JenniferJune 5, 2007 7:30 pm

Hello, everyone!

Yep, we’re back. Some of you may be wondering how it went: the trip to Vienna, the flight back home. Vienna, of course, was wonderful. We had a place there which was billed as an apartment but was really one big room. It did have a small kitchenette, thankfully. Also, it mercifully had a partial walk-in closet just right for a crib. – When we first arrived, we were rather mortified to find the crib right there in the room, right next to our bed, across from the kitchenette. The place was supposed to be a ‘suite’ thus we figured it’d have another room, perhaps other walls. Luckily, we found the closet. Anyway, Vienna was marvelous. I cannot tell you how much apple strudel, kinder egg chocolate, and manner wafer cookies I stuffed down my gullet. Plus, there were the walks everyday (I love pedestrian cities!), the gardens, the naschmarkt. It was the Vienna we love – with a two year old, which made things rather interesting.  

Then there was the trip back home. You remember the one: 9 time zones, 23 hours of straight travel, 4 planes. Economy class. Oh, and did I mention that it was solo with a two year old? That was the kicker. I do love my child. Adore her. Thankfully. Even now.

Just let me give you a little taste of what May 4th was like. Picture this: we’ve already flown on three planes, traveling 19 hours, leaving Vienna at the crack of dawn. (Blessedly, Chris went with us to the airport.) We are now almost on the last plane on the final journey to Phoenix (where we will be coddled and brought back to health by Kim, my sister). Stella-Grace has had, oh I don’t know, at least three screaming fits already (one for each plane), but hasn’t completely snapped. Well, it happens: the big snap. You see, on the third flight (the one from Dulles to Chicago), she had finally succumbed to sleep, was deep into REM, when we touched down. Because the flight had been delayed getting out of Dulles, we were told that we would have to race to our connecting gate (our initial connecting time was going to be 45 minutes, and that was when the plane was on schedule). Thankfully, it’s only three gates away. So, we’re racing. Well, fast hobbling. Me, with a huge backpack, purse, baby carrier, baby blanket, Greenie the bear, and a large bag of S-G’s food along with a rather disgruntled bleary-eyed two-year-old. Said two year old doesn’t quite grasp the importance of getting to the gate on time. Greenie, the bear, understands completely.

Okay, you get the picture. But, oh, there’s more. So much more. All I can say is be grateful you weren’t a passenger waiting for the Phoenix flight out of Chicago. Yep. Confined space. At the gate. (And, of course, the flight is NOT leaving on time.) Equals screamage. Yes, screamage. At the top of one’s lungs screamage. Ear splitting, eye swelling screamage.

So, I’m doing all I can to stop it. Out of the backpack (the one, I might add, that is packed exclusively with S-G ware, not my own) comes books, crayons, little people, stickers, crackers, chocolate, all to no avail. Let me repeat, chocolate to no avail.

There’s this new kick that S-G is on, perhaps you’ve heard of it, it’s called the "I’m too sad" response. Usually it’s woefully said between tears, but on this particularly outing it was shrieked. Now, to the ears of the untrained, it may sound like garbled howls, but, oh, I know my baby and I could make it out (call it the miracle of nature).

So, here we all are, all the Southwest passengers waiting to board, all there in one cozy little confined space with my child (Child? What child? I’m sorry, at this point do I have a child? I thought I was a young, unfettered, urban professional. Oh right, that was in my dreams.) SHRIEKING at the top of her lungs. If you have never heard this particular shriek, oh are you in for some fun! Perhaps I’ll tape it and send it to you via e-mail audio. Surely it can be used as a prison or SEAL training exercise. You know the ones, used to induce disorientation and panic.

So, we’re here. Me sitting beleagueredly in a chair, hands flying from backpack to item in backpack to child trying to assuage this, this screaming thing in front of me. Up runs – literally runs – a flight attendant (I don’t know, perhaps while they were in the air she heard the screams from the ground) with a can of apple juice and one of water.

