Sunday, March 11, 2012

Let's Talk Special Needs Adoption

I have been mulling over this blog post for a long time because I think it is important to have a discussion about what is considered a special need in international adoption, specifically from Bulgaria. I am going to come right out and tell you that at the end of this post you will not have a definitive answer, but maybe some food for thought instead.

There are many different definitions of special needs. Parents, social workers, placing agencies, foreign partner agencies, and foreign governments all have their own views of what’s considered a special need. While some prospective adoptive parents might list needing glasses or having a food allergy as special needs they would accept or consider, these conditions may not even be on the radar of a foreign government in terms of special needs. On the other hand, being a member of a large, healthy sibling group that must be adopted together might be a special need in the eyes of that same government. A social worker may consider Down Syndrome a significant special need while the family hoping to adopt a child with just that extra chromosome might only think of his or her accompanying heart defect as a special need. A placing agency may tell you that children’s advanced age is sometimes their only special need and a foreign government may refer a child with repaired club feet as healthy.

When I meet new families now who are just starting their Bulgarian adoption journeys, they often tell me that they are open to mild and correctable/moderate special needs. Of course, what this entails for each of these families is hard to know. Our story went like this:

In our very first home study, our approval read as follows, “Craig and Viviane Martini are approved to adopt from Bulgaria one to two children of either gender between the ages of 0-36 months at the time of referral, preferably as young as possible, and in good health relative to orphanage care. The family might consider on a case by case basis a child or children who have some minor correctable needs, such as allergies, missing/fused fingers or toes, cleft lip, and needing glasses.” Looking back on it now, the only thing on this list that the Bulgarian MOJ would probably have considered a note-worthy special need is cleft lip/palate.

Later when we revised our parameters, the home study read, “The Martini family is approved to adopt up to two children of either gender as healthy as possible relative to orphanage care and with minor and correctable medical and emotional needs including, but not limited to, allergies, asthma, cleft lip/palate, club foot/hand, delayed development, diabetes, exzema, fused fingers and toes, Hepatitis A, hearing impairment, hernia, hypospadias, needing glasses, premature or smaller in size, between the ages of 0-36 months at the time of referral with a preference for a child 0-24 months from Bulgaria.”

At that point, MOJ had also created a special needs document we filled out. We said yes to the following conditions: child born of incest, child born of rape, jaundice, umbilical hernia, lactose intolerance, any scars from delivery, Mongolian spots, raised angioma, small nevuses and burn scars, blind in one eye, vision problems correctable with glasses or surgery, cleft lip/palate, ear infections, heart murmur, ASD, VSD, hernia, parasites, missing fingers or toes, webbed fingers or toes, asthma, allergies, bronchitis, pulmonitis, digestion problems, poor nourishment, controlled seizures, hypospadias, and anemia. We also said maybe/would consider to 50 other conditions. Once we had submitted our updated paperwork after a year’s wait, we were matched with Emilia within four months. Emilia has a heart defect (VSD), failure to thrive and significant developmental delays. We did not know until we brought her home that she also has a moderate milk allergy and is anemic. In addition, Emilia has some factors in her family history that could be of concern and might have deterred other families from accepting her referral.

As many of you know, I have the list of registered dossiers through the end of 2009 which at one point was accessible on the MOJ site. This list shows when a dossier was submitted, when registered, the country from which it came, as well as the number and maximum age of child(ren) requested. By my most recent count and unless these families have dropped out of the program, there are still 5 families waiting from 2006, 11 from 2007, and 24 families from 2008. I think it is safe to assume that they have requested fully healthy children who are developmentally on target and that there may even be an ethnic preference expressed in the requests. Unless dropped out, there are 34 families remaining who want to adopt two or more children and 183 families registered in 2009. It’s certain that the greater the number of children and the narrower your age and health parameters, the longer your referral wait.

