Isaac is adorable. It is his super power. He doesn't throw tantrums. He begs sweetly instead and no one in this house can resist his signs please and sweet puppy eyes. He recently learned where we keep the free access snack and fruit. One morning he pushed a chair up and got out three bananas.
I exclaimed, "Oh my, you little stinker!" I did not do it in a scolding voice. Rather admiration. He melted. He just melted into a pile of silent and brokenhearted sadness. Holly ran to him, looked me in the eyes and scolded, "Mama, he is NOT a stinker. You should not call him names!" He looked up at me, tears rolling down his cheeks, and my heart broke a million times. I scooped him up and we sobbed together.
Children do not understand name calling as an affectionate exclamation. They only see it as someone they love is calling them something that is a bad thing.
That is when I stopped calling him my little stinker and Holly my sweet monkey butt and Lily so very impossible.
Now Isaac is my little super hero! Holly is sweet ballet dancer! and Lily is the impossible astronaut! (Her idea.) It is just as easy to use a positive name in the situation as it is to use a derogatory one.
Holly later explained to me that Isaac is a big boy trapped in a baby's body and he is so invisible sometimes that we forget how big he is inside. She's spot on. That's pretty much sums up Isaac. He is so sweet and silent too that it is easy to forget that he has these HUGE emotions going on, like all almost 3 year olds do.
I want my children to know by my words that I love them, to know by my hands that they are loved, to know by my voice that they are heard, and that they will come to know how much I love them by my writing. Someday they will find this, maybe I will be there and maybe I won't. Life is like that. I want these daily exercises in recording our activities and my thoughts to be my love letters to them. This writing can't be that if I call my children lazy or stubborn or fat or any other words out of frustration with them. They may have moments when they are tired and refusing to participate in what we are doing, but that is human. They may have breakdowns or bad days, but don't we all? I do. Less and less though the more I model for them centering myself and gaining control over my own words and actions because they see that, they hear that- not empty words but the action of my being. I am their mother after all.
So if I seem overly adoring of them, this is why, I love them so very much. I want them to know me and know that. I would not want their future employers to read this and say, "Wow, no way and I hiring that lazy brat who refused to do their spelling worksheets and take out the trash! No way!" Not that we do spelling worksheets like that. You know, unschooling. Ha!
No, this is a record of sorts, as are my public facebook pages, for all to see into our lives. Sometimes it isn't pretty, but it won't be ugly like that. It will be brilliant and sparkly and three kinds of awesome.
A blog about farming, unschooling, feminism, 22q deletion syndrome, cooking real food, homesteading, permaculture, and motherhood.
Monday, 19 August 2013
That One Time I Called My Child a "Stinker"
Holly's Grateful Today.....
We played with collected cicada carcasses, sang itsy bitsy spider and twinkle little bat, and snuggles while wishing on summer breezes. Today was good. Get Mugged made a fantastic cuppa with added caramel and whipped cream, a friend brought me some house plants (which Lily claimed for her own), and dinner was good. Today had some frustrating phone time, but overall, a perfect summer day. There seem to be a lot of these lately. Can't say I have a problem with that. :)
Sunday, 18 August 2013
Comparing Blessings
Which one is more full? Can you tell by looking? Nope. |
Holly came along and was the quiet one, but she crawled early. She then walked late. She refused to talk until she was two. She refused to potty train. Refused. We cloth diapered. We wore her. We gave her watermelon. Constantly measuring her progress against my peers kids and the child development books. Also a HUGE baby and child. (No one panic, she is now 5 and uses the potty.....) I slowly learned that each kid is their own person, their own timelines apply, and I would just need to roll with that.
Then Isaac was born. I knew from Holly's babyhood that sometimes kids just take their time. As it became more and more apparent that Isaac was falling behind in milestones and growth, he stayed in premie clothes and then in newborn, 3-6 month sized at a year old. He was diagnosed with 22q deletion syndrome at age 5 months. As a baby it is easier to pass at the playground. Everyone we don't know just assumes he's actually a newborn. As he got older, even crawling, the playground introduction is always followed by, "How old is he?" and the answer is greeted with politeness, but the shock or realisation on their faces says enough to make my gut drop out and make me want to throw up. At that point I usually blurt out his dx and start making excuses, explaining hypotonia.....but it makes me feel ill. It does. Random strangers don't have a right to his medical information. His life should not be his mother making excuses for him. Eventually, he'll begin to understand what that means and it isn't good.
