cancer


Sarah said I have a type. And then I as we hugged in pain from the news, Steve said the same thing, “you have a type.”

I guess by that they meant that I loved sharing my life with a partner who also shared my curiousity, creative sense of play and exploration, and whose work complemented my own as we supported each other’s pursuits. The implication, however, was that they often worked with materials that were toxic, or shared the habits of their generation such as heavy smoking and drinking, suffering the consequences of the indiscretions of youthful hubris.

The sad part is that there are no guarantees on longevity. None of us gets an assurance on how long we have on this earth, on how much time we have to spend with our loved ones. And no amount of love, no matter how deep, will keep them here on this earth if their fate is meant to be somewhere else.

[N]o amount of love, no matter how deep, will keep them here on this earth if their fate is meant to be somewhere else.

Not Again

Steve had been feeling sick since late September and was finally able to get a telehealth doctor’s visit in late October. That lead to an immediate trip to the ER due to pleural effusion and three days in the hospital. More follow-up doctor’s visits and then another visit to the ER and a week in the hospital, collapsed lung, more thoracentesis, CT scans, pathologies, and finally a confirmed diagnosis – stage IV non-small cell lung cancer adenocarcinoma. Followed by biopsies, colonoscopy/endoscopy, and PET-CT and finally a meeting with the oncologist.

Treatment would be palliative to keep the cancer from spreading further. Depending on the analysis of tissue from the biopsy, it would include immunotherapy, or a combination of immunotherapy and chemotherapy. Prognosis was dependent on the outcome of that treatment – months or years.

In dark times like this, sometimes a morbid sense of humor results. “I thought I had a 10-year warranty on our marriage!” I said to Steven as we shared a quiet celebration of our 8th anniversary this week. “And I intended to renew it with another 10-year extended warranty!” Geez.

Preparing for the holidays

This past weekend Steve was able to fit in some moments of normalcy between naps and directing from his stressless recliner as visiting family members helped with chores that culminated in decorating a much smaller Christmas tree that I’d ordered. At half the size of the 12′ tree we’ve had the past few years, the smaller 6-1/2 footer allowed me to manage its assembly and grandkids to help with decorations without a ladder. The job was done in a matter of hours instead of days. Although not the grand tree we usually had, it put a smile on Steve’s face and that’s what mattered to me most.

The new 6-1/2 ft tree was decorated with help from family including grandchildren. It replaced the 12-1/2 ft tree that normally fills the room but that takes two adults on ladders to do. This smaller tree was put up and decorated in a day and still managed very nicely to make everyone smile with gratitude and appreciation.

And an anniversary

When we first started dating, he’d show up at my door with two roses in his hand and a silly grin on his face. It always made me smile in return and lightened my heart. Steve gives the best hugs and so it has been my goal to return those hugs and their healing power as much as I can and he’s willing to accept them as his body fights back.

Copper orange roses for our 8th anniversary.

So on our 8th anniversary this week, I brought him a dozen copper orange roses, a box of chocolates, and a Hallmark card. These were what he would have brought me but driving hasn’t been his option for the last two months. So I did it for both of us. His lip quivered a bit fighting back tears as he read the card and saw the roses. I split them up – 8 in one vase for the years we’ve been together, and another 4 for blessings going forward.

Dinner and The Voice

We sit here and watch the finale performances for this season’s The Voice. We’re in the new bed I bought, a split adjustable king bed that would allow Steve to raise and lower his back and legs to help him breath and get a bit more comfortable. 

This afternoon, while I was in online meetings and student reviews in my home office, Steve was riding the tractor down the hillside out back with John following so they could hook up the plow blade for the inevitable snowfall we anticipate for the winter, yet haven’t seen much of yet.

I was part horrified when I learned of his joyriding out back while holding back my critique as he looked at me painfully while trying to eat his dinner. He’d been asking me to make this dish he saw on Facebook – baked honey sesame chicken which was basically a sweet and sour chicken – and so I made it. But that pained look told me he was struggling to eat it – not because he didn’t like the taste, but because as soon as he starts to eat, his stomach says “no more.” 

“Did you feel almost normal when you were riding around on the tractor?”
“Yes, almost.”
“Then it was worth it.”

“How have you been feeling?” I asked. “Crappy all over,” he replied. “It’ll be okay,” I replied. But he broke down. He didn’t like this crappy feeling, he said between tears. “Did you feel almost normal when you were riding around on the tractor?” I asked him, touching his arm gently. “Yes, almost,” came the reply between the slowing sobs. “Then it was worth it,” I whispered.

