Where Else You Can Find Me

Saturday, August 16, 2014

Best Laid Schemes

It's almost that time, y'all.  School is about to start.  We have one week and two days until we're back in a routine.  You know that saying  "The best laid schemes of mice and men..." Yeah, I had all these plans similar to my list of things I was "fixin to" do before school let out.  You can read that here.  I found the "new schedule" I'd written up on the first Monday of summer vacation.  It went like this:

Do you know how many times we followed said schedule? Exactly none.  I had these great visions of proving my parental prowess, and failed miserably.  You know the area in which I excelled? Letting my kids have free rein over their day.  There were several that I didn't even have to make breakfast...we had brunch instead.  That's one less set of dishes, my friends. 

By this time last summer, I'd written our letter to the teacher.  It's a good one.  You can read that here.  This summer, I'm wondering if I even need the letter.  Big Brudder has changed and grown to a point that has me beyond pleased.  Is he "typical" ? No, but more often than not, I feel like "he's got this."  The NT (neurotypical) Wee One is going into big kid school; I honestly feel like he needs a letter to the teacher more than BB.  He's definitely more challenging at the moment.  His apple doesn't fall far from the maternal tree, bless his heart. Maybe this year instead of letters, I'll give those tiny little liquor bottles and gift certificates for a massage.

I'm ready for routine. I'm ready for my boys to miss each other at the end of the day. I'm ready to miss my boys at the end of the day. I'm ready to clean my house (did I jsut say that?) and to be able to enjoy the clean for a couple of hours. I'm ready to rock this school year like the awesome helicopter mama bear (did you know bears fly helicopters? They totally do!) I am.






Sunday, August 10, 2014

Here's what this Autism Mama wants from YOU

The good news is it doesn't cost you anything!  That's a bonus, right?  There is this great sociological principle called Verstehen.  The definition as below is from sociologyindex.com

VERSTEHEN

Verstehen is associated with the writing ofMax Weber. Verstehen is now seen as a concept and a method central to a rejection of positivistic social science (Positive School, although Weber appeared to think that the two could be united). Verstehen (ferchaen) is the use of empathy in the sociological or historical understanding of human action andbehavior.

Basically, Verstehen is taking empathy one step further.  It is saying although I don't walk the walk in life you do, I will put myself in your shoes.  I will listen and hear you. 

An example where I would love to see this is when we discuss anything at all!  This means, politics, religion, vaccines, wether I would change my child's neurology or not, wether I homeschool (or in my case definitely not), wether I buy all organic, choose gluten and casein free or not. Everything.

In having a discussion on FB (one of the rare ones where people didn't get irate over the topic of neurology I came to this realization. There has to be room at the table for all of us.  We, every single one of us, need to embrace and support one another, not despite our differences in opinion but because of those differences. There is so much to be gained by actively listening to those with a different perspective.  I would never ever change my kiddos neurology.  But you know what?  I recognize he can tell me he loves me, can tell me (most of the time) when he's ill.  My son doesn't have PICA (the desire to eat not nutritive things), he doesn't smear his feces. If he did, I recognize I might feel differently.  Our walks are different.  Everyone's walk is different.  You came to your point of view because you are uniquely you. I respect your walk. 

Do I always practice what I preach? Nope. I'm trying.  I'm trying really hard to remember that just because we disagree, that disagreement is not an indictment on my personhood.  Feel free to remind me of this. 

So let's quit calling "BS" when someone expresses a point of view we don't share.  Know that my point of view isn't one of popping rainbows and unicorns.  Someone else's is not that of bitterness and anger. Instead, let's take a breath, practice VERSTEHEN, look at how that other human we are sharing this world with came to their point of view, and play nice. If we do this, even just sometimes, I promise you we will be nicer human beings to be around. 

Xoxoxo and 

VERSTEHEN on my friends!

K

Thursday, July 10, 2014

You know what they say about opinions...

You know that old saying about opinions...well, my full moon brain is in full effect and these are the opinions I've been thinking about in the wee am hours.

