Thursday, December 23, 2010

Rebirth [ree-burth, ree-burth]

n.
Renaissance; Renewal; Resurrection; New Beginning

Most faith traditions throughout human history have acknowledged some version of the “circle of life” – birth, life, death, and rebirth. This is the season where Christians focus attention on that concept through the birth of a child, symbolizing the hope of a new beginning for humanity. In the last few years I have thought about this only in the context of Susan’s own birth, life, death, and “resurrection”. But as we navigate through this second year and into a third without her physical presence, I have become more aware of how this concept also applies to me. While I have not “died” in the sense that we usually mean it, a chapter of my life has in fact passed away and I am experiencing a renaissance. I’m feeling very much alive in a very new way. It’s exciting, challenging, and maybe a little scary.

As it applies to me, the “labor and delivery” of my own rebirth started slowly at first, but has picked up momentum. Somewhere along the line a new “me” has begun to emerge – a mix of who I have always been, minus who I can no longer be, with added features of who I can yet become. This “year of seconds” since Susan died has not been without its challenges. In fact, it has affected me in ways I did not expect. Labor and delivery indeed. But I have found my way through it mostly because of Jane and my wonderful relationship with her. Jane has graced my life with new awareness and new reasons to “be”. I think she would say something similar about how the relationship has affected her. Jane and I aren’t deliberately trying to change each other. But by being together, we are doing just that.

A new relationship at this stage of our lives is a fascinating experience. It retains many aspects of the original love recipe but it’s also seasoned with life experience. The result is a tasty new set of savory sensations. And like all new culinary creations, it brings anticipation along with questions. Is this what we want it to be? Is there too much of this or too little of that? Have we prepared it properly? How do we know when we’re “ready” for the next course? And taste-testing along the way yields delighted exclamations like, “Oh my! This is really good!”

One of the major differences in establishing relationships with new mates later in life must surely be what we inherit from each other as part of the bargain. When we’re young and just getting started, there’s not as much life history to assimilate with a new partner. There are the families of course, and that’s often a significant factor. But later in life, there are decades worth of friendships, experiences, roots, habits, children, and “stuff” to absorb into a new life style. This adds both clarity and complexity to the newness. Clarity, because we have a better idea of what we want and need (or don’t want and don’t need) from a new relationship. Complexity, because we still have to figure out how to merge what’s already been established.

The list of changes in our respective lives has grown over the ten months we’ve been together. Jane and I have formed a new living environment with different things in different places, different routines, and a developing set of new shared experiences. They are all inextricably rooted in our old paradigms and inevitably compared to them. Our minds are busy processing all of this, occasionally demanding us to take a deep breath and catch up to the realization that this is all good, and good for us. One of my realizations is how healthy I feel in both body and spirit (and how long it’s been since I have felt that way). It’s not at all stretching the point when I say I feel “reborn”.

I suspect – indeed I hope – that all of us are experiencing some version of this renewal. Susan will never be truly gone from us. She is in fact an active participant – a midwife perhaps – in all of these new beginnings. There is no dishonor or betrayal of her life and legacy. Quite the opposite. She and all of our departed loved ones are a vital part of the new life that is being reborn in us. It is because they lived that we experience renewal in the ways that we do. I really like that notion. Isn’t that how faith traditions view their icons and ancestors? Isn’t that what we’d like to be for those whom we will leave behind?

Just like our bodies are continuously shedding old skin cells and replacing them with new ones, we have a continuous opportunity to ask ourselves: What elements of my life am I ready to release to history? What new elements would be relevant to my needs today? Becoming aware of these things invites epiphanies that can revitalize us.

Birth, life, death, rebirth. People who have come and gone long before us already knew what we must learn for ourselves.

Bless you all in this season where darkness turns back to light as a reminder of new life and new awareness. Happy Winter Solstice! Merry Christmas! Happy New Year!

Tuesday, May 18, 2010

Springtime in the Rockies

Her name is Jane. We’ve been together for almost three months. We’re teaching each other new ways of looking at ourselves and the world around us as we accumulate shared experiences – one at a time. Both of us feel like it’s springtime again in our lives. I’m suddenly aware of many others who have felt the same fresh breeze of new love in their own worlds. They smile at me or nod knowingly or write positive affirmations. My friends tell me I look and behave “differently” (which truly surprises me – I had no idea). I find myself responding to questions like: “how are you?” with an enthusiastic “terrific” or “faannnntastic” – and meaning it.

As a widower, I am keenly aware of a delicate balance between honoring the treasure I’ve lost and rejoicing over the treasure I’ve found. When I was evolving in my readiness to pursue another relationship, my early (and irrational), silent fear was that loving another woman would somehow be dishonorable to Susan. The idea almost seemed adulterous. That’s clearly a fallacy – and I’m over it. I’ve had nothing but encouragement from friends and family – including Susan’s family. We are being accepted by the people in each other’s communities with open arms and warm hearts. And I had clear instructions from Susan herself (those who knew her can start grinning now) that I was expected to do exactly what I’m doing. In fact, Jane and I both have a sense that Susan was somehow actively involved in getting us together because it feels so “meant to be”. That sense makes this all the more special. It turns out that I am honoring the treasure I’ve lost by rejoicing in the treasure I’ve found. They are not mutually exclusive. What I learned in partnership with Susan is “paying forward” into what I bring to my relationship with Jane. We have arrived in each other’s lives at seemingly just the right moment. We seem to be doing exactly what we are supposed to do.

Anyone who has ever experienced this time of year at altitude knows what we mean when we say “It’s springtime in the Rockies”. It can be warm and beautiful one day, complete with gorgeous spring flowers and budding trees. The next day could bring a storm with heavy, wet, branch-breaking snow. We often refer to spring weather as “unstable”. The sudden changes can be daunting, and stressful. But spring storms also leave behind a wonderland of beauty. (The mountains are breathtaking after a fresh snow.) The indisputable promise of summer is still there. Spring moisture makes everything colorful after a drab cold season. If springtime is a metaphor for new relationships, then the springtimes that Jane and I have already experienced in our lives have prepared us well for this one. As in all new relationships, we’re making adjustments to the lifestyles we had before. We’re accommodating each other’s schedules. We’re learning what the other is like at various times of the day, what foods we enjoy or dislike, what we watch on TV, what brands we buy at the grocery store, our tastes in music, and a multitude of other, sometimes mundane details. We’re also realizing the similarities of our Midwestern heritage (we grew up 100 miles from each other), the many ways in which we’re alike, and how often we have the same thoughts at the same time. The adjustments can be daunting, even stressful – the realizations delightful. Because we’ve been here before, we know that the beauty of the relationship itself is what’s really magical.

We recently took a brief trip to Montana and Wyoming to visit Patrick. We came back through Yellowstone and the Tetons – a first for Jane (and I don’t think I’ve ever been there during this time of year). Soon it will be warmer and greener with less precipitation – and way more people. So it was special to experience these places (and the wildlife that inhabit them) in snowy, cold, overcast conditions – and in their never-the-less silent majesty. The steadfastness of the changing seasons, complete with their unique splendor and their onerous challenges can help us appreciate the meaning and beauty of life’s odyssey. Jane and I hope to have many seasons together. But no matter what, we are experiencing life in all its glory – right now. Capture the moment. It’s springtime here in the Rockies – and it’s faannnntastic!

Monday, March 29, 2010

Bricks and Patience

How do you build something that will endure the test of time?

Brick by brick.

