2009 Year of Pleasures #13

Mirror on the ceiling

We stopped for the night in Las Vegas and spent the night at the Tropicana. We thought that a major hotel right there in the heart of the strip would be a sure bet. It was stunningly scuzzy. I think I can tell you all you need to know by showing you this picture and then telling you that we were actually in one of the upgraded rooms.

I can now officially say I’ve stayed in a hotel room with mirrors on the ceiling. I think they must be more fun when you share your bed with a baby. He spent hours blowing raspberries at the baby in the mirror.

Today is one of those bitter days.

Atti’s teething about four teeth at once, he’s had a low-grade fever on and off for nearly a week, and I cannot do anything to make him happy.

In the past couple of weeks it seems like a little lightbulb has turned on for Atti. All of a sudden he’s interacting with us so much better. He can start to communicate with us, to follow simple instructions, he’s aware of so much more. Which is of course a good thing, but it brings some big fat complications.

Now that Atti is aware of what he wants to do, he’s also aware of what he can’t do. I keep hoping that it’s just the teeth, but lately when I put him down for tummy time he just starts throwing a fit. Instead of working and muscling his way over to a toy, he starts to cry and bangs his head. And instead of my sweet, peaceful, content baby, I suddenly have a very bitter little man.

I keep trying to remind myself that in parenthood, everything will pass. For good and for bad, everything will pass. So maybe I’ll be in for a rough few months, but I shouldn’t let myself think that this is how it’s going to be forever. But boy is it tempting. He’s more dependent on me right now than he even was as a newborn. At least then he would sleep, or I could pop him in his sling. Now I have to lug around a 20 pound sack of flour, all day long.

When someone you love is going through therapy, there’s a standard pattern of behavior. They work and work and work and seem to get nowhere, so you agonize that they’ve reached their limit and whatever ability they have right then is all they’ll ever have. You worry and grieve about their options and what this means for you as a caretaker, and just when you’re ready to give up and settle in to what your new life will look like, they have a breakthrough. The elation you feel is more than can be described in words. The clouds part, heaven itself seems to shine down upon you, you weep with gratitude and pledge to always remember this feeling and never be so pessimistic again. You commit to celebrating achievements and to stop focusing on limitations.

And then time goes on, they work and work and work and seem to stagnate, and no matter how big the previous breakthrough, no matter how glorious you felt before, you will still eventually face those feelings of hopelessness again. You will still have visions of yourself dealing with this same problem 10, 20 years from now. You still count up all the things you’re sacrificing.

And then they have another breakthrough, and the sun comes back out from behind the clouds.

The sun will shine again for me, I’m just getting tired of living in this gloom.

The Music Man

I spent part of today finally downloading every video we’ve ever taken of Atti’s whole life off of the video camera, and onto the computer.

So in honor of my massive feat of organization, I give you my favorite video ever:

Atticus listens to music.

I wish I could say it worked that well every time, but still, it’s the most powerful trick I have in my arsenal.

Netflix just sent us Nick and Norah’s Infinite Playlist, and the whole time we were watching it I just kept thinking I was watching Atticus all grown up. A sweet, sensitive, music obsessed, quirky kid. I hope so.

I’m the most powerful woman in the world

Three little examples of how I am figuring this out:

1.
Every few days Atti will have obvious pain in his gums. So far he’s got two little bottom teeth and a new one just started poking it’s head out of the top. One day last week he was just inconsolable. Tylenol wouldn’t work, cuddles didn’t help, Bear was so frustrated there was nothing he could for him. I picked Atti up and started massaging his gums with my fingers. After just a few seconds he looked up at me with surprise and broke into a huge grin. Oh how my heart melted. I fixed it. Mama made it better.

2.
Atti has to get at least two shots a month, this month he’s had to get eight. His usual nurse knows our routine and when she’s all done with his shots and he’s cleared for cuddles she always says, “OK mom, it’s singing time!” since she’s watched as month after month I pick him up and start to sing and he stops crying before she’s even cleaned up. This month we had a new nurse for one of the appointments and after his shots were finished I started to sing his favorite song. The nurse just snapped her head up and said, “Wow. *That* worked.”