Still when my friends were posting pictures of their 9 month olds walking, cheering with joy at these first steps, I held back tears and my own fears as Isaac was still just crawling at 28 months. I would sob at night. I would question the decisions I made for his therapies. It would consume me at times and block out all other joy in my life.
I stopped doing that. Isaac started walking and I've been too busy trying to keep up. That day was so full of wonder and happy that I thought I would have a heart attack and my face would fall off from smiling.
It got me thinking about my own internal dialogue though. Stop comparing to other "healthy" kids. That part was easy, all I had to do was embrace and rejoice in how adorable Isaac is and how amazing each and every milestone and every day is full of love and happy. Isaac IS healthy, he is making progress, he is amazing.
What is harder is to stop comparing to other special needs children. This goes two ways actually. I found my heart reeling with fear when another kid, a full year younger, with a more severe diagnosis was walking when Isaac was just still struggling to crawl.
Then we'd meet a non mobile 14 year old on a ventilator and I would feel relieved about our situation. Then I would feel guilty for feeling better about ours by comparing to someone else's struggles. How horrible of a person could I be? Then I would get whirled up into fundraisers and fanpages of kids with Isaac's diagnosis who were actually very sick. I felt out of place. How could I offer our story to the collective support groups when Isaac, while slow on physical and verbal milestones, has never had a single surgery and never been hospitalised with an illness, not even RSV even though he had it last winter (just an ER visit). I'd do my part offering prayers, all the time guilting myself into sleeplessness because my kid is healthy. Compared. Someone would get another diagnosis or hospitalization that would send me into another guilt spiral. Why them and not us? Why do we keep escaping the symptoms of Isaac's diagnosis?
I'd read books about special needs families, hoping that folks that I don't know in real life might offer me a more objective perspective, a 22q adult narrative, a therapy book. I kept coming back to comparing what we do, what options there are, Isaac's current health state. Comparing statistics, comparing politics.
Compare.
That's the snare. I don't want my joy to be stolen by guilt and every time I compare in either direction I am racked with guilt and horrible feelings. There will always be kids healthier than Isaac and there will always be kids sicker with greater struggles than us. We will slide between, walking the line and stumbling, slipping like it is wet sloppy mud. Just like Holly and Lily fighting over who has the most orange juice in their lunch cup, the fighting stops when I assure them that if they drink all they have, they will get more as they each need. Their needs will be met to the best that I can provide. They can relax and settle into saying what they are thankful for and eat and play. Their jealousies forgotten. I can meet my families needs and prepare so if they get worse we can be ready, hopefully.
Since being in this much better place in my own mind, I have found a depth of relationship I had never known with other families. I have found my voice.
That doesn't mean our struggle isn't real and it doesn't mean our joy isn't also a blessing. I used to think it was this grey area we fall into, this fog of in between, but that's not it at all. The world is not black and white with shades of grey and no one is promised perfect health always. We all have our own stories and our own struggles and we do the best we can to make the best life we can manage. Isaac is not a fog of grey, he is orange monkeys, and sea glass green, and bright neon pink Dora sock puppets, yellow bananas, melting raspberry Popsicles, summer peaches, and bright sparkling silver trumpets, and delicious blue skies thick with fluffy clouds laughing as he swings too high on the tire swing! This is the life!
Through my children I have learned to stop comparing and be with them in that sparkling moment, their fleeting childhood, that magical place where their mother's love is enough and then some.
Saturday, 17 August 2013
Pictures and Stuff from August
Iowa State Fair, Peaches, Beyonce and Anastasia the peahens, Jessica teaching Isaac about the wonders of the cordless power drill (his is Holly's toy), and Isaac walking up the slide and posing a smile that I think makes him look like Wil Wheaton. I can totally see Isaac saying, "Don't be a dick." It is a good law that more people should embrace, especially online. Sportsmanship, y'all.
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