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I’m Not Alone

morning candles

It’s been almost seven years since I moved my Dad to California, knowing that his cardiac disease was catching up with him. We’ve had quite a few scares since then: a small stroke that temporarily interfered with his ability to speak, a strange seizure, numerous falls and illnesses. During one of those scares, my husband was in Mexico, unreachable, and I was alone at the hospital with Dad, afraid.

I hate being alone when Dad’s life is at risk. I can handle the decisions that need to be made. I can handle the physical challenge of the long hours. I can be strong for Dad so that he is not afraid.

But I want to be able to cry and have someone to hold and comfort me when am afraid. I just don’t want to be alone.

Yesterday my first morning thought was of all the people who are, as one friend puts it, “holding me in the light.”

In recent days, I have heard from a college friend with whom I have been out of touch in recent years. My spiritual and artistic cousin, Lynn, has become the angel who perches on my shoulder with frequent, loving messages, like this one:

Whenever I read your ardent posts as I did just now.. and look at your exquisitely poignant and palpably tender photographs.. I am reminded again and again of the Rumi stanza..  that I am sure you are familiar with but I can’t help writing:“Let the beauty of what you love be what you do.” –Rumi    

 Mostly, I want you to know this New Year’s eve that even though it may seem I am in the background I am a part of that large net beneath the high wire you are walking– where by the way, you are dazzling in your diamond light.  I am not quite breathing with you, but almost…

My dear friend, Lisa, who spent the day on the 18th hanging out with me and cooking for me, is in Italy with her family where she is lighting a candle in every church she encounters. When traveling, Lisa normally devotes her laser-like focus to something food-related, like tasting lentil soup in Turkey, but on this trip, she says she is thinking of Dad and me. She wrote:

It is making me feel slightly better — but marginally so — wish I could be with you to help you through this important time. Your dad is a great man, and you are the best daughter and friend anyone could hope for. Miss you.

Yesterday I wrote my oldest friend, Ellen, about how she had rescued me when we met as lonely adolescents. She wrote back:

I have loved walking this current path with you. I have felt your sadness and pain. I have cried with you. I have wondered, and asked, and railed with you. I have grown with you. I have deepened and broadened who I am with you. I want to be there with you, but also know that you would be caring for me, and worrying about me, while at the same time you are caring and worrying about everyone else in your life. It’s your nature.

This is a hard path. But it’s far harder on Dad as he struggles. The love and support of family and friends makes all the difference. It holds me up so I can hold him up.

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Planning Care for the “Biologically Tenacious”

Henry S Campbell

As Dad has weakened the past few weeks, I’ve been preparing myself for his final days. That means coming to terms with what his dying may entail (ugh) and what his loss will mean to me and my family. A tall order.

Enter my husband who reminds me that, “Hey, don’t forget. This is your Dad.” Sure, Hospice thinks weeks to months, and it looks like he may have weeks to months based on all indications. But still. We’re talking about the guy who has survived war, heart attacks, strokes and high risk cardiac surgeries.

This phrase struck me in Sidney Callahan’s post about her mother’s long, long illness with Alzheimer’s in the Over 65 Blog published by The Hastings Center: “biologically tenacious.”

My husband’s grandmother was biologically tenacious. Like Sidney’s Mom, she still enjoyed eating and was comfortable, even though she hadn’t spoken or seemed to recognize people in years. And Gigi always said that she had “a bad heart,” something that amused us as the pages turned on the calendar, long past her 100th birthday.

I also have to be prepared – or at least set up for – Dad’s body persevering even if his mind and heart would prefer to move on. He is still a Marine, and some inner core of him doesn’t know the meaning of “quit.”

In practical terms, I have to have a reliable team of caregivers to help me care for Dad safely here, which means being able to transfer him safely until such time as he is confined to bed. I have a great partner in Visiting Angels, and an independent caregiver who was suggested by a family friend, but I’m not in a reliable groove yet.

This is a practical challenge when someone is facing the end-of-life: scheduling. If my husband wants me to join him with his folks to see Les Miserables, I have to have a caregiver who is capable of transferring Dad alone. On a weekend, if my son wants to run with Todd, leaving me alone in the house with Dad, I will need them to stay close to home in case I need help. The toughest transfers are on and off the john, which really takes two people. And unfortunately, there is no pattern as to when Dad’s urge might strike.

