatric orthopedic doctor. Caius has arthrogryposis and because of that qualifies for free medical care at Shriners Hospitals for Children. We recommend Dr. van Bosse in the Philadelphia Shriners if you can do it. As an orphan with a pre-existing condition you will also qualify for Medicaid. (His medical issues should NOT cost you your savings! We spend about $20 a month on medical stuff since we don't live close enough to Shriners. We paid twice that during serial casting since we paid a copay every other week. We don't pay much now that we're done with all the major stuff.)
 
Caius will need serial casting, specifically the Ponseti method that any good orthopedic doctor worth anything will be familiar with. This method is where you go in to have a limb casted and shaped slowly over time. It's like having braces on your teeth and getting them adjusted. Every week or two you go in, have the cast removed and get a new one placed. Slowly this stretches out whatever joint is stiff and stuck. (Arthrogryposis is a joint condition.) Wrists, elbows, knees and feet among other things can be serial casted to avoid surgery.
 
 
Serial casting. Image taken from Plymouth Hospital.
 
Remember "Laurel" who was adopted six months ago? She's 16 years old and has AMC just like Caius. She just reached the half-way mark on serial casting. Half way done!
 

Sitting pretty with her new casts on.
 
 
We did serial casting on Roland's elbows and knees and feet. I'm thrilled with the results and I'm also thrilled we're done with it so he can take real baths again! Roland responded really quickly, partly because of his young age and partly because his AMC was not a more severe kind.
 
I hate that Caius' picture has him all covered in clothes! That's what we get for getting pictures during winter. But you can tell his legs are not quite as bent as my son's. One looks a bit higher like maybe there's some hip involvement. An x-ray will tell you if the hip needs anything done to it. And I cannot tell because of the giant warm sweater if Caius has straight arms or slightly bent. (If my son's hands had been covered I wouldn't have known from his picture how they were either. They turned out to be straight.) I want to guess Caius has slightly bent arms. Having bent arms is way more functional. We have since done serial casting on Roland's arms until they were able to bend enough to feed himself. Now that he's out of casts we do daily stretches on them.
 
And that's about it. If you were hoping to totally completely avoid all doctors, well AMC kids do see the orthopedic doctors a lot initially but then less and less as they get older. You will also want to see a physical therapist and occupational therapist (who usually share the same building and your orthopedic doctor would give you a referral for them) who can give you ideas of what kinds of exercises to do at home. We go once a week and the therapists just play with the kids, but it gets them moving and doing more and more!
 
Daily life consists of getting up at around 7:30am (the orphanage trains kids to sleep or stay quiet through the night), changing his diaper, putting on his KAFOs (leg braces) and letting him walk around the house, feeding him breakfast (it goes faster than if he feeds himself, but he can feed himself), playing (or preschool twice a week) until noon, lunch, nap, stretches after his nap, playing with his sister when she gets home from school, "helping" me fold clothes or do a household chore, splashing in his bath which he loves, putting on new clothes (he "helps" but can't dress himself yet and will need to figure out how to do it with limited mobility), learning to brush his own teeth (yeah they don't do teeth brushing in the orphanage), sometimes if we're being super parents he gets an extra stretching session and then kisses and hugs goodnight and he sings the goodnight song.
 
Stretching takes around 10 minutes. It would take five minutes if *someone* would cooperate!
 

 
I can't tell you how wonderful it is to have an AMCer. We have two--Roland's new big sister also has AMC. She also walks, goes to school, gets ready for bed and all that too. Although she doesn't get stretches because she's older (five years old in kindergarten which she says makes her a "growd up") and she either does her own stretches or naturally gets stretches as she plays and moves around. She also wears leg braces.
 
 
 
I feel like I'm always telling people how our lives are perfect--rainbows, butterflies, sunshine--because that's how I feel, but it's not always easy. I hated going to the doctor initially. I worried over serial casting. We had a sleepless night or two. And the initial transition after bringing our son home(especially the first three days) was hard on all of us. But adoption is wonderful. Our baby boy is wonderful. AMCers are super smart (above-average intelligence if you believe Dr. Hall, the famous geneticist) and super great. And if you want to adopt a little guy who will only ever know you as mommy and daddy, and adjust a lot better since he's so young, I highly recommend Caius.
 

 
~~~
To donate towards Caius' adoption please go here. 


Wednesday, February 20, 2013

Drake has a family!

Drake has a family!
 

Prologue by Bring Hope:

Last year we advocated for a little girl with arthrogryposis named Rita. Since we could not raise funds for Rita at the time because of her situation, we instead started a sharing campaign. Hundreds of "shares" happened across Facebook and blogs. Rita was famous in a matter of days! (In fact Rita caught the eye of one mommy who later went on to adopt our other AMCer, Victoria!)

When Kelly contacted Bring Hope to say she had been planning on adopting Rita, we were overjoyed as it marked the first time we could celebrate one of "our kids" finding a family in the same month we were spotlighting that child! That was very encouraging to us. (That was the first time it happened, but not the last!)

But our friend Kelly was not content to merely stop with changing the life of one girl. We watched her champion the cause of many orphans. (In fact I see Kelly sharing Sadie's file just about every day!) When Kelly saw that Melissa wanted our little Drake (as Melissa very subtlety commented "I WANT HIM" on that post, heh) she immediately sent Melissa encouragement and resources. We are privileged to be one of those resources.

A lot of the following story happened behind the scenes as the family prepared to commit to Drake and we attempted to help them raise the necessary commitment fees without spilling the beans on who they were commiting to! But now we are happy to announce how it worked out! Below is the whole story told by Drake's new mommy, Melissa.
~~~


