I’m Going with Them Dad. Okay?

Fireworks.  Looking for inspiration I came across some fireworks pictures I snapped last July 4th.  This picture shows a typical firework just after the in-air explosion to 3.2 seconds later; revealing the path of each burning ember.

fiework-6262Metaphorically speaking, I see Savanna’s development the last 6 months like the firework picture, several areas of growth exploding independently, creating a wonderful overall effect, but also showing signs of stall as the burning embers drift with the wind – propellant exhausted.

Like the firework picture, I actually see Savanna as she was 6 months ago and how she is now – all at the same time.

I hear her opine on and on about different subjects!  To the point I find my self asking her to be quiet sometimes.  I hear grammatically proper and phonetically correct sentences.  I hear an exploding vocabulary, with nearly unlimited parroting.

Phrases such as ‘fwench fwies’,  are quickly being replaced with the correct phrases.  Suddenly, her social interaction and behavior looks normal?  Her physical ability now allows her to ‘hang with the boys’ for the most part, feeding the positive social interaction.

I praise her advancements since our last outing to the play place, playground, or the stairs that lead to the Speech Therapy facility.  I do not praise mediocrity but rather encourage exceptional performance and behavior; both with our boys and Savanna.  She responds to that fuzzy but hard line.

I am amazed!

I also still hear the struggle in her language.  I hear the difficulty pronouncing complex sounds.  I hear echolalia.  I see the inappropriate grading of physical gestures towards her brothers.  I see the undeniable speed difference with which she processes and reacts to new environmental input.

Like the drift evident in the fireworks picture, I see her coasting for the moment.  And when she can’t respond to the fuzzy but hard line like her brothers, well….

I am concerned.

I am both amazed and concerned at the same time.

For the first time, I have observed Savanna realize her challenges with expressive speech.  Watching her put up emotional walls and turn inward was profound.  My mind raced forward 10 years regarding her emotional health.

Discharged in September from facility-based ABA, she has progressed to a level where she can function in mainstream environments, or so we think.  Similarly, she was discharged in November from in-home OT services for the same reasons.  These 2 months were like letting go of the bike when you have been running along with your 5-year-old for miles holding them upright…. And suddenly; there they go; on their own.  And all the ‘what if’ scenarios start to play out…

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Her BCBA at the ABA facility recommended that we start in-home ABA services to surveil her progress.  Her developmental pace is what we now monitor.  Is she keeping up or does she need help?  A neuro-psychological evaluation in the coming years will help us identify specific areas which might need extra attention.

Right now, life with Savanna is such a blessing and joy as she seems to fit right in with her peers.

Well, there are moments of course that are very unpleasant, like when she goes # 2 in her pants.  Yeah, that sucks – still.  It sucked a lot less when she wore a diaper, but she has mastered #1 and I find she loses that mastery when the diaper goes on or when the routine changes, so now what?  We are going on a year of #2 training.  She has no desire that I can see to accomplish this task, despite all our incentives.  I feel defeated in this area for sure.

She is in fact, only 4 years old.  While I see her as a professionally trained child with nearly 2000 hours of formal therapy, most see her as just a 4-year-old little girl with a short haircut and cute sunglasses.  She has what?  She is missing what?  She can’t see what?  Really?

Yes, really.  That is amazing I know!  God be praised!

Savanna follows much more than she leads, which is okay I guess.  She does initiate activities Austin enjoys, like building anything Lego, coloring, etc.  She will mimic just about anything Austin does.  Thankfully, she still sits to go pee pee! But, I won’t be surprised if she decides to stand up like Austin, lol.

She is also great at being mischievous.  A hidden talent, no doubt.  A short example:

Not long ago, we went to ‘Hot Wobby’, Savanna lingo for ‘Hobby Lobby’.  I only needed a picture frame that was already in my mind.  They (her and Austin) walked away around the corner and I thought to myself, “they will be okay” as I let them go.  I could not find my frame, and then I heard ‘the devious laugh’.  I turned the corned and found them with a couple hundred gift cards and envelopes scattered in two distinct piles in the aisle.  It almost looked competitive, like who could make the bigger mess!  I was too embarrassed to even take a picture.