The whole "would you change your child" thing.  Disclaimer: I come from the perspective of a mom to a profoundly gifted, child with Aspergers as well as a cleft lip and palate. Just because my child is on the "high functioning" end of the spectrum does not mean that he does not face challenges and obstacles that often far exceed what I feel like he can handle.  Looking back to when Big Brudder was two, my answer probably would have been different.  That was a time when he wouldn't eat...for days...I mean days at a time.  His meltdowns were hours if not the whole day long.  But you know, if I'd had a magic pill and changed him, changed his neurology at that very early point in his development, he wouldn't have some of the best coping skills out there.  Due to his cleft lip and palate, my son has had countless surgeries.  Several summers ago, he had a hole drilled into his hip where they took bone marrow and injected it into his gum-line.  You know what that kid did?  He rocked his bone graft like a champ.  This kid, he is a survivor. He is a champion of champions.  Does he still perveserate on things?  Oh, the perveseration that goes on in this house.  Between me googling sofas and him asking me every three minutes about something he's focused on, it's a miracle anything really happens around here. Does he still stimm?  Like crazy, but he's learning when and where it's acceptable to do so.  Does he still meltdown?  Honestly, not really. On the very rare occasion, but he has learned to cope and use the skills he's been taught to work his way through. This kid avoids eye contact like the plague, but you know what he taught himself to do when he was three or four years old?  Look at people's noses so that he was meeting the social expectation of listening.  Two years ago when I was speaking with his principal about an issue that was happening at school, I had a realization.  I understood, in that moment, that through the struggle of an awful school year, he had grown by leaps and bounds.  This kid is ready for whatever life throws at him.  He can handle more than most grownups I know.  Does that mean he has friends? Not a real one.  He's got a few that tolerate him. Maybe, I would change that for him.  I would make kids see him.  See past the squawks, see past the awkward gate, see past the inability to hold a real conversation. But, ultimately, he's got this. He's got whatever it is that life throws at him. No changing him.  Besides, he is where the unstoppable force and the immovable object meet.  No changing him even if I wanted to.

I've also been thinking about intent.  So many people get so angry and frustrated (me too) by small things people say or do "to us."  Lately, I've been thinking about the intent behind those actions.  Surely, you've been given parenting advice.  One of my faves was "He'll eat when he's hungry." Yeah, no he won't.  That made me so, SO, SO mad.  But, should it have?  If I had had the clarity to take a step back from those situations, I could have asked myself, "Does this person mean me or my child harm by saying this?"  Same goes for the "you can hardly tell he had a cleft."  That is said meaning well.  And, it means that my kid is gorgeous.  Because he is. Along those same lines, a friend of mine blogged the other day (I had also written a FB post about this, so I'm totally not stealing her thunder, but you can go read her blog about it HERE  ) is all the "what not to say" open letter type stuff.  I get that when people say things, it can be taken a different way than they mean, but let's be honest.  If you stop. Really, truly stop and look at the intent behind those words, shouldn't you a. be thankful someone said anything rather than ignore whatever situation you are in?   b. be thankful that didn't say eff you, or if they did be thankful they said what they truly meant? I can keep that in mind, unless of course you question my kid's dx.  Then, we've got trouble and I might take off my earrings and flip flops. ;-)

Autism and vaccines:  Find my thoughts on that click here but not if language offends.

Finally on the autism communities' us vs. them vs. them rife:  stop it.  Stop it now.  Our walk is our walk, your walk is your walk, their walk is their walk.  Parenting is hard, typical, ASD, HFA, severe autism and a myriad of other stuffs. No one has the the exclusive on hard. Get over it.

So, now you know my opinions on everything almost under the sun.  If you've waded through this, you deserve a treat.  Go get you some chocolate or coffee or something. 

xoxox
k



Cleaning

So, I've been doing a little cleaning.  Well, a LOT of cleaning.  In the spirit of trying to get my house a little less disgusting, I also cleaned out my old computer files and came across some real gems.  I'm not even being sarcastic there.  In the tab that says things I've been hoarding, there are some great resources.  There are two versions of a food diary and a calorie index that we used when we were tracking big brudders weight and moods for food aversions.  Ironically, we thought the aversions had to do with his cleft lip and palate. Nope. Anyway, these paved the way for some good food chaining and helped us figure a few things out.  I hope they help y'all too.

xoxoxo
K

Friday, May 30, 2014

20 things I was fixin' to do before school let out...