I’ve become keenly aware how emotionally comfortable I was most of the time during my years with Susan. To be sure, we had our ups and downs – both as a couple and as parents. I had many days and nights of angst over that 32 year period. But no matter what, we knew it would be OK because our relationship was cemented in deep, trusting love. After the first few months (maybe even weeks), the foundation of our love was never in doubt, particularly as time went on and our lives became more and more entwined. It’s amazing to look back and see what we built over that time – and how many building blocks it took – all placed one at a time. Being single again has forced me to identify as an individual rather than as part of a couple. I’m essentially getting to know myself again. What’s changed? What’s the same? It’s a pretty interesting and refreshing experience. And a new relationship means starting over – brick by brick.

I’ve been dating a remarkable woman for about a month. I had completely forgotten the emotional roller coaster that is present in building a new relationship. It’s like being a teenager or a 20-something again. In fact, that’s what Jon said I sounded like on the phone! My heart does flip flops and I feel euphoric when I’m in communication with the object of my new romantic interest. Then, when we haven’t been in touch for what seems like a long while, I begin to conjure up all kinds of stupid stories about how I’ve said something to screw up the relationship, or she’s having doubts, or something’s not right, or . . . I just really like talking to her and being with her and I can’t wait for the next encounter! More than once I’ve heard a voice saying to me “Rob, you’re pathetic! Get a grip!” Then, I get an email or a text or I’m with her and my heart goes pitter patter all over again. To be sure, we don’t know where this relationship is headed – the uncertainty is very real and it adds a measure of vulnerability to this experience. (But how can you feel love if you’re not also willing to feel pain?) The necessary time to build something worthwhile and enduring is in conflict with my impulse to hurry. But relationships are journeys not destinations. The more disciplined voice in my head keeps reminding me to do this one step at a time and savor the experience - brick by brick. Isn’t that how we’ve had to do our grieving? Fortunately, my new special friend is wise in the ways of patience and it’s a common (and enlightening) topic of our conversations.

Experiencing all of these emotions has brought back some vivid memories of my early relationships, including when Susan and I were just getting started. Given my age now, I had assumed all that stuff was behind me – an artifact of youthful immaturity and the absence of life experience and wisdom. Apparently, age alone does not make those feelings go away. The good news about dating at this stage in life is that our hard-earned wisdom really does help keep us reasonably centered and stable. We both know from our life experience that everything is going to be OK no matter what. But the emotions are more intense than I ever would have imagined. It’s invigorating, thrilling, exciting – and unnerving! And it feels like it’s taking so damn long! The reality is that it’s only been a month. How many bricks can that be?

In our fast-paced, high-tech, quick-gratification world, there still remains an ancient truth: Anything built to last still has to be built one brick at a time on a solid foundation. If we choose to, we can call upon the necessary patience to not only persevere, but also to find peace in the process.

Sunday, February 28, 2010

China!

The trip was an extraordinary experience - not always easy or enjoyable - but remarkable. February, as I knew, isn't a particularly good time to visit. Cold, cloudy weather added to the air pollution was a constant downer. We didn't see the sun and clear air until (believe it or not) Beijing - which was a delightful surprise. But what it lacked as a relaxing vacation, was more than replaced by exposure to a fascinating culture and people with more similarities than differences. There were plenty of differences though, some of them pretty annoying. Still, my mind went from "I'm not coming back here"; to "if I come back I'll . . ." ; to "when I come back I want to . . ." It was terrific to spend that kind of time and have those experiences with Jon. He's pretty conversational in Mandarin and it solved an endless number of problems. I thought of Susan a lot - mostly about how she would never have done this trip in this way! Maybe we'd have done a more comfortable, english-speaking tour - but never like Jon and I did it. However, she'd have gone nuts with the shopping opportunities!

Thursday, January 28, 2010

Smoothies, Coffee, and China

I joined eHarmony a few weeks ago. It’s one of several on-line matching services that help people find new relationships in a safe and expedient manner. It felt like a HUGE step for me at first – equal parts of fear, excitement, and dread with a dash of guilt. But the experience has been instrumental in helping me prepare my outlook for the future – the future that Susan and I discussed many times – my future. So I have carefully written my profile and posted some pictures on eHarmony. It’s been a fascinating experience on many levels. I’ve already been “matched” to several hundred women (all in the Denver area – amazing). Most of these matches have now been closed - either by them or by me. It’s not as easy as it might seem. It’s still going to take time. I did have a face-to-face meeting with one person. We progressed through the communication steps and agreed to meet at a Jamba Juice a few weeks ago. We had a very nice conversation even though she is clearly not “the one”. So I guess my first “date” in well over 30 years is now under my belt! It’s gotta be easier moving forward. I was set to have another encounter for coffee last Sunday with another woman. She had to back out at the last minute and says she would like to reschedule after I get back from China. We’ll see. (I’m already feeling hardened to the realities of seeking new relationships!)

But my focus hasn’t been on new relationships lately. After the first of the year I finally got serious about planning my trip to China and that has occupied most of my attention for the last four weeks. I leave tomorrow and I’m ready to go. I know I’m in for an adventure (after a very long plane trip) – but I really have no idea what to expect. I’m just looking forward to seeing Jon and traveling with him. He’ll meet me in Shanghai and we’ll be off on a big loop through the country. No matter what we experience, it will be unique and memorable. My friends and I have been chuckling about my trip preparation – or rather the lack of it prior to the new year. Susan would have been 99% packed and ready months ago. It just takes me a while to get mentally ready before I spring into action! It’s all come together nicely – but I admit it’s been a little hectic.

All of this illustrates how far we’ve come in a year. We’re moving on with our lives but we haven’t left her behind. She’s right here with us. In fact, I’m discovering her presence in new and pleasant ways all the time. She’ll be with us in China. She’s with Patrick in Bozeman (he’s living and working there after having graduated last month). For all of you who knew her, she’s no doubt with all of you in some meaningful way. And – she’ll be my “chaperone” for all those future smoothie and coffee dates! Onward we go!

Thursday, December 17, 2009

Decorating for the Season of Life

Today is the first anniversary of Susan’s passing. I have vivid memories of the weeks and months leading up to the moment she took her last breath. I look at the weeks and months since then with wonder and amazement - I don’t remember ever experiencing such a roller coaster of thoughts and feelings as I have in the past 365 days. And when I ponder the whole experience over the last six years, I’m astounded. It’s been an extraordinary ride – and it’s not even over.

I’ve decided to decorate our Christmas tree as part of my observance of the day. In our long life together, I was always responsible for getting the tree up, getting it straight, and doing the lights. Susan always did the decorating. She had a flare for it and knew the story behind each ornament that came from family members or those we had purchased in some Christmas store in our travels. The decorating part was always a little tedious for me (we’ve collected a LOT of ornaments. Besides, we all know it needed to be done right!) Last year, our good friend (the other) Susan helped us hastily decorate the tree in the days immediately after Susan’s death. It felt like it needed to be done. This year I will do it in honor of her, even though I don’t have the flare and I won’t know all the stories. But I do know her story. It feels like the right thing to do.

Just a few weeks ago I was ambivalent about decorating at all. I was approaching this cold, dark season with a sort of gloomy demeanor. All I wanted to do was to get through this “year of firsts” and get to spring as quickly as possible. But somewhere between our anniversary on November 18th and Thanksgiving on November 26th, a little switch flipped in my head. I can’t explain it. The only trigger I can think of was Patrick saying “let’s put up the decorations”. A little voice in me said “of course”, and that was that. No hesitation about it – let’s put up the decorations. We got the outdoor lights in place and hauled up the indoor stuff. But we didn’t get around to doing the indoor things before Patrick returned to Bozeman to finish out the last seminar of his (final) semester. I’ve been both procrastinating and too busy to do it before now.

