Reading
So, I am almost finished with a fantastic book, and I can’t wait to see how it ends. I can’t break my posting streak, though, so take this short blurb as today’s entry.
So, I am almost finished with a fantastic book, and I can’t wait to see how it ends. I can’t break my posting streak, though, so take this short blurb as today’s entry.
I got a lot of advice after my son was born and we learned of his Down syndrome. Suddenly, there were experts (“experts”?) at every turn, offering words of advice on everything from what to feed him, which therapies to start, and even tips for hiring a special needs attorney.
I remember bristling at that suggestion, thinking that if it ever came to the point where we thought we needed an attorney, then the situation would be so off base that we would just remove him from whatever was causing the problem.
Alas, first time mothers often make mistakes on which they later reflect in amazement.
I never imagined that I would have to spend hours revising IEPs, or that I would worry incessantly about the words I chose, so as to not affect the reputation of my family and negatively impact a situation for my other children. I never thought I would have to nitpick every last detail about my son’s schedule, both at school and for extracurricular activities, to ensure the highest level of inclusion. Some days (years!) I worry more than others; some activities cause more stress than others, while still other situations leave me banging my head against the wall. And, on the flip side, sometimes I find myself in a complete state of astonishment because I don’t have to work at all to find the right balance for Alex because the party on the other side of the scenario just gets it (church programs and dance studio, I’m referring to you here…). That situation doesn’t occur often, but when it does, I find myself happy but also frustrated, because shouldn’t it be that “easy” all the time?!?
Beggars can’t be choosers, though. I’ll enjoy these rare occurrences whenever they arise.
I’ve seen the term “Warrior Mom” applied to mothers of children on the autism spectrum, but I think it is fitting for all mothers who are fighting for their children. While mothers of children with special needs might find themselves with more cause to battle schools, government institutions, healthcare companies (the list could go on and on, I’m sure), all moms who advocate for their children are Warrior Moms. Our armor? The tough skin that you have to develop to take all the nonsense, set backs, and other struggles that come with this territory.
And let’s not forget the dads! I so rarely hear about the fathers of children with special needs and their advocacy efforts. They may not be the vocal parent at the conference table, but they are just as involved in the process. Advocacy is definitely not a one-person show.
While Alex has been blessed with many great teachers, therapists, and cheerleaders, we still spend a lot of time making certain that he has every opportunity available. I tend to be a “pick your battles” kind of mom, except when it comes to matters of inclusion. I don’t mess around there. I’m trying to relax this summer, and take a break from the constant looking-over-shoulders that I find myself doing during the school year. So far, it’s been difficult to step away; it’s now to the point that I feel that I’ll miss something if I let my guard down for even a few weeks in the summer. It’s pathetic to think that, right?
I’ll always feel that way, though. I suppose it’s just one of the many pieces of this big advocacy puzzle that we’re still trying to put together.
Another challenging day in the ol’ duck pond.
Alex is really feeling the transition from the structured school routine into the less structured summer routine. Yes, we have a schedule for summer, but it’s not as defined as his schedule during the school year, so it takes him weeks to adjust.
I wanted to take the kids back to the zoo today, but Alex didn’t want to go anywhere because he thought it might rain (it was kind of cloudy). We compromised, and decided to visit the library and grab some ice cream before heading to his speech and occupational therapy appointments.
He loves the library, and who doesn’t enjoy a good ice cream treat, so I thought we’d have a great afternoon. It was, for the most part, but my kids have learned the art of screwing around in the car, with the thought that Mom can’t do anything about it because she’s driving.
Ugh.
I can not stand to hear screaming kids in the car. It’s nonsense. It’s not safe. It makes me crazy. Yet they continue to do it. I’ve stopped the car, taken away privileges, yanked electronic devices out of their sticky little hands, but I have yet to find the magic solution to their minivan shenanigans.
So, imagine the headache I had when we finally got home this evening, after hearing them yell, laugh, scream, and fight in the car in between all of our destinations today. It was ridiculous. I escorted them inside, said hello to my husband, and then said goodbye as I walked out the door to go have dinner, by myself.
I had a lovely meal at Pei Wei, dining quietly and uninterrupted, and even read a couple chapters in a book that I’m really enjoying but have a hard time squeezing into my schedule. It was glorious.
And now, I’m back home, the headache down to a dull roar. The laundry needs some attention and the dishwasher needs unloaded, and I’m certain there is something I could be doing for Team Alex, but I’m going upstairs to take in another couple chapters of my book.
Here’s hoping for a more peaceful Tuesday.
I don’t know if I’ve ever met anyone who does not enjoy some type of ice cream.
I was born in a smallish town, which had several family owned ice cream joints. We could walk down to the end of our street and get an ice cream cone out of an old caboose. It was awesome. After we moved to Columbus, we lost that piece of small town charm. We had a Dairy Queen right across the street from our first home, and that was cool (and it was before DQ went super corporate, so that location was more of a hybrid), but it wasn’t the walk-up type of ice cream joint.
I still miss that.