Cr@p in a basket.  It's the last day of school.  Here's 20 things I was fixin' to do:

1.  Get my ladies check up.

2. Go to the dentist.

3.  Color my hair.

4.  Fold and hang all the laundry on the "guest bed"  aka folding table or as hubs calls it, the giver of socks.

5.  Clean closets.

6.  Clean the bathroom.

7.  Blog more.

8.  Finish my children's' book.

9.  Find an agent for said children's book.

10.  Have lunch with my friends.

11.  Mop my floors.

12.  Clean off the coffee table.

13.  Go furniture shopping.

14.  Stock up on sunscreen.

15.  Stock up on snacks.

16.  Get our summer lessons ready.

17.  Loose thirty pounds.

18.  Shave my legs.

19.  Organize my pantry.

20.  Read a book.

I'll totally get right on that checklist on August 25th.

I've totally got 2nd and 4th graders in my house.  Whoa.

Thursday, March 27, 2014

One in...

So they came out today.  The new autism numbers from the CDC.  They are already outdated.  Am I scared of those numbers?  No. Not the numbers.  Do I feel like Autism is an epidemic?  No.  Do I feel like there needs to be a cure for autism?  Nuh-unh.  For if we cure autism, we simultaneously rid the world of some amazing minds.  Amazing people.  Amazing experiences. Amazing opportunity for growth.  If we were all NT, if there were no people with downs syndrome, no people with physical differences, what a boring world this would be.

What I wish the CDC would focus their money on instead of promoting the idea of an epidemic, is spend time with Autistic children, Autistic adults, parents of Autistics.  Find out how to best serve the needs of this community.  My son won't stop having autism when he turns 18.  Find out what this community needs.  Find out what the schools need in order to better serve our children and all special needs children.  Find out what the people who service adults with autism truly need. Find those things.  Make those things a priority.


Friday, March 21, 2014

My week so far...

Fist a note, I'm typing this on the iPad, so if it's wonky know that it's not my fault.  I really do have fairly good grammar skills and spelling.  No I don't have good spelling; that's why we have spellcheck and autocorrect, right?

So I've been really angry this week.  Ranging in everything from anti-vaxers using autism as a reason for not vaccinating their kids to the mommy wars I've seen started by moms of gifted kids on a blogger who wrote all kids are gifted.  Basically, no one was going to be able to say anything that wasn't going to piss me off.  My thoughts on vaccines are it's an individual choice and there are several valid reasons not to vaccinate without using autism as one of them.  What that says to moms like me is "I would rather my child die from polio or another terrible, preventable disease than be like your child."  I'm not gonna lie, that hurts.  

Now, the mommy wars. Can we stop?  For one damn minute and be kind to one another?  A mom whose kid didn't get the letter saying she qualified for gt, wrote a blog about how all kids are gifted and all kids are talented.  The response from moms of intellectually gifted kids was insane and bordered on bullying.  As a mom, it made me so mad to see these "gifted" parents act like children.  I have two "gifted" children, but I understood what this mom was saying.  There are all kinds of giftedness and all kinds of talent.  These moms in an attempt to explain why gifted programs are necessary for our intellectually gifted kids acted pretentious and in my opinion did more harm than good.  They even began saying gifted is equal to not bring neurotypical.  Let me tell you, there IS a difference.  I have one twice exceptional (gifted plus Aspergers) and one neurotypical gifted child.  They are vastly different scenarios.   I had a moment where I was tempted to call them out, but thought better of it.  Because isn't that exactly what was making me mad?

Then, it happened.  Last night I watched Parenthood for the first time in a long time.  Max Burkholder's character Max has Aspergers.  On last night's episode, Max was going on an overnight field trip and didn't want  his mom, played by Monica Potter, to chaperone.  Despite her hesitation, she let him go without her.  Because after all isn't it huge that a kiddo wants to grow up, wants to do it alone?  That's progress and we have to let our kids find their wings.  Then it happened.  THE phone call.  You have to come get him.  I wasn't expecting what happened next.  I totally should have.  This isn't the first time I've watched this show.  Doesn't it exploit my emotions every darn time?  The scene was my worst nightmare while also being one of my greatest hopes.  Max tells his parents the vile things the kids have done and breaks down.  It was beautiful.  It was raw. It was perfect.  I know my kid will continue to be an easy target for kids who are trying to figure out who they want to be in this world.  So, when the bullies strike (notice I don't say IF), I hope my son feels safe enough to say me the things Max said to his mom.  I hope that I have the courage to take off my seatbelt, crawl into the backseat and hug him anyway.  

I think that scene hit at what my real issue has been all week.  Fear. Frustration.  Wanting.

Xoxoxo
K