Smiling wanly, I grab them. "Thank you," I say, "I’ll try." Do I think this is going to work? No. Does she think it’ll work? Yes. Does it work? No. The "I’m too sad!" comes out loud and strong as does the batting away of the cans.

Next, a jovial man saunters over looking extremely confident, and childless. "Let’s pull out the big guns." I hear him say through the screams. In his hand is a Twix bar.

Now, did I mention that even chocolate didn’t work with this child (whom I would at this point refer to as rabid, that is, if she weren’t my own)?

"Hmm." I offer it to the child in front of me.

Oh, the joy of yet an even more resounding scream and a plaintive, "NO! I SAID I’M TOO SAD!"

When I turn around, the man-of-confidence is gone.

We board the plane (mercifully, unlike the European push and shove, people with children have priority) and grab the two seats in the second row on the left side. By this time, S-G is at a low-grade muffle and quiets when the once-spurned (but not holding a grudge) can of apple juice is produced with a straw. The "I’m too sad" cry is now replaced with the "I can do it myself" command. For those of you who don’t know, on Southwest you pick your own seat. They aren’t assigned. Well, we are in primo seats (second row). Yet, for some reason, not one person sits next to us, not in the whole row (even in the seats across the aisle). Two do sit in front of us, one behind. Bubonic plague could not have cleared the area sooner. Of course, once we are in the air, S-G flakes out and sleeps the entire flight. It makes for a blissful journey … except for the child way in the overcrowded back who screams all the way home. I tell you, some mothers! Why have children when they can’t control their own?!

The following Wednesday, after my Doxil treatment on Tuesday (we’ll get to that later), Tasha, my niece, exclaims, "You look better after the chemo than when I first saw you."

"Yeah" I explain, "that was just chemo. When I first saw you I had traveled across country with a two year old."   

On to the Doxil front … well, Cranmer, my oncologist, read the CT scans that I got upon my return home and decided on one more round to be followed by a re-evaluation of the situation next month (which means 18 more ounces of that ever pleasing barium shake they serve – yum yum). Apparently, almost all of the nodules (which, he oh-so-sensitively announced to be "hundreds of") in my lungs have remained the same size, except for one which has grown slightly. Thus, I had another treatment of Doxil two weeks ago. This go-round, while Chris was still in Vienna heading his delegation, Tasha came to head mine. Tash is my oldest sister’s daughter. She had some time between her studies at nursing school to administer to me, the chemo-infused.

Now, let me tell you, I love Tasha. Adore her. But, again, like the trip from Europe, I had a painted scenario of how things were supposed to go and I held on to it. Clung to it, actually. I should preface this by saying that I have grown accustomed to a certain level of care giving. My sister, Kim, is a prime example: the care giver who immediately – almost telepathically – knows my needs and caters to them. Caters with a smile. Kim is an angel on earth. Which, of course, is all good and well when you’re knocked out with nausea or debilitated by pain, but, and get this gentle reader, I wasn’t. I was feelin’ gooood! Goooood! But did I let a little thing like boundless energy get me to be appreciative? To be grateful for my lot: that I had a 22 year old babysitter and companion with whom to talk? OH no! Not me! Nooooo way! I had expectations. I had an agenda in my head and a description of how my caregiver should be. Even if I didn’t need one. And it wasn’t as if Tasha didn’t help. She did. But she didn’t help telepathically. The audacity! So, I was blessed, truly blessed, to have Tasha here, but instead of gratitude what did I show? Anger. Resentment. Why? Because she didn’t follow the script. And the crazy thing is, I was well enough that I could do things! Two days after chemo, I pulled our huge trashcan from the garage to the curb in the blazing hot sun … while carrying Greenie and followed by a two-year old. I was well! Am well. Yet did I acknowledge it? Did I thank God for this blessing? Nooooo! I wanted things to be different. I had a script. So I spent a lot of the time disgruntled, silently going through the litany of things that weren’t being done, at least not how I imagined they should have been. Tasha wasn’t Kim. Of course, she didn’t need to be. She just needed to be Tash, precisely right for right then. Still, I clung on.

