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.

Atti’s Birthday Present

Hanging Toy

Back to business around here, it’s time I share this little project in detail.

If you’re much of a sewer it’s probably instinctual, but if you’ve been meaning to pick it up here’s how. This project really couldn’t be much simpler, and it’s a super easy first project.

Hanging Toy Tutorial
Cut four strips of fabric 1 1/2″ x 6″, sew into a tube using a 1/4″ seam allowance, and turn right side out.

Hanging Toy Tutorial
Thread a piece of batting through the tube. I cut mine about 1/2″ x 7″ and then rolled it up.

Hanging Toy Tutorial
Trim the batting, fold the raw fabric edges in, and sew a small square of velcro to each end. If this part is a too fiddly for you, you can use a fabric glue.

Hanging Toy
Alternate a fabric ring with a wooden ring, and then dangle over baby’s head.

I got my wood rings here, and I used a couple of different sizes. They make absolutely fantastic teethers, they’re easy to hang onto and Atti hasn’t managed to gag himself with it yet. He’s is already too strong for the type of velcro I used, so you might want to take that into account when you’re standing in the aisle at the fabric store.

I’m working hard on preparing some things to go up for sale in my shop, and since I still have some wood rings leftover, there may be one or two of these up for grabs.

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.

2009 Year of Pleasures #6

A boy and his cat

Our boy cat has completely adopted Atti. They always have tummy time together, Lobo sniffs out any new therapist that comes by the house, when Atti’s crying Lobo comes running.

And big fat Lobo is always around when it’s feeding time.
PA274645

Like a lot of preemies, Atti has some digestive issues. The other night his stomach was hurting him badly so we brought him into our bed to try to soothe him. Nothing we did worked, he was in pain and just couldn’t be comforted. So then Lobo hopped on the bed, laid himself down on Atti’s legs with his front paws extended onto his belly, and started kneading. It was the only thing that got Atti to feel better long enough to go to sleep.

The therapists call him the therapy cat. I’ll hold Lobo in front of Atti whenever we’re trying to get him to scoot or reach and Lobo will almost always just sit and take it.

Of course, sometimes he gets sick of it just like any other big brother.
big brother

Recovering from the party

If I admitted that I just now finished doing the dishes from Atti’s party on Saturday, would that burst your image of me? It’s all about priorities ladies and gentlemen, and dishes are rather far down on mine these days.

Birthday Boy

The party was great fun, small but chaotic nonetheless. Since it’s just his first and he doesn’t have real friends or anything yet, we just had the immediate family over. We grilled hamburgers in between rain showers, I made homemade french fries and salad, and then I decided I had to have a cookie bar. I have no idea what possessed me, we ended up giving cookie plates away to friends and neighbors since we made more than any of us would ever want to eat, but it was still fun to do.

I used Martha’s Cookie of the Day resource and we made Mudslide Cookies, Pink Grapefruit Sandwich Cookies, and our own recipe for Peanut Butter Cookies. The pink grapefruit cookies are out of this world. Holy Cow! They’re outrageously good and no one had ever tasted anything like it. Those will now be on our greatest hits list.

Once again we went overboard on the cake. We made a burgundy fondant cover, carved the cake into the shape of pages, covered it with a creamy peach fondant, and then cut and painted the sides to look like gilded pages. I had plans of sculpting little characters from his books, but yet again I ran into my own limitations. Fondant and gum paste just do not work like polymer clay, so I’m struggling to figure out how to make it do what I want. We were a little bummed we couldn’t make it look like our vision, but we feel like we’re getting way closer each time.

Birthday Boy with Felt Crown

Of course Atti had to have the felt crown from Amanda’s book. The best part was that since I was so busy with last minute cookie baking to consider a birthday hat, I only started this about an hour before guests arrived and I finished it with time to spare.

Too Many Presents
I asked the family to not get us toys. He has plenty of toys. We’ve broken our own No Plastics rule to get him toys that will aid his development, he does not need more. Instead we asked for books. There can never be enough books in our house. But everyone took pity on poor Atti with his humdrum granola mom and bought him whatever they felt like anyway. Everyone actually bought him great stuff, and were way too generous. I was really touched by the efforts they made to go along with my love of the natural. We got wooden trains, wooden buses, wooden blocks, books, and even the plastic toys light up and play music just like Atti likes best.

It was hilarious to see the reaction around the table when we opened up the gifts from us. A storybook about fuzzy bears, a toy I made, and a CD of Ladysmith Black Mambazo music. Bless their hearts, they try, but I don’t think they always understand why I do things they way I do.

Hanging Toy
I’ve been meaning to make him these hanging toys for months, but I kept putting it off. I waited a little too long, I think he’s a little advanced for them now, but I’m still happy I finally got this one out of my head and out into the world. I wanted him to have something to bat at and chew on from his car seat that wasn’t made of plastic, and I couldn’t find anything. So this little chain alternates a wood ring and a fabric ring so I could still use them to attach things where I wanted, and the wood is a fantastic teether. I’ve got a tutorial coming up for these this week, and I’m also planning on having some available in my next shop update, which I’m hoping will be at the beginning of next month.

Amy Butler covered toybox
I also made him this toybox to corral all the toys that seem to have been breeding in the middle of the night. We’ve hardly bought a thing, but between toys on loan from therapists and family members concerned for how much fun we let this kid have, we have more toys than I know what to do with.

Toybox in place
I made it just the size to fit into this one odd little cranny I have. I put it on wheels so it’s easy to pull around, and the sides are soft so Atti can crawl right inside if he needs to to reach the perfect toy. I took notes as I built it to do a tutorial, but it would be a pretty long and specific one, I’m thinking instead of making it a pdf download available for a couple bucks. If anyone’s interested than give a shout in the comments so I can see if it’s worth the effort.

Of course once the party was over, literally as the guests were walking out the door, I felt my sinuses start to plug up. As soon as my big deadline was met and I had a couple days to relax before starting the next big thing, that’s when I get sick. And as my sisterfriend Schelle says, Mommies don’t get to be sick. So I’ve been doing all I can to keep the baby happy without actually expending energy or allowing anything to touch my achy body. I have a ton of wonderful emails I need to get back to, but I’m going to plead sick day and get back to my couch bed. Luckily I’ve been so busy with the party that I haven’t been watching TV, which means that my Tivo is stuffed and waiting for me.

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