Category: Epilepsy

What Happened to Happy?

It’s very interesting, as we live this life with Aaron, how we see all the ups and downs that go along with autism and Epilepsy and developmental delays.  We not only see the ups and downs, but we deeply experience their effects on him personally and on us as well.  Certainly anything that affects Aaron impacts Gary and I, too, and what a ride it can be!

Aaron really wants to enjoy happiness, but he wants it on his terms.  Sometimes that’s just not possible.  There are occasions where Gary and I walk a fine line as we attempt to provide a happy environment for Aaron without giving in to his every whim.  It’s like being on a boat.  We can be trolling along, happy and peaceful, and then all of a sudden we run upon choppy seas that threaten to overturn us.  Some days we can see the storm coming with Aaron as we read his mood.  Other days the storm swirls in out of the blue, unexpected, catching us off guard and then demanding all of our skills that we hoped we’ve learned over the years of parenting Aaron. 

This past Sunday night, Aaron and I were in the kitchen after playing Skip-Bo.  He was thinking of the next day as he said, “Mom, tomorrow’s Paradigm.  Let’s not let me go!”

I laughed at the funny way he phrased his comment, and then he laughed, and all was well.  The next day he was more adamant about not wanting to go.  Aaron loves Paradigm, but his dream life would be to stay home every day playing on the computer or watching movies.  That’s not going to happen and he knows it, but he still tries to test those waters.  He did go to Paradigm, but he did slam the van door and so I prayed as I drove away that somehow he would have a good day.  Barb said he was VERY grouchy when he came in but then settled down and had a really great day.  Yay!  Not yay for VERY grouchy, but yay that the rest of the day was great. 

Aaron pushed my buttons when he got home, blaming me for ruining his dream life and other ills as well.  Supper didn’t suit him, so Gary and I actually enjoyed a nice meal alone with uninterrupted conversation.  May as well see the silver lining in the cloud.

Later, Aaron and I had a talk, where I got firm and Aaron saw the light.  He was nice the rest of the evening…..almost.  Then came bedtime.  Why do so many things happen at bedtime?!  For instance, a couple weeks ago it was time for bed and Aaron knew it was time for bed.  If anyone knows anything about time, it’s Aaron!  But he was watching a movie, not wanting to quit until he was at some magic point, and so I did all the bedtime chores I do for him….and still he sat at his desk, engrossed in the movie. 

So I said goodnight, with some aggravation in my voice, and went to my bedroom.  I locked the door because I figured I would be followed.  Sure enough, I soon heard Aaron’s heavy steps coming up the hall.  He knocked loudly on the bedroom door and then said, “Mom!  I want to say goodnight in my room!”  You see, I hadn’t said our goodnights in the proper Aaron way.  I sighed and opened the door, where Aaron repeated what he had said about saying goodnight in his room.

“Come on!” he commanded as he walked briskly up the hall toward his room, before I could object.  But I did.  “Aaron,” I protested.  “I already said goodnight.”

“But you weren’t happy,” he explained.  How perceptive, I thought.  So, very tired and just wanting sleep, I followed him to his room.  He went into his room, turned toward me, and reached out for a hug.  I complied with an obligatory hug, not a heartfelt one.  I was still aggravated….and Aaron knew it.  I even said goodnight, but Aaron stared hard at me and then said, “You’re still not happy!”

So out went his arms again and this time I had to smile, more inside than out, as I gave him another hug.  I tried to make this hug more sincere, and I even did smile an outside smile as he stared at me again.

“Are you happy?” he cautiously asked.  And I assured him that I was happy, so that he would be happy, and I finally was released to go to bed…..at last!  His insistence on going to bed happy really was the right thing to do, much as I didn’t want to participate at that point, and his perceptions were also pretty amazing. 

Back to Monday night.  On Monday night I found myself wishing with all my might that Aaron wanted to be happy.  You see, Gary and I are getting ready to paint Aaron’s bedroom.  Gary has patched Aaron’s walls, but on Monday night Aaron wanted to show Gary a huge mark on his otherwise repaired wall.  Gary was shocked to see the mark.  We both think that Aaron made that mark on Monday morning when he was mad at me, but Aaron wouldn’t own up to that at all.  In fact, when Gary asked Aaron when he had made the gouge in the wall, Aaron hit the roof.  Boy, did he ever react!!

Aaron accused Gary of accusing him of making the mark.  “Well,” Gary replied, “who else could have made it?”  Aaron was beyond furious.  He became livid.  Gary and I both ended up in Aaron’s room, where Aaron erupted over and over.  He was in a full meltdown, and it wasn’t pretty.  It’s actually very amazing to see the progression of his thought processes when he’s out of control like that.  I’m just thankful that we don’t see this scene very often.  He never owned up to making the mark, but he sure did fling out all sorts of insults and angry comments.  I told Gary to go on to bed, and I sat with Aaron for awhile.  He was mad at me, too, at this point.  He watched a movie for a few minutes and then commanded me to leave his room. 

What happened to happy?  It was totally gone at that point!  I went to our bedroom, where Aaron followed and barged in, yelling some more and refusing to leave.  He did finally leave and he did stay in his room.  He went to bed around 12:30.  I’m sure he wrote down the precise time in his journal. 

He went to Paradigm the next morning.  I praised him for his maturity.  When he returned home that afternoon, I could tell that he was still struggling with some anger.  Yet when Gary got home, Aaron was fine.  We had supper and a pleasant evening, which was so welcome after the awful anger of the night before.  Aaron asked me to tell Gary what I had told him about being mature, so I told Gary how mature Aaron was to go to Paradigm without a fight.  Aaron stood there rubbing his hands together as I praised him to Gary, so happy at those words…..at last!

Yesterday after supper, Gary and Aaron took a walk out in our back yard with Jackson.  I looked outside and felt warmed by the sight of the two of them walking together.  What a picture of reconciliation!  The restoring of relationship is something we do fairly often with Aaron.  We must….because we love him and because it’s right.  All of us have these family moments and life moments where we have to come together again with those who have angered or hurt us.   Gary and I have to be the adults in these situations with Aaron.

But I guess that’s not always true, is it?  Didn’t I just tell about how Aaron came to get me when he knew I wasn’t happy?  How he insisted on being happy before we went to bed?  So I know that there are times when Aaron can and does get it right…..and I have it wrong. 

Our boat is once again sailing calmly.  He knows that tomorrow is Friday and that I’ve agreed with his request of a Papa Murphy’s pizza for supper.  Yet I know that the winds can change direction at any time, and another storm can blow upon us.  I know that I will once again, at some point, be asking what happened to happy.  Let’s pray that happy hugs are all it takes next time to bring the ship upright and make it steady again.    

Let’s hear it for happy!

And hugs!  Lots of happy hugs!