I want to be able to be a daughter and support my Dad every step of the way, but I know I must also make time for my mental and physical health. I don’t feel any resentment at the commitment I’ve made to move him to my house and have him spend his last days here, but I know, if enough time goes by, I might feel that way.

Semper Fidelis, Dad. I will find a way to make this work for both of us.

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Taking Stock of My Journey with Dad

Henry Campbell Dec. 23 2012

I’m one of those people who likes to take stock and tidy up as the new year approaches. But instead of cleaning my office as I have in years past, my attentions are here on this blog. Looking at the “About” description, I realized how its content has changed as Dad has aged and weakened. It started as a celebration with a few funny bits and occasional bits of advice thrown in. I wrote from the head, thinking, how can I capture useful insights from this experience for me to remember and for others to benefit from?

Last summer, as Dad’s health began to fail, I started writing from the gut. I wrote about my experience, about feeling vigilant, not just about Dad but about everyone in my life. I wrote about not sleeping. I felt a little like a mother hen trying to keep the chicks safe in the nest.

In the process of seeing Dad start to slip, I became more aware of and grateful for family and friends, especially my amazing husband of 30 years. My post on our anniversary, “30 Years of Opposites: Happily Ever After,” became my most-read post of the year, with over 300 views.

In October and November, The Henry Chronicles took on a more somber tone with the loss of my “other mother.” In the last month, my posts have expressed my desperation to turn things around and my anger at God when I could not. Without planning to do so, I find myself writing almost daily in the quiet hour after the night caregiver leaves and my Dad calls out that he is awake and ready to get up. One morning I thought about all of the people who have been supporting Dad or me, and I said thank you to “Team Henry.”

I’m no longer trying to be smart or useful. I’m just trying to get through this time with as much strength for Dad as I can. I keen online because I can’t help it. By releasing the terrible pain and fear that comes with caring for someone in the last months of life, I feel better. Maybe it’s self-therapy, online.

I do draw great comfort from the small company of friends and followers who read my little posts and share their own experiences, or offer a supportive word. I’m kind of amazed that, in this frenetic holiday period, people are willing to read something that isn’t about the fun of the holidays.

I may be hanging on by my fingernails, but I am hanging on.

The “About” page now ends with: These days, this blog is about coming to grips with the impending end of his life, a search for faith and understanding, and a longing for strength so that I might offer him the same unconditional love that he has always given me.

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The Petty Jealousy of the Paper

Sunday papers

It’s Sunday morning and the front paper is mine. My nighttime caregiver awakened me at 5:45 a.m. saying she needed help getting my Dad to the john, which takes two people to do safely. Just a few months ago, I would have gloried in having the paper to myself for 90 minutes.

Until this winter, I rose every morning at 7:30 a.m., made coffee and stepped out on the front porch to retrieve the paper, quickly noting the weather before brushing off the grime caused by runoff from the planter.  I devoured the headlines of the New York Times, knowing that Dad would latch onto it as soon as he came out for breakfast. I was jealous of these few moments alone, when I was in control of my time and my paper, if only for 20 minutes.

Then I heard it: the snap of the brake release on his walker, the slow sibilant shuffle on the wood floor, the clink of the lever that flushed the john.

But on the days when 8 a.m. came and went with quiet, I wondered, “Is this the day?”

Fifty years after the first of Dad’s three heart attacks, I started every day steeled against the possibility that I would find Dad dead and that he would not awaken again, not ever.

I feel awfully small for that little jealousy over the paper. The prospect of losing Dad soon is no longer possibility or probability. It’s near certainty. (When you’re talking about a man who has survived Iwo Jima, three heart attacks, three open hearts and three strokes, you learn not to place bets on prognosis.)

Yesterday I read through the booklet that Sutter Hospice gives you when you are admitted, “As the End of Life Nears: A Caregiver’s Guide.” I read this:

As your loved one begins to accept his or her own mortality, you may notice that they start to withdraw physically and emotionally from the ‘outside’ world. A person who once loved television and the newspapers may cease to enjoy these activities. In addition, he/she may not want to interact with people. You may even notice a steady withdrawal from people the patient loves most. Withdrawal from the outside world is a natural part of the dying process…. (H)e/she will most likely begin to sleep more…. This is a normal process and even though your loved one is asleep, important work is being done on the ‘inside’ in preparation of the transition from this life.

