Category: Family

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!

Lights On. Lights Off.

There is something laying on the floor of our garage right now.  It’s a baggie that contains some coins….some coins that Aaron needed to take to his day group today.  The bag is on the floor of the garage because Aaron put it there.  Well, he didn’t just put it there.  He threw the bag down on the floor.  He threw the bag down on the floor because he was angry.  He was angry because he didn’t want to go to Paradigm today.  He didn’t want to go to Paradigm today because of something that happened there on Friday.  He didn’t have to go yesterday because of a doctor appointment and then a fun day with me…..so he doesn’t want to go today, either.  Are you following me?

It’s how we have to follow Aaron.  Living with Aaron means living with autism, and living with autism means that we often follow Aaron as he goes down one trail, switches to another, and back tracks to the first one, but is soon off on a wild tangent, and off we go.  Living with Aaron and living with autism means that we must understand, as best we can, the things that Aaron can’t easily or sometimes ever express.  At times it’s a fascinating journey.  At times it’s a funny journey.  And at other times, it’s a very frustrating journey.  It’s really wild when all those emotions are mixed up into one ball.  Boy, can we bounce from one to the other!

Anyway, back to the bag of coins on our garage floor.  Aaron was awake a little after 5:00 this morning.  I heard him go to the bathroom, but he never went back to sleep.  He was in the kitchen watching me scramble Gary’s eggs well before 6:00.  He ate some sausage and I took his coffee to his room.  He came several times and stood behind my chair as I had my morning quiet time, sometimes talking and sometimes just staring.  He showered and took his pills.  And just under the current of his swirling mind, I knew what was there.  He didn’t want to go to Paradigm.  But when he saw that I was really going forward with our morning routine, like cleaning his glasses and handing him his wallet, he was not happy anymore.  On the way to the van, he turned and threw the bag of coins on the floor.  He left them there as we got into the van, and I am leaving them there for him to pick up when he comes home.  But he went to Paradigm, was met by the manager who rubbed his back and calmed him down (I hope), and hopefully will come home with happy stories.  And he will pick up the bag in the garage, because he needs to do that.  It’s a small lesson, but a lesson regardless.
 

Sometimes we don’t necessarily understand what makes Aaron do certain things, but we know that these actions are set in stone.  We are fighting a losing battle to try to change them.  Like his sausage this morning.  Aaron got his own silverware because he knew that Mom wouldn’t do it correctly.  I knew what he was thinking as he reached into the drawer and pulled out his fork but also a knife and a spoon.  Who needs a spoon for eating sausage?  Aaron does.  There’s no need to make a big deal about it or try to make him put it back.  Why make it an issue?

And the family room lights.  I don’t turn them on in the morning because we’re not sitting in there and so we don’t need the lights on, right?  But every time Aaron walks through that room, headed for the kitchen, he flips the lights on.  I flip them off at the first opportunity.  He flips them back on.  Lights on.  Lights off.

This morning he walked into the kitchen.  Lights on.

I soon took his coffee upstairs.  Lights off.

He followed behind me.  Lights on.

I came back downstairs.  Lights off.

He came behind me again.  Lights on.

I carried my own things upstairs.  Lights off.

He finished taking his pills and then came upstairs.  Lights on.

Sigh.

On the days that he is home and wants to eat lunch, he will eat only if it’s 12:00 or shortly after.  He will not eat at any time before 12:00.  Not 11:48.  Not 11:55.  Not even 11:59!!!!  And if I ask him what time he wants to eat, he replies, “At the time for lunch!”  As if Mom is a little thick headed, you know.

One day recently he said, “Mom, I’m sleepy.  I think I’ll take a nap at 12:00.”

I said, mistakenly, “Well, it’s almost 12:00 now.  You could go ahead and lay down.”

“But it’s 11:53!!!” he exclaimed.  “It’s not 12:00!”

Well, of course.  Whatever was I thinking?!

Wheel of Fortune is another one.  It starts at 6:30, so Aaron has decided that he will turn the television on at 6:28.  Again, not at 6:25 or 6:26 or even 6:27.  No.  Only….ONLY……6:28.  He will stand in front of the TV, literally staring at the clock, until it is SIX…TWENTY…..EIGHT!!!! 

It actually makes Gary and me smile. 

Movie credits.  Oh yes, movie credits.  When Aaron watches a movie in his room, he watches the entire movie.  But to Aaron, the entire movie means from the moment the DVD begins until the moment the DVD is over…..completely over.  That means watching the credits…..every single bit of the credits, until there are no more credits to watch.  He stares at them intently, too. 

 
So yesterday, after Aaron’s doctor appointment and after eating lunch at Abuelo’s, we went to see San Andreas.  He saw it at the theater on Friday, but he really wanted to see it with me.  Yesterday worked out perfectly for that.  For one reason, the theater wasn’t full at all and so I wasn’t as stressed about Aaron’s noises and rubbing his hands together when he got excited.  And this is a VERY exciting movie.  We had a good time, and when the movie was over I could tell that Aaron didn’t want to get up.  Why? 

