Sibling fight!

Why is it that food fights are fun and email fights are not?

I was quite smug last night when I told a friend that I thought my brothers and I were really communicating effectively with one another. She had just returned from 10 days of overseeing her mother’s recovery from pneumonia and surgery, during which she was repeatedly second-guessed by her out-of-state sister.

Then I got an email from one of my brothers today, who reacted to an email sent by another brother. I won’t get into the details but I’ll share the zinger with which he ended his message: “…have the two younger sib’s simply cut out the two older sib’s from having a voice?”

I thought we were past this.

But the truth is that it is very, very hard for people who act like grownups in most situations to behave that way when something triggers half-buried resentment. We are all suddenly six.

There are a lot of “perhapses” that come into my mind. Perhaps the brother who sent the original email should have called instead of sending this particular message by email. Perhaps the brother who seethed over the email should have picked up the phone and expressed his concern to the sender, or to me (since I was supposedly colluding in the decision in question). We could have done better.

When we are stressed, as we are in no small part by Dad’s deteriorating health, we are reduced to the ugliest side of our personalities and temperaments.

It’s hard to keep one’s eye on the real issues here: how to make sure that Dad feels loved and safe, and how to preserve and perhaps strengthen our sibling relationships for the time when Dad is no longer there to bind us.

Right now I’m working on that last part.

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My husband, the unsung hero

(Before you read this post, stop remembering the Andy Kaufman version of the Mighty Mouse theme song. I mean it. Stop. It. Right. Now.)

My husband and I have always had a 50-50 arrangement, if you average it over time. Statistical nerd that I am, I know that the average can mask a labile distribution of responsibility for household and familial duties. Sometimes it’s 75-25, sometimes 25-75, and occasionally even 90-10 (as in the time when we were preparing to move and my husband managed to break his knee on a guys’ trip).

Every time someone says to me that I’m an angel for taking care of my Dad, I remember that the guy holding my halo in place is my husband.

When I stop to take inventory, I realize that it’s a whole bunch of little things he does that accumulate to make a difference. When he comes home from work every evening, he asks if my Dad has his glass of wine. While I scramble to do my “magic” in the kitchen (anyone who knows me knows this is not a joyful experience), he’s contributing the comfortable routine of my Dad’s life. Dad used to have a couple of scotch and waters before dinner that over the years morphed into a glass of red wine. Dad’s almost lost his taste for wine at all, but that pre-dinner libation is a nicety in the not-so-nice world of advanced age.

Sometimes my husband “covers” for me if I have a morning meeting or am entertaining a couple of girlfriends. I’ve never detected a moment of resentment if I ask him to fix Dad’s breakfast or put his dinner on the table.

Taking care of Dad severely limits our flexibility to accept invitations from friends or go out of town for the weekend, things my extrovert husband would enjoy. But he never complains. Ever. I’ve never detected resentment, though he would be well within his rights to feel some.

And he shares his space often, as family members come to visit my Dad.

Perhaps most significantly, he doesn’t try to fix my problems when I feel down or a little worn out. Earlier in our marriage, we learned that my sharing a problem led to him trying to solve it, when sometimes all I wanted was the opportunity to vent. He sits with me and empathizes. I feel held inside even if we are not touching outside.

Next time your mental jukebox plays, “Here I am to save the day!” remember the great men who are out there standing behind the “angels” like me.

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What makes caregiving so hard?

I thought I knew what hard is. Hard was being nine months pregnant, diagnosed with pregnancy induced hypertension (ankles bloated to the exploding point), and getting ready to present the first full-scale consumer awareness study to the hospital system execs for whom I worked. Hard was working full-time, while trying to be a good mother of  a one-year-old and  studying for my M.B.A. during nap time and at night. Hard was working a full day with two hours of commute time on either end.

Being responsible for someone who needs your help and care, it seems to me, isn’t exactly training for the Olympics. But it can feel that way sometimes.

My Dad doesn’t need assistance with the basics. He dresses himself, puts his hearing aids in, eats independently, and has the toileting thing pretty much under control. My caregiving gig is a lot easier than many.

