I am my brother’s keeper. And so are you.

I’m thinking of my brother Joe on his birthday today. For two weeks each year we are the same age, but on New Year’s Eve he takes a step ahead of me again. In the back of my mind, all through my life, I’ve known that one of my roles is to be my brother’s keeper. It is only in recent years that I have been able to see him more fully for who he is in his own right, separate from me.

What we all wouldn’t give, those of us who know him, to have fuller access to the brilliant mind we have only been able to see at a glimpse. When Joe was preschool age, in a program focused on teaching such life skills as toileting and eating with utensils, his teachers one day realized he was reading. My parents credit Sesame Street and The Electric Company–as well as Joe’s intelligence–for that self-taught accomplishment. When we were teen-agers, he used to sit on the living room floor each afternoon and write a sports report on a manual typewriter, perfectly capturing the voice of sports reporters. He still reads the newspaper every day, follows politics, listens to religious talk radio (that one’s a puzzler for us), watches sitcoms from our childhood, and tunes into every televised game the Seattle Seahawks and Mariners play. He adores dogs. When we were kids, he taught ours to chase cars. Some of you might remember him running along the side of the road in front of our house, barking at cars as they drove past, our terrier mutt Fritzie at his heels. (The 70s were a different time, eh?)
 

Joe was not accurately diagnosed (with autism) until we were in our early 20s–which means that his entire formal education failed to address many of his actual needs or develop his intellectual potential. Academics were basic and played a minimal role in his schooling, which is outrageous to me now but did not seem wrong then. Joe was already 10 when we passed the law that guaranteed a free and appropriate education to all children, and I think my parents were grateful that he was in school at all.

While the shifts in understanding and acceptance of autism that have happened in our lifetime are wonderful to see, wondering how things might have been different for him and our family if he’d been born at a later time is a mental path I rarely travel down because it is too painful (and pointless). A lack of services and understanding have limited his life to a degree I can hardly express. The world is a dangerous place for a young, mute man who cannot/will not comply with social norms, such as following directives from police officers. My parents have done what they felt they needed to do to keep him safe in it. (Maslow’s hierarchy of needs for the lose.) 

It has long seemed wrong to me that Joe’s care has been primarily the responsibility of our family alone. I am my brother’s keeper, but Joe is his own person, with his own feelings, needs, habits, and dreams. (After “graduating” from high school–which meant only that he turned 21 and was no longer eligible for educational services– he told our dad that he wanted to go to college, “like Rita.”) Joe belongs to the world as much as any of us do. What happens to the Joes in our society who do not have a safety net of family? What happens to Joe if the one beneath him frays and cannot hold? How do we value and care for those among us who cannot fit into all of our round holes? Or any of them? How can we better support them in being their full, autonomous selves?

Joe is my brother, but he–like any of us–is fundamentally yours, too. We haven’t done very well by him, in many ways. Later today, he’ll be opening a dog calendar from me. It’s what I give him every year. He’ll hang it in my parents’ utility room and faithfully turn its page on the first of every month, and he’ll be happy to have it. He seems to love those calendars. It’s fine for what it is, but I sure wish I–we– could give him more, and that in the pages of the days in the coming year he might find, in addition to cute dog photos, a life with more independence, freedom, and connection to his fellow humans. I hope that, for Joe, as we are coming to know better, we can do better. I hope it’s not too late for the boy who was born too soon.

 

6 thoughts on “I am my brother’s keeper. And so are you.

  1. Kate says:

    Happy belated birthday to Joe. I hope he had a wonderful day. I recently listened to an interview on Wisconsin Public Radio of a philosophy professor on his book – written on the importance of family. Your post parallels some of what he was saying. I wish I could find the interview (and the name of the book he had written). It (as well as your post) have me thinking a lot about family in the micro and macro sense.
    Kate recently posted…2018My Profile

    • Rita says:

      Oh, I’d be interested in that. Sorry for the delayed response–the re-entry into regular life was a bit brutal. Hope it’s not been the same for you.

  2. Marian says:

    Like Kate, this post has gotten me thinking about family — the lengths we go to do what we can for them, what we hope for them, what we see in them — as well as community, because of course, you’re entirely correct: we ARE all our brothers’ and sisters’ keepers, we’re all connected; any hard-hearted notions that we aren’t are entirely missing the big picture. And yes, there have been leaps and gains, but there’s still a lot of work left to do, especially when it comes to the needs of the caregivers. That seems to be a common thread that is still not being adequately addressed by society/government, even here in Canada.
    Thanks for sharing this, Rita.

    • Rita says:

      Yes, I see the issues of caregivers in the experiences of my parents and in Cane (in dealing with his daughter’s needs). There doesn’t seem to be much feeling among those currently in power in the US that we have obligations to each other at all–unless it is to behave in ways that those in power want us to behave. But don’t get me started on that…I might not be able to stop.

  3. Shirley says:

    I was married for over 25 years to a man that has Asperger’s Syndrome which is a form of autism. My ex-husband was not diagnosed until we had done so much damage to our relationship and while I could not stay in the marriage we remain friends. We have a son together and in so many ways this man still feels like family to me and I know that I am a part of his support system. Thank you for sharing Rita. I can identify with your thoughts so much.

    • Rita says:

      Thank you for taking the time to write. I’m so sorry for your experience; my life has been impacted by autism in numerous ways, and I understand what you’re saying here. That lack of understanding that comes from not knowing what you are dealing with–it is so hard (for everyone involved), and it can create damage that can’t be repaired. I’m glad that you have been able to make your way to a place that sounds peaceful.

Leave a Reply

Your email address will not be published. Required fields are marked *

CommentLuv badge

This site uses Akismet to reduce spam. Learn how your comment data is processed.