I’ve been thinking about what I might do today for some time. I decided weeks ago that I’d take the day off. I consulted with friends about how to make my observance meaningful. There is of course, no “right” way to do this other than what feels right to each of us as individuals working through our own process. But most people I talked to agreed that doing something deliberate, perhaps with a sense of ritual, would be important. I’ll talk with Jon and Patrick, re-read what I’ve written about this experience, review all the cards and mementos that have been waiting for me to revisit, light a few special candles, and play some favorite music. And, I’m going to do what Susan might do if she were here. I’m going to decorate the Christmas tree.

The significance of that little switch that flipped in my head is about much more than the Christmas decorations. It now feels like I can move on in my grieving process with less sadness about our loss and more focus on what Susan has meant to me; with less incredulity at what has happened and more awareness of how I have grown from the experience; with more appreciation for what we have successfully endured and less apprehension about when I will ever find unbridled joy again. I’ve already begun reaching out to build new relationships. I have a sense of hope and excitement about the future. It feels good. It feels like I’m decorating for the next season in my life. And the voice inside my head is saying "of course".

Tuesday, November 17, 2009

Sentiments about Sentiments

Yesterday would have been my mother’s 100th birthday. She was an especially sentimental soul and always remembered important dates in her life (especially losses) with melancholy nostalgia. I often thought she was way too wistful. Now I have a somewhat more tolerant perspective.

I reconnected with a childhood friend yesterday. He used to live across the street from me. I became a member of Facebook a few weeks ago – surprising even myself along with the younger members of my family. I don’t know if it’s a function of my age and/or my situation as a new widower, but I’m feeling a strong urge to reconnect with my past. Facebook is helping to satisfy the yen (although it’s only as good as the impulses of my peers to join as I did).

This childhood friend and I were very close through our elementary years but had drifted apart before we graduated from high school. Never-the-less, the shared memories haven’t lost their importance. Most of them are of us as typical neighborhood playmates. But one is seared in my memory and came roaring back as I recalled those childhood years. When I was about 6 or 7 and my friend was about 5 or 6, his little brother was hit and killed by a car – right in front of my house. I have a horrible image in my head of their mother standing at the scene of the accident in hysterics, and watching helplessly as the fatally injured toddler lay on the street next to his mangled tricycle. I didn’t know how to process that at the time. And all of a sudden, I have a new perspective for her grief and what she must have experienced in dealing with such a tragic and sudden loss. My loss pales in comparison and yet I feel like a member of a very unique club whose members have had very unique experiences and to which none of us really wishes to belong.

As my family and I were sharing emailed thoughts about my mother, we agreed that our loved ones – even our children, are only on loan to us from God. In addition, my brother offered up a passage written by Khalil Gibran. It includes these lines: “The deeper that sorrow carves into your being, the more joy you can contain.” “When you are sorrowful look again in your heart, and you shall see that in truth you are weeping for that which has been your delight.” It’s a very similar sentiment to what I mentioned in the last post – the more loss we feel, the more it means that we had something worth grieving for. And it was never mine to begin with.

My friend Peg suggests that I am defrosting from the numbness that has protected me up to now – which I no longer need – and that my pain is therefore more noticeable as I continue to heal. My friend Alan, having himself traveled this road, says the same thing using “the Novocain is wearing off after a dental visit” analogy. The comparisons are accurate and they both frame the situation in terms that promise the pain will ease.

Tomorrow would have been our 31st wedding anniversary. I’m feeling a little wistful about that - with no remorse. And I’m glad that my mother showed me how.

Sunday, October 4, 2009

That's Life

My grieving process reminds me a little of when Jon and Patrick were little. Susan and I were aware that we were always moving from one parenting phase to another. Just as we got used to one, it seemed another was upon us. It required flexibility and patience. Through it all, we experienced life with its full range of emotions. That’s what this feels like now.

The last few months have been very busy and active. Everyone, including me, anticipated that “busy-ness” would be good for me – and it no doubt is. But my active involvement in things outside home and work has brought with it a new intensity of emotion that I didn’t see coming. I am experiencing Susan and her loss in a variety of ways, triggered by a variety of – well, activities. I guess that’s what you get when you choose to live life actively.

Susan and I had no idea of course, how we would connect after she died. We discussed it often and both of us believed that we would – somehow. The only model that I had in my head was the scene from “Sleepless in Seattle” where Tom Hanks interacts with a vision of his dead wife in the living room of his houseboat. But I’ve discovered that I can connect with Susan in a wide spectrum of ways. I have difficulty explaining it or offering examples other than to say that it reminds me of the “Where’s Waldo” books that we read with our children. We find Waldo amid a kaleidoscope of colorful, busy images, often difficult to spot – but always there. I have only to think of her and I know she is with me. It is bittersweet. I deeply appreciate her spiritual presence – and I deeply miss the tangible interaction. She will always be with me and she will always be gone. One of my daily meditations reminded me of the great irony of grieving: the more loss we feel, the more it means that we had something worth grieving for. Other entries remind me that she is “in the air that surrounds us, the sunshine that bathes us with its warmth and light, and the life that surges within us”. Like water that might have boiled “away”, it is still water in a different form and still “there”. Like God, she is in nature, she is in others, and she is in me.

The “busy-ness” began in August with a trip to visit Susan’s family and celebrate the shared birthdays of Jon and Susan’s mother. It was a little weird and a little sad to be there without Susan this first time. As soon as we returned, Patrick got immersed in student teaching, Jon got ready to go to China for the school year, and I got involved in my first show in six years.

Rehearsing for shows has always been intense. But I discovered that memorizing dialogue, lyrics, and movements is now much harder than it seemed before. I can’t imagine that aging has anything to do with it! Eventually I learned my part and had an enjoyable experience. But I was performing without Susan for the first time in over 30 years – we always supported and encouraged one another’s performances even if we weren’t performing together (which we did a lot). There were a variety of emotional triggers for me with this production. The show was dedicated to her memory. Opening night was on my birthday (another “first” without her). A very sweet teenager whom Susan had helped in earlier performances came up to me to express her appreciation and sadness. Before the Saturday night performance in the traditional cast circle, our good friend and director, Dennis, remembered Susan in an emotional tribute. They all combined to create not just a busy activity, but an experience that made me feel fully alive.

In another touching event, a long-time choir member and friend, Don Elliott, made a shadow-box display for the glass hummingbird I gave the choir in memory of Susan. He finished it in time for the first choir rehearsal in September. It will be mounted on a wall in the choir room. Don died very suddenly and unexpectedly a few days ago, making his effort even more special.

I have become keenly aware of this “year of firsts”. Jon, then I, and now Patrick (today) have all experienced our first birthdays since Susan died. In addition to the date of Susan’s death, our wedding anniversary, Thanksgiving, Christmas, and her birthday are still coming up. As we approach the darkening season and the memories of intense care-giving, decline, and death just one year ago, I know that the sense of progress I felt earlier this year was an important “phase” to help us get ready for these milestones.

Very soon, I will be immersed in church committee work for the foreseeable future. My job with the City of Denver is professionally stimulating. Plugging back into life in these ways is better than being idle – and it is also creating more powerful feelings of appreciation and sorrow.

