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reflection


day in the life

Highlighting the everyday life of a couple living well with a slow-growing cancer. Life isn’t always easy, and there will certainly be sorrows and losses along the way. But being alive is good. It is very good.


Wednesday, May 28, 2008

Countdown

Five more days until I get to meet our newest granddaughter, Lydia! Until then, my life at work is crazy busy. We’re in crunch week of Heaven Can Wait, a 5K walk/run founded nine years ago by a local breast cancer survivor.  

 

               This year the event will more than likely pass the half million dollar mark in total funds raised to benefit our Cancer Services Department. Amazing for a small town like Bend.    

Gary gets roped into these events as my volunteer personal assistant – we’re a package deal. He’ll help me set up on Friday evening at the athletic shoe store where registrants will pick up race packets … we’ll work together at the store on Saturday … and then report at 6:30 am to the park on Sunday in preparation for the main event. 

    

 

And then I’ll board a plane Monday morning for New Jersey and leave all the “clean up” work on my desk, and will try not to think about how high the pile is while I cuddle and play with grandchildren.

 

Five more days!  

 

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Monday, May 26, 2008

Extended family

We just got back from Gary’s family reunion. For 39 years, the Johnsons have been camping out on Memorial Day weekend with anywhere from 80 to 120 people in attendance – a wonderful blend of four generations.

 

Over the course of the years, a few things have changed. I’m not a coffee drinker, but we’ve gone high-tech from the early days when someone threw a handful of grounds into an old cast iron coffee pot and set it on the open fire until it boiled over.

 

A few years back, someone got smart and divided the family members into groups for meal preparation and clean-up. Almost every year there are new engagements or marriages, and almost certainly there are new babies. The most noticeable variation this year was a couple of our nieces who changed their hair color from blonde to dark brunette … but they’re still blonde, if you catch my drift.

 

So although there are changes, not much really changes. Which is one of the things I love about the family reunion. We still hang out around the campfire and get caught up on the latest family news. We still play table games and lawn games and take the little ones to the playground, marveling at how much they’ve grown. We still eat way too much food (the Johnson women know how to cook!). We still have Skit Night on Saturday and a Sunday morning worship service.

 

On the drive home, Gary commented on how encouraging the weekend had been and how good it is to get together. Whether they realize it or not, our extended family is a critical part of our support system.

 

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Tuesday, May 20, 2008

Testing the limits

Gary took the last two mornings off from his usual hike up Pilot Butte because his calves were pretty sore. They’re sore because we hiked Tumalo Mountain in the snow on Sunday.

 

We’ve climbed Tumalo Mountain in the summertime and knew it would be a challenge in the snow. It’s a favorite place for local snowriders. With snowboards or skis strapped to their backs, they hike to the top and throw themselves over the east edge. No pricey ski passes; no waiting in lift lines. Sometimes you just have to see what you’re capable of doing.

             

 

With Gary, it's defying the side effects of cancer treatment and refusing to give in to exhaustion. Like I said, sometimes you just have to see what you’re capable of doing.

 

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Saturday, May 17, 2008

Trailblazers

Gary was in an all-day training today. He’s now an official, card-carrying cancer support volunteer with the Cancer Hope Network, a non-profit organization that provides one-on-one support to people undergoing treatment for cancer.

 

Thirty-four local people participated in the training these past two days. The new trainees will be added to the Cancer Hope Network database. When a newly-diagnosed patient calls CHN, they’ll be connected to a trained volunteer with a similar cancer experience. Gary was impressed with the other survivors he met who have gone through so much and yet are willing to give of their time and efforts to help others.

 

I’ve heard Gary compare the cancer journey to hiking a new trail. He points out that whenever we consider a new hike, we like to talk with someone who can give us an idea of the terrain and what to expect. “It’s the same with cancer,” Gary says. “It’s good to talk with someone who has walked the trail ahead of you.”

