BRIAN'S HOME!!
We spend Wednesday with just our immediate family (a rare occasion in itself)..eating dinner, catching up with each other and playing with Levi.
Here, Levi shows off his latest crawling maneuvers.
Austen and Brian spend a few hours just talking and going over gyro-copter plans. Then all three boys stay up way into the night playing MineCraft
Thanksgiving Day? I make the boys - all of them- Brian, Cody, Austen, Calvin and Levi..pose for entirely too many pictures. It hits me that this may be the last year with everyone home. Brian and Cody both graduate this Spring. (Brian from UT, Cody from..well..home!). I do not know where they will be living at this time next year.
Selfishly? I hope they stay in Texas. That way..I can see them on all the holidays! After all, it's all about what mom wants..right?! (sigh) no one else agrees either!
But if... they live..in say...Michigan..or Pennsylvania..or Massachusetts? Well I just hope they find a nice family to spend the holidays with!
So I take all these pictures. I lose the camera. So...no pics.
On Friday we wake the boys up at noon. It is our family tradition to put the tree up after Thanksgiving..and leave it up until Epiphany.I think the boys all sense it may be the last year..because this year? They do not argue, moan or groan like they have the past few years.
Here Brian and Cody decorate our tree.(Brian took pity on me and let me use his camera phone)
..and now Austen? He is placing the baby-proofed ornaments on the bottom of the tree. You know..things like..NOT GLASS!
The Boys Pose for a variety of tree-poses. I was fired..because, they obviously, take MUCH BETTER PICTURES than me. Here are my dear, charming, unruly boys. Gotta love them!
This pic was taken shortly before they all took off to hang-out with friends and girl-friends for the rest of the weekend.
and finally?
The Advent Candles
Advent is one of my favorite parts of the season.
I know the colors have changed over the years...but I love the tradition of gathering around the candles in the evenings and reading the Christmas story. One week at a time. Lighting the candles along the way.
It is a time to reflect, to meditate, to wait.....and to enjoy some of the magic of the Season.
A few years ago, my good friend Leticia passed away just before Thanksgiving. Advent was a season Leticia treasured..and I hope to pass this tradition on to her daughter/my god-daughter Katherine.
Most years, Katherine helps me set up the candles..but this year? She is having her 10th birthday party! So I promise Katherine I will set up the candles..and on Sunday, (the beginning of advent)...... We are roller-skating!
Katherine and I agree to light the candles together during her Christmas break.
What's for dinner?
Saturday- broccoli/cheese soup, grilled turkey sandwiches
Sunday- barbecue for friend's birthdays?? and veggie burgers
Monday - not sure..community dining? I'll be at Cody's soccer game.
Tuesday- lasagna, salad, french bread
Wednesday - Swiss steak, pasta salad, salad
Thursday-veggie tacos
Friday -make your own pizza
Friday, November 26, 2010
Monday, November 22, 2010
Baby Free Zone?!
also known as our Den In Progress.
Several years ago Big B and I moved to the Tx. Hills. Our intention? To build a log cabin along the river.
1 year later we were still in the single-wide trailer that came on the lot. Still arguing over floor plans (and budget and time frame)...for the log cabin. We decided it was healthier for our marriage to buy a double-wide.
We spent the next 4 months looking at homes and finally found a floor-plan we loved. It had a living room with den attached, dining room, kitchen, morning room/laundry, 2 bathrooms and 3 bedrooms.
Then? We stumbled on this same house (only the den was a bedroom!)...for sale in Bandera.
If we bought the one off the lot? We would save almost 30 grand.
It was a no brainer. We would replace the green carpet, and turn the bedroom into a den. It would be less expensive to remodel than 30 grand.
So..you guessed it. Here we are 12 years later..and we still have green carpet...and we still have no den.
The den was originally going to be used for piano/violin lessons. Well..we just gave lessons in the kitchen or living room instead, until I stopped teaching.
Last summer Big B and I decide we really could use that space after-all.
Guests have no privacy on our pull-out couch in the living room. The teens and young adults needed some space to have an electronic explosion. (not literally..think Wii, guitars, lap-tops and..okay..electronics being taken apart) I do not want the explosion in the living room.
Big B and I agree. It is time!
Instead, we start a garage.
..and along come Levi...and also? Jack (2 years) and now Charlie (3/4 weeks?)..for community dining..and now Malachai (1 year) and Reini (3 years)..a couple days a week. Meaning?
The babies are everywhere!
Don't misunderstand. We love having the younger crowd around. Cody and Austen play with them, tease them, carry them, feed them, and try to protect the house from little fingers...and in return? The babies adore the boys.
Reini shows her adoration by hiding under the piano when it is time to leave. Everyone looks and Reini is not to be found. When she is...it is always followed, with loud wails, tears and No..No..you CAN'T find me! Try again. (more sobbing) Jack continues to bring the boys random items...blocks, little people, cars. Malichai throws things at them...and Levi shows off his latest noises. This week? Levi can make spitting sounds that sound like a boat motor.
Sometimes , all this baby love can be a bit overwhelming for the older kids.
For example, last Thursday, Cody, Austen and friend Devin tried to write a timed essay. While for some people, essay writing is a cinch, this is not the case with these guys. Especially timed...because in years of self-directed learning..no one ever chose to write timed essays.
Until now. Why? Because these young men are practicing for ACT, SAT and Accuplacer.
So...back to the essay. I start the timer. The boys look at the writing prompt..and Levi and Malachai have a squealing contest.
Then? Malachai starts throwing cereal from the highchair. The cereal repeatedly hits Cody in the head. This causes Malachai to laugh hysterically, causing the boys to lose all concentration, because cereal on Cody's head is way more interesting than writing about reasonable expectations for the ethics of leaders.
While Malachai throws cereal..Levi makes boat noises..louder and louder and louder.
...and yes the boys managed to write essays. They almost made sense.
The boys and I agree. The time for a den is NOW.
So Big B, Cody and Austen remove walls, replace walls, add a huge entrance (that will be blocked by a baby gate!). We are not normally baby-gate people..but this is to keep the older boys in..really. The boys continue by putting up sheet rock..and we paint the floor (YES we pulled out the green carpet..but cannot afford the floor we want) a blue/grey.
This is to be the older kids space. The baby-free zone. The one and only zone in the house, where they can be teens/young adults...without playing with babies. This den..is their line in the sand.
Here's hoping we finish it soon.....
Several years ago Big B and I moved to the Tx. Hills. Our intention? To build a log cabin along the river.
1 year later we were still in the single-wide trailer that came on the lot. Still arguing over floor plans (and budget and time frame)...for the log cabin. We decided it was healthier for our marriage to buy a double-wide.
We spent the next 4 months looking at homes and finally found a floor-plan we loved. It had a living room with den attached, dining room, kitchen, morning room/laundry, 2 bathrooms and 3 bedrooms.
Then? We stumbled on this same house (only the den was a bedroom!)...for sale in Bandera.
If we bought the one off the lot? We would save almost 30 grand.
It was a no brainer. We would replace the green carpet, and turn the bedroom into a den. It would be less expensive to remodel than 30 grand.
So..you guessed it. Here we are 12 years later..and we still have green carpet...and we still have no den.
The den was originally going to be used for piano/violin lessons. Well..we just gave lessons in the kitchen or living room instead, until I stopped teaching.
Last summer Big B and I decide we really could use that space after-all.
Guests have no privacy on our pull-out couch in the living room. The teens and young adults needed some space to have an electronic explosion. (not literally..think Wii, guitars, lap-tops and..okay..electronics being taken apart) I do not want the explosion in the living room.
Big B and I agree. It is time!
Instead, we start a garage.
..and along come Levi...and also? Jack (2 years) and now Charlie (3/4 weeks?)..for community dining..and now Malachai (1 year) and Reini (3 years)..a couple days a week. Meaning?
The babies are everywhere!
Don't misunderstand. We love having the younger crowd around. Cody and Austen play with them, tease them, carry them, feed them, and try to protect the house from little fingers...and in return? The babies adore the boys.
Reini shows her adoration by hiding under the piano when it is time to leave. Everyone looks and Reini is not to be found. When she is...it is always followed, with loud wails, tears and No..No..you CAN'T find me! Try again. (more sobbing) Jack continues to bring the boys random items...blocks, little people, cars. Malichai throws things at them...and Levi shows off his latest noises. This week? Levi can make spitting sounds that sound like a boat motor.
Sometimes , all this baby love can be a bit overwhelming for the older kids.
For example, last Thursday, Cody, Austen and friend Devin tried to write a timed essay. While for some people, essay writing is a cinch, this is not the case with these guys. Especially timed...because in years of self-directed learning..no one ever chose to write timed essays.
Until now. Why? Because these young men are practicing for ACT, SAT and Accuplacer.
So...back to the essay. I start the timer. The boys look at the writing prompt..and Levi and Malachai have a squealing contest.
Then? Malachai starts throwing cereal from the highchair. The cereal repeatedly hits Cody in the head. This causes Malachai to laugh hysterically, causing the boys to lose all concentration, because cereal on Cody's head is way more interesting than writing about reasonable expectations for the ethics of leaders.
While Malachai throws cereal..Levi makes boat noises..louder and louder and louder.
...and yes the boys managed to write essays. They almost made sense.
The boys and I agree. The time for a den is NOW.
So Big B, Cody and Austen remove walls, replace walls, add a huge entrance (that will be blocked by a baby gate!). We are not normally baby-gate people..but this is to keep the older boys in..really. The boys continue by putting up sheet rock..and we paint the floor (YES we pulled out the green carpet..but cannot afford the floor we want) a blue/grey.
This is to be the older kids space. The baby-free zone. The one and only zone in the house, where they can be teens/young adults...without playing with babies. This den..is their line in the sand.
Here's hoping we finish it soon.....
Thursday, November 11, 2010
Epilepsy (long post)
Cut the dreads?!?!
Austen is debating joining the local law enforcement Explorers program. This would mean...(music please) cutting the dreads. But he is not sure.
As unimaginable as it may sound for a child of mine, Austen thrives in paramilitary environments. His experiences with Scouts and Civil Air Patrol have proven this. But...these programs (Scouts aside/Explorers included) usually have an emphasis on career exploration. Careers..that Austen are drawn too. AND careers whose doors remain closed for Austen.
Why? Because Austen has epilepsy.
It is estimated that 3 million people in the United States are affected with seizure disorders today.
According to this article The Scope of Epilepsy and Seizure in the United States
The severity of epilepsy varies from person to person. In an ongoing study sponsored by the Epilepsy Foundation on the impact of epilepsy and the cost of the illness, several distinct patient groups were identified. In about 60 percent, no additional seizures occurred after one year. In an additional 15 percent, several seizures occurred over time, but eventually ceased.
And in an unfortunate subset, amounting to about 40 percent of the total epilepsy population, seizures persist despite treatment and are considered intractable.
40 %! That is crazy. My sister, Tania is one of those 40%. My son, Austen..appears to be in the 15% (we are hopeful, fingers crossed) but it is too soon to tell.
Today, I am sharing Austen's story.
