I have been debating with myself about posting about Boo. You see, there is just so much that we are still learning and discovering about our sweet boy and his educational diagnosis of PDD-NOS.
PDD-NOS is the acronym for Pervasive Developmental Delay - Not Otherwise Specified. PDD-NOS is sometimes included on the Autism Spectrum but not always. And even though he does have PDD-NOS, we have not been told that he has Autism. It's kind of a weird, confusing thing to me actually.
But to explain what he does have and how we have gotten to where we are right now, I'll go through the basis of his history. When he was born (at 39 weeks via scheduled c-section) he was not breathing. The umblical cord was tied in a knot. Much like the knot you make when you are tying something. Just a simple knot. But a knot that was cutting off vital oxygen and blood to him. We were told that had we scheduled the c-section for later than we had, he could have died. As it was, he wasn't breathing and had to be resuscitated and given blow-by oxygen. I didn't get to see him for three hours. It was horrible. They got him to breathing well on his own and by the sixth hour (I believe it was around that time) he was able to stay in my room with me. Prior to that, he had been able to come in but had to go back for further monitoring. His apgars were something like 2,9,9. The only thing he had going for him during that first set of apgar scoring was his heartbeat. That's it.
He recovered well from his birth and was a nursing pro. When he was just shy of three months old, he began having bowel and reflux issues. We thought maybe it was just reflux. We took him to a doctor who deals specifically with nursing babies and allergies/intolerances. She diagnosed him with MSPI (milk, soy protein intolerance), so those things were eliminated from my diet. But he still was not getting better, so we eliminated more and more things. Eventually, I went on TED, the Total Elimination Diet. I was able to only eat turkey or lamb, baked or boiled potatoes, sweet potatoes, rice or millet, squash, pears, and pear juice. That's not a lot of options. It was hard, but I did it. After two weeks' time, I was able to add items back in one at a time (much like you do when you are introducing solids to your baby for the first time) and then had to watch him to see if he began reacting to it. What we were able to determine was that he had intolerances to not only milk and soy but also to beef, eggs, nuts, hmm, there were more things but now I cannot remember them... Eventually (around 7-9 months of age), he was able to tolerate most of those foods in my diet in small quantities. He stopped nursing around 9 months old and we had him on a soy-based formula, then switched to regular formula. He began babbling and even saying a few words by a year old. Around 13 months though, he started reacting to something again, and at that point, we eliminated all of the foods we knew he had issues with prior to that. We even had him on goat's milk for awhile because he seemed to tolerate that but eventually, he began reacting to that as well, so we switched to rice milk for him instead. It was around this time that his world went silent. He didn't talk or babble anymore, but he was also learning to crawl and so we thought maybe his energies were tied up in mastering this feat. More and more though, he withdrew and after awhile, he wouldn't make eye contact either. He didn't play with the other kids, didn't really even acknowledge them. We made an appointment with his pediatrician.
His pediatrician ran a battery of tests to try to determine a physiological reason for his delays and regression. But there wasn't a physiological one. He referred us to our city's public school program.
At 19 months old, he had his first evaluation with the school system, at which point, he was diagnosed with PDD-NOS. Basically, PDD means across-the-board developmental delay. He was behind in EVERYTHING. From social and play skills to cognitive abilities to gross and fine motor skills. He had learned to walk just one week prior to the evaluation. The NOS part of the diagnosis means that there isn't a physiological explanation for it.
So, we started services. We had a wonderful home teacher, Jane, who came out about once a week to work with us and Boo and he gained quite a bit of ground while we worked with her. We worked with Jane from May 2009 until October 2010, when Boo enrolled in a traditional classroom setting.
We had two options for his classroom. One was more of an ECSE (Early Childhood Special Education) format, where most of the children have IEPs (Individual Education Plans) with a few peer models thrown in for balance. The other was basically an inversion of the first. Mostly peer models with a few kids who have IEPs. We chose the second one, feeling that it would be of the most benefit to the boy.
He has done wonderfully! He is still behind quite a bit socially but is catching up. His motor skills are just minimally behind, his play skills are also still fairly behind but we have seen some recent improvements in that as well.
He had a hard time waiting for his turn to bowl, though no meltdowns there either. At one point, our lane broke. I don't know what the deal was, but of course, it was Boo's turn. I had just spent the last two kids' turns telling him that it was almost his turn and when we finally got up there, he got his ball and I had to stop him. "Not yet, Boo. The lane isn't ready. They are going to fix it though." So, he stood there patiently and my heart grew with pride about how well my little Boo Buddy was waiting. He stood there and held that 8 pound bowling ball for a full five minutes (it felt like an hour to me!) until they decided that the lane was unfixable and then worked us into another lane that already had three kids bowling in it.
And then lastly, a shot of Boo with two of his classmates.
One really recent development with Boo has been in his communication. Although he doesn't really talk much about things that he has done, seen or experienced, I try to prompt him for information. After school one day recently, I asked him if he had played with Master C (the birthday boy in the above photos) and our conversation went like this:
Boo: "No. I play wif [Master M],"
Me : "You played with [Master M]?"
Boo: "Yes. I play wif [Master M]."
Me: "What did you play with [Master M]?"
Boo: "We play cars. Vroooooooom!"
Me: "You played cars with [Master M]! That sounds like fun. Was it fun?"
Boo: "Yes. Fun play cars wif [Master M]!"
That was the longest "conversation" we had ever had. It still might be.
I just love the way he talks! He has some really unique ways of saying things and he is very obsessed with letters and numbers. Some examples of Boo's language:
"Open hand!" This is said when someone is holding his hand or arm to keep him from running off. Instead of saying "let go", his command is "open hand". It would get the same result if obeyed, but is just a different way of saying it.
"Mommy, you home. I home." This is what he says to express that he missed me while I was at work. It doesn't matter if we are in our house or if I am picking him up from Grandma's or whatever. If he missed me, this is what he says. He also says this to express love. It's a situational phrase.
"Mommy, I find your blue!" He says this as he runs to me, holding either my (blue) phone or my (blue) camera. I tell him, "thank you Boo, for finding my blue phone!" He will look at me and say, "Blue phone!" and I will hold it up for him to look at and then repeat the phrase.
"Can I cars, please?" He just said this a moment ago. He wanted to go play with his cars, but he doesn't always use verbs in his sentences, so we give him permission as we rephrase his question, "Yes Boo, you may go play with cars."
He knows all of his alphabet letters on sight and can put the alphabet in order when using manipulatives. He also knows his numbers by sight up to 19 and can count up to 49 now. He also rote spells his name, his sister's name, JoNo's name (well, an abbreviation of JoNo's name but says it as the full name), as well as Mom and Dad. He does get stuck when spelling Dad or just refuses to spells it.
His Magna Doodle Jr. is his best play toy. I keep that in his backpack at all times if possible. No matter where we are or what we are doing, I can almost always get him back on task (or at least out of a meltdown) by using this toy to practice letters or numbers. He also knows the sound that each letter makes. He will spend quite a while "reading" letters off of signs or walls or whatever he can find. He loves it! A while back, I was dropping him off at church and he sat down and started "reading" the wall. "J-E-S-U-S-L-O-V-E-S-Y-O-U" It's all just one big long word to him, although he does recognize the words as separate items when I am reading to him.
And that is Mr Boo in a (VERY large) nutshell. He is such a joy to have around and to experience life with. The world is such a different place from his prospective. I love seeing things from his point of view. ♥ ♥ ♥
I am also going to link this up to Company Girl Coffee and