When MissG was diagnosed I grieved. I sought a diagnosis for MissG because of problems she was having. Problems with communicating and in social situations. Problems due to sensory overload. Problems caused by my expectations of how she should behave.
The reality is my grief was based on my own false expectations. On what I thought society wanted from me and my child. On what I thought I was losing, based on what media and health professionals told me about Autism.
But I now realise that I didn't know anything about Autism. About its creativity. Its persistence. Its resilience. Its beauty.
I am not worried that my child may never speak out loud. I am not worried that he might have some challenging behaviours. I am not worried that he may have difficulty processing sensory information. We have 2 Autistic children already and we know how to support them. What we don't know yet, we will learn if and when we need to. The fact is that parenting any child, Autistic or not, presents its own set of challenges and requires learning new skills and ways of thinking. I am not worried about facing those challenges.
I am only worried that if he is Autistic he will face bullying, discrimination and stigma.... that people will not accept him for who he is. That he could grow up knowing that in some peoples eyes he will always be less.... broken.... inferior.
But not to me. To me he will always be just fine as he is. His neurology does not make any difference to me. I love him. I will not be disappointed if he is Autistic. Sure, it would mean another intense parenting journey. Sure, it would mean more work finding the right supports for him. Sure, it would mean more learning. But why would that be a problem? He is my son. I would do anything for him. Just as I would for any of my children. Just as you would for yours.
I am not the only parent of Autistic children who feels this way.
"We cannot afford for the focus of Autism be about parental grief. Our anger and our sadness and our grief need to be directed at the targets which are worthy of it. Those targets should be the ways that Autistic people are disabled by their environments. And we need to attack those targets with ferocity. To disable the environments which keep Autistic people from thriving."
from love explosions
"When I try to imagine how my child feels about life, I take my childhood and try to imagine my life minus those experiences. But that's a fallacy. Anytime I try to subtract my experiences, I will feel a sense of loss. That same sadness happens when I imagine what I think is a "normal" childhood, an ideal childhood, that comes with a list of all the experiences a child needs for a great childhood. Karate, Valentines, kindergarten, music lessons, ballet, team sports, schoolmates, formal dances, first car, spring break, college visits. Any missed experience means that I have to cross that item off his list. A missed experience means a less-than- ideal childhood. Always. For any child. It's a flawed paradigm.
This paradigm is the same one that causes us pain when we think certain children with certain qualities are "Normal" and any difference is "Not Normal." It can only set us and an entire group of children up for isolation.
Children with a disability do not have a life minus. They have a life period. It's their life. It's not some other child's life, the parent's life, or their peers' life. It's their life.
A complete childhood has nothing to do with specific experiences. A complete childhood does have certain qualities: connectedness, optimism, playfulness, a passion for things that interest them, a feeling of proficiency at things they want to do, and a feeling of being loved wholeheartedly for who they are right now. That list is the one that matters."
from Mama Be Good
Autistic adults have spoken out about grieving Autism too.
"You didn't lose a child to autism. You lost a child because the child you waited for never came into existence. That isn't the fault of the autistic child who does exist, and it shouldn't be our burden. We need and deserve families who can see us and value us for ourselves, not families whose vision of us is obscured by the ghosts of children who never lived. Grieve if you must, for your own lost dreams. But don't mourn for us. We are alive. We are real. And we're here waiting for you."
from 'Don't Mourn for Us' an article by Jim Sinclair
Look at this picture. How could anyone honestly ask me if I am worried this baby will be Autistic like his older brother? Look at them! How could I be worried when my Autistic son is a strong, intelligent, persistent, brave, tenacious, caring, funny, generous and thoughtful young man who has big dreams and expectations for his life?
Why would I worry about having 2 sons like that?