Sunday, April 6, 2014

Wednesday, September 25, 2013

'Bout time

I don't follow the conventional rules of blogging. With my last post dating February of 2012, I am definitely not a "regular" blogger, I do not follow many other blogs, and those that I do follow, I rarely make comments. I'm not sure my blogging style is "casual" either, since my posts tend to be weighty (at least in my eyes) and significant. I don't even consider myself much of a writer. More often than not, I sit down and I wing it, letting my thoughts and usually my sarcasm tumble into words on my screen. This post is no different.

The last time I wrote I had just met with my doctor in Baltimore, one year after my transplant, and I was medication free and cleared for ALL activity. At the time that meant occasionally working out in the garage (we have a small workout area set up), getting on the mat with the wrestlers I coach, and the freedom to participate freely with my girls in their active lives. I had no idea it would take me to the place I find myself today. Let me explain...

On October 6, I am joining a team that is participating in the Tough Mudder Race in Auburn, Wa. This event wasn't even on the radar until a good friend of mine invited me to join his team. At that moment, and over a nice glass of IPA I might add, the idea sounded ridiculous and totally within reach at the same moment. At the time I was training to train, but this gave me purpose. Those of you with a competitive spirit know what kind of mental switch takes place when you prepare for competition rather than simply maintain a training schedule.

The Tough Mudder is a 10-12 mile race, peppered with intense military style obstacles that are tougher on the mind than the body, but the body has to be ready. So for what it's worth I've been training, hoping that my my body and my mind are ready.

This isn't the end of the story however. A good friend of mine has started a charity foundation called Team Julia. It is a non-profit agency that raises money for cancer victims as well as cancer research. Team Julia works through race participants to encourage people to donate money. So far Team Julia has represented Ironman participants and complete Ragnar teams among other races. Now it is time to add the Tough Mudder to the list of Team Julia events.

So many of you donated generously when my family was in great need. I know the financial burden of treatment, loss of pay from missing work, and unforeseen costs related to serious illness. If you are willing and able, please consider donating to Team Julia as my sponsor for the Tough Mudder.


I can't thank all of you enough for your support over the years. Your prayers are felt, your well wishes heard...now it's my turn.





Wednesday, February 29, 2012

I'm cured. How are you?

I've thought it more times than I've said it when people ask how I am. It is a little quick and even flippant which is why I've restrained from saying it frequently, but it couldn't be more true. A year ago this month I took a day off school to get a blood transfusion so I would be ready to coach a middle school match that afternoon (note that I took school off and not wrestling). Now, I'm worried more about how long to marinate my steaks than I am about my health. Incidentally, three days in a teriyaki, garlic, and sesame oil marinade is magic with rib eyes and flanks.

Last night we celebrated a season finished as the Squalicum Wrestlers, their families, and the coaches participated in our end of the season banquet. This was no ordinary season with a changing of the guard for a head coach and my full return to coaching as an assistant. I made this season more about me than I will ever do again as a coach, but my selfish ambitions were robbed by a group of wrestlers that reminded me why I coach in the first place. This was a year of exceeded expectations, capped by a young lady that made it to the state finals when her season goal was just to wrestle on day 2 of the tournament and simply place in the top 8.

Not to bore you with wrestling details, but there is an indescribable feeling as a coach to be in a pressed shirt, a tie, and a pinstripe suit waiting for your wrestler to battle for a state championship.When I traveled to Baltimore, MD to visit with my doctor in January for a standard 6 month check up, I did my best to describe to him this feeling of coaching in the finals. He listened and patiently responded.


He told me that seeing me in his office...cured, is the same feeling we as coaches feel when all the months of hard work and preparation, sweat, and tears produce a champion.

So here I am, cured! I am back to teaching and coaching which means long hours and caring too much about my students and my athletes. It means that the precious few hours I spend with my family are in fact few, but God is faithful in guarding those times so my girls can enjoy a healthy dad and Kelly can love a healthy husband. It means that plans for our future contain fewer "ifs" and more "whens".

My life is very seasonal as a teacher and a coach, and unfortunately my walk with Christ is seasonal as well. There are times where I am committed to reading my bible daily and praying constantly, but now is not one of those times. I could blame it on schedule or the emotional recovery of an intense wrestling season but they are just excuses. A second lease on life should mean a renewal of faith and commitment to living for Christ, but I think I am still riding the emotional high. Anyone that has experienced an amazing season of redemption, whether physical, spiritual, or emotional, can ride the waves for a while but eventually the waves crash on the shore and the ride is over.

I need to renew my daily walk with my creator. Time in the word, time in prayer, time in worship, grounding myself for service, seizing opportunities to act in faith, praying for more opportunities. God allowed me to be cured because he is not done with me on earth, and that is the ONLY reason he didn't take me. Those that know, know how close it was.

I tell my athletes that practice is the most important time and place for success. You can only perform as good as you practice, and unless you have rehearsed winning in practice it will be nearly impossible in competition. It's time to take my own advice, and program my spiritual muscle memory to respond when the wave dies and the ride is over.