But deep inside, I wondered how many more of these “close to normal” moments there would be in his future. 

Silken Windhounds, Louie (white and tan) and Ralph (dark grey and black) curl up beside Steve as he watches the singers on The Voice between short naps.

As I write this, Steve munches on some Lays Waves potato chips, craved from the power of suggestion as The Voice’s Blake Shelton did a shtick where he steals the Voice award by swapping the award sitting on a pedestal rigged with an alarm with a bag of Pringles. Steve looks happy. And if I didn’t know better, I’d say all was normal as both Ralph and Louie are curled up with their heads against his side. How I long for this moment of normalcy to last.

Warning: This post includes a reference to my own political views. If any criticism of the recently removed occupant of the White House, aka #45, will upset you, please go elsewhere for your reading. That is, unless you are truly interested in learning about the pain this has caused within families and would like to try and heal that rift. Thank you. – MJF

I often wonder how our conversations would have gone if my Dad were here to have seen how the past 10 months have panned out. We had come to agree not to speak politics, especially at the dinner table. I still remember the day more than four years ago when he asked me why I was screaming when he kept dismissing my concerns about then candidate tRump. I told Dad it was because he terrified me. I could feel the evil he, tRump, was projecting, the cold heartless disregard for others, the narcissistic boasting of lies that his speech pattern revealed, unable to string together a coherent thought while weaving in complete and utter nonsense soaked up by his base who somehow thought being tough meant beating up the opposition. All critical thinking having been abdicated in exchange for a toxic masculinity in what became the cult of the schoolyard bully of tRump.

Mom and Dad in happier healthier times. Summer 2010 visiting the Detroit Zoo as part of a family celebration of their 50th Anniversary.

I remember tearfully and loudly exclaiming how could Dad even consider following him after the toxic expressions of anti-semitism, the admiration of dictators and despots, the complete disregard for human decency and process. My dad dismissively waived off my concerns saying it was just his candidate being boastful, that it would never get that bad. And maybe, I hoped do, too. That the checks and balances of government, and that the fourth estate would be enough. But then came COVID19. And he became so adept at the flippant lies that the cultish base he dog-whistled to had finally been fully brainwashed. And the evil we saw spread in its rabid attack on democracy had reached its peak.

Dad passed away May 1st, 2020 after a brief and ugly battle with cancer, and full of the awful indignities that go with it. And I did my daughterly duties and cared for him, cleaning him up, feeding and bathing him when his body turned against him. As his body began to degrade around him, I remember Dad asking me “What happens after you die?” And it crushed me. Raised Jewish, there is no hell or purgatory. But there is guilt. I chose not to add to his pain. Instead, I asked him questions that were meant to help him reflect and guide him to his own conclusions. He was in a room filled with books that explored this very thing…my mother, who had passed away nearly four years earlier, was a voracious reader of all things spiritual. Yet he had never picked up a single one of these books except to place them on the shelf. So, after a few bits of back and forth that didn’t seem to satisfy him, I simply responded “You’ll be with mom once again.”

The writer of the article linked below is hoping to find his lost (to the cult of tRump) parents long before they die. I hope he is successful.

https://qr.ae/pNlwHD


When a terrible disease ravages someone you love, the mourning process begins long before they finally pass on. Kübler-Ross (1969), in her study on death and dying, described five stages of grief including denial, anger, bargaining, depression, and acceptance. But Kübler-Ross was initially focusing on those who were dying, and not so much on those who were dealing with personal loss of any great significance, which she later came to recognize.

These stages are not linear, either, and can occur in any order, if at all. Women tend to experience all five stages more than men. They can be cyclical, too, with two or more occurring in an almost extreme emotional roller coaster. For both the dying and the loved one, getting to the point of acceptance does not always happen at the same time. The dying often reaches the stage of acceptance before their loved ones. But if and when both reach the point of acceptance, where communication and reflection can be experienced, a more dignified death can be found.

I’d add a couple of additional stages, or at least notable elements, to the stages of pre (and post) grieving. That includes fighting to maintain control of the details in their lives. The opposite is the disruptive feeling of vulnerability when control is lost which can lead to related stages of despair and anger.