Savanna was proud of herself and the look on Austin’s face turned from priceless to fear as he realized I was there.  He knew he did wrong and immediately covered his butt with his hands, because Yes, I am one of those parents!  Savanna still has both frontal lobes but, sometimes I wonder about the function as she didn’t get the ‘wrong’ at all?  lol.

Noteworthy is the increased tolerance and patience from her brothers including her twin brother.  Not just the expected empathetic response to your sister being hurt, but truly being patient with her knowing she isn’t behaving appropriately.  Just when I think they do not ‘get it’, I see the interaction when a friend or classmate comes over who has no awareness whatsoever of Savanna’s challenges.

It is then that I realize the real affect of Savanna on them.  Heavy is my heart during these moments of reflection.  What will they be burdened with when I am gone from this earth and Savanna needs a lot of help?  Their preparation is under way already.

In June we ‘graduated’ a pre-K and 1st grader to Kindergarten and 2nd grade.  Savanna regularly proclaims “I will ride the bus Sunday!” (she means some day).  She is right.

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Early into summer, I thought Swim Lessons would be a good idea!  Savanna’s relationship with the water is sinusoidal love-hate.  This period was one of hate unfortunately.   Challenged by her own behavior, she had difficulty responding during the lessons, despite this cute picture.

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Despite all the protest and hassle, Savanna did learn. And, she demonstrated that later in the summer.

Vacation!  FL-VA-KY this year.  Destin, FL, was our first stop for some time in the white sand with Rebecca’s family.  Still enrolled in facility based ABA at this point, Savanna’s day included immersion in all things ‘appropriate social interaction’.  She was happy showing off her skills and getting all the positive praise.  She loved the beach and the pool, but not the ocean.  NOT the ocean.  I don’t know why.  She didn’t even like us being in the ocean.

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She talked constantly during our stay in Destin.  Proving she generalized a skill, she learned everyone’s names quickly, 16 other people besides our little family of 6.  She initiated a lot of conversation.

But still, she was three.  And, so was Austin.  This picture during our attempt at a group picture, pretty much says it all – or a lot of it anyway!

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Our clown show arrived at Grandpa Ken and GranShe’s in VA house where Savanna once again amazed them with her independence, happiness, and seemingly new-found language.  Our boys love their house as it is on the lake with a large piece of mature woods, perfect for adventure and exploration.

Savanna was in a period of love with the water at this point, despite her recent protest at the ocean!  Once unthinkable, I now envision her someday riding the inner tube, or whatever, by herself.

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A quick stop in KY to see more family.  Savanna was such a joy during this trip.

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Returning from our trip, we ushered off the other kids to school.  While it felt good to put them on the bus, the unrelenting waves of unnecessary financial solicitation began; whereby the school and the PTO ransom the emotions of our children to puppeteer our check-writing hand.  I wish they would just ask straight up for money and stop the nonsense.  Soon after, the homework followed.  You know, the homework that always leaves you wondering what do they do all day at school?  (Austin is such a character in this picture!)

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We have a lot of Veteran’s in our family and to them, I say Thank You!

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We have 4 birthday’s in our house during the fall.  This year, Mommy celebrates the big Four O! (I am sure she is glad I added this, lol!)  Then Austin and Savanna turned 4!  Their journey: amazing!  God’s plan is at work.  Finally, Brandon turned 6.  He is the middle child, enough said. HaHa! Austin is a little poser!

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This picture of Brandon’s SpiderMan cake is a great one of Savanna.  Photographing her is often challenging.  Her eye contact is far less than her brothers – it is a constant battle.  Just about every photo moment takes about 100 pictures to get a decent one, and she often is still looking away.  Not today!  (Yes, Daddy made the cake – that’s right!)

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Despite the cute rainbow dress in this picture, Tom Boy best describes Savanna’s typical behavior.  She usually wants to wear Austin’s underwear, Austin’s socks, Austin’s pants, Austin’s shirts, and for sure Austin’s Jackets.  Her latest wish is Austin’s shoes, (that are like 4-5 sizes too big.)

