What's with the plural, anyway?

    Astute readers such as yourself certainly have noticed by now that this blog is riddled with first-person plural pronouns, as in--

          We feel a bit like we're sailing off into the unknown

               I knew our adventures were beginning last week...

               Now that we're past the halfway mark... 

          ...we might sail through the rest of the treatments just fine...

          Soon, it [ringing the bell] will be our turn...

    "What is up with this?" you may have been wondering.  After all, you know as well as I do that I'm not the one with a brain tumor, well, I don't think so anyway, and I'm completely sure that I'm not the one getting proton beam therapy.  

    In any case, I admit that there is a heavy use of we, our, and ours in this blog when I'm talking about P.'s condition and treatment.  I assure you, though, that all the rest of the caretakers here at the Hope Lodge are talking the same talk.

    I guess this is inevitable.  When any family member has cancer, it is more than a little bit like you do, too.  And when you are the primary caretaker for that person, the warp and woof of your loved one's day and yours have an enormous amount in common.  If your caretaking duties go a step further, and you have been pretty much completely lifted out of your own world, like say, by moving 400 miles away from home for two month's of treatment, you'll find that your sense of self is even more intertwined with your caretakee's.

    In fact, if you were to walk into the waiting room of the proton center or the kitchen of the Hope Lodge right now, it might take you a while to figure out which person in each couple was the patient and which one was the caretaker.  In part, this is because a lot of cancer patients actually look pretty darn good, like P. does.  But, I have to say, that it is also because some of the caretakers look rather worn out, almost like they could be the ones getting treatment.  During our time here at the lodge, I know two caretakers who have been rushed to the ED because their own health issues needed urgent attention, others report fairly often that they have had to stay in their rooms for a couple of days because they caught a bug, and still others have talked about getting in touch with their doctors about lining up some badly needed health care for themselves once their loved ones' treatments are concluded.

    Thus all those plural pronouns.  We're just all in this together.  For better or worse, and all that.

    This linguistic twitch is probably just temporary, a little like the bald spot P. has on the back of his head where the proton beam has been pointed.  His hair will grow back, and my use of plural pronouns will become more appropriate. 

    In the meantime, though, dear reader, I know that you know somebody right there in your own town who is heavily involved in caretaking duties at the moment.  You might have given him or her a kind thought or two, or even put in a optimistically-worded email or call.

    Let me urge you to take those caring thoughts a step further.  Bring that caretaker a nice casserole.  Take him or her out for a coffee break, or offer to take on an afternoon of caretaking yourself so that person can get caught up on work or, better yet, on sleep. 

    Don't just think kind thoughts.  Do kind deeds.  They will be appreciated.

   

Hello Goodbye

    The residents at our Hope Lodge are an ever-changing lot.  Every few days, we meet a couple of newbies who have just checked in.  You can spot them in the kitchens, nervously opening and closing drawers and cabinet doors, trying to find a measuring cup and hoping that they are going to get the hang of communal living soon.  (Actually, they hope that they will hang onto just plain living, given that everybody here is a draftee in the Cancer Army.)

    And, as some folks come on board, likewise, every couple of days, somebody else finishes up his or her long, long course of treatment.  Having rung that bell, these couples say goodbye to the rest of us at the lodge who are still doing time with the proton gizmo, the photon gizmo, or some other techie cancer zapper.

    When we were the newbies ourselves, with only a couple of treatments under our belts, we would chat with the old-timers, the ones who were coming close to wrapping up their 35 or so sessions.  We would say something like, "How wonderful that you'll be going home in just a few days!  You must be so excited!"

    To a person, they all mostly just looked back at us, slightly glassy-eyed.  Their replies were never as exuberant as I would have expected.  "Yeah, sure," they'd say.  "We're happy," they'd add, without a smile. 

    Where were the "yippees!" and "hurrahs!" I'd wonder.  Weren't they glad to be done?  Didn't they want to go home? Or were they just hiding their glee not to rub our faces in the fact that we were still hitched to the zapper machines with weeks left before we'd get sprung?

    Now, a couple of months later, we're the old timers ourselves, with just four treatments left to go.  And I understand their reactions completely.

    Some people, we now know, aren't all that jubilant because, while they may be finishing up one round of treatment, there is something else in the works (surgery, chemo, etc.).  Others are subdued because they know that they are still playing the long odds with cancer, so they are going home hoping that nobody is going to be writing an obituary about them at some point that starts with that awful phrase, "After a long and courageous battle ..."

    Some folks, like us, got the luckier outcomes.  We don't have another round of treatments to go through, and P.'s doctors feel confident that his proton treatment constitutes a near-100% chance of a complete cure.

    I can tell you, though, that we lucky ones are looking back just as glassy-eyed at the new folks who are telling us how great it is that we are going home soon.  Not because we aren't really, really, really happy to be finishing up, or that we aren't eager to get back to our lives.

     It's just that, after this many weeks of living in an alternate universe, we're all just tired.

    Next week, nonetheless, however wearily, we do plan to set off fireworks.  Since the lodge forbids flames of any kind, we'll have to make do with virtual sparklies. Preview below.

   

   

Waiting for the bell

 
   Those of you who have remained blissfully unaware of the cancer treatment world probably don't know about The Bell. 

    I too didn't know a thing about The Bell until we were getting ready to come here to the Really Famous Hospital for P.'s zapper treatments.  But we know about it now.  And we're waiting to hear it peal.