So, my question is, how do I accept God’s gifts? How do I acknowledge them? For so long I’ve wanted things to be "just right," "just so," the way that I think they should go. The thing is, I’ve missed it. I’ve missed the gifts that were right there – are right there – right in front of me!

It wasn’t until Tasha left, when I awoke from my bed and didn’t see her outside, dangling her legs in the pool, that I missed her. Heart longingly, achingly, missed her. That’s how I’ve lived my life with a lot of things. That’s how I lived my life with Tasha’s mother. In my script, Julee (my oldest sister) wasn’t supposed to be manic-depressive. She wasn’t supposed to act the way she did, going off on wild tangents. Yet my soul needed her – needed her there. Just the way she was. Not until Julee was gone. Not until a long time after her suicide, after I’d written about it endlessly in notebooks and on the computer, did I realize how very much I missed her. How there was a hole. And how, just maybe, the way she led her life was precisely what I needed. Precisely right not only for her, but for me, too.

Maybe that’s what this lump on my leg is doing (not to mention the "hundreds" of nodules in my lungs). Maybe I’ll miss it when it’s gone. Maybe its existence is precisely what I need. Precisely now. Perhaps instead of guarding myself against it, or pretending it doesn’t exist, I should just love it. Let go and love it in all its splendor. I mean, how else would I know what to value if I didn’t have it? It’s given me the greatest of gifts: it’s allowed me to see.  

That doesn’t mean I don’t fantasize about being a fetterless passenger in the airport or a healthy patient catered to with frosty drinks and chilled cups. I do. But do you know what miraculous thing is starting to happen now? I’m starting to get it sometimes. I’m starting to realize how grateful I should be. (Usually at the cost of realizing how ungrateful I was.) Oh sure, it doesn’t happen until days or sometimes weeks after the incident, but it happens nonetheless. And I’m starting – starting – to take myself a little less seriously and realize that I’m human. When I realize this, it’s okay that I didn’t completely see how fortunate I was to go to Vienna with child, and come back. That I didn’t appreciate how very blessed I am to have a niece who will drop everything and come stay with me, even when I’m a hag-monster. And that’s okay. I’m human. I’ll try harder next time. Life is good. And it’s flawed. And it’s perfect. All at the same time. Pretty much how humans are. Now I just have to work on loving. Loving the whole. It’ll come. It always does.

So take care, you all. If there’s one bit of advice I would give to you before your travels: buy ear-plugs.

I love you,

Jennifer

JenniferFebruary 5, 2007 8:01 pm

Jennifer

Hello, everyone!

Thanks so much for your prayers, kind words, irreverent humor, and loving support.  It has made this adventure much more manageable.

Alright, that said, I haven’t been wanting to write this e-mail.  In fact, I’ve been using just about every means of procrastination available not to write this e-mail.  No, don’t worry, it’s not due to some dire medical prediction.  It’s something much deeper.  Something at the heart of me and why I’ve been in such a funk lately.  It’s my Ego.  That damned Ego-Me entwinement.  Still, I’ve decided to ‘fess up, because, in the end, that’s all I can do, right?  And we really don’t have time for games, not anymore.

That said, first some good-news (further procrastination):

We got a house!  Yes, folks, finally.  We’re currently under contract.  It’s a great ‘60’s brick/stone house on two acres.  There are loads of saguaros, great mountain views, and a wash (read: lots of wildlife).  Plus, it’s in Northwest Tucson and right by my favorite shopping haunts (you can never be too close to a Trader Joe’s is my motto).  The house has some funky ‘60’s elements so I’m currently trolling e-bay for retro furnishings like ‘atomic’ fiberglass lamps and eames-style furniture.  We are due to close on the 22nd of this month.  We’ll also have our apartment until mid-April.  So those of you seeking warmth in the desert, book early.  I figure we should have some furniture in the new house by early March and the apartment is completely furnished.  Come one, come all.