Really?  Surely you know.  The credits!!  Aaron would have gotten up if I had insisted, but I knew that watching San Andreas in the way that mattered to Aaron meant watching it to the bitter end…..which meant to the very long, last credit.  Everyone had left the theater, and the cleaning crew stood in the back waiting on us to be finished, but Aaron and I did it.  We watched every single line of every single credit for every single miniscule part of San Andreas.  Aaron put his hands on the back of the seat in front of him, enthralled at getting to watch big screen credits all the way to the end.

 
 
This is what we often do as parents of Aaron, and as we live with autism.  I entered Aaron’s world at that moment.  It was actually funny and endearing.  We left the theater laughing, and I laughed even more when Aaron bent over as he rubbed his hands together furiously, asking the ticket taker why San Andreas was “fictinous,” as Aaron says.  The stiff, unsmiling ticket taker was rather put out at this odd situation and made some curt comment, which totally didn’t faze Aaron.  That poor guy missed out on a wonderful opportunity.

I’m learning more and more to enjoy those opportunities to enter Aaron’s mind and to follow him on his paths. I am blessed to partake of Aaron’s world on most days, but there are many times when it’s hard and frustrating.  Which brings me back to the bag on the garage floor.  Hopefully, as he picks the bag up off the floor, Aaron will talk to me about what was really bothering him.  Hopefully, he will learn that he needs to correct his own wrong actions.  Until the next time he takes off down that trail of frustration, but we’ll deal with that as well.

Lights on.

Lights off.

 

 

The Pieces of a Beautiful Life

Two weeks ago, Gary and I were finishing the last leg of our drive to West Virginia as we traveled home for my mother’s funeral.  Has it just been barely over two weeks ago that she breathed her last breath?  So much has been packed into this short time that it seems like she left us much longer ago.  That’s how my mother lived her life, though.  Like my brother said at her funeral, Mom squeezed every bit of opportunity out of each day that she lived.  So much was packed into her life…..so much that will impact so many for eternity.
As Bob and Jan, and John and Jeanie, planned Mom’s funeral, they incorporated two very sweet and personal elements into the service.  Jeanie asked each of the grandchildren to write down their memories of their grandmother.  At her funeral, Jimmy read every word that had been written.  It was a very moving and sometimes humorous part of the service.  Then Jan asked each of us to bring our quilts that Mom had made us.  Each hand stitched quilt that we brought was hung over the railings at the front of the church, adding a beautiful background as we remembered our mother.
 
Something really stood out to me as I listened to the grandchildren’s memories being read.  It’s the same thing that I noticed during her visitation at the funeral home the night before her funeral.  That night, we stood in line for nearly three hours as person after person hugged us and told us of what our mother had meant to them.  Most of their stories were fairly simple.  It wasn’t that Mom had done earth shattering acts of great note.  She wasn’t interviewed by the newspapers, seen on television, or given big awards for her acts of kindness.
So what did people talk to us about as they shared my mother’s impact on their lives?  It was her service to them, her love, expressed in so many ways.  It was meals she cooked, her home she opened to so many, stockings she knitted, clothes she sewed, miniature roses she delivered in Cracker Barrel syrup bottles, boiled custard that she cooked because a friend loved it, sending out missionary prayer letters, making dozens of quilts for others, and so much more.
It was her great sense of humor….her ability to lighten any situation with an attitude of light heartedness that was often amazing.  It was her word fitly spoken to so many, especially to those who had messed up and made poor decisions.  She comforted without judging, and extended help where others might have looked the other way.  Story after story we have heard since Mom died.  What a balm to our hurting hearts!
The grandchildren’s memories were more of the same, on a more personal level.  Again, what is striking is that no one mentioned my mother’s education or her job.  Not that this isn’t important, because it certainly was a great accomplishment for her to have a Master’s degree and to have a supervisory position with the State Board of Education.  Yet with all of her educational goals that she met and with her very responsible job, my mother maintained our home and our family in an incredible way.
It was, again, the seemingly small acts that all the grandchildren remembered the most.  Guess what was mentioned most often by her grandchildren?  It was the Cheerios that she kept in the coffee table drawer in the living room.  So many of them talked about that memory and of how much fun it was to go to their house, pull out that drawer as a little child, and eat as many Cheerios as they wanted.  Other memories were of the toys, the laughter, sitting on the front porch, all the play time in the yard, her cooking, gardening, sewing, and her unconditional love.  It was how she filled her home with joy and filled their lives with personal touches for each grandchild.
In her memories of her grandmother, Andrea wrote, “I remember how she patiently showed me how she pinned her fabric together in preparation to sew her gorgeous quilts by hand.”  As I sat in the church during mother’s funeral service, I looked at the quilts that we had hung on those railings.  Each one is full of hundreds of fabric pieces, placed together in ways that make a gorgeous design.  When you step back and look at the finished project, you see how each piece combines to make a perfectly beautiful work of art.
So it is with the life that Mom lived.  Each act of love that was remembered and many that have been forgotten, have all fit together to produce a beautiful life.  It’s the handiwork of God in our mother’s life that has blessed and profited so many of us over the 88 years that she lived.  Her life was a pattern that I want to follow.  A pattern of service and kindness that means more to people that any public acclaim ever will or could produce.
Like she so often sang:
          I’d rather have Jesus than men’s applause.
          I’d rather be faithful to His dear cause.
          I’d rather have Jesus than world wide things
          I’d rather be true to His holy name.
 