I think what’s hardest for me is the emotional burden – dodging obstacles, holding others up who worry from afar, and coping with the no-end-in-sightedness. I am constantly anticipating problems and talking steps to circumvent them, for example, clearing my Dad’s path of trip hazards and pre-emptively clearing dishes so that my he will not take it upon himself to do so, toodling from the breakfast table to the counter with dishes in both hands (and thus without either cane or walker). When a medication stops working and needs to be adjusted,  I run the gauntlet of conversations with doctors and care staff, trying to get accurate information about the situation (clarifying, clarifying, confirming) and calling and finally badgering someone into changing medical orders.

Dad is unstable enough that my brothers now worry from afar. I understand their vigilance, having felt just the same way when home in California during my mother’s four month hospice period in 1999. When I report setbacks, which have been more frequent during the last month, I get messages from my brothers asking if this is a crisis and whether they should book flights. I know their messages are code for, “Do you think he could die?” I try to reassure them. Understanding that you are going to lose someone is to begin grieving. I know they hurt. [Brothers who read this: this is not a complaint. I really appreciate your increased vigilance.]

We’re not there yet. Several times of late I’ve been asked what I will do when “this period is over” (code for “when Dad is dead”). I don’t know. I can’t plan. If I get my head in the future it will be even harder to manage the day-to-day. So I am actively avoiding long term planning.

Right now my whole world is the next two weeks, in which I hope we will stabilize Dad’s underlying congestive heart failure condition so that his weight swings and shortness of breath resolve, at least until the next unsettled period.

This shouldn’t be that hard. But some days it is. Fortunately, today is not one of them. So far.

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Turn off, brain, and let me go the f* to sleep!

The lovely view from where I didn’t sleep

Just when I feel overwhelmed by my Dad’s declining health, it seems that the sleep gods conspire against me.

My anxiety – and accompanying sense of hyper-vigilance – built to a pitch over the weekend, even while my husband and I attempted to relax in Northern California’s playtime paradise of Lake Tahoe.

Over the past month, the medication that had been working so well to control the symptoms of Dad’s long-term congestive heart failure sputtered and stalled in its effectiveness. His weight dropped from 204 lbs. to 188.5 over three weeks, and then, when we cut back the dosage, spiked back up to 198 in less than a week.

My brother, who came into town to “spell” me for my anniversary trip, called me Saturday night. His voice was choked with emotion as he explained that Dad looked as weak and worn out as he’d seen him. When he asked Dad how he was doing, Dad replied, “I don’t think I can pull through this…”

That night, I left my cell phone on in case my brother needed to reach me in an emergency. Then starting at 1:30 a.m. that night, I started this exchange via text with my young adult son, who was finishing up packing for a 5 day cruise the next day. What’s funny about this is that I just couldn’t let go. I felt utterly driven to ensure that my son did not – gasp! – make a mistake packing:

Him: Do I really need a carryon? I was just gonna keep it simple with a rollaboard.

Me: It if fits that’s fine

Him: Fits what? I was gonna check it

Me: Rollaboards can go in the overhead bin. Then it can’t get lost. If you are going on a cruise your bag will never catch up if it gets lost. When you connect there is more of a chance of it not getting on the 2nd plane. It’s up to you but it’s safer

Me: ‘nite

Him: I have the red one, will that fit? [The red rolling bag is ginormous.]

Me: No. It has to be one of the small black ones. Sounds like you don’t have a choice unless you have a duffel that qualifies as a carry on. Southwest is pretty good about getting bags there so you’ll probably be fine. Don’t check your computer – keep it with you.

Me (again): The carry on can’t be longer than 24″ [Note: I have now gone on SWA via my cell phone to actually check the limitations.]

Me (again): Be careful not to oversleep

Me (yet again): Can I go back to sleep now?

Him: Yeah, sorry, I’m just gonna check it

Me: OK but keep your computer with you. Put your name and home address on a piece of paper inside the checked bag. Make sure it has a luggage tag too or put a paper one on it at the airport. Travel safely.