   To fill you in, these bells are affixed to the walls outside radiation and chemo rooms all around the country.  On the last day of someone's treatment, family members crowd around to snap pictures while the patient rings the bell.  Everyone in the room erupts in applause--doctors, nurses, technicians, and, most of all, other patients who know just what an accomplishment is represented by that golden sound.  

   Blog entries about the bell abound, as in here and here and here.

   So it's big deal, this bell ringing.

   As the weeks have gone by, we've watched a lot of other patients get to ring the bell as they've wrapped up their 30 or 35 or 40 sessions with the proton beam.  This often involves cake, watered by tears. 

    Soon, it will be our turn. We're on schedule for P.'s bell ringing ceremony soon, since he's got only nine treatments left to go.

    I've got the camera ready.  Think we'll get all weepy, too?

    You betcha.

The Best / Worst Lists

    Now that we're past the halfway mark in P.'s treatments (yay!), I feel we've logged the requisite time and experience to pass judgment on the best and worst features of what we've been dealing with to date.  I'd like to end this post on a positive note, so let's get the top five not-so-great items out of the way first:

    Worst List # 5:  Shopping just isn't the same here.  How's that for a trivial-sounding issue, given that we're here dealing with the Big C?  I know I'm coming across like the Princess and the Pea on this topic. But, while I don't give a fig about shopping in general, cooking and beading are my release valves for this pressure cooker we're in right now, so I'm longing for access to the same range of foodstuffs and bright shiny beading objects that I can get at home.  For example, there doesn't seem to be a tornado crimp within a hundred mile radius, and the region's lack of the world's most magnificent grocery chain merits an entire post of its own, coming soon.

    Worst List #4:  There is a lot of cleaning to be done every single day.  I knew that would be the case, given the more-or-less communal living situation we're in and that fact that everyone here is dealing with cancer.  Some of the folks getting treatments just aren't up to doing much housekeeping, of course, and their family members are often dealing with overwhelming caretaking duties.  Others, less burdened by illness, simply weren't raised by my particular mother (i.e., the Majestic Goddess of Universal Cleanliness).  So, along with a couple of others here, I'm logging in a lot of hours with the scrub brush and the bottle of disinfectant down in the kitchen, trying to keep things hygienic, especially for the stem-cell transplant patients.

   Worst List #3:  Schlepping back and forth to the hospital over and over again.  It takes us 37 minutes, door to door to get from the lodge to the Really Famous Hospital by public transportation, and it's about the same by the shuttle.  So this really isn't a ridiculously long ride.  It's just that the doing of it each and every day Monday through Friday is getting seriously old.

    Worst List #2:  It's cold, really cold, outside and it pretty much has been this way for the entire time we've been here.  If this stint in treatment far from home had landed us here in June and July, we probably would have been griping about wasting the few short summer months in the aforementioned treks to the hospital.  But at least we would have have been able to go for leisurely walks among this city's lovely neighborhoods and parks while we were complaining.  As it is, we're not walking in a leisurely manner at any point; we're dashing through the frigid February outdoors trying to get inside as quickly as possible.  As I type, it's 22 degrees outside.  You skiers out there may be scoffing.  Go ahead.  I know I'm a wimp.

    Worst List #1.  We're here because of a brain tumor. 

    Ok, you're sick of hearing me kvetch and so am I.  Here then, is my list of the top five good things about being here.

     Best List #5:  We love the art museum that is a just a mile or so from the lodge.  In a city famous for superb museums, this one is a standout.  We go every Wednesday evening, when admission is by donation only (yes, we do make a contribution--we're not complete freeloaders).  We decided at the outset to start at the beginning and work our way forward chronologically, so we commenced with the Old Egyptian exhibits and went on from there.  In our four visits to date, we've made it through the Etruscans, the old and new Greek exhibits, the old and new Romans, and we're partway through all things Asian.  Simply awesome stuff, especially the Greek vases and the Chinese ceramics.  However, if we're going to make it to the rooms with the contemporary work by the time P. is done with his treatments, we are definitely going to have to pick up the pace.  Since art that was made five minutes ago is one of my special pleasures, I am motivated to keep going.

    Best List #4:  We have a place here at the Hope Lodge.  Some people now at the lodge previously had to stay for some length of time in random hotel rooms while waiting for a room here.  They report that it was as gloomy and as isolated as I feared that type of housing situation would be.  I continue to be thoroughly grateful that we are here for the whole of P.'s treatment regime, even if I am sort of the Cinderella of the kitchen (see griping above).

    Best List #3:  My cousin has been a wonderful friend and native informant here.  Since L. has lived in this city for 20-plus years, she has deep expertise in what is worth going to and how to get there.  A special plus is the fact that we share many of the same interests and preferences.  I should mention, too, that she has been fabulously patient with us, even when we keep calling her for help when I break things (e.g., a tooth, my glasses).  She always has good suggestions for how to find an expedient remedy.  She is a discerning restaurant guide; we've had terrific Thai and Indian meals here, both very high on my list of great cuisines.  And she's been good company during a complicated time in our lives.

    Best List #2:  P. continues to be experiencing few side effects.  Having gone through 19 treatments now, he's had plenty of time to watch for the potential bad by-products of having a particle accelerator pointed at one's head Mondays through Fridays.  But, so far, he's doing great.  His doctor says that, since he has made it this far this well, we might sail through the rest of the treatments just fine.

   Best List #1:  The doctors say to expect a complete cure.  And so we are.  

   Bonus Item:  I do know how to bead without any tornado crimps whatsoever: