Stevens-Johnson Syndrome: Thinking your child is going to die and what that does to your head

Kyle and Stevens Johnson Syndrome

I put some sad music on. Nothing like Arvo Part’s Spiegel im Spiegel to do the trick. I am trying to find that space. I need to heal that space. Whenever I go to that space my words immediately become clunky, jumbled and paralyzed. I do not know how to say it or what to say. I keep trying. I see it. I see last year. And when I think about last year, everything I see hits me in a giant, suffocating wave. I feel like drowning and I try to push through. I am clumsy as I keep trying to tell our story. At the very least, I want generations of family to feel inspired, to feel blessed, to be grateful that their predecessor Kyle was a freaking super hero and so was Eli, his rockstar brother. I do not want our story lost. Most people know that Kyle was very very sick last year. Stevens-Johnson Syndromewas the mean ugly train that took us for a very scary and terrible ride. In bits and pieces I have awkwardly tried to tell our story. It still feels trite. I still feel awkward. Right at the moment I think about this past year or try to write about this past year, I short circuit and in my body I sense how I think I would feel if a semi-truck were barreling towards me and in my mind I see that the semi-truck is seconds from impact. Bam! Time stops. I feel that feeling you get, you know, that the terror you sense when you are watching a horror movie. You know that something bad is going to happen. You see that something bad is going to happen. You want to reach into the screen and say, “Hey, don’t open the door. Really! Please do not open the door! He has a knife. Seriously! Step away from the door!” The person cannot hear you and there is nothing you can do except cover your eyes. And before the semi comes crashing into me, I hold my breath and slam on the brakes.

Kyle and his amazingly awesome Doctor: Stevens-Johnson Syndrome

I want to get it all out.  Most people do not know that Kyle had two overlapping cases of Stevens-Johnson Syndrome. His nose took a bigger hit on the second round.  For starters, I want parents to know what it is like to sit alone in a hospital room day after day. I want them to know that they will be ok no matter what. I want people to know that they need to keep the hospital room peaceful. I was scared into peaceful and then I did not want to do anything to tip that balance. When people saw Kyle and came unglued, I asked them to leave. Even then, I was blessed with resolve. He was scared out of his mind. He heard the doctors say it was very serious. He felt their fear and confusion. The very least I could do is give him some peace. I want healthy siblings to know that we parents love them just as much as their sick and needy brother or sister. I want people to know that doctors do not know everything. Trust yourself. Trust your instinct. Even if you are a pain in the ass, do not be afraid to ask questions, change doctors, change nurses or simply speak up. I want you to know that I saved Kyle’s eyesight because I spoke up. It was that simple. I listened. I paid attention. All he needed was an over-the-counter lubricant. The nurses thought sleep was more necessary than waking Kyle up every two hours. I told them not to worry that he would not wake up. And it would not matter if he did. I insisted. I pushed. I got his eye doctor involved and the nurses pushed back. I pushed some more. Kyle’s eyeballs were shedding all of their skin. His eyeballs were scabby and raw. All he needed someone to do was open his eye and squeeze the lacri-lube lengthwise along each eyeball every two hours, then every four hours, then every six hours, every eight hours until months down the road (now) when he no longer needs it every single night. Sure, at the time, he also needed stronger eye medication, however, to prevent his eyes from completely gluing shut, all he needed was that over the counter eye lubricant. What the over-the-counter eye lubricant did was prevent his eyelids from adhering to his eyeballs. Once the adhesions glued themselves onto the cornea there could be irreversible damage. Each day the Ophthalmologist would come in with a dental-tool-like instrument, open Kyle’s eyes and scrape out the inside wherever there was a new adhesion forming. It was horrific. Kyle was so brave. The nurses resisted. They were not wrong that Kyle needed his rest. I was right. I did not want him to go blind. As parents, as advocates, that is what we need to do. We need to persevere.