Arthrogr...what? A few short weeks ago I had no idea how to pronounce arthrogryposis, much less know what it was. Another unfamiliar diagnosis listed below a waiting child's name.

Enter Drake...

Someone on facebook posted Drake's link from Reece's Rainbow and I said I WANT HIM! Of course, I didn't really know what I was saying....I had seen his little bitty figure transform into a smiling little boy waving at the camera and was amazed! Fast forward and now there are even more videos and this little boy astounded me!

That one comment "I WANT HIM" (and yes, I did comment with all capital letters) led another mom to message me and let me know that she would answer any questions I had about arthrogryposis (there's that word again) and that there was a terrific support group for families who have adopted children with this diagnosis. We visited and I contacted another mom, Alexis, to ask her a few questions...

I was hooked! My husband and I, and our 3 children, were just about to submit our dossier for Lance, a 2 year old with severe CP in Drake's country and I just could not get rid of that tugging that Drake was special...I had butterflies for him, just like I did for Lance. I talked to my husband, who wonderful man that he is, told me his concerns but didn't say "no" (That's almost a "yes", right???) So we talked about it a lot, did a little bit of math, and realized that to add Drake to our current adoption without stalling the process for Lance would cost an additional $7000.00 and have to be less than 2 weeks since we were almost ready to submit our dossier.

$7000.00- that's nothing to save a life/ a soul! Right?

Well, here's the thing: My terrific, wonderful husband said "$3500.00 in 2 weeks and we will move forward confident that God wants us to adopt Drake."

Oh my goodness!!!! THAT'S A YES!!! RIGHT? Ok...wait, what was that "little" part about $3500? How on earth are we going to raise that in less than 2 weeks?

Well, God is faithful and with some help from Bring Hope and SEVERAL other people we have never met in real life, we had raised $3520.00 in LESS than 1 week.

God provided not for the adoption of another child... but for our adoption of "Drake"! To see God's love poured forth for this little boy half a world away, who has no idea any of us exist, is more powerful than any words can express. My God, who knows the number of hairs on little "Drake's" head, has seen fit to bring him into our family. We are so grateful for the friends we have met in a few short weeks who have taught us about arthrogryposis and encouraged us in our journey. Thank you for your willingness to reach out and provide hope and help for children with arthrogryposis....thank you for your willingness to provide hope for Drake!