3.
In his physical therapy, there are a couple of exercises that we return to over and over again, because they’re important stepping stones on to more mobility and because he refuses to do them. There’s one exercise that requires him to kind of do an oblique sit up. For most babies it’s instinctual, but for mine it involves a lot of training. We’ve been working on “trunk righting” (or sitting up without falling over to the side) for nearly eight months now with very little change.

Then one day I was playing with him and making a K-k-k sound, just to introduce the consonant to him. I’d come forward towards his face with each K, and then I’d boop his nose with my nose and say “Kitty!” He just thought it was the funniest thing he’d ever seen in his life and laughed until he gave himself the hiccups. I noticed that he liked it so much he’d start to bring his head up to mine, meeting me halfway with a little sit up so I’d boop our noses together. As an experiment I turned him to the side and watched as he suddenly mastered doing that sideways sit up we’ve been working on for his whole life, just to touch noses with his mom.

Heaven knows there are enough frustrations and failures in the day to day of parenting. I’m writing these down to remember that when I succeed, there is no other feeling like it on earth.

I love you guys…

How can I even begin to thank you guys. I cannot express how wonderful it is to be so thoroughly cheered on by old friends, new friends, readers, and the whole of the internet. It is a powerful feeling to have all of you behind me and I really do feel the strength of all the prayers and good thoughts and hopeful intentions. Please forgive how horribly behind I am in my emails, but believe I treasure every one.

We’re coming to terms with things over here, and a couple of my oldest and dearest friends managed to say some things that really made me discover some faith in myself. Crysta rewrote that whole paragraph I wrote about Atti’s strength to become her speaking about me. And dear dear Jana reminded me of how I have tackled things in the past. I thought it was so funny, I do so love my moment of drama, but now it’s time to get down to business and find that action plan Jenny pointed out.

I’ve been thinking pretty much non-stop about what the doctor has said. I really wish I could just write her off as a quack, or hate her somehow so I could work on proving her wrong with all the spite in my heart. But she’s not a quack, and I’ll adore her forever. I’ve decided that it was her job to convince me of the odds against him so that I would be absolutely ferocious about pursuing treatment. I can’t afford to waste time hoping that it’s just a phase or thinking he’s just a little bit slow, I have to understand down to my core just what he’s fighting against so I can give him the support he needs. Her job was to scare me into action.

But I also think that she just doesn’t know this kid. The other day I was firmly entrenched in my couch bed, eating coffee ice cream and ignoring the shower for the mumblemumble day in a row, and I just had no emotional resources to be an interactive parent. Normally when it’s Atti’s tummy time I keep a pretty tight reign on him. He likes to roll over and hang out on his back, so on a regular day I stay close to keep flipping him back over. During my pity party I just let him go. There were toys scattered all over the floor and I watched as he rolled from one end of the carpet to the other, pulling himself along like an army commando, huffing and puffing and scooting along to get to the toy that played the music.

He’s going to do it. He’s going to figure it out. I just have to find a way to give him the freedom he needs, and the support he needs at the same time.

I’ve been hiding from the internet

I guess I need to find a way to accept this. Atti has now officially been diagnosed with Cerebral Palsy.

We knew he was at risk since before he even left the hospital. Sometime before he was full term he didn’t get enough oxygen to his brain, and spots of damage were formed. It could have been because he was so tiny that his body was just incapable of getting the air where it needed to go, it could have been one of the five times that he pulled the respirator out of his throat, we’ll just never know.

At the time the doctors told us that they expected it to be mild and that he would most likely be able to retain function. We had another visit with his Neonatologist on Wednesday and she said that it was now officially CP and no longer just your garden variety preemie delay, and that it seemed to be manifesting more severely than previously thought. Her best guess now, based on statistics, is that he may eventually walk, but probably only around the house. He’ll probably need a wheelchair. He may have trouble eating and speaking, drooling, using the bathroom. There’s just no denying it anymore. My sweet miracle baby is going to spend his life fighting this disability.

I am very much of two minds about this.

Part of me knows with a deep conviction that he will be able to surprise all the doctors. This is my kid. He is stubborn, he is willful, and he is not going to be content to not do something he wants to do. This is the same kid that set hospital records by ripping his respirator tube out five times before he was even old enough to have hand eye coordination. This is the kid that allegedly has limited fine motor skills, until he wants to get that eye patch off. This is the kid that will do anything it takes to make music come from whatever is in front of him. I cannot imagine that this boy will be content with doctors expectations and not drag himself towards more by sheer force of will.