Easy E sadly sits at the hospital

Every single second was a fight. It was not any easier once we were home. It was worse. It was hell; months and months of hell. I think everyone else assumed it was better. Maybe because I did not know how to tell them it was not. Kyle came home disfigured and traumatized. Eli was shell-shocked, Dave was in over his head and I was freaked out and exhausted. I could not sleep. It was like we had a newborn, a newborn that could talk and tell us how much it hurt. And this newborn was scared, emotional, distant and crazy. We spent months giving Kyle round-the-clock medication. He went back into the hospital for surgery to remove scar tissue from his tongue. Getting this surgery was another giant challenge. It was a challenge that consisted of trips to new doctors and new specialists. There was a moment where we thought about leaving that stupid, ugly growth. “Hey, at least no girl would ever want to kiss him with that thing. We can have it removed when he is twenty-one.” We joked. People assumed I was specifically avoiding their calls. What they did not realize is I was avoiding everyone’s calls. I did not know what to say.  Sometimes I worry that people are still mad at me because of how I acted the months after Kyle came home. I wanted to tell them how scared I was. I always seemed fine. I was hiding and it sucked. This being said, there were those who found a way in and for that, I will be forever grateful. Thank you for fighting for us. I want you to know about them. Those folks who quietly stood by our side, those who loved us and assured us that Kyle would look normal again. I want to tell you about the people who Kyle let in. They have changed our lives forever. Kyle went through steroid withdrawal, narcotic withdrawal, he lost his friends and I did not know how to keep mine. We made Kyle go back to school when he was not ready. He had missed so much school we thought he should try. No one realized how bad he still was. I do not know if I will ever forgive myself for sending him to school. Shortly thereafter, we had to pull him right back out. His immune system was wrecked and because it was wrecked once he was in the student population he became very ill. Looking back I know I was in shock. If I saw him now I would know how completely ill he still was. Then, I had to fight for his grades. I had to fight for him to be re-tested. He looked freakish and we had to fight. We were at the pediatrician all the time. The eye doctor saw him twice a week at first, maybe more.

This is how Kyle looked when he went back to school. We were crazy for sending him.

I cannot remember. It all sucked. It really, really sucked. Eli cried. He cried a lot. He heard other kids making fun of his brother. He never wanted Kyle to know how sad he was. Every thing made Eli think Kyle was going to die, that Kyle would have to go back to the hospital. It terrified him and then he cried some more. That was our day to day. I could not complain. At least Kyle was alive and we were all surviving. This is the beginning. There is so much more to tell.

Easy E & Kyle
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I needed to Fix Myself

I was pregnant here. You can see the beginnings of my pregnant belly. 6.17.06
Dave & Me. Thanksgiving 2011

As I crawled in bed late last night Dave, who was already in bed, said, “I read what you posted. Wow! That was a lot. That was really good. You are a good writer.”

Thinking he was talking about the post I had just written on Overweight Women, confused and perplexed I said, “Well, thanks, um, didn’t you edit that post earlier?”

“No. The one you posted on Facebook.” He responded.

“Oh. My Fix-You Post.” I said and because I was tired and caught of guard by his thoughtful comment, I mean, (I don’t think Dave would feel especially compassionate about the overweight woman who was smoking while carrying her catheter bag into her dialysis appointment), I continued, “I am working on my archives. That was one of the last posts I wrote  before I quit blogging and it was one of the first posts I was able to recover from the sever-back-up Vortex. It was always a favorite.  I didn’t read it today. It is too sad.”

I turned over, smiled and was grateful that he had read it.  Dave’s feedback meant more to me than almost any other feedback I have ever been given. Go Dave!

The “Fix-You” Post was so sad  because I was so sad and right after that I quit blogging.  I quit blogging because my heart was broken and I spent the next five years trying to put my heart and the rest of me back together. It was more than blogging. I stopped and changed everything. I put my two feet on the ground and pointed them forward.

