Tag Archive | caregiver

Classical Music, and the Reason and Will to Live

Is “caregivee” a word?  Well, if not, it should be!

As I’ve mentioned before, my father presents a classical music demonstration in his community every other week.  He does so by creating a YouTube playlist of performances around a certain theme, then writing up a short blurb that is edited by my brother or me and printed/copied by the community’s Activities Director (the soon to be world-famous Andrea), and then streaming them over wireless to an AppleTV box attached to the flat screen in the common activities room.  Very 18th century meets 21st century.

Anyway, this is his favorite project and the thing that he lives for.  If you are a caregiver, you know how important it is that your loved one have an organizing principle in their lives beyond taking medication and watching old movies.  This is his.

The “reason to live” is the slightly younger twin brother of the “will to live”, which is something we all pray for regularly, whether consciously or not.  They are inseparable.  In Judaism, I believe that this is what “Refuah Shlema” refers to.

Below is an excerpt of my dad’s latest presentation, done Wednesday.  It is his 2nd pass at Mozart, whose Eine Kleine Nachtmusik was the soundtrack to many of my childhood family road trips in my dad’s faux-wood station wagon(s).  If you don’t like classical music, enjoy instead the depth of the curating effort of a man armed with an iPad, a YouTube search bar, and a reason to live.

The Classical Music Hour

with

Andrea and Steve

Wednesday, March 5, 2 PM

MOZART REVISITED

WOLFGANG AMADEUS MOZART is perhaps the most popular classical music composer. He produced over 600 works, including 6 major operas, 41 symphonies, 28 piano and 5 violin concertos, many of them acknowledged as masterpieces in their categories.

Although a few samples of his work were introduced during the past classical music hours, a more detailed, more comprehensive examination seems to be justified.

The next 45 minutes, you will watch a great variety of Mozart’s masterworks, such as:

OVERTURE of the ABDUCTION FROM THE SERAGLIO, Vienna Symphony Orch. – Fabio Luisi

http://www.youtube.com/watch?v=GrFbiw77_90

MADAMINA Arie from DON GIOVANNI, sang by F. Furlanetto

http://www.youtube.com/watch?v=INF9r5jju0A

CHAMPAGNE Arie from DON GIOVANNI, performed by I. Kovacs

http://www.youtube.com/watch?v=wW_L6Fo7Fjk

THE QUEEN OF THE NIGHT Arie from the MAGIC FLUTE performed by E. Miklosa

http://www.youtube.com/watch?v=H_xfC9RXicU

OZMIN’S Arie, THE ABDUCTION FROM THE SERAGLIO, sang  by  Jozsef Gregor

http://www.youtube.com/watch?v=rvDZ9Ikvc7U

THE FAMOUS PIANO PIECE, TURKISH MARCH, played by pianist R. Brautigam

http://www.youtube.com/watch?v=HMjQygwPI1c

PIANO CONCERTO #20 – Romanze, played and conducted by Mitsuko Uchida

http://www.youtube.com/watch?v=qhNITXBguSs

VIOLIN CONCERTO #4, performed by Julia Fischer

http://www.youtube.com/watch?v=9Hqyxy9u4W8

SYMPHONY #40, first movement, Berlin Philharmonic, conducted  by T. Pinnock

http://www.youtube.com/watch?v=pIsMmuf9Q3Y

SYMPHONY #41 “JUPITER” – Chamber Orchestra of Europe, conducted by T. Harmoncourt

http://www.youtube.com/watch?v=zK5295yEQMQ

TURKISH FINALE from the ABDUCTION FROM THE SERAGLIO

http://www.youtube.com/watch?v=Tw84smtNE1Q

Caregiving Success: It’s Not Entirely Luck

I consider myself pretty self-aware; given how much introspection it takes to keep myself on the rails, I better be.  Every once in a while, I allow myself to take some credit for my father’s improved situation and my kids turning into warm, emphathic, smart and kind people (credit shared with my brother and wife respectively, of course).  So many things are out of our control in both situations that when a chapter ends well, you take a small victory lap even if you know already that the book itself is going to be a tragedy.

Brief side note: I have a good friend down the street who convinced me to buy an outdoor gas grill that I could connect directly to the line in my house.  Best thing I’ve bought in ages.  His logic was simple: as a father of daughters, you control so little in life that you need something that you actually do control.