Me (again): Got your passport? Keep that with u too

Him (now at 2:02 a.m.): Found a duffel, using it instead & I’m not bringing a computer

Me: OK but if they make u check it remember to keep your passport with you, preferably in something by your feet. Passports can get stolen out of backpacks in bins. Students get targeted by thieves.

Me (finally): OK goodnight. I love you. Have fun.

Him: Gnight mom! Love you too & I’m sure we will

You can guess how the night went after that. I didn’t fall gently back into slumber.

On Monday, I made a record 20 phone calls to my father’s doctor, to friends and family who visited my father at his assisted living apartment, and to family to report in. At the time, Todd and I were attempting to complete a 7 mile hike.

That night, I was awake from 3 a.m. to 5:45 a.m. I’d drift into sleep and pop right back out of it.

I know I am not alone. Over the weekend, a dear friend lost someone she’d known and loved since childhood. She texted me last night, “Just took pill… haven’t slept in five days.” My brother who had been upset over the weekend texted me Tuesday, “I slept finally last night, though I had a 90 minute break in the middle.” Another close friend posted on Facebook: “Being the ‘sandwich’ generation and responsible for taking care of both parents and children sucks! Why do both generations have issues at the exact same time?????”

Five question marks is about right.

“Grief is a journey, I’m told,” my friend texted last night.

Yes, it is. But I am fortunate to not be on the trail alone.

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30 Years of Opposites, Happily Ever After

Today, my husband and I celebrate 30 years of marriage. You know that old saw, “And they said it wouldn’t last”? The Episcopal priest who married us, who’d known me since I was nine, actually expressed his reluctance to read the banns because we were too different. He based this opinion on the results of a psychometric questionnaire that he had both of us complete.

He was right that we were different, and we still are.

  • My husband is a true extrovert who comes home from a party so jazzed up that he can’t go to sleep; I collapse in a heap, worn out from having to be that extroverted.
  • Members of his family, men included, cry easily. Crying was pretty much trained out of us in my family, which faced most hardships and losses with stoicism.
  • My approach to strong disagreement, like my mother’s, was to yell, with the occasional “god dammit” and “hell” thrown in for seasoning. Then we forgot about it. My husband learned to conquer other people’s anger by withdrawing. He prefers to stew a bit before sorting things out.
  • My husband is an ESTJ in Myers-Briggs parlance and, if you’re in to that sort of thing, a Virgo. His world view is pretty black and white – it’s right or it’s wrong. He’ll give people a long leash, but if feels they’re taking advantage of him – bam! – they will get an unambiguous shove back. He likes to know the rules up front, and he likes to follow them. I, on the other hand, am an ENTJ with a healthy dollop of Gemini sauce. Rules, schmules. How I react depends on whether I’m feeling extroverted or introverted at that moment. But always, I tend to put logic before feeling.
  • He likes things neat. I like things clean.
  • He loves to listen to music all day long. I love quiet.
  • He’s definitely conservative, in the sense of can’t-stand-the-idea-of-our-son-getting-a-tattoo. I figured it was inevitable, but I find I actually appreciate the fact that the tattoo honors that interconnectedness of people and the earth (I just didn’t think it needed to be emblazoned on one’s body).

I could go on, but you get the idea. It’s not a marriage made in heaven – I see Fr. Dave’s point – but it wasn’t made in hell, either.

What it has been is interesting – and, for the most part, good. My Dad often says that he views his life in distinct phases that feel discontinuous. Our early marriage years were horny and busy, very much about having fun with each other and fun with other people. The second phase of our marriage, after our children were born, found us fully engaged in demanding careers, squeezing every drop out of our schedule to put into parenting.

Those mid-kid years were tough, so tough that we ended up doing three years of marriage counseling. Where we learned – guess what? – how different we are. We were there because we had grown distant, because we had become great business partners, but weren’t such great lovers. Something had to change.

But the miraculous thing is that things did change. We reassessed, listened, got over our anger, and regrouped. We found better ways of being together that worked for both of us and honored our differences.

