May 22, 2012

The New Faces of International Adoption?

For several months, I’ve been thinking about a blog series on unrealistic adoption expectations. Off & on, I’d draft rough notes on the topic. But in the last week or so, I’ve really gotten motivated to move forward with the series. One of those motivators was seeing the new movie “What to Expect When You’re Expecting”.  I knew that one of the couples in the movie adopted a child and I was eager to see how that was portrayed in the movie.

Wow. What a disappointing, unrealistic portrayal of international adoption. I know it’s Hollywood, and we shouldn’t expect much, but still, this kind of thing only serves to increase the unrealistic expectations of first -timers thinking about adopting internationally.

(Slight spoiler here for anyone concerned.) The desperate-for-a-baby mother and the freaked-out father choose Ethiopia.  Just a few days or weeks (!) later they get a referral for and a picture of an adorable, six week old, perfectly healthy baby boy. There’s an “awwww,” from the audience, of course.  Months later they travel to Africa and arrive at the care center with a large group of other adoptive families (each and every family carrying an infant baby carrier!). There is a short ceremony where they all stand in a line and repeat an oath about caring for the child and keeping them in touch with their Ethiopian heritage. They then exchange a lit candle for their baby and are pronounced to be a family. More awww’s from the audience.

Easy enough right? Apparently many people assume so.

Here’s a (paraphrased) conversation I had with a prospective adoptive family not too long ago. This is a conversation I seem to have over and over again:

Excited Family: We are really interested in providing a family for a baby girl from Uganda!

Me:  Well, baby girls aren’t usually available for international adoption in Uganda unless you are open to fairly significant special needs. Are you open to adopting a child with special needs?

Somewhat Less Excited Family: Ummm…no….I don’t think we’re equipped to care for a special needs child. We’re really hoping to adopt a healthy baby.

Me:  OK, well, that isn’t possible from the Uganda program. Most orphaned baby girls in Uganda are now able to be adopted in-country.

Deflated but Insistent Family: Umm, ok. But you know, we really feel called to provide a family to a child in need, and we feel like we are supposed to adopt a baby who is sitting in an orphanage waiting for a family. Cause, you know, there are 147 million orphans in the world. We want to make a difference. What country should we be looking at…? 

You see where this is going?

I have absolutely nothing against this family or other families who start out their adoption journey the same way. We shouldn’t be mad at them. Most of the time, they are sweet, concerned families who truly don’t understand that these aren’t the children that are waiting to be adopted.

Many of these well-intentioned families have seen their friends bring home healthy infants for the past 10 years from China, Ethiopia, Guatemala, Vietnam, etc. They’ve heard the statistics that there are 147 million orphans in the world. Perhaps they went to a Christian conference where leaders were shouting from the rooftop that it’s a Christian’s duty to rescue one of the millions of children waiting in orphanages. Certainly they’ve watched the popular “gotcha day” videos where teary-eyed moms hold their babies for the first time and read the popular blogs. Understandably, they dream of similar videos and blogs of their own. It’s no wonder these families are fired up and ready to rescue a baby. Except that in reality, these waiting, adoptable “healthy” babies just don’t exist.

Friends, it is time to paint a more realistic picture of what international adoption looks like today.

I am not aware of any adoption program, anywhere in the world where healthy, adoptable infants are sitting in orphanages waiting for families.

The fact is that there are far more families wanting to adopt healthy babies than there are adoptable healthy infants. In the U.S. I have heard that right now, for every healthy, adoptable infant, there are 20 – 40 families waiting.  That’s right, families waiting for babies, not the other way around.  I’m assuming this statistic is for white infants. I have recently heard that the wait is less for African American infants.  I don’t have numbers on internationally adopting families, but I know typically they are waiting several years for the “popular” countries.

I suppose there are always going to be families lining up for years to adopt babies, and I’m not going to tell someone that it’s necessarily wrong to do so. I tell the families who contact me that if they are completely set on wanting to adopt a healthy baby, and only a healthy baby, they need to get on a waiting list with a reputable, ethical agency and be prepared to wait a long time.

Or, they can shift their mental expectations from a “perfect” baby  to one who might not make Hollywood’s casting call.

I don’t feel that it’s ever right to try and guilt-trip someone into adopting, but it is good to offer people different perspectives and to challenge preconceived ideas. Not every family can or should adopt a special needs or an older child, but I would ask those families who say they “really want to make a difference” to think about ways in which they can make the biggest impact on one of the thousands of desperate, adoptable children who are waiting, waiting, waiting, right now.