Anyway, I am also keenly aware that much success in life and caregiving stems from luck.

Yesterday, Today and Tomorrow Sandwiched Man

My family and I were away for February vacation for a whole week.  For many people, trips away provide a welcome opportunity to pause, change life’s rhythm (usually to slow it down), and put down the metaphorical glass of water.  Meaning, even a not-very-heavy glass of water eventually is a back-breaker if you have to carry it forever.  

Being a parent and a caregiver simultaneously increases the degree of difficulty on putting down the glass of water, but it can be done.  For a short time.  And not for a week.  

Once you get up to a week, you start handing problems to the tomorrow version of yourself.  Fans of the show Seinfeld might remember the episode where Seinfeld talks about “Tomorrow Jerry”.  I use this construct a lot; at some point, you have to delegate your problems today to the tomorrow version of yourself.  (Trust me, that sentence works.)  Most days, I thank Yesterday Peter for some of his good choices or empathize with his prior plights enough to give him a pass for things he handed to me handle today.

A week with an elderly parent means that if you help parcel out medication, as I do, your parent is going to run out by the time you get back.  This time I prepped a few days extra, but that ran out on Sunday.  So after driving back from New Hampshire, I had a date in Framingham with my father’s prescription bottles.  Today Peter was on the case.  But then he got tired enough that the snowy, windy weather encouraged him to have hot chocolate instead and delegate the pill distribution to Tomorrow Peter.

Then Tomorrow Peter turned into Today Peter with a medication disbursement deadline.  Today Peter was also faced with the just-announced merger of his company where he was among the few survivors, as well as prep for an upcoming Board presentation on the somewhat radical financing structure that he was recommending for his Temple.  And this is how Today Peter found himself on multiple conference calls in his car, while driving to help his father in Framingham, while cursing Yesterday Peter and his poor planning.  I pulled into a liquor store parking lot just off Route 9 for a few of these.  At least I was able to stop off to pick up my father’s Vermouth and replenish the house beer supply for when I visit.

Today Peter arrived at his father’s apartment around 4pm with only a few minutes to take care of parceling out pills before the next wave of conference calls.  My father sensed the time pressure, sensed my anxiety and knew that my time was limited.  So he did the logical thing, which is to recommend that I have a drink with him.  

At first I turned him down.  Then I realized that I was crazy to turn him down.  So we had a quick shot together.  It was fantastic.

Now that I am looking back on how Yesterday Peter performed in that situation, I want to thank him.  It became a great memory and a nice reminder that my father isn’t just someone who I am caring for — he is my father and sometimes knows what I need.  I’m sure Tomorrow Peter will agree.

Sandwich Generation Scourge #259: Relatives Speaking Nonsense

If you are a caregiver, you have a person like this in your life too.  She means well and is a good person.  Probably loves her kids and has many redeeming qualities.  Connected to you by blood and the memory of many family events, some of which you even recall as not completely awkward and uncomfortable.  Someone who has come through for you in the past.

But not always – because this person can be counted on occasionally to give your loved one spectacularly bad advice.

In my case, this advice was related to taking medication.  Because apparently doctors are all trying to make money by prescribing antibiotics like Dificid, which is the pill that currently separates my father from the runaway symptoms of the stomach bacterial infection C Diff.  Also, once the symptoms are gone, you don’t need to take more pills.  After all, if I have a headache, and I take aspirin, and the headache goes away, I don’t take more aspirin, right?  I mean, clearly doctors are just trying to make money.  Everyone knows that.

My father relayed this advice that he’d heard to me and I went ballistic.  Sometimes I do this.  Generally my style of persuasion is finesse, not brute force.  As a sandwich generation person, I try not to go to the yelling mode with either my father or my kids, but sometimes there is no choice.  Plus, I was angry.  My father has a penchant for making his own medical decisions, most of which consist of trying to second-guess which prescriptions he should take that week.  I have worked really, really hard to talk him out of this habit and put the medication process on auto-pilot.  It has worked.  This is better for everyone.  And then now this

So I somewhat (but only somewhat) more gently pointed out that this infection had come back many times, that he should stick with the plan, and this relative should stick with what she really knows a lot about, whatever that is.  Etc.  Then he said, “Peterkem (Hungarian for ‘my Peter’, sort of a term of endearment), of course I am listening to you.”  Almost as if to say, “I know that this advice makes no sense.  I am not a dummy.”