I’ll be learning lessons from the design of my mother’s life for the rest of mine, I’m sure.

Keeps Me Singing

It was probably over 55 years ago that a soloist with a beautiful voice went to sing in a revival service in the little town of Oakvale, West Virginia.  She sang the hymn “I’d Rather Have Jesus,” and then she sat down to listen to the sermon preached by Jimmie Jones.  Her heart was disturbed as she listened to the gospel being preached that night.  She thought of the song she had just sung, and of the words that came out of her mouth in such a perfect performance…..words that she knew she didn’t really mean.  For it was just that – a performance.  She sang beautifully, but she sang a lie.  She knew that she didn’t really know Jesus, and that she didn’t really mean it when she sang about wanting Jesus more than anything this world affords. 
 
This woman was my mother, and that night changed her life and the life of our family.  She went home and urged my dad to go with her to listen to Jimmie Jones preach.  Mom didn’t know that my dad had already trusted Christ as his Savior.  It wasn’t long before my mother made the same decision.  She bowed her head and confessed her sin, and asked Jesus to be Lord of her life.  God changed my parents tremendously.  They raised their five children to know and serve the Lord, and they left us a spiritual heritage that has more value than anything this world affords.  And “I’d Rather Have Jesus” became my mother’s signature song…..one we heard her sing many, many times over the years.  One she sang with honesty for the rest of her life because of the work that God had done in her heart.
Last week we said goodbye to my mother for the final time on this earth.  We had really lost her a long time ago to the horrible ravages of Alzheimer’s.  She no longer had her memories, her personality, or any of her other faculties.  But even Alzheimer’s cannot take the Lord away.  He has promised to always be with us, and He always keeps His promises.  We saw evidences of His presence with Mom as she struggled in various ways.  What sweet comfort it brought to know that deep in her heart and her mind, God was ministering to her in ways that we could not. 
Two weeks ago, on the day before the call went out to family that mother was dying, we saw a profound picture of God’s grace in her little body and in her heart.  Jan and her daughter, Bethany, had gone to spend some time with Mom in the care home where she lived.  Mom was sitting in the commons area, her head down and her eyes closed, unresponsive to the voices and the noises around her.  Suddenly, on the television that was playing, a man started singing “Amazing Grace.”  Bethany looked down at her grandmother and saw that her lips were moving.  Surprised at this, she and Jan leaned down and put their ears to Mom’s moving lips.  Here is what they heard coming from my unresponsive mother:
         
         
         
         
My mother was singing!  Jan and Bethany wouldn’t have believed it had they not heard it for themselves.  She was clearly singing this beautiful old hymn.  She was singing about Jesus, whom she was soon to meet.  God’s prompting, God’s presence, was there with Mom in that room.  Jan and Bethany joined her in singing, and then Bethany said, “I love you.”  Mom clearly said, “I love you” to Bethany, her eyes still closed.  Then Jan said, “I love you, Mom.”  And Mom said, “I love you” to Jan as well. 
Those were the last words that my mother spoke.  The next day the family got the call that she was dying, and on Monday, May 4, my mother met Jesus.  Jesus, the sweetest name she knew.  Jesus, who filled her every longing.  Jesus, who kept her “singing as I go.”  Singing as she got ready to go to heaven. 
Like my brother, John, said at her funeral…..how appropriate that Mom’s walk with the Lord began with a song many years ago.  And her life with the Lord ended with a song…..a song that surprised us all, but was such a gift of grace and hope from God. 
A gift and an example that we will always, always cherish. 
 

In The Blink of An Eye

I’m thinking of my dad today for some very special reasons.  It’s been 6 ½ years since he went to heaven after fighting cancer for 8 years.  Dad was the one of the godliest men I have ever known.  He was so kind, selfless, and loving.  He was firm in his faith, never wavering through all the ups and downs of life, including his two bouts with cancer which finally took his life.  Yet despite his strong faith and his deep trust in the Lord, Dad seemed to have a great fear of death. 

None of us looks forward to dying, so on many levels we could understand his dread.  As he weakened and the end was coming nearer, he still seemed to struggle more and more with his uncertainties.  Finally one evening my brother John spent some time alone with Dad, talking to Dad about what was on his heart.  It was during this conversation that John was able to gently lead Dad to really express his concerns about dying.  One of Dad’s biggest issues was that he wondered what he would say to Jesus when he first saw Him.  We all just smiled and shook our heads when we heard that.  There he was again, not worried about his own pain but instead concerned about what he would say to his Lord.  And how like Dad that was!  He was always the ultimate planner and organizer, so for him to face this uncertain encounter with no plan or idea of what it would be like was very hard for him to handle.  Plus it very much showed his humility as he felt completely unworthy to stand before Jesus. 