Austen is our numero tres son. Other than a few minor concerns about his growth (or lack there-of) and some delays in walking. Austen was a healthy baby. In early pre-school years, the concerns started to grow. Austen was ALWAYS sick. Asthma, pneumonia and bronchitis...along with numerous allergies.
The Spring before Austen started kindergarten, my friend Cookie and I loaded all three boys into her car for a month long trip to D.C. and back. We camped and visited family along the way. We stopped in numerous museums..and Austen chatted non-stop about being an army doctor.
When we visit the memorial wall in D.C...my little boy stands still..for a very long time. I stoop down in front on him. He has been silently crying. Austen looks me straight in the eyes. This should not happen. I have to be an army doctor. Maybe some of these names would not be here if I had been there. I dry his tears and think of his constant bronchitis. I assure him these men had doctors as well...but that I'm sure he will help people in the future. But first..don't you think we should start Kindergarten?
Austen started kindergarten wearing size 4T. He missed often due to bronchitis. When he was in class, he was in trouble. The teacher did not know what to do with him. He was always day-dreaming, wandering off or running around the room. Once? He danced on the desk! Just before Christmas, it was agreed that Austen should try Kindergarten again in a year..and by the way the teacher says, we think he is adhd..please consider putting him on medication. Here is the name of a psychiatrist we recommend.
Austen came home. We read books, he fished. We played with horses at a nearby girl-scout camp. We cooked, we painted. We went to LOTS of doctors. Pulmonologists, allergists, cardiologists (his lips were turning blue)...and we went to an assessment center through our local university health system to see about the adhd concerns. I had my doubts..but something was up, that was for sure.
It was discovered that Austen was CAPD and maybe ADD. Meaning..he had been trying to lip-read in the classroom. Hence..the constant running around. Still..all was well. No meds needed. Keep in touch if anything else comes up.
This continued..this learning at home..and constant illness for a couple of years. We dragged Austen to the activities of his brothers. Karate, Soccer...Austen would proudly cheer his brothers on..before falling asleep at the dojo or soccer fields. Why? Because he was SO TIRED and his head hurt. Austen always has a headache.
Just before his 9th birthday a friend of mine pulled me aside. She was Austen's scout leader..and she trained paramedics in the paycheck world. Nicole, she said, something is not right. He is getting more and more confused. He is wandering off and looking geuninely shocked at us. Sometimes..I think he doesn't know who we are. It's almost like..I don't know..a Hodgkinslike look or something. What are the doctors saying?
She is right. I know she is right. But the doctors have ruled out their major concerns..and keep trying to help him breathe. They don't know. I respond.
On his 9th birthday, Austen has a small party. Among the gifts received..a cool video-game. The boys are only allowed to engage in 4 hours of electronics a week. Austen is determined he will use all his 4 hours on THIS GAME...and he does.
The next morning, as I'm lying in bed. I hear tip-toeing in the next room. It is Austen.
That little sneak. I think to myself. He thinks I won't hear him playing. (His 4 hours are up for the week). I stay quiet to see if he is actually going to play the game. Yup..I hear the sound of the game..I hear race-cars...and the volume is quickly turned down..and I hear banging? Austen..AUSTEN.
He appears to be ignoring me..and I am stunned at how shameless he is. I walk into the living room to scold him..and there he is. Curled on the left side in a fetal position..game in hand...body banging. Austen is having a grand-mal seizure. I time him. (I learned this with my sister years ago). At 45 seconds he stops. I carry him to the couch and wake up his brother Cody.
Come on. I tell Cody.We have to take your brother to the hospital.
Cody rides in the back. He nurses Austen's head in his lap. Austen has no idea what is happening. We drive for an hour to the nearest emergency room. Cody keeps giving me an update. Mom..he's still breathing. Mom..he twitched. Mom..he's still breathing.
As we pull into the parking lot. Austen opens his eyes. Oh. he says.
Austen looks around..and looks at Cody. What are we doing here?!
You had a seizure. I respond. We're here for you. Come on we need to get you checked out.
Austen grins, he shrugs and skips into the E.R.
Once I convince the triage nurse that Austen REALLY DID HAVE A SEIZURE...they agree to run an EEG ..mostly to humor mom.
..and then? He seizes again. Then again. EEG records abnormal activity not just when he is obviously seizing..but even while he is just telling jokes to the nurses.
We are now welcomed into our new home away from home, at Methodist Children's Hospital and the Texas Neurological Institute. Austen meets his new best friend. The neurologist who continues to work with him today.
Over the next couple of years Austen's seizures get worse. We discover he has been having drop seziures, petit mals and nocturnal seizures for a while. Hence..the purple lips, day-dreaming and constant fatigue.
Austen begins the medication maze. We start with depakote. As the depakote dosages increase and the years pass, Austen becomes less focused in his thinking..he starts to have memory problems, his amonia levels get too high. It is time to switch to lamactal.. Austen spends 3 months being withdrawn from depakote and increasing lamactal. Then the lamactal rash starts. Another 3 months and daily visits to the nurologist..to lower, then slowly increase lamactal again.. Lamactal doses continue to be increased year after year. At his worst Austen is averaging 6 seizures a day. He begins hyperventilating and develops leg tremors.
Yet he remains optimistic. He knows he is better off than some of his friends at the T.N.I building...and even though he can no longer play any video games, go to arcades, movies that flash,etc...he feels really sorry for Joe. When I ask him why he says..Mom..he can't wear headphones! So..in Austen-land. All is well.
Austen's headaches continue.
This picture was taken during one of Austen's harder years. Here he had been home for almost a month due to uncontrolled seizures. Cody shows him how to play guitar.