Problem solved.  Until the next spectacularly bad advice floats over the transom. 

Sandwich Generation: the symptom is the cure

Here is a screen shot my father took from a Skype session I had with him last night.

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Sophie and Daddy use the magic Skype machine

You can see my daughter Sophie in the shot – she was talking to him (this was about an hour after my last post about his C-Diff returning and feeling a distinct sense of whatever the opposite of the relief is).   You can see in the picture how happy they both are about it and the connection that’s formed.

Sometimes you can employ one side of the sandwich, so to speak, to help you with the other.  That is, the symptom is also the cure.

#bummedoutedness

My father’s C Diff is back.  He had some stomach “issues” last week (yes, that’s a euphemism for problems that require bleach to fix), and after 2 days had pased, he finally let me know about them.  To be honest, I think the main reason he confessed is that I was standing in his apartment, and the signs are impossible to miss even with your eyes shut tight.  So, confronted with my presence in the living room, he decided to fill me in.  Such is the advantage of having him close by and visiting regularly, I suppose.

Anyway – the tests confirmed what we’d suspected after last week’s incidents.  Getting the results, as you might imagine, required several phone calls to chase them down since, as I now know, doctor’s offices labs don’t perform stool samples; they send them out.  

So now we are moving on to treatment.  This starts with another round of antiobiotics that’s going to run “only” $800 – luckily, we are into a new calendar year so that takes us out of the coverage donut hole as described here in my earlier post on Medicare Part D.  

When you get C Diff 6 times, it’s pretty obvious that drugs alone can’t kill these bacteria, so alongside that, the accompanying protocol is what’s known as a fecal transplant.  Yes, it is what it sounds like.  

But augmenting your weakened stomach flora with healthy ones from another person’s gut is remarkably effective and, fortunately, not as yucky as you think.  Generally, it can be a non-surgical outpatient procedure using a GI tube.  Plus, we connected with the rocket scientist gastro-enterologist at Mass General Hospital during a time of my father’s seemingly perfect health back in December, so we are prepared.  And he’s generally feeling fine, with his symptoms under control and a high energy level despite not having Dificid yet.  So, all in all, I have great cause for optimism.

And yet — I’m experiencing a palpable sense of what I can only define as “bummed-out-ed-ness.” (soon to be a trending hashtag on Twitter).  I am.  I honestly expected to be past this thing.  I had repurposed the brain cells I’d targeted at C-Diff-related-thinking into more productive purposes.  I had mentally said goodbye and good luck to Dr. Jenny Sauk, the aforementioned rocket scientist gastro-enterologist at Mass General Hospital.  I allowed myself to luxuriate in the thought of a future free of conjuring the emotional energy required to demonstrate a can-do spirit, even though down deep lives the nagging feeling that this particular disease (a) wants to kill him and (b) isn’t going to take no for an answer.  

In a strange way, I am relying on him for some degree of emotional sustenance.  After all, this is a man who survived the Nazis, the Communists, colon cancer, and so far, this thing.  I suppose as caregivers, we have to acknowledge a symbiotic relationship; our parent’s willingness to fight on reinforces our strength to help them fight on.  The sandwich generation piece of this is that our children’s willingness to learn reinforces our strength to teach them.  In either case, if either side withdraws their energy, we need to be ready to feed it from our own reserves.  My reserves are high right now.  But I must confess that I had let down my guard against having to tap them again so soon.

In other words – I’m experiencing #bummedoutedness.  Look for it on a Twitter feed near you. 

3 Caregiver Lessons I Learned from Bad Fiction Novels

I’m certain that in the course of writing this Sandwich Generation blog that I’ll be waxing poetic about my father’s various heroics in certain situations and how much I admire him.  However, that’s not going to happen today.  Instead, I want to highlight his terrible taste in books.

Let me start with his obsession with W.E.B. Griffin, and in the particular, the Brotherhood of War series.  I know he is obsessed because he bought the whole series (The Lieutenants, The Captains, the Majors, the Colonels, etc. etc.) in paperback multiple times.  For someone who grew up in Depression-era Hungary and used to keep dead batteries in a drawer in his desk, because “you never know”, this is quite a statement.

