I used to read that the “co-morbid” conditions of T.S. were far more frustrating than the tics themselves.
As defined, co-morbid means the annoying other conditions that make you want to poke your eyes out with ice picks the simultaneous presence of two chronic diseases or conditions in a patient. For kids with Tourettes, this could be ADHD, OCD, Autism, ADD and insane awesomeness.
Stink deals with the last two on the list, and let me tell you, it’s been a crazy year. If I was able to guide him through the chaos, drama and joy that accompanies kinder through sixth grade, let’s just say that seventh grade has proven to be the final leak in a boat that was destined to sink without a major overhaul in the floorboard.
Having a kid with T.S. and ADD, while being a working parent with a little bit of ADHD herself (I know… biiiig shock) is kind of like fixing a boat’s floor while still on the water. It can be done, but the progress is slow. (Not to mention tiring. How many buckets of water can you scoop and throw over the side while steering the ship and feeding the crew?)
The best bet to fixing that leak is to get that boat out of the ocean all together. Take a break from the swells and breathe while your vessel chills out on dry docks. Get a professional boat repair man (or woman – no prejudice here!). Invest in his advice, buy the supplies to keep it fresh and clean once it’s back on the water, and absolutely join a hole-in-the-boat support group. After all, there’s a decent chance that at some point that gash in the floorboard will come back. You’ll want another mama to cruise by in her motorboat when this happens. You’ll want that lifeline and the invitation to a cup of coffee in her well stocked cabin to catch your breath until your own boat works again.
Since life is not apparently perfect, I’m kind of stuck in the middle between shore and open water. I’ve been organizing my own life, to help organize Stink’s, and we’ve made progress. I am avoiding a lot of frustration by accepting life on life’s terms. I am not focusing on what he’s behind on in school. (Um, everything.) Instead, I’m focusing on helping him get caught up with the goal that he’ll be doing this himself at some point.
This means coming home each day after school and doing his work in the same spot. It means having him diligently utilize his planner so that he’s not relying on his own brain to remember every little detail of his “overwhelming” (his words) seventh grade schedule.
The challenge with using a planner is that you have to remember to take your planner home. And then, here’s the real rub: you have to find it in the first place. And when that task seems too monumental, you just throw yourself on the floor and scream like a Carolina fan reach out to an educator who knows you’re doing your best to help your kid.
Here’s an email exchange I had yesterday with one of his educators, minus the teacher’s name because, you know, these teachers have nothing better to do than stalk their ADD student’s mom’s blog.
Hi Teacher Fabulous-
Andrea


Yes, I will pick it up today after school if that works for you? If not, you can leave it in the office. Whatever is best.
I have to supervise out front after school. I’ll do my best to remember to bring it out there with me so you can get it then.

As a co-morbid condition mama, I can totally relate. I’m used to the missing planners, unwritten-in planners, missing assignments, etc. I’ve mostly given up on the planner thing since I can’t get my child to use it anyway.
FYI – Check in the school office to see if they have any extra planners. I got one there and paid $5 for it. Then, of course, we found the missing one a couple days later.