But I guess - that’s life.

Friday, July 17, 2009

Up

In this story, we view a man’s life from when he discovers his earliest childhood passions, meets his soul mate, and forges a wonderful life with her through joys and sorrows – until she dies. The man is deeply saddened by her absence as well as by unfulfilled promises and dreams. But an opportunity to keep those promises, see those dreams come true, and pursue new ones, comes his way unexpectedly. He goes along reluctantly and begrudgingly until he realizes that pursuing his new life and keeping his old promises might be one and the same. He becomes renewed and thrives again.

Patrick suggested we see this movie last Saturday night. He had seen it before, so I suspect he already knew that its similarities to my own life would not go unnoticed. This might even be a way for him to deal with his own grieving process – by intersecting his and mine with shared events. The movie was a poignant experience – as well as funny and creative. For example, if you know anything at all about stereotypical dog behavior you’ll have some good belly laughs. It’s a fine film and I recommend it.

I have had many other poignant reminders lately. The youngest son of some special friends got married last Friday. The wedding (in a beautiful, outdoor, mountain setting) underscored the passage of time, the physical absence (but also the spiritual presence) of Susan, and the timeless rituals of life. It was also my first wedding as a widower – which was a little weird.

I don’t often need to identify myself as a widower. But twice this past week I found myself explaining that Susan had died. Once was to notify the office of one of her specialists who had called to suggest it was time for her to be seen again. The other was someone at work whom I had not seen in a while and who inquired about her.

The daily meditation for July 13 (from “Healing After Loss” which I mention in the book list below) quotes John Hassler: “He’d begun to wake up in the morning with something besides dread in his heart. Not happiness exactly, not eagerness for the new day, but a kind of urge to be eager, a longing to be happy.” The author of these meditations, Martha Whitmore Hickman reflects, “Then one day we may think to ourselves, ‘Wait a minute. This feels different!’ . . . we realize we inhabit a new land where we are happy and content more of the time than not.”

This feels like an accurate description of where I am on this path – and where I’ve been for a couple of months. I still have moments when I have trouble believing that all this has really happened. I still have moments when I miss Susan terribly. It still feels like grieving, and it still looks like I have a long way to go. But I’m much more aware of how far I’ve come. I am more cognizant of the “circle of life” – being born, living, dying, and being reborn – than I have ever been before. It’s the fundamental commonality of all religious traditions. It’s beautiful, sad, inspiring, and awesome all at once.

Life is good. Everything is as it should be in the Universe. Things are looking “Up”.

Wednesday, June 17, 2009

The Passage of Time

I’m remembering six months ago today and the life-changing weeks, months, and years leading up to that moment when Susan took her last breath. I’m awed by the powerful transformation from winter into spring, both in nature and in our human experience.

Tuesday, May 19, 2009

Trips of a Lifetime

Throughout the many years in which cancer was a part of our lives, Susan and I tried to create as many memories as possible (a term coined by our friend Martha). One of our favorite things to do was to take trips. Together, we were able to visit places in Colorado, Alaska, Washington, Maine, Montana, Wyoming, Tennessee, New York, California, the Caribbean, and Europe. (As I reviewed the list, I was surprised at how many places we traveled!) In addition, she took trips to Minnesota (by herself), Israel (with a group), and Illinois (with Jon). Those trips are full of precious recollections as we tried to live a lifestyle that could most closely resemble an early retirement.

There have also been several other important trips since Susan died, where she was with us in a different way. As I reflect on them, I notice that they are helping me travel through my own passage as I adjust to life without her physical presence.

Susan and I had intended to visit Washington, D.C. in April or May of 2008 but the brain tumor got in the way of that. So in late April of this year, in honor of that “last trip not taken”, I did it for both of us. It was a great trip and I managed to cover a lot in less than 5 days. It involved a lot of walking. Had Susan been physically with me, we’d have been limited to whatever could have been done with a wheelchair and a bus tour. But she was definitely with me in spirit and it was good to revisit this great City. There were all kinds of reminders of our life together and of our shared pleasures. I found myself “talking” to her a lot.

Early in the cancer journey, we feared that Susan might not even live long enough to make Patrick’s high school graduation in 2005. But of course she did – and almost made it to his college graduation – which was the day before this past Mother’s Day, 2009. Jon and I watched Patrick take a trip down the aisle with his class in commencement ceremonies at Montana State University – and Susan was there too. (He will officially finish in December after student teaching this fall.) Neither Susan nor I were ever particularly enthralled with big commencement events and Patrick was of the same mind. But such milestones have become more important to us and Patrick agreed to participate in honor of his mother. Ever the great planner and role model that she was, she had written a letter for the occasion which I gave to him the night before. Jon, Patrick and I enjoyed each other’s company in Bozeman (a great college town), then loaded up Patrick’s stuff for his return to Denver and a major lifestyle change.

Two days later, and a little over a year after putting his life on hold to be Susan’s caregiver, Jon proceeded with his plans to pursue international service. After a 52 hour trip, he is now at a volunteer center in Kenya working with kids in a small village (his blog address is: http://www.woeai.blogspot.com/). He’ll be back in Denver on July 31. Shortly after that, the three of us plan to take a trip to Downers Grove to visit Susan’s family. Then Jon will be off to China in late August where he’ll study Chinese and teach English at Chongqing Three Gorges University. Naturally, I have a trip to China in mind some time after the first of the year!

The trip theme continued last Saturday when I attended a memorial service conducted by the hospice that cared for Susan. They were honoring those for whom they had cared over the last year or more. The staff emphasized what a privilege it had been for us to allow them into such an intimate part of our lives. The service ended outdoors (on a gorgeous spring day) with the release of white doves, one for each honoree. It was symbolic of Susan’s trip across the threshold to that beautiful paradise we all hold in our hearts.

Several of us will be taking a “trip” back to the Montview Garden Columbarium this Memorial Day weekend to place a Butterfly Plant near Susan’s crypt. It was one of her favorites and it seems fitting to have it there, reminding us of the circle of life and death and life again.

All of this reminds me that our trips, excursions, expeditions, jaunts, and journeys are an important part of the fabric of our earthly life. They’re helping me stitch together that huge whole she left in our lives with a unique pattern and texture that is shaped just like her.

Sunday, April 19, 2009

Foresight and Style

Among the many incredible gifts Susan left us was her foresight about what we would need after her death. Her long journey allowed her lots of time to contemplate those needs. Some of the initiatives she took were in partnership with me – such as remodeling the house and minimizing the attention it would require for a while. But she did other things that, even though I might have been aware of them taking place, are only having their impact now. In addition, she taught me how to be more proactive, to look ahead, anticipate, and prepare for things that were never on my radar screen before.

She had an extensive wardrobe. To be more direct, she was a self-admitted clothes horse. But she also had a great sense of style which not only kept her well-dressed, but also kept me from looking like a clueless geek (at least in the eyes of most, I hope). Packing for any trip, no matter its length, was an obstacle course of decision-making for her, complicated by the choices she had. Which shoes should I take with which slacks and which tops? Are we going to any dressy places? What if it rains or snows? What if . . . ? It always took her hours to pack and she was always mildly chagrined that it generally only took me about 15 minutes or less.

Because of steroid-related weight gain, much of her earlier wardrobe became unwearable. Throughout 2008, and to spare me from having to do it, she and her friends worked hard to go through everything and give away most of what she no longer needed. In one particularly meaningful time period last fall, her sister Barb came for several days to help. It was an emotional time and they were as close as I’ve ever seen them, making it a meaningful step in the dying process as well as an exercise in practicality. I will be eternally grateful for Susan’s proactive nature.

