Taking a trip with the kids is nothing new for us – we’ve tried to fit some kind of real trip in to the kids’ schedule every year, as we try to keep things as ‘normal’ as we can, even in the situation. None of these really have been big ‘vacation-trip’ things like a lot of other families with children our kids’ ages do, though.
But, to every thing and all. We’ve decided to take the plunge and plan a real vacation-trip. Continue reading →
I… think it’s actually been a while since I last talked about the Monster and curling. Whoa.
Quick recap – for those who haven’t been around for a while, I curl semi-competitively myself. R and the Monster have been curling in our local club’s Middle Rockers program for the better part of two seasons now, and the Monster is the only child with a developmental disability that is in the program. This has us running into interesting issues now and again, due to the Monster’s deficits, but… when you go from a place of ‘assume competence’ and ‘adapt where you can’… Continue reading →
Before anyone worries – it’s just been a very busy couple of weeks here, on this side of the screen. (All the better reason, if you don’t follow the Facebook page or the Twitter account, to do so – I’ve not been wholly quiet while I’ve been gone.) . But I’m going to try, now that things are calming down offline, to get back to a regular cadence and…
What? What have we been up to? Oh!
For starters, we took in an inclusive religious service last weekend, in advance of Purim. Continue reading →
As I mentioned last week, the Monster and I were offered the opportunity to catch a Ravens game, thanks to the kindness of a donor at The Arc Baltimore. Last night was the game, and so we went.
I love football. (I love most sports, frankly.) As I mentioned, I grew up getting to go to sporting events now and again – from baseball to football to hockey and basketball – and seeing sports live is something I rather enjoy. We’ve taken the Monster to baseball games, largely minor-league, previously… and it’s definitely easier when you are in a smaller facility where you can walk about and still see the field (and definitely more so when you’re going to these events as part of a group of children in similar situations). A football stadium is not one of these kinds of things. Continue reading →
I’m going to do something that might be… ill-advised next weekend, but reminds me a lot of my childhood.
A fond memory of my childhood was going to sports events with my father. Dad had season tickets to the local basketball and football teams, and we had neighbors who gave us tickets to go to the occasional baseball game. As a result, I spent a lot of time seeing sports live – the way they’re really meant to be seen – and… well, given that I grew up further north than where I live now, a lot of the football, therefore, was outside in the winter, bundled down in a seat and cheering on my team, and as a relatively neurotypical child, I could easily handle being out there in the cold and crowd for a few hours. Continue reading →
One of the truisms about having children in general – and especially when you have children with special needs – is that being a parent can do horrible things to your relationship in terms of giving time for one another.
I’m not saying that I regret having kids – the Monster and R are wonderful critters who make life fun, and I adore being a father and spending time with them. But, it definitely puts a cramp on spending meaningful time with my wife, both in terms of mood and energy, and when you factor in the attempts we make to still sustain independent lives for ourselves in addition to our marriage… it’s a lot.
So a while ago, the wife and I decided that we had to make an attempt on a regular basis to actually get away and spend time together. Continue reading →
It’s been a few months now of ABA for the Monster.
I’ll admit that… well, we came into it without my having a very good idea of what we’d get out of it, to be honest. I’ve heard about ABA – applied behavior analysis – before, and we’d not availed ourselves of it because we didn’t know how to fit it into our lives. That my insurance through work happens to pay for a lot of it was the kicker to get us to rearrange our lives to fit it in, and we’ve gone with the theory of ‘that which is not harmful and might work is worth trying’, so… Continue reading →
Long before the children were a thought, my wife and I managed to get away twice on cruises. It’s fun enough to me – most of an all-inclusive coupled with actually getting to see different places – but as we’ve had children, that’s not been as much of a thought to me. And then throw in the Monster’s Autism, which makes any trip scary enough… and we’ve not really gone anywhere.
So when Autism on the Seas announced that they were doing a ship-tour nearby, coupled with a discussion of their services, we jumped at the chance to both window-shop and hear about something that might make it possible. Continue reading →
I started out this morning on this topic on Twitter, and realized I probably should just expound on it here instead.
When we’re out and about, we usually refer to the Monster as “non-verbal”. I took him with me to a meeting on Thursday night, and one of my friends commented that she doesn’t understand why I refer to him as “non-verbal” when he’s clearly able to speak.
Today being the first day of Rosh Hashanah, we went to shul as a family.
(No, don’t be shocked that I’m on the computer. :p )
Granted, the Monster’s school is closed today for the holiday, more perhaps a function of the number of observant staff than the student body. It’s slated to be open again tomorrow, and he’ll go to school for his therapies then. R’s school doesn’t close for the holidays, but he has an excused absence.