So, where are we now? We are officially committed to Drake, we are waiting for our apostilled docs to come back, and we are hoping to send our dossier for translation in about 2 weeks.
We estimate that our adoption of our 2 precious sons will cost a total of $30,000.00. So far God has provided for our adoption so abundantly and we are only about $9600.00 short of being fully funded!!! We can't wait to see how He chooses to provide for the rest ;)

~~~
To donate to Drake and Lance's adoption please go here. To find out how you can obtain help with your adoption of a child with arthrogryposis please leave a comment on this blog and we will be happy to assist you!

Monday, February 4, 2013

Meet our February Child: Drake!

We still have a matching grant going on until February 15th for Anthony. (His 14th birthday is on the 15th.) All donations are doubled until then. Our February child (featured below) cannot receive funds at this time so please direct your monthly giving to Anthony if your heart leads you. He still needs over $1,000+ to deplete this grant. To donate go here. Thank you.

Meet Drake!

Drake is an almost-five year old boy living in Eastern Europe. We often can't mention the specific country name, even though that is not against any rules. It is just an extra precaution so that someone cannot Google the country name, find the child and possibly be offended that their country is not represented well. (We don't dress our orphans like THAT!!) We'll just say his birth country rhymes with Dulgaria. And we have friends who have adopted from this country who have good things to say.

It's rare to see a description of a child to be so thorough. But to quote his listing: "[Drake is] now sitting up independently, pulling up onto his knees in the bed and is working hard to learn to get himself to a complete stand position. When placed against support, he can stand and hold on to something. He can get around independently in a walker and wheelchair. He is working with a physical therapist and learning to crawl. He drinks from a cup independently and eats from a spoon. He plays appropriately with toys and will mimic any action that he’s shown. He still prefers to use his left hand, but he is beginning to manipulate objects with his right hand as well. He enjoys playing board games with other children. He differentiates between familiar adults and strangers. He responds appropriately to praise and to correction. He repeats words that are said to him and is beginning to spontaneously talk. He understands what is said to him and follows verbal directions." His complete listing is found here.

Keep in mind that Drake had a rough start in life and is delayed a bit. "Catching up" developmentally is expected as time goes by. 

From some insider information we've received Drake is one loved, happy little boy. People want to see this little man in a family! And when an orphanage provides physical therapy and works one-on-one with a child, let's just say we all feel a little more hope for humanity. 

So let's talk Drake. From an AMC prospective he's doing well. Before very recently we did not have an update on him and this post was more guess after guess on what we estimated he might be able to do. There are more pictures and videos that we received as recently as last month so some of our guesses were spot on, while others of our expectations were exceeded!  

First off let us just point out that his diagnosis is listed as Freeman-Sholden syndrome (by which they mean Freeman-Shelden syndrome), which is a specific type of AMC discovered after genetic testing. Most of us at Bring Hope have met and spoken with Dr. Judith Hall, the top geneticist who specializes in arthrogryposis and all 400+ types. For one thing the dignosis of this type is hard to do as Freeman-Shelden is the most rare of the distal (mostly affects hands and feet) forms of AMC. Second of all, if the orphanage doctor in "Dulgaria" was able to correctly type this we would be very impressed. (We'd bake him/her a cake.) But to be on the safe side we would encourage a second opinion. His AMC may not be as severe, and after learning more about him... we all doubt it is.

Secondly everything Drake is doing physically is right on target for a very independent, highly functional AMCer. We don't doubt he'll be walking one day. We don't doubt he'll be an independent adult one day. Heck we don't doubt he'll be president! But maybe there's a rule against that if you're not born here. Well he'll vote for the president one day at least. But only if he's adopted! And if you adopt him he may even vote for the party you like! 

I really wanted to do this post on Drake because where he is located makes for easier travel and an easier process than the typical process that we just experienced adopting our son. Easy travel and a shortened process is just feeding my jealous flame over here. :) Adoption is hard. Travel is hard. Leaving other kids at home is hard. This would be less hard. Starting physical therapy from scratch is hard. Starting medical stuff on an adopted kid who has never had medical stuff done is hard. Drake would be less hard. Also he is available to just about anyone. You have a million kids? No problem! You are single? Sure! You are grandparents? Give those grandkids a tiny uncle! Seriously he just needs a family. No home manipulation, wheelchair ramp, special needs experience required. None. He just needs love. We'll hold your hand through the rest. Us AMC family members will take you in and make a place by the fire and help you do this. We'll tell stories and listen to yours. You can do this. 

Since Drake cannot receive funds until he has a family in place, we will just continue to advocate for him. Want to join us? Just share this post (or his RR profile) on Facebook, in your blogs or on any social media site. Print it out and pass out flyers to people in your church (who are required to care about orphans and stuff), your family, neighbors and coworkers. Random people on the subway! Put up billboards! Produce a commercial!! Sky writing!!! 

I'll just be sharing on Facebook because I'm way less motivated than you people. 


Thursday, January 31, 2013

What Happens If You Care A Whole Awful Lot

When we started advocating for orphans with arthrogryposis in January 2012, we had no idea what to expect. We created a group on Facebook, Bringing Hope to 12 in 2012 and we believed we could make a difference. There were a lot of orphans with arthrogryposis multiplex congenita that needed to find forever families. All of our contributors are either moms of children with arthrogryposis or adults with arthrogryposis, so who better to advocate than us?