I wrote to my friend Jim, “I have been worrying about him sleeping too much and becoming dehydrated. You’ve written all those great words about the descent/ascent, the bridge, etc., and I took it in but I don’t think I really thought I was there now. But that’s were we are, isn’t it? He is withdrawing. It isn’t just my brothers who have to let go. It’s me.”

And Jim responded:

Sleeping is sweet.  Think about how treasured one’s naps are.  It is just his biological body adjusting and slowing down.  It is about letting himself accept his body doing what it needs to do so his spirit can be set free.  Honey, it is the way for each of us. You are providing an environment and space for him to to do this without judgment or demands. 

It is NOT about letting go. It’s about telling him he can fly to where he is meant to go, and that you will never let go of him in your heart.  I promise you he will be in your heart until the day your spirit treks along with his.

It’s about loving him so he can let go of this human experience.

Betsy, of course you can let him be born anew into eternity.  You let your kids be born into this world. You’re helping him be born again. It is not easy; it is not without labor pains.

He is withdrawing not from you but from this reality, so he can be in another one and still be very alive in you.

Stop picking on yourself. Just be present; open your heart to everything non-rational, and be open to him claiming his own eternal destiny.  Your heart will break: love knows not its own depth until the hour of separation.  But our faith suggests Easter is an ever present reality, as he will be for you the rest of your life.

While you sleep, Dad, I’ll read the paper, but I’ll be thinking of you in your dreams, flying to heaven.

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Now For the Heavy Lifting

Dancing with Dad

I can’t believe it’s only been a week since we’ve been on hospice. So much has happened, and things have changed so rapidly.

Nine days ago I wrote my plea for hospice. The next day, I wrote my thank you. I also wrote things like this to my brothers:

Dad isn’t doing great, but I do think he will stabilize with the tender ministrations of hospice. These people are GREAT with comfort care. Statistically, people with advanced illness live longer with hospice than without hospice. He could well rally and “graduate” from hospice (be kicked out of the program). Or he could continue to have accelerating problems. 

The day after I sent that message, my Dad stopped being able to walk. He walked to breakfast with his walker in the morning, and by afternoon, his legs were unable to support him. My carefully laid plans about the period ahead were shattered. Some time ago, I wondered what I would do if my Dad got to the point my mother did, when she needed to be physically lifted from her chair, to a wheelchair, to bed. I had said to myself, “I don’t know what I’d do if if my Dad gets to that point.” After all, my Dad weighs 200 lbs.

Now I know.

I rapidly went from expecting to need night time care, to needing afternoon respite, to needing almost 24 hour care. It isn’t safe for my Dad or for me to transfer him alone.

Hospice told me that their preference is for Dad to be in bed if he can’t assist with transferring by pushing himself up with his arms and helping to stand. But I just can’t face him spending the rest of his life – short though it may be  – in bed. He’s too “with it.”

So we are settling in, and making adjustments to keep him – and me – safe.

Long ago, I danced on my father’s shoes and he kept me from stumbling. Now we are doing a dance of a different kind, as I raise him to his feet and we shuffle together to the wheelchair, bed or chair. It may not be the graceful father-daughter moment that we had when I was five, but it is still sweet. I will not let him fall.

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My Back and Forth Faith

pendulum

Last Sunday, I shared how generally pissed off I was with God. If I learned anything from marriage counseling a dozen or so years ago, it’s that arguing isn’t a bad thing. In fact it’s healthy. It’s how you argue that matters. Do you argue to hurt, or to be heard? Do you listen as well as assert?

On Christmas, Maureen Dowd published a column about losing her friend Robin and Father Kevin O’Neil’s meditation on dying.

I underlined two of Father Kevin’s phrases in particular:

“A life of faith is often lived ‘back and forth’ by believers and those who minister to them.” and…

What I do know is that an unconditionally loving presence soothes broken hearts, binds up wounds, and renews us in life. This is a gift we can all give, particularly to the suffering.”

Back and forth, that’s me. At times in my life, I have felt the presence of God directly. I have asked him for what I want and need, although perhaps he heard the longing of my soul even more than my words. And He answered. At other times, we have been estranged. And recently, we’ve been fighting.

Although it appears Dad is not going to rally – as he has time and time again – he is comfortable, and I am settling in to his new reality and mine.

As friend Jim says, “So glad you are ‘turning it over’.  Remember, the descent (which I prefer to call the path to ascent) is like going down steps of a stairs.  Sometimes one by one, and sometimes several.  Nothing you can do about this but be present and loving.  It is nature and his human body with his spirit trying to discard it so it can move forward.”