The result? I admire my husband’s integrity, his stability, and his rock-solid values, which include commitment to me. He laughs and cries more freely than I do, and both his humor and his empathy have helped me to be a happier, healthier person. Though we have been very angry with each other on occasion, he has never treated me poorly or tried to wound me. I know a lot more about music than I would have, although I am still hard pressed to “name that band,” or remember lyrics. Our kids, now young adults, are better people for having had parents who learned to listen to them and each other through our differences; they could not be more forthright, and they actually continue to seek our counsel. And our house is both neat and clean. Call ours reconcilable differences.

While this particular post honors the differences that have challenged us through the years, we had a lot of commonalities that provided a foundation. Belief in God (shaky at times, but nonetheless there), priority on family, empathy and respect for one another. And love.

It’s 30 years later, and we’re 55. I feel like we’re in phase three of our marriage, and I look forward to the phases to come. I enjoy being with him more than I did 10 years ago, and as much as I did 30 years ago. Having said that, I don’t feel at all like I did in my mid 20s. I’m not the same person. Neither is he. But we’ve found a way to be together.

It’s like getting married all over again.

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Road Trip: The Hot Pavement of Memory Lane

Horseshoe Bend image/yakimamemory.org

Sun-drenched has always struck me as an oxymoron here in toasty Sacramento where people often say the old cliche, “it’s a dry heat,” with more than a little acid in their tone. Samuel Taylor Coleridge recognized the sun in a less friendly form in a favorite quote of my Dad’s from The Ancient Mariner: “All in a hot and copper sky,/The bloody Sun, at noon,/Right up above the mast did stand,/No bigger than the Moon.”

During a hot spell, old time Sacramentans would have opened their windows at dawn and shuttered them at 9 a.m. to keep in the cool. At night, they might have dragged their mattresses out into their one-car garage and slept under a wet sheet, hoping for the Delta breeze to come up. Damn the mosquitos.

Having spent most of my formative years in the cool Pacific Northwest, “hot” was reserved for road trips. Every so often, we drove over Chinook Pass and headed to Yakima to visit my grandmother and great aunt. The first part of the drive was spectacular, past sparkling streams of snow runoff, through fields of lupine and Indian paint brush. But then came the hellish drive on the winding canyon road that snaked beside the Yakima River, where no breeze penetrated, and where the sun was amplified by basalt ridges thinly felted with dead, brown grass.

When two of my three brothers were along, I rode pressed next to my father and mother on the bench seat in front. Where the fabric of my shorts left off, skin adhered to the plastic or leather upholstery. My mother, never modest, unrolled the window, unbuttoned her sleeveless blouse and let the breeze of the open window serve as fan. When it got to be too much, my mother advocated a stop to “hot our feet off,” often near Horseshoe Bend. Bliss, even if it was cut short by having to put our shoes back on and pile back into our then-hotter car.

Our summer drives often included a trip to Boise, where my mother grew up, or McCall, Idaho, where my mother’s uncle maintained a summer home. Driving to Idaho was a lot like driving to Yakima in our pre-air-conditioning-era car, but without the benefit of a river for relief.

Remembering those drives, I fully understand the meaning of the ad slogan, “the pause that refreshes.” Coca-Cola never tasted so good as when you were sweating profusely. I remember the excitement of pulling up to a gas pump in the Horse Heavens, past Rattlesnake Ridge, and being given a dime or a quarter. The gas station in my minds’ eye had an old fashioned (1950s) machine that looked like a big cooler or a small freezer. You reached in and pulled out one one of the frosty bottles, held by metal clamps that were released when you inserted your coin. Six ounces of caramel-colored, fizzy heaven.

I don’t remember those drives as especially comfortable, but I remember feeling secure between my Mom and Dad, with my brothers in the back seat, passing the time by playing “red car.” There’s something to be said about the days before air conditioning.

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The Caregivers’ Special? Wine and Cereal

Image

When my kids were little, the ultimate in lazy cuisine was what we called “the babysitters’ special”: mac & cheese. Out of a box.