Something else that was heavy on my Dad’s heart was the fact that he would be leaving my mother.  They had been inseparable during the 22 years of retirement they had enjoyed together.  Then when dad was put in a hospital bed, Mom slept in their bed right beside him and they held hands through the rails.  Dad knew that Mom was really showing the signs of Alzheimer’s in ways that we hadn’t seen.  He kept trying to find ways to tell us about it without Mom hearing him because he was so worried about what she would do when he was gone, and he wouldn’t be there to help her.  Part of his letting go was hearing our words of assurance that Mom would be cared for and that he didn’t need to worry about her.

But it wasn’t just that Dad was burdened about leaving Mom alone.  It was also that he was very concerned, almost fearful, of him being without her in heaven.  He was so close to her, so dependent on her in many ways, that the thought of being without her……even in heaven…..was nearly unbearable to him.  So on the night that John talked to Dad, he told Dad to remember that God said a thousand years to Him is but a day.  John said, “Dad, I really believe that when you go to heaven it’s going to be like you blink a couple times and then Mom will be right there with you.”

I don’t know that anything comforted Dad more than those words and that thought.  Later that night, as Mom and I sat with him in their family room, he very softly and slowly shared that thought with us…..and he sweetly smiled as he said it.  His soft, gentle smile….full of the hope that the separation from his Beth wouldn’t be so long after all.  We all know it was that night when Dad felt released to go on to heaven.  He knew that everything would be all right, and that Mom would join him in the blink of an eye.  Several days later he left this earth for heaven.

I’m thinking of my Dad today, and definitely my mom, for another very special reason.  Today my mother also left this earth for heaven.  She and Dad are finally together, whole and healthy at last!  I can’t imagine the joy they’re both experiencing right now to be with Jesus, and to be together for eternity.  Jan told me that Mom opened her eyes, eyes that had been shut for days.  It was as if she saw something.  Then she closed her mouth, closed her eyes, and was gone.  Did she see heaven?  Did she see Dad, grinning from ear to ear?  Did she see her Savior?  What precious and awesome thoughts those are!   

So while we cry at having to say goodbye to our last parent, we can’t help but smile and be so happy for her and for Dad.  Oh my goodness, I would love to have seen that reunion!  Someday we’ll join them there, and we’ll have so much joy and so much fun.  But until then, while we will sometimes weep and we will often miss them both, we can smile at God’s sweet goodness and rejoice over the certain hope we have of life together in heaven.  
 

Hey Mom, you and Dad have a great time up there! 

When we all get there, I do hope the Lord lets us sing “Oh, It Rained, Rained, Rained” again, just to torment dad. 

We’ll all see you in a couple blinks of an eye.    

Spilled Water

Today Aaron had a dentist appointment to have his teeth cleaned.  He was happy about it, not because he likes having his teeth cleaned but because he knows that afterwards it means we hit the Pizza Hut buffet down the road from the dentist’s office.  Aaron and I happily walked into Pizza Hut, only to find one very busy server working hard to keep up with a rapidly filling restaurant.

We waited a long time while this poor overworked server was on the phone before she was able to break free.  She told us just to go ahead and pick a seat, but asked us first what we would like to drink.  Aaron quickly told her that he wanted water WITH lemon…..because Holly, who had just taken care of him during our trip to Houston, put lemon in her water. 

“Mom!” Aaron had said to me earlier this morning.  “Do you know what Holly puts in her water?”  Then he proceeded to tell me how Holly put lemon in her water.  “Can I put lemon in my water when we eat at Pizza Hut?” he asked.  And I told him that he could.

So when the busy server asked for our drink order before we seated ourselves, Aaron jumped on it and made sure that his water would have a piece of lemon.  When we sat down, and our waters came, Aaron said, “Holly squished her lemon and poured the juice out.  Will you do that to mine?”  So I squished his lemon and he watched me pour the lemon juice out into his water.  He was happy.

We walked over to the buffet line, where the salad in the large bowl at the salad bar was nearly gone, and there was no pizza left on the pizza side.  Poor busy server!  We were able to fix small salads…..Aaron’s with way too much dressing before I could wrangle the dressing ladle from him.  Soon we were able to get some pizza, too, and we sat there eating and chatting.

I looked up at one point to see that five Amish young women had come in and were waiting to be seated.  With them they had two small children.  They were such refreshing and lovely young women, I thought.  I watched as others stared at them, and I hoped I wasn’t doing the same.  It must be hard sometimes to always stand out as being different.  Finally they were shown to the seats right behind Aaron and me.  I pretty well knew what would happen when they walked past us. 

“Mom,” Aaron said.  “They have on hats.” 

“Yes,” I answered.  “That’s part of their religious beliefs.  And don’t stare or point.”

“I was watching her,” he continued.  “You’d say I was staring?”