 

I would think having a personal cancer trailblazer would be incredibly encouraging. Along with that, I believe that being a personal cancer trailblazer can be an important part of living well.

 

So often it turns out that we’re the ones who benefit most when we focus outward in service to others.

 

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Thursday, May 15, 2008

The last lecture

I just finished reading a little book, The Last Lecture, by Randy Pausch, a computer science professor at Carnegie Mellon. Pausch has a wife, three young children … and pancreatic cancer. He’s been told he has just a few months left to live.

 

Gary and I watched a YouTube version of Pausch’s last lecture given at Carnegie Mellon. After doing push-ups on the stage floor to demonstrate that he was probably in better condition than most of the people in the audience, Pausch talked about how to achieve one’s childhood dreams.

 

Pausch’s book is an expansion of his lecture. Its short chapters have titles such as “No Job is Beneath You”, “A Bad Apology is Worse than No Apology” and “Don’t Obsess Over What People Think”. The lecture and the subsequent book were created for the benefit of his young children – so they could remember their dad and know that he loved them; so they could take in his words to live by.

 

I like this guy’s attitude. Pausch has determined to live life fully for the remaining time he has left on this earth. And what a great way to live … whether one has cancer or not.

 

Read the book.

 

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Sunday, May 11, 2008

Mother’s Day thoughts

Gary and I are sitting in a sunny spot along the Deschutes River eating our Mother’s Day picnic. Geese are honking their arrivals and departures, the wind is blowing through the tall trees and chicken sandwiches never tasted so good.

 

We’re a bit overdressed, but it’s because the Deschutes River Trail was Plan “B”. Originally we set out to climb Tumalo Mountain, just 20 miles west of town. We layered up and grabbed our snowshoes, but at the base of the mountain the wind was blowing snow crossways. We climbed a little distance … and even though we were dressed warmly enough, we turned back because the plan was to sit and write and enjoy the great outdoors while eating lunch. 

 

So here along the river we are soaking up the warmth of the sun and I was thinking about our children and about my mom and mother-in-law, both widowed. We mailed cards and gifts earlier this week to our mothers and we’ll call them both. Our daughter, Summer, who just had a baby girl two days ago, texted this morning: “On our way home from the hospital to begin our new life as 5.” Our son, Jeremy, will call later today (or at least he’d better!) and I’ll phone Summer after she gets settled in at home with their new baby.

 

Gary and I were just talking about how we raised our children to be independent and are so proud of the young adults they’ve become ... and yet there’s this little piece deep inside my heart that says, “Don’t get so independent that you don’t need me any longer.”

 

But that’s exactly what’s happened. They don’t need us any longer in that same sense. And that’s a good thing. They have their own lives to live, just as we set off on our journey of building a life together several years ago. We didn’t forget our parents, but our days were wrapped up in raising our children and in providing for their needs and making memories for them.

 

And so as we take stock of how much we have – even after the dust has settled from recent setbacks and losses – we are grateful for the influence of our mothers and grateful for all the ties that link us to a living and breathing family structure that nurtured us and taught us how to pass that nurturing down the line.

 

And on this day, we are particularly grateful for our children and children-in-law and grandchildren.

 

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Friday, May 09, 2008

Welcome to our world, Lydia

The phone woke us out of a sound sleep last night. Our daughter, Summer, was headed to the hospital to have a baby. Josh, our son-in-law, called shortly after noon today with the news that Lydia Hope had made her entrance – weighing in at 8 lbs., 2 oz! Mother and baby were resting well.

 

Josh and Summer have a 7-year-old daughter, Lilly, and a 5-year-old son, Titus. They’ve both been looking forward to having a baby sister (well, actually … Titus was hoping it would be a baby brother). They lived in Bend until about a year and a half ago when our son-in-law moved our daughter and grandchildren to New Jersey.

 

I emailed my sister-in-law: “Where is New Jersey … somewhere in Eastern Europe?”