We make the best of it. Big B says obnoxious things. For instance..one day when Austen's left leg kept trembling Big B..looked at Austen and said.Hmm..I think you like a girl. Shake your leg if you like a girl.
Austen would grin ..Dad..it's not funny. Stop. And then he would laugh.
We learn that Austen's triggers are flashing lights,needles (and this is a kid that needs LOTS of blood work), messed up sleep cycles and math.
It's a sequencing thing..so we cook and play games in place of any formal math work.
Many of Austen's asthma meds disrupt his sleep patterns. Our family physician and neurologist work closely to come up with a reasonable medication cocktail to enable Austen to function with the best life-style options possible. As his sleep becomes manageable..and his nocturnal seizures decrease, Austen finds the energy he never had.
Austen discovers gymnastics and roller hockey.
We are upfront with the gymnastics instructor. Not a problem, says the awesome gymnastics coach. He's most likely to have a seizure after he works out. We have mats on the floors. He'll be fine. The neurologist agrees...and encourages us to help Austen develop his risk-taking abilities...and so we do.
We realize Austen likes Roller Hockey because he can wear a helmet and blend in with everyone else. He becomes an active skater at the Boys and Girls Club. He rides bikes. He swims...and he has friends. We add karate to his list of activities.
Austen's friends are crucial. I have never seen so many supportive kids in my life. Birthday parties are planned in places Austen can attend. (I.E...no roller-skating and pizza places with flashing lights). Questions are asked to know how to help if and when. Austen's friends are protective of him.
..and then there are the brothers.
They are supportive, they are protective, they are obnoxious. I walk into the living room one day when Cody and Brian are trying to teach Austen what he looks like when he is having a grand-mal. The boys think this is great fun..and they could scare mom! I start to protest..but I realize, they are supporting Austen in their own, twisted, brother way. So I leave it alone.
Just before Austen's 11th birthday the neurologist calls me into his office. He would like us to consider surgery. Austen is on the same dosage of depakote needed for a grown man. The neurologist is concerned about liver damage...and if Austen is going to have surgery it needs to be either now, or after puberty.
We begin a series of tests.
More psychological, more EEG's, sleep apnea, MRI's, educational (to see what areas of his brain are affected). We discover Austen is dyslexcic, dyscalculic, and dysgraphic in addition to having memory loss. We contemplate putting him in school. The specialists advise us to keep him home. We are informed by the school district he would be a home-bound student if he were registered. After all (all medical and educational professionals agree) Austen shouldn't work on more than 15 minutes of formal academics at a time. It is too hard on his body. More testing..and...
It is decided that Austen is not emotionally ready for the surgery.
We have a no brain surgery for now ice-cream celebration.
In time, Austen gets better at managing his own lifestyle. We plug along with minimal book work. His short-term memory is shot. We think this is because of meds..but we are not sure. We make sure to show him pictures of people before any function so he can remember who they are. We tell and retell family stories over and over. We continue to read to Austen. We visit lots of museums and see lots of plays. Austen continues with karate, gymnastics and roller hockey...and then he gets pneumonia again.
When Austen is 12- almost 13 -our family physician refers him, again , to a pulmonologist. Austen is diagnosed with chronic pulmonary disorder and his meds are changed again. And you know what? They start to help...and as Austen's breathing becomes more regulated, the frequency of his seizures seems to decrease.
The headaches? They continue.
Austen joins Civil Air Patrol when he is 14. He flies planes, he becomes an element leader. AND he is really good! I love to watch him drilling others.
There are certain things people do that- when they have a gift..or simply really enjoy doing-makes them. beautiful to watch. I love to watch my son Brian do katas and complicated math problems. I love to watch Cody play soccer and work out computer programs. And I love to watch Austen when he is choreographing a drill..or working with a drill team. He is beautiful.
Just before Austen's 15th birthday, his neurologist decides to take him off of his meds! We are stunned.
I know, he says. It makes no physiological sense. Let's just say, serendipity has struck again.
He pats me on the shoulder and gives me a wink. This is the way to decrease his meds. Call me if there is a problem. Otherwise? Austen..I hope to never see you again.
Here is Austen lighting a camp-fire for brother Brian's 20th birthday camp-out.
I would like to say that was the end of the story.
It is not.
Austen returned to the ER last Spring with a migraine that led to an altered mental state. This led to another round of testing with neurologists and cardiologists. But Austen is still off of meds...and for the most part his memory seems to have returned.
It has now been determined that Austen has Bickerstaff Encephalitis. Essentially, his brain stem swells as a reaction to pulmonary stuff (originally). One of the times his brain was swelling, he received lesions on his left-frontal lobe. Causing permanent scarring -hence epilepsy. The brain swelling occurs off and on. This is Bickerstaff. We now know that this swelling is triggered by numerous food additives.
Today Austen is 16.
He sits in my living room reading Peter Pan as I type. He still works as Junior Staff at the Boys and Girls Club.
He quit Civil Air Patrol a year ago.
Austen realized he would never be able to be in the air-force and decided to turn his attention another direction. He spent a year directing all his attention to Odyssey of the Mind..and now he is searching, yet again. My son will not be an army doctor, an airforce search and rescue guy..or Drill Sergeant. But Austen is amazingly social, bright and resilient. He contemplates opening a cafe, being a museum curator..or maybe..maybe..he will be president...
Austen misses the structure, the leadership training, the camaraderie and the challenges of the Civil Air Patrol environment, yet he seeks to grow. Austen seeks to soar beyond his limitations..and accept the ones he cannot change.
