Showing posts with label Love that Max. Show all posts
Showing posts with label Love that Max. Show all posts

12 April, 2012

Autism: Around and About and Aware

We are on week two of spring break around here, and my lovely pre-teen son is taking nicely to sleeping in until 9:30am (thank you to Sage who is getting my girl to kindergarten this week!) While it usually feels a little frantic and unstructured during spring break, this year feels like some mostly calm time I've been able to spend with each of my kids, and around visits to the movies, day trips and the museum,  I've been keeping myself busy.

It's Autism Awareness month. Since we are well aware of autism in this circle we have moved on to Autism Acceptance month instead. Thinking Person's Guide to Autism has a great "Slice of Life" series where we have given the same set of questions to autistics all over the spectrum. These are people in your neighborhood, in your classrooms. They work in the cube next to you, and skateboard at your local park. They are individuals, not statistics. Those 1 in 88s and 1 in 54s and all of that data that's been flying about? 'Those people' have always been with us, but we are getting better at spotting autism earlier, which will hopefully get everyone the support needed to be a happy, healthy, valued, and productive part of society. I know that "awareness" is still important because there are people that are ignorant, misinformed, or disinterested...even my spell check does not recognize 'autistics' as a word, and we have a long way to go, but we are focusing on acceptance around here.

I have another post up at Dandelion. I'm a regular contributor there,  or at least I am when I can get my act together. Dandelion is a great resource for Bay Area parents, and is not just autism focused.  I write there about three times a month. They have a very active events calendar, and happily take new events, so if you have a special needs benefit, auction, speaker series, or sibling group, head to their calendar and ask to have it added.

Last month Care.com asked me to write an article about Learn the Signs, Act Early campaign that the CDC has put together. It can be very emotional when you think your child is developing differently than other kids, but the important thing to do is keep your head on and check-in with a professional who can complete an evaluation of your child's development. With good information you can get your child every support he or she needs. I have more to say on this, and some good tips that I figured out when we were still figuring out our boy when he was very young.

The wonderful Ellen Seidman, who writes Love That Max turned over her Parents.com column this month to celebrate Autism Awareness/Acceptance. Shannon wrote a lovely post about Parenting Autism in the iPad and Internet Era.
Ellen asked me so great questions, including what are three things I want other people to know about my kid. My number one answer was: “Just because he can’t talk doesn’t mean he can’t hear you. Kind words, mean words, he hears all of it. With my son, and with any person with disabilities we should start with, “Hello.”” You can read the entire post here. 
I'd like to thank Ellen for hosting us in her column. I feel lucky to have her on "my team."

And I am nominated at Babble.com as a Top Autism Blog for Parents. Thinking Person's Guide to Autism has been nominated in the "write-in" section too, so stop by and give us a thumbs up if you think jennyalice.com or thinkingautismguide.com serves parents well. Maybe one of these days I will either a) make it on a list that does not require someone to vote or b) stop feeling like I need to chase votes once I am on a random list. Next year I am going to create a list of Top Autism Blogs in My Family. I am pretty sure I will make the cut :) I was happy to see so many of my fine friends and their amazing words honored already, and knowing that we are all serving this community is a great feeling.

There are lots of other exciting things in the works. TPGA  has been all over the radio across the country, so if you thought you heard Shannon Des Roches Rosa, you probably did. And we are working on more venues for book readings. I was thrilled to find out last week that an education class for teachers is using the book as classroom text. If you know anyone who is interested in using the book as a text in an educational setting please contact me: jennifer dot myers at gmail dot com. I am happy to help get the book out to you.

My voice is hoarse and my house is a mess, but my heart is full and my kids are happy.
Be well friends.


12 August, 2011

Home Again

I went to BlogHer11 last week. I road-tripped with one of my bestest friends AND her mom AND her girls, and managed to be packed and ready to go at 5am. We slid past the San Luis reservoir at daybreak, and in record time were able to gobble delicious Mexican food in Southern California. I even managed to sneak a quick visit in with my Dad over those delicious enchiladas. Another couple of hours, and  I got to meet the cool group of people at Oceanhouse media. If you don't have any of their apps go check them out. Road tripping with someone who has a plan is an awesome thing. We were efficient, on time, and uhm, she drove the whole way to our destination. My stay in San Diego/La Jolla was lovely of course. Our hostess has created a welcoming, easy-to-slip-into type of place--she even has homemade jam; it is a tough place to leave (and I thank you again for having us.)

I had the best bunk mate ever. We talked, and talked, and talked, and then she told me a story about the axle on her car? Maybe, and I fell asleep. Sorry I'm so rude. Sorry I "snore lightly." But mostly I'm really sorry that we don't live closer, because She made me laugh so hard that other people couldn't even type. That tweet by Liz Ditz above should say "laughed so hard she couldn't talk for 5 minutes", but it's also likely that SJ could make me laugh hard enough to get knifed five times too. It's not often I get to have that many uninterrupted conversations with someone so smart and sassy who also has such a depth of character.  She even convinced me to do a little cooking demonstration thing with Knorr with Marco Pierre White. It was fun, Chef White was very gracious, and I got some cool free samples of Knorr stock and a signed book, and an apron which I actually really needed. And Chef White did not shame me when I basically needed a half cup more of parmesean on my risotto. I really love risotto, especially with parm and asparagus, and cooking with friends is one of my favorite things.

I danced at the evening parties. I even fell on the dance floor like I did at that wedding when my brother threw me across the wood in a reckless Tango move.. but this time I was the designated driver, so it had more to do with my tiny heels and my amazing dance partner Jen Lee Reeves, of BornJustRight. Who also made me laugh quite a bit, now that I think about it.

And of course there was that great Special Needs mini-con on Friday. I was honored to help the unstoppable Julia Roberts (not that one) from SupportforSpecialNeeds.com. I didn't do much, but she did a fantastic job setting everything up, and the 80 or so people that came were some of the vibrant, deep-thought, hilarious bloggers I know online. The speakers on the panel were Shannon Rosa, Auriela Cotta and Robert Rummel-Hudson. I think I can call Robert Rummel-Hudson a friend now, and not just because I brought him little tiny ice cream bars at one of the breaks, but because we share the same passion for wanting to come together as a group, united as parents of special needs kids, in our desire for positive change, and take on those completely uncomplicated things like health care and insurance reform.

BlogHer is one of those magic places that helps blur the lines between IRL (in real life) and online  friends, and that's a good thing, because as we get more wired in, with Google+ and Twitter and Facebook, it's hard to say I'm not "close" with someone just because I can't meet them at our Thursday morning coffee. As I sat next to Laura Shumaker at the mini-con, and later at dinner, I realized how lucky I am that I can probably hang out with her as much as our schedules allow (and we are totally going to do that as soon as my children get their buns back in school), but with BlogHer, and the whole interwebs thing, parents of special needs kids don't have to feel so isolated anymore, and anyone can hear all of the wise things Laura has to say just by visiting a website.

Things might get sort of tough sometimes, but we can find each other in the middle of the night online. On those late nights when we think that we are the only person with a ten year old who is wandering the house checking for ways to get outside, it's nice to know I have friends on another coast who can offer advice or support. We never would have had the opportunity to help each other 20 years ago, and two years ago we didn't even have a mini-conference. Talking with Ellen, from Love That Max and Shannon, of course, I know we can build on Julia's good work this year and create an entire day..let's expand that mini-con, I think we have a lot more to say, and even more to do.
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