It’s 7am and Jonah’s already attacked me – he asked for “train-a” (he’s been putting an “uh” sound on the end of a lot of his words lately) so I told him it was a school day but we could go to see the train after school. This is a pretty standard conversation in our house so I didn’t expect it when he tore at my face, scratching me near the corner of my eye and mangling my glasses. For the second time since I bought them on October 23rd, I’ll be at Lenscrafters today to get the glasses fixed. I think I’m going to be their best customer. Now the almost-brand-new glasses are really mangled – no matter how I try to push and pull them back into shape they sit crooked on my face. I look and feel like a broken doll.
It’s “special persons day” at Jonah’s school which means both my mother and father will be there, and Jonah’s classroom is preparing a special Thanksgiving feast; I pray to God and little baby Jason that Jonah’s a good boy, at least for most of the time.
This past weekend Andy took care of Jonah (with help from my mom) while I went to NYC for an adoption conference for work. Because I am adopted I especially enjoy talking to the prospective adoptive parents, agencies, and attorneys – I was an exhibitor at the conference because we facilitate adoption advertising, and because I did not have Jonah for a day and a half I enjoyed the guilty pleasure of freedom. In addition to manning an exhibitor table, I was on a panel of parents who spoke about “raising a challenging child.”
All the other parents on the panel had adopted special needs kids – the kids had separation trauma, fetal alcohol syndrome, bipolar disorder, you name it. One couple had actually adopted 15 kids (!), 3 of which they had to place in a home because of violent or out of control behaviors. Jonah’s all I’ve got, and to place him is something so hard to comprehend that I’m wild to try everything/anything else we can, as quickly as we can, to seek another way.
Would I have deliberately adopted a special needs child? My first reaction is to say hell no, but when I was pregnant I told God (naive little big-bellied me) that He could give me a disabled child or a gay child, that I would be okay with either.
My running joke now is that Jonah is probably both disabled and gay.
Someone I met on an autism group on Linked In sent me an obviously self-published book they wrote about their “journey home from autism” – and a children’s book they’d written as well. Very kind, to send me the books for free, and I haven’t read them yet, but I’m going to use this as an opportunity to bitch that I’m tired of the whole Jenny McCarthy “you too can rescue your child from autism” schtick. Most of the time I think these “rescued” children were mis-diagnosed in the first place. I believe that 50 years from now it will be apparent that what we now call “the autism spectrum” is actually about 10 different things. Jonah was unquestionably born with autism- our family physician noticed issues before he’d even had his first immunization, and in hindsight I can easily see how he was very different from neurotypical babies. How can that be the same thing as the child who develops normally for however many months, gets a shot, and suddenly “falls off the planet,” losing all his or her social, verbal, and other developmental accomplishments? It can’t. The symptoms might mimic each other but the underlying cause and condition isn’t the same.
If anyone had figured out a real, viable way to “rescue” these kids from autism, we’d all be on that fucking bandwagon, trust me. But what works for one child doesn’t work for another, and the “here’s our amazing story of how we pulled our precious child out of the bowels of the hell that is autism” books are a dime a dozen nowadays. You can’t throw a stone at a bookstore without hitting something written by people who want to share the inspirational tale of tirelessly helping their child become “normal” again.
The parents of kids with autism don’t need to feel guilty about what the Superparents accomplished that for some unknown reason the rest of us haven’t been able to. Since the market is flooded with these Superparent success stories, I think what parents need is for someone to write: this sucks, and I don’t know what to do either, and I’m trying hard, and I’m afraid, and I understand, and I’m in the same boat, in the same perfect storm. I’m drowning too.
I understand. I’m drowning too.
Dear Amy,
I’ve just read most of your blog posts from today’s back to the first one in August, and I cannot comprehend how you are able to do what you do day after slogging day. I am very grateful that respite help is kicking in from various agencies to give you some relief and that Andy is helping you by sharing in Jonah’s care again. Take whatever help in whatever form this universe has to offer you and know that you deserve every single bit of that help.
Please don’t deny your strength because you cry from frustration, exhaustion and fear. The definition of courage is acting despite fear. No fear; no courage. You are one courageous, strong woman and a loving mother. I know that whatever decisions you make for your son will be made from your loving heart for his welfare and best interests.
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Amy,
You are welcome at LensCrafters any time to have your glasses fixed…that’s what we are there for!
I have not commented before, but I have been reading your blog since the day we met, October 23rd. (I helped you with your glasses!) You are an amazing woman and I had no idea what you go through on a daily basis.
Thank you so much for your honesty…it makes me realize how fortunate I am to have two healthy boys. I hug them a little more each night because of you. Jonah is a lucky boy you have you for his mommy.
Thank you for introducing me to your life.
Susan
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Thank you, Susan and Channah! I really do appreciate your support and kindness.
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One of the strange aspects about autism is an apparent disconnect between pain and communicating that there is pain. Typical children will say Mom it hurts. A child with autism might take a swing at the nearest person and resist moving from one setting to another. When asked the child will react as if saying the words it hurts has no relation to the pain. Sometimes children in chronic pain will not sleep but will stay up jumping or moving around or breaking objects. If asked a child can point to where it hurts but will not voluntarily say my toe hurts or whatever is wrong. Children who have possibly the roughest time are those with gastro-intestional or gut problems. The doctor who came to talk in the psych ward was describing the gut issue and pointed out that most with this problem end up going to Boston for diagnosis and treatment. Fortunately, Boston is only a few hours of driving away.
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Actually the doctor in the psych ward didn’t say anything at all about the “gut issue.” I think I’m savvy enough to notice if Jonah is bending over, holding his tummy, or exhibiting other signs of being in pain. I realize sometimes behaviors are signals that he is not feeling well. I am not stupid. No shit he can’t tell me he hurts. I’ve mentioned this before. I am taking him to doctors piecemeal because we can’t get in a medical institution for any length of time for a run of medical tests, not anywhere. Trust me, I’ve tried. And he sleeps fine – like a rock, actually. What are you basing this comment on? You mixing me up with another person? I don’t know why I haven’t unapproved your comments but if you continue to piss me (and my readers) off, I will.
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Amy I am so glad you had some time away in NYC! I hope you enjoyed your quiet time! Let’s get together soon for lunch or a smoothie! I miss you…and start work soon so let’s meet this week while I have the time!!! Jonah is welcome!!! 🙂 or not if you need a break!!!!!
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thanks for giving expression to a piece of my mind !
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