Some of the conditions in which these sweet children wait are unimaginable, and it’s not difficult to find their heartbreaking stories online if we really want to know what life is like for the less than perfect. These are the children with the lists of diagnoses you didn’t check off on your home study checklists. They’re the kids with the not-so-cute referral photos, but who are often old enough and bright enough to understand that they aren’t wanted because of their age or special needs.

Many of them live a tortured existence in adult mental institutions. Some of them are diapered and tied to their beds for the rest of their shortened lives. Can you imagine any child tied to a bed for years? No love or caresses, no kind words, no intellectual stimulation of any kind. And all because they are considered “retarded,” untreatable or sometimes even cursed in those countries.

These children are waiting right now. While people are lining up to adopt babies who won’t even be born for three more years, these children are growing up without a family and some of them are dying because no one will consider them.

Why? Why aren’t more families saying yes to these children?  Without passing judgment, without blaming anyone, I’m just really feeling that it’s time we in the international adoption community begin to bring this issue to the forefront of our discussions.

I’m interested in what kind of ideas and discussions a series on special needs adoption will stimulate. I’m thinking that a follow-up post might be on the most common reasons people give for not being willing or able to adopt older/special needs children and how regular families, just like yours (and mine), have gotten past these obstacles and are providing families for waiting children. I’m really interested in hearing from all of you.

Thanks so much for reading –and considering.

(Please take a look at this beautiful video recently released by Rainbow Kids! )

May 19, 2012

Benja’s EEG/MRI update

We got notice that Benja’s EEG and MRI show a NORMAL (though still small) brain!  YAY!!

No signs of seizure activity so we’re assuming at this point that his previous seizures were febrile seizures.

This is such a relief!

We have an appointment with genetics on Monday to find out the results of his genetic testing. Then in June we go back to the craniofacial surgeon to talk to him about his plans for Benja’s mandibular distraction and cleft palate repair. We are also waiting for a call back from audiology about a more thorough hearing test and possible hearing aids.

Benja got AFO’s and a standing frame and is currently working on putting weight on his legs with hopes that he’ll show interest in standing and eventually walking.   We’ve been joking that he’s going to be a hurricane once he is walking.  He is already such a handful!

We’re having so much fun watching this sweet boy grow and develop!

 

 

 

May 1, 2012

Saving Beth

Update:  BETH HAS A FAMILY!

Friends, please look at this beautiful child and spread the word about her need for an adoptive family.

Baby Beth is almost two years old. She has unrepaired spina bifida and will likely DIE if she doesn’t receive medical treatment and a forever family ASAP. It is truly a miracle that she is still alive now.

In case you aren’t aware of what spina bifida is, she has a hole in her back exposing her spinal cord. Spina bifida is usually correctly shortly after birth. Children with un-repaired spina bifida are at great risk for infection and usually don’t survive. Beth also has hydrocephalus (build up of fluid in her head) for which she has received a shunt. My friend Sarah is parenting amazing two children with spina bifida. I have cared for and transported internationally two children with un-repaired spina bifida and there will be many people happy to talk to anyone interested in learning more about what caring for children with spina bifida looks like.

I’ve been told that they don’t think Beth will be able to walk because of damage already done due to her unrepaired spina bifida. Miracles do happen though!!

Each of the children with spina bifida I have had the privelege of knowing have been the most amazingly smart, beautiful children who have touched my heart in such a special way. (Read about one of the babies I transported HERE. It’s the only one on this blog or I’d share the other.) Spina bifida has always been on our “of course!” list of medical conditions when we have adopted. We’d love to adopt a child with spina bifida someday. If we weren’t so newly home with our babies I’d be figuring out how we can adopt this beautiful little girl. PLEASE spread the word and help us find her forever family before it is too late.

Interested families should contact Nina at nina.t@chiadopt.org

April 30, 2012

AHHH!!!!!

I’m so excited, I’ve got to share!

I’ve been feeling a bit frustrated and frankly, just not satisfied, with the information we were given when we had Jovia evaluated by the orthopedic specialists when we first came home. They told us to never expect her to sit up and that prosthetic’s would likely not be an option for her.

This morning I sat down determined to do some more research. I’ve been looking for “the best” specialist for kids like Jovia. Someone who has experience with other toddlers without limbs. This is a tiny market, there just aren’t many of these kids. But wouldn’t you know it, the first article I pulled up had a picture of a little boy in Oklahoma, without arms and legs, walking! It listed the man who created his prosthetic’s as Kevin Carroll, the man made famous by Winter the dolphin’s prosthetic tail.

I decided to take a risk and send a email to this prosthetist to see if there is any way he’d be able to evaluate Jovia if I could somehow get her to Oklahoma.