Chill Down


I pretty well knew the track we were headed down yesterday morning as soon as Aaron walked into the kitchen after he got out of bed.  Funny how that works, but I’ve lived with him for a long time.  Not only was it what he said, and the tone of voice in which he said it, but it was also his physical appearance.  He looked very tired, his eyes dull and not bright.  
“Mom,” he began.  “I just want to stay home today and chill down.”
“Uh, that would be ‘chill out,’ I almost said……but I wisely kept my mouth closed.  Aaron wasn’t happy, I could tell, and any appearance of correction when he’s in that mood never goes over well.  In fact, it usually only gives him something else on which to focus his anger.  So I remained silent, and he told me again…..in case my ears weren’t working correctly……that he wanted to remain at home and “chill down.”
I hoped that fixing his hot coffee would help.  It didn’t.
I hoped that carrying it upstairs for him would help.  It didn’t.
I hoped that some empathy from me would help.  It didn’t.
So I knew that it was time to leave Aaron to himself.  Besides, I had to shower, so I hoped that his time alone, drinking his coffee, would do the trick.  It didn’t.
I knew it didn’t help because soon Aaron was back in my room after my shower, declaring that he wasn’t going to Paradigm.  I told him that was fine, but this answer also made him angry.  He proceeded to tell me that he hated this staff and that staff at Paradigm.  Those words coming from him always disturb me, but I’m not surprised.  When angry about something, Aaron will often begin to talk about some person who has made his life miserable, in his opinion.  On this morning, it was three of the Paradigm staff.  
As Aaron talked, he told me that they wouldn’t let him sit outside and play in the leaves and sticks the way that he likes.  I tried to explain why they wouldn’t allow that, telling him about his plan of care and all the effort that went into keeping him safe.  Alone time, liability issues, and even his safety meant nothing to him at this point.  He was solely focused on how mistreated he was and how he hated those particular staff members.  
So I brought up the subject of going to a different group, which was a silly thing for me to do.  This doubled Aaron’s anger.  He may say he doesn’t want to go to Paradigm, but neither does he want to entertain even the mention of attending another day group.  Things between us at that point were definitely “chilling down,” and not in a good way.  There was a chill in the air and things were going downhill fast!
Aaron banged a few things in his room, but didn’t break anything.  And like a moth to the flame, he kept coming back into my room to talk…..or mostly to rant, which he did quite well, saying the same things over and over.  No amount of logic on my part made a bit of difference to him.  He stood in my bathroom and kicked the cabinet out of utter frustration, so I marched up the hall in an effort to gain some composure, and then stood in his room.  He knew what this meant!  He followed me swiftly, and I turned with fire in my eyes as I offered to break something of his.  He said no, and he settled down.  
But he was still on that one mental track, not reasoning at all with anything that I said.  I called Barb at Paradigm to talk about Aaron sitting outside and she explained things to me.  She said she would look at his plan of care, and Aaron had decided to go to Paradigm, so I continued trying to get ready.  I was taking my elderly friend, Nora, out to run errands after I dropped Aaron off.  I called her to tell her that I would be late.  Nora doesn’t handle “late” very well, so it took some time to get all that straight.  But Nora told me, when I informed her that Aaron might not go to Paradigm, that I should just make him go.
“Easier said than done, Nora,” I told her.  “Easier said than done.”  Nora has no idea of what it’s like to deal with Aaron.  Her words were not what I needed to hear.  If we could only make Aaron do whatever he needed to do at any given moment, how wonderful that would be!  But one does not MAKE Aaron do much of anything.  I was thinking of all this as I finished putting on my makeup.  Aaron had looked at the clock, seen that it was time to go, and had turned off his computer.  But when he came in my room, he saw that I was NOT ready to go….and off he went again.
“Mom, I’m ready!!”
“Can’t we go NOW?”
“I turned off my computer!”
“You’re taking forever, Mom!”
“Mom!  You don’t need make-up!”
“You’re taking forever!”
“Mom!  You don’t need earrings!”
“You’re taking forever!”
“You don’t need to brush your teeth!”
“See?!  You’re taking forever!”
My lungs must be in great shape from all the deep sighing.
These issues of the brain and behaviors are so very difficult on some days.  I can’t see what makes Aaron unable to process emotions, information, and logic like I do.  Why was he fine the night before and yet wakes up in this foul state of mind?  Why is it impossible for him to follow reasoning, no matter how simple it is?  I could understand a wheelchair, or being blind, or so many other special needs that Aaron could have.  But all this brain business is so very complex.  
The symbol of autism is perfect.  That puzzle piece completely describes Aaron, and us as well, as we all try to put together the pieces of the puzzle that make up Aaron’s brain…..sight unseen.  It takes lots of understanding.  It takes knowing Aaron very well.  It takes many shots in the dark, prayers in our hearts as we try to reason with him, and all the patience I can muster on some days.  
And lots of sighing.
Well, Aaron went to Paradigm and happily talked to me on the way there about the continuing story he makes up as he sits in the mulch, or in the sticks and leaves at Paradigm.  It’s a story he’s worked on for many years as he sits in his relaxing mode, like a soap opera that goes on and on for years, building as he creates it in his mind.  And it hit me!  That’s why Aaron doesn’t want the staff to bother him.  That’s why he sometimes won’t get up right away to come inside when he’s told to do so.  He can’t have his story interrupted until he’s at some point that only he knows.   Silly me!  Why didn’t I think of that?
So at Paradigm I talked to Barb and she totally understood.  She showed me Aaron’s plan of care, showing that he could have that alone time outside within certain bounds.  I talked to one of the staff that Aaron said he hated, and she was so understanding and kind.  Like Barb said, working with this population means you have to be like a duck.  You have to treat Aaron’s behaviors like water off a duck’s back.  
See how happy Aaron was as I took a picture of him with Barb and her daughter, Casady?
Barb, Aaron, and Casady
See how intent he was as he asked to clean a zucchini last night?  He wanted to help!  That’s always awesome.
 
And this morning, he not only gave Gary a big hug before Gary left for work, but I got this picture from Casady of Aaron and Natalie hugging at Paradigm.  Casady said, “Aaron’s affection game is strong today.”  Let’s hope it stays that way!
 
Did Aaron’s two small seizures last night rearrange those neurons in his brain?  Who knows?  I’m just happy that Aaron didn’t want to “chill down” again today, even though tomorrow may very well be another story.  
Aaron’s writing more than one story, that’s for sure.   And some days, I’m just trying to piece it all together. 

My Other Body

Last night Aaron came up to me and said, “Mom, the carpet in us kid’s bathroom is wet.”  I asked him why the bath mat was wet.  He answered, “Because when I finished my shower, I dried my other body.  Then my feet were wet when I stepped on the rug.”

I just smiled.  I wanted to ask him about his other body, but instead I just enjoyed the unique way that Aaron describes things and expresses himself.  And I’ve been thinking since then about how many different ways Aaron reacts to life around him.  He has many ups and many downs.  Sometimes it really is like he has various bodies.  Then Gary and I feel like we have a variety of bodies, too, in any given day as we react to how Aaron is reacting.  We do get jerked around a lot, waffling between pleasant moments and pulling-out-our-hair moments.