Not content with that, he insisted that I buy him the series again for his Kindle.  Which I did.

He also recommended that I read it.

The last book he tried this with was “The Panther” by Nelson Demille.  Horrendous.  It’s the story of a married couple in the CIA (I think) who is sent to Saudi Arabia (maybe) to kill or capture a terrorist mastermind called the Panther (probably).   Hundreds of pages meander on with no action but plenty of cringeworthy puns about sex and violence.  Every chapter ends with some variation on “…so we settled in and waited for happen.  Maybe.  Or maybe not.”  The book is filled with barely disguised racism, celebrates ignorance, and there are pages where Demille just mailed it in and lifted passages from his other books, which he then passes off as reminiscences.

You would think that I would have absorbed the lessons from this particular experience.  But I am a caregiver son who is grateful to have a father who still reads and recommends books almost at age 90, so I shrugged it off.  So he loaned me one of his 3 copies of “The Lieutenants”, and I started reading.

It’s 90 minutes of my life I will never get back.

Ostensibly, it’s about U.S. Army lieutenants in World War II, which is a topic my father knows nearly everything about.  But that’s actually not what it’s about.  It’s mostly about American army officers’ post-war exploits in post-war occupied Germany, how terrible the Soviets were, and how the Germans actually really weren’t that bad.  They were perfect gentlemen in the way they treated these guys when they were POWs, for example.  W.E.B. Griffin says so.

One particular prison camp scene where the American and Nazi officers have a leisurely drink together was my tip-off that I was not going to dig this book.  To make matters worse, the characters — many of them, each less likable than the first — run around talking about “niggers” in the Army and showing surprise when a troop of “fried chicken eaters” turn out to be decent soliders.

I guess I have 3 points.  The first is that just because your parent thinks you will like something, you might not.  I know now to approach any book my father recommends with a lot more caution.  Apparently, even unconditional love has limits.

The second is that his book recommendations remind me that my father is a product of his era, and like the rest of us, fulls of imperfections large and small.  A good man, I believe, but a flawed one just the same.  If I am really honest about it, he has always been a little bit racist.  Demille’s humor really appeals to him, I’m sure.  He has had a complicated relationship with relationships.  Of course he’d rather read puns about stereotypically dysfunctional ones.  On certain occasions, he’s suggested that America’s best foreign policy strategy would be to kill everyone in a particular country, because what’s the difference — it’s really the oil we want.  Books celebrating war just help reinforce that reaction.

It’s probably a 21st century sensibility to see the irony of someone who survived World War II being so enthralled by a book that whitewashes the Germans — I know.  But since it is 2014, I’m not sure what other lens to apply.  And when you are a caregiver for someone, it is easy to forget that this person who so needs you is actually a real and imperfect human being.

The third and most uplifting lesson is that he wants to connect.  Wanting that connection with his kids was not really his thing in my childhood, and I suppose if I could have had it then vs. now, I might have taken it then.  I don’t know.  I have to make the best of what I have right now — as in today.

Postscript: I returned the Lieutenants, and placed it next to its other 2 green-colored-cover brothers on his shelf.  I told him what I thought of it.  He nodded, apologized a little, and then moved on to the next favor.  Caregiver tech support never ends.

Medicare Part D meets Kung Pao Chicken – A Cautionary Tale

If you are a caregiver and familiar with the administrative horror show that is Medicare Part D, you can save yourself the 10 minutes you would ordinarily spend on this space.  If you are not, you will be glad you invested the time, because inevitably, you will find yourself fighting with an insurance company while racing the clock.  Trust me, you want to avoid learning this stuff on the fly because those 2 things just go together.

On their 65th birthdays, seniors in the U.S. get access to Medicare.  It’s actually a few different programs, which vary from great to “huh?”  The great part is Part A, which is basically comprehensive medical insurance that helps cover inpatient care in hospitals, as well as skilled nursing facility, hospice, and home health care.  Then there’s Part B, which pays for services (like lab tests, surgeries, and doctor visits) and supplies (like wheelchairs and walkers) considered medically necessary to treat a disease or condition.  It also helps pay for lift recliners and a variety of other stuff that is advertised on cable channels during showings of old movies.  Smart marketing.