Another related stage involves trying to make order in one’s life. Especially when the world around you seems to be in chaos, small efforts to create order can take on an outsized importance. Cleaning out cupboards, putting away old records, sorting through old photos, are just a few example of how the person facing loss may attempt to build a sense of order in a life that seems otherwise out of control.

Recently, I heard this statement made by someone who is facing the inevitable loss of his longtime spouse who is in the late stages of Alzheimer’s disease. I’ve paraphrased it per my own cloudy memory.

I feel like I’m in a carnival outhouse sitting out in a field, and the circus is packing up to leave without me.

While he didn’t elaborate, he was trying to express his feelings regarding the situation he found himself in now. I’ve been thinking about this and cannot help but connect it to my own experiences and ruminations.

First and foremost, there is the overwhelming feeling of vulnerability, of literally having your pants down in a crisis, or a formidable change that is going on around you. You’re stuck. It is hard to move forward without first finishing the primary business at hand. Panic sets in and it is hard to make decisions. Yet you’re also worried about being left behind, and by the act of moving to a new location – mentally, emotionally, and physically – and the unknown that comes with that. But even more so, it is a fear of being left behind by the ominously fast progression of a disease that robs you of the one you love, again mentally, emotionally, and physically.

The carnival/circus represents fetes of apparent magic, gravity-defying acts, seemingly impossible, often nonsensical, frightening in their dangerous distortions of human entertainment, and the funhouse mirrors that twist and distort our vision of reality.

The world around you no longer makes sense and you feel vulnerable, scared, afraid of being left behind, fearing for your loved one and a future you cannot envision without them. It literally scares the shit out of you… And yet you know you have to keep moving to survive. Because that’s your role here.

Of course, the circus could also represent your loved one, the person who was the highlight of your life, with which you shared the literal stage of life, it’s bright lights, music, the comedy and drama of a life fully shared. Either way, it all seems so unfair.

Anger rushes forward. Anger at what fate has thrown you, your loved one, the cruelty of the disease. There is no preferred or better way to die of a disease. Cancer kills the body slowly while eating away at the person. Alzheimers eats away the person while leaving the body to deteriorate at a slower rate, until the parts of the brain that operate the body begin to lose their synaptic connections.

Either way, these diseases are cruel – to the loved one who suffers them, and to the lover who must endure the pain of watching, of frustrating efforts to try and overcome the diseases’ manifestations, the cruel teases of normalcy and strength that suddenly appear and then, as a wisp in the winds, they disappear to the mists that hid the light in their eyes.

Whether you want to or not, you are, and will be… the survivor. The one who will carry the stories forward until they can be shared fully with a new generation. You will be needed by others who will benefit from your wisdom, humor, insights borne of long experience. The fates have determined that your place is here…in this world…where you are still needed.

The journey along side the dying of a loved one is dark and painful. But it also has its moments to be cherished. The fleeting glimpse of a smile, a flash of humor, the small gestures that show you are still connected to this loved one. You have been chosen for the honor of being beside them on this journey to the end of this life. You, however, will stay behind, their partner only until the gates of passage open to the other side. Until death do you part.

It sucks. It hurts so badly, the pain is physical, palpable. Breath… breath… You are still alive. And they will always be with you, and waiting on the other side to greet you when your turn comes, naturally, when the fates determine it to be so. In the meantime, treasure each moment with your loved one as a gift. Soon enough, there will be only memories that you will hold onto tightly, then share with others when the right time comes.

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Sweet Pea, our nearly 15 yr old Borzoi, in a glamour shot from her healthier days.

January 8, 2016, 11:11 pm

Sweet Pea died today. Steve and I took her to the veterinarian this morning after making a difficult choice. She had not been well for awhile, but had begun declining more rapidly in the last month or so. She’d grown more frail, wasn’t eating as much, or sometimes not at all, and could barely make it up and down the stairs. Lenny, in the meantime, had begun to show his own distress by whining and barking to get Sweet Pea, or one of us out of bed to help her go outside, to eat, or whatever was going through his little puppy sized brain. He was driving us all crazy by doing this at all hours of the night. We were growing impatient, exhausted, and frustrated. We knew what it was about. But neither one of us wanted to make the decision. Sweet Pea would tell us, we would say to each other. She would let us know when the time was right.

But sometimes we don’t want to pay attention, to make the difficult choices. Sometimes, we think, that if we just ignore it, life will go on without having to face the painful moment of truth. I know that’s bullshit. I have seen it up close and personal. But it doesn’t make me immune from the desire to shield myself from the reality of her – or anyone else’s – suffering. It hurts too much to acknowledge it.