Last Sunday, Aaron’s week started out nicely.  He found something very special as we walked around the back yard.  Only Aaron would find a turtle virtually hidden in our thick grass, up near our patio.  I walked right past the turtle and then heard Aaron saying, “Look, MOM!!”  I turned around to see him holding the turtle, poking his finger in to where the turtle was hiding his head as I warned him that he would get bitten.  Aaron proudly held his find before he and Gary turned the turtle loose in the finger of the lake that comes onto our property.  The turtle was still for a moment and then with a dive took off into the welcome water.  Aaron was delighted, although he still was hoping he had found a turtle pet. 

 
Later that night he talked to both Andrea and Andrew on the phone.  He always has to tell Andrea about his latest movie that he’s watching, describing it in detail.  She always shows great interest whether she really is or not.  I would say she’s usually not.  Neither are we, honestly.  I have no idea how many movies it is now that Andrea is either supposed to rent to watch, or watch with Aaron when she comes home.  Aaron probably won’t forget.

He talked to Andrew about racing, which is so unusual.  There was a time when Aaron was very jealous of Andrew.  He didn’t want to see him on ESPN when we watched an NHRA race, but now Aaron really enjoys seeing Andrew.  It was fun to hear Aaron say, “Hey, Andrew, I see you on TV!”  And Andrew acted surprised by that, to which Aaron affirmed that this was true.  “Yes, I see you on TV!”  So Andrew said, “Well, maybe someday I can wave and say hi.”  Aaron’s face broke into a huge smile.  “You would do that?” he asked.  “You would wave and say hi on TV?”  Andrew assured him that if he could ever do that, he would.  “On TV?!” Aaron asked again.  It was a sweet exchange between those two brothers.  Aaron, who is the oldest, seeming again like the baby of the family in more ways than one.

On Monday, I worried that Aaron would have a hard time going to Paradigm, but he did beautifully that day…..and all week, actually.  After the huge adjustment of returning to his day group after being gone for a month while he was sick, this second week of smooth sailing was so welcome.  Even with Bryan gone this week on vacation, which meant that Aaron wouldn’t be helping work on houses, he still had no problem going every morning.  Except for a little on Friday, but more on that later.

He came home on Monday in a very good mood.  All was well and happy for our evening…..until I walked in the kitchen and saw him with a second glass of iced tea.  I let him have one glass while we watch Wheel of Fortune, but he’s famous for trying to sneak in two glasses.  I caught him in the act as he was putting the second glass to his lips, so I told him that the glass of tea was his special treat then.  I wasn’t going to fix him anything else.  And the tide turned.  The mood darkened, dramatically.  He became belligerent.  The past few happy days came cascading down into defiance from Aaron.  He hovered behind me on the computer, saying whatever mean thing he could think of without totally crossing the line.  He gave his fake sinister laugh to add some effect.  He would walk away for a minute, only to return and repeat his actions.

I finally had Aaron come into Gary’s study and sit on the floor.  Gary and I talked and talked to him, not seeming to really make any headway at all.  It was just amazing to see how his thought processes just don’t process at all like ours do.  He wasn’t connecting the dots in any way like we do.  It was just another lesson in frustration for Gary and me.  Another evidence of Aaron’s different bodies, if you will.  How quickly he can go from joy to anger, and how tremendously hard it is to reason with him.   

Sometimes our bodies are tired, as are our spirits, and such was the case Monday night for Gary and for me.  I’m thankful to have Gary by my side.  He fills in many gaps for me, and I do for him as well.  We’re a team…..a tired team on occasion.  Finally that night, things calmed down and all was well when Aaron went to bed.  We can only pray that something we said stuck in that brain of his.  We know we have to keep trying.

Aaron had times of showing compassion this week, which always makes us very happy because typically Aaron is all about Aaron.  He told us that he gave one of his bean burritos to Jennifer, his friend at his day group.  And he gave her his water, according to him.  He wanted to take some zucchini from our garden to Barb, which he did.  He’s been known to sneak produce out of the house in one of his deep pockets, but this time he did it with my permission.  He does sometimes love to share. 

When we talked to Andrea later in the week, he was very concerned to find out that she was sick.  She ended up having pneumonia in both lungs!  He wanted to talk to her, but I resisted because I knew she really didn’t feel like it.  But Aaron asked her right away if he gave her his sickness when we visited her in Houston, and he showed real concern for her.  That was sweet to see. 

On Friday morning, I had to go to the air base for some routine blood work for my yearly physical.  I left early, but the lab was busy and so it took me longer to get home than I had planned.  I knew when Aaron called me, sounding very down and sluggish, that we were in trouble.  It was confirmed when he said he didn’t want to go to Paradigm.  I got home to find an angry Aaron, but a dressed Aaron.  You see, his routine was all messed up because I hadn’t been at the house.  He slept a little later than usual, had to get his own coffee, and was just generally unhappy about the whole state of affairs.  But of all things, miracles happen, and Aaron ended up going to his day group willingly.  Another crisis avoided! 

Then came seizures on Friday night/Saturday morning.  Just three seizures and not as severe as they sometimes are, but still sad to see.  Aaron’s body gets jerked around physically, that’s for sure.  He slept later than usual yesterday morning, but woke up fully functional.  That was a relief!  Yet he was grouchy because of the seizures and not feeling well, so I had to tread lightly for awhile.  Just another example of the many bodies of Aaron.

He made me laugh this week, as he often does……some days more than others.  One morning I told him it was time to leave, but he told me to wait a minute.  I repeated that we needed to go and he told me again that he was almost done…..just wait a minute.  I looked in his room and found him, of course, watching the movie credits from the movie he just finished.  He was rubbing his hands together, a sign of delight, and as always I laughed.  The credits cannot be interrupted, so I waited until he was down to the very last word and then he happily turned the DVD off and away we went. 

 
Then today, as we watched racing and he tried to catch a glimpse of Andrew, he ended up sitting like this.

 

Yes, that’s our cushioned ottoman lid on his head.  Good balance, don’t you think?

But perhaps the sweetest thing was when we sat down for lunch today.  He said he would pray, which he doesn’t often like to do.  He almost always says two phrases when he prays.  The phrases may vary, but there are almost always just two.  Short and sweet.  So we held hands and Aaron said, “Lord, thank you for this food.”  He paused, then continued.

“Please help me feel…..I mean, help ANDREA feel better.  Amen.”

That was his sweet body……and a sweet moment to cherish. 

Home From the Hospital

Friday, June 19, marked a full week that Aaron had been in the hospital for low sodium and pneumonia.  He was feeling better that morning.  He still had a wicked cough, but his fever had been gone for over 36 hours and he was generally feeling much better.  In fact, the better he felt the grouchier he became.  As he felt better, he missed home more.  He missed his life and his routine.  He was more alert and aware of how abnormal this hospital life was for him.  So the better that Aaron felt, the harder he made life for those who were caring for him.  All he could talk about that morning was going home.  He didn’t like anything that anyone tried to do for him, including me.  He tolerated his chest X-Ray, his pills, and his other morning interruptions…..barely.

I saw his doctor in the hall and told her that she better put on her very thick skin when she came to see Aaron that morning.  She just laughed, and I told her I wasn’t kidding.  Aaron was grouchy, in all caps.  GROUCHY!!  And wanting one thing…..home!  So later she came in with a huge smile, and of course Aaron told her immediately that he wanted to go home.  She told him that she had good news for him, then, because home is where she said he could go.  Then he smiled along with her, for the first time that morning, and life was good again. 

Of course, when one of the aids came in a few minutes later, Aaron looked at her and said, “I don’t need you now!”  And I made him apologize, even as she just laughed and knew that Aaron was very happy to be leaving.  He just had a very blunt way of letting that fact be known.  The Occupational Therapist came in to give Aaron a shower and try to give him some shower pointers, but he actually just showed her how he showered and didn’t really listen to much of what she said.  Physical Therapy had Aaron walk up and down the stairs one time, which he willingly endured because it was just another block to check before he headed out the door.  

Soon the wheelchair containing happy Aaron was on the elevator, along with our cart full of a week of accumulated “stuff”, and before long we were in the van, waving goodbye to the nurses and driving away.  Going home at last!  But a stop at McDonalds was first as Aaron asked for a burger and fries on the way home.  We picked up lunch, and headed home to eat and to settle in to the life that Aaron had missed.  

Aaron was very, very weak.  He needed lots of help with walking, with stairs, and with the bathroom.  He was home, but life wasn’t going to be normal for some time.  He finally ate, and slowly we made it upstairs to his room.  He was so happy to be there at last.  He wanted to watch his new Tremors movie for real, on his DVD player instead of the portable player.  So he sat down in his chair, and he got his things around him fixed just right.  His clock next to his desk had to be positioned just so.  The items that he keeps near him on his bed were placed just right, with his stack of books on the corner of the bed.  On top of those was his notebook in which he kept his record of what movie chapter he was watching.  His pen was placed precisely on top of the notebook.  His back scratcher was set beside that pile of books.  His Gecko from Glenda was settled in front of his clock.  He looked around and checked to see that things were exactly as he wanted them as I stood behind him silently watching, and silently marveling at his precision with every item.

Then he saw a DVD that needed to be put on his shelf of DVDs.  He asked if I would put it there, so I leaned over and placed it at the end of the row.  He just stared at it, and I waited.  Nope.  It wasn’t right.  So I repositioned it several times before finally finding that he wanted it leaning a little at the top, and he wanted his special large rock to be placed near it so it wouldn’t slide out of place.  There!  It was finally according to Aaron’s specifications, and I was free to leave while he watched his DVD, content that all his things were in their perfect place as they should be.  At home.  Where he should be, and where he was so happy that at last he was there. 

Aaron spent much of that first weekend sleeping in his chair in the family room, his animal print blanket stretched over him.  He coughed a lot, and he tried to walk by himself, but it was very slow going.  He needed lots of help with everything.  Coming home was wonderful, but it didn’t mean that Aaron was well and strong right away.  For that reason, he was pretty disappointed.  He loved being home, but he wanted his old body back as much as he wanted his old life back.  Both would take awhile to return to normal, and despite our reminders and assurances, Aaron had some frustrations. 

 
“I’m just so tired of myself!” he blurted out on Saturday, overcome with frustration at his weak body.  That made us so sad, but we could only offer encouragement that every day would be better.  And it was.  He enjoyed visits from friends, including Rosa and her mother, Louise…..complete with pizza and balloons!  He enjoyed his room and his family room chair, watching Wheel of Fortune, and being with Jackson, and just everything.  And each day was better than the one before.  Each outing found him getting a little stronger, his stamina increasing slowly but surely.  After several days, he and I played Skip-Bo, with Aaron checking his watch to keep track of time, just like always.
 

Perhaps what he loved the very most, and what he had missed the very most while in the hospital, was his own comfy bed.  The first night back at home, when it was time for bed, I was helping him get everything ready.  Every blanket was perfectly placed, every wrinkle straightened out, the pillow put just in the right place, and then the sheets were pulled back so that he could place his snake and his skunk under the covers.  But now he had decided to add a new member to the mix.  He wanted to add the soft green frog that Andrea had sent him while he was still in the hospital.  So he rearranged Mr. Snake and Skunk in order to make room for Mr. Frog, stood back to observe and to rearrange, and finally he was satisfied. 

 
He climbed in his bed, after writing his “Time to Bed” in his log book, and I pulled his covers up around his face.  Then he smiled the sweetest smile in the world as he moved his legs back and forth in his wonderful bed that wasn’t a hospital bed.  He was the picture of utter contentment.  He pulled his arms from under the covers and held them up to me, so I leaned down and gave him a goodnight hug.

“Good night, Aaron,” I said as I hugged him.  I arranged the covers up around his face again, and there was that smile.  He looked at me for a few seconds.

“Mom?” he asked.  “Do you want to say good night twice?”

What a precious moment!  Of course I said yes, and so out of the covers came his outstretched arms.  I leaned down to hug him one more time, thankful that our Aaron was home in his own bed.  The hospital stay was scary.  His health was uncertain.  The outcome was unknown for days.  I had stretched my arms on this bed days earlier as I asked God to heal him.  Now here Aaron lay, smiling and hugging, wanting to say good night twice.  It was his way of telling me how very happy he was to be home.  I understood and I agreed.

I left Aaron to his dreams.  And I didn’t go to sleep until I thanked God that on this night, I got to say good night to Aaron in his own bed…..twice!

Aaron’s Hospital Stay

Aaron came home from his day group on Thursday, June 11, in his usual way, bounding in the hall door from the garage with talk of what he had done that day at Paradigm.  It was later, as I stood in the kitchen fixing supper and he sat in his family room chair, that I noticed him coughing.  It was just a dry cough, nothing major, but it was persistent.  So I leaned around the corner and asked him if he was all right, and he answered in his usual droll way that he was just fine.  But as we ate supper awhile later, Gary and I noticed that he was very slow.  A couple days earlier, on Tuesday, Aaron had four seizures.  That wasn’t unusual for him, but on Wednesday he was himself again.  To be more lethargic on Thursday was concerning to us. 

During Wheel of Fortune he wasn’t animated or excited at all.  I felt his forehead and noticed how warm he was.  Sure enough, when I took his temperature it was 102.4.  The next morning I called McConnell Air Force Base to make a same day appointment.  Aaron kept sleeping until I finally went in his room and roused him enough to take his temperature again.  It was still 102.4.  He had a very hard time waking up enough to take his morning pills, and then went right back to bed.  As I continued to check on him I became very concerned at how he couldn’t wake up, so I finally made the decision to take him to the ER.  McConnell agreed with me, so I worked to get Aaron awake enough to dress.  I then had him sit on the floor of the hallway upstairs and scoot down the stairs on his bottom.  He would scoot down one stair and fall asleep until I jostled him……then scoot down another stair and fall asleep…..all the way down the stairs. 