 

She wrote back: “I think it’s in South America.”

 

We were lucky to have six very fun years growing up in the same town with our grandchildren. They were both aware that Grandpa had some sort of illness and had to eat a healthier diet, but of course they didn’t understand cancer. They loved coming to our house for sleepovers. From a 2005 journal entry:

 

“Lilly and Titus spent the night Friday night.  And in the morning we baked healthy cookies—my little helpers with chairs pushed up to the kitchen counter—and we watched Ice Age for the second time and they still didn’t want to go home, so they helped me pull weeds in the yard, only I pulled and they dug holes in the soft damp dirt and when we finally took them home with dirt in their fingernails their mother was pleased they had helped Grandma in the yard.” 

 

And now there is a third grandchild, only this one was born clear on the other side of the world. I will fly back to New Jersey soon to meet our newest grandchild and to spoil the older two for a few days. And I will count my blessings, which have just increased.

 

Welcome to our world, Lydia. Do you know how loved you are … even before we get to hold you?

 

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Sunday, May 05, 2008

Personal touch

I mentioned our friend who just this past week learned her colon cancer had metastasized to her brain. For the past couple years, she and her husband have been attending the DEFEAT Cancer program founded by Dr. Archie Bleyer. When he heard the news of her metastases, he immediately called her. Friday morning at work he previewed a DVD of a television discussion with three cancer survivors – Lance Armstrong, Elizabeth Edwards and a journalist who is almost two years out from colon cancer metastases to the brain. Dr. Bleyer was thinking of our friend at the time and arranged to get a copy to her.

 

I’ve mentioned the good doctor before, but you need to know a little more about him.* He was Chair of the Pediatrics Dept at the prestigious M.D. Anderson Cancer Center in Houston in the 1990s; he’s a founding member of the LiveStrong Young Adult Alliance; he’s been awarded more than $75 million in research grants – just to mention a few of his lifetime achievements.

 

He is 65 years young (I once saw him let some visiting foster kittens loose in the Cancer Center, placing one hapless kitten on the desk of one of the oncologists). He is brilliant but personable; he takes the time out of his incredibly busy schedule to connect with local cancer survivors.    

 

Our friend has begun her daily radiation treatments. Those of us on the Cancer Services staff stop to chat with her and her husband when we see them in the waiting room. I was thinking how much the personal touch would have meant to us when Gary was first diagnosed—if staff had greeted us with hugs and unhurried conversations; if one of the docs had presented us with a DVD that he thought would be insightful and encouraging.

 

It’s the personal touch that a good deal of the medical professionals don’t have time for ... and understandably so. But speaking from experience, it’s the personal touch that helps a cancer patient and caregiver feel a little less frightened. For where there are people who seem to care, there is hope.

  

*Unrelated, side story: Gary and I traveled with Dr. Bleyer to a Lance Armstrong Foundation conference in Austin, Texas last fall. The conference ended at noon and Dr. Bleyer was flying back to Houston to pick up his wife, Mo, who was visiting friends. Our flight took us to Salt Lake City, then we would meet up with them at the Portland airport for the last puddle-jumper flight home to Redmond/Bend.

 

We were sharing a cab to the Austin airport but didn’t realize at the time that Dr. Bleyer's flight left at 1:00. So at 12:00, he's heading upstairs to pack. We checked in at the airport and he ran past us as we were walking toward security– "I'm going to miss my flight … can you make sure Mo gets home from the airport!” The last we saw of him was with shoes in hand, pulled aside at the security point. Boy, is Mo going to be unhappy.

 

You can imagine our amazement when we deplaned in Portland and Dr. Bleyer was sitting with Mo in the airport waiting room!

 

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April 2008

Dispensing goodness

Cancer community – Part II

Cancer community

Barn door analogies

Homemade soup day

Mice and tumors

Waiting room magazines

Weekend date

First entry