On to the hospital front:

Apparently, the CT scans that I had in late December showed that, as my oncologist put it, the “nodules” in my lungs (which, he says, are too numerous to count) have “progressed.”  Thus, we are off to “bet on another horse.”  That horse is Gemzar.  Gemzar is an approved chemotherapy drug.  It just isn’t widely used on sarcomas.  So, after an initial false-start in which I was primed for treatment and then told that we had to wait a week to see if it was approved by my health insurance, I am on it.  Chemo is now every Tuesday of each week for 3 consecutive weeks followed by a week off. 

Which brings me to the bit that I’ve been avoiding – no, not just avoiding, burying – because it’s such a freakin’ blow to my ego.  (Which, I suppose, all in all, is a good thing.  Ego blows can be nothing but good.  Still, they’re painful.): 

Alright, so … on the 9th of January, I go to the Cancer Center for my first Gemzar treatment.  I’m all psyched.  I mean, hey, the other times were spa days: no pain, little hassle, interesting talk with friends, and a few cups of tea.  And chocolate.  So, I am ready to enjoy the day.  Even the fact that I had to wait 2 hours for blood work and that they misplaced my orders didn’t dissuade me.  This was spa day.  So, at a quarter to one, after squeezing in lunch due to the blood work debacle, my friend, Shirley, and I head up to the Central Pod.  (I kid you not.  It’s called a ‘pod’.  They recently moved the Center to a new swanky building a few blocks away and now they have a player piano and pods.)  So, we go upstairs.  To the pod.  We’re told that my treatment today will be in a communal room.  The communal rooms have four different treatment stations, one to each corner, with a recliner and I.V. hookup (not to be confused with an R.V. hookup).  The room’s full except for the empty chair to the left of the door.  We go and get situated.  I look around the room.  To my right is an attractive younger woman getting an infusion.  Her rather anguished-looking husband is beside her.  To my left is a 50ish man dressed in flannel.  His legs are jumping up and down (the spasms are a result of one of the nausea drugs he was given before chemo).  Okay, fine.  All is well.  Then I look directly across from me, catty-corner.  There sits a large, loud, middle aged, dark-headed woman.  Immediately, I get uncomfortable.  No, not just uncomfortable – pissy uncomfortable.  I haven’t even started the drug and already I’m having a reaction.  To the large woman across from me.  When I say large, I mean obese, and when I say reaction, I mean vitriol.  Literally, vitriol.  I am watching this woman – trying not to watch this woman – and spewing thoughts (not out loud, blessedly).  They go something like this: “Of course you have to be hooked up to oxygen, just look at yourself.  Look at your ankles, all swollen.  Look at your legs.  God, I bet you can’t even get up without help.  Sitting there, all high and mighty.  No wonder you have cancer.  You deserve it.”  Then, I watch her some more.  Watch her with the nurses and I become incensed, “How dare you order those nurses around.  God, you’re so rude.  And why are the nurses being so nice to you?  Why are they taking this?  Can’t they see what you are?!”

No shit.  That’s what I’m thinking.  No, spewing.  Spewing.  Internally.  At this woman.  A complete stranger. 

If you haven’t guessed it already, this is the part that I don’t like talking about.  This is the part that isn’t supposed to happen.  Not by me, anyway.  I’m above this.  I’m enlightened.  I love everyone.  Well, it happened.  By me.  To someone else.  A complete stranger.  But we’ll get to that later.