These pictures are the best.  Taken on September 20th, their birthday, Austin is her Angel for sure.  Yes, Savanna is able to interact with him on his level, but he is patient and tolerant of her as she learns.

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Girl toys? Not so much.

Swords.  Power Rangers.  Ninja simulation.  Lego blocks.  Yes!

Girl pajamas, sometimes.  But, only over top of the boy ones, lol.

Here she is just wanting to do what the boys are doing, shortly before Halloween, field testing the Halloween gear of course.  (Almost none of this gear actually survived to see Halloween.)

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Then Halloween arrives.  Sigh.  Oh yes, Daddy’s favorite Holiday – not!  A day of memorial has morphed into extreme candy entitlement.  An elementary study of the foundation on which we celebrate some of our ‘Holidays’ reveals significant migration from the original intention.  We participated anyway because it is in fact Rebecca’s favorite Holiday, second only to Christmas.

Here is a cute video showing Austin taking his daily medicine from Savanna.  You can see in the video that Savanna hit Austin hard with the plastic sword on accident.  She displayed zero empathy and zero outward understanding she made a mistake whatsoever.  This kind of behavior is still a bit of a problem.

And then Brandon… He decided to start a game of ‘Hit the Butt’.  Yes, I know, judge me.  I have let it go because Savanna loves it so much.  Here is a little snippet of what that is like on the platform swing.

By the time October 31st actually arrived, most of our costumes showed significant signs of wear and (ab)use, as the daily play routine 3 weeks prior included mandatory use of all-things-Halloween.  Luckily this event happens at night.  Savanna did well, still quite slow, but she participated far more than the previous years.

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Thanksgiving was great this year as we hosted family from CA.  By now, Savanna was really warming up to Mommy.  She has really been a stinker in that regard, being a ‘Daddy’s girl’ to a fault.  (it was an ABA goal…to address Mommy)  But, mommy handled it well. And finally, the pendulum changed direction and we started hearing her ask Mommy to “come help”, “come see”, “take me with you”, “No!  I want Mommy to brush my teeth, wash my hair, etc…”

Here she is in a video compilation performing in a ‘Sing-A-Long’ for Thanksgiving at her school. A familiar daytime place presents 3 opportunities for nasty falls in the evening as her visual field cut gets the better of her at night.  Knees scraped up, she begins to derail emotionally as I usher her into the staging area.  Only Mom’s in there (Mom’s I don’t know), I feel the eyes of judgement from all around.  For a second, I contemplate giving up and giving in.  Then, I get right in her face and we work it out with tactical technique and surgical conversation I re-engage Savanna in the activity.  I promptly leave without looking back while Savanna cries, knowing she will be okay.  The onlookers thought I was a complete a-hole Dad for sure, but Savanna responds.  And respond she did!  Tristan, 7-years-old, captured these video snippets.

 

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Recently we were in KY for Christmas and were eating lunch at Aunt Kathy’s house.  Savanna wanted Mommy to come see something.  Mommy assured Savanna that she would ‘come see’ once done eating.

Savanna could not wait.  She came to the table, security blanket in hand (finger in the loop formed by the tag), and grabbed Mommy’s hand proclaiming “Mommy! You are done.  Come with me!”

Everyone got a good laugh, and was impressed at some level.

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November was epilepsy awareness month, with a special week in December for Infantile Spasms.  It passed quickly for me this year. Watching my Facebook news feed turn purple, I failed to address it out loud this year in any meaningful way.

I often struggle with Savanna’s amazing progress given the prognosis that comes with such a devastating neurological condition.  Why?

I could leave that life behind and operate under the assumption she is healed or cured.  But science doesn’t see Savanna’s situation as healed or cured; the same science that provided the course of treatment that helped her.

It may just be semantics to some, but I see Savanna on a path to resolution, not healed or cured or even on such a path.  My wife recently told me 99% of people would think I am wrong; that stopping the seizures is equivalent to cured or healed in their minds.

