Once upon a time I was a really judge-y a-hole. I thought I knew everything about everything and this wasn’t even my teenage years. Gaaaaah, I was exhausting. One of the things I knew nothing about but thought I did?
Until not only Samuel, but Abraham as well were diagnosed with it. No, scratch that. That’s a lie if I’ve ever told one. I still didn’t know. And quite frankly, it was the beginning of one of the hardest uphill battles I’ve ever fought. Alone but with people, together but on opposite sides of the river. Different but the same words to apply to two of my three boys who just rode the struggle-bus-wave at school something fierce. It was hard to swallow because it was personal and I felt like I had failed them in some way, even though it had nothing to do with me but was about to consume my life. Our lives. Each of us in different ways.
Samuel’s diagnosis, as a Type 1, meaning he has inattention but not hyperactivity, was an absolute dream in terms of handling it. He was put on a small dose of Ritalin and it was an overnight change, where he went from testing below grade level in every subject to making the honor roll no less than three months later. “He’s not dumb, he just needs a little help,” his sweet fifth grade teacher had told us. Learning about what he needed and why completing homework and turning it in was so hard made a lot of difference in understanding him better. Isn’t that what we all want? To be understood better? He started to gain self-confidence, boosting his self-esteem. You could see a visible change in him, almost immediately but also over time. Not to say he hasn’t had some ups and downs that have needed revisiting and adjusting. Sam still continues to be so much easier to handle.
So, enter Abraham, who has been marching to the beat of his own drum since the moment he was born. Yesterday he asked me for a picture of that day, and you know what? I don’t have one. He was my fastest delivery, being born less than an hour after I finally got to the hospital because nobody believed that I was in labor and then when the nurse checked me I was dilated to 8. When they told me I couldn’t have an epidural or any other sort of pain meds because I was too far advanced, I broke down crying. I had been trying to keep it together for so long, thinking it would be coming. It wasn’t. He got stuck and the doctor had to help him get his head unstuck and I just screamed in pain. I remember it like it was yesterday, all the pain and commotion, but I don’t remember his face. I hardly saw it. He came early, was whisked out of the room so fast. I had only gotten to hold him for about five minutes and then he was gone but I didn’t even notice because then I was surrounded by doctors and nurses. I was hemorrhaging and they were working fast.
I don’t even know how much time went by before I realized he never came back to the room. And then it was a twilight zone because they started lying to me in ways I would mimic later, when my kiddos asked for something I knew I wouldn’t deliver on. “Maybe in a bit, not right now, etc” kept being fed to me. I remember wanting my Mom there but she wasn’t. Hearing false information in a hospital should be a crime. And you shouldn’t feel alone when you hear it.
****** You’re probably wondering why I’m rambling on about all of this. It’s most likely because I’m defending why I’m so Mama Bear with him. Ku thinks this is why and I don’t think she’s wrong. ******
Not even two hours later, after being told maybe and soon and a whole bunch of other no-in-disguise words, he was off, on a helicopter, to Children’s hospital. See, he couldn’t breathe on his own, he was considered a preemie and they didn’t have what he needed to keep him alive at St. Josephs. And then I was mad, because my doctor wouldn’t release me to go to him. You guys, I was straight up mean to that doctor and he took it like a champ. I’m still not even a little sorry, though.
Skipping forward, he was in the NICU for three a half long weeks where I was by his side day and night, practically forgetting I had four year old Samuel at home, being cared for by my ex’s family. It’s the one thing I’ve ever sincerely thanked them for. I wouldn’t allow pictures in there, not that we had many visitors, which I think I still struggle with, inside. I was so alone during one of the hardest months of my life. He was on a morphine drip, intubated, and not improving for so long. I could hardly take it and yet that’s what moms do; the hardest work and almost always on their own.I still see him, so little and helpless in the incubator, muted and fighting for his life. I was willing his lungs to do their job for so long, and yet I couldn’t make him better. When he was finally home, I would stare at him in the night, convinced that something would happen and he would stop breathing, because joy forebodes fear because that’s what we are taught in the movies.
I taught him baby sign and he was full on signing sentences before he was even eleven months old. He started walking on his tiptoes. He taught himself to read at four years old. He learned cursive on his own, at home, because it was interesting to him. He has a signature, friends. And he’s barely eleven.
He’s also type 2 ADHD. Which means hyperactivity.
It isn’t even what I would consider severe but holy moses, it’s so true for him. He will sit and watch a movie but his body will not stop moving. In fact, from so many talks with his doctor and counselor, he needs the movement to focus his mind. And this has not come without difficulty at school. Difficulty and distractions and distracting. To say it’s interfering with his learning is an understatement, even though he is still so smart.
We’ve been lucky in that a) I believe it. The other side of his family did not. Frick, some of my own family didn’t either. The fact of the matter is that while ADHD has almost certainly been not only one of the most misunderstood medical conditions, it’s also been misdiagnosed and over-diagnosed in many cases. Not in Abraham’s. I mean that sincerely. It wasn’t something we could change with just eliminating things like food dye from his diet. That doesn’t mean it isn’t true. I know that works for some kiddos.
It doesn’t mean that getting more activity in with your little isn’t the answer. It just wasn’t the sole answer for him. It isn’t a pass to just medicate and while Sam was such a big win with his, we have tried so many different kinds, stimulant and non stimulant alike without finding the best helper.
You want to know what one of the biggest helps has been? Having had some of the BEST teachers for him that understood or tried to understand him, that believed in his intelligence and that worked alongside us to help him thrive. It was such a weight off our shoulders to feel like we had an army behind us. Except, fairy tale elementary school is over and we have entered middle school and all its chaos and we are all drowning at our house.
We have entered a season of school struggle in a way we aren’t used to. Yes, middle school was tough for Sam, but it was Sam tough, so that still makes it sort of mild. I call him the meanager and that’s mostly from those rough years because he couldn’t figure out how to excel in school anymore. Getting him to do his homework, keeping him up on his assignments and learning how to actually study were so hard. Now, it all applies to Abraham and we are RIPPING OUR GAWWWWD DAMN HAIRS OUT.
I mean it. It’s been friggin tough as hell. It is straight up square peg, round hole time and all of us are at our wit’s end. I mean, I scheduled a meeting with his teachers and it was fruitless. Unfruitful. Without fruit? I’m saying I walked out of there feeling like I could have gotten more done trying to teach a giraffe their ABCs. It’s no wonder he’s having a hard time. If I feel like they don’t care, I can only imagine he feels like they don’t care because he’s pretty intuitive and you’d basically have to be blind to not see it. I even called, ten minutes after leaving and on my way to work, and spoke to his vice-principal and expressed how wasteful my time there had felt, was promised a call back and action, a commitment to helping him, etc. It was like being in that hospital room all over again, hearing fake news told to my face without an ounce of meaningfulness.
Today, I took my voice back and I Mama Bear’d it because I am not playing around. I don’t want to be that person that loses their patience with their kiddo over something they haven’t figured out how to control yet, because that’s bananas and not right. It’s not cool to get mad at a child with diabetes for having their blood sugar in the wrong numbers because they aren’t directly in charge of metabolizing their glucose and making insulin. <— wait, did I say that correctly? Do you get my drift?
What I’m saying is, if you have a little with either type of ADHD, or if you have ADHD, hear me on the following:
You are smart.
It is real.
You are not defined by it.
Use your voice.
What about if you don’t? You probably know someone who does, so read up a little on it, so you don’t sound like Vee2013 who was just a judge-y a-hole. Don’t tell people it’s made up because it isn’t. And offer some love.