Again I just cautioned Aaron not to boldly stare, so he continued eating.  Finally, we got up for one more trip to the buffet, and as Aaron was getting out of his side of the booth his arm knocked over his nearly full glass of water.  His water with all the squished out lemon juice went all over the table and down onto my side of the booth.  Thankfully I had already stood up, so I didn’t get wet.
 

Aaron apologized profusely, so I told him it was fine…..and told him not to be so loud…..and he reached his arm up to me.  I leaned down as he still sat there and he gave me a big hug.  The older man in the booth beside us stared even more than he had already been staring.  And as I turned to see what kind of mess we had, I made eye contact with one of the young Amish women.  She looked quickly away, but I knew she was watching us and probably wondering.  I knew that I felt the way she must often feel.

For the rest of our meal, I sat with Aaron on his dry side of the booth.  Our poor harried server never did make it over to clean up the mess, and that was fine.  I felt really sorry for her.  Besides, this gave Aaron and me a chance to sit close together.  He leaned his head on my shoulder, so happy that Mom wasn’t angry and that all was well.  I knew he felt so badly about what had happened, but I assured him that it was fine. 

He was very happy that I offered him my water, but I took my straw out so he wouldn’t get my cold.  He quickly grabbed his straw that was laying on the table in the mess of spilled water, ice, and soggy napkins.  He was content as he ate his pizza, not minding that the server never made it over to clean our table.  While he ate, he sang songs from Phantom of the Opera…..quietly……and he drank every drop of my water.

 
I was now facing the Amish women as I sat beside Aaron.  One of the young women that was facing me was pregnant.  I looked up at one point and our eyes met, and we both smiled at each other.  I wondered what she was thinking.  I wondered if she wondered about Aaron.  Wondered if she wondered what my life is like, just the way I wonder what her life is like. 

Aaron and I finally went up to the register to pay.  I had to run after Aaron at one point because he walked rapidly over to the buffet.  He was just ready to reach in with his bare fingers and grab some bread sticks for the road before I was able to stop him.  Oh Aaron!  You know better! 

Aaron and his messes that he makes!  In the short time that we’ve been home from Houston, we’ve had several of those messes to deal with and try to correct.  They may be physical……like me on my knees cleaning up certain spills and missed aims, if you know what I mean.  Or they may be messes created by his behaviors.

That’s why I was on the phone this morning with Bryan, one of the Paradigm staff that takes Aaron with him to work on houses.  Aaron loves working with Bryan, but on Monday Aaron had a meltdown at Paradigm and was mean to Bryan.  I wondered what Bryan would say when we talked, but he was amazing.  He really loves Aaron.   He really understands Aaron, as much as any of us can understand him.  And he knows that all he can do…..all any of us can do…..is clean up the mess and move forward.

Sometimes we have to sit in the mess awhile, like Aaron and I today in our watered down booth.  Sometimes there are no quick fixes or easy solutions.  Aaron sees the mess and the havoc it creates, but it’s important for him to know that he is still loved in the midst of it.  He is still cared for despite it all.  He felt bad about the water today, and he usually feels badly about the outbursts he has.  Yet he can’t always stop it when he’s upset, any more than he could stop the water that spilled so suddenly today. 

The damage is done, but I can still sit closely enough for him to put his head on my shoulder, and know that he is forgiven and loved.    Believe me, sometimes I want to run to another room….another house….another state!  But that’s not the solution, for Aaron or for me. 

We stay in it because we are all Aaron has.  God gave him to us for a reason, messes and all.  And we do love that big, crazy guy. 

Spilled water and all.

The Slow Train

Imagine that every day when you drive away from your home to run errands or to go to work, you must cross a train track.  Imagine that every single time you come to that train track, there is a train on it, traveling ever so slowly.  You must wait on that train to pass before you can cross the track and continue on your way.  Then when you drive home later, the same thing happens.  Any time you try to cross that train track, no matter the time of day or how many times you have to drive over that track in a day, the same thing happens.  Over and over again, you must stop and wait on that train to slowly pass.  You begin to dread it and you find yourself very irritated about this slow moving train.  Some days you handle it better than others, but eventually on a bad day, you find yourself saying, “I hate that train!!” 

 
This is how I sometimes feel about autism.  Not Aaron, mind you…..but autism itself.  I love Aaron so much.  I love how unique he is…..how he views the world while opening up his view to me……all the many, many lessons he has taught me over the years as I have lived with him….all the times that he has made me laugh at the funny things he says. 

But some days it’s like running into that slow train every day.  On those days, if I’m tired or troubled, it can be especially difficult to remain upbeat or to see the fun in Aaron’s way of living in his world.  That’s because his way of living in his world usually involves me to some degree, and often that involvement causes me to stop what I’m doing and do what he wants…..or demands.  Just like that slow train that impedes my day, at times Aaron’s rigid routine makes me stop what I am doing while I meet his needs.

For instance, his bedtime routine at night.  At night, when I am more tired.  He absolutely does not want to go to his room to get things situated unless I go with him.  He wants me to help get his blanket on the bed just right, close his blinds, set his clothes out for the next day, and say goodnight in his room near his door…..not out in the hall or on the right side of his bed, but in his room near his door on the left side of the bed. 