Cuts and broken bones heal.  Healing involves restoration of health, like ‘as it was before without loss’.  Removing brain cortex to gain seizure control is not a healing process in the true sense of the word, but one of resolution.  And no one truly understands the condition of the remaining cortex, as the underlying etiology is unknown to a large extent.

One could argue she is past the age of her West Syndrome, thus classifying this as resolved.  The cold truth is that Savanna is still very early in her journey with epilepsy.  Relief of her seizure burden by removing the offending tissue only guarantees seizures won’t come from that area of the brain ever again, nothing more, nothing less.  Her risk of experiencing more seizures is elevated.

Savanna remains seizure free, nearly 2 years and 9 months.  She also remains medication free, more than 2 years now! (Still an Engel/ILAE 1a surgical outcome for sure.)

I will always watch for seizures.  I can’t even look at another baby or child the same way, let alone Savanna.  The innocence is long lost, stolen in the dark of night.  In broad daylight I work each day to regain a little bit of security.  I do this without anger toward God.  I do not believe he wanted epilepsy to be part of her life.

I believe God’s plan is for each of us to find the good in life.  I consciously choose not to look away from Savanna’s past partly because it fuels my passion in actively helping others navigate once finding themselves on a similar and unlikely journey as a parent to a child like Savanna.

Segway to Dance Party!  This is a girl who had global discontinuities on her EEG (proverbial EEG ‘flat line’), global hypsarrhythmia, and really nothing at all normal happening in her brain at 12 weeks old.  Look at her today!

As long as we are able, we will make the pilgrimage back to KY and VA to visit family over Christmas.  At Grandpa Ken’s and GranShe’s house, we went on a ‘hiking adventure’ in the woods, well kind of anyway.  I encourage Savanna to go with her brothers.

Then, Savanna paused, turned towards me and proclaimed:

“I am going with them Dad. Okay?”

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The Emotional Roller Coaster

First, some housekeeping notes:

November is Epilepsy Awareness Month.

The Infantile Spasms Community on Facebook, is recognizing November 3-9 as Infantile Spasms Awareness Week.  The professional community is recognizing December 6-10 as Infantile Spasms Awareness Week.  This is sponsored by  the Child Neurology Foundation.

I intend to share stories from people affected directly or indirectly from epilepsy.  If you would like to share your story of how epilepsy touched you or your family, please contact me at ken lininger @ gmail com. (no spaces in the name)

Many of you know, we did battle IS in the beginning.  Savanna exhibited classic signs of Focal Cortical Dysplasia.  That is, intractable simple/complex partial seizures even though successfully controlling the IS.

Continue reading

Sunshine After the Rain

There is nothing like a 3400 mile road trip to bring out the best behavior in everyone – all stuck in the van for what amounted to north of 64 hours.  My apprehension taking Savanna on such a long road trip was high.  Her demeanor the past three months tempered my expectations.  In addition, results from the Bronchoscopy and EGD scope of her esophagus showed nothing was wrong.  Rebecca took her that day, and I was home with the other kids.  I remember getting the call, and actually feeling depressed.  I desperately wanted something found to be affecting her that could explain her lack of eating and near constant agitation.  Despite the fact she is not having seizures, we cannot live like this.  For the first time, I actually thought maybe we made a mistake with the brain surgery.  It was like a dark cloud was following her (and me) and the rain just wouldn’t let up.  I said a prayer that day for God to give me strength to carry on.

Yes, there was some less unhappy time, even some photo opportunities in the past 3 months.  But, I remember no discussion prior to surgery other than the common complications and rare unintended consequences, such as infection, hydrocephalus, and paralysis.  I did learn how to help her regulate her behavior, but it required a lot of heavy sensory input from me, and it was exhausting.  I just could not do it for more than 2 or 3 hours at a time.  At which point, I just had to put her down.  She could not just be held without a lot of stimulation.  Here is a short video of what she looked like during most of her time awake since the surgery (just before the trip)

Travelling in the car proved easy really, as Savanna really enjoyed the constant motion and movement which is known as vestibular sensory input.  Knowing how to regulate her behavior externally through my actions, I actually expected an easy car ride.  But she wasn’t just easy to manage, she was really happy at times.  It was refreshing to witness.  At the hotel, the alternate personality emerged, (and so did the Ativan®).  An hour or two was all we could endure at that point, and we had to intervene.

