Welcome

Hello! My name is Shannon Taylor. I'm a former editor living in the woods of Wisconsin with my husband, four children, and lots of pets. I created this blog as a place to gather my thoughts and share ideas as I squeeze in some writing whenever the kids aren't looking.

Featured Posts

Recent Comments

  • Mary Stoltman: Awesome! You are hilarious….glad it missed us.
  • Diane: To give you an idea how crazy it is…no snow in White Bear Lake, dusting of snow on roofs in Oakdale and...
  • Tim: Yep…no snow over here in Bloomington, MN. Commute was no issue either, once I got dug out of Prescott. I...
  • Shannon: Tim said there was green grass 20 minutes from our house. Crazy! The snow day part was fine, but we could...
  • Patti: Beautiful scene, but belongs in January! Funny that we didn’t get anything here- just an hour away! I...

Books We’re Reading

What Alice Forgot

Book Club

Pink Rabbit

Bedtime Story

homemade_life

Inspiration

craftaday

For Fun

Becoming a Writer

On Writing

By 2g1c2 girls 1 cup

Site search


November 2011
M T W T F S S
« Oct   Dec »
 123456
78910111213
14151617181920
21222324252627
282930  

Fun Activities for Kids

Categories

The Road Less Traveled

I haven’t written anything for A Mom’s Year for more than a week. I’ve never had writer’s block before, but when Will got an official diagnosis of Asperger’s my words dried up. Even though we’d known for a long time that something wasn’t right with his wiring, being told that Will has autism felt like getting the wind knocked out. And because no one in this family ever does anything by half, Will also got a diagnosis of ADHD (minus the “H”).

So once again we find ourselves on the road less traveled and there’s a lot to learn about and figure out and try to understand.

Part of the figuring-out process has included working out what and how much to say about all of this—here and in regular life. The thought of making a big announcement feels odd and stilted—I mean, he’s still Will. But at the same time it’s weird for me to write about Christmas projects or chat about the weather when this is all I can think about.

My truth has always been found in books and poetry, so it was no surprise that I got my answer in an article by writer and illustrator Anne Sibley O’Brien: ”We’re the myth makers, the image seekers, the story bringers. Our calling is to brave the hero journey, deep into the universe of our individual and collective unconscious, to return with the treasure that will save the kingdom: meaning.”

I don’t want to lay Will bare for all the world to see, but if my experiences as his mother can help anyone at all, then I will gladly share what I can. I have no idea what’s going to happen, but the thought of shaping all of this into something meaningful makes me feel a lot better.

And already I am feeling so many instances of God’s grace as we stumble forward on this not new but newly-defined path: in the dedication and compassion of teachers and staff at Will’s school, in the stories of friends who are parenting their own children with autism, and especially in Will himself. My Grandma Charlotte, who was a mother of eight and a grandmother and great-grandmother of many, once said, “I love all my grandchildren, but there’s something about Will.” Yes there is, and bless you for seeing that, Grandma. I see it, too.

So there you have it. The word autistic still makes me wince, but I think I can go back to talking about our regular old life and Christmas and everything that’s beautiful and wonderful about this time of year.

Related Posts Plugin for WordPress, Blogger...

Comments

Comment from Kristin
Time November 29, 2011 at 10:55 pm

Shannon, you hit the nail on the head: he’s still Will! And he’s awfully lucky to have you two for parents, because you will see the silver lining and doggedly learn how to meet the challenges. Thanks for posting. Your family will be in my prayers, especially as you decide how to talk about it.

Comment from Shannon
Time November 29, 2011 at 11:02 pm

Thank you, Kristin. I’m already feeling more peaceful because now we know what we’re dealing with instead of just speculating. There’s lots of hope out there.

Comment from Stephanie
Time November 30, 2011 at 1:04 am

I only know you through your blog, but you seem to be a very strong, close and loving family and I’ve no doubt you’ll all successfully face this challenge together. Will is such a handsome, happy little boy in that photo! A true treasure.

Comment from Shannon
Time November 30, 2011 at 7:42 am

Stephanie, that is so kind of you to say. Will truly is a treasure, and those big blue eyes and lopsided dimple of his will, I’m sure, help him a lot through all of this. ;-)

Comment from Shannon
Time November 30, 2011 at 7:43 am

By the way, the photo is from Lily’s birthday luncheon at the American Girl store. You’d never know from the photo how much Will was suffering from having to be there!

Comment from Judy
Time November 30, 2011 at 10:56 am

Shan; Will has always been one of my favorite kids, moreso now than ever. I’ll take him, Aspergers and all!!

Comment from Denise
Time November 30, 2011 at 5:38 pm

Hi Shannon,

My son Carter also has Aspergers. We also knew something was off with him and got many diagnosis that didn’t make any sense. This was the first one I knew was correct. The way I look at it is it’s a label to help me help him. I only tell him the good about Aspergers, that it makes him SO funny and SO creative. I never tell him it will hinder him in any way. I love the way his brain thinks and life with Carter is always so much fun. A person I follow on Facebook and have read his books is John Elder Robison. He is an adult that has Aspergers and wrote a few books that really helped me understand how Carter’s brain works. I wish you all the best.
Denise

Comment from Jennifer
Time November 30, 2011 at 11:23 pm

Shannon, you are so wise and such a wonderful mom. I admire the way you are looking to books and poetry for guidance on this journey. Even though I don’t know him well, I knew from the way you and Tim talked about him that there was something so sweet and whimsical about Will, some qualities that made him unique and especially loveable. I know this diagnosis must be scary, but with his family’s support, Will is going to be fine. Can’t wait to see you all on Saturday. Lots of love, Jennifer

Comment from Shannon
Time December 1, 2011 at 9:04 am

Thank you, thank you for all the kind and supportive messages. I can’t tell you how much it helps to hear about other people’s experiences and to have you say such sweet things about Will. He makes me smile every time he comes in the room, and that’s saying something, isn’t it?

Comment from Marilyn
Time December 5, 2011 at 10:48 am

I’m never quite sure how to best support a blogger friend, so I guess I’ll just say that I find you, your blog and your family (through your blog) to be lovely. I continue to feel that way, and I’m glad you’re back.

Comment from Shannon
Time December 5, 2011 at 11:11 am

Thank you so much, Marilyn. I think you know exactly how to support a blogger friend. :-)

Comment from Lynn
Time December 6, 2011 at 12:12 pm

Shannon,
I love all the things that you write about. You are truely a wonderful person. Will does have that special way about him. There is something about Will that when you see him, you just have to smile and call out a Hello to him :)

Comment from grampa jeff
Time December 6, 2011 at 1:04 pm

That’s cool that you remember grandma saying that, pretty smart lady. Will is so smart and curious and wonderful.

Write a comment





Featuring Recent Posts WordPress Widget development by YD