Last night, after two nights of sleeping down on the coach through the night, Sweet Pea decided she wanted to join us…one more time. Before this, the trek up the stairs would be wobbly but possible. It was the trek down the stairs that scared us all. Her legs barely held her up, and her unsteadiness made it a nerve racking and time consuming experience to get her back down the stairs. So we were grateful that she had not attempted it for the previous two nights. But not tonight.

The spirits had been talking all evening… I’d been seeing 11’s for most of the day. Michael sent me a photo that showed 5:11 in the LED clock on the TV set top sitting on Keith’s cherry cabinet he’d made for them in Needham. And again I’d look up to see 11 elsewhere…clocks, emails, texts. Something was up.

So when Michael texted me again at 9:11 pm, I thought it was simply an acknowledgement of the pattern I’d shared with him. But not long after, I heard shuffling and then a bang, then whimpers in the hallway. I jumped out of bed to see what happened. Sweet Pea had fallen at the top of the stairs, collapsing in front of the bathroom and had her nail caught under the doorframe molding. With some difficulty, I freed her from the doorframe and coaxed her up so she could make it to the bedroom. I went back down and fetched her pillow bed that I’d brought down before to convince her to stay down there. She looked forlornly in my direction, her cataract cloudy eyes trying to see me in the fog. This might be it, I thought. Maybe she’ll die in her sleep like Gemorra did so many years ago.

But the night passed and Lenny’s constant whimpering reminded us of the grim decision we would have to make once daylight came. She could barely stand, let alone make it down the stairs. At first I tried, but gave up, so Steven took on the challenge, pleading with her to try, telling her he’d catch her if she started to fall. She made it and went outside to pee, retaining the last bit of dignity the old girl had left. She even ate a little when she came back in, constantly escorted by the ever whimpering Lenny. But then she made her way to the couch, using her last bit of energy to climb up there. Her breathing was labored and I could see the time had come. I couldn’t make her suffer another day.

She passed peacefully in the vets office. They put out a white blanket for her to lie upon, though she missed it when she reclined after her anesthesia. At one point I thought the anesthesia had done the job, without the final injection. But she was breathing still, though so shallow it was hardly visible. Then the shot in her leg, and within moments she was gone… Gone to the other side, relieved of her pain, greeted happily by a healthy and goofy big Stanley. Given a warm and social greeting by her old master, Keith. I picture them enjoying some romping and fetching games followed by a good round of coach-potatoing together like they did all the time before.

Steven and I gave our last tearful goodbyes…he was really fond of her, she reminded him of several other big white dogs he’d had as furry companions in his life before me. And, with a trim of her tail feathers and an imprint from her paw as a memorial from the vet, we left to toast Sweet Pea over bacon and eggs and…toast.

Although my neighbor referred to her as "Satan's Spawn," Sweet Pea did have her playful side.

Although my neighbor referred to her as “Satan’s Spawn,” Sweet Pea did have her playful side.

Later, after letting my grown daughters know about her passing, I posted a photo and the news on Facebook. I felt somewhat awkward about the outpouring of sympathy. Yes, Sweet Pea was my longest living Borzoi, having made it nearly 15 years. Yes, she had helped me through some difficult life transitions. Yes, she had been “my” dog and furry companion. And yes…even better, she had befriended Steven…a sure sign that he was the good guy I thought him to be. I even imagined Keith sending her back from the cemetery that hot summer’s weekend over 2 years ago when she got loose for 30 hours and nearly died in the 100 degree heat so that she could help me to decide on the merits of Steven’s character. She did not share her inner sweetness with just anyone, and was especially particular when it came to men. There have been only two men I knew her to show deep affection for – Keith and Steven. I guess she knew who were the right men to be trusted in my life.

Stanley (left), Keith (laying down across the couch), and Sweet Pea (on Keith's chest)....aka the Keith sandwich on Russian rye.

Stanley (left), Keith (laying down across the couch), and Sweet Pea (on Keith’s chest)….aka the Keith sandwich on Russian rye.

In the photo above: It’s hard to believe when I look at this picture..my heart both sinks in sadness, yet breaths hope, too. Everyone is gone from this earth but hopefully reunited on the other side. Stanley on Mother’s Day 2011, Keith on 9/1/2012, and Sweet Pea on 1/8/2016. Even the couch – brought back from Fiji – is gone, having been turned over to the dogs, and later dismantled, the leather salvaged for me to use in making books. Maybe I should make some more…

September 8, 2014

So what does grief look like after 2 years? It is a full moon tonight as I contemplate this question.