First stop on the trip was my Dad’s place in VA.  They live in a modern log cabin on Lake Anna, a man-made nuclear power plant cooling reservoir.  Lake Anna is nearly 17 miles long, populated by people who love being near the lake.  The obvious enjoyment of lake living overflows from their property onto elaborate docks complete with second story living areas, slides into the water, dry docks for several different types of watercraft, duck blinds, and even an airplane hangar or two.  It seems more developed each time we visit.  Rebecca had to work in DC, so I took all four kids out on the pontoon boat with Grandpa and Grandma 2 days in a row.  We pulled them around on the tube until they just didn’t want to tube anymore.  I even took Savanna out on the tube with me, and she really enjoyed it.   Before, after, and sometimes during, was challenging with Savanna as usual.

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Then on the third day there, a miracle happened.  Her morning was typical.  Inconsolable for about 5 hours, then nap time, and then she awoke and didn’t cry!  Like the sunshine after the rain, Savanna was happy. It was like a new beginning that day.  I didn’t know what to think or even how to appreciate it?  It was a relief at first.  She wasn’t screaming and crying constantly and I assumed that she would start crying again soon.

She became a Mommy’s girl instantly.  She wanted little to do with me, especially when Rebecca was within sight or earshot.  How selfish was I to be a little depressed by this particular behavior, being the only one who could seem to regulate her for any length of time in the past few months.  The coming days saw another leg of the trip (550 miles to Louisville, KY) where the other grandparents and family live.  She could not have been happier once at Rebecca’s parents’ house.  She smiled.  She laughed.  She was very deliberate with her actions and movements.  Her cry changed to one of ‘look at me!’ rather than the boo hoo of ‘why is this happening to me?’  The shallowness of my thoughts during those first days would soon be overshadowed by the change we saw.

I really think God was watching us and was acting.  I tried to explain to those around her our first night in Louisville that this had just happened.  My words felt like they became awkward, as none of them have really seen her in the last 3 months.  I should have just kept quite.  Looking back, what did the past really matter anyway?

The joy of peace and happiness filled the air.  All seemed right in the world.  I learned on this trip not to disturb such joy with unnecessary conversation.  I am still learning how to choose the right words to formulate responses to questions from many different types of people.  I am still learning how to exude happiness, elation, and even satisfaction about how great she is doing compared to where she was less than 1 year ago.

I have immersed myself in her every detail of her condition and care, delving deep into how persons like Savanna ‘recover’.  I have results from Early Intervention testing, advanced genetic testing, detailed clinic notes from many types of doctors, and feedback from therapists who spend most of their time with kids like Savanna.  I spend time helping others work through similar situations, providing support, just trying to listen.  All of this activity brings gravity to Savanna’s situation.  Yes she looks great.  Yes, only Savanna knows what she is going to do in this world.  Yes to all the anecdotal advice we are given.  But my vantage point gives my a different perspective.

A broken bone healing is how I think many see Savanna’s situation.  During this trip, the cast came off, function resumed, and now she is ‘normal’.  Just put her back with the other kids, right?  What is your problem Dad?  What, she won’t eat?  Well, you need to learn how to feed her – don’t you know?  Okay, maybe.  Maybe everyone is right and I am over thinking some things [but I don’t think so].

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Most professionals would agree that the broken bone example is over simplification, despite how she is acting at the moment.  On this journey with Savanna, I am learning how to converse with people about her situation at various levels.  Numerous times on this trip I found myself misguided in conversational direction.  I was too argumentative with my know-it-all attitude, and too late to change course aside from shutting down the conversation.  Live and learn.

Character flaw aside, I really enjoyed also watching Tristan, Brandon, and Austin spend time with their cousins and especially Savanna’s happiness with her Mommy.  I felt blessed by the end of the trip.  We let Tristan have a camera during the trip and just let him go to see what he would capture.  Attached are some of the photographs he captured.  Each day I see a little man emerging in Tristan.  I wish I could just freeze him just how he is so I could have more fun with him at this age, but life goes on.