If I am on the computer he will come to stand behind me and he will hover.  He is waiting for me to come up to his room for the bedtime ritual.  If I tell him to go on and brush his teeth and take his pills, he will do that and then return to stand behind me and hover some more.  I just know that he will not go to bed unless I stop what I am doing and go with him.  There’s that slow train, every day the same.

Or getting his coffee in the mornings.  When Aaron comes down to the kitchen, he wants his coffee.  I don’t mind that at all, unless he’s demanding.  But he will linger as he waits for the coffee to finish perking, if I’m making fresh, and he will linger as he waits for me to pour the coffee.  And he really wants me to carry it upstairs right away.  The other morning he was hovering, wanting me to pour his coffee.  I poured his cups of coffee and went back to what I was doing.  I always carry his coffee up to his room because he is so shaky that he spills it.  So he stood there, hovering, waiting for me to carry his coffee upstairs. 

“Are you carrying my coffee to my room?” he asked.  I told him that I would get it in a minute.  He walked in the living room, but soon was back in the kitchen…..hovering again. 

“Are you getting my coffee?” he asked again.  So I told him to go on upstairs and take his shower, and I would bring his coffee up while he showered.  This didn’t suit him at all. 

“Mom!” he said with impatience.  “Aren’t you getting my coffee?”  He started walking away, but I knew we weren’t done….and I knew I would need to carry his coffee upstairs now.

This made me very irritated on this particular morning.  I rinsed my soapy hands off under the running water at the sink.  And thinking he couldn’t hear me, I muttered, “I hate autism!”

But Aaron did hear me.  He heard my careless remark, and he did not like it…..not one bit.  Since that morning I have had to do some damage control.  I’ve explained to Aaron several times what I meant when I said those words, assuring him that I did not mean that I hate him.  I reminded him that Granddaddy died of cancer, and that I hate cancer.  I told him that Grandmother has Alzheimer’s and that I hate Alzheimer’s.  I’ve explained that I hate his seizures.

Explaining to him why I sometimes hate his autism has been a little trickier.  I’ve talked to Aaron about how sometimes life for him is very stressful because of his autism and how it makes some situations difficult for him to handle.  Aaron really doesn’t want to go into great detail about those things, though.  And I don’t either, because I don’t want him to feel that I think his life is bad or hard.  I wish I could take back that moment, and that I hadn’t said those words in my frustration.  Yet on the other hand, at least it’s opened up some conversation between us and enabled me to talk openly to him in a way I don’t normally do. 

Aaron and I were watching a movie on Saturday night, one that he had looked forward to watching with me.  Suddenly he turned to me and said that he was having a dream, and then went into a big seizure.  Gary and I stayed with him, and when he was able we went upstairs to his room so he could go to bed.  The movie would wait until another night.  I got his bed covers all ready while he brushed his teeth.  His head was hurting from the seizure, and he was slow and weak.

Despite how he felt, though, he went about his bedtime routine as he normally does.  I watched him carefully place his stuffed snake and skunk in the bed, under the covers, just right…..and then pull the covers up just to a certain point.  I watched him open his notebook and record the time he was going to bed, so meticulously.  I watched him make sure that his back scratcher and other items were on his desk where they belong….that his clock light was dimmed…..that his glasses were just where he always leaves them beside his watch that he was sure to remove from his arm. 

His routines are his life.  Even when he feels terrible after a big seizure, he still maintains his definition of normalcy and routine.  I do admire him for that.  He’s so determined despite how his body works against him.  So strong even though he’s weak at times like this. 

Yes, I do hate autism and how it has altered Aaron’s life in huge ways.  It has also altered my life in huge ways.  But I do need to be careful not to let my anger at autism be a cause for hurting Aaron’s heart.  I think he understands my statement from the other morning.  I still wish I hadn’t said it.  Lesson learned, I hope. 

That train will be on that track every single day.  I can’t change its path or its inconvenience in my life.  But I can change my attitude, and when I feel like muttering useless words I need to pray instead……count to 10 or to 100……go sit in the flower bed with Aaron for some mulch therapy……clap a few times like Aaron does to relieve my tension…..whistle or whoop out loud with Aaron…..

Poor Gary.  I don’t know if he could handle two of us in the house.

 

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. 

Still Our Sweetie Poo

I got one of those phone calls yesterday that I don’t like to receive.  It was Barb, from Paradigm, trying to tell me about an incident with Aaron.  It was hard to hear her, though, because she put it on speaker and I could hear Aaron in the background.  He was yelling as he tried to explain his story, and he was crying, and no one had to tell me that he had just had a meltdown.  My heart sank.  It’s been awhile since we’ve seen this with Aaron.  I felt drained when I got off the phone, and I wasn’t even there when Aaron lost it.  It’s just very discouraging to feel like things are going along so well, and then BAM, he hits that wall again. 