I do not know what Austen's future will hold. Will he stay relatively healthy? Will he get sick again?
I do know that Austen is a strong-spirit. I am lucky to be his mom.
So..the question, for now remains. Will Austen keep his dreads?
Austen is debating joining the local law enforcement Explorers program. This would mean...(music please) cutting the dreads. But he is not sure.
As unimaginable as it may sound for a child of mine, Austen thrives in paramilitary environments. His experiences with Scouts and Civil Air Patrol have proven this. But...these programs (Scouts aside/Explorers included) usually have an emphasis on career exploration. Careers..that Austen are drawn too. AND careers whose doors remain closed for Austen.
Why? Because Austen has epilepsy.
It is estimated that 3 million people in the United States are affected with seizure disorders today.
According to this article The Scope of Epilepsy and Seizure in the United States
The severity of epilepsy varies from person to person. In an ongoing study sponsored by the Epilepsy Foundation on the impact of epilepsy and the cost of the illness, several distinct patient groups were identified. In about 60 percent, no additional seizures occurred after one year. In an additional 15 percent, several seizures occurred over time, but eventually ceased.
And in an unfortunate subset, amounting to about 40 percent of the total epilepsy population, seizures persist despite treatment and are considered intractable.
40 %! That is crazy. My sister, Tania is one of those 40%. My son, Austen..appears to be in the 15% (we are hopeful, fingers crossed) but it is too soon to tell.
Today, I am sharing Austen's story.
Austen is our numero tres son. Other than a few minor concerns about his growth (or lack there-of) and some delays in walking. Austen was a healthy baby. In early pre-school years, the concerns started to grow. Austen was ALWAYS sick. Asthma, pneumonia and bronchitis...along with numerous allergies.
The Spring before Austen started kindergarten, my friend Cookie and I loaded all three boys into her car for a month long trip to D.C. and back. We camped and visited family along the way. We stopped in numerous museums..and Austen chatted non-stop about being an army doctor.
When we visit the memorial wall in D.C...my little boy stands still..for a very long time. I stoop down in front on him. He has been silently crying. Austen looks me straight in the eyes. This should not happen. I have to be an army doctor. Maybe some of these names would not be here if I had been there. I dry his tears and think of his constant bronchitis. I assure him these men had doctors as well...but that I'm sure he will help people in the future. But first..don't you think we should start Kindergarten?
Austen started kindergarten wearing size 4T. He missed often due to bronchitis. When he was in class, he was in trouble. The teacher did not know what to do with him. He was always day-dreaming, wandering off or running around the room. Once? He danced on the desk! Just before Christmas, it was agreed that Austen should try Kindergarten again in a year..and by the way the teacher says, we think he is adhd..please consider putting him on medication. Here is the name of a psychiatrist we recommend.
Austen came home. We read books, he fished. We played with horses at a nearby girl-scout camp. We cooked, we painted. We went to LOTS of doctors. Pulmonologists, allergists, cardiologists (his lips were turning blue)...and we went to an assessment center through our local university health system to see about the adhd concerns. I had my doubts..but something was up, that was for sure.
It was discovered that Austen was CAPD and maybe ADD. Meaning..he had been trying to lip-read in the classroom. Hence..the constant running around. Still..all was well. No meds needed. Keep in touch if anything else comes up.
This continued..this learning at home..and constant illness for a couple of years. We dragged Austen to the activities of his brothers. Karate, Soccer...Austen would proudly cheer his brothers on..before falling asleep at the dojo or soccer fields. Why? Because he was SO TIRED and his head hurt. Austen always has a headache.
Just before his 9th birthday a friend of mine pulled me aside. She was Austen's scout leader..and she trained paramedics in the paycheck world. Nicole, she said, something is not right. He is getting more and more confused. He is wandering off and looking geuninely shocked at us. Sometimes..I think he doesn't know who we are. It's almost like..I don't know..a Hodgkinslike look or something. What are the doctors saying?
She is right. I know she is right. But the doctors have ruled out their major concerns..and keep trying to help him breathe. They don't know. I respond.
On his 9th birthday, Austen has a small party. Among the gifts received..a cool video-game. The boys are only allowed to engage in 4 hours of electronics a week. Austen is determined he will use all his 4 hours on THIS GAME...and he does.
The next morning, as I'm lying in bed. I hear tip-toeing in the next room. It is Austen.
That little sneak. I think to myself. He thinks I won't hear him playing. (His 4 hours are up for the week). I stay quiet to see if he is actually going to play the game. Yup..I hear the sound of the game..I hear race-cars...and the volume is quickly turned down..and I hear banging? Austen..AUSTEN.
He appears to be ignoring me..and I am stunned at how shameless he is. I walk into the living room to scold him..and there he is. Curled on the left side in a fetal position..game in hand...body banging. Austen is having a grand-mal seizure. I time him. (I learned this with my sister years ago). At 45 seconds he stops. I carry him to the couch and wake up his brother Cody.
Come on. I tell Cody.We have to take your brother to the hospital.
Cody rides in the back. He nurses Austen's head in his lap. Austen has no idea what is happening. We drive for an hour to the nearest emergency room. Cody keeps giving me an update. Mom..he's still breathing. Mom..he twitched. Mom..he's still breathing.
As we pull into the parking lot. Austen opens his eyes. Oh. he says.
Austen looks around..and looks at Cody. What are we doing here?!
You had a seizure. I respond. We're here for you. Come on we need to get you checked out.
Austen grins, he shrugs and skips into the E.R.
Once I convince the triage nurse that Austen REALLY DID HAVE A SEIZURE...they agree to run an EEG ..mostly to humor mom.