Everyone is out tonight. Dad’s back at his assisted living apartment (which he insists on calling “The Hacienda,” even though that’s not its name). My husband is on his way to a guys’ weekend in Montana. My son is working in Tacoma, WA, where he attends college during the year. My daughter is at a rehearsal of a play she’s in, which opens tomorrow in Davis, CA.

I don’t have to do anything. Which includes cooking.

What appealed to me? A bowl of Cheerios and Byron Pinot Noir 2010. (I doubt this is what the winemaker had in mind for a pairing.) And I’m deliriously happy about the whole state of affairs.

I think I’ll live dangerously and eat my dinner in bed.

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A Love Letter to My Sister Wife

If you stumbled across this blog post searching for something salacious, now is a good time to exit the page. My oldest, best friend is leaving this morning after a three-day visit, during which she gave me a card with this message:

If I was a Mormon Fundamentalist, I would want you as my sister wife. Thanks for being my friend.

She’s upstairs sleeping in my son’s room as I write this, and I realize how much I will miss her when she catches her airplane to go home in a few hours.

Compared to many caregivers, I have it pretty easy. My Dad still gets himself out of bed, dresses, and toilets unassisted. Nothing I do for him is physically demanding. But, I will admit, it is emotionally demanding.

My most important task for my Dad, in many ways, is to boost his spirits. Most days, he rises like a balloon full of fresh helium, rolls into the kitchen to greet me and may even burst into loud, gravelly song, “Summertime… and the livin’ is easy…” Within a couple of hours, however, the balloon begins to deflate and he expresses dismay about how old he’s getting, or how weak or shaky he may feel. On a bad day, he may ask what’s to become of him next, or lament that he is so dependent. He doesn’t outright say that he’s ready to leave this world, but I often feel that’s the part he leaves unsaid. I do my best to help him feel supported and loved, and try to do little things that temporarily buoy him.

Quiet, intimate time with true friends – especially friends like this one – help me to refuel. Most of our weekend was spent talking, a fair amount of it accompanied by a little wine. She won’t go home raving about all of the cool activities we enjoyed but I hope she enjoyed it.

In the wake of her departure, I feel content, like a cat sitting in the sun, petted by someone who loves me.

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Worth repeating: family communication tips for caregivers

Full disclosure: that’s my hand holding Dad’s, and the blog post below was originally published on the Ray Stone Seniors website. The article was inspired in part by my recent blog post about my experience with family communication, but I thought this had some great tips worth sharing.

With more people living longer, many of us find ourselves balancing caring for our children with caring for our parents, often, while working full-time. Family communication – with parents and siblings – can either become an obstacle to ensuring that parents and caregivers get the support they need and want, or an opportunity to deepen relationships. According to “The Elder Care Study: Everyday Realities and Wishes for Change,” 60 percent of former caregivers reported that their relationships with the elderly relative they cared for changed for the better due to the experience. The same study found that working together to support an aging parent drew some families closer, while a lack of support or help had the opposite effect.

What’s working for these families who report coping well, despite the extra work of caring for an elder? Intentional family communications aimed at fulfilling the older person’s wishes can go a long way toward turning this period of greater dependence into a period that will be remembered as a loving, if difficult, time.

Research and our experiences at Ray Stone Senior Living suggest these 5 techniques can increase the likelihood that caregivers will succeed in achieving better balance, and strengthened relationships:

