Sweet kid (May 1)
There is something so acute about life with Lucas – I want to hold on to each sweet moment, knowing life could get harder. And yet, so many amazing and hilarious and dull and tiring and then deeply awesome moments have to slip by without documentation because life keeps moving before we get a chance to sit down and write. Like spring break. It was amazing – we went to Long Beach and flew kites and saw sea lions and once again created an accessible adventure for our family. In fact, these days I am constantly convinced that this moment of parenting Lucas is the best yet. (You may already know this about me, but I am prone to hyperbole. I am also sometimes convinced that parent-caregiving is sapping the life-blood out of me and that I will never get enough sleep to hold a regular conversation. More on that another day.)
One of the most moving things about this moment in our Lucas’s life is that he has become so expressively caring about Burke and Ida and me. When I come home from my yoga class, he asks, genuinely, “How was your yoga class Mommy?” On the nights that Burke or I go to a class or meeting that keeps us out past his bedtime, he asks us about it in the morning. I’m pretty sure he doesn’t actually care about our answer, but that he is asking to demonstrate that he’s paying attention and caring about us as more and more “equals” in the family. It melts my heart every time.
A few days ago Lucas didn’t have a nurse on a school day, so I was with him all day long. I went to school with him in the morning, then brought him home midday so I could take care of him and Ida in the afternoon. I tried to make a little more “learning” happen at home, so I gave him a writing assignment. Creativity isn’t his strength – he likes research and the telling of facts – so I gave him the assignment of writing a list of five things he liked about our spring break. I set him up at his computer and went to the kitchen to clean up from lunch. Lucas proceeded to type in hundreds of nonsense characters (ie: 11111111111//////???11111111111/////, ten time over.) Then he hits the “read” function, and it takes his computer forever to read through it all. I got frustrated with him – this is his classic delay tactic when he doesn’t want to write. I erased it all. Went to the kitchen and he started to write a list. “1. I liked….” Then I saw him erase it and proceed to the nonsense-character-stall tactic again. I went over, turned off the volume and sat next to him and helped him think of three things to write on the list. I walked away, and he repeated his resistance tactics.
I got mad, and we ended up in a power struggle. I rarely get mad Lucas, and I hate to admit that there was something that felt good about the whole situation. I am the adult here! I can set boundaries and force my kid to practice things that are hard-but-good for him! But the truth is it’s not actually how I want to relate to Lucas. Even if it is my job to sometimes push him, I don’t want to do it from a place of power-over and frustration.
We made it through, and we found something of a compromise – Lucas doing the bare, bare minimum to meet my requirements; me enforcing the time limit I had set for his computer time. As soon as he finished writing, I told him it was time to shut his computer down since he had used all his computer time messing around on the writing exercise. He generally only writes on his computer because we tell him he has to before he can play his games, so this level of harshness from me took him by surprise. I could see him get sad, and it broke my heart. I probably would have caved and let him play if we hadn’t had a real-life timelines – I had to get him down and changed and fed at that moment if I was also going to have time to feed and change Ida and get all of us out the door in time for family choir. I could see his chin start to tremble as he tried not to cry. I felt terrible as I disconnected his vent so I could pick him up out of his wheelchair and lie him down on the couch.
In these transitions, when he is briefly disconnected from a ventilator, Lucas doesn’t have the air to speak. We’ve developed a few thumbs up and clicking signals he can make to communicate in these moments – sometimes we tease him about something, then tell him to give one click for yes and two clicks for no. This time, as I picked up a near-to-tears kid and held him in my arms for a second before I set him back down on the couch, he blew me a kiss.
And in an instant, as if he had hit a reset button, he shifted everything. I set him down and connected him to his ventilator. And I gave him a hug. I was so floored and humbled and yet not at all surprised that in a power struggle, my stubborn, determined Lucas was also the more patient and zen of the two of us. He softened and forgave me first.