Friday, October 21, 2011

"Forgive me if I don't shake hands."

...says Doc Holiday in the epic Tombstone. I will shake your hand, but don't be offended when I break out the pocket sized hand sanitizer and apply. It's not you, it's me! I am now a germophobe.

It starts simple enough with bottles of hand sanitizer at every sink, plus several strategically placed throughout the house. One in each car, plus the aforementioned pocket bottles that travel with me. But it doesn't stop there. I've have said goodbye to buffets, potlucks, communal bowls of candy, and the box of donuts in the break room. Every door handle, faucet tap, table top, or chair arm poses unseen danger. The next time I take communion in church I will bring my own unleavened bread and flask of wine...er, grape juice. The tough one is shaking hands, because I really like that. So when I bathe my hands up to my wrists in 62% ethyl alcohol with aloe, don't take it personal.

Obviously, I have reason to be cautious as my immunity is rebuilt over the next two years. I will receive childhood immunizations all over again starting next July (one year after transplant) and then follow up shots throughout the the year up until two years out. As for my exposure to illnesses like the common cold, I need to go through the process of getting sick and allowing my body to build it's own defense, just like an infant would. That is why I will be able to return to work at the end of this month. I HAVE to allow myself to be sick so that I can be healthy. I only pray that any sickness I do experience in this next year will be mild and forgiving, allowing me to build my immune system but not wipe me out completely or worse, put my overall health at risk.

Post transplant life is good, freeing, liberating. I am no longer bound by blood counts or the lack there of. All numbers are higher than they have been in years and steadily increasing, but we are training ourselves not to watch them like a sports ticker. What we are watching is my kidneys and liver to make sure they are tolerating the meds and showing no signs of Graft vs. Host Disease or GVH. Another interesting precaution is sunlight. A sunburn can trigger severe GVH for the rest of my life, so come summer time I'll be the guy in the wide brimmed hat, wearing SPF 50, drinking beer under the umbrella at the beach. I suppose I live in the right part of the country to protect myself from sunlight.

With constant improvement and recovery, I am finally returning to work healthy for the first time in a year. Tomorrow I will be walking into Shuksan Middle School preparing to face the reality of spending my days with pre-teens. Fortunately, it is a staff work day tomorrow so I get to ease into my classroom and the school before students arrive. Shuksan Staff, I can't wait to see you guys again.

With my new found vigor, I have been training again. Training for what, I'm not sure yet but I'm pretty competitive so I'm sure I'll have to kick someone's ass at something down the road. On my training route the other day, I realized that in-spite of saying that I am thankful to God for my health, I hadn't actually told Him, "Thank You!" So in a brief moment of solitude on a path-side bench at Northridge Park in a cathedral of trees, I thanked Him. I praised Him for His greatness and His orchestration of the plan for my life. I praised Him for creation and that the beauty of the forest pales in comparison to His handiwork in us. I prayed that my new lease on life would be a testimony to His power, His grace, and His love for us. Amen

Sunday, August 14, 2011

I usually don't take bone marrow, but when I do I prefer "Dos Equis."

The most triumphant moment in sports is the come-from-behind win. At a point in a contest when the scoreboard and the clock are as much an enemy as the opposing team, that is when a competitor makes a choice. It begins in the brain where in spite of the odds, the choice is made to fight no matter what the outcome yet never forgetting that victory is always the goal. The fighter mentally then transforms him or herself physically to where the body responds to the brain with almost subconscious accuracy and ability. At this point, the mind considers injury and exhaustion mere speed bumps as the body performs at almost superhuman capacity.

Sometimes the effort falls short. The rally caps are flipped over, the wide receiver crumbles in the end zone after feeling the football scrape the tips of his fingers, or the wrestler falls mid-scramble as time expires. Even in a loss, the fight is remembered and is memorialized among it's witnesses.

Then there are the victories. These are remembered by all, and quite often heroes are born from such stories.

In order to come from behind, there has to be deficit. There has to be insurmountable odds. Only by a missed shot can there be a rebound and a put back. Only through a lopsided scoreboard can there be a come-from-behind win. Only through the breakup of a great band can they reunite. Only through sickness can there be healing. Only through death can there be resurrection.

I think once again of our friends Rob and Bree-Ann whose young daughter Reese is undergoing chemo to clean up after a brain tumor that was surgically removed. Talk about being in the trenches. Of course I can make no guarantee, but in 10 years or so I see a beautiful young girl and her family with a come-from-behind story that brings indescribable faith and joy.

Ten years ago, I could have never imagined how my own odds would shape me. Three out four quarters were mild battles, fought methodically with each team claiming narrow leads on the scoreboard. Then in the fourth quarter, the opposing team struck with a vengeance and nearly claimed victory. But the game was not over, and the good guys brought out their secret weapon (Bone Marrow Transplant) in the fourth quarter.