Don’t get me wrong; we have great options for ice cream here, so I’m not complaining. I love treats from Jeni’s and Graeter’s, as do my kids. But, sadly, neither one of those fine establishments has a Smurf cone. Ah, the Smurf cone; a childhood favorite. This concoction consisted of blue soft serve ice cream, a marshmallow hat, and candy eyes. Perfection on a cone.
Today, I saw several posts from Facebook friends that mention an ice cream place not terribly far from my house. It seems to have that element that I miss about my trips for ice cream as a child, and I’m very happy to hear that they have a Smurf cone. I am definitely excited to check it out.
Seriously, I might have just declared tomorrow as National Ice Cream for Lunch Day.
Another busy Saturday in the books.
A t-ball game, a couple hours at the water park, and then another baseball game. I am one tired mama.
Tonight, though, I have the “sunburn chills”, on top of my normal exhaustion. I am rather notorious for haphazardly spraying myself with sunblock (although you can bet every square inch of the kids is appropriately coated), and the end result is always funky, sunburned stripes.
I look ridiculous.
Bright pale, with random splotches of beet red. Faaaantastic.
Tomorrow, I shall invest in sunblock lotion and cross my fingers that I do a better job the next time I venture out in the sun, which may be a while. I do not like the sun anyway (#palegirlproblem?), and getting burned is so awful for your skin, so perhaps I would be better off hibernating. Well, ok, maybe hibernation isn’t the answer, but long sleeves, floppy hat, and giant sunglasses will definitely be in order.
Here’s to a shady Sunday, at the very least.
Friday night. Dance rehearsals. Finally, dinner time.
So, this happened today:
Seriously, school hasn’t even been out a full week yet, and I’m already dealing with this crap.
Transitions are just the worst. Any parent of a child with special needs will wholeheartedly agree with that, and I suspect that a lot of other parents would concur. A change in the schedule brings about an array of difficult behaviors. It just takes one of the kids to start a chain reaction; when one acts out, they all jump on the Let’s-Make-Mom’s-Head-Explode bandwagon. By the time that we get used to summer, and these behaviors level out, it will be August and time to go back to school. And that will bring another transition. Fun!
After today, I hope the time quickly passes.
Don’t be a hater. Don’t remind me of how many wonderful memories can be made over a summer break. I get that; not every moment of our break will be like today. I’ll enjoy those precious moments just as any other mom would, but until you spend a day with my monkeys (when they behave as they do for me, not as they do for everyone else!), keep your fluffy, sparkly, rainbow-laced comments to yourself.
There may be a ban on bubbles around here for awhile, but I’m certain they’ll find some other mischief before the summer ends.
The foundation for which I work is hosting a video contest, #WhyWeBuddyWalk, to illustrate the reasons families like mine are inspired to participate in Buddy Walks across the country.
I never realized how difficult film making can be! There is definitely a reason I am a writer. I had ten years’ worth of Buddy Walk photos, plus three video clips, to sort through to create a 30 second submission for the contest. Yikes! Although two friends (and great Team Alex supporters!) contributed video clips for our video, we decided to only use a clip filmed in my backyard in order to stay within the 30 second parameter of the video-maker-thingy. (See what I mean? Totally a writer.)
Anyway, this can only begin to illustrate #WhyWeBuddyWalk, but I hope you’ll enjoy our video.
To donate to Team Alex and the 2014 Columbus Buddy Walk, please visit our team page here.
Team Alex, the Buddy Walk team honoring my son, will walk in our 11th Buddy Walk this September. Eleven?!? Doesn’t seem possible, yet here I am, working on my 11th campaign to raise money for the Down Syndrome Association of Central Ohio. Our team’s goal this year is to raise $7500, none of which is specifically earmarked for Alex; rather, all of the funds raised will benefit our entire Down syndrome community, providing valuable programming for individuals with Ds and their families.
Last year we started proclaiming the third day of the week as $10 Tuesday. This is a fun and simple way to not only raise money for our team, but also raise awareness for the event and our mission. So, each Tuesday, you’ll see me post to Facebook and Twitter an announcement to remind everyone to visit our Team Alex page to donate $10.
Of course, the option to donate more than $10 is always there, and we hope that you’ll even register to walk with us on 9/21 to show your support for Alex and his peers. The event is fantastic; what could be better than a big celebration of inclusion and accomplishments?
We also hope that when you see these posts signaling the arrival of another $10 Tuesday, you will be moved to share the posts and help us raise even more awareness of the event (and, ok, raise more money). It’s so easy to share a Facebook post or retweet a statement on Twitter, and those simple acts can really do so much.
So here we go, with another $10 Tuesday! Click here to make your donation or join our team. On Facebook? Please click here to “like” our Team Alex page so you can stay up to date with all of our fundraising efforts. On Twitter? Follow me here to stay connected.
Thank you for reading today’s post (psst…I’m on a journey to blog every day for a year; I haven’t missed a day yet in 2014!), and I hope that if you are moved to support Team Alex and DSACO you will click through the links to learn more. If you are interested in getting involved with our fundraising efforts, please don’t hesitate to contact me.
Go Team Alex!!
Beautiful weather. Good food. Great friends. Quiet reflection and appreciation for the sacrifices made by our military personnel and their families.