{Side note: I don't feel one ounce of guilt for letting him use my phone in order to feel less anxious or to let the people around us enjoy a semi-peaceful meal, so I'm not even going to entertain anyone's opinions on that aspect of my parenting}
The meal progressed with very, very minimal ticking from Gerry. His head turning and fidgeting was in full force but his vocal ticks had taken a backseat to whatever game he was playing on my phone and, to an outside observer, there was nothing amiss. The conversation turned to Gerry's TS diagnosis. Typically, I don't like to discuss it within ear shot of Gerry. One, because I don't want him to feel like I'm talking about him or his diagnosis like it's something to be ashamed of and two, because bringing attention to his tics makes them more pronounced. However, the question of his upcoming CBIT therapy came up and the conversation just took that natural flow. And, of course, because we were talking about it, Gerry started ticking more. His goat noise made an appearance, as well as his newest "groaning from deep in the back of his throat" tic. At that point, when they became more noticeable, someone at the table asked if I'm sure it's "not just attention-seeking behavior".
My first instinct was to be annoyed. I'm pretty sure that if my kid wanted attention he wouldn't choose to get it by making loud noises and moving his body weirdly. That simple question made me so angry. Do they not know how much I've stressed about this dinner the last few days? Actually, how much I stress about every single social situation these days? Do they not understand how hard we work to come up with things to distract him when we're out in public so that his tics aren't so noticeable? Do they not know how embarrassed he gets when he's in public and making animal noises that he can't help? He's not doing this for attention.
So I was angry on his behalf and I'm pretty sure I just gave a short "No. It's not for attention". But then I sat back and really thought about it. I tried to see Gerry as someone else would, someone who isn't his mother, someone who doesn't also have TS and has put up with decades of people not understanding anything about the condition. And I went from being angry to being understanding. The question wasn't asked out of annoyance or as a dig at my kid. It was a genuine, thoughtful question. And it's not that person's fault that there isn't much known about TS or that what little information there is out there is mostly unhelpful.
Tourette tics are not attention-seeking behavior. They legitimately cannot be helped by a TS person. Most people with tics will attest to the fact that their tics worsen in certain situations, one of those being when their tics are brought to their attention (like Gerry's were when we talked about it with him sitting right there). My brother-in-law made a very good point: bringing up his tics kind of makes them into the "elephant in the room". Once they are mentioned, it's pretty much all the TS person can focus on. I'm a 35 year old adult who has been diagnosed for upwards of 25 years and I still have a hard time suppressing my tics when I talk about them, so I can only imagine how difficult it must be for a 6 year old newly diagnosed with the syndrome. It's like chugging a gallon of water and then trying not to think about how badly you need to pee.
Another comment was made that "He never does that at my house." This can mean one of three things. (1) He's doing it and you just don't notice it or don't know that what he is doing is a tic, (2), he's comfortable/focused/distracted enough in that environment that his tics aren't obviously evident, or (3) he's suppressing his tics when he's there.
Now, a disclaimer. Neither of these comments was made in a negative or judgy way, regardless of how I perceived them at the time. It was family who love us and love Gerry asking legitimate questions and making legitimate observations in order to try and understand his syndrome better. And there is absolutely nothing wrong with that. The lack of information out there coupled with the fact that Tourette Syndrome doesn't affect any 2 people in the same way doesn't make it a very easily understood condition. I welcome questions about it because it shows that the people around us care. I may not love discussing Gerry's particular "journey" in front of him, but I'll never turn down the opportunity to answer questions or to educate another person about it. And as he gets older, I want him to feel comfortable talking about it to others, as well.
There's no shame in our tic game. :-)