In the past year, I have had the honor to be a part of a group that is teaching me with every post, every discussion.. I have learned so much about international adoptions--not only about the conditions these children are living in--but most important, the people who believed in a child they never met and said yes, you are mine. Many of our new AMC famiilies, I have only had the chance to meet online. But I am forever connected to them because of arthrogryposis, because of adoption, because they cared a whole awful lot./

We will continue to advocate for a new child each month in 2013 and we cannot do it alone. We need your voices and your support. Sharing the stories of our children is just as important as putting money in their adoption funds.. We know it can get better and it all starts with a simple “share” or email with a link to a blog post. If you can financially support each featured child, any donation does make a difference./

Anthony, our featured child for January, could really use someone to care a whole awful lot. Anthony is a 13-year year boy living in an Eastern European Institution. He needs parents, and he needs them fast! In Eastern Europe if he reaches the age of 16 he will become un-adoptable. Given that he has all extremity arthrogryposis his ability to become an independent adult in his society is very, very unlikely. He will likely be an some level of an institution forever. He doesn't deserve that, no child does. You can read more here.

If you can’t make a donation, then “donate” a promise to share the blog post with your networks. We never know how the families will find their child.

  • Share on Facebook
  • Tweet to your followers
  • Post an update on LinkedIn
  • Repin our photos on Pinterest

Monday, January 21, 2013

Anthony has a matching grant!!

Our focus child for January has ZERO dollars toward the cost of his adoption! 

Lets change that! 

Remember it will cost around $20,000 to complete the adoption process for Anthony. 

I've had adoptive parents tell me that they were able to commit to their child because they knew a significant portion of the money it would cost to complete the paperwork had already been fundraised. 

So lets help lessen the financial barrier to Anthony getting a committed family! 

For every dollar donated between now and February 15th will be matched up to $1500 total!  

So $1 becomes $2
$5 becomes $10 
$12 becomes $24 
$50 becomes $100

Every.Single.Dollar WILL help!! 

He has waited for THIRTEEN YEARS 

He Turns 14 on February 15th so lets get $3,000 into his account by that time! 

Lets ensure he doesn't have to wait in 2014 too! 

Tuesday, January 1, 2013

Meet Anthony!

The first child we are spotlighting for Bring Hope to 12 is a young man named Anthony! 



Anthony is a 13-year year boy living in an Eastern European Institution. He needs parents, and he needs them fast! In Eastern Europe if he reaches the age of 16 he will become un-adoptable. Given that he has all extremity arthrogryposis his ability to become an independent adult in his society is very, very unlikely. He will likely be an some level of an institution forever. He doesn't deserve that, no child does. 

This young-man has all kinds of great qualities! He is full of energy and is a ham. He can read and write. He follow directions. He loves chocolate with nuts, the colors yellow and brown, likes soccer and cars. He picks up english quickly. He has a huge smile and loves to laugh! 

He has had some treatment for his arthrogryposis which included a year of serial casting on his legs and feet. He has been seen walking when he is in casts but otherwise utilizes a wheelchairs for mobility. He can self-propel in his wheelchair. 

He is VERY anxious to be adopted. When Americans come to his orphanage to adopt other children he asks to be adopted and yet he continues to wait. He remains hopeful his family will find him but understandably is getting frustrated. 

Here is a VIDEO of Anthony. 



He turns 14 in February, which means he has just 24-months to adopted or he will remain institutionalized for life. An adoption from his country normally takes around 9-mons but could take longer. A family will need to commit to him in less than 15-mons to have enough time to complete the adoption and still have enough time to allow for delays in paperwork. 

An international adoption will cost upwards of $20,000! Most people can afford to take care of another child and would willingly adopt but reality is they don't have $20,000 laying around. 

Anthony needs our help...he needs your help! 

Please consider donating to his adoption here and if your finances don't allow for that please just SHARE this blog post. Publicity on social media and the internet could lead to his family finding him and sharing is FREE and takes 30 seconds or less! 30 seconds of your time could change his entire life FOREVER! 

If you're interested in adopting Anton please contact us or click the "contact us about this child" at the bottom of this page: http://www.eliproject.org/children/anthony/ 

Adopting an older child with special needs can be scary but we know several families who have adopted much older children with arthrogryposis so if you're interested in adopting Anton and would like to connect with these families please let us know! 

Here are more pictures: 



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Saturday, December 1, 2012

Introducing our December child: Kyle!


Kyle
 
We introduced Kyle a bit early because of sweet Francesca's death last month. Kyle is also in Africa and also has AMC. He makes our 12th child for Bring Hope to 12 in 2012.
 
An update:
 
January - Joel (now Roland, orphan no more!)
February - Laurel (now Alexandra, orphan no more!)
March - Victoria (has a committed family!)
April - Igor (his family MEETS HIM TOMORROW!)
May - Alexis (her family brought her home recently!)
June - Elizaveta (still without a family, but $1,000 closer to finding one)
July - Lily (had a committed family and we were able to raise their funds)
August - Raymond (still without a family, but $2,000 closer to finding one)
September - Aubree (still without a family, but $1,000 closer to finding one)
October - Rita (got a committed family the month we advocated for her! A first!)
November - Francesca (passed away during her month)
December - Kyle (unlimited potential!)
 
For the final month of Bring Hope to 12 in 2012, would you please share Kyle's link with your Facebook pages and blogs? We'd really appreciate it.
 

Contact Ruth Cox for more information on Kyle. Her email is yakorphans@gmail.com.