There were still a lot of clothes (and shoes) left after she died. After several months of not being ready, I finally decided that the time had come to deal with them. I asked Peg to help – because I knew Peg would take charge, make me her assistant, and tell me what to do. She'd already helped Susan with the bulk of her earlier giveaways in 2008. The act of handling and recording the items as we categorized them was not in itself particularly difficult. But it set the stage for a conversation that we had not been able to have since Susan died. Peg was the first one on the scene just minutes after Susan took her last breath. Like so many others, she had spent time with Susan in the prior weeks and had gained some pretty incredible insights. Discussing those was an emotionally cleansing experience for both of us. I realized in talking to Peg, that Jon and I (and Patrick when he was here) were so busy being stressed-out, exhausted caregivers, that we were unable to appreciate any of the beauty and mystery of her dying process. As a result, I intend to circle back with others who spent special time with her during those final weeks. I think it will help me appreciate a more beautiful picture than the one we saw at the time – and I hope it will be good for them too.

There continues to be no particularly good answer to “how are you doing?” Everything I’ve read about the grieving process indicates that it takes its own time – and I’m finding that to be true. I do feel progress. But almost the moment I acknowledge it, something else reminds me of all that has transpired and I realize there is much more healing to come. It’s a little like hiking in the mountains or in a very hilly area. Just when you think you’ve reached the topmost peak and expect to see a panorama of the world, you discover that there are other, sometimes higher peaks that are still obstructing the view you were hoping to see. I have to remind myself that it’s still a beautiful view, made so by all of the caring, supportive people around me who seem to understand what I’m experiencing.

One of my “summit” moments was particularly remarkable – at least to me. I’m sure only a few people would truly understand it or not think I’ve gone wacky. It was the morning of March 31. I was on my way to work by train. I had finished reading my newspaper and was sitting quietly, aware of the rising sun over my right shoulder and appreciating the beauty of a spring morning in Colorado. I must have been thinking about her because I suddenly felt Susan’s presence leap into the huge hole that her absence has left inside me. At least that’s what it seemed like. The feeling was pleasant and comforting. It stayed with me for most of the day and made me feel like she was intimately close rather than in some elusive, external place waiting to be discovered. In retrospect, it almost seems silly – except for the impact it clearly had on me at the time and the way in which I remember the moment. Part of my awareness that day was a deep sense of appreciation for the courageous and dignified way in which she chose to live with that terrible disease. I’m so impressed with all the things she did for us in preparation for her departure in spite of what she was experiencing herself. I was also aware of the reality that she will always be with me – just not in the way in which I yearn to be.

So – how am I doing? Some days are OK. Some days it seems unbelievable that she’s gone. Every now and then I have a rare melt-down. But the reminders of her wonderful life are everywhere.

And somewhere in the world beyond, she is a model of foresight, organization and style – making things ready for us when our time comes to join her.

Wednesday, March 11, 2009

Untangling My Strands of Yarn: Reflections On Grieving

It’s been almost three months since Susan died. I’ve been wanting to post my thoughts during that time but I haven’t been able to get them out. I think I finally figured out why. The other night it came to me just before I went to sleep.

In the last few years of her life, one of the things that brought Susan great joy was knitting. Some of you have artifacts of her work, and some of her work is yet to be discovered by future grandchildren or others at some other time. She was prolific until the last couple of months, often working on multiple projects simultaneously. Occasionally, when she picked up a project that she had set aside, she’d find the yarn in a tangled mess. The tangles were particularly difficult when she was using more than one yarn at a time and knitting them together. She would often enlist my help in getting the yarn(s) untangled so she could proceed. This recollection has become a metaphor for my grieving process. My thoughts and feelings have been in a tangled mess, needing some time and patience (and help) to get untangled. The eventual result of Susan’s untangled yarn was always something beautiful – and useful. And so it is that I hope the path of this grieving process will take me to a beautiful, more comfortable place of reconciliation, where more recent events are overwhelmed by memories of our entire 30-plus years together.

My tangled feelings have evolved over the weeks. I felt pretty much OK in the first week or two after her memorial service. Patrick went back to school and Jon was in Uganda, so I had time for introspection. I went back to work and choir and felt more or less normal. But then I began to notice myself wanting to talk to her, to share some story, thought, or event – only to be disappointed at the realization that she wasn’t there. I’d roll over in bed and be surprised to find her gone. Gradually, it began to sink in to my psyche that her physical absence is permanent and that I have work to do in order to get used to it. There are so many things I’d like her to know. They’ve been so snarled up in my head that I didn’t even realize I was experiencing so many different feelings. These are the strands of my tangled yarn:

First of all, the memorial service was incredible. There were somewhere around 400 people in attendance, including a huge family turnout (both from her side and mine) as well as friends and colleagues from our life together and from our respective professional lives. I was particularly gratified by the showing of so many people from my work community – many of whom I would not have expected to take the time to come. Susan’s pre-planning paid off in a big way. It was not only a fine tribute to her, but also a celebration of our humanness as a community. Our friends who spoke or read or sang or played really poured their hearts into it.

There are still lots of tasks to complete. Part of me wants to wave a magic wand and take care of them right away. But part of my growing realization is that the important stuff will get done, the less-important stuff will get done in its own time, and the stuff that doesn’t really matter will eventually fade from my concern. There are of course the financial details and the legal records that must be completed and changed. I’m finally getting near the end of that. Then there is the disposition of Susan’s belongings and figuring out how to run the house. There are so many things she did that I either quietly appreciated or took for granted – but that I am otherwise clueless to replicate. My colleagues at work now have to point out things like the stain on my shirt that Susan would have caught before I left the house! Part of the loss is knowing that many things won’t be done, or won’t be done in the same way. And all of this is taking longer than I ever would have anticipated.

I’m occasionally having what I can only describe as some degree of post traumatic stress disorder. The final five weeks or so were incredibly intense. I sometimes have flashbacks of both the more difficult and tender moments. The night she got so upset and belligerent and wanted to “go home and find her husband” sticks out as bittersweet. The morning she silently placed her hand on my cheek while we gazed into each other’s souls is a treasure. Remembering what she went through is agonizing. Remembering her when she finally let go is indelible.

Then there is the big hole in the fabric of our lives. Her absence is palpable and I miss her terribly. I yearn to interact with her. I try to talk to her at her crypt. Yet, she’s still here in some way – the chills I experience, the dreams I have, the hummingbird images I notice, and the things that remind me of her must all be evidence of her presence. Somewhere along the way it became clear to me how strong our life partnership was and how challenging it is to function without her after 32 years of doing virtually everything together. Sometimes I feel at a loss to make a simple decision because she’s not here to consult. Other times I realize how liberating it is to make decisions for myself and then feel a brief sense of guilt at the realization that she might have preferred something else. Not being in partnership with her is going to be a hard habit to break.

I’m struggling to keep the entire 32 years in perspective. I have difficulty remembering what life was like before cancer. And yet the cancer journey, particularly the way she handled it, became such a defining aspect of her and our partnership. How can such a curse, such a scourge of the human experience also provide such growth and enrichment?