The other part of me is paralyzed with fear. But more for myself than for him. Motherhood is demanding at the best of times. I was just starting to feel like I was figuring this out, even with therapy every single day, even with his dependence, I was getting a routine down. But now. Oh dear.

Suddenly this requires even more of me than before. And I’m realizing that all the plans I had for myself, all my own dreams and goals, are now going to have to go away. We’re going to have to double up on Atti’s already extensive therapy, and now instead of having everyone come to me, I’m going to have to take him all over the county to his appointments. All of the therapists I’ve grown to love so much are going to move on to other cases and I’m going to have to start over with a whole new crowd. This all just got a whole lot more serious.

No parent wants to see their child limited. Even in the best case, if he does manage to walk and talk, there are still doors that are now firmly closed to him. He’ll never join the military (Whew!) He’ll never be an athlete or fly a plane like his dad. But we’re realizing that every parent eventually has to come to terms with their child’s limitations. Every child has talents and inclinations, and limitations of their own, and every parent has to eventually accept that their baby is not going to live the life they had scripted for them.

I see it all the time in my work with the teenagers at church. In the teenage years kids begin to choose their own path and it is so hard for parents to sit back and watch. To watch as little Johnny shows no interest in whatever life his parents wanted for him and decides to pursue fillintheblank. Maybe the parent had dreams of Harvard and the child does not enjoy school. Maybe the parent wanted a professional basketball player and the child tops out at 5’3″. It happens to everyone. And they all have to accept it.

We’re just having to accept it a whole lot sooner than most people.

Now if you’ll excuse me, I’m going to go crawl back into my nest of blankets on the couch and resume my deep deep depression.

One year ago…

I must have been sleepwalking through this year. I have absolutely no idea how this happened.

First picture

For three months this little picture was all I had to take home with me. The nurses took this picture for me when I was still too sick to leave my hospital bed and see my baby. Atti didn’t even have a name for his first three days of life because I insisted on meeting him before giving him one.

Since I was discharged from the hospital, this little picture has been taped up to the wall next to my bed. To focus on while I pumped breastmilk, to keep me company during those long nights away from my baby, to remind myself that it really all happened.

Even now I still occasionally find myself forgetting that I really am a mom. The whole thing was so bizarre – after eight marathon years I was pregnant for less than 7 months and whisked through delivery so quickly that it took less time than a standard doctors appointment – I still have trouble shaking off the disbelief.

Atti at one year

Having a disabled child was one of my biggest fears going into motherhood. I have big dreams for excellence for him. I want a fancy school, I want a love of knowledge, I want music and language and exceptional skill. The thought of having a child who wouldn’t be able to pursue those things was so terrifying I couldn’t even speak the words out loud. I believed with my whole heart that I did not possess the strength or talents needed to parent a child with special needs.

But since this is my life, and I have a long history of getting exactly what I thought I didn’t want, a special need baby is just what I got. And yet, I surprised myself. It’s wonderful. And I’m doing it. I used to talk to other mothers of special needs kids, and I never believed them. They’d tell me how much they loved their child, how they were so blessed, how it was hard but they were so grateful, and in my head I’d just think, “What an amazing woman. She is a saint. If this is what she needs to believe to get through her day, then good for her.” But now I know it’s so very true.

I don’t want anyone to think I’m any different than they are. I have no more reserves of patience or love than anyone else. There are days when I resent all the appointments. There are days when I want him to be more independent. And there are days when my heart breaks because he doesn’t understand why he’s being tortured with more shots and exercises and work and medicine. There are nights I sit up terrified that he’ll never be able to use his left arm or leg, because he isn’t using them now, and that could mean 1 of 87 different things including everything in between permanent paralysis or laziness. Every little thing he does sends me swinging between depression and elation as I look towards his future. And then he’ll give me that smile that’s just for me. He’ll stare into my face while I sing him a song, he’ll bring his face up to mine to ask for a kiss. And all I can focus on is what’s in front of me. I drift off into that baby bliss sleepwalking state and I get through it. And it’s wonderful.