In his frustration, he broke his watch and he broke his brand new two day old glasses.  This is very typical of Aaron when he gets that upset.  He will break something that’s important to him, and then afterwards he’s just eaten up with remorse.  The remorse comes from all of his behaviors when he loses his temper, but he knows that breaking things comes with repercussions.  He won’t get a new watch right away.  He didn’t know if his new glasses could be fixed. 
 

The repercussions with people’s hearts is an area that he is not quiet adept at understanding.  He’s doing better with empathy as he’s gotten older, but he is usually very narcissistic and only thinks of himself when he is in a rage.  I guess many of us are that way when our emotions take control, but Aaron is often that way even when he is even keeled.  Thinking of others and what they are feeling has been long in coming for Aaron’s autistic mind.  He’s getting there, very slowly, sometimes more than others.  For instance, not long ago he found out that Andrea had a migraine.  The day that she and I were talking on the phone and she mentioned it, Aaron was frustrated that our phone call was taking my time away from him.  I chided him when I got off the phone about how uncaring he seemed.   The next day when she called, he said to me, “Tell Andrea I cared for her migraine!”  He was very pleased with himself that he cared, because even he knows how hard it is for him to feel that emotion, and because he felt guilty that he had not felt it at first for his sister.

He came home yesterday, face and eyes all red from crying.  He told me what had happened, so we discussed it as much as I felt that he could handle.  He lets me know when he has had enough.  Barb and I talked privately when Aaron was up in his room, and Melinda and I texted.  I felt like I had a good grasp of what had happened, although part of it was still fuzzy.  That’s why I tried to talk to Aaron again after Wheel of Fortune was over, but he did not want to talk about it further.  The book was closed, in his mind. 

I was almost asleep last night, at 11:30, when I heard our monitor on the nightstand beeping.  It meant that Aaron had turned his unit off in his room.  And it wasn’t long before our bedroom door opened and Aaron strode in to tell me that he had turned his monitor off and he had no intention of turning it back on.  There!

“Oh boy,” I thought.  “Here we go.”

Aaron has these residual effects from his behaviors…..effects that show up hours after the incident is over and hours after we have talked about it.  I followed him to his room, noticing his agitation.  He turned and told me that I was mean, that Dad was nicer, etc., etc.  I knew that my second conversation with Aaron was the cause of this, but I couldn’t take it back.  He thought I didn’t believe his version of the story….that I would make him leave Paradigm……and on and on.  And he assured me once again that he was NOT turning on his monitor.  That was the biggest sign of his rebellion that he could come up with at the moment. 

I left his room frustrated, and Aaron was frustrated, and the monitor stayed off all night.  This morning, I left Aaron alone when he got up.  Even when he stood staring at me silently, I did not speak to him.  I poured his coffee and carried it upstairs.  I got myself ready and I opened my bedroom door, and finally he walked in and told me that he was not going to Paradigm today.  I knew that was coming, so I asked him if he would go on Monday and he gave an exuberant yes. 

So many of my decisions at these times are uncertain.  Is it right to not make him go today to his group?  Do I still get him his Friday goody bag?   Was this outburst because of his new seizure drug….the one that can cause anger?  Do I take him off this drug?  Or do I wait awhile longer to give it more time? 

Well, I didn’t make Aaron go to Paradigm.  I know this is his typical response to such stressful situations, and I know that he does need time to emotionally recover and to sort it all out in his head.  His big, impulsive hug for me later showed me how thankful he was that I let him have some time and space today.  I still don’t know about the new seizure drug and what to do there, but I think I’ll give it some more time.  I think.  I did not get him his Friday goody bag.  He hasn’t even asked about it because he knows that he really messed up.  My mother heart wants to take care of him…..to blame the autism….to quote the professionals about his emotional deficits.  But I know he also needs consequences, and so the goody bag will not happen today.

I did take his glasses to the optometry shop.  “Wow!” the technician said.  “He sure did a number on them.”  I didn’t have Aaron with me because I wanted to explain what had happened, but not in front of Aaron. 

“Yes,” I agreed.  And I wanted to add, “You should see the number he’s done on my heart, and on the hearts of others.”  But of course I didn’t say that. 

By some miracle, the young man brought Aaron’s glasses back to me later, all fixed and ready for Aaron to wear again.  I wish it would be as easy to fix the situation of yesterday, but that will take more time. 

Later, Aaron and I took Jackson for a walk around our neighborhood circle.  It’s a beautiful day, perfect for a walk.  When we got home, Aaron quickly grabbed his mulch bucket and situated himself out in the flower bed for some mulch time.  He stayed there for nearly an hour, relaxing and sorting out his thoughts with each little piece of mulch that he broke.  It’s time that he needed…..quiet, peaceful, reflective time for him. 
 

Wouldn’t it be wonderful if mulch would cure autism?  Or if mulch time would give me all the patience and wisdom that I need?  I would say, “Scoot over, Aaron!  Make room for me!  Will you share your bucket?”

I know every parent of autistic children can understand how helpless I sometimes feel.  How embarrassed at my son’s behavior.  How frustrated and then sad at his response. 

Then I think of Barb, who loves Aaron and who said, “Tomorrow’s a new day.  We’ll just put this behind us and go forward.”