I have read dozens of reports for kids matched through the main procedure and for waiting children. Some needs that I recall as being most frequently listed: mental illness/retardation in the family, mild/moderate mental delays/retardation in the child, moderate to severe speech delays, congenital diseases that are now cured, heart defects, strabismus, limb differences, hydrocephalus (with or without a shunt), spina bifida, short stature, epilepsy/seizures, premature birth, cerebral palsy, cleft lip/palate, and hearing impairment. Some children are described as having anomalies in the phenotype, but genetic testing came back with no issues. Quite often there are children who are physically healthy but noticeably delayed in development or children developmentally on target with physical disabilities.

So what is a special need? Obviously it depends who you ask, but in my opinion as an adoptive mother who has watched Bulgarian referral statistics very closely for the last two years, it would be foolish to submit a request to MOJ for a toddler with needs like glasses, a missing finger, or lactose intolerance and consider it a special needs adoption. However, a child with a correctable heart defect and developmental delays may be on the special needs radar of MOJ as would any child upward of seven years old. I don’t recommend to anyone that you indicate openness to special needs with which you are not comfortable. However, I do suggest that you educate yourself about what certain special needs might entail. Don’t just read the potentially scary Wikipedia entry, but also try to connect with parents who have children with a particular special need to see what it’s really like. You may be surprised. I also advise that you keep a realistic outlook on the referral wait you might expect, especially if you are just starting out on your adoption journey or are newly registered. Unless the process changes, for a healthy or nearly healthy Bulgarian toddler with few developmental delays, the wait seems to be at least 24 months now, sometimes closer to 36. For children with moderate, correctable or severe special needs and older children, the time to referral seems to be 12 months or less.

Saturday, March 10, 2012

Consignment Palooza

Today I went to my favorite bi-annual children’s consignment sale at a local elementary school. You have to get up early to arrive when the doors open, but it’s worth it. Meanwhile, Craig and the kids met up with his cousin and his little boys for breakfast. I think they had a nice time doing some daddy talk and entertaining the kiddos.


As always, I came across some great finds at the sale.

Rex

2 short-sleeved shirts

2 long-sleeved shirts

3 pairs of shorts

1 pair of shorts overalls

1 pair of corduroy pants (looks brand-new)

1 jacket (looks like it was never worn)

Emilia

1 jacket

3 zip-up sweaters

4 pairs of shorts

1 skort

1 pair of pants

2 short-sleeved shirts

1 long-sleeved shirt

1 pair of tights

Some of these clothes are brandname (Gap, Carters, Children’s Place, etc.). I just can never believe the variety, quality and price you find at this sale. Anyway, I know you’re waiting for it… my grand total for this loot of clothing… $17.00.

Thursday, March 8, 2012

Farewell, Baby Shoes

My lovies have outgrown their first pairs of shoes, the ones they wore out of their orphanages the last time they passed through those doors. Rex outgrew his right around Christmas and Emilia hers last month.

I think I will save these shoes for them as they touched their native soil and show just how small their feet were when we brought them home.

Monday, March 5, 2012

Emilia - Fifteen Weeks Home

I know I am quite behind, but Saturday marked fifteen weeks home for Emilia. I am not sure what’s new to report with her. She continues to be a cuddle bug when she has access to mama or daddy and she is also a thrill-seeker. You can throw her as high up in the air as possible and she loves it. She enjoys swinging, whether it’s by her arms or in an actual swing. She likes to climb and bounce.

Emilia’s receptive language seems to be expanding. She now almost always responds to us calling her name and she will come if told. Just today, I was looking at a book with her and telling her all about tigers and she began imitating the t-sound very consistently. Come one, language, come on, I know Emilia can do it, she is just holding off for some reason.

This is one of my favorite Emilia faces.

She makes it when she is surprised, sees something that excites her, or when told no.

Emilia had some bloodwork done last week and her iron levels have increased enough that she needs to take her iron supplement only through the end of March and then is done with it. Her thyroid function has also improved though it is still a bit elevated. We will re-test for it in the summer.