Ideally, your parent has supplemental coverage on top of Medicare.  This is extra insurance that covers things that Medicare won’t under Parts A, B and D.  Especially for Part D.

The big gap in Medicare until about 10 years ago was in prescription drug coverage.  While you were in the hospital, medication is covered, but the minute you busted out (more on this in another post), you were on the hook.  Along came the mid-2000’s Republican Congress looking to cement elderly voters as leaning GOP, and Medicare Part D was born.

Part D should be better than it is.  It’s totally run by third-party insurance companies so is not the single payer model that Medicare is.  Sometimes these are the same carriers who have your separate long-term care insurance policy.  Sometimes your father knows the difference.  Most time he doesn’t, can’t explain it to you, and stashed the policy information deep in a drawer somewhere.  I’m just saying.  Plus it’s different in every state, so when you move, it can’t move with you.

When my father was discharged from the rehab center where he spent almost a month recuperating after his C-Diff-inspired hospital stay, his Vancomycin regimen became our responsibility.  Like most Americans, I have spent a decent part of my adult life on antibiotics, so when I got the prescription from his rehab center medical group, it seemed like a lay-up.  I even placed an order for takeout Chinese food from my dad’s favorite place near the CVS.

It was a muggy, rainy night in New Jersey and after placing our order and informing the nice man behind the counter that I’d be back in 15 minutes, I went into CVS holding the prescription.

“OK, I found the medication,” the pharmacist told me.  “But do you know that this medication is $3,000?”

“What?  How can that be?”

“Well, it’s a Level 5 drug and the doctor didn’t get a Prior Authorization .  Also, the prescription is for liquid but we only have capsules.  For liquid you need to go to a compounding pharmacy.”

I understood none of this.  That morning I had woken up naively believing that springing my father from rehab would be a good idea.

It tuns out that a compounding pharmacy is one that mixes medications from certain compounds in a variety of forms.  Good enough.  So eventually I got into my dad’s car and drove to the nearest compounding pharmacy, which was in a low rent strip center in Hamilton, NJ.  To find it, I had to rely on Google Maps on my cellphone, which drained the battery to nearly, but not quite zero.  There I told the pharmacist my tale of woe.  He looked up the medication.  Still a Level 5 drug.  Still no prior authorization.  Still $3,000.

He was able to figure out for me who I should call (AARP Insurance, my dad’s supplemental carrier), what information I needed, and what tactics I should use to overcome the inevitable denial that was coming (“tell them he’ll end up back in the hospital without it,” he said).

He also let me borrow the phone at the counter because of my aforementioned cellphone battery issues.  This worked great until I’d been on the phone for more than 30 minutes, after which point he and the other staff members kept reminding me impatiently that I’d taken up one of the only 2 phone lines in the store.  After 45 minutes, they told me that I had to get off.  I honestly thought I was closing in on success, so kept pushing them off.  (I was wrong, but didn’t know it).

After an hour, a woman behind the counter hung up my call, and then as I freaked out because I (wrongly) was convinced that I was about to break through, denied that she had done it.

If you are an experienced caregiver, you know this story.  You have grown accustomed to feelings of powerlessness.  Whether dealing with advancing age, health conditions, or insurance bureaucracies, you have come to accept feelings of inadequacy that stem from the situation, not from anything innate.  This was my first brush with it with my emotional guard down, and as I stood outside the compounding pharmacy on a muggy, rainy, August night, I was shocked.

As an added bonus, my cellphone battery had now completely drained, so I had no way of calling my father to explain why my 30 minute CVS errand was now taking almost 5 times as long.

The ending: I called the doctor’s office once I got home that night, and told their answering service that yes, it was an emergency even though their policies said that they couldn’t alert doctors for prescription questions.  I finally got the “Prior Authorization”, and got them to change the prescription to pills instead of capsules.  My father got his Vancomycin dose a few hours late, but at least it was the same day.  I wrote down all of the phone numbers, insurance plan numbers, etc. and put them into a document that my brother and I share online.  The medication didn’t cost $3000 — but the out-of-pocket was almost $800.   Part D coverage is different for different medication types at different “levels” based on which version of the plan you’ve signed up for.