And Melinda, who also loves Aaron, and who said, “Aaron informed me that I am NOT his sweetie poo anymore!  Well, he is still my sweetie poo.”

That makes me smile, and it makes me thankful for those that work with Aaron and love him even on the bad days.

We will, and we do, move forward.  Today Aaron said, “Mom, I’ll turn my monitor on tonight.”  It’s his way of telling me that he’s better now, and that he is ok with me…..mean old Mom of last night. 

Yep, it’s a new day and we will go forward.  And I just hope Aaron knows how many people cared for him when he messed up.

He’s still our sweetie poo!

 

 

The Meat Goes ON the Rice!

I stood in front of the greeting card display a couple weeks ago, locating the various categories of Valentine cards that pertained to me.  Husband….sons…..daughter…..friends…..special ones.  I paused at the “mother” category, and then skipped over it as I continued my search for just the right card for each person on my list.  Sometimes it takes forever to find just the right sentiment, and today was one of those days.  I decided on several cards, but there were still some unchecked names on my list.  “Well, I would just have to go to another store and see what choices they offered,” I thought as I went on my way.

I later made a new list in my “brain notebook” that sits in my cool ThirtyOne notebook holder.  It’s the notepad that’s just like the one Mom used…..the one she called her “brain”……..with all of her lists and her scribbled notes.  Just like Mom.  Like my mother used to be.  And there she was, once again, in my life and in my memories……although she is still living, but not like we all knew her. 

My new list consisted of items that I hadn’t been able to find on this day of shopping, and among them were three Valentine cards yet to be chosen.  As I looked at those names, I knew that one was missing, and I felt guilty.  My mother was not on that list.  I had overlooked that section earlier that day, on purpose.  Why get a card for my mother?  She is now deeply affected by Alzheimer’s.  She doesn’t know any of us.  She doesn’t even know that she has children at all. 

Not only that hard fact, but my mother doesn’t know what Valentine’s Day is all about.  It wouldn’t affect her one bit to not receive a card, and it wouldn’t affect her one bit TO receive a card.  And further, my mother doesn’t even know what a card is or what it is for.  It’s all tragic and sad and completely impossible to believe that this is true of my mom.

 
My mother was beautiful, and she was gifted in so many ways.  She was an extremely hard worker, and organized to the max.  She even washed her dishes a certain way, and taught her four daughters to do the same.  I thought of this fact one night last November when our dishwasher sat broken and useless in its place in our kitchen.  I filled the kitchen sink with hot, soapy water and began to place the dishes down in the suds.  I smiled as I thought of how Mom taught us to wash the dishes in a certain order and even to put them in a particular place in the sink.  Obsessive?  Maybe.  But it makes sense, the way she taught us, and I thought as I washed my dishes that night…..in my mother’s order……that I bet each of my sisters would load their dirty dishes into their sinks exactly the way that I was placing mine that night. 

My mother’s teaching and her influence go far beyond how to load the kitchen sink, certainly, but it’s in those practical ways that I find myself often drawn to her.  One of our favorite stories about Mom that make my family laugh is the one about the time that Mom and Dad had all of us over for dinner when we were visiting.  Mom had cooked beef in gravy with rice on the side.  She set the line up as a buffet, and she watched carefully as either Bethany or Martha….don’t remember which……put their rice on the plate and then put the meat on their plate separately from the rice.  Mom pulled herself up to all of her maybe 5’2” frame and announced loudly, “The meat goes ON the rice!”  We all wanted to burst out laughing, and we did roll our eyes when she wasn’t watching……but we all loved her for it.  That was Mom.  “The meat goes ON the rice!” is now one of our favorite sayings.

Now Mom doesn’t even know what rice is…..or meat…..and often doesn’t know what to do with the meat and the rice that might be on her plate.  Jan sent us a video last night of a recent visit with Mom.  She wasn’t sure that we would want to see it, but we told her yes……please send it and let us see our little mother.  It was heart wrenching and sad to see her so completely unaware of anything and anybody.  To see her showing fear, shaking and scared.  Our mother is gone.  The woman who bore us and raised us, and instilled in us so many amazing values that were her own, is now gone.  But her body is here, and she is loved by all of us……and excellently cared for by Bob and Jan, and John and Jeanie.

It’s all we can do…..love her and care for her and definitely to pray for her.  And for me personally, to buy her that card.  Yes, I added her name to my list and I went to the “Mother” section of the Valentine cards.  I found just the right card, surprisingly enough…..one that talked about what my mother had done, not what she was doing now.  And what she HAS done is plenty!  All of her children and grandchildren are reaping the benefits and blessings of all that my mother HAS done in her life well lived. 

I really know that I sent her that card, not for her, but for me.  I needed to remind myself of all that my wonderful little mother was, and of all that she is still doing in my life today.  In that way, I honor her, though she is unaware of that. 

Remember now:  The drinking glasses are washed first, then the plates and the silverware…..with the silverware in front and the plates behind them….

And the meat goes ON the rice, for crying out loud!