Emilia sleeps quite well through the nights now all by herself in the kids’ room. We may have the occasional night of hysterical laughter for an hour or hear some whimpers or leg-kicking through the wall, but most nights, there’s no need for us to get up and check on her. Emilia continues to eat well and explore gritty foods. She can now eat Arborio rice cooked in coconut milk and mixed with fruit puree with no problem. I think I will try soft orzo next. Emilia refuses anything from a fork or fingerfood still. I attempted to give her a very soaked piece of pancake yesterday and she acted like I was trying to kill her. It might be a long while before real solids are part of her diet.

Overall, Emilia is doing great. I think she gets a little more secure and comfortable here with every passing day. And I just can’t wait to see what spring has in store for her.

Sunday, March 4, 2012

Rex Is Three

This week we celebrated Rex's third birthday and unlike last year when the day was filled with tears for me, this year we had planned a lot of fun.

We started the day off at home with a lazy family morning. I prepared German potato cakes for lunch and Rex had four. He loves those things. After nap we headed to Great Wolf Lodge for an overnight to see if the kids would enjoy the indoor water park. They did like it, but the tremendous noise and the unexpectedly large crowds were a little overwhelming. Nonetheless, Emilia decided it was as good a place as any to take a nap.

We had a wonderfully relaxing evening as a family at the lodge with none of the responsibilities that sometimes take over at home. After dinner we just played and then cuddled on the king bed until the kids fell peacefully asleep.

When we returned home, we had planned a small gathering with family and friends. We had cake and ice-cream and lots of excitement. Rex was showered with many wonderful gifts. He played with his new guitar and his top for a long while. And the balloons from Ms. Rie were a big hit, too. Once again, Emilia partied a little too hard and passed out on the floor.

I really cannot believe my little boy is three. He is so amazing, growing and learning at his own pace in his own style all the time. He brings such joy to our lives and we could not be more grateful to be the parents of this handsome toddler.

Happy birthday, son. We love you beyond measure.

Saturday, March 3, 2012

Rex - Twenty-Nine Weeks Home

Thursday marked thirty-one weeks out of the orphanage and twenty-nine weeks home for Rex.

The last two weeks have been pretty quiet. Rex’s focus has been on communication. He has been signing eat for months and now has added music and swing to his repertoire in quick succession. He uses both signs pretty accurately, independently and reliably. Rex is also imitating the signs for on, shoes, and tickle though he still isn’t always sure when they’re appropriately used. In addition, we are hearing some spontaneous verbalizations for ball and bubble. All of Rex’s therapists are very excited about this development as are we. Rex is now able to respond correctly to some short commands, such as “go get…”, “come here”, and “let’s go.” When we met with a communication/speech expert this week to discuss and test some communication devices for Rex, she noted that Rex has very good receptive language - finally someone who agrees with me on that matter.

In other developmental areas, Rex has been working on puzzles. He can take big pieces out and also put them back in though he sometimes needs a little help figuring out where each piece should go. He very easily locates hidden objects and when applying the right focus, can even find an object hidden under one of two cups with the cups being switched around. I hope he never runs into a hustler on the street doing that game.

It seems that we have merged into a new stage of behavior with Rex as of late. When he was newly adopted, many of his poor behaviors like raging and hitting himself were related to his inability to process sensory input and his lack of communication skills. Now that he has made so much progress in both areas, his tantrums are more like those of a typical toddler though probably a bit more intense. He is trying to assert his autonomy and get his way, so Craig and I are entering the territory of having to set firm and consistent boundaries for our little boy. He doesn’t like it one bit, but that’s part of love, too.

Rex’s scab from the new, accident-induced lip stitches finally fell off and the repair looks very good. His plastic surgeon said that we should know in about a year how much of a scar will remain, if any. He also mentioned that Rex’s initial cleft lip repair in Armenia was done in a very outdated manner, so it will be a surgical challenge when the time comes for his lip and nose revision. But I’ll worry about that later.

Not much else new, so I’ll leave you with a photo of my two favorite guys:

Thursday, March 1, 2012

Баба Марта

Emilia and I put on our martinitzi this morning and have been showing them off all day:

Chestita Baba Marta, everyone!