I’m not joking when I say that not 10 minutes later an Oklahoma phone number popped up on my phone.

No way. I ran to the bathroom to escape the kids and answered the phone.

It was Mr. Carroll’s office. Not only is he willing to see Jovia, he is going to be in a city ONE HOUR away from us on May 17th and wants us to bring Jovia over so he can meet her!!!!!

Our baby girl is going to be evaluated by one of the best prosthetists in the country in just two and a half weeks!

I’m so excited to hear what he has to say. Even if his answer is the same as our first evaluation, just knowing she’s been seen by the best specialists will make me feel so much better.

I am blown away and thanking God for such a miracle and answer to prayer. YAY!!!!

April 29, 2012

I scream, you scream…

we all scream for ice cream!

And that is exactly what happened at the park today.

Out of nowhere I heard a high pitched tinkling of music coming up the road. As the sounds of the truck grew closer, screams of “ice cream!” started rippling through the park and children abandoned their playing to race towards the parking lot. Parents started scrambling through their purses and pockets with one hand while attempting to hold back wild children with the other. Yes, that includes me.

I only found $2 so I told the kids we’d all have to share an ice cream cone. That didn’t seem to phase them…they were so intent on getting something, anything, from that ice cream truck.

As we walked up to the truck I saw a sign propped up in front that said “Free Ice Cream, Courtesy of —–(local realtor). Woo hoo! Ice cream for all. As the news spread the cheers grew louder and the line grew longer.

The three who were with me were overjoyed to get their ice cream out of the truck window. We don’t live in a part of town that gets an ice cream truck so this was quite a treat. It was a fun surprise to our afternoon.

April 29, 2012

Benja’s EEG/MRI/CT

Just an update on Benja’s continuing medical evaluations. 

He recently had an EEG.  It was at noon and they wanted him to nap during the test.   Benja and I looked at the technician like she had four heads when she asked if he was ready to sleep.  In a room with three people, a TV, multiple computers,  in the middle of the day, strapped to a board with a gazillion wires coming out of his head.   Right.    I told them there was no way he would go to sleep.  So they did the test while he was awake.   She said they got what she needed so hopefully it was OK.    He was strapped down for probably a total of 2 hours.   About a hour to get all the wires stuck to his head and then another 20-30 minutes for the test and another 20-30 minutes to get them all off.   He wasn’t crazy about it but did OK.   They did a really poor job of getting all the glue off his head and two hair washes that night didn’t get it all off either.  Finally some baby oil and a good comb through got it all off.   Now we’re waiting to hear the results from the neurologist.

We spent that night near the hospital in a hotel because we had to be at the hospital at 7am to get checked in for his MRI/CT done under anesthesia.    I hate when he has to be intubated.   Because of his jaw/airway issues they make a huge deal about it at the hospital with multiple anesthesiologists, lots of questioning and discussing, explaining the increased risks, the difficulty of intubating him, etc.    It all makes me nervous.    I sat in the surgery waiting room for several hours while he had the tests done and then a nurse came out to get me.   She said “Is Benjamin your baby?”  I told her yes and she said “Girl, you have THE CUTEST baby!”   I agreed.  When I went back to see him the nurses were passing him around the nurses station.  :)   They said he did great waking up and besides a sore/scratchy throat and being tired the rest of the day he was great.   Now we’re waiting on the craniofacial surgeon to call us with results of the MRI/CT and let us know if we can schedule his jaw surgery!

April 24, 2012

Some pictures…

Some cuteness from the past week or two:

April 24, 2012

Jovia Dancing

All of our kids greatly enjoy the the Gummy Bear Song but Jovia gets particularly animated when she’s dancing to this song.  :)

April 14, 2012

Better late than never…

I know it’s late – almost a month late – but the babies are now TWO!!!

We had a wonderful birthday party for them here at home with many of their family and friends.   They both thoroughly enjoyed their cake and opening presents.   They are growing and changing so quickly!   

 

April 11, 2012

Benjamin can roll!

Benja can officially roll over!  Until recently he’s been like a little turtle, once he was on his back, he was stuck on his back.  His PT told me that Ben just had to learn to roll.  That was our big assignment to work on.   We started practicing with him every day – it took about 2 weeks but one day he just figured it out!

I’m happy he can do it but he’s become a handful ever since he learned.  Diaper and clothing changes are such a struggle cause he goes crazy trying to flip himself over!   He also has decided he no longer needs to sleep at nap time now that he has figure out how to get himself up to play after we put him in bed.   He’s such a silly boy.  :)

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