In terms of dinner: the Chinese food was cold and soggy when I got it, and microwaving the Kung Pao Chicken did not help the situation much.  Then I drank 2 beers when I finally got home.  Strong ones.  Quickly.

The moral of the story is this: find out all of your parents’ Medicare Part D coverage information BEFORE you need to know it, and always remember that anything besides the standard medications likely will require additional authorizations that only your doctor can get.  And above all, do not order Chinese food before picking up complex medications.  You are tempting fate, and as caregiver, this almost never works.

Blood (Not What You Think)

Here’s a quick story of how my Sandwich Generation moment (sort of) intersected with another’s.

My kids’ last elementary school science night was a few days ago.  The first session we attended was devoted to blood – specifically, what’s in it (plasma, hemoglobin, platelets and 3 types of white cells, by the way).  That we focused on blood was not the important part.  The element that matters in this story is the presenter, who was a student’s hemaologist grandfather.  I found his style and manner of speaking ideal.  Unfortunately, my sensibilities and those of a 7 year-old differ slightly, so I suspect many of them were bored.

The subject matter caught my attention, but even more so was the way his son behaved.  At least I think it had to be his son.  His impatience with his father’s imperfect presentation was palpable.  He corrected and interrupted him frequently.  HIs tone is one I can only describe as a cross between exasperation and embarrassment.

His father took it well and kept plugging away at his program.  But it got me thinking.

Fast forward to the next day when I found myself in my dad’s community room attempting to troubleshoot network connectivity problems with the overmatched and harried assistant executive director (Terry) responsible for the “independent living” wing where my father lives.  My dad’s latest classical music presentation had been hamstrung by technical problems that could have been caused by a variety of factors, so Terry and I were trying to troubleshoot.  Or, rather, I had on my nerd jacket and trying to decipher the problem while Terry told me stories.

One that he told me, after which he asked for my help, was about the a recent community trip to CVS (estimated distance: 1.5 miles) on the group bus.  Apparently my father had been a participant on that trip, which I know from speaking with him is one of his favorite outings of the week.  The fact that he does not have to shlep all the way out there (remember – estimated distance: 1.5 miles) never ceases to amaze him.  It makes him feel like royalty.

On that trip, Terry told me, as if this physical challenge of my father’s was news to me, that the smell from his incontinence had permeated the bus sufficiently that other residents had complained about it… and could I please speak to him about doing something about it?

Now, I know this issue is a chronic one for him.  It has been since 2004 when he started taking Lasix, which is his congestive heart failure (CHF) medication.  Basically, CHF is caused by excessive fluid, so the drug drains it.  There is only one way it can drain.  You get the idea.

I took him to Mass General last month for a C Diff check, and all I can say is that I know what Terry was talking about.  Plus, the weather that night ranged from really cold to “are you kidding me”, so opening the car window for very long presented its own set of challenges.  I usually give him non-stop grief about this issue.  My brother does too.  Don’t get my sister-in-law started on it.

So what did he say when I brought up Terry’s comment to him?  Nothing.  Because I didn’t tell him.

I figure that part of my role, aside from parceling out medication and checking that nothing scary has taken root in the refrigerator, is to take his side whenever possible, even when he is wrong.  In this case, he was almost certainly in the wrong.  But so what?   He already does his best with this.  I have done everything I can short of conferring with my brother and deciding that he’s not capable of making his own decisions about getting dressed.  And aside from having to pick my battles, I feel like I have to give him credit for generally making pretty decent decisions, and for a generally improving trend of decision-making overall.

When I had showed up for our weekly dinner that night, he had put on a nice oxford shirt and dress pants just because I was coming over.  This is a man who wore robes nearly non-stop just before and just after he moved here.  That doesn’t happen anymore, and not because I continued to yell at him about it.  He still has the capacity to self-correct, which if I devalue, makes everything (my brother’s and) my problem.

Back to the blood, which is how we started this.  I don’t know if I would have reacted as the hematologist’s son did had this been in front of kids, even my kids.  It is hard not to snap at parents.  Maybe I would have.  But I hope not.  I hope that if my father had been up there talking about and showing off his lifelong passion for blood or anything else, I would have listened quickly, helped out politely, and looked on with a lot of pride.

