Wednesday, June 24, 2009

It's Tuesday, right?

So here I am again, thinking, "Why did I say I would write by every Tuesday? Did I not realize what I would be doing on the 23?" Oops. Peyton and I spent today traveling to visit family in Denver and for those of you with kids, you know what the day before a long trip is like. My good intentions of having everything packed two days in advance didn't pan out quite like that, but I thought I was doing pretty good to be done before midnight last night, especially since we had to get up at 4a.m. today!

I enjoy parenting so much more now, and am thankful even in the difficult moments for the joy Peyton provides. Traveling was such a fun adventure with him today and I loved watching the experience through his eyes. The best part of the day was when he quickly turned to me, urgently wanting my attention, and said, "Mom! I see God! He's out there!" He was looking out the window of the plane at the clouds with amazement and awe. I wish I had gotten him to go into more detail - I hope he will remember it so he can explain it better tomorrow. His look and the urgency of his demand for my attention was thought-provoking.

His comments over the last two days keep me laughing. He was over at a friend's on Monday, and the little girl he plays with there is a three year old enamored with princesses, princes, and fairy tales. I heard from her mother that she will lay on her bed, close her eyes, and then call for her dad to come and "kiss her awake." I hope they don't mind that I tell this, but you have to know that part to understand the next part. The mother told me upon my return that afternoon that she overheard Peyton say from his reclining position on one of the children's couches, "Come kiss me!" I guess he said it not once, but multiple times, until he got a response (though assuredly not the one he was hoping for). The little girl's response was, "What? Why? Are you a princess?", to which Peyton responded, "No! I'm a king!" I think the funniest part of the scenario is not necessarily what he said, but imagining him lying there on the couch, waiting for his beautiful princess to come and kiss him, yet with all the innocence of childhood (I hope!). How come we never hear the king's side of the story?

I am sure the above creates an appearance that life has carried on into more jovial times and that we are moving on, and we do have joy and happiness in every day, but it amazes me that grief can coexist with these blessings. Imagine for a moment that a cloud is not a representation of trouble, but of beauty. It is as if there is a lining to every beautiful cloud, but instead of a silver lining to the clouds, there is a faint shadow around most every cloud. I wouldn't say it's even a shadow, but a blurred edge, where the defined blurs into the undefined until you don't know when you stopped looking at the cloud and began to see the sky. I know that sounds a little odd, but so to is the mind set right now. It is a strange place in the middle ground between here and there. Some moments I am so caught up in an experience, enjoying a bug with Peyton, or a conversation with a friend, and the next I am carried away in a breath by something that reminds me of Drew. He seems to be a part of every thread of me. I read something that put this into perspective for me today and validated my theory that I was addicted to Drew (and of course, still to Peyton). The article I read said that the oxytocin a woman's body produces at birth creates an immediate addiction to her baby. Any interaction with that baby then only enhances that addiction. If I was addicted to Drew and he was so abruptly gone, it only makes sense that I would go into shock and withdrawal. As with an addict (in this case, to nearly the best possible thing created!), even when you have not "fed the addiction" in a very long time, it takes very little to bring that urge rushing potently to the surface, creating an intense desire and simultaneously an angst over the realization you can't have it. How do people manage that feeling?!? I know the loss of Drew was much different than dealing with an addiction, but it helped me understand how the desire for him could be a part of every thought, whether conscious or unconscious and how at times the longing can overwhelm me.

To close, I have to share where I have found joy over the last week. We shared a wonderful weekend of camping with some dear friends two weekends ago. It was Peyton's first camping trip and he nearly bubbled over with excitement all weekend long, fizzing out only when he hit the car seat on the way home. One of his highlights was swimming in the kid-friendly lake nearby. On Saturday, as we were winding our way along the forest trail to the lake I saw a patch of clover nestled among the roots of a tree. As Peyton chattered along behind me, I found myself slowing down to peer into the patch, in faint hope of spotting a four leaf clover as I walked past. It occurred to me as I realized there were none to be seen that had I found one I would have been so fascinated with my treasure. What feelings come to mind when you remember the childhood hunts for the elusive clover, and what did you feel if you were successful? What if you spotted it when you weren't even looking for it?
Drew is my four leaf clover - different, yet beautiful; unique among so many; a treasure often discovered where you least expect, and one you would never return; and with a magic that can cause you to marvel without explanation.
I have never felt the richness of life like I do now. For that I am blessed.
My sons, I love you, and Jordan, I love you more!