We slowly made it to the van, and later at the ER a male nurse helped Aaron out of the van and into a wheel chair.  Still he slept.  We got him on the exam table and he slept again.  Somehow he stood up for a chest X-ray, but he slept through the doctor’s exam, the blood draw, insertion of the IV, and even the catheter.  The doctor found an ear infection, so I thought that Aaron’s body was just fighting hard and the sleeping was his reaction to that.  I felt like we would soon leave with an antibiotic prescription, go home, and get Aaron well. 
 

 
Yet the concern on the doctor’s face as he kept coming in the exam room was raising my own concern as well.  Finally he told me that the blood work had shown Aaron’s sodium to be dangerously low.  It should be at 135-136, but Aaron’s was 121.  Then he said that Aaron would need to be admitted to the hospital to address the sodium issue, and to find out what else was going on with him.  My mind was whirling as I called Gary and as we tried to decide if Aaron would stay at St. Teresa Hospital or go elsewhere, although that decision was made for us by insurance.  We would stay at St. Teresa.  It wasn’t long before we were on an elevator headed up to the small ICU unit, my mind still trying to adjust to all this.  I looked down at my very sick son and wondered about the “what else” that the ER doctor had mentioned.  What else was going on inside his body? 

 
There Aaron lay, all hooked up to monitors and tubes, his body struggling against that unknown something that was making him so sick.  He tried hard to wake up enough to answer nurse’s and doctor’s questions.  He sometimes showed his definite personality, like when the nurse asked him a question about his bowel habits.  He gave her a rather disgusted look and just answered with a “Hhmmpf!”  When Gary was there, and I left later that evening to run home, Aaron asked me to bring him his watch and his glasses.  He didn’t wear his glasses a lot during those first few days, but he put his watch on his arm right away, pushed way up the way he likes it.  It was a piece of normalcy in this crazy place in which he found himself. 

 
Over the weekend, when friends came to visit, Aaron would cry.  He showed emotion that was rare for him.  He told me later that he was sad.  I told him that we understood, but I didn’t tell him about my own sadness.  Or about those icy fingers of fear that were trying to grab at me.  It was not only sadness but fear I was feeling as I watched the blood draws…..the strong antibiotics flowing through the IV into Aaron’s body…..the fevers that sometimes rose to 104.5……the CAT scan…..the X-rays…..the spinal tap……the kidney specialist and the infectious disease doctor…..the testing for West Nile and tick borne disease…..the low sodium issue. 

 
Early on Saturday morning, as I have done many times in the past during stressful times, I asked God to give me a special verse.  I asked Him to speak to me in the way that I needed at this time.  There in that hospital room, with Aaron sleeping nearby, God gave me Ecclesiastes 11:5:  “As you do not know the way the spirit comes to the bones in the womb of a woman with child, so you do not know the work of God who makes everything.”  That was it!  I didn’t know what was going on here with Aaron.  I didn’t know the work of God but I do know God.  I know that He loves us and I know that He has a work that He is accomplishing.  I know that I can TRUST Him, regardless of what else I don’t know. 

It was very hard to watch Aaron suffer.  Hard to see the pain in his face when he coughed….the struggle to deeply breathe and to talk……the pain of needles and tests.  It was easy for me to let fear take over as I helplessly watched our Aaron and wondered still about the “what else” that was so elusive to find in his body.  Soon another principle from scripture came to my heart.  “In everything, give thanks.”  I went home one evening while Gary sat with Aaron, and I knelt by Aaron’s empty bed in his bedroom.  His stuffed snake and skunk were still in the bed where he had left them.  I stretched my arms over his animal print blanket and I asked God to please heal our son.  I told God that I didn’t know about this work that He was doing, but I did trust Him.  And I thanked Him for this time.  That kind of thankfulness takes great trust in the One whom I was thanking, for sure, because I hurt for Aaron so deeply.  But I also know God and I know that He can be trusted.

It was a turning point for me.  My mother heart still hurt deeply all through that week in the hospital.  One night, with eyes closed, Aaron said, “This is not fun.”  There went my tears.  And later, eyes still closed, he said, “I love you, Mom.”  I leaned over his bed and he got as big a hug as I could give him.  But I purposely stood there and voiced thankfulness to God, hard as it was, for this work that He was doing and that I didn’t understand. 

 
Aaron’s chest X-ray finally showed pneumonia in his right lung.  It was determined that he had Aspiration Pneumonia.  Apparently, he aspirated some saliva during his seizures that previous week.  He responded to a new antibiotic, was moved out of ICU to a private room, began walking with the help of physical therapy, and was soon clamoring to come home.  I don’t know who had the bigger smile, Aaron or his doctor, when he was finally told that he could go home.  On Friday, a week after being admitted to the hospital, he was wheeled out to our van and we took off for home…..after picking up his choice of McDonalds for lunch on the way.  He is recovering his strength and his spirit, and some grouchiness, too. 

There is more to write about this experience.  About how Aaron’s autism affected his hospital stay, and about his tender return home to his world and his routine.

We’re so thankful for this outcome, but if it had been different, I pray that we would still be thankful.  Thankful for the work of God who makes everything, even when don’t know or understand His work.  When it’s all said and done, there is no better place to be than in His will as we watch His work and trust in Him. 

 

Because He Lives

While enjoying a dynamic Easter service this morning, I was struck with the words from the familiar song, Because He Lives.  This old song by Bill and Gloria Gaither, written in 1970, can be sung by memory for most of us.  As I joined the congregation in singing the words to the second verse, my mind thought of Aaron.  It struck me forcefully and yet sweetly how much these words give me comfort concerning Aaron, in a way I hadn’t really contemplated this deeply before.  The reality of what a living Savior means to us as we deal with Aaron’s future and the seriousness of his seizures washed over me with great peace and hope. 

 

How sweet to hold a newborn baby,

Aaron, soon after birth
 

And feel the pride and joy he gives;

Aaron
 

But greater still, the calm assurance,

Aaron – Video EEG
 

This child can face uncertain days because He lives.

Seizure day
 

Because He lives, I can face tomorrow;

 

Because He lives, all fear is gone;

Seizure day
 

Because I know He holds the future.

Newborn Aaron
 

And life is worth the living just because He lives!  (Bill and Gloria Gaither)

 

No matter what each of us is facing, we can face it with the calm assurance that Jesus lives, and in Him we will have all we need to face whatever the future holds

Shaky, But Not Shaken

Yesterday Aaron rushed in the house when he came home from his day group.  He had a huge smile on his face, but he had something else, too.  He was wearing bright yellow shades, as he calls them, and he was quite happy with his new look.  His huge smile was as bright as those sunglasses that Bryan had bought him that afternoon.  He let me take a picture to send to Andrea, Andrew, and Megan, and he was happy with their responses. 
 

Now today we’ve gone from that happy scene, to this:

 
Most of you know what this picture means.  Seizures.  How quickly things can change.  Poor guy!  Such awful seizures…….and all the awful side effects and results that go along with them are what he’s facing today.  Gary knew before bed last night that it would be a seizure night for Aaron, but I wasn’t so sure.  Well, he was right so here we are again as I listen to Aaron breathing deeply while he sleeps on the couch, his fourth seizure over as I hope there are no more.