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Our trip back to Houston was without incident, and Savanna has remained for the most part happy.  She seems much more engaged with her surroundings when she isn’t just wondering around on the floor crying.  She is exploring, learning, and having fun.

We accepted the arrival of our Au Pair, Ruth, from Australia.  Ruth is a great addition to our family and the kids have warmed up to her quickly.

I am learning each day how to better appreciate a little sunshine after the rain.

-ken

Our baby is home….

Savanna was discharged early Friday morning and we made it home by lunch time.  It was so nice to be home, feeling like we were back in the driver’s seat again with her care.  Savanna is doing better, but still has a long way to go in terms of recovery.  She is in a lot of pain, and the best we have to manage the situation is ibuprofen and Tylenol.

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The past few days have been rough trying to manage her pain.  It comes and goes.  We seem to get good moments all of a sudden, and then as quickly as it became good, it deteriorates into crying and fussiness.  She has absolutely no interest in taking a bottle, so we are back to bolus feeds only (through her feeding tube).  This is tricky when she is just agitated beyond consolation, and squirming like you would not believe.

I decided to make some adjustments to her medication to see if we could level out her mood without too much sedation.  I split her onfi back to TID (tri-daily) versus morning/bedtime only.  And I went ahead and started scheduling .5mg of ativan, TID.  This has helped tremendously.  She is much happier and playful, with a lot less ibuprofen.  Once we get completely off the dexamethasone (steroid for her stridor), that will help this situation too.

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She used to crawl by doing a bunny hop, versus alternating opposite leg/arm movements and now she is crawling like a normal baby.  Albeit not much, but when you see it, it takes your breath away at first.

She is eating, like a horse.  She is chewing well.  Against normal intuition as a parent, dicing food into incredibly small pieces enables babies to simply swallow food versus chewing.  One piece just the wrong way and she chokes or her gag reflex kicks in full force.   So, the O/T (occupational therapist) we have recommended giving her larger pieces, so she would not naturally want to swallow the food, but rather naturally realize she has to chew it first.   Even if she doesn’t swallow it at first, that’s okay, she is getting over the aversion to having food in her mouth.  This has been a long process with Savanna.  A process that honestly, we almost didn’t even notice with our other kids – that is how different they are from a developmental standpoint.  It is all good.

One step at a time.

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These guys are three pees in a pod.  They are the best of brothers, and worst of enemies when it is time for ‘warfare’ – aka ‘playing wrestle’.

Tristan, Brandon and Austin are such good helpers.  They love to do things for Savanna to help us.  Most of the time, it is a good help.  Sometimes, like when Brandon wants to spin Savanna on the sensory swing, things get a little out of control.  I picture in my mind puke spraying out from Savanna splattering the walls all around her as she spins wildly…. and then… well, I slow down the swing of course.  We have yet to see the puke, but I have to admit, she likes to spin.

They just crack me up with their antics and how Tristan (the oldest) can interact so well with Austin, (Savanna’s twin and the youngest).  He is so protective and makes sure Brandon does not hit him too hard, or ‘wrestle’ him too hard.  They drive me to my wits end, especially when Savanna is having a really difficult time.  Then they turn right around and do things that are so touching and so thoughtful.

Sometimes, I have caught myself making parenting mistakes with Tristan (oops! did I say that out loud?)  Yes.  When my patience is the thinnest, I act my least thoughtful.  I am so focused on something going on with Savanna, that I have said things in a voice that was not called for, but was heard.  These situations are difficult.

Like seeing a picture you shouldn’t see…you can’t ‘unsee’ it.  Once I hurt his feelings, it can take a long time for him to get over it no matter what I do or say.

In the beginning, he (Tristan) would ‘forgive’ (more like forget) pretty quickly, but not now.  He is older and smarter.  His feelings are genuinely hurt, and most times it goes into the next day.

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I am learning as a parent and person in this situation.  It is still a work in progress, but this ‘stay-at-home’ situation is far more difficult than I thought it would be when I signed up for it.  With that, of course, goes the reward far beyond what I could ever achieve in any company, at any level.