Tuesday, June 16, 2009

I'm still here

I have determined that I will post once a week.  I need to set myself some goals to get out of this zone I seem to be in.  I have so much I want to do here and so much to share, that I get overwhelmed, don't know where to start and thus, decide not to start.  As such, I have decided to set an achievable goal... or at least I hope it's achievable!  I will be posting once a week, with Tuesday as my start day.  If I haven't posted in a week by Tuesday, I will then.  Now that I have written this and it's captured in ink, I will be more likely to do it!  

I am hoping to change this blog around a bit in the next month.  I want to do two things - to fill everyone in on our current happenings, and to share my thoughts on what grief is like on the inside.  I hope to ask for your input, and am looking forward to your responses already!  Now I just need to get this site going better!

Most importantly, I need to add two things to this post.  1) Peyton is doing very well!  I am thrilled to be able to say this and yet am reluctant to put it into writing!  We are hopeful he will continue to heal so well.
2) We are planning a fundraiser to show Drew how much we love him, and to try to make a difference for the kids and the families that have yet to go through this.  We feel very deeply about this and will be working towards making a difference any way we can.  My sister-in-law, Nicola, and a dear friend, Aisling, are the main coordinators, with Jordan and I playing a back-seat role.  You can find out more at A Day For Drew (www.adayfordrew.com).  I will be adding more to this blog on that note in the future as well.

Please bear with me as I seek to turn this blog into something sustainable and hopefully interesting/helpful to those who visit.  Thank you again for visiting us!

(I have promised an update on our genetic situation and Peyton's results, but am waiting for a meeting with the genetics specialist to post more.  Well, sort of.  That's sort of an excuse, but I am getting closer to being able to post this - it takes a lot of emotional energy and I need to dose it right now.  I haven't forgotten!)

Wednesday, May 13, 2009

May 14th

2008





Today was not May 14th, but it might as well have been.  I am sitting here in Drew's room where our computer now is, along with many of Drew's things, and where his crib was last year at this time.  At this time last year, on Wednesday night, Drew was sleeping peacefully (I hope) in his crib, and Jordan, Peyton and I were sound asleep too.  I would have just finished his last feeding of the night, rocking him close in the rocking chair and loving the silence and comfort of that last feeding.  I would have just put him down, snuggled up with his special blanket that he always wound his fingers through and with his little bear next to his face where he inevitably ended up putting it.  I know I was only the distance of 4 inches of wall away from him, but from this vantage point, it was way too far.  I wish I had been in here watching him, holding him, near him, as if somehow I could have prevented him from having that first seizure.  We were sound asleep... completely unaware of how soon our life would change.  

On the Wednesday of this week last year, Peyton, Drew and I went out to the Zorn's ranch with the Mom's and Tot's group from our church for a hay ride and a day with the animals.  We went with great anticipation and I'm sure a little chaos getting out the door!  It was a spectacular spring day, and I remember carrying Drew around in the Baby Bjorn for a good portion of the day, trying to protect him from the sun while trying to keep up with Peyton.  Peyton was in his glory, feeding chickens and gathering eggs, riding a horse, playing in the hay, climbing on tractors, and running around unfettered in the warm spring air of the countryside.  Drew seemed to be enjoying himself too, smiling lots, and content to be carried around and to be part of things.  He spent quite a lot of the afternoon in the laps of special friends who felt it no burden at all to give some extra cuddles.  The only strange thing about the afternoon was that he didn't seem to want to eat, and though he had been in the heat of the day, he didn't seem to want to drink much either.  After shedding a little worry, I gave up fighting on that and wrote it off as an issue of too much distraction, that could be overcome once we got home.  