It’s a beautiful spring morning here.  I’ve opened some windows, enjoying both the gentle breezes and the sweet sounds of birds outside.  In our front yard, just off the front porch, we have a large Golden Rain tree.  I noticed the other day, after some stout winds, that we had some small twigs scattered around the yard under the tree.  Nature had once again done her pruning work on our tree.  At other times, during strong storms, we have had very large branches scattered over our yard.  I was thankful that this wind only brought down small twigs that I will rake and throw away. 
 



















Yesterday morning, as I finished reading Psalm 21, I was struck with verse 7.  David wrote, “For the king trusts in the Lord, and through the lovingkindness of the Most High he will not be shaken.”  Pondering that verse, my mind went to our Golden Rain tree.  That tree has been shaky, many times, as it’s buffeted in the Kansas winds.  Yet while it’s been shaky over and over again, it is not shaken.  That tree still stands tall and strong, minus some branches and many twigs, but not destroyed. 
 

Shaky sometimes, but not shaken.

I find myself there in life, over and over again just like our tree.  I’m especially thinking of that fact today as Aaron lays nearby, recovering from his latest seizures.  Things sure do get shaky sometimes in life.  I’m tossed around by the winds that come my way…..that come to all of us at one time or another…..or multiple times.  I know that God can use those winds to prune me, to take out of my life attitudes that I don’t need, and to shape me to love Him and serve Him more.  God’s pruning occurs best in the shaky times.

However, I’m not shaken.  That’s because I, like King David, have trusted the Lord.  I realize that through God’s lovingkindness……there’s that word “hesed” again……I will not be shaken.  God’s love is a covenant love, never ending and never wavering toward me, His child.  The Hebrew word for “shaken” here means to go off course or to waver.  That’s what I never need to do because I am wrapped in the unconditional love of God.  I know that He does what is best, always, even when I don’t understand it. 

I may look at life through tears.  I may look around me and see the tossed about twigs that come from going through the shaky times.  But I also know that because of God’s faithful, enduring love…..because He is sovereign and never makes mistakes……that I can still be found standing strong, unshaken.  Just like our tall, beautiful Golden Rain tree. 

Shaky, but unshaken as I watch Aaron sleep this morning.  I know that Aaron is in God’s loving hands as well.

Tomorrow?  Tomorrow will be a day for wearing bright yellow shades again. 

 

 

Headed Down Pity Path

I’ve been trying to decide how to write this blog post….or if I even should write it.  Yes, I think I should.  But how to do it in a way that doesn’t make Aaron look “bad” or make me look selfish.  Yet the truth is, Aaron isn’t bad but I am sometimes selfish.  I’m human and I get tired, but I also have to acknowledge where my roots often rest…..and that’s sometimes in soil that grows some undesirable attitudes. 

Tuesday night saw Aaron having four large seizures, so I was up four times with him.  I did sleep some between the episodes, which I often am not able to do, but still I was tired that morning.  I stayed up after Aaron’s last early seizure, and later I did the usual clean-up.  I stayed close to him as he lay on the couch for the rest of the morning, waiting to see if he had another seizure.  I had the laundry going and was able to do some other things while I sat there at the kitchen table.  I was on Psalm 18 that morning in my study time, which was perfect for me.  My favorite verse is there….verse 29.  “For by You I can run upon a troop; and by my God I can leap over a wall.” 

I felt very thankful as I sat there.  God seemed to be prompting me to focus on thankfulness.  I was thankful that Aaron was for the moment seizure free, warm, and safe.  Thankful that this wasn’t the day I was to take Nora to an important doctor appointment.  Thankful that my washing machine and dryer were just steps away, convenient and functioning.  Thankful that Aaron’s seizures aren’t far worse, as so many of our friends experience with their children.  Thankful that I don’t have to work, because it would be nearly impossible for me to do so.  Thankful for coffee.  Very thankful for coffee!

Later, Aaron woke up and he struggled to get off the couch.  After a few minutes, as he sat with me at the kitchen table, he told me that his arm was hurting.  I think he sprained it during one of the seizures.  Soon I asked him if he would want to eat, and we figured out together that some Cream of Chicken soup would hit the spot.  He was worried, though, that with his right arm hurting he would not be able to lift the soup spoon to his mouth.  Therefore, I demonstrated to him how he could eat by bending close over the bowl.  Aaron sometimes doesn’t like us to use our hands to demonstrate some action.  Don’t ask me why, but sometimes it irritates him.  So when I bent over to show him how he could eat, he snapped at me.  “You don’t have to show me how to do it by going like this….” he said with irritation as he copied my movement. 

It was as if he had thrown cold water in my face.  I knew that he was feeling terrible…..I knew that he has never liked physical demonstrations like this……I knew that his autism makes him very blunt…..but I also knew at that moment that I felt very hurt.  I just looked at him, and he knew very well that I was not happy.  I didn’t say a word, but got up and fixed his soup.  I got him all settled there at the table so he could eat, and I coldly told him that I was going upstairs to take my shower. 

For some time, my thoughts were headed down Pity Path.  How could Aaron treat me so rudely after all I’ve done for him?  It was very easy to rehash all of my sacrifices for Aaron, and very easy to nurse my hurt.  I was mostly silent toward him as the afternoon wore on around us.  He seemed to be fine, watching a movie, so I slipped down to Dillon’s to run an errand I had hoped to run that morning, but couldn’t because of Aaron’s seizures…..how I had to sit with him and didn’t get to accomplish what I wanted when I wanted……how my day was interrupted and my schedule trashed…..

See how it went with my thoughts?  Where was the thankfulness I had experienced earlier?  Where was my, “…..with God I can leap over a wall?”  I’ll tell you where it was.  It was buried under my self-centered thoughts, my tired body and mind, and my feelings of being very unappreciated by my son.  I had some major adjusting to do over the next hours, and some soul searching, as well. 

We all have many moments of feeling just as I did on Tuesday afternoon.   As a parent, spouse, sibling, friend, worker on the job, volunteer at church…..no matter where we are…..we will get our feelings hurt.  And as the mother of a special needs child who also has autism, it’s easy to be hurt a lot.  Aaron doesn’t have filters or feelings like we do.  He must be reminded over and over to be kind, to think of other’s feelings, to react in a nice way instead of a blunt or harsh way, and on and on.  He is very self-centered, and this is a huge reason why it doesn’t work if I am that way, too. 

I think it was important for me, personally, at that moment to step back and remove myself from Aaron and the situation.  The danger I faced, though, was in nursing my hurt instead of focusing on what God would do.  What I allow my thoughts to focus upon will determine my attitude, and will even determine whether I sin in the situation or grow in it.  To be hurt was normal.  To let my roots sink into the hurt as I planted myself in it would not be beneficial or right. 

