Monday, March 30, 2009

Max & Lucy


I have the pleasure of watching a cute little girl named Lucy. Don't you just love that name? When she comes to play, Max has such a good time. He instinctively knows to be careful, and he has taken great pleasure and pride in sharing his toys and trying to make her laugh or play with him. He told me last time she was here that he wondered if she would let him sit with her and snuggle in the bean bag chair. That is precious, because he only does that with me. I am encouraged to see this nurturing side of him. Thanks to Lucy's mom and dad for trusting us to take good care of her. We sure love having her!

You are What you Eat?

I have a cute little friend that I love to hang out with. She is beautiful and tiny - but of course she doesn't know it! We had a chance to escape to our favorite fast food spot, KFC. After we ordered I looked down at our drinks:



Guess which one is mine? It's just a coincidence, right?

Tuesday, March 24, 2009

Milestone #1- Celebrate with Us



We are celebrating! This is the longest that Darrell has been out of the hospital AND the lowest dose of prednasone that he has been able to tolerate since his diagnosis in July 2008! He fought off a cold (this is big, because it means his weakened immune system is still fighting) and is feeling "pretty good".

I just wanted to post how grateful we are to our friends and family and all those who have sent good thoughts and prayers our way. We are especially grateful for the priesthood blessing given by Bishop Curtis and the promises made. Darrell and I have clung to that blessing as we have moved forward. As a family we want to express our love to Bishop Curtis, Bishop Merrill, President Bradshaw, Bishop Walker, Brother Brown, and all those worthy priesthood holders that have blessed and guided us through this challenge.

I have read that a trial is when you really have to decide where you stand. You simply can't sit on the fence when you make life decisions. This has strengthened our resolve, fortified our faith, solidified our marriage. And we have the gospel as our roadguide to help us through. Without it, Darrell's illness would just feel like an unfair break without any hope of survival. But we have hope, we have strength and we have resolve. If you have any questions about our faith, The Church of Jesus Christ of Latter-Day Saints, please click on the picture of the Temple on the right-hand side and get your information straight from the source. It will change your life, if you let it.

Check back for Milestone #2 - 1 year post diagnosis on July 3rd....yes we can.

Tuesday, March 10, 2009

Now Take It, That's for You

Do you ever see a movie that leaves you with one line you just thought was hilarious? Well we saw Don't Mess with the Zohan. This was classic Adam Sandler - which means parts were stupid and other parts were just comic genius (in my humble opinion). Click here to see the scene with the classic line...

The kids and I repeat this with food and even gaseous emmissions (smell it, smell it, now take it - that's for you!)

Thursday, March 5, 2009

Eric wins Essay Contest!

Mesa Public School District held an essay contest and all English students could submit their original pieces. Eric put his heart into his essay and his English teacher convinced him to submit it. The news came yesterday that he got 1st Place in the personal narrative category! Now this isn't first place in his class, or at Mesa High School. This is for all schools in the Mesa School District. He will be recognized at an awards assembly on May 6th. You can feel the emotion as you read his essay:

Orchestrating My Place of Peace

“One hundred twelve degrees, 5:32 p.m.”, scrolled the electronic banner in front of the hospital. As the sun banished behind the distant horizon, I reluctantly pulled into the busy parking lot. A symphony of thoughts conjured up an electrical storm of neural impulses in my head. “What changed, is everything alright? Have his kidneys turned around?” The Banner Gateway Hospital sign loomed nearer as I approached the intimidating, gloomy building. When I finally reached the door, it slid open with a welcoming light. The smile on the receptionist’s face gave me a ray of hope and radiated a positive aura at the hospital entrance. “Room 215?” I questioned. “Take the elevator and it will be to the right” replied the optimistic man. The vast elevator opened to reveal a beautiful interior with glass and granite handrails. Upon the second floor the elevator opened and I was greeted by two plasma televisions, both displayed challenging diseases and life-changing trials. “Wow, I couldn’t image having to worry about those trials”, I pondered. “It is a good thing that he only hurt his leg. They can fix that up and we’ll be back to our normal lives.” On the way towards room 215 were a series of closed doors and hand sanitizer dispensers. “210, 211, 212, 213, 214”, I mentally counted. Finally, room 215. I took an uncertain breath and pushed the door open to reveal my mom perched upon the edge of the room’s couch next to a sanitary white hospital bed that supported my dad.

Upon seeing me, my mom quickly put in place her most cheerful expression and stated, a little too happily, “Hi Honey”. I sat next to my mom, and waited expectantly. As she took a moment to pause before speaking, my Mom turned to my dad and said, “Shall I tell him or should you?” My Dad simply shook his head and quietly whispered, “It would be best if you did”. Before my Mom could speak, the door swung open by a small commanding figure who wasted no time with introductions. When he sat at the foot of my Dad’s bed, the electronic bed shifted to accommodate his weight. He leaned forward and earnestly began talking. Words that sounded like a foreign language rolled naturally off his tongue. Words I had never heard before and didn’t understand. Words like lymphoma, t-cells, non-hodgkins, and stem cell transplant. I stared at the doctor’s mouth as the words tumbled out. When the words cancer and chemotherapy finally penetrated my ears, I suddenly understood what was happening and that enlightenment hit me like a thunderbolt. I continued to watch the doctor as he described a diagnosis, prognosis, treatment plans, and a transfer to another hospital. The room spun and my mind raced. Was this what I had been summoned to witness? I finally understood. My dad had cancer.

A few months had passed since I learned the news about my father’s condition. I felt so helpless, but there was one thing I could do to cope with the chaos. From my place on the piano bench, I created beautiful waves of chords that resonated and filled the air in the small home. The music’s emotion could be clearly detected by the casual listener as I set the music with a swaying “A”-based arpeggio. When the base of the song was established, the higher-pitched melody crept in, and created a reflective feel to the piece. I concentrated intently. Ironically, I felt no control over the notes that seemed to magically flow from my fingertips as I closed my eyes and let the music simply guide me. The swirling, seemingly random thoughts and flashbacks of my father’s illness that float unconnected within my mind were tied together in a pattern of organized, complete musical expression of notes and chords. Collections of keys that built in tempo vigorously, increasing amplitude gave way to soft, light chords, held until the desired resolution that only I could feel, seemed to express what I could never put into words. As the final haunting notes were dispersed throughout the home, my mother’s voice broke the silence. “That was beautiful, honey. But I have never heard you play that piece before. In fact I‘ve never heard you play so much. Where are you getting your inspiration?” I simply turned my head to deliver the words of my heart. “I am orchestrating my place of peace”.



This has been such a hard year for our family, but Eric has turned a trial into a triumph. Congratulations honey, we are so proud of you.