It has not escaped my attention that we’re all grieving together and that everyone who cared about Susan is experiencing something proportionate to her place in their lives. I’ve had lots of conversations with lots of friends and family. Everyone is taking good care of us and each other. Our good friend Susan (TOS or “the other Susan” as we joke) loaned me a really good book of meditations on grieving. (I’ve referenced it under “Good Books to Check Out”.) All of these things reaffirm what I know to be true: we’re going to be OK. People have been walking this path ever since humans have had the capacity to feel. We’re doing what we’re supposed to do and all is right with the universe.

My yarn feels a little less tangled and I’m hopeful that we can eventually knit something beautiful to fill that big hole in the fabric of our lives. I hope your grieving process is moving in that direction too.

Wednesday, December 17, 2008

New Beginnings - For All of Us

The Susan we knew and loved passed away today. Her long journey is finally over and we are confident that she is at peace. It’s important to note that she did not “lose her battle with cancer”. She beat cancer years ago when she chose quality over quantity of life and lived with the disease far longer than expected. Indeed, her life is nothing short of a triumph. Now we all embark on a new journey – life without Susan’s presence, but with the memories of her that have shaped our lives. Her obituary will read something like this:

Susan G. Moody was known for her zealous effectiveness in everything she sought to accomplish. It was therefore no surprise to anyone who knew her that she lived a full life for more than four and a half years after being diagnosed with terminal stage IV melanoma. Her cancer journey was characterized by her ardent emphasis on the quality of life, not its duration. She died in her home on Wednesday, December 17, 2008 in the presence of loved ones.

Susan, 55, and who lived in Aurora, Colorado was a retired Community Health Nurse Manager. She held two bachelor’s degrees (Zoology and Nursing), two certificates (Medical Technology and Science Education), and an honorary master’s degree in Nursing Leadership bestowed by Regis University in 2004 when she fell just short of completion due to her illness. She began her professional life as a medical technologist for 15 years followed by brief service as a public school science teacher. But her true passion was in public health nursing where she became a subject matter expert in women’s health issues, especially for the under-served population. After first working in the Chicago area where they lived for eight years, she and her family moved back to Colorado where she worked for the Tri-County Health Department for several years before joining MCPN (Metro Community Provider Network) as a Clinic Operations Manager.

Susan was an avid gardener, knitter, jewelry maker, seamstress, reader, and singer. She was a soprano soloist in the Westminster Choir at Montview Boulevard Presbyterian Church, a member of a jazz/gospel ensemble group known as “The Stage Crew”, and appeared in numerous musical productions over many years. She was also an Elder in the Presbyterian Church USA and was elected to Montview’s Session. She served on a committee of the Diana Price-Fish Foundation, a cancer support organization; and on the board of Self Improvement Opportunities, an adult education provider where she also tutored GED students.

Susan married Rob Moody in November of 1978 after meeting him through her sister in 1972. Together, they raised two fine sons, Jon age 25 and Patrick age 22 both of Aurora. Besides her husband and sons, she is survived by her parents, Wallace and Nancy Given of Downers Grove, Illinois; a brother Scott Given also of Downers Grove; and her sister Barbara Wise of Hampshire, Illinois. Her extended family includes numerous cousins, nieces, and nephews.

A memorial service will be held at Montview Boulevard Presbyterian Church, 1980 Dahlia Street in Denver where she will be interred in Montview’s Memorial Columbarium. Memorials and contributions can be made in her name to:

Montview Blvd. Presbyterian Church Music Program
1980 Dahlia Street
Denver, CO 80220-1239

Visiting Nurse Association Hospice at Home Program
Attention: Bob Crump-Bertram, Chaplain
390 Grant Street
Denver, CO 80203

The Melanoma Research Foundation
170 Township Line Road, Building B
Hillsborough, NJ 08844

Wednesday, November 26, 2008

For Real

On Thursday, November 13th, Susan had a significant new pain crisis that has turned the page on a new chapter of this journey. The standard treatment for pain of course, is to increase pain medication, in this case morphine. The hospice philosophy, which is all about comforting the dying, accepts no excuse for pain. Pain interferes with the important emotional and spiritual work that is being done in preparation for the transition out of this life. The tradeoff with pain management is sleep.

So Susan has been more asleep than not since that Thursday night. Even in wakeful times, she’s still in a world of her own. But she’s perfectly aware of what’s happening and has grown in her level of acceptance. The reason for the pain is undoubtedly disease progression, which means we’re getting yet closer to the inevitable beginning of a new journey for her as well as for the rest of us. Underscoring that reality has been the breathtaking speed of change in the household. Suddenly, we have a hospital bed in the living room, and we’re using more oxygen. Jon and I are taking turns eating and sitting with Susan who is essentially uninterested in food and no longer able to sit at the table. One of us sleeps in the living room with her at night. We have meals and pastors, and professional caregivers coming and going on a regular basis. Friends and family are right here with us both physically and spiritually. Sponge baths and changing the bed and lots of laundry are now the norm. Susan hasn’t been upstairs since Saturday morning because getting her up and down stairs has become too adventurous. Her favorite recliner in the family room seems like a distant memory. Just in the last few days, our lives have been transformed into the picture of in-home hospice that many of us probably imagine – and maybe dread. She has swiftly become bedridden and dependent on us for nearly all of her needs. Susan and I have discussed this picture many, many times over the last 4 ½ years – and here it is for real.

A wonderful friend of ours, Helen, offered an amazing metaphor to all of this. Helen suggests that Susan is in labor again. But this time it’s to give new life to her soul as her body dies. As I was sitting in the living room reading and contemplating our circumstances, trying to decompress from all of the new stressors that this has produced, I suddenly became keenly aware of what in-home hospice is all about – and it’s a lot like trying to make childbirth as comfortable as possible in familiar surroundings. Much of the stuff you’d expect in a hospital room is right here in our living room. We even have one of those over-the-bed tables on wheels that can be raised and lowered and upon which hospital meals are served. But it’s still our living room – with new meaning to the term “living” – not a stark, unfamiliar, and unpleasant place. I’m reminded that most of the literature we’ve read about the hospice movement emphasizes that dying is actually part of living – for all of us. We need not treat it as a failure of some sort. Doesn’t it make more sense to acknowledge its reality and deal with its inevitability by exercising as much control over it as we can? Prior to “modern” medical technology, isn’t that what people used to do? Die at home? Give birth at home? Susan occasionally wakes up, looks around, makes an observation, and resumes her slumber. The other day she commented “we have a nice living room!” Point made.

Jon’s prior CNA experience in a nursing home has proved to be invaluable. He’s teaching me all the tricks. But the new chores that Jon and I have taken on are unpleasant and exhausting – and not just for us. Susan, even though she’s not the same coherent person we’ve known, clearly doesn’t like any of this either. We had hoped to avoid this stage. But the fact that we’ve had so much time to prepare for this is a gift. We’ve read a great deal about hospice and the dying process – and I’m beginning to understand why it can be an honor to be a caregiver to a loved one.

Uncertainty is still part of the process. Though things have changed rapidly in the last 13 days, we still don’t know when she will be able to let go. She doesn’t either. We only know we’re closer than we were before. Patrick was here for a few days last week and will return for the Thanksgiving break. Instead of the usual Thanksgiving custom, the four of us will be giving thanks in a very special and memorable way – for the gifts of life and love, and especially for the extraordinary legacy of Susan Diane Given Moody.