Christ gave up a lot for me.  How often do I react to Him with unthankfulness or pride?  He didn’t hold on to his position as God’s Son, but emptied Himself of all that and became sin for me.  That’s the best example I can follow as I experience the hurt and the tiredness of being a special needs Mom….or any of the other many roles I have in this life.  It can’t be about me, or I will be continually frustrated.  It must be about honoring Christ, and caring for Aaron.

Understanding how Aaron feels after seizures…..understanding his autistic way of viewing the world….is very necessary, as well.  So is training him and reminding him of his actions, and how they can hurt or help others. 

Understanding how I feel after Aaron’s seizures…..understanding my sometimes selfish way of viewing the world…..is also very necessary.  Both must be recognized and dealt with before being allowed to get out of hand. 

Well, back to my verse in Psalm 18.  I didn’t exactly leap over that wall with God.  He more or less had to lift and shove me over it.  I wanted to sit at the base of the wall and lick my wounds, but He wouldn’t let me.  I’m glad for that!  Glad that He is patient and persistent with me.  Glad that He shows me His love.

Just like we have to be with Aaron.  It won’t be the last time, either.  For me or Aaron, either one. 

I’m Glad You Took Care of Me

Aaron had two doctor appointments this week.  On Tuesday we went in for his yearly eye exam, and on Thursday we went to the dentist to have his teeth cleaned.  He very much prefers the eye exam.  For one thing, nothing hampers him from talking to his heart’s content at the optometry clinic.  No one has their hands in his mouth, doing uncomfortable procedures, and so he can talk and talk…..which he definitely did.  He charged right up to the check-in counter at the eye clinic and didn’t even say hello before he started telling the two receptionists all about Fallen Skies and alien skitters and the skitter-in-charge, named Cochise.

It’s just amazing how Aaron will launch right into his tall tales without one word of hello or a few words of explanation to get him started.  Nope, he just barrels right in to his review of whatever is currently on his mind, oblivious to the confused looks of those to whom he is talking.  Or he’ll mention his day group, Paradigm, or someone at Paradigm, as if these ladies know all about this place and those people……which they don’t, and so once again they are confused.  This is why one of my job descriptions is that of interpreter.  I definitely multi-task big time as I try to sign forms, go over insurance, check for information changes, and explain skitters. 

Thankfully these ladies were delighted with Aaron.  Their give and take with him only encouraged him to continue with his stories, and I had to urge him to finally hush and follow me to a chair.  His forced silence was short lived.  He was immediately called back to begin the exam, so he hardly missed a beat before he was telling a new person about Falling Skies and skitters and that he broke his glasses the week before.  He made me laugh as he did one of the eye tests, putting his hands up to the machine as if he was gazing at something exciting.  Maybe he thought he would see another skitter? 

 
The eye exam went well with patient Dr. Fisher……our friend, Brandon.  Of course, Aaron just had to tell him that he got in trouble for calling Stephanie a babe at Paradigm.  And there I was, proud Mom, wondering if I should explain.    Then it was on to get his new glasses.  Trying on glasses is Aaron’s least favorite part of this process.  It ranks right up there with trying on clothes.  He just doesn’t want frames that make him look like Clark Kent.  After that fact is established, he could care less.  And going over insurance is really boring to him.  Again, two understanding technicians and lots of laughs helped tremendously.  Soon we were eating lunch at Chili’s and all was great in Aaron’s world.

Thursday was teeth cleaning day.  The dental exam is really, really Aaron’s least favorite thing in the world to do.  Most of us don’t like teeth cleanings, and Aaron is no exception.  It’s uncomfortable for Aaron, plus he can’t talk and so it’s a long process of frustrating scraping and rinsing and forced silence.  I used to go back with him, but now I let him go alone.  I urge him to be mature…..plus it’s best for me to have an element of ignorance about what really goes on back there, on Aaron’s part.  I know he gets frustrated and impatient.  Once he bit the hygienist.  He said it was an accident.  I wasn’t totally convinced. 

Another part of it is that Aaron doesn’t want us to talk about how he doesn’t do a good job with brushing his teeth.  That’s why we have gone every four months for cleaning, and now have decided to go every two months.  Aaron starts getting angry if I talk about his teeth at home, if I try to help him at home, or when the dentist or hygienist is talking to me about Aaron’s teeth.  We try to keep it low key but with instruction for him, too, yet nothing really helps. 

Later, as he took full advantage of the Pizza Hut buffet, we mentioned his teeth just a little.  Most of the time we talked about whatever entered his mind as he thoroughly enjoyed the pizza and the salad.  I laughed at the dressing on his nose and the look on his face, and I had to tell him many times to talk softer as he was talking in high gear once again, like he was making up for the lost moments when his mouth was silent at the dentist’s office. 

 
We went to Sam’s for a few things.  On the way home we stopped at my elderly friend’s apartment.  Aaron hadn’t seen Nora’s new place.  I dropped off a sweater to her that I had repaired.  She was delighted to see Aaron.  Once again I was the interpreter as he told her about skitters and Paradigm this and that, and she stood there clueless.  She gave him a piece of candy, and he thanked her.  “Are you glad I said thank you?” he asked me as we left.  “Are you glad I told her hi?”  I told her that I was very thankful that he had practiced his manners.

Manners were a little absent later that night, however.  A lot absent, actually.  Like a light switching off….or on…..Aaron’s mood changed dramatically.  We haven’t seen that kind of change in a long time.  He instantly went from happy to angry as he prepared to go to bed.  He decided to focus on his teeth. 

“Mom, you make me feel like I’m bad in my mouth!  I’m not going back to them!!”

He slammed our bedroom door, and he slammed his bedroom door.  Then I heard him stomping up the hall, where he barged in our room yet again.  “I’m not going back to them!” he angrily said….referring to the dentist.  And he called me a name, several times.  This was surprising because Aaron has been so mellow lately.  I wondered if this foul mood was related to his new seizure drug, which can cause anger.  Or was he going to have some seizures.  Often, mood changes precede seizures. 

And sure enough, he had two hard seizures during the night, and another one yesterday morning as he lay on the couch.  He chewed the end of his tongue again, and wet the bed.  I wondered what he thought as he silently watched me yesterday morning in his bathroom, on my knees cleaning up the pee that was on the floor around the toilet.  He was unsteady when he got up and he told me this had happened. 

I thought about his anger the night before, and the name he had called me.  It would be easy sometimes to show anger right back to him, and I certainly have done that.  But that night before I had remained mostly silent, knowing that it was futile to reason with Aaron when he was so angry.  Now before our issue was resolved, I was on my knees cleaning up his mess…..because I love him.

Just like God loves me, I thought.  Here, once again, in my life with Aaron I have another example of God’s love for me, expressed unconditionally.  God loves me when I’m happy…..He loves me when I’m angry……and he cleans up my messes and he soothes my heart over and over again.  How can I do less with Aaron?

I washed all of Aaron’s bedding during the day as he slept on the couch, and was reminded again of God’s love for me as I love Aaron.  I’ll be doing this again, too, and so will God with me.  Faithful love is what God shows to me, and is what I need for Aaron, as well…..even with the still fresh reminder of Aaron’s anger the night before. 