  1. Start by putting the opinion of the elderly parent at the center of the dialogue. AARP Foundation’s “Planning Guide for Families” cautions that families “should never make a plan or interfere in the lives of their loved one without their knowledge or consent.” Don’t expect, however, to learn what your parents do and don’t want in one fell swoop; be a good listener and look for opportunities to engage them and clarify their wishes when triggering events arise, such as a conversation about a neighbor or friend who is having health problems or making changes due to aging.
  2. Identify a primary contact person. Kathy Quan, R.N., B.S.N., P.H.N., author of “The Everything Guide to Caring for Aging Parents” suggests that identifying a point person to act as a clearinghouse of information can help avoid miscommunication and rumor mills. That central communicator will be charged with making sure that all family members get the same information at the same time. She also suggests having a conversation about ground rules for back-and-forth exchanges, such as: ensuring that everyone is heard, limiting the length of uninterrupted comments (“speeches”), avoiding finger pointing, and not reverting to old, unhelpful family communication patterns.
  3. Divide duties. The Elder Care Study found that 86% of family caregivers said they receive help from other family members, but almost half added that they didn’t get as much help as they would like. Often, women feel they carry more than their fair share of responsibility, but they may not challenge this pattern out of habitual gender roles. By making a list of activities that could be supported, family members’ different abilities and resources may be more fully utilized. Expressing empathy and appreciation for siblings’ contributions also can go a long way toward fostering positive relationships – and possibly more offers of help.
  4. Take advantage of technology-enabled ways to communicate (but pay attention to etiquette). Many families find email an efficient way to keep everyone in the loop – not just about medical problems or changes in medication or routine, but reminiscences that may be shared in the course of the day. Email is also great for attaching documents and photos, as well as passing along greetings from Mom or Dad to other family members. However, email is a poor choice for sensitive discussions or voicing a concern or criticism. Some families also use a family website or blog to stay in touch – not just about parents, but about extended family happenings.
  5. Don’t forget to keep Mom and Dad informed, too. Returning to point #1, the goal of all caregiving efforts should be to honor aging parents’ wishes while keeping them safe. As medical and physical challenges increase, it can be easy to slip into conferring with medical or other professionals as if the older parents are not in the room. Insist that others still treat your Mom and Dad as if they are central, even if it can be frustrating to slow down or repeat information. After a discussion, it can be very helpful to recap it in writing in the form of a letter or note, especially if your parent has any short-term memory loss.

Caring for one’s parents as they age can be tiring, but it can be a time to honor these loved ones by giving back some of the love and support they have shown you along the way. It may even strengthen family relationships into the next generation.

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Family communication: seeing eye-to-eye through our diversity

Nephews, brother, sister-in-law, niece and Dad – out on a walk

Writer’s note: If you find this blog post of interest, you might want to check out a discussion on the NY Times New Old Age blog in which readers comment about communications techniques they have found helpful – a response to the article, “How Do You Keep Track of It All?”

My brothers and I look so little alike – and are so little alike – that it’s a matter of family jest. The brother who is closest to me in birth order and I once had to show our driver’s licenses to prove we were related to a woman who knew us both yet was unaware that we were related. My eldest two brothers are 15 and 10 years older than I am. The family unit they grew up in – which included a younger sister who died of leukemia in the 1950s – was a different one than the one my younger brother and I knew. It would be easy for us to have different ideas about “what to do” about our parents as they aged.

Instead, we seem to be in lock step.

Going back 15 years, when my mother’s dementia grew worse, and later, as she struggled with late stage lung cancer, my brothers and I evolved a system for communicating with one another. That system reduces stress for my Dad and makes it easier to ensure that he is getting the care he wants – and avoiding the care he doesn’t want. It also provides me with emotional support, and now it seems to be helping my brothers and I to imagine how we will be a family after my father’s eventual death.

That “system” started when my brother who is nearest in age called to suggest that we rescue Dad for a few weeks (by taking Mom on vacation) during the period when my mother had become increasingly agitated. Dad’s angina was increasing as her anger and confusion grew. Later, when my mother was eventually hospitalized and near death, our sporadic phone calls were replaced with much closer coordination by phone and email. We took turns staying with her in the hospital and took notes during our “shift”, briefing the next family member who arrived to sit by her bedside. On at least one occasion, our notes enabled us to correct what would have been a grievous medical error since her chart became so large that it was split in two – and some important information about her medication was not transferred to the active chart. When my mother came home with hospice, we tried to keep one another informed of her status as we rotated for three-to-five day stays at my folks’ house to oversee her care and my father’s recovery from his third bypass surgery.