..and then? He seizes again. Then again. EEG records abnormal activity not just when he is obviously seizing..but even while he is just telling jokes to the nurses.
We are now welcomed into our new home away from home, at Methodist Children's Hospital and the Texas Neurological Institute. Austen meets his new best friend. The neurologist who continues to work with him today.
Over the next couple of years Austen's seizures get worse. We discover he has been having drop seziures, petit mals and nocturnal seizures for a while. Hence..the purple lips, day-dreaming and constant fatigue.
Austen begins the medication maze. We start with depakote. As the depakote dosages increase and the years pass, Austen becomes less focused in his thinking..he starts to have memory problems, his amonia levels get too high. It is time to switch to lamactal.. Austen spends 3 months being withdrawn from depakote and increasing lamactal. Then the lamactal rash starts. Another 3 months and daily visits to the nurologist..to lower, then slowly increase lamactal again.. Lamactal doses continue to be increased year after year. At his worst Austen is averaging 6 seizures a day. He begins hyperventilating and develops leg tremors.
Yet he remains optimistic. He knows he is better off than some of his friends at the T.N.I building...and even though he can no longer play any video games, go to arcades, movies that flash,etc...he feels really sorry for Joe. When I ask him why he says..Mom..he can't wear headphones! So..in Austen-land. All is well.
Austen's headaches continue.
This picture was taken during one of Austen's harder years. Here he had been home for almost a month due to uncontrolled seizures. Cody shows him how to play guitar.
We make the best of it. Big B says obnoxious things. For instance..one day when Austen's left leg kept trembling Big B..looked at Austen and said.Hmm..I think you like a girl. Shake your leg if you like a girl.
Austen would grin ..Dad..it's not funny. Stop. And then he would laugh.
We learn that Austen's triggers are flashing lights,needles (and this is a kid that needs LOTS of blood work), messed up sleep cycles and math.
It's a sequencing thing..so we cook and play games in place of any formal math work.
Many of Austen's asthma meds disrupt his sleep patterns. Our family physician and neurologist work closely to come up with a reasonable medication cocktail to enable Austen to function with the best life-style options possible. As his sleep becomes manageable..and his nocturnal seizures decrease, Austen finds the energy he never had.
Austen discovers gymnastics and roller hockey.
We are upfront with the gymnastics instructor. Not a problem, says the awesome gymnastics coach. He's most likely to have a seizure after he works out. We have mats on the floors. He'll be fine. The neurologist agrees...and encourages us to help Austen develop his risk-taking abilities...and so we do.
We realize Austen likes Roller Hockey because he can wear a helmet and blend in with everyone else. He becomes an active skater at the Boys and Girls Club. He rides bikes. He swims...and he has friends. We add karate to his list of activities.
Austen's friends are crucial. I have never seen so many supportive kids in my life. Birthday parties are planned in places Austen can attend. (I.E...no roller-skating and pizza places with flashing lights). Questions are asked to know how to help if and when. Austen's friends are protective of him.
..and then there are the brothers.
They are supportive, they are protective, they are obnoxious. I walk into the living room one day when Cody and Brian are trying to teach Austen what he looks like when he is having a grand-mal. The boys think this is great fun..and they could scare mom! I start to protest..but I realize, they are supporting Austen in their own, twisted, brother way. So I leave it alone.
In this picture Brian is putting sunscreen on Austen. During this vacation Austen was fighting headaches and a medication rash the entire trip..but he was determined to have a good time...and he did!
Just before Austen's 11th birthday the neurologist calls me into his office. He would like us to consider surgery. Austen is on the same dosage of depakote needed for a grown man. The neurologist is concerned about liver damage...and if Austen is going to have surgery it needs to be either now, or after puberty.
We begin a series of tests.
More psychological, more EEG's, sleep apnea, MRI's, educational (to see what areas of his brain are affected). We discover Austen is dyslexcic, dyscalculic, and dysgraphic in addition to having memory loss. We contemplate putting him in school. The specialists advise us to keep him home. We are informed by the school district he would be a home-bound student if he were registered. After all (all medical and educational professionals agree) Austen shouldn't work on more than 15 minutes of formal academics at a time. It is too hard on his body. More testing..and...
It is decided that Austen is not emotionally ready for the surgery.
We have a no brain surgery for now ice-cream celebration.
In time, Austen gets better at managing his own lifestyle. We plug along with minimal book work. His short-term memory is shot. We think this is because of meds..but we are not sure. We make sure to show him pictures of people before any function so he can remember who they are. We tell and retell family stories over and over. We continue to read to Austen. We visit lots of museums and see lots of plays. Austen continues with karate, gymnastics and roller hockey...and then he gets pneumonia again.
When Austen is 12- almost 13 -our family physician refers him, again , to a pulmonologist. Austen is diagnosed with chronic pulmonary disorder and his meds are changed again. And you know what? They start to help...and as Austen's breathing becomes more regulated, the frequency of his seizures seems to decrease.
The headaches? They continue.
Austen joins Civil Air Patrol when he is 14. He flies planes, he becomes an element leader. AND he is really good! I love to watch him drilling others.
There are certain things people do that- when they have a gift..or simply really enjoy doing-makes them. beautiful to watch. I love to watch my son Brian do katas and complicated math problems. I love to watch Cody play soccer and work out computer programs. And I love to watch Austen when he is choreographing a drill..or working with a drill team. He is beautiful.
Just before Austen's 15th birthday, his neurologist decides to take him off of his meds! We are stunned.
I know, he says. It makes no physiological sense. Let's just say, serendipity has struck again.