It is estimated that since Eli was born (he is 10) that I have had at least twenty miscarriages (I stopped counting). I could have chosen to adopt. I could have talked Dave into using a surrogate (probably not) and  even now that I am much older, every single month I still ask myself, “What if I am pregnant?”  It never leaves.  It just does not and so it is what it is. What I want you to know is that I use my pain to see opportunity. My heartache has morphed  into gratitude and  my lack of control has taught me to let go. And yes, getting here has been anything, but easy.

Opportunity.

Opportunity is what it was and opportunity is how I spin things now.  The one opportunity I did walk away from was my daily interaction with wonderful people who came to Crazyus.com. Without a word or an explanation, I unplugged and I walked away. Bloggers and readers alike were always kind and good to me and believe me, when I left, I missed all of them.  As I sit here and type I know that I would be over the moon if I ever could have that same internet connection again (get the play on words . . . internet & connection . . . he he he). Seriously, it would be beyond my dreams!

The opportunities I did have way back in August 2006 were my late miscarriage and imminent mental crash. It was time for me to accept the fact (or at least start accepting) that I may never give birth again and this was a not-exactly-how-I-had-envisioned-my-life opportunity to stretch.

Peggle

Here is how it went. We sold our house. We moved into a tiny tiny condo in Park City, UT. Dave would go to our land, work on our new house everyday, Kyle would go to school and Eli would go to pre-school. I, well, I would sit home and sleep or play Peggle. I spent hours and hours every single day playing Peggle. I played Peggle so much that I finally confessed my Peggle Addiction to Dave. He already knew. He mentioned an article he had read about combat soldiers who play Tetris. “They play it to help with Post Traumatic Stress Disorder.”  That was all I needed to hear and I kept on playing. I played Peggle for months and months and months. I loved my high scores I loved watching where the orange ball would go.

Eventually and still in my Peggle fog, we pulled Kyle out of first grade because he was so far ahead. He had gone to an accelerated kindergarten the year before and in October when the Principal at his new school told me it was fine for Kyle to “hang out” until the end of the school year (doing absolutely nothing, except getting in trouble), Dave and I knew something needed to be done. Because I was on Peggle-Auto-Pilot Dave took the lead and found a Homeschooling group (I was not about to Homeschool), which led him to this Hippie Montessori School. Dave went over to the school and loved it. I resisted for a few weeks until he finally dragged me over to check things out. Miss Diane, the long haired sixty-five year old director was wearing leggings, Uggs and a denim shirt. The school is in a house-slash-barn and I saw lots of feathers, Indian gear and Dreamcatchers. Because nothing is ever completely ideal, the school would end up being this crazy, dysfunctional, magical-talking-stick-duct-taped together Fairyland, but in that moment Miss Diane grabbed my sad sad face, kissed it, then looked me right in the eyes and said, “You will love it here. I know you will.”  She hugged me and welcomed me into her crazy-Hippie-Montessori-Planet. As confused as I felt, I knew and to this day know, that Miss Diane loves and accepts me, crazy parts and all. We paid our overpriced deposit, filled out our paperwork and signed Kyle up.

Miss Diane & Kyle

 

In late 2006 Diane and the Another Way Montessori School Community was everything this Adams Family needed to heal our broken hearts. No one knew anything about us. We had a clean slate and I loved it. We were simply the weird family, who was building a house up the street. And really at Another Way, everyone is a little weird and outside-of-the-box. Because of this we all fit into this little Park City Island of Misfit Toys. I loved it! I loved getting caught up in fundraising. I loved learning about Yellowhawk, the Indian. I loved that Sausha’s dad is Bart The Bear’s Trainer. I did not love that the dog-wolf hybrids came to the school, but my kids did.  I loved learning about the Talking Stick and I loved that Another Way was NOT Peanut Free. I sent my kids with their Peanut Butter and Jelly Sandwiches to school and I loved that I could.