I worry all the time about how disability plays into all of this. Power struggles are all the more complicated for us, since I am not only the adult, but also the physically able one, the one on whom his life depends moment to moment. Part of me worries that he has to forgive me quicker than a kid who could wrestle the tablet out of my hand and run away. I’m not just his mom in this situation, but also his arms and legs and caregiver. I hope one day he can read this and reflect back and tell me what he thinks of my parenting. (And I hope I’ll be open enough to listen.)
I am pretty confident that we’re doing a good job holding all this. He knows Burke’s and my love is unconditional, and that certainly our life-maintaining caregiving is absolutely unconditional. I am pretty sure that even though these power dynamics are real and unavoidable, Lucas is confident that he can be fully himself with us. There are times when he is not all sugar and sweetness (his stern “Get out Mommy!” comes to mind – usually when he’s excited to have Burke read him his bedtime story and I joke that I’m going to take over). Anyway, when he blew me that goofy and forgiving kiss, I felt so deeply lucky to be able to know Lucas so intimately. He is truly exceptional.
And he really did immediately shift his mood. I helped him get a book to read on the couch while I did his care and got Ida ready. The three of us somehow made it out the door and got to family choir on time. And Lucas was not just feeling OK by then, he was in a spectacular and goofy mood. He talked more in choir than ever before, joking with the choir director and making up new song lyrics with her. He was so proud of our new lyrics (“This train don’t carry no fuzzy bow-wows”) that he insisted that she tell the band that we had heard play the song about our new verses. He told some fart jokes, talked about dinosaur fossils, and when we sang Lucas belted out – Lucas style – his favorite songs.
Comments (8)
Judi
May 6th, 2017 at 6:05 pm
Lucas was just born with an abundance of empathy. Something the rest of us need more of. Not surprising that we can learn a lot from
him about expressing your frustration with others and then just moving along.
Lots of love and hugs to all.
Adele Rolider
May 6th, 2017 at 2:10 pm
Krista: I wanted you to know that I read this blog post before I had to go through an MRI, scary for the test itself as well as the results(waiting to see dr.). But it was so so healing to read your words and feelings and experience with Lucas, and really take it in.
thank you!!!!!!!!!!!!!love adele and love to Burke, Lucas and Ida.
liz roberts
May 6th, 2017 at 11:24 am
Another moving, powerful story illustrating your incredibly insightful, respect-filledl, empowering, and loving approach to parenthood and showing Lucas’s gentle, wise, and brilliant spirit. Such an inspiration to read your astute and principled reflections. Love you all!
Kristin Lasher
May 2nd, 2017 at 4:52 pm
Way to go Lucas and mom. Being the big strong parent, sometimes in my case, without Krista’s depth of thinking and wondering about that power, I missed many opportunities to allow for the soft ending. Lucas, you are a kind person. You are forgiving and resilient. We could all learn so much from you. Sure hope your mom gets some more sleep, however, as she wears me out just thinking about her day. xoxox Kristin
Jacoby Ballard
May 2nd, 2017 at 6:35 am
Oh Krista, what a beautiful story. You and Lucas bring me to tears.
Sending the whole family so much love.
Jacoby
Sally Tripple
May 1st, 2017 at 8:34 pm
Lucas and family. : You guys are amazing. You are managing to relate to each other as individuals and value each other no matter what. I love reading your posts and look forward to more blogs by Lucas in the future. Sally Tripple
Judy
May 1st, 2017 at 7:38 pm
Hello Lucas and hello mama. I was glad to see an update about all of you and to read the latest. mama, you amaze me with what you do although I have nephew who is autistic and that family has so many challenges too. My nephew does not sleep! Dad is stay at home to do day care and Mama is a vet who brings in the bucks. Their story reads a lot like yours regarding going on trips, keeping Jack from getting away from them, finding the right school and the right pet, etc. etc. I just admire all of you so much.
Lucas, mind your mama and help all you can too. Thanks for letting mom share with us so we can send our love and prayers. Your friend in Albuquerque, NM. judy
Beth Bauer
May 1st, 2017 at 5:49 pm
Brought tears to my eyes :) You are doing great and Lucas is a true MTM warrior!
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