When we got home, I'm sure I fed the boys dinner, but I don't remember much of that part of the day.  I do remember getting them ready for bed, and listening to Daddy read to Peyton while I read and sang to Drew.  I tried to put him to bed but he didn't want to settle.  I picked him up a couple times, cuddled him, tried to feed him again in case he was still hungry, and then put him back to bed.  The same thing repeated a couple times and then he finally settled to sleep.  I thought it was attributable to being overstimulated all day long.  (Was I oblivious?  I know the logical answer to that, but can't help but ask.)  Jordan and I came in to look at and wonder over him before we went to bed, as we liked to do every night with both boys.  I remember looking at him, so peaceful, and feeling so content, so blessed, and so excited about the future.  It wasn't long after that he woke up for a midnight snack and I remember holding him, both of us barely awake, but aware of the comfort of each other's presence.  I remember thinking over the day and planning for the next day as I fed him, anticipating the adventures the next day would bring.  I remember holding him close to my chest, head looking over my shoulder as I patted his back, and I can still feel that feeling of having him heart to heart.  Then off to bed again.  Separation.  That feels like a lifetime ago, and like a mistake I wish I could take back.  It was at that point that I said goodbye to the dream of the Drew I knew to that point.  Not to Drew himself, because I would never take back last summer, but to what I hoped for him and what I dreamed of about him.  

1:15 a.m. Drew woke up crying strangely, in some kind of discomfort.  The cry was not one of hunger or the desire to be cuddled.  It seemed that he might have been teething all day so I thought that was what it was and decided to go give him some Tylenol to see if that would help settle him.  I have gone over that scene a hundred times in my head, sad at how poorly I handled it - how unobservant I was to what was really happening.  I didn't realize he was having a seizure until I tried to give him his pacifier back in hopes of not disturbing him too much by picking him up or turning a light on, and he couldn't keep it in his mouth.  I tried again.  He still couldn't keep it in.  At that point, I was fully awake and instantly alert - I turned the light on low to check him.  He was shaking in his crib, helplessly flailing about, with a look of what might have been confusion in his eyes.  Shock.  Act.  Move.  Think.  Go!  I picked him up and took him into our bedroom, trying not to wake Peyton up by yelling at Jordan, but wanting to scream at the top of my lungs for help.  I put him on our bed and turned the lamp on, waking Jordan up.  I remember thinking, "I never imagined calling 911.  I guess this would be the time to do that.  All those years of thinking those are the numbers you never accidentally want to hit - overwritten in less than a moment."  Drew lay there, still shaking, looking to the left, and if I didn't know better I would think his eyes were saying, "Please help me."  

The paramedics were here in less than 5 minutes.  They assessed him, gave him medication and rushed him out the door.   I was in the front seat of the ambulance as it whisked my baby to what I hoped would be help that could fix the problem.  I remember sitting in the front, watching the trinket dangle from the rear view mirror, joking nervously with the driver (what was I thinking?  Shock does strange things).  When we got to ACH, Drew was swarmed with a team of caring medical staff, while a nurse came near to check on me and make sure I was ok.  Did I need a glass of water, anything?  It took them over an hour to stop his seizure and I can't even tell you what I was thinking.  I just remember trying to move his blanket closer to him in case that could provide some of the comfort I couldn't get close enough to provide.  

After multiple tests that night and so much medication that he was on life support, off we went to ICU, turning a corner that we will never go back around.  I called the family in the middle of the night this night last year, needing their prayers.  I hope I never have to do that again, and that I never get one of those calls.  

I desperately miss my littlest boy tonight.  I love him so much.  Doesn't the grief get easier at this point you could ask?  My answer would be that the constancy of it changes, but the intensity of the grief is almost more painful in the doses that come.  I don't cry all day, and I laugh often (Peyton is still my dear Peyton!), but I do wear waterproof mascara every day now where I only wore it on special occasions before.  Why?  Because I never know when I will get to experience something that will open the bottle of tears, through which I am drawn back, closer to Drew for a moment.  I never mind the tears, I just wish they brought back more than a memory.

I will be ok in the morning, because "joy always comes in the morning."  My eyes will be red, and there will be an empty tissue box, but perhaps I will dream a sweet dream of the little one I love tonight.  If this prompts a tear, turn it into a prayer of thanksgiving for me, that God allowed us to experience both Drew and His love through Drew.  Drew, I will love you forever and more!  I love you.

Peyton and Jordan, I love you too, and am so thankful for you.  You are rocks in my life.  Thank you.  



