Tuesday, August 24, 2010

to the boys

i've been thinking about my boys.  thinking about their lives- their extra challenges in being a part of this particular family.  their life with someone who is wired slightly differently.   the one they look to, the one who sets the tone, the one who doesn't always act the part or accept her role as the oldest.  how they have to live with the disproportionate time spent- how they know nothing else.  it's hard and sometimes i get mad for them.  and sometimes i get mad for me.

this weekend we were in north carolina at my parents mountain house.  "we" is me and the kids- mike was climbing mount whitney on the west coast.  so i was on the single parent path- which can be exhausting- especially with those kids who alone seems to need two full time parents.  so i was feeling stretched- i was feeling thin.

the last night we were there, i had put the boys to bed- ok- i had put them in their bed and gone on to help move zoe along.  i found her setting up a chess game (which she doesn't know how to play) and reporting that she was going to play checkers with ama (my mom). but it was her bed time- and i might not ordinarily have cared that much except that i'd found her sitting outside in the full moon feeding the dog dog biscuits at 2 am the night before- so she needed to go to bed and so did i. i told her it wasn't happening and that she needed to brush her teeth, and get her pajamas on and go to bed.

you'd think i'd asked her to eat nails.  she was enraged.  not at having to go to bed- but at me for being the one telling her to go to bed. and it blew up into this nasty mess for her and she couldn't let it go. i however kept relatively cool - for once. but the point of the story is that it took a long time for her to settle out and for me to try to help her shrink it back to reality and in the meantime- bryn had come out of his bedroom and had been asking for me. 

tell him, i'll be there when i can - i told my brother.

a few minutes later i heard- bryn still wants you and is calling for you.

tell him i'll be there soon.

again.  and my reply the same.

finally, i got her to bed and went quickly down to see him- but it was too late, and he was sound asleep.


so this is dedicated to jude and bryn.  really, to all the little brothers and sisters of kids who have needs- special needs- different needs- needs that take a lot of time and energy away from the other kids. it's for all the times you guys get quiet and real good when zoe's having a meltdown.  its for reminding her - nicely usually - that she's alread told you that four times or to stop flapping during the funny part of the movie- even though you're only five.  it's for those forgiving looks and extra hugs and kisses you give me when you know things have been rough. for bringing me your blankies when i have a migraine. it's for driving 45 mins each way three times a week for your sisters therapy - in 100 degree weather - and trying not to fight. it's for all the times you love her and except her just as she is.  it's because you love her and she is who you bounce off of as you become your own people. and because you say things like, " mom, i love you all the way to saturn and then to the moon and then back to saturn and then back again" in your squeeky three year old voice, even though  i never made it down to kiss you one more time that other night. 

5 comments:

Candie said...

A prayer went out to you, the boys, and Zoe tonight. I pray comfort and understanding. I can't say I understand because my daughter is the only child in our home but I can only imagine how difficult it must be.

Unknown said...

My little sister had special needs and because of the home I grew up in, I became her parent. It was hard and I identify with the pain of that existence. What I think makes all the difference is knowing that no matter what, you are loved and supported and I have a feeling your boys know that. I will definitely say a prayer for you guys tonight.

Unknown said...

It is always amazing to me when young kids show that kind of tolerance and kindness to other kids who are having a hard time of it... just when we, as adults, are ready to throttle the kid with the bad day. Are we born with that, and lose it over time? I ask because I don't have that kind of tolerance, if I ever did... just the self-control not to throttle when I really want to.

Barbara said...

Hi Kris. I just want to say how much I've appreciated reading through your blog tonight. This is the first time that I've really felt that I'm not the only one who has experienced the wide range of feelings that come along with having a child with special needs.
I have a son who has nonverbal learning disorder. He's now 20. It's been a very long, and emotional road for all of us. There have been so many ups and downs along the way.
Reading your blog took me back to what it was like for us 9 years ago. They were tough years.
We've come a long way. My son is now an adult, but he still requires our daily support. Still, I look back and see how far he's come.
Things do get easier ... a little easier anyway.
I have a blog, but it's just about life in general, not just my son. Reading yours makes me really wish I had of kept a journal all through those years.
Thank you for your posts. I look forward to following along more.

Kris Reid said...

barbara-
thank you so much for sharing that! just hearing that you've been there and have survived is a huge encouragement!! i'd love to hear more about your son- send your blog address and i'll check it out. so glad your years have gotten easier- thanks for reading!!

Post a Comment

Note: Only a member of this blog may post a comment.