One day I believe he’ll be able to pursue all the things the “normal” kids do. He’ll be just as intellectually capable as other kids, and one day he’ll be healthy enough to play ball with his friends, probably. But I just don’t care about that anymore. Atticus is no longer forced to measure up to my dreams of his life, or what the other kids his age are doing. Now he’s on a scale of his own. Every single day I’m astounded at what he accomplishes. What he puts up with. What he smiles through. How much he loves. He’s just such a sweet brave little boy. I can’t believe how wonderful this year has been.

Happy Birthday my sweet little man.

P.S.
The mohawk now has a life of it’s own.
Crazy hair

Ideas that are nice in theory

I’ve described myself in the past as being about equal parts hippy dippy flower child and hard boiled cynic, and that really fits in most aspects of my life. I think I’d describe my taste as equal parts modern designer and Handmade antique. I can’t fully commit to the handmade aesthetic, and I can’t fully commit to the sterile modern design either. Luckily my wishy-washy-ness has been really helpful with how my particular journey into motherhood has transpired.

Oh I had goals. I had the loftiest of goals. Attachment parenting, cosleeping, cloth diapering, no plasticing, organic everything goals. And even though every single person around me thought I was out of my mind, including occasionally Bear, I stuck to my guns. California has a reputation as being full of the organic lovers, but it varies greatly by the region, and once you get south of LA it’s all a very conservative, frequently wealthy, “Ah, just buy it, it’s easier.” kind of mentality.

But I wouldn’t listen to the skepticism. I had my plans, including preparation for an unmedicated birth, and nothing was going to dissuade me from them.

Until Atti was actually born.

There went my unmedicated birth – it was far more important that we both make it out alive. There went my beautiful dreams of breastfeeding – no matter how many hours a day I attached myself to the pump my milk supply dried up before he even made it home. There went my ideas of attachment parenting – it’s a little hard to wear a baby and an oxygen tank. No cloth diapers – I spend hours every day doing physical therapy, I have to limit as many household chores as possible.

The one that really hurt my heart was giving up on the No Plastics rule. He still has the fancy bottles, so I suppose that’s what is most important, but I’ve scoured the internet and I’ve never found a toy made of wood or cloth that lights up and plays music when you hit it. And that’s what he needs to motivate him to do physical therapy.

I still try though. We coslept until he was too big to fit in the bed, I try to wear him as often as possible (he’s sitting on my lap as I type) and I make all his baby food from organic fruits and vegetables.

Baby Food

Really, I’ve been pretty surprised to discover just how ridiculously easy his baby food has been. It takes me maybe one afternoon every five months, and costs maybe $25. WAY cheaper than buying in a jar, and I know there’s no preservatives, no sugar, no salt, and all the vitamins haven’t been processed out.

And yet this was the parenting choice that people really went nuts about. This was what convinced people I was a total extremist. I don’t know exactly what people think is so complicated about making baby food, but just in case you’ve toyed around with the idea let me explain.

1. Chop food into chunks and either boil or steam. If it needs to be cooked at all. Most fruit doesn’t need it, avocados don’t need it.

2. Run the prepared food through a blender or food processor to make a nice puree. If it’s a little thick, thin it down with some of the cooking water.

3. Pour the puree into ice cube trays and freeze.

Done.

Early this week I sat down with a mess of apples, nectarines, squash, and carrots, and in about three hours from start to finish I have enough baby food to last him for months.

Pouring into the ice cube trays creates perfect 1oz serving sizes, so I just grab a couple of veggi cubes and defrost. Then I don’t have to worry about throwing out a ton of food if he isn’t cooperative. I also supplement in with fresh mashed bananas, fresh mashed avocado, a bunch of cereals, and yogurt.

The reason I wanted to adhere to all those parenting philosophies was because I was convinced they were better for a child. And I still am, but they weren’t better for *my* child. Or I should say, *this* child. If I get to have another one I’ll try all over again. But at least I can rest easy that I gave this baby what he needed, and that was the whole point.