Miss Diane is a world renowned ski instructor and we love that she taught our boys to parallel ski. No snow plowing allowed. I love that the boys learned to ride and groom a horse and I loved that the horses were at the school. It was not very long after we signed Kyle up that Miss Diane convinced us that Eli needed to be there too. It was easy. It was safe. If I needed time to breathe, the boys could stay late.  As Dave and I continued to do infertility treatments I always knew we could leave the boys with Diane. I really believe we found our very own Modern Day Hippie Commune. It was disorganized, unpredictable and I loved it. The friends I made there are friends I will have for life.

As I was talking to one of those friends earlier today I was mentioning how our choices take us to where we need to be. I mentioned my second act, the-what-I-did -after-my-miscarriage-broke-my-heart act. My friend is my very same age and has had similar struggles and I said to her, “You know how you always tell me to put my feet on the ground and point them forward? Well, when I moved to Park City, that is what I did. I had no idea what would happen. I was so sad. And then I started opening my heart ever-so-slightly  and there you were, a better friend than I could hope for. You got it and  understood this crappy infertility road and since the moment we met at Another Way, you have always been willing to travel the road with me.”

Grateful.

Grateful is what I am. I am stubborn. I desperately want to control all outcomes. When I let go, when I point my feet forward, people and places always come into my life that heal me and are so much better than anything I could have imagined. Because I got out of bed and put my feet on the ground, I could begin to heal.

Eli the Very Serious Equestrian and Miss Diane
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Alligators in my Dreams

Celebration, Florida

With my hands tied I cannot speak about what I have been processing lately (my childhood, it always goes back to my childhood). I would love to share about my one friend (my texting buddy) who is struggling and I am dying to write about that really off-guard moment (with family), which triggered a pain that took me all the way back to Mr. Eide (our next door neighbor) and my five-year-old-girl alligator dreams. I had so many freaking alligator-in-the-backyard-pond dreams that I began to refer to them as if they were my very own middle-of-the-night television series. Even when I would run into my mom’s room screaming, I would sob, heave, sniff and sob some more, “Mom, I had that same one two nights ago and it still scared me!” I would shake and shiver uncontrollably until she calmed me down and then I would spend the rest of the night sleeping in her bed until I had so many dreams that my mom and step-dad began making me a bed on the floor. Today I am not ready to get into it. Be advised, however, that anything I write now is totally being controlled by my alligator pain [wink wink].

 

It is probably not so crazy that as I write I still am feeling those crazy alligator knots. The knots come from five year old aligator-dream me, nine year old me and most definitely fifteen year old me night-terror me. Yes, when I was fifteen I had the craziest night terror ever. My parents found me standing in my closet with my pink blanket covering my head. They were afraid to come into my room because my screams were so loud and shrill. As they tried to wake me I screamed, “The Titanic! It is going to get me! I am in a little boat! HELP! HELP! H-E-L-P M-E! The Titanic is going to get me! HELP!” Yes, I really was standing in the closet with a pink blanket over my head and yes, that is really what I was screaming. And no, the knots did not leave after that. I believe I carried those knots all the way to twenty-one year old me. And when I was twenty-one and on a Mormon Mission, the powerlessness became so suffocatingly huge that were I to survive, those knots had to begin untying themselves and so they did. Ah yes, life likes to remind us that we are human and so on occasion, like now, something brings the knots into view and I am reminded that I still have some work to do. Damn Knots! And why does everything we do have to go back to something that happened to us when we were children? Why?

Maui

Sadly one of the things that happens when these knots show up is that I feel powerless. When I feel powerless I always experience writing paralysis. Stupid writing paralysis! Yet as I think and not write, I think about how cool the past five years has been and how happy I am that I opened this internet door again. I would not be so bold as to call myself the Little Engine that Could, but more I would call myself The Little Website That Has A Goal To Write Every Single Day and is Not Quite Meeting Her Quota.

Thank God there are no alligators here.

Alligators in the Pond
Guys’ Weekend: Kevin & Easy E

 

Guys’ Weekend

 

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Thanks to Bachelor Ben, Eli & Jack are having a play date

My friend Kathi and Bachelor Ben

I have not watched ABC’s The Bachelor at all this season. That being said, who am to say that I won’t. See, in those moments when I am drifting through the channels, if I land on The Bachelor, I promise you, I will stay on The Bachelor. I have completion issues. Even if I start watching an episode half way through, I will watch it to its end and if it is some delicious-Bachelory-reality television, I tell you now, I will finish the season. Bachelor Ben, there is still time.

This season, however, I really do not have to watch. See, early on The Bachelor came to town. Not only did it come to town, but the Bachelor People stayed at the hotel just down the street from me. Not only is it the hotel down the street, it is also the hotel where I have a gym membership. Celebrity sightings are a plenty. Hillary Swank nearly saw me naked in the Spa last year, for instance. No big deal, right? Right. We live in Park City, otherwise known is Little Hollywood. Ok, I have no idea if Park City has ever been referred to Little Hollywood. What I do know is that not only is Park City a major ski and vacation destination, it also hosts the Sundance Film Festival. And somehow over the years, Park City is a magnet for all sorts of Hollywood folk. As I type, the 2012 Sundance Film Festival is in full swing. Even before the festival blazed its way into town, celebrities of all different shapes and sizes were knocking at our door.

Continue reading “Thanks to Bachelor Ben, Eli & Jack are having a play date”

Thinking of Michelle

Kyle & Eli February 9, 2007

It was a really weird, last-minute-holiday-shopping type of day. I was buying Christmas and Kyle’s Birthday presents. With the Winter Solstice staring me in the face, it was dark early and I must admit that I let the darkness creep inside too. I was hungry, needed some sugar or caffeine and wanted to get back to Park City.

I waited and waited to make a lefthand turn out of the 33rd South Salt Lake City Red Balloon, and the holiday traffic was not letting up. Tired of waiting, I took a right instead and found myself trying to navigate a different route back to the highway.

It was really no coincidence that as I drove West down 33rd South, then made a righthand turn at 2000 East and saw La Puente Restaurant sitting there on the Northwest Corner, that I started thinking about Kyle’s pre-school friend/cousin, Sam Williams.  La Puente was the last place I saw Michelle, Sam, Ben & Ana.  Kyle & Sam are the same age and Ben & Ana were roughly the same ages Kyle and Eli are now.  Back in 2007 it was the Williams Family and their tragedy that nearly brought me back to blogging.  I have wanted to write about this, but it never felt right until now.

My Boys Today

It all began when Kyle was in pre-school.  He came home  one day, excitedly handed me an eight and a half by eleven lined sheet of paper with the name Sam and a phone number written so big the letters filled the entire sheet. “Mom. Mom. You know Sam?”

“Yes. I know Sam.”

“Guess what?”

“What, Kyle?”

“Sam says we are related and that we are cousins. Here is his phone number. We need to get together.”

Sure enough and as crazy as it may sound, Sam and Kyle are most definitely related and yes, they are second cousins, depending on which side you are coming from. A few days after Kyle brought home the phone number I saw Michelle, Sam’s mom, at Pre-School pick-up and as she stood outside with the sun glistening on her face she said, “Beth, did Kyle tell you the news?”

“I believe he did.” I replied as we both laughed.

“It is true. We are related. Beth, your mother-in-law, DeAnne, is my first cousin. Last weekend I was at Aunt Jean’s in Saint George . . .”

“I know Aunt Jean.” I excitedly interrupted and blurted out.

Michelle continued, “Well, I was at Aunt Jean’s and I asked her why she had a picture of Kyle’s parents on her piano. She told me, ‘well, that’s Davy, you know, DeAnne’s son.’ Then she told me how we are all connected, how Dave’s mom lived with my parents a long time ago and that she knew you and Dave. It is such a small world.”

“So small that sometime you find out that you are related, right?”

“Right. Sam thought it was really great and could not wait to tell Kyle.”

With this new piece of information Kyle’s friend, Sam instantly went from pre-school buddy to Kyle’s family.

Kyle & Zeke

As time and life goes, the pre-school year ended and I was not great about staying in touch.  And then one evening, as we often did with them back then, our friends Kat & Alan asked if we wanted to go out to eat.  Because we were burned out of Rubio’s and Cafe Rio, they suggested La Puente and we were on our way.  Once seated, Michelle and and I almost immediately noticed each other. She and her kids were sitting close by.  Once Kyle realized a fellow family member was sitting so close he burst out of his seat to greet them.  Then Eli, Kyle, Sam, Ana, Ben & Zeke (Kat & Alan’s son) made their way over to the “Arcade” (the entryway of the restaurant that has a few video games and gum ball machines.  Kyle and Sam quickly retold their story, proving once again even to Ana & Ben, that yes, we are related. “Sam told us about you. We are cousins, right?” Ana said making sure we all understood that she and Ben knew that we were family.  The kids had a blast. We literally had to drag them out of the restaurant with apologies that it had been so long and promises that we would see each other soon.

Shortly after that, we moved to Park City. And if you know anything about Utah, once you move to the other side of Parley’s Summit, you might as well live in Antarctica. It is strange how a half hour drive over a high mountain pass transports you into another world.

. . . Several months later found Dave, the boys and me in Hawaii for the very first time. We were there for nearly a month. Our trip magically began in Oahu and ended brilliantly in Kauai. By the end of our trip I was convinced that we would somehow find a way to move to this island paradise. The sunshine and ocean waves were the Natural Xanax I needed to conquer my seasonal Winter Blues.

Our last day arrived much to quick. We had to check out of our condo hours before our flight departed. With our bags packed, I did the one thing I always do in the morning and that is read the online news, especially the local news. I saw the initial article: Pregnant Woman and Two Children Killed in an Accident. With no other information, I needed to check the news again because somehow in the back of my mind I knew it was Michelle. I know the area well. I know the underpass the family was driving under. I knew she was pregnant. All the facts were adding up.

We had to check out of our condo and I had to wait to find out. As my boys spent their last day in paradise I knew a family back home was hurting.

Lydgate Park. Kauai.

At the same time I was reading the news the behind-the-scenes communication was happening in the Dorny family (Dorny is my mother-in-law and Michelle’s maiden name) and I received an email from my Mother-in-law with a link to an article telling us the very sad news.

I remember the weirdest things from the funeral. Dave and I were very tan. I was wearing a new Apple Green shirt I bought at Banana Republic. The line was long and I was surprised to see so many non-related people I knew. As we came closer to the caskets, we saw pictures and trinkets. The closer I came to the three caskets, the smaller I felt. My throat was tight. We stopped by Ben and Ana dressed so beautifully. We stopped and I thought about my own boys. I thought about loss. I thought about how childish I am and how short life is. We moved along until I stopped at Michelle’s casket. Of course I am crying as I write this. I was a small space in her world and I was overcome. She lay there. It was obvious that she was pregnant. I stopped and I could not move. She is a mother and she was gone. I could not stop thinking of all the times we met at pre-school. I liked her before I knew we were related. She was cool, calm and kind. I see the sun shining on her face as we talked outside the preschool. I stop and catch my breath.

I wanted to pull her up. I wanted to walk her right out of that room and tell her, “You can’t go. Not yet. Life got busy and we drifted apart. We are family.” And then it was our turn to say hello. Thank goodness. Michelle’s mom grabbed my hand, welcomed and thanked me. How can she be thanking me? And as Dave stood by Michelle’s dad it was eerie. Dave is physically a younger version of her dad. They are tall, thin and broad shouldered. Thank goodness they look so much alike because within seconds we were ushered over to the rest of the family and yes, they all look like Dave. We talked with all the aunts and then it was time to go.

And this is how they died.

On a quiet Salt Lake City Street a drunk 17 year old boy was driving alone, driving on the same road I found myself on, 2000 East. Somewhere around the I-80 underpass this boy lost control of his car. The Williams Family had no time. In a flash their life was forever changed. Almost immediately, Sam’s dad watched the last breath leave his mom’s body and in that moment he decided to forgive and then he moved forward.

Let me tell you, Kyle, Eli and I visited Sam after the accident. We knew it was not easy, yet Chris took a breath, forgave  and allowed his family to heal. I admit that on sunny days it is much easier to move forward. And on dark days, I still fight not to slip back. In my life I have been an idiot. Things that roll off will sometimes creep in. In those moments especially, I am aware that it is not always easy to heal or forgive. As I think about standing there wanting to desperately pull Michelle back into this world, I know I have to keep trying and keep healing. That is all we can do.

Then because I was not able to make a lefthand turn, I found myself turning right on 33rd South. I turned on 2000 East  right by La Puente. A few moments later I found myself driving under the same highway underpass. I was so focused on finding my way back to the highway, I was not sure how I got there until I was there. And then I thought about Michelle and healing. Seriously, it was like she was sitting right there next to me. In a drive under a dark highway underpass, I knew it was time to share my space in this. It was time to remember how grateful I am that  I met Michelle, how grateful I am that Kyle survived his ordeal, how grateful I am that I was able to have children and how grateful that somehow I am healing and the only way I heal is by forgiving and forgiving myself.  Really! Life is way too short not to heal and let go.

 

 

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Because I myself, am not sure where I stand with religion, I struggled with wether I should post the following video link. I guess you can take it or leave it. This being said, I want honor the Williams family and so I am posting it. Chris tells the story of his loss and healing like no one else can. I think it is pretty cool. The message of forgiveness is amazing!

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Happy Birthday Kyle!

Happy Birthday Kyle! We love you!

Kyle at the beginning of the 20 minute visit

Today, on his birthday, I keep trying to write a letter to Kyle. I want it to be profound. I know he knows I love him and that I always have his back. I have held on so tightly and I am just starting to let go.

I have spoken about Kyle and his battle with Stevens-Johnson Syndrome before and today I need to say more because Kyle wants me to tell you more. Now coming out the other side of our personal horror movie, Kyle wants you all to know that he is ok and not only did he survive SJS and continues to survive SJS, he has learned a lot. Just other night as I was tucking in him in, we were talking and he said, “Mom, I am really glad you write about Stevens-Johnson Syndrome. I am really happy you tell people about me. I think people should know about it. And you know what, Mom?”

“What, Kyle?”
“Do you think I will ever know anyone else who has had Stevens-Johnson Syndrome? Because I would really like to meet them.”
“I bet we can make that happen.”
“Really?”
“Absolutely!”

As I turned out his light he paused and said,

“I bet it will be a great book, Kyle.”

I shut his door and walked away, thought about where we have been and where we are now. People always say to Kyle,

“You must have something really important to do on this planet because you have been through so much.”

I never know if that is their kind way of saying,

“Dude, your life really sucks,”
or if they see what Dave and I see, one strong, resilient and amazing kid. Whatever is behind those words, I would like to think that it is true, “Kyle will do great things.”

He already has.

Kyle in the Middle of the 20 minute visit starting to crash

Nothing I have done has ever come easy and as I have mentioned, having kids was no different. For years after Kyle’s birth I suffered PTSD. (Long story I should post). The favorite part of his birth story he likes to tell people, “My HEART stopped. I was NOT breathing. They hit that BLUE hospital light. Called the resuscitation team. I was DEAD for FIVE minutes until they were able to bring me back to life.” His story is usually followed up with a, “YES, I was really DEAD for five minutes.” And then Eli says, “Mom, really? Was he really dead for five minutes?” I always come back with, “Well, he was not breathing and his heart was not beating for five minutes. You tell me.”

In those crushing moments when I am in say, a truck stop bathroom, painfully once-again miscarrying, I breathe in and think, “You are so blessed. Many people cannot have children and YOU have those two amazing boys. Remember, they saved Kyle! Get up, pull yourself together and go outside. Your boys are sitting in the car waiting for you.” That is what I do.