Tuesday, May 5, 2009

Peyton's home

I guess that means we are all home.  We have actually been home for a couple days, but we have been trying to reconnect and avoid all distractions for a while, so I have not yet updated this!  I may be in avoidance mode, not wanting to sit down and write because so much has gone through my mind that I don't know where to start, or I may be in some state of denial or ??? - don't even know what to call it - where I don't want to sit down and write because I don't want to say something and then have to take it back a day later.  It feels like if I wait a bit maybe everything will settle down and Peyton will get to stay home for good!  As if I have any influence over what happens!!!  Silly the way the mind works on overload.

I feel a little like a fly buzzing around frantically.  Almost in circles.  Perhaps aimlessly, though not in the fly's mind.  Flying at that pace until it drops.  Then it drops.  I think it's survival mode - it's what I go into every time we come home from the hospital and some times it lasts longer than others.  It seems like things should be easier now and we should be moving past the idea that we have had to deal with some challenging things, but my mind doesn't know how to sort through this one.  Neither Jordan nor I know whether our grief process (over both Drew and the loss of our idyllic future) has been postponed, or abbreviated.  It has been a blessing in some ways to have had something to change our focus, as we have poured ourselves into supporting Peyton; however, in other ways, it has been so hard to mix the two groups of emotions, each with their own wear and tear.  I think that is partly why I feel like the housefly right now - I don't know where to settle, and what risks settling in one particular spot will bring with it.  I think I will just keep flitting about for a bit, until landing seems like a good idea.  

We are so glad to be home!  There isn't a day that goes by where Peyton doesn't mention at least once or twice how glad he is to be home.  He is doing amazingly well - Amazingly well!!  I am sure I wouldn't be bouncing (literally bouncing) back the way he is.  He had his bowel resection done two weeks ago today and the surgeon said he would be well on his way to recovery and able to resume most activities by 3 weeks, but to hold off on more significant activities until the 4 - 6 week mark.  He also said Peyton would know his body best and would slow down if he needed too.  Last Tuesday he was zipping around the hospital like he had never been better, and the nurses were just waiting for him to show that he was getting tired.  He didn't tire until he hit the bed.  He was a little sore the next day, but trying to restrain him that Tuesday would have been like trying to restrain the wind.  You try it!  By Thursday he was feeling better than he had in months.  We spent Friday, Saturday and Sunday outside, trying to clear the cobwebs and basking in the sun.  It was wonderful, and even more exhilarating to see Peyton brimming over with life. 

Last summer, we promised Peyton that as soon as the snow was gone this spring we would get him a two wheel bike.  He never noticed how fast the snow melted before, but he couldn't let any of us not notice it this year!  We finally held true to our promise this weekend and he got his bike.  He would bring that thing to bed with him if he could.  He rode it out the doors of the bike shop and was attached all weekend long.  We thought he would get tired, but he just kept going.  Today is the only day in the last 4 where he didn't beg nonstop to ride it and that is only because he was sure a tornado was going to hit (strong winds and rain, and a very active imagination).  I am sure we will be out and about tomorrow morning!  He seems to be recovering very well and hasn't complained of tummy pain or nausea at all since his surgery - Praise God!  We hope this will be the end of the complications and that he will not need any more surgeries.  The surgeons can't guarantee anything, but they said there is reason to be hopeful right now.  I'll take that.  Hope is good.

Here are a few shots and a video clip documenting the big day, they made me smile.
 
Eager anticipation...
Riding the new bike out of the shop.
Can you get that out any faster?  Be careful Mom!
Proud new rider
I think this is a rite of passage...

Video clip of Peyton's first official bike ride:



I am still working on trying to get an audio piece posted to add to that story I promised, but I will have to try again when I can think more clearly.  Hopefully that won't be weeks from now!!!

Drew - wherever you are tonight baby, I love you forever, and more!  I miss you like crazy-crazy!  I wish I could give your fuzzy head a kiss tonight and smell your forehead.  God, take special care of my Drew tonight.  Thanks for blessing my son with the gift of being in your presence and free from these cares. 

Monday, April 27, 2009

Technical difficulties - stay posted

Ok, I was going to post a radio clip and some pictures of our day Friday but am going to have to wait until I can either get home for a minute or two, or get to a different computer and try again. If I get a chance to do this while here, you will hear the story - if not, it won't be long after we get home. Sorry for the delay!

Saturday, April 25, 2009

My bubbling river

I have often likened my little Drew to a sunbeam and if he is that, then Peyton is a river. He is like a river that meanders slowly and gently at one moment and at the next is roaring over the rocks, splashing everywhere and getting everything in its path wet. It shoots over falls without thinking twice, easily cuts through new territory out of necessity, and moves around rocks, not stopping to think about the size of the obstacle encountered. It sprays into the air sometimes, mixes with the sun to create beauty everywhere, and brings life to the surrounding environment, not intentionally, but by proximity. It may be cold and deep, still and quiet, loud and abrupt, or warm and gentle. It doesn't do anything to attract attention intentionally, but something about it draws people to watch it.

Peyton has brought us smiles this week, and pride, as he deals so bravely with his lot. He has also caused me frustration and confusion, if I am completely honest. He does not (DOES NOT!!!) like the NG and oxygen tubes they put in his nose after surgery. Between the NG tube and the pain meds, he has challenged all of my mothering skills and then some for the last 5 days. Friday he was crying about something, which brought me in closer to investigate. He responded, "I don't need you, I need NG out!" If you came to visit, you might have thought he had surgery on his nose instead of his stomach by his indications of what was bothering him. I tried every trick in the book to distract him, and more to comfort him, all unsuccessfully. I think the nurses are never sure what mood they will encounter when they venture in! He has perfect manners some days, but is more than prickly others. If you ask him how he's doing if he is experiencing any discomfort at all he may bite too! I guess I might ask people to allow me a little latitude too if I had gone through half as much, but he certainly proves how much a situation like this can impact all elements of your being.

We are hopeful that Peyton will be discharged later this week, if everything continues to mend as well as it has been. Since he got the NG tube out on Friday, he has done a 180 in both personality and recovery. He was so ginger with his movements because he didn't want to bump his NG tube that he wasn't pushing himself at all. It might have been a mixed blessing for his recovery. A few of the nurses who were on last week but had the weekend off came by to see him today and were so surprised at how well he is doing. We missed the doctor this morning, but I'm sure if he knew what Peyton was up to today he would be thinking of kicking us out of here. We just need to check on a few more things and I am not eager to rush things at this point. Peyton has an area that is swollen around the incision, but it looks like it might just be how they sewed things up - none of the nurses have been too worried about it. Hopefully it won't slow our discharge date down. He needs to be able to tolerate a full diet too, before we can leave. His tummy bothered him anytime he ate today, so hopefully that is just due to his tummy learning what to do with food again. I can't imagine the shock to the gut from having everything taken out, pieces removed and then everything put back in - that just sounds wrong and definitely something that I would think would take more than a week to recover from but kids can't stand to be down long! He was already trying to hop on one foot this afternoon (OUCH!), let his sneezes out gingerly (he wouldn't let himself sneeze until today) and proving his speed had not been affected. I was talking with a friend in the hall and Peyton excused himself for a moment. He had been running in the entry hallway for the unit (the only somewhat safe place to expend that type of energy indoors) and decided his reindeer slippers were too slow. He was back a minute or two later with his running shoes on and then had to put them to work! You would not know he was laid up a couple days ago! Amazing.

Now it's time for a quiet moment or two before bed to unwind. Thanks for following and I am going to work on that story shortly...

Abby's Special Day

Today is a special day for a dear little friend of ours and I wanted to share her day with you. Many of you have been praying for Abby, a little two year old with the same disease as Drew. Her Mommy and Daddy are working hard to make it possible for her to stay at home and that is the goal of this special day for Abby. God has blessed my life with the friendship of her mother, Jen, and Abby's smiles often remind me of Drew.
They are going to have a fundraiser for Abby tonight in Calgary, down south of the city at the Deer Run Community Centre. Everyone is welcome. If you see this before tonight and wish to join us, please do! I have included a link to the information about the fundraiser, that includes directions if you decide to come. I will be there and would love to see any who can come!

There will be an update about Peyton tomorrow. He is doing well, but is very sore right now. We have the most wonderful story to tell as well! God blesses our family in so many ways and with so many wonderful people!!! I am so glad He has opened so many doors to our family, and we are thankful for all the prayers for peace and comfort.

Please pray that Abby's fundraiser will be a success and that her parents will be surprised at the outcome!

Here are the links to information about Abby's special day (and some great pictures of this adorable little lady!).

http://www.facebook.com/home.php?#/event.php?eid=51294124353

http://www.momentswithabby.blogspot.com/