My thoughts continue this way pretty much all of the time that I’m getting treatment.  Which, by the way, is no tea party.  First off, they give me compozine.  It’s supposed to be an anti-nausea drug that works on the mind.  Welp, it worked on my mind.  Did it ever.  Within minutes of receiving it, my thoughts turn to death.  Cancer-death.  Luckily, Shirley immediately flags the nurse.  While she’s dosing me up with Benadril (to counteract the compozine), the nurse explains that this reaction isn’t uncommon in young people.  “You just want to jump right out of your skin,” she explains.  Then comes the infusion itself.  Before plugging me in, the nurse warns me that the Gemzar might hurt.  Of course I’m thinking, “No, not me.  I can just counteract this through thought.”  Yeah right.  This time I let the nurse know what’s going on and she alters the saline to counteract the pain.  While she’s doing this she informs me that some patients liken the sensation to ‘shards of glass’ entering their veins.  Ah, the thrill. 

So, we finally escape the hospital.  Me being one drugged up puppy and Shirley right-minded and driving us home.  (Chris, S-G, Rufus and I were spending the month in her apartment.  She had returned home briefly in between jaunts.)  

Okay, jump to the next morning (early, before Stella-Grace awakens), I’m having tea and gazing out the window, trying to pull it all together.  What the hell happened yesterday?  And why?  I think back to the treatment.  I think back to the room.  I try not to, but I think back to the woman (the large one who started it all).  And then I begin sobbing.  Sobbing, just like that.  Hard solid sobs.  I walk over to Shirley, who just happens to be in the kitchen eating her granola, and tell her about the woman.  Very reluctantly, I tell of my thoughts about the woman.  I’m talking about this, trying to get it out, and not wanting to get it out.  I mean, whatever will Shirley think of me?  Me, Jennifer.  You know the one.  The one who doesn’t do anything wrong.  The one who’s perfection embodied.  What will happen if she figures out that I’m flawed?  What will happen if I figure out I’m flawed?  Still, in the end, I have to tell her about it.  So, I go on and on.  All the while, Shirley proves very insightful and reassuring (and she seems to still like me, even though it’s pretty damned obvious that I just might not be perfect.)

Then, just like that, in between sobs, I get it. 

Or at least part of it.  I get that I don’t hate that woman.  I get that I don’t actually feel those things towards her.  I don’t know why I feel those things but they aren’t at her.  I don’t know her.  In fact, I want nothing but ease and comfort for her.  I do.  And my heart grows, and I realize that I love her.  Not her, per say, because I don’t know her, but her generally.  All of her.  And it’s a comfort.

Somewhat taken aback, I ask Shirley about the vitriol.  Where’d it come from?  I mean, if it isn’t towards that woman, who is it towards?  And then, I kind of get that, too.  See, for a long time now, my teachers have been telling me about how we humans project things onto others which we feel towards ourselves.  That’s why, they always explain, you have to figure out what’s wrong with you in a relationship before ending it and going on to a new one, or you’ll just replay the same scenario with someone else.  Well, I was always like, ‘yeah, yeah, sure’ – it might be like that for other people but not for me.  (Did I forget to tell you that I’m perfect?)  So, I kind of get it now.  It wasn’t the woman I was thinking all those thoughts about.  It was me.  Is me.  And I don’t even fully understand that, but it’s true.  Many, many times I’ve thought those things about myself.  Including the swollen ankles bit (my right ankle and lower leg swell due to the lump in my calf).  Have I ever fully accepted what’s going on?  Do I look at myself in disgust, just as I was viewing that woman?  Yes.  And that’s a hard one.  I look at myself in disgust.  And I don’t want to.  That’s as plain as it gets.  I don’t want to.  And part of that not wanting to is accepting what I’m thinking right now and trying to open up to it.  Because, and this is the freaky bit, if I allow myself to recognize that I view myself with disgust, then compassion starts to seep in.  And that’s what I need.  Compassion. 

It’s bizarre.  I feel like I’m going through this apprenticeship.  It isn’t all that fun all the time, yet it has to be done.  It’s similar to my time at the Neighborhood Playhouse and in Romana’s pilates program.  Break them down before you build them up. 