Half Full (Part 1)

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Although I am in the midst of the intense experience called “caring for one’s parent”, I am also aware that in many ways, I am lucky to be in this situation at all.  C-Diff is not a disease that everyone survives, and certainly not everyone who is 89 years old and has 5 recurrences.  But then my father has been giving death the slip for a long time now.

And, whether by good fortune, planning, or both, I also can look at the situation of taking care of my father and feel like the glass is not just half full.  It might be closer to 2/3.  Here’s why I say this (and have been encouraged to say it):

  • My father’s mind isn’t just sharp.  It’s activated.  He reads newspapers online in multiple languages (Hungarian, German, English).  He leads a bi-weekly classical music seminar in his community where he streams YouTube videos over AppleTV to an ever-growing crowd.  He Skypes with my brother regularly.  He remembers nearly everything from his photo albums from 60 years ago.  This is big.  And he nearly always wants to learn.
  • My brother and I are a great partnership.  Yes, I am local and he is out in California, and yet I could not ask for a better partner.  Our relationship works now at a level that I could not have conceived of only a few years ago.  We work at this and communicate frequently, so this is not entirely luck.  Many siblings actually disagree about what to do and how to do it, which leads to paralysis, which then leads to bad situations persisting.  I learned a lot about partnerships in one of my businesses and have applied some of those lessons to being in this one.  But having a brother?  I can’t take credit for that.
  • Ditto for the support I get from my family.  It is easy to mess this up.  I have to balance things carefully (hence the title of this blog) to keep it that way, of course.
  • Jewish Family and Children’s Services have great support and programming for this exact situation.  We got connected with their Elder Experts service, a pricey (more on this later) but invaluable service that helped me find him a place to live, a local doctor, and connected me with Schecter Holocaust Services, which pays for some of his additional home care because he is a Holocaust survivor.  WIthout them, I probably would have moved him into an apartment, which likely would have been an unmitigated disaster.
  • We have sufficient financial means to pay for housing in a nice community near me, which is not easy since I live in Wellesley, MA, also known by its slightly derogatory nickname “Swellesley”.  He actually lives in Framingham, which is a lot cheaper than being here and still feels really swank for someone who grew up in Depression-era semi-rural Hungary.  He is in independent living, which is a lot cheaper than assisted living, which itself is cheaper than skilled nursing.  JF&CS pays for his weekly HomeInstead visits, which when they finally began liberated me from being his housekeeper.  And we have insurance which paid for his post-hospitalization stint in the rehab center (Medicare would have mostly dropped him after 20 days), so that didn’t wipe him out.  Some of these stemmed from good choices he or we made a long time ago, which I guess has some degree of foresight to it.  And a lot of it was luck.  My mother was a bit of a day-trader in her day, so not all of their financial decisions were good ones.  The decision to take out Medicare supplemental insurance definitely was.
  • We were selling his house in 2013, not 2010.  Total dumb luck.  People forget sometimes how the difference between financial success and failure is timing.  Never has this been more true than in the housing market in the past 5 years.  We hired a really good broker who specializes in this kind of transaction (vacant house from a senior owner who lived there for many years and then moved on), and she did a terrific job.  For our part, my brother and I were hyper-responsive to anything she asked us to do and let her drive the bus, so to speak.  Could she have sold the place so quickly and for such a good price in 2010?  Doubtful.

I could go on, but you get the idea.  Here is one last story to illustrate it.

When he was in the rehab center and I was shuttling back and forth to NJ from MA, my visits ranged from a few days to a few hours.  During my shortest visit, my father was in the physical therapy room and I was about to leave.  He had been there for over 2 weeks and physical recovery was coming slowly; he still had C-Diff, the power of which neither of us fully understood, so we didn’t know why he was so drained and tired all the time.  As I started to leave, he started to cry, which is very unusual for him.  He was convinced he was going to die in rehab as my mother had 2 years earlier.

I told him that we were destined to have 1 more bowl of clam chowder together at Legal Seafoods and that all he had to do was hang on long enough to make that happen, and the rest would take of itself.  When I said it to him, I believed it.  I don’t know why; I just did.  I told him it was written in the stars.

Several weeks later, after he left the rehab center, had survived 2 weeks on his own mostly alone in the house, moved to MA and gotten over the latest bout of C-Diff, we finally had that meal at Legal’s.  We were very fortunate to be there.  I am fortunate to be in this situation.  I know.