Everyone grieves differently. For me, grief is a different creature than it was last year, or even the year before. For me, it lurks deep in the crevasses of my emotions, boiling in the depths far below the view of the outsider, or even – at times – myself. Yet at the right moment it bubbles up like a volcano, racking my body with sobs, an emotional sink hole in an otherwise softly curvy road in life’s journey.

A week ago yesterday marked the second anniversary of Keith’s passing. The actual day of the anniversary, Sunday, September 1, 2014, passed with little fanfare, a relief that the day was finally here and soon to be gone. I took part in the “Ice Bucket Challenge” where I wrote two checks – one for Keith’s scholarship, and one for the American Cancer Society – and then prepared a Tequila Sunrise to toast in Keith’s memory, followed by dumping the bowl of ice over my head, all recorded for sharing on FaceBook, as is the custom for this challenge. It was a cathartic ending to a difficult, yet sometimes fulfilling, week.
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Keeping a Steady Head Despite the Anticipation
For me, it was the anticipation of the anniversary date, brought on by the pattern of activities that occur annually at this time of year, that made it more difficult to maintain an even emotional keel during the week before. And some changes in my work made this passage even more pronounced.

This summer I was offered a new opportunity at the college, to serve as Faculty Director for the Center for Teaching and Learning where I could test out my newly minted doctoral studies in community college leadership. The opportunity marked the end of my reign as Program Coordinator in Graphic Design, a program I created upon my arrival from Fiji back in 1997 and had guided to success ever since. To step down from that position, while still maintaining my teaching position (and teaching just one class) was a major shift both mentally and emotionally. It meant turning over the reigns to one who I had helped mentor to take over. But I never thought I would see such an opportunity so soon. I was truly excited by this new endeavor. But it also meant stepping further away from a life and identity I had built with Keith.

That is part of the crux of this. It is all about Time, with a capital “T.” Time, in this case, is like a long winding road that sometimes loops around on itself. My life with Keith now lies further back on this road. And each new step I take building a new life takes me further and further away from him and the journey we shared together. As sad as that sounds, the reality is that he is not here, physically at least, traveling on this road with me now, and I’ve come to terms with that. There are others who are on this journey with me, my children who still connect me to Keith. Many dear friends and extended family members. And then there is one especially sweet and gentle hillbilly of an artist who has joined me on this road I travel now.

It is all about Time, with a capital “T.” Time, in this case, is like a long winding road that sometimes loops around on itself.

But each year, the summer winds down, and the last milestones that passed with Keith in his last weeks and days in that Summer of 2012 march across my calendar again – his birthday, our anniversary, and then that last week…

On the college calendar, all faculty come back from summer for Welcome Back week. The last two weeks before classes start are among the busiest for everyone on campus, but especially in the office of my new job.

Yet so marked are these late summer dates in my mind, that I can’t help but count them down. Friday before Welcome Back week… when the hospice nurse urged me to try and go to my doctoral class meeting in Grand Rapids after we had spent the morning talking about installing a hospital bed in our bedroom so that Keith would no longer have to climb the stairs. Keith had expressed his concern to the hospice nurse about being too much of a burden on me while I attempted to go back to teaching in Fall. For me, it was an admission of my failure, that the end was near for Keith, that I could not save him. It broke me emotionally and I cried all the way to Grand Rapids and back, even screaming at the top of my lungs in the cocoon of my car.

Then there was the following Wednesday afternoon when I attempted to try and pretend I was doing something normal by going to the Faculty picnic. I lasted only an hour, leaving after the VP told me that she didn’t expect me to be there, to go home to be with Keith. She was right. I couldn’t face all the happy people excitedly telling stories of their summer adventures. This year’s Welcome Back festivities brought all those memories back to me again, especially that picnic. But this time, I mostly enjoyed seeing all the smiling faces.

It was a good day. A mother-daughter bonding day, a day when we didn’t need to spend lots of money to enjoy each other’s company.

Then there was the memory of the days that followed – Thursday being told to prepare for Keith’s imminent passage, Friday spending the day between the bedside vigil in the dark room where Keith lay, and spare moments with my brother and sister-in-law who had come to help rescue me and the girls from well-intentioned visitors. And then there was that final day… sending my youngest grown daughter upstairs to wake her sister to give Keith his meds. Feeling the urge to follow her moments later… walking into the room in time to see her as she said “I think I just saw Dad take his last breath.”