He pats me on the shoulder and gives me a wink. This is the way to decrease his meds. Call me if there is a problem. Otherwise? Austen..I hope to never see you again.
Here is Austen lighting a camp-fire for brother Brian's 20th birthday camp-out.
I would like to say that was the end of the story.
It is not.
Austen returned to the ER last Spring with a migraine that led to an altered mental state. This led to another round of testing with neurologists and cardiologists. But Austen is still off of meds...and for the most part his memory seems to have returned.
It has now been determined that Austen has Bickerstaff Encephalitis. Essentially, his brain stem swells as a reaction to pulmonary stuff (originally). One of the times his brain was swelling, he received lesions on his left-frontal lobe. Causing permanent scarring -hence epilepsy. The brain swelling occurs off and on. This is Bickerstaff. We now know that this swelling is triggered by numerous food additives.
Today Austen is 16.
He sits in my living room reading Peter Pan as I type. He still works as Junior Staff at the Boys and Girls Club.
He quit Civil Air Patrol a year ago.
Austen realized he would never be able to be in the air-force and decided to turn his attention another direction. He spent a year directing all his attention to Odyssey of the Mind..and now he is searching, yet again. My son will not be an army doctor, an airforce search and rescue guy..or Drill Sergeant. But Austen is amazingly social, bright and resilient. He contemplates opening a cafe, being a museum curator..or maybe..maybe..he will be president...
Austen misses the structure, the leadership training, the camaraderie and the challenges of the Civil Air Patrol environment, yet he seeks to grow. Austen seeks to soar beyond his limitations..and accept the ones he cannot change.
I do not know what Austen's future will hold. Will he stay relatively healthy? Will he get sick again?
I do know that Austen is a strong-spirit. I am lucky to be his mom.
So..the question, for now remains. Will Austen keep his dreads?
Tuesday, November 09, 2010
Lazy Day Bliss
It is starting to feel like Fall here in the Tx. Hills - also known as the land with no seasons.
This morning we awoke to a howling wind. Levi is up and ready to play at 4 a.m. Somehow, he hasn't gotten the message there has been a time change. No explaining will do. Levi is not interested, in the least, in day-light savings.
I place a kettle on the stove. Cinnamon tea it is. I place a Louis Armstrong c.d. in our kitchen c.d. player...and this seems to have set the tone for our day.
I absolutely love days with no agenda.
Austen is still recovering from hunting over the weekend.Too much time in the cold..his asthma is in full swing.Yet he is grateful. You know,he says with a grin, I'll take this kinda sick over a migraine any day. At least I can still function. Cody is swollen, bruised and bloody (it's soccer season).
We are finally finished with transcripts, grants, soccer paper-trail, etc. Working on Cody's transcripts motivated me to be a little more organized with Austen. So..Sunday night I started putting Austen's transcript together. Oh my.
I show him what he has accomplished (in that highschool transcript checklist sort-of way) so-far. Austen is still a sophomore, he has completed the equivalent of 2 years of highschool English, 3 years of science, 2 years of social sciences, and numerous electives..but math?..and .. you know Gov't and U.S history. Well..We do have another 2 1/2 years. We agree to switch math programs that might be more effective for Austen.
So anyway..after all this paper-trail, trying to be organized stuff..on top of just feeling puny. We decide a lazy day is in order.
The boys have spent the morning reading.Cody snuggles under the blankets in his room to read Hamlet, Austen sprawls out on the living room floor to read The Story of US (Thirteen Colonies). He is next to Levi. Levi has spent most of the morning trying to learn to craw. Occasionally Levi and Austen get distracted playing peek-a boo with a quilt..which for some reason Levi finds hysterically funny. I rotate laundry, pack stuff to give to the Ronald McDonald House, start some minestrone and play on the computer.
Occasionally we converse with each other. Austen wants to know if I know what a privateer is. He is enamored with the idea of a pirate that works for a king. I mean, really. What could be cooler?
At one point, Cody wanders into the living room. We discuss whether to give away an old science set. Before long I realize that the boys and I have spent over an hour in conversation. A range of topics from telescopes, netflix, suicide... privateers.
Cody decides to make omelets for lunch. Austen is not far behind.
Now? The kitchen has been raided, bellies are full. All studying seems to have ceased..and we are planning a movie/ Terminator-Sarah Connor Chronicles marathon for the rest of the day...complete with left-over Halloween candy.
Ahh..lazy day bliss.
What's for dinner:
Monday: community dining at Balsley's (or Balsley take-out for those at soccer) Spaghetti!
Tuesday: minestrone, grilled sandwiches, sliced tomatoes and cucumbers
Wednesday: three cheese tortellini, salad
Thursday: honey chipotle salmon, wild-rice, broccoli with cheese
Friday: make your own pizza
Saturday: swiss steak, bread sticks, spinach salad
Sunday: linguine with Alfredo sauce, stuffed clams, green beans, sliced fruit
This morning we awoke to a howling wind. Levi is up and ready to play at 4 a.m. Somehow, he hasn't gotten the message there has been a time change. No explaining will do. Levi is not interested, in the least, in day-light savings.
I place a kettle on the stove. Cinnamon tea it is. I place a Louis Armstrong c.d. in our kitchen c.d. player...and this seems to have set the tone for our day.
I absolutely love days with no agenda.
Austen is still recovering from hunting over the weekend.Too much time in the cold..his asthma is in full swing.Yet he is grateful. You know,he says with a grin, I'll take this kinda sick over a migraine any day. At least I can still function. Cody is swollen, bruised and bloody (it's soccer season).
We are finally finished with transcripts, grants, soccer paper-trail, etc. Working on Cody's transcripts motivated me to be a little more organized with Austen. So..Sunday night I started putting Austen's transcript together. Oh my.