Sunday, November 9, 2008

Urging Us On

When I was about 15, I walked the Lincoln Trail as a boy scout. The Lincoln Trail retraces the path that Abraham Lincoln walked between Springfield, Illinois where he was studying law and New Salem where he was living in the mid 19th century. It’s 20-plus miles – a pretty long trek for a youngster, especially if the youngster isn’t in the best of shape. But my brother and my cousin had both done it and I wanted to do it too. Hiking the trail earns the scout a medal and a big sense of accomplishment. Besides being dead-tired toward the end of the long day, I remember feeling lonely during the journey, even though I was with a small group of others who urged me on. I probably wouldn’t have made it without that support.

This memory could be a metaphor for our cancer journey. Susan, Jon, Patrick, and I are all experiencing this trek in our own ways, and I think it feels a little lonely for each of us even though we have lots of people urging us on. I don’t know how people do this without the encouragement of others because getting to our destination is a long trek. As with many life experiences, hiking the Lincoln Trail must have been part of my preparation for this time in my life.

Lately, the show of support has been particularly evident from all of you. We’ve gotten loving, non-invasive messages in all kinds of ways and from all sectors of our lives. Some of the messages have become dependably regular and are our bedrock. Some of them have been unexpected and gratifying surprises. The number of people who are with us on this journey is astonishing, and humbling, and touching. It illustrates the best of our humanity as we travel the circle of life together. It is what will help us make it. In spiritual terms, all of you equate to the presence of God in our lives – and God is mightily present.

In the last month Susan has gone from what had been pretty stable pain control to sudden, severe new pain. After a couple of weeks of increased doses and being “out of it”, she seems to be in a little better control of the pain for the time being. Her memory and cognitive abilities are still pretty variable from one moment to the next. She struggles with the loss of function. We know pain management will be an on-going challenge. Stability and mobility are growing issues and all of us are fully exercising our coping skills as we strive to keep her safe, comfortable, and at peace with the situation. It’s already been a long hike and we don’t know how far we have yet to go. The sense of accomplishment we seek at the end will be helping Susan finish her earthly life in peace and comfort. But we’ll make it – because we have you urging us on. God is with us. Thanks be to God – and to you!

Sunday, October 5, 2008

Letting Go and Holding On

One of the challenges Jon and I have noticed about this journey as caregivers, is how very difficult it is to find the right balance between assisting Susan with a task and assisting her with her dignity. It’s very hard for Susan to let go of things that she can sometimes do, but sometimes can’t or sometimes shouldn’t. It’s usually little things – like carrying a glass of water around the house or a handful of stuff up and down the stairs. It could be something very important to her but not so much to us when we have so many other priorities on our minds. Sometimes, it’s no problem at all. Sometimes she can’t do it safely and knows it. Sometimes she can’t do it safely and doesn’t know it but Jon and I do. And sometimes we’re mistaken. Part of the dying process is learning to let go of things and we talk about that a lot. But as Susan points out, it can’t be done overnight, especially for someone who has always been so competent. Knowing exactly how best to get someplace or where to park doesn’t go away just because you’re not the one driving. Taking things away from her – even with all our good intentions as caregivers – sometimes results in some verbal wrangling, albeit brief, that only adds to the stress of it all.

I think parents and teachers get lots of practice at the process of helping, then letting go as children grow, develop, and master new things. Experiencing that is both scary and rewarding. But this is just the opposite. We’re not talking about someone’s development; we’re dealing with someone’s decline. We’re not the ones letting go – she is. I noticed the same difficulties when my sister was the primary caregiver to our mother. The caregiver wants to help, to take annoying tasks away, to keep the loved one safe, and to balance all of that with whatever the caregiver needs to do for himself. But the loved one wants to reaffirm her own value as a competent human, to offer thoughts, ideas, and expertise in the activities of daily life no matter how trivial. It turns out that helping someone who is not always helpless is a steep learning curve.

Because of Susan’s decline, it’s very difficult to tell from one moment to the next if we’re dealing with a sharp, rational thought process or if we’re dealing with the effects of the brain tumor. She is often confused and frequently has trouble converting her thoughts to the right words – but not always. Short-term memory is a big problem. In addition, her mind is tormented by an overwhelming, sometimes anxiety-producing flood of thoughts. Some of those thoughts are constructive, accurate, and right on the money. Sometimes they’re not. Often, they are things we don’t think she needs to worry about. But when we step in to rescue her from being a hostage to her own unnecessary control needs, we sometimes get a backlash because she’s unwilling or unready to give up the dignity of having thoughts and choices. It’s very stressful and takes a lot of energy for the caregiver to figure out the right response. In fact, it’s probably impossible – which adds an element of guilt for not getting it right.

Her decline is more and more obvious. For several weeks, pain management has been a growing issue. We’re constantly trying to determine how much regular, baseline pain medicine she needs in order to avoid too much breakthrough pain yet not so much that she falls asleep in the middle of a sentence. The more morphine she takes the more cognitive function she gives up. The less morphine she takes, the more she’s in pain. Her balance and mobility are much worse. She uses a walker more and more, even in the house. Her risk of falling is considerably higher. She uses oxygen occasionally for shortness of breath (that was particularly handy for our recent visit to the higher altitude of Estes Park). And yet she continues to formulate future plans and future projects and hold on to as much as she possibly can. It turns out that the dying process is much more complicated than I ever anticipated, even though we’ve been informing ourselves about it for years.

How will Susan know when it’s time to let go and die in peace? How will the rest of us know when to signal to her that it’s OK? There is only one answer that consoles me: We have to let go of our human concerns and hold on to our faith in God, Nature, the Divine, or whatever superior force we rely on to help us cope with life’s challenges.

Let go – but hold on. It takes a lifetime to master.

Wednesday, September 3, 2008

How do you say good-bye . . .

. . . to your parents, your sister, your brother and all the rest of your loved ones when you’re dying?

Susan’s parents were here for a brief visit in early August, followed by her sister Barb with her husband Jack later in the month. Her brother Scott and his wife Jan will come for a short visit in late September. In each case, we all know that it may very well be the last time they see Susan again.

But as sad as that sounds, there are blessings in all of this – just as we’ve said about the whole cancer journey. How often do we take the opportunity to really pay attention to our loved ones, to listen to them, and appreciate them rather than taking our relationships with them for granted? When you add the element of dying into the mix, everything changes – especially if it’s not following the usual order of the older folks dying first. Susan and her family are as close as they’ve ever been – and that’s a good thing.

So, how do you say good-bye to loved ones when you’re dying? Maybe it doesn’t matter as long as you somehow focus on what makes them your loved ones to begin with.


By the way – how is Susan doing?

We continue to experience ups and downs, often several times in the same day, with a gradual downward trend. Everything is slowly happening as expected. Susan’s pain is pretty well managed most of the time, but her cognitive abilities and emotional reactions to things are noticeably affected. She has trouble with short term memory and gets easily confused or upset or overwhelmed. Someone is always with her when she leaves the house and most of the time at home as well. Her balance and mobility issues require a cane or a walker. But she continues to maintain a great deal of control of her day-to-day tasks. She is continually knitting multiple projects, mostly for others.

Jon is at home most of the time on weekdays and I primarily do evenings and weekends. Jon has a part-time job and is taking a class – both of which help keep him alternatively occupied. Patrick worked at scout camp until early August, and then was part of the care-giving mix for a couple of weeks before returning to Bozeman last weekend for the beginning of his semester. It’s a unique challenge for him to be there and not here. My work is going well and my co-workers are wonderfully supportive. I try to take a little time for myself now and then but my plate is full and I will sit out of choir for the time being.

Jon, Patrick, and I can tell you that this is hard and getting harder. I watched my sister deal with the challenges of eldercare with our mother. There are lots of similarities. But as my sister pointed out, such difficulties are not unexpected when your parent is ninety-something. When as in our case, it’s your soul mate with whom you had retirement dreams, or your mother who would relish a chance to someday hold your own children – there is an extra overlay of emotional difficulty. We’re exercising our coping skills, practicing our faith, and feel deeply appreciative of a supportive community.

Thank God for all of you!

Friday, August 22, 2008

Stateside and Back

We have a guest blogger for this entry. This posting is from Lisa's Peace Corps Blog, writing about her recent visit in late July. Rob


I tactfullly avoided mentioning to too many people that I would be making a stop in the states for a bit, just as I have been tactfully avoiding writing anything about my trip there. Well, I think it's about time I talked. It's strange to think of an experience as both rejuvenating and energy-sucking. B/c that was what America was. Essential and exhausting, wonderful and heartbreaking.We have all changed so much whether we were aware or not: Susan, me, Jon, Sarah, family and friends. It's amazing how distance can put such a real and invisible gap between what we all understand about one another. And how that enables us to just grow up more, i guess.Susan was my reason for going back where i came from. So I went. Things were different. Some of it was sad and real. But it was what it was.I saw both a different woman and the same woman in her. I saw a woman who still loves her crafts, who still wants to be with her friends and get her nails done and have the classic "Moody" conversation that we have at their dinner table, usually on the verge of politics or religion, or life in general. I also saw her frustration in losing her independence in all these activities as well. The ultimate reality that it will not get better, and wondering, just how the hell do you say goodbye to someone...for good? I managed to leave there with thoughts of not being sad for Susan because she knows what she wants and how to go about her plans as best as she possibly can. But plans are just hopes. And we hope we can carry them out against all odds. I cannot honestly say that i am not worried for her within the next few months, but I was happy to see that she is able to make her decisions, able to prepare herself and her family and enjoy what time has left to her. I saw her trying to embrace her own person, on her own, as well as giving what time she can to others. I think all of us would want to give this time to those we love. And I can see Susan doing this both because she needs her family, but also because she knows that we need her. What greater show of empathy for those of us behind her than to get time with her, cause that's all we got to work with. Jon, Patrick and Rob are a bit of another story for me. I do worry for these men and how they will cope. I also (saw) 2 different Jonathan's back home. A caretaker, all business at times and just as frustrated as his mother was. His trade-mark patience could wear-thin. He even found it hard to "please" me one time when I snapped at him for no good reason. That's when I thought that I am not so sure that he is aware of what he is doing exactly. And that is his very best. His best to love himself, the best to love his mom and take care of her, the best to alleviate any stress on the family. His best to hold it together as a part of his world changes before his eyes. And this all just made me realize, for only the millionth time what a good heart he has. And how proud I am to be a piece of it. And it would be a lie if I said that being in Uganda wasn't some sort of escape for me. It is. I have another focus here, another life, really. That is the best and worst part about being here, maybe: the separation from my point of origin. But, this is life. Everyday we all die a bit, we grow a bit, we lose something and replace it with something else. What is most important is that we learn a lot and play a lot, like my papa preaches and do what we can to connect to others. Can I end this on a morbid note? "Love is watching someone die"And I hope that I can get a chance to be with those I love when they end their time here. Life is nothing special if it does not hurt. And I am ok with this.
Created for your enjoyment by Lisa B at 7:31 AM

Sunday, August 10, 2008

Here's to Jon!

Our oldest son, Jon just turned 25 – an age when most people are focused on their own lives, their own future, and developing their own ways of meeting the challenges of life. Most of us did not have to deal with the reality of a dying parent as part of our early adult experience.

Jon graduated from Colorado State University in December of 2006 with a B.A. in History. His plan at the time, along with his long-time girlfriend Lisa, was to enter the Peace Corps and serve the world in a uniquely meaningful way for a couple of years. He and Lisa applied and were both accepted. The screening process was long, and even after their initial acceptance they each had to endure a multitude of psychological and health tests. Never-the-less, the process was leading them to Africa where they both wanted to go. They wouldn’t have been serving in the same place, but they’d have been on the same continent doing what they had long committed to do. But in the summer of 2007 after months of delay, Jon was finally informed of the Peace Corps’ reluctance to proceed while his mother was dealing with a terminal illness. At the time, we had no way of knowing where Susan’s disease process would take us, or when. But the Peace Corps has a great deal of experience in these matters and knew that the loneliness and isolation of an assignment in Africa would be arduous – and that any major family crisis, let alone her death, would threaten his experience and that of the community he would be serving.

While Lisa’s plan moved forward, Jon took the disappointment in stride and looked for alternative opportunities closer to home. He ended up joining an AmeriCorps program called the National Civilian Community Corps. He left in late January for what would have been a year-long assignment based in Maryland, just a week before Lisa left for the beginning of her Peace Corps assignment. She went for an orientation in Philadelphia first (where she and Jon were able to rendezvous), then went on to Uganda where she is currently serving. It was shortly after that when we found out about Susan’s brain metastasis and that we had entered a new chapter in the journey. After several months doing post-Katrina projects in Biloxi, Mississippi, Jon decide his calling was at home. He arrived back in time to join me in the emergency room on a day when Susan was dealing with the medical crisis that helped us decide to enter hospice two days later.

Jon put his life on hold and chose to be with Susan as a caregiver. He has training as both a certified nurse aide and as an emergency medical technician which has come in quite handy. Early in the hospice journey the going was relatively easy and his presence was simply appreciated. Now, looking back over the last three months I can’t imagine doing this without him.

Jon’s role is more complicated than it appears. If he were just being employed as a companion, he might be able to go off duty and retreat to his own living space. But he’s also a family member dealing with the end of his mother’s life. There’s no “time off” for that. Though he found being thousands of miles away very difficult, he’s now dealing with the challenges of being so close. At any given time, he’s taking Susan where she needs to go (he’s not very fond of the craft and fabric stores she frequents), doing chores around the house, helping her with her meds, or observing her symptoms and behavior. (Such observations are critical for the hospice team in order to monitor changes and make necessary adjustments for Susan’s comfort.) All of that has become much more complex and challenging in recent weeks. Susan, by her own admission and because of her brain tumor and meds, can sometimes be a pretty crabby patient. Jon usually bears the brunt of her physical and emotional symptoms because he’s with her so much. But Jon is also processing his own journey. He’s trying to figure out what to do and where to go after Susan is gone. He’s trying to keep up with Lisa and her separate experience in Uganda, both to lessen the anguish of her absence, and to be supportive of her. He’s experiencing losses and learnings that most young adults don’t experience until much later in life. And I know he has days when he wonders why he has to endure all of this.

We all have our ways of coping. Jon works out a lot. He plays with the dog, he has two part-time jobs that get him out of the house, and he is exploring future opportunities. At Jon’s Eagle Court of Honor in 2002, I said I had begun seeing him as my own role model, rather than the other way around. I don’t know how I would manage what Jon is handling if I were his age. But I admire the heck out of what he’s doing. I know that as difficult as this is on so many levels, that he’s been gifted with the unique ability to do this and do it well. I believe he’ll be an even better person for this experience, difficult though it may be.

When I told Jon I was writing about him, he asked “is it good?” He’s not looking for accolades. He’s not that kind of guy. But I think we all need support in dealing with this journey at the end of Susan’s life. Some of my support comes from him. He deserves our support too. So please raise your glasses and join me in a toast.

Here’s to Jon!