A prayer, then:

Help me, God, to be fully present

Help me to feel calm so that I can calm my Dad

Help me to radiate so much love that it warms him to his toes

Help me to support the others who love him on this awful journey

Help me to understand

Help me to love

Help me

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Ceding Control

Henry Campbell, Christmas morning 2012

My dear “Caregivers’ Social Club” buddy called yesterday after taking her husband to the hospital. Acutely aware of his advancing Alzheimer’s, she had felt something was wrong and then noticed a sudden downturn in strength. She learned that he has had a slow bleed in his brain for some time.

She was filled with recriminations for herself: How could she have missed it? How could she not have listened to her growing feeling that he was “off?” What if she had figured it out sooner?

We are the careful caregivers. The careful caregivers are observant, especially when it comes to the primary focus of our attentions. We aren’t doctors but we could play one on TV. We rack up successes: bladder infections we caught early, raspy noises that turned out to be pneumonia, disabilities we were able to reverse by advocating for physical therapy. We dance in front of disaster.

Then one day, we can’t dance fast enough.

It isn’t that we don’t want to, or haven’t tried, or aren’t good at it. We’re champions at it.

We butt up against the irrefutable reality of a chronic illness that ultimately goes only one direction: down.

Crossing the threshold of hospice represented a change in care for Dad, but it also signified a change for me. Though still vigilant, I stopped fighting and accepted where Dad’s journey is going. I am putting supportive care in place so that I can focus on loving him and listening to him rather than trying to fix everything.

I am not giving up, and I am not giving in. I am giving it over. With four visits from a hospice nurse in six days, I have a clinical partnership to help address symptoms as they arise. I am coming to terms with God’s role in all of this – though I still don’t understand how this difficult process of dying is a great plan. I am beginning to recognize that I am not in control of the speed or shape of this final journey. I am no longer fighting but I am not beaten.

Today I am praying for my dear friend as she faces a difficult decision about whether to approve surgery or not. She’s a careful (and loving) caregiver, and she wants to make it right.

To C: I am with you, my friend. There is no “right decision” here and it may not even be possible to discern the best decision. I wish I could say, “You’ll know what’s best.” But that’s one of those things people say that isn’t always true. Surgery or not, the future is a bitch. You will pick the least worst of the choices ahead of you. You will keep in mind what is kind, and ethical, and what your husband would want. This is an awful decision to face, one you never anticipated and one you could not have prevented, even as careful as you are. I love you. Call me if I can help.

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A Christmas Album, Shared with Dad

Rainy Christmas morning, shared memories with Dad at the breakfast table …

1953, my sister Midge’s last Christmas…

brucemidgesnowman1953

Midge got a dolly

Scott got a rifle

christmasdinner1953

1954… brother Dean arrived on the scene…

christmas1954

1956 in Kingston, Ontario… Nana in the foreground (I’m still in Mom, about 3 months along)

Christmas 1956

1959… I’m on the scene, 18 months old, in our house on Old Spring Road in Kensington, MD

Christmas 1959Christmas 1959

Christmas dinner 1959

Dad at the head 1959

Probably 1960… brother Dean and I show off our snowman

Christmas snowman 1960

Christmas dinner in Everett, 1966

Christmas dinner, 1966

And our last family home in University Place (Tacoma), 1969

Christmas morning 1969

Cassandra Eileen Campbell 1969

By the tree, 1969

Christmas 1971… and man, was it the 70s!

1971 - big snow year

Sandy dressed for snow

Christmas dinner 1971

1973… Dad surprised Mom with the diamond wedding ring she never had, the ring I wear today

A diamond ring for mom

Gathered round on a Christmas Day, 1985

Christmas day 1985

Maddie had so much fun hunting a Christmas tree with Nana and Papa, circa 1991

Maddie Christmas tree hunting

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Keeping Watch Through the Night, with Faith

Screen Shot 2012-12-24 at 7.38.35 AM

[Updated] I felt very dark in my faith two days ago, shaken, as I watched Dad’s discomfort while he prepares to transition from this world. And I wrote about it on this blog. But as I have said before, “Team Henry” doesn’t just support Dad. It supports me. And three of my most stalwart supporters responded with long and thoughtful emails. They meant a lot to me, so I am posting them here for the world to stumble across. I don’t think I’m at a place of peace and acceptance yet… maybe closer to Jim’s, “Well, dammit, Thy Will Be Done.”