In the past six years that Dad has lived partly with me and partly in an assisted living apartment, I’ve sent periodic “Dad Reports” to my three brothers with details about his spirits and physical health. Instead of quietly nursing resentment when I felt they weren’t doing enough to reach out to Dad via mail or email, I point blank asked them to step up their outreach to him. Our efforts were greatly enhanced by a “Presto” machine that automatically prints out emails sent to my Dad’s email address, thanks to a gift from my eldest brother.

As I have become more concerned about my Dad’s failing health, I have shared recent blog posts with my brothers, including my long rant after reading Joe Klein’s cover feature for Time magazine, “How to Die.” And it was that most recent outreach that uncorked a cascade of emails from my brothers that truly surprised and moved me. Not only were they aligned around preserving my Dad’s comfort and dignity, but they vocalized a commitment to our family unit.

My first reply came from “brother #2”:

I guess I’ll start by saying that for the past year I have been expecting a phone call from my Betsy or the staff letting me know that Dad had passed – I know that phone call is inevitable, and I know that every time I go up to provide respite for Betsy, I might be the one making that call to the rest of you. Selfishly, I don’t want that duty but if I have to be the one to make the call, I will respect Dad’s wishes. I know that he has lost everything he loved or took pleasure from in life, and has become a dependent. He can’t hear us, and I know it galls him.

Is there value in a rush to the ER? Well, the medical profession can certainly prolong a life that has become burdensome and often painful, but they cannot turn back the clock and give life in abundance. And ultimately, all the tests in the world probably won’t offer much that will give him a more abundant life.

I am conflicted by these thoughts – I like the family we have become and the strength that we siblings have found through Mom’s hospice. In many ways, I think that Dad has been the glue that bonded us all together, and I am fearful of losing more than just Dad when he passes away. But that’s not a reason to withold from Dad the end he wants.”

Then brother #1 weighed in:

(Brother #2) has done a good job of capturing my thoughts and feelings on this subject. And like him, one of my worries is that Dad’s passing will dissolve the glue that has kept the four of us close as siblings. I have the longest experience of the four of us with the reality of Dad’s mortality, going back to when Mom and I drove Dad to the Navy infirmary at Pearl Harbor when he had his first heart attack. I recall well how worried Mom was that Dad wouldn’t come out of the hospital alive, but yet he did, and he has hung on tenaciously for nearly 45 more years. As much as it distresses me, his race is almost run, and he has fully earned the right to let go when he thinks the time has arrived. Like (brother #2), I wouldn’t want him to die in distress, but neither do I think it’s fair to him to prolong his life if he wishes otherwise. 

It obvious that the time is drawing closer to when we will lose Dad, and as prepared as I have been for years for him to die, I still dread the reality. We have all been so incredibly lucky to have had Mom and Dad as our parents, and with Mom gone it will be even more wrenching to lose Dad as well. So, I think we should continue to dialogue about our courses of action and be available for one another. As the oldest sibling, I feel a good deal of responsibility for the three of you, even given the fact that you are all strong adults and don’t need me to look out for you. But old feelings and habits are hard to break…”

And lastly, brother #3:
“I have been acutely aware of Dad’s heart condition these many years, and recall thinking when we were off hunting by ourselves that something could happen anytime.As Dad approaches 96, he has clearly run a great race; he recognizes his time is coming and is at peace with that. I have always believed his end would come with a final MI/cardiac arrest; but who knows. Should we find ourselves in a situation where hospice is appropriate – perhaps the heart failure finally becomes unmanageable – then hospice would  be a good choice, and without further intervention other than palliative. On the other hand, if a condition presents that can be reversed or managed to maintain quality of life then I agree the right thing would be to obtain the care.
I agree with (brother #1’s) observation that Mom and Dad helped us to form a strong family. It’s unimaginable to me that we would somehow fall apart after Dad is gone. I enjoy being with each of you and will always love all of you.”
Not only did I find my brother’s emails restorative, but it gave me hope that we will find a way to enjoy one another into the future, despite our differences. Without this effort to communicate with one another, I am certain that the future would have seen us drifting apart, separated not only by physical, but emotional distance.

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