Developing a Social Life

It’s amazing what not having a child in the hospital can do for your social life. For the nearly two years that we’ve lived here, I’ve been fairly isolated. First by being new and in the middle of house renovations, then by scary personal problems, then by the intensive needs of my little guy. It’s pretty hard to meet someone under the most stressful conditions of your life and seem at all like a sane and fun person to hang out with. Honestly, without the gift of the internet I probably would have made myself a little Wilson by now.

Now I’m starting to settle into the groove of what my little guy requires. Bear even joked the other day that I’m so used to the constant stream of appointments that I don’t even bother to put them on the calendar anymore. And I’m finding the idea of getting out and making friends appealing again, instead of just one more thing to try to squeeze into my day.

On Monday I finally got together with my “new best friends” from church. We’ve known since early on that we’d all get along so great, but along with my own drama of the year, one friend had a daughter graduating and going off to college with all the work that comes with it, and the other friend’s husband was in a major car accident and has been recovering from serious injuries ever since. It was not exactly an opportune time for any of us. But we finally succeeded and it was so restorative to me. We had a great lunch, we passed around my teething fussy baby, we talked all about art and culture. I just got home and wanted to let out a big sigh. It was just what I needed.

The Saturday before that my sister Traci and her kids came into town, and I was just sad we couldn’t see them longer. But how can we compete with Disneyland? It’s not the first time we’ve had to steal a few hours away from the mouse, and it certainly won’t be the last.

But on the Friday before that, I got to see one of my very dearest friends for the first time in six years.
High 5

Jana is one of those friends that you’re lucky to find once in a lifetime. The kind of friend where months (or years) can go by and you can pick right back up where you left off. Where you may not get to talk as much as you like, but they make you feel so secure in your friendship, so truly loved and “gotten” that you feel buoyed up just knowing they exist in the world.

Baby love
Check out Jana’s death grip on Grant. These boys loved each other.

Jana’s in the middle of a big prolonged move back to Hawaii in preparation for her husband returning from serving in Iraq, so she stayed with me for a day before driving up to visit her brother and shipping her car off before flying to Hawaii, with her three year old son Grant, setting up house and getting her car about a month later.

Jana and grant feeding ducks

Oh, and she just finished running her first marathon. Can you believe her? She’s like a cartoon version of the ultimate capable woman. “Oh sure I can be a single parent while my husband is off creating roads and bridges and infrastructure to help the Iraqi’s, and I’ll handle a complicated move on my own while being a crazy great parent to my sweet little Grant. But how am I possibly going to fill in my free time? How about a marathon!”

Atti and me at the park
We’re more “indoor” types of people.

I’ve been so lucky to find the friends I have. The only problem is that they’re all scattered from one end of the country to the other. Jana is particularly gifted at making the distance not seem so far.

Sorry for the unexplained absence

Wow, how’d a whole week go by?

August 14th was our nine year anniversary, so this time last week Bear and I dropped the Rookie off with Grandma and Grandpa and spent a night just the two of us in a hotel next to Disneyland. It was wonderful. We went to Downtown Disney and leisurely shopped, we ate at a very fancy Spanish restaurant where we had a table on the balcony with a perfect view of the fireworks, and best of all, I actually got a full night’s sleep for the first time in six months.

But by the next morning I couldn’t get out of the room fast enough. I was shaking from baby withdrawal. These mother emotions are powerful things. We’re always trying to get them to be more independant – “just have some tummy time while I do these dishes.” “Please, it’s time to go to sleep already.” – and then when they show those baby steps toward independance I just want to snap him up and hold him close and never let him grow up. He had a great visit with the grandfolks. He played in the bath, he played games with singing grandma, and he got snuggled to bits. Yet when I called to check in on him, I got the biggest smile of the night just by hearing my voice. It’s a pretty amazing thing, being the person he loves most.

Since we got back into town I’ve been struggling to catch up. My house is in shambles, there are drifts of laundry strewn throughout the house, I still haven’t managed to make it to the grocery store, and I’m trying to hurry up and finish a couple projects before I’m tortured to death by the projects burning holes in my head waiting to be started. I have mountains of emails to return, but I don’t get much time every day with two hands free, so that keeps getting pushed off in favor of blogging because, even though I may have to type this one handed, at least there’s only one of those to worry about. It’s such a harsh tradeoff. I desperately needed that break, and yet that break makes things even harder when you get home.