My younger daughter and I got together on Sunday, the day before the 2nd anniversary. It was a good day. A mother-daughter bonding day, a day when we didn’t need to spend lots of money to enjoy each other’s company. We enjoyed looking in antique shops, eating a cheap but delicious BeBimBop at Cosmos, and wandering Ann Arbor chatting away about everything and anything.

I know that when Keith died, she was worried about losing her mother, too, as I made my own way through grief. Her older sister had her new husband to lean on. My younger daughter’s concern seemed to grew when I met my new friend Steven. It has been a long winding road, but a certain balance has begun to evolve. I am seeing the way forward to build a new life with a new partner and new job, balanced with the life that existed before and which provides the foundation for my future, and the evolving dreams.

Sometimes the Winding Road Bends Around on Itself

But it’s not without tears. That winding road of Time, when the events flip back over upon themselves, repeating their position on the calendar, mock my grief which had sunk deep out of sight into those crevasses. Then, occasionally, it explodes as it did this year in a sobbing release. It occurred this time on that Wednesday before the semester started, the same day as that faculty picnic. I had tried to remain stoic and put on a happy face throughout the week, and most of the time I actually felt happy! The new job was starting and I was immersing myself in learning as much as I could about its operations and mission.

But I could feel the cracks occasionally fissuring away at my strength. Steven was trying to help. He had arranged to get my car serviced a week before at his son’s shop in Gladwin. And now he was even getting new tires put on after we discovered the cause of a slow leak in one of the tires, a metal screw that probably came from the roofers at Perry Road.

In discussing the cost of the tires, I had pulled out the papers from nearly two years ago in October 2012 when I’d brought the car to a company Keith had used before to get two new tires. Back then, the kids had been concerned saying my rear tires were far too worn to be safe and urged me to go. It was just 5 weeks after Keith’s passing and I went to the tire place thinking it should be a straightforward affair. It was… as long as I didn’t pay attention to the charges. Looking at the receipt now nearly two years later, Steve and I discovered I had been charged for two overlapping warranties amounting to nearly $140 in extra charges.

On this night, after getting the exact same tires put on for nearly $230 less, Steven was angry at the original tire company that he believed had taken advantage of me. Extending the conversation, he was equally impatient that the roofers had not taken better care to clean up the nails and debris from their installation at Perry Road. Yet another item seemed to irritate him that wasn’t done more carefully at Perry Road, too, and he expressed a frustration that some people may have taken advantage of my more vulnerable position.

…Keith had been my protector, running interference and taking care of those things to his satisfaction while allowing me to focus on other things that helped make our lives run smoothly…

But the reality was that back then… during those six months after Keith’s passing, I did not have the strength to push for details. I just wanted things done. And if it caused too much of a drain on my energy to try and resolve an issue, I backed off. I had learned that life was, indeed, too short to waste one’s energy on arguing. And the reality was also that, as a woman, I was indeed taken advantage of by certain vendors, especially the tire company. It’s a common theme experienced by many women.

Even more than that, though, was the fact that Keith had been my protector, running interference and taking care of those things to his satisfaction while allowing me to focus on other things that helped make our lives run smoothly, things that I was more expert in. He would take care of the car and tires. He would have made sure that the roof, or the drain tile, or the clean-up was done satisfactorily. Steven, though well intentioned in expressing his dissatisfaction over these issues, feeling they were an affront to my wellbeing, had succeeded in reminding me how vulnerable I had been without Keith.

It reminded me how much Keith had protected and cared for me in these situations… and, yes, how Keith had protected me from at least one unscrupulous “friend.” Steve’s frustration reminded me how far away from Keith that time’s winding road had carried me, only to flip around and hit a moment of painful memories… And then the dam finally broke on the wall of tears that I’d held back for the previous week. A gentle embrace held me while I sobbed until I had no more tears left. And then life went onward and the grief receded to the deep crevasses again.

Life is good. Life is blessed. Next month I should be defending my dissertation, another milestone on the winding road of this ethereal journey of dreams.

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Above: My brother is met by a White Heron who hung around on the beach near Sarasota, Florida during our visit in May 2014. I have often thought that the Heron, whether White or Blue, was Keith’s animus.

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