One of Shirley’s teachers told her that the bigger the Ego the better.  The harder the fall.  And more exhaustive.  Apparently, our human job is to build up the Ego, our soul work is to let it go.  Well, I must be a straight-A human student because I have plenty of Ego.  (In fact, I have enough for 2, maybe 3, people if anyone’s looking.)  And it’s hellish letting go.  The whole thing has got me so confused.  It’s never what I think it is – life’s lessons, messages.  Right now I don’t know which end is up.  My shaman friend would say that this is a good thing, that what we think we see is only a dream.  Yeah, well, why doesn’t it feel any better? 

Still, I gotta go through it.  This apprenticeship.  There’s no other choice.  So, if you call or e-mail me and I’m not some beacon of unending optimism, you know why.  It’s weird, I’m not frustrated about the cancer or the lack of recovery (although it does piss me off that it hasn’t happened yet).  My real frustration, my real internal wrath, is about not “seeing.”  Not letting go yet.  Yet.  I suppose I am an optimist after all. 

Still, there’s more, more to write.  About Stella-Grace (who has now become enamored of play-acting.  Frequently, she is Sparkles, the dog, but the majority of the time she insists on being called Bebe.  Chris is Boddy, pronounced Bawdy.  I’m Doogadoga.  Really.  It’s catchy.  I’m seriously considering changing my name.)  Anyway, I have a lot more to talk to you about, but I figure that you might want a rest from me right now.  There’s this whole thing about us all being saints that I’m trying to understand, but that’ll come later, in another e-mail.  Probably next week, so beware.  Right now, I’ve got to sit with this disgust-compassion idea, because, believe it or not, not until I wrote this e-mail to you did I fully understand what was going on.  And for that I am grateful.  You have given me the chance and the opportunity to understand.  By being there.  By listening.  To my funk.  So thank you.  From the bottom of my heart, thank you.

I love you,
Doogadoga rose
JenniferDecember 6, 2006 11:59 pm
May I introduce my dear friend, Jennifer. She is the most spunky truth-teller I know.
Jennifer
Hello, everyone!

 
Just thought I’d check in with you.  Thank you for your continued loving thoughts and white light.  You all are a blessing and I am truly grateful.  Again, thank you.

 
First off, for the really great news: On Friday, Stella-Grace, Rufus and I (Chris was in DC) went hiking.  Hiking!  Yes, me (alone, without any help) with a 33 pound baby strapped in the front-pack, hiking through the Catalina State Park.  Okay, so I took the easiest route (the Romero Ruin trail), but, still, there were steps.  Up (and down) 80 steps — me and baby.  It was wonderful.  Plus, we saw three roadrunners.  If you would have told me during the dark days of summer when I was writhing in pain and couldn’t lift my legs off the hospital bed, let alone stand, or when several medical ‘experts’ informed me that I might never be able to walk "the same way" again, if you would have told me that I would be hiking come December, I probably would have thrown my walker at you.  Life is good.  And living is amazing.  I had been hiking with Chris — in fact, we went hiking the day after my first chemotherapy treatment (it was a very slow hike) — but this was the first time that I had carried Stella-Grace on my own.  The first time since July, right before the spinal fusion.  It’s just so cool.

 
So, the chemo has begun (dum, dum, dumdum).  I am not a cueball-head yet, but the molting appears to have started.  (Stella-Grace, when she finds an errant hair — on her clothes, on her stuffed animals, in her food — keeps saying, "Dog hair, dog hair!"  I shake my head, while pulling the long, brunette strand away, and say, "No, baby, it’s mommy’s hair." To which she inevitably responds, "Mommy’s hair, baby’s hair." Such support, and only 20 months old!)  I’m experimenting with the idea of shaving my head entirely and getting someone (probably a tattoo artist) to do some funky henna design on it.  (Medusa comes to mind.)  It’s an idea. rose

 
But before I get into the chemo nitty-gritty, and I know you’re all just so excited for that, I want to put out a request.  For housing.  So, here goes: If any of you know of a cozy, aesthetically pleasing hacienda in Tucson that is for sale, or thinking of going on the market, please let me know.  Yes, it’s a buyers market now (thankfully) and Chris and I are doing the usual househunting, but with limited success.  Anyway, our wish list includes: a house in the North/Northwest of Tucson, by the mountains, with mature vegetation, some land (1-3 acres or so), good school district, cozy, warm, older, ceramic tile, with a casita, and local wildlife (inside and outside the house).  So, if you know of anything, please let me know.

 
I’m sure you’re all wondering about my new friend (dum, dum, dumdum) ’The Chemo.’  Well, before you read the following, remember that this is from someone who did NOT want chemo, someone who, when they told me about the B-52 killer chemo I was "supposed" to have heard a very distinct, very loud, "GET OUT!" directive.  And this is from someone who followed that directive.  Just so you’re with me here …

 
Okay, so I’m pulling into the Safeway parking lot a week prior to my first go at chemo and, I kid you not, I hear this voice say, "This is exciting.  It’s going to be an adventure."  This voice was not talking about shopping.  So I put the car into park and sit back.  "What?" I say, knowing full well what the reference was to.  "Chemotherapy." is the answer.  Right.  I’m sitting there, trying to take this in.  I wasn’t really angry, it just wasn’t exactly what I had expected.  "What," I finally ask, "what do you mean an adventure?" "You’ve never experienced it before.  It’s a first." Now, if this would have been a year ago, even a couple of months ago, I would have shut that voice up so fast, it wouldn’t have even registered.  But, you know what?  I let it breathe.  In fact, it kind of intrigued me.  And, in the subsequent days, that voice provided me with a great source of comfort.  I’d been agonizing about the treatment and if it was the best option, and then, all of a sudden, there was the answer.  It was the right thing, for right now.  Yes, this way of thinking is trippy.  Yes, it’s unconventional.  But, hey, it’s a comfort.  I take that where I can get it.  I am not suggesting that chemotherapy is some grand "adventure" we cancer patients are just chomping at the bit for.  The human side of me would have certainly passed on this one.  Still, it’s my adventure, for now.

 
The voice is a great source of comfort as is the bear.  Yes, the bear.  Okay, just to get a little more trippy on you … A few times in my meditation, prior to the first go at chemo, I started seeing a bear.  A big, brown bear.  Alright, I’ll back up a bit … When I went into the hospital for spinal fusion, particualrly right before my surgery, I saw a white tiger lying on my torso.  Okay, I didn’t ’see’ it in the "I see that the doctor is standing there in front of me" way.  But, I did see it.  More importantly, I felt it.  Don’t ask me how.  It was just there, all sprawled out, this big ole black and white striped tiger.  (Sometimes it was a cub frolicking on my lower abdomen.)  Yeah, it’s weird, and, yes, I was on a lot of meds, but I wasn’t delusional.  And, more importantly, the tiger was a comfort.  For some reason, I knew that if the tiger was there, I was safe.  So, there appears this bear, right?  Well, I go along with it and start investigating the meaning of bears.  And, apparently, bear medicine is very potent.  So, I decide that this chemo is just that: honey for my bear.  So, the bear has helped.  The honey’s helped.
                                                                                totems
As has my support team in the hospital — particularly Chris and my dear friend, Shirley.  They’ve been coming to the hospital (chemo is every two weeks, so far two treatments down) and have helped infuse the whole process (chemo bags included!) with love, support, and healing.  We even have tea.  In real tea cups.  I kid you not — as the I.V. drip is going, we dine on hot tea and brownies or chocolate chip cookies.  (My sister now refers to each chemo treatment as my "day at the spa.") The nurses are terrific as well.  They even hooked me up with a nurse who is a Reiki master and practices healing touch.  Due to hospital protocol she can’t physically touch me in that capacity, but she can infuse the bags with healing.  The whole hospital process (it takes about 6-7 hours) is really interesting.  That little voice was right.  I’ve certainly never experienced this before.  Ever.