Seeing Savanna learn and progress, knowing that I am big part of that effort, just can’t be explained in words.  There are not words that I can put together to characterize the emotions involved, especially since this last surgery.

So, overall, Savanna is progressing and doing well.  We are really anxious for the next few months to see what happens.  We continue to learn as a family what it takes to care for someone like Savanna.  More challenges are forthcoming.  Just as I have said before, God is preparing us for the future with the situations of today.

A special thanks goes out to Grandpa Squiz, Grandma Lou, Mama Barbara, and McKenzie and Eric for being there when we really needed help.  They allowed us to devote 100% of our time to Savanna during the operation and recovery period in the hospital.  Their help was a blessing.

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Sometimes, Less is More: Less Brain Tissue with Focal Cortical Dysplasia Is More Freedom From Seizures.

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We have been blessed with witnessing a profound new beginning for Savanna after her first resection at 13 months of age. Today, God willing, we are expecting a new child to emerge from the operating room again as she undergoes … Continue reading

A Day to Give Thanks, to God.

An update on Savanna’s situation.

She is 4 weeks post-operative, and she is well.  We have started to titrate down some of her medications, but she is still on basically the same panel of medications that she was prior to the operation.  This is keeping her quite sedated.  We are starting to reduce the Onfi first, and see how she responds.  Despite the level of sedation, we are happy to report significant changes.  The biggest change we have seen is the engagement in her environment.  She seems to see her world differently now than she did prior to the surgery.  I looked at her over the crib rail one day and she smiled at me without any stimulation or sounds from me.  To most of you that may sound silly or trivial to bring up, but for me personally, it was profound.  She had never done that before and more importantly, it was a sign that at some level, her brain is working correctly.

She has periods where she tolerates sitting up in a bumbo seat or bouncer or something similar.  It is really rewarding to see that type of progress.  We still harbor a guarded optimism for her immediate outlook as we know some of the facts.  We know that the Sabril could be helping to suppress the Infantile Spasms.  Should we lower that dosage and the Spasms return, it would be another fork in the road of her journey to put it nicely.  Also we know that if Savanna would not have struggled as much as she did during the surgery, the surgical team would have expanded the resection.  While not trying to be an eternal pessimist, it is important that we have some emotional preparation for what the future may hold.  Another surgery is quite probable, and a life-long battle with seizures is also quite possible.

Unfortunately, we are still seeing abnormal activity at times.  Just last night, she was having a really difficult time sleeping, and I witness about 6 hours of what I would consider a seizure-filled period.  I am not positive that what I saw was seizures, but it would appear she has some partial activity still in the background, and it occasionally spikes enough to cause complex or clinical indications.  I am certain that a VTM/LTM is in her near future to diagnose what we are witnessing.  She has become quite cross-eyed lately and it is asymmetric in nature.  What is weird is that the opposite eye is effected than prior to the operation.

We are told she may be experiencing many circumstantial situations as she develops a new baseline.  In the mix too is that she is growing, and with infants, things can change fast as we have learned.  So, it may be possible she doesn’t reach a baseline for quite some time.  We have scheduled clinic visits to see the doctors in the neurosurgery, neurology, ophthalmology, and genetics departments next week.  We will send our blood samples to a couple of different labs to sequence her exome and our genome.  We are starting therapy again for motor skills, speech, and cognition.

I have included some pictures here that are from the last couple of weeks.  She truly is an angel and while we live the myth of Thanksgiving nowadays, we are very thankful this year for what God has given our family.  The true story of Thanksgiving has long since been white-washed and papered over with liberal textbooks.  It is a day that requires some inward thought about the real story, our past, and the future of our country.

For those of you who might want a closer look at what she underwent 4 weeks ago, there is a hidden link on our website that shows a few pictures from the surgery. [taken down, as of 2-2013] I am not posting the link, to the pictures, just to the website.  The link is the homepage picture.  It is mobile friendly.  Warning: they are graphic.

www.kenandrebecca.com

Have a great Holiday this weekend, and hope this email finds you and your family well.

Mom and Dad

(Ken and Rebecca)

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