Last night, when Aaron could no longer keep his eyes open, I helped him get in bed.  His covers were all clean and fresh.  He was ready to get in bed when he remembered that he needed to fill out his notebook.  He had written the time that he got up that morning, so now he wrote the time that he went to bed.  It was 9:52.  Then he asked me to put his snake and his skunk in the bed.  I laid Mr. Snake under the covers and Aaron stood there staring at him.  Then he told me to scoot him over a little, which I did.  Aaron stared again.  And I had to move Mr. Snake once more until he was finally in just the right place.  Then the skunk went in the bed, just right, and finally Aaron got slowly under the covers.

He gave a huge smile as he felt the weight and the warmth of the covers on his tired body.  We hugged and Aaron smiled again.  Then he laughed, and I asked him why. 

“I told Dad I’m glad you took care of me when I had a seizure,” he slowly said. 

All thoughts of anger and name calling vanished at that moment.  I was thankful for the privilege I have to take care of Aaron, and I told him that.  He smiled again as I pulled the covers up until just his smiling face was showing.  I turned off his light, and I closed his door…..and I thought of what a difference a day can make. 

What a difference knowing God makes, too.  I’m glad God takes care of me so that I can take care of Aaron.  And I’m glad that He continues to use Aaron in my life to teach me so many things about Himself. 

Our SUPER Hero

The first one was at 11:46.  The second at 1:33, and the third at 2:48.  Aaron’s seizures last night…..and how I hate them!  I was able to give him some Ativan when I heard him stirring about an hour after the first seizure.  I think the Ativan helped the next two seizures not to be as severe as they usually are.  I lay in bed during those hours, comfortable but unable to sleep as I listened to Aaron through the baby monitor.  I used some of that time to pray, and to ask God to ward off my fearful thoughts about Aaron and about our world.  I prayed for family and for friends as well. 

I don’t remember exactly when Aaron got up from bed this morning, but I am sure that he knows.  I am also sure that he wrote it in his special notebook that holds those important times that he faithfully records, every single day.  He looked more than a little worse for wear as he came into the kitchen, staring at me sitting at the table.  He told me that he didn’t feel well and I told him that he had some seizures, which he never remembers….thankfully.  He took his pills, and I gave him something for his headache as well.  Seizures cause such awful headaches.

Poor Aaron.  Today was movie day with his group, which he loves, and which he would now miss.  So much for his extra-large popcorn with extra butter and extra napkins and anything else extra that Aaron can grab…..such as toothpicks.  But he was comforted later after I texted Barb to ask what movie they were watching today.  I told Aaron that the movie today was to be Sponge Bob, and Aaron lifted up his hands in surrender as he backed up and said, “No!!  Sponge Bob is NOT my favorite!” 

Some things work out like that for Aaron, and some things just don’t.  We can’t pick and choose on what day his seizures will occur, of course.  It’s just extra sad when he has to miss something special because he’s too sick to go, again. 

I was tempted to just stay home all day with him, but as the morning went on he seemed to be feeling pretty good.  He came into my room and I asked him how his head was feeling. 

“It’s becoming fine,” he answered.  I just love the way Aaron phrases responses like that.  It’s uniquely Aaron, and it makes me stop and smile.  He smiled when I asked him if he wanted to go to McDonalds for lunch, and use his gift card that Aunt Sandra gave him for Christmas.  I even got brave and decided that we would eat inside the restaurant, hoping that he didn’t have a seizure there.  He didn’t.  He was mostly slow and quiet, which is typical on the day following a night of seizures.  He lacks his usual zip.  He’s rather flat.  But he did notice the little girl sitting in the booth nearby with her grandmother, and when she noticed him, they waved and Aaron smiled.  It made me thankful that I had decided to go inside to sit.
 

We went to our vet for dog food, and there in the Dillon’s parking lot we saw this huge truck/limo that made us both laugh, and become very curious.  Aaron wanted me to drive behind the truck/limo so that he could try to decode what the personal license plate said.  And inside Dillon’s, as I chose a head of lettuce, Aaron found his favorite……artichokes!  He stopped to look at the Chinese food in the deli as he always does, and as always I had to tell the server that we weren’t buying…..only looking.   Of course, we had to stop to look at the lobsters, shrimp, and crab legs on ice in the seafood department.  It’s best not to be in a hurry if I go to Dillon’s with Aaron.

 
But it pleased me to see him being happy over such mundane things that we take for granted…..especially on this day after his nighttime seizures.  Giving him a little fun doesn’t cost me much at all, but it sure brings priceless joy to my heart, and to his as well.

Just two evenings ago I was telling Andrea on the phone about Aaron’s seizure that morning.  It always makes the kids sad to hear about his seizures.  I told Andrea, though, that it was such a blessing that Aaron doesn’t seem sad over his seizures, really.  He doesn’t talk about all the things he can’t do or how hard it is to be different.  He doesn’t seem to grieve the loss in his life that makes the rest of us sad for him. 

But don’t you know, that very evening, Aaron said, “Mom, I wish scientists could stop my seizures so that I could be normal.”  This comment stopped me in my tracks, and left me struggling for words as Aaron repeated it again in case I hadn’t heard him.  I assured him that I understood, and that I wished scientists could stop his seizures, too.  I walked upstairs with my load of clean towels, swallowing the lump that was suddenly in my throat.  So Aaron does sometimes think thoughts that he doesn’t often share.  He does wish that he could be “normal.”  I was thankful that he expressed himself in a way that he usually doesn’t…..in a way that he finds hard to do.  But his simple comment made my strong outward reserve crack some, and I had to walk away quickly lest he see my tears.

A couple months ago, Aaron excitedly shared with me yet another story from a movie he was watching.  Suddenly he paused as he described the super hero, and he told me that this hero looked like this:

 
This pose was so out-of-character for Aaron that I just laughed and laughed, which delighted Aaron.  He didn’t even mind that I took his picture.  There he was, Aaron posing as this certain super hero.

In reality, though, as I’ve pondered that funny pose, I realize that Aaron truly is a hero.  At least in my book he’s a hero.  He’s a hero for enduring so much pain and so much hurt and so much disappointment over the years……so much physical and emotional hardship.  Yet he continues to go through each day in his Aaron way, hardly ever complaining.  He pushes through each day despite his seizures and his social difficulties.  He sure is an example to me when I feel overwhelmed or tired or discouraged.

I know many parents of special children who would agree with me on this when it comes to their kids, no matter their age.  I hear their stories often.  Children with seizures, Downs, autism, and so many other issues.  Children who just pick themselves up and keep on truckin’.  And parents who love them with all their hearts.  They are heroes as well, and they are all around us. 

So today, and every day, I know that we live with our special SUPER hero.  He teaches me not to give up, on him or anything else in life.  We’ll keep plugging along beside Aaron, trying to care for him and provide for him.  Trying to understand him and to instruct him, especially when his mouth or his hands get out of line. Trying to explain him when necessary, and to defend him if needed. 

And trying to help him believe that he IS normal and wonderful and special……just like a SUPER hero should be.