Update on progress: If you've read
this and
this (my last couple serious blog posts) about our struggles with diagnosing and treating the challenges our son has, then you'll know what I'm talking about here. We did start seeing a psychiatrist at Yale. He is starting a six week comprehensive developmental assessment. Yay (spoken in a very sarcastic tone). Testing is just what we need. (I'm going old school here) NOT! Can you imagine anyone testing Mateo? Okay, well, I guess not cause most of you haven't met him. But just trust me when I say, it ain't happening. I literally told the doctor "good luck with that!" I should probably be more optimistic and helpful, but I am finding it pretty pointless to go this route. But we're going to stick with it for now.
Here comes the controversial part. Sidenote: I have to be controversial once in a while because that's when I get all the comments :)
We really want to start Mateo on medication. Okay, well, maybe I said that wrong. We don't
want to start Mateo on medication. We really feel like he
needs to be on medication.
I am going to try to talk about Mateo's special needs without revealing too many specifics. Let's see if this works out. I know it can be quite shocking to even think about medicating a three year old for behavioral problems. But, believe me, this is not something any of us take lightly. Everyday I watch him struggle and lose functioning because his "problem" is eating away at his brain. It's not for my benefit that we would medicate our son, it truly is for Mateo. I want him to grow and develop and learn. But right now that is being hindered by his "problem". And it will get worse if we continue to ignore it.
The decision to medicate our son (for his benefit) is after exhausting many, many, many, many other options. We've tried counseling (for us as parents) and therapy for him. We've tried cutting out sugar completely from his diet. We've had lots of blood work done to test for other conditions that could be mimicking the "problem". We've gone to tons of parenting workshops, adoption counseling, attachment conferences, and talked to many professionals. We even had a 12 week in-home behavioral service come into our house to observe us and give us suggestions. We ended after 5 weeks because the worker, literally, had no advice for us. She had never met a kid like Mateo. Not many have.
It will be a long road finding what works and balancing benefits with risks and side effects. We will need lots of understanding and support. The psychiatrist we're working with is on board for medication, but waiting to confirm the symptoms he feels the need to treat. I don't really know how long this will take (I'm hoping not too much longer) or what he will want to "treat". I'm worried we will disagree with his opinion and have to start all over again somewhere else. But we'll take it one step at a time. I'm hoping in the next six weeks, Mateo will show this doctor what he is all about and give him lots to consider. He is a very complicated little guy with a lot going on. It is hard to get to know him, understand him, and separate what is what. That is the biggest challenge. But I'm hoping this doctor "gets it". There is a huge shortage in child psychiatry and even less of them take insurance. We don't have a lot of options, other than paying thousands of dollars out of pocket. If this psychiatrist doesn't work out, I might start soliciting for money. Be prepared! ;)
Most of my commentators are supportive and just generally awesome (thank you for that!). But I do welcome respectful feedback on this topic as I know it is controversial and there are many opinions about it. As long as it is respectful and not derogatory in any way, I will not delete the comments. I may have more on this topic, in which I'll post later, but for now, this is it. Let's see what you all think!