And now that Kyle is feeling better and back in the swing, I am starting to breathe. Because he wants me to tell you about Stevens-Johnson Syndrome battle, I think I can. What we have gone through has bound us together like some super crazy soul-strengthening polymer that you just cannot separate and not just Kyle and me, but Dave and Kyle, me and Eli and all of us. Because Kyle gave me the space to say these things, as I re-read what I have written, I think this post may be a little more for me than it is for him. Hey, but that is Kyle, sometimes misunderstood (especially when he was younger) yet you will not find a sweeter, more compassionate, more perceptive and thoughtful kid.

Just one year ago Kyle was still in Primary Children’s Hospital. After sometime he was finally able to get out of bed and leave his room. After this huge freedom had been given, each day Kyle would not-so-patiently wait for his friend to arrive. “Mom. Mom. Call him. He is not here yet. Call him.” Even on Kyle’s sickest of days, those days when his ice pack covered eyes were also covered by a blanket that was wrapped around his head and covered with a pair of sunglasses, just to make sure no light got in, well, even on those days, he always thought of his friend.

When his friend arrived, Kyle would sit up and say,

“Hey, do you want to go for a walk?”

His friend would always respond the same way,

“Yes. Whatever you want to do. Will you be ok?”

Then all of us would help Kyle get up and we would walk to the playroom. Kyle would often say,

“Mom I am so glad he can come see me. He understands and I do not feel so alone.”

Just a year prior, his friend  suffered a serious brain injury and was still not back in school full time. He and Kyle would walk and talk, his friend patiently waiting while Kyle grabbed tissues along the way and his friend did not seem to mind watching Kyle spit out all the dead Zombie-parts-looking tissue he was shedding from inside. Nor did his friend mind Kyle’s moveable IV stand, his feeding tube, red-shedding-eye-tissue-sticky-oozy eyes and all that gross and thick mucus membrane Kyle’s body was letting go. They walked and talked and for those moments, it seemed like all the things weighing Kyle down disappeared, and in those moments, I could breathe.

Once in the playroom we often had to pause and again catch our breath. We would look around and see all of the children. Many of the kids we knew would be fine, many were dying, and if they were not dying, their lives had been forever changed by some terrible accident or illness. We knew early on that we had not cornered the market on bad things that happen to you. And in the playroom there was this coming together, where all the other families understood that too.

On one of the many random days we were in the playroom Kyle and his friend wanted to play Apples to Apples. There were about ten times as many volunteers as children so Kyle and his friend asked them all if they would play. The boys also noticed a little girl in a wheelchair and asked her and her mom if they wanted to play. She seemed a little out of it. The boys (because children can just ask these things) asked and found out that she had also suffered a TBI (traumatic brain injury). It was early on and I could see the fear and confusion in her mother’s eyes. Patiently the boys waited as her mother explained things over and over again.  I ached for them:

“Her short term memory is really bad right now. They say it will get better.”

I could see her hoping those words were true. Kids aren’t dumb. All three  knew they had a long way to go. And as I sat there, I was grateful that as Kyle, his friend and this little girl asked each other the Apples to Apples questions,  their pain seemed to disappear.

After 20 minutes Kyle was done.

That is how Kyle is. Even when things completely suck, and believe me there are times still that they suck so much that I have a hard time talking about it, and people, I do not have a hard time talking about anything. Kyle is always able to manage perspective. On those dark and very painful nights when we were alone in his hospital room he would always say something like,

“Mom, thank you for being here. I don’t want to be alone. Thank you for talking to my doctors. I am so glad you are here. Mom, are you ok? Mom, it hurts so much and I am scared. Thank you for making sure I am ok.”

In those moments when I had no idea what the hell was going on or what was going to happen, Kyle always managed to appreciate the people in his life, and as you are learning, life has not been easy for him. He knows life is not always smooth and because he knows life is not easy he gets how awesome it is to have people in your life who love you and who have your back. And guess what? Kyle will always have yours.