And so here we are in the fourth quarter (at least of this game), and everyday we feel a little closer to just downing the ball and running off the field as we watch the last few seconds tick off the clock. My doctor here in Baltimore is confident that my previous conditions, Aplastic Anemia and PNH, are history and that I am now quite simply a Bone Marrow transplant patient. I am still taking some meds for a year or so but already, at day 44 post transplant, my blood counts are higher than they have been in years with all counts steadily increasing.

My sister has every right to be proud of herself for her bone marrow absolutely kicking butt in my body. Incidentally, here is an interesting fact about Bone Marrow donation. Since the donor is female, the chromosomes in my blood are now XX instead of XY. One of the doctors jokingly said I could commit a crime, leave blood at the scene, and blame Kari. I suppose I should start drinking Dos Equis beer and become "the most interesting man in the world."

My own come-from-behind story is still being written, and I would be cheating my creator if I did not give him thanks and praise for the miracle at work in me. I just hope the miracle does not end with the restoration of my body, but continues with the daily renewal of my faith and the faith of those around me.

Monday, July 25, 2011

Moving Out

So, here's the thing about bone marrow transplants. They are BOOOOOORIIIIING! The word "transplant" conjures all sorts of images of doctors clearing the halls, knocking over trays of hospital food to get the precious marrow from the donor to the recipient in time. It couldn't be further from the truth. It's just a big red bag that hangs on the IV pole and drips away. The most exciting part of the day is the number of times the nurses check vitals looking for any reaction to the marrow.

The good news is that my stay here in Unit 5B of the Weinburg building has been boring from the beginning. The nurses like to say here, "Boring is good," which means no surprises, no complications, no major concerns and that has largely been the case. I battled a fever just a few days after the transplant that cooled quickly with aggressive antibiotics, but that has really been the only bump on a very smooth road. Even the effects of the chemo have been very tolerable with the worst behind me.

The next major step is seeing blood counts start to recover and that may not happen for at least another week. I haves lived with low counts for so long that I don't feel an empty tank, but I am no less excited about seeing blood counts start to come up. Once the counts start to appear, it will be easy to tell if it is the new marrow that is working and not my own trying to bounce back. Because my own marrow produced abnormal red cells, the new marrow will produce healthy blood cells which they can easily test for.

Now boring may be good for the transplant, but it's driving me nuts. Sure I'm reading, watching movies, taking naps, doing what I can to let time go by, but checking out and coming in as an outpatient is sounding better and better all the time. The good news is that barring any surprises, I will be checking out this coming Sunday to start the next phase of the recovery process. I'll stay in campus housing and come in just during the day for treatments. It doesn't sound very different, but getting out of this unit having a little more independence will make a huge difference for me.

I do need to recognize Kari, my sister, in this whole process. She was a trooper and in spite of her anxiety before, her exhaustion the day of, and her soreness during recovery, she gave cheerfully and willingly. Thanks to Lach who marched her around DC just a few days after the procedure, she recovered quickly (the doctors told her it is good for her to be up and moving). I love my sister, and I will never forget what she went through for me.

The waiting game continues, and prayers for continued patience are appreciated. Obviously we are praying that counts start to come up and that I can remain relatively free of complications, but waiting sometimes is harder than anything else.

Friday, July 8, 2011

Grace, Love, and Warm Cookies

Every once in a while, God throws us something special. It feels less like a divine moment and more like getting a full size candy bar while trick-or-treating or catching a free t-shirt that's been shot from a cannon at a college football game. He reveals to us exactly how and who he uses to answer our prayers. The prayer and the answer is between Him and me, but the message is universal. Our hope and our faith are justified in an instant when secret Santa stands up at the Christmas party and says, "It was me, I hope you like it...it had 'you' written all over it!"

It does confirm my faith in the Almighty, but that may not be God's only purpose. What God says to me here is that he loves me and he wants me to be happy. God is in no way proving himself to me. Instead, he is sending me a care package from heaven and the cookies are still warm. Like a father longing to embrace his son from far away, He just wanted to show me how much he cares for me.

So far this process has been uneventful and verging on boring...at least for me. "Boring," my nurse said, "is a good thing around here." I am tolerating the chemo well, although I am only two doses in and expecting my third this evening. It is amazing to me how such a little bag that takes only an hour to run can turn people upside down, physically and psychologically. So far, nothing has been as bad as I have anticipated. Whether that continues remains to be seen.

One of the positive turns in this process is that I may be released from inpatient to outpatient status much sooner than originally thought. That means I would live across the street in hospital outpatient housing and come in for daily treatments. Things need to continue to go as well as they have so far, but it is a possibility none the less.

"The Donor" is en route via road trip in a hippie hybrid car (just kidding Lach, I love that car) and should be in town Monday. According to the hospital staff, I'm being born again...again. They refer to transplant day as my new birthday. July 12 is easy for me, just another bag dripping from my IV pole but my sister has a rough go. She'll be under anesthesia, but recovery can be a little uncomfortable.

I can't sign off without thanking everyone for your prayers and support. Through all of you, God has revealed to me new measures of His love. I only hope each of you can experience the same Grace, Love, and warm cookies that God has shown me.