I feel a lot of shame in the confession that I’m about to
make, but it represents a personal epiphany that I need to think (write)
out. As I process, I’m hoping to
gain personal clarity, but also offer insight into the mind of a mother raising
a child diagnosed with autism.
First, I know, in my Mamma gut, that Matt has more than
autism. I’m not referring to the 7
formal diagnoses he has from the list of specialists we have visited. Rather, I feel there is something that
we have yet to unearth, understand, or recognize. That said, I know that autism is one explanation for
what we observe in our son that “makes sense” and helps us to socially excuse
his behaviors in a way that most people can wrap their heads around. Mind you, I realize there is so much that I don't understand about autism—it is still a mystery to me even though see it up close and personal on a daily basis—but it is becoming a commonly accepted and
recognized label that helps me help others make sense of my Matt.
So I’m sitting on a plane flying home from England and I
started to read a book called “I Know You’re in There.” I simply read the forward written by a
boy who “used to be” autistic and I ended up in tears. He talks about his parent’s patience
and persistence in helping him find a cure for his ASD and how grateful he is
to have outgrown it. I immediately
prickled…not because of what he said because I long for it to be true, but
because I recognized at that moment that I am not his mom—I am not doing
everything I can for my son right now and the reason is what I feel some shame
about.
I think I avoid autism. I think I avoid the uncomfortable space that research takes
me to. It forces me to look at
Matt like a subject and not my son, but it also forces me to face the uncertainty
of his future, stare at what we have yet to understand, and accept that there is
still so much we don’t know. That
prospect is both exhausting and overwhelming, but in addition to that, it
scares me. Instead, I find myself
compensating for his challenges rather than looking for ways to fix them. I seek for solutions to symptoms versus
cures.
I’m not entirely sure why I do this—perhaps because I tell
myself he isn’t broken and doesn’t need fixing. Perhaps because a lot of the “cures” are still just
theories…unproven by science, but worked for someone who knows someone who had a
son who did something similar to Matt that went away when he made this simple
change. Perhaps it feels
hard to me—requires a lot of work that I don't know will pay off.
Perhaps I don’t like change and dread instability (trial and error). Perhaps because I can’t fathom it can
be simple. Perhaps because I think
a lot of it just sounds plain crazy. And, perhaps I don't know how to do or feel strong enough to do some of what I know will be required of me to really help him.
I purport that I would try anything, but I find myself
avoiding looking for creative possibilities because I cannot wrap my head
around them. I find myself
resistant to research and reading because it requires me to face my fears about
autism and Matt’s other disabilities, and to be open, vulnerable, and
emotional. Research sounds
logical, and it often is. In this
case, however, it is anything but logical—it is deeply, deeply emotional
because it is about my son.—my biggest challenge, my hardest mountain. He brings out my demons and somehow
reveals the best my soul has to offer at the same time. I cannot figure out how to do what I
need to—search far, wide, weird, and deep—to discover exactly what my Matt
needs without feeling like it might bury me.
I say that with tears flowing freely, recognizing that this
confession might make me sound horrible, but comforted by the fact that this
also represents a new resolve. I
have to do things differently if I want to get different results. I don’t even know what the first step
is. No one can hand it to me, gift
me the knowledge, figure it out on my behalf. This is my journey because I have to do something with what
I learn—implement by trial and error some of the different theories until we
find the things that work for our unique little man. I would love to delegate this, but instead I will continue
to thank the dream team we are currently surrounded by and try so hard to be
more open and listen more, read more, learn more without judgment, reservation
or fear.
Stephen Covey always said “R&I Julie. R&I.” Resourcefulness and initiative. Time to put on some big girl panties and exercise a little
R&I.
Last week at the office I was grateful to have two experiences of getting to help during appointments for special needs boys.
ReplyDeleteThe first was a boy who was 14 and was deaf and knew some limited sign language so I got to interpret and communicate with him. He is mentally and emotionally at the level of a four year old or younger. When he discovered I was someone who could sign with him, COMMUNICATE in his way with him, he lit up. We connected. And when I looked in his eyes, I was surprised to see my own son- he had such a familiar feel.. That way he looked at me struck my heart. And then he smiled the most beautiful, genuine, big, gap toothed smile and had happy squinting eyes. This was one part of the appointment- one beautiful part shared between him and me and his mom. The remaining 75% of the appointment, we struggled through with difficult communication and basically just surviving and getting him on his way trying to keep him happy!
The second boy was just eight and in a wheelchair and I'm unsure his special need/"label" but he couldn't use words and was communicating through
movement by turning his head and clenching his teeth so we couldn't see his teeth. And he was strong, physically STRONG. Mom helped hold his hand and I held the other and like earlier in the day, I made eye contact and I don't know any other word for it except that we CONNECTED. And I saw him as he truly is, beyond his outer shell.. This scared, "normal" child who is there and aware and happy and loved. Again, it struck my heart as he looked into my eyes and soul.
I wanted so badly to help him- to help him not feel scared, to help him communicate.
I don't usually get the opportunity to be present for the special needs patient appointments but I was so grateful for those experiences that day.
You know that look and connection I'm talking about- and while it was a first for me, I bet you've experienced it ten fold with your own child.
I don't have much I can say from limited experience with this, but I'm rooting for you, and for Matt, and Todd and Addy and Liam! You guys are so loved. It's so easy to look back on our lives and be able to connect the dots. The tough part is not being able to do it looking forward. Trust it will all work out exactly how it is supposed to and your answers will come as you're ready. I heard someone say once something like "the teacher appears when the student is ready."
Love you lots and I so appreciate you opening your heart and getting to learn and live and love with you.
This is the Steve Jobs "connect the dots" quote I was referring to from his Stanford Commencement address in 2005- the whole thing is great but this part is my fave:
ReplyDeletehttp://www.quotationspage.com/quote/40889.html