 
Sure, there’s some nausea, sleeplessness (due to the steroids), bloating, hot flashes (now those are wild!), numbness in my feet, and fatigue.  (Come Saturday, I’m wrecked.  It feels like a really bad hangover.) Still, all in all, it’s been pretty easy.  The week after chemotherapy is the hardest, but, in an odd way, also the most interesting.  How will my body react?  What will I have to do?  (Last week, I gave myself daily injections — to increase my white blood cell count — for six days.  A month ago, if you would have told me that I’d be jabbing away at myself with a great big needle, I would have laughed.  But now it’s a piece of cake.)  Plus, maybe this week (and this is my human side talking) I won’t feel the nausea or fatigue.  Maybe …

 
The other day (while talking to Chris about our, thus far, fruitless house search), I said, "It’ll all work out.  It will.  It always does." And he said, "No.  No, it doesn’t always work out." Maybe … Yet I KNOW it does.  It may not be what we envision to be the best, or what fits into our perception of what is ‘for the best,’ but, in the end, it all does work out.  It does.  It has to.  Because, in the end, there is only forward movement.  And that forward movement is love.  Plain and simple.  It may take me three hundred lifetimes, but I’m moving forward in every one.

 
It’s weird.  I had this realization a couple of weeks ago that God/the Universe/Buddha/whatever you want to call it, doesn’t hate or judge us, or even have an agenda for us to follow or ‘be damned.’ It’s really not like that at all.  Really.  The Universe just loves us.  And I mean really loves us, like some big ole Aretha Franklin thick-armed hug love around us loves us, no matter what.  NO MATTER WHAT.  That means no matter what we do, or don’t do, we’re loved.  It really freaked me out (I was raised a Southern Baptist after all.).  "You mean there are no judgments?" I asked.  "Nope." Actually, I’m still reeling from it.  If there are no judgments, what do I do?  How do I live?  And who’s the one who keeps judging?  Who is that incessant voice in my head pointing out when I do something ‘right’ and especially when I do something ‘wrong,’ if it isn’t God?  It’s almost too much for me to fathom.  I’m so wedded to this idea that there is some magical (and elusive) ‘right’ thing to do or ‘right’ to live that I just haven’t found yet and that when I do, boy oh boy, will everything sparkle.  But what if I’m loved no matter what?  What if there is no ‘right’ path and everything sparkles, if I’d just see it?  How do I live then?                                                                                         rose

 
I still haven’t figured it out.  All I know is that there is love.  And when, in those brief moments of clarity when I realized that there is no judgment, I try to ask myself, “What feels best?”  And, you know what?  I’ll be damned (there I go again with the judgments) if it’s not love (or some form of love dressed up as a smile, or a patient response, or some blunt advice, or time).  Don’t get me wrong, lest you can’t recognize the Jennifer you knew mere months ago who made you do Magic Circle and Flow at the same time (and would do it again if I could – hahaha!  That’s manicial laughing, in case you didn’t recognize it), I’m still flying off the handle and chewing on things I have no control over and worrying.  I’ve, also, been known to use the Chemo-card (as in “What do you mean, ‘can I watch the baby for a minute’ while you go to the bathroom?  Can’t you see I’m on my fifth consecutive hour of watching the first season of Project Runway!  I just had chemo!”).  Of course, the best one (as my friend, Shirley, reminded me) is the D-card (the Death card).  I flip that one out, too, from time to time when I’m really feeling self-righteous or want to see someone (usually my husband) crawl.  What can I say?  With cancer you think comes complete enlightenment?  (See, there’s the C-card and the E-card together.  Very tricky.)  Still, in the end, it’ll all work out.  Because, after it’s all done, there’s love.  I know it.  I’m just trying to realize it.                    tea

 
Take care.
I love you,
Jennifer