I show him what he has accomplished (in that highschool transcript checklist sort-of way) so-far. Austen is still a sophomore, he has completed the equivalent of 2 years of highschool English, 3 years of science, 2 years of social sciences, and numerous electives..but math?..and .. you know Gov't and U.S history. Well..We do have another 2 1/2 years. We agree to switch math programs that might be more effective for Austen.
So anyway..after all this paper-trail, trying to be organized stuff..on top of just feeling puny. We decide a lazy day is in order.
The boys have spent the morning reading.Cody snuggles under the blankets in his room to read Hamlet, Austen sprawls out on the living room floor to read The Story of US (Thirteen Colonies). He is next to Levi. Levi has spent most of the morning trying to learn to craw. Occasionally Levi and Austen get distracted playing peek-a boo with a quilt..which for some reason Levi finds hysterically funny. I rotate laundry, pack stuff to give to the Ronald McDonald House, start some minestrone and play on the computer.
Occasionally we converse with each other. Austen wants to know if I know what a privateer is. He is enamored with the idea of a pirate that works for a king. I mean, really. What could be cooler?
At one point, Cody wanders into the living room. We discuss whether to give away an old science set. Before long I realize that the boys and I have spent over an hour in conversation. A range of topics from telescopes, netflix, suicide... privateers.
Cody decides to make omelets for lunch. Austen is not far behind.
Now? The kitchen has been raided, bellies are full. All studying seems to have ceased..and we are planning a movie/ Terminator-Sarah Connor Chronicles marathon for the rest of the day...complete with left-over Halloween candy.
Ahh..lazy day bliss.
What's for dinner:
Monday: community dining at Balsley's (or Balsley take-out for those at soccer) Spaghetti!
Tuesday: minestrone, grilled sandwiches, sliced tomatoes and cucumbers
Wednesday: three cheese tortellini, salad
Thursday: honey chipotle salmon, wild-rice, broccoli with cheese
Friday: make your own pizza
Saturday: swiss steak, bread sticks, spinach salad
Sunday: linguine with Alfredo sauce, stuffed clams, green beans, sliced fruit
Thursday, November 04, 2010
In the beginning
(John1:1) In the beginning was the Word, and the Word was with God, and the Word was God.
Over a year ago I attended a 1/2 day Biblical Story-telling workshop. The speaker told of a challenge he received in college to memorize his favorite Gospel.He chose Mark. I have thought of this often in the past year.
It is no secret that the bible was never meant to be read. It was meant to preserve the stories. As in oral -storytelling tradition stories. (okay..I know, I know..the letters from Paul, etc.) Still..most biblical stories are meant to be told. Not read.
I am drawn to John. Always have been. But really? It's the longest gospel. I'm not that talented. So I tuck the idea in the back of my mind and leave it there.
Then? I begin reading some of St. Teresa of Avilla's Interior Castles. I am working on letting go of anything that holds power over me. Primarily..ideas of social status, and memories. Memories that are good, bad..or simply never were. I take these ideas/memories and hold them individually and collectively...and then I pray. I pray for guidance on letting these things that hold power over me go. I pray and listen...and as I listen? I keep coming back to the book of John.
So..I am trying to memorize the book of John. So far? I am comfortable with story telling John 1:1- 5.
Yeah..back to the not that talented. Yet I am compelled to try. And somehow? This feeble attempt to know John...well..is helping me enjoy (okay all you Eckhart Tolle fans) the here and the now.
So..as for the here and the now? I would like to tell a tale of another beginning.
It was the beginning of my marriage to Big B. We were young, naive, broke..and hopeful..that we could really make this work.We dared eachother into this venture..and then headed to the flea market (because we like flea markets..) to search for wedding rings.
Fast forward a decade+. I have lost my ring .Rumor has it , it might be on a ship in Corpus Christi somewhere. Brian has broken his at least 3 times. We spend a few years without rings. For the last year and a half? We just keep talking about looking for some replacements..you know..when we have time.
So this weekend? We made the time! We spent the weekend in Port Aransas with the Van Bibbers , Balsleys, Devin and Austen.
Cody chose to hang at sardinemama's house for the weekend. Brian and Angee? Studying still.
Pictured here are Jack and Rhonda early Sat.(Sun?) a.m..
and pictured here are Austen and Devin with newly discovered costumes from a yard-sale.
On Saturday, we messed around in souvenir shops..when I thought. Aha..we should get beach rings! We can afford them...and the mission began.
We went from shop to shop- Big B and I ..dragging all the other families (complete with the wolf and dragon boys)and I would explain our plight.
Here's the thing, I begin. We (motioning to Big B and myself) lost our wedding rings a few years ago. We would like to replace them while we are here..but we are on a budget..and sort-of irresponsible..so we might lose them (break them) again. Still..we enjoy being here (Port A) and would like to try. Could you help us?
And most places did. Shop 1? We found cool rings made of shells. But they only fit me. Shop 2? Wooden rings..but Big B didn't want flowers. Shop 3? Nope. Then? (and by now we have lost everyone else..they were much more interested in t-shirts) Shop 4: Two women helped us dig through a bucket of womens rings. Finally Big B finds one with waves. He grins. This is it. I like this. We decide it is perfect because we have spent 20 years "riding the waves of life together."
Another search through the bucket of mens rings..and we find the match.
By this time the rest of the crew have wandered into this shop. The woman behind the counter directs us to place our rings on eachother's fingers. She waves her hands in a grand gesture and announces that we are officially rewed.
...and we are off to enjoy the rest of the weekend.
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