My best and oldest friend, Ellen, the one who “saved me” with her friendship after we met by the lockers in 7th grade, sent this:

When Dad was dying, and he was in the hospital for the first time, and he was terribly paranoid, it was the first time I had ever seen my dad afraid, the first time he was not the strong one in our relationship. I was shocked that he could not access his faith to comfort him on some level. I remember trying to say the 23rd Psalm with him, pulling up the words from some deep memory: “Yea, though I walk through the shadow of death, thy rod and thy staff, they comfort me.” I didn’t see it working. Where was God?

After he died, I had a crisis of faith. What good is faith when it’s not there for you at the end? Where is God in those moments? Is there a God? I don’t know…

So, some things have become apparent to me, and maybe they are apparent to you already, but I would feel better trying to share them with you.

One realization I have had in the passing years is that the life cycle of everything includes decay of some kind. As a being nears its end of the cycle, parts of it start to fall apart, or wilt, or stop working. A plant changes how it looks. It goes to seed. It starts to turn brown. It’s leaves begin to fall off. It’s the same with people. We all wear out towards the end. It’s the way we are made.

Unfortunately, there does seem to be pain with this change. Maybe plants and trees and animals feel some pain as they change, too. Who knows? If living is about learning and growing and developing and becoming, then there is all of that in the dying process, I guess. Maybe the pain is a part of the change process helping us become whatever we must be for the transition.

I also have spoken to people and read things that have helped me to begin to have a smidge of understanding about what is going on physiologically, especially in our brains. Maybe the deterioration, or the pain, or whatever, makes it hard for us to access the prefrontal cortex, the seat of logic and reason, and where faith probably lives on some level. If so, it’s sad that we find it difficult to hold onto that which could give us strength and solace. Add in a potpourri of drugs, and it must be even harder to access faith from a logical or reasoning place.

We are all afraid of that unknown that dying is. I am afraid of the steps to dying, the pain I have watched others experience. The agitation. I am afraid of how my death will hurt those I love. Am I afraid of what happens after I die? I have friends who believe nothing happens, and then I know those who believe that if we have been good enough, we go to heaven. I don’t believe in hell.

That weekend that Mom died Lynn told me about Eben Alexander, a neurosurgeon who had a near death experience and wrote a book about it. The title is “Proof of Heaven,” and I have since read the book. I can’t say it was fabulous, or that it changed me or even answered all of my questions, but it does seem to be reassuring in the fact that there is a heaven of some kind, for all of us, that is it another dimension of our existence.

I do not want you to have to go through the process of losing your dad. I think this pain is very hard, and on the heels of losing Mom, I would not want anyone to have to go through this. I do not want you to have to carry around the sadness that I am carrying, even though we both know it will ease some as time passes and we become accustomed to carrying this weight. I know having these experiences with death, and losing those that are so much a part of us, it shapes us, adds dimension to us, affects our path forward.

I have cried out to God, too. I have had my faith rocked. I have been there. I would wish you some peace instead of angst. I would hold you, and cry out with you, and be your mother, and friend, and sister, if I could. I love you, dear one.

And my friend and mentor, Jim, offered insight and practical advice (in bullet form!), as always. (When he refers to “his” 34-year-old father, he is speaking of his role as a hospice chaplain in Kauai.) From Jim:

  • God is with us, actually inside each of us even when we do not sense it, and remove enough of our own clutter and misgivings and pain to be fully conscious of divine love inside us.
  • God doesn’t have a dossier on each of us that reads how long we will live, how we will deteriorate, whether you get cancer or I get Alzheimers. We are spiritual beings having a human experience, and that experience is governed by the natural order which is haphazard, and evolutionary, and our individual biological destiny gene defined more than most anything else. But the soul was, is, and shall be.
  • It’s perfectly natural for us to wonder how a loving God could allow this or that, but fairness as we want it to be does not come with free will and nature.
  • I have asked for most of my life, “Why did you set it up this way God?” In my dotage I have come to accept that I will get an answer…I will see and understand only when my spirit is set free from my human experience.  Meanwhile, I have to trust, have faith in God’s unconditional love, and try to be a loving other in the world. And to be perfectly comfortable in having a fit from time to time about why it is this way — why my 34 year old father of three kids is dying of brain cancer, or my lady in the Alzheimer’s unit is so very lost.  Very hard to accept that we are not in control; that we have to ultimately turn it over to the embrace of the Divine.  Meanwhile we care for each other in the fullest sense we know how, offering love and our own broken heartedness with the words of the Christ  “Thy will be Done.”  You can even go so far as to say, “Well dammit, Thy will Be Done.”
  • I am sure you understand the chaplain was asking the question so he could get a sense of where your Dad is both spiritually and religiously so he can approach your Dad accordingly.  What the chaplain’s job in this team is, is to do anything he can to help your Dad have peace of heart and peace of mind. Sometimes this is expressed in religious language; often not.  Your Dad does not have to have all the answers to all the questions right now. He needs heart connection because that ultimately answers the unanswerable questions and ensures him peace of heart and peace of mind so he can release. Whether he connects in any way to a traditional notion of God, he sure does to your Mom and he wants to go and be with her.  So for him, there is a there there, and he has his heart set on arriving.  Leaving is generally harder than entering, for each of us.
  • Turn all your mixed feelings over to Divine Love.  Literally, write each one on pieces of paper; put them all into a bowl or pot.  Take a lighter and burn the scraps safely and as you do, tell the Divine to take care of this messy stuff so you can take care of your Dad and your self.  Each moment now, even the most gritty ones is precious. HUGS

And this, from my beautiful cousin, Lynn:

You are in my heart during this time of unbearable agony.  The Love you are feeling is God. Everything even the agony is part of that love. This is your path now… with your father. You are meeting it. Valiantly. You are supported. You are not alone.  

Is it possible for you to lie beside your father, maybe holding his hand, without words, and breathe together with him…  when you breathe in,  breathe in Love, when you breathe out surrender all your feelings to God/Universe, just let everything go.  Continue to breathe with your father’s breath and in that stillness you will feel God.   I love you, Lynn

[Updated] And more from beloved Jim:

Sometimes at the ICU or Emergency rooms, I encounter folks who are facing the worse — a loss that they wish were not so.  While friends and loved ones gather, no one can truly cut through the individual despairing that is happening.  Yet the presence of others is a comfort because it reminds those despairing and bracing for the worse that they are not alone completely, although the comfort does not abate the broken heart.

The same with God when we cry out for very understandable reasons, “Why are you…make it better…make it stop!”

Yet the presence of the Comforter is there deep inside whether we recognize it or not.  Not unlike what the Christ felt on the Cross when he said, “My God, My God, why has thou forsaken me” — that profound sense of broken heartedness that comes to us humans.  Yet God was there, and cut through what seemed like an ending and made it a beginning.

Turn it all over to God — see if you can make your cries personal — for me I have to talk to Christ Jesus, or the Holy Mother, or the Holy Spirit whom I equate with the female aspect of God.  I just ask them to be present with my loved one, to help them ease across that bridge over the river of life, to hold there hand in a way I no longer can, and open their inner eyes to what Steve Jobs saw at the moment of his death and exclaimed, “Oh WOW; Oh WOW”

Death will be your Dad’s final victory, Betsy.  HUGS

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Remembering Christmasses Past

christmas eve

Growing up, Christmas was about much more than the presents, decorations or food. Certainly we had all of the trappings; I remember gently hanging silver foil “icicles” over the branches of our tree, and helping Mom to place on the mantle her collection of angel figurines on a bed of “angel hair” lit from below. But at its heart, Christmas was a religious observation.

My Mom was a devout Episcopalian. We went to church and Sunday school every Sunday, and if we were sick, Mom read the week’s lessons and prayer service at home. And Christmas Eve meant attending midnight mass, which actually used to be held at midnight. When I was very young, we attended the Washington National Cathedral (I think). I drifted to strains of “Silent Night,” snuggled against Mom’s silky seal skin fur coat, surrounded by votive candles and swags of fresh greens. That distant memory of light, music, smell and touch is about as close to heaven as I can imagine.

Through the years, the scene was repeated — at St. Mark’s in Seattle, St. Patrick’s in Eastmont (near Everett) and St. Andrew’s in Tacoma.

This is a different kind of Christmas Eve. My Dad and I will be at my house, but he is not strong enough to join in the festivities at my in-laws. Much less attend Christmas Eve service. My advisor Jim reminds me, “Each moment now, even the most gritty one, is precious.”

Mom, tonight you are closer to me than ever, though you have been gone for almost 14 years. Keep the candles burning for Dad. He is trying to find you.

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