I hear from a lot of parents and readers who talk about how we've become an inspiration for them in some way, and I am always touched by that, even when I don't feel like I deserve it. Well, the parents in the article, Michelle and Jim Foard, have become heroes to me. They are fierce advocates for their son, and they're not ones to sugarcoat the challenges he faces. When something's hard, they say it's hard.
You know how I feel about the "glass half full", "he's my special little guy", "handicapable!" Holland crowd. If that sort of sunny-side approach is what they need, then I certainly think they need to embrace what works for them. But I don't have much use for it, and I certainly don't think broken kids need it, either.
Michelle and Jim understand something that I think most people don't get, and that includes a lot of parents, even some with special needs kids. They understand that their son has limitations that have to be respected, but they also seem to understand that within those limits, their greatest gift to their son is the expectation that he will one day be able to fit into the world.
The title of the article comes from something Michelle said, in the last paragraph:
Michelle and Jim have risen to the profound occasion of raising their son. "We want to give Jimmy every possible chance to excel," says Jim. "We love him. He's perfect. But he's going to have some very serious issues we're going to have to deal with for the rest of his life." It's a future they've learned to make peace with. "It's life now," explains Jim. "It's part of everything we do." Michelle searches for another way to explain what it's like to be Jimmy's parents. Ultimately, you learn to embrace "a different kind of perfect," she says, and "a different kind of normal."
When I first read the article, I wrote to the author, Charlotte Meryman, to tell her how much I enjoyed it. We exchanged a few emails and had a pleasant conversation, and while I don't remember telling her about my site, I either must have said something or she found it on her own and shared it, because last week, I received an email from none other than Michelle Foard herself.
She expressed some of the same things I've felt, about how "usettling" it is to have all this personal information out there in the world about her family and how hard it is to receive unpleasant emails from strangers. Until now, she was unfamiliar with the whole blogging world, so all of the faceless, anonymous bile of the internet is new for her.
I hope she won't mind if I quote her email, but she said something that made me proud, both of what I'd written and of what you people said in response, and I thought you ought to read it:
So after reading a barrage of angry emails and stupid remarks, it was nice to see that someone out there really got the gist of what the article was about and could relate to our situation. So thank you and your other "bloggers?" for reaffirming that going public and being completely honest wasn't a crazy stupid mistake.
So there you go. Good stuff happens here sometimes.
6 comments:
Schuyler is so lucky to have you.
I'm so impressed by this family (and you) for opening eyes to what raising a special needs child is really like. It's a wonderful article. (And anonymous people who write mean emails are just grown up bullies.)
As always, I respect your positions, and I can see why you hate the "Holland" crowd. At the same time, I still have trouble judging any parent - especially ones with a special needs' child. It's an incredibly difficult life to adjust to, and it's nearly impossible to make all of the right choices all of the time; to know when to push and when to let go of the "ideal". I try to give the benefit of the doubt that they're doing the best they can in their own unique situation. I would hope someone else would do the same for me.
Hi Rob, I found your blog via another blog via another blog. Don't you just LOVE it when you come across a gold mine when you are being transported across the blogsphere? ;) Thank you for sharing this magazine article. I really enjoyed reading it because I love the concept of "a different kind of normal." Being Deaf, I could very much relate to that concept. I look forward to reading the next installments!
Since I've only come across your blog tonight, I read your earlier posts about who you are, who Schuyler is and what this blog is about. When I saw the video of Schuyler signing, my heart swelled with pride seeing her use my native language. It makes me proud that sign language can be a source of communication for people of varying abilities.
Schuyler is a beautiful little girl. I can see why she is the light of your life. You and Julie are doing a fabulous job raising her and providing her "a different kind of normal life." =D
Rob, you write from the heart, which is what I think a lot of us find inspiring. You talk about the doubts you have as a parent - and it may be news to you but the parents of kids without monsters have similar worries about their kids and how they'll fit in to the world. That's not meant to diss you or Schuyler's difficulties, it's to point out that a lot of what you write resonates with people because it's common ground.
& it doesn't hurt things that you are a good writer. (I'm really looking forward to your book.) There's enough vulnerability mixed with humor in your writing to capture the audience. It also doesn't hurt that Schuyler is damned cute and engaging.
Whether you feel like you're 'normal' or not, you've captured the interest of people all over the world and allowed us a view of someone else's life - different to our own. You allow us to feel like we belong as part of your village, and that's a great thing. I'll be expecting timeshare rights to that island.
Nexus
That is great, it must have been exciting to get an e-mail from someone you admire so much.
Kind of a bright spot amidst a difficult few weeks for you, with tire blow-outs, toothaches and such.
Now I want to know how his speech therapy and assisted communications stuff is turning out!!
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