“Woe to the man whose heart has not learned while young to hope, to love and to put its trust in life!” (Joseph Conrad)

December 30, 2007 at 5:23 pm | In breast cancer, cancer, health | Leave a Comment

I haven’t blogged much this week because I am out of town, “getting my affairs in order” as it were.   My father got married yesterday, and we’re in South Carolina to celebrate with him.  As we have other family friends nearby, we decided to head up to the Charlotte area afterward and spend a couple of days with them, too–giving me a chance to really enjoy the holidays with those we love before going in for surgery.

Dad’s marriage, and being around family I hadn’t seen in some time, was a tonic to my soul. I have to admit I have in the past been prone to cynicism (stop laughing, all you who have known me 10 years or more)!  It reminded me of my own marriage nearly 10 years ago.  Those who undertake marriage are always investing faith in the future, depending on love and trusting in another to keep promises. That’s a really hard thing to do!  It was especially hard for me, and I imagine for many of my generation, the kids of the 70s and 80s, over half of whom watched our parents divorce–then remarry, then more than half of those divorced again!  My father chose, instead of bitterness, hope.  He chose to risk happiness instead and I have not seem him happier.

When Jay and I got married, Dad made a toast in which he advised us, as we go through life together, to always remember what brought us together in the first place.  That advice has proven invaluable to me.  By not dwelling overmuch on the little things–who forgets to put the trash out, who nags a bit much….but focusing on the forces that brought us together years ago, we’re able to go on happily.

When I met Jay, I had been through a fair amount and had pretty much lost faith in other people.  Jay gave it back.  He won my trust, and that’s huge.  I knew that I didn’t have to be perfectly strong, perfectly self-sufficient, perfectly perfect, with Jay.  He respected my accomplishments but came with many of his own.  He loved me, but didn’t idealize me.  I wore myself nakedly to face him, and he loved me anyway.  That has kept me confident and positive throughout this cancer experience.  I knew I could fall apart and sob on his shoulder, and he’d support me. I knew–and know–that he’d do anything it took to be by my side.  And, for those who’ve never been through something like this, that is worth more than a lifetime’s worth of hauling garbage or putting the toilet seat down.  Maybe everyone else out there already knew that, but until I met Jay, I didn’t trust my own judgment to understand.

I don’t wish cancer on anyone, ever, but I am grateful that I have been able to be weak for a spell and rely on my husband to stand strong for me.  I know it’s been really hard on him, too, and I am grateful that he has never passed that on to me (though I can sense it in him).  Cancer has reminded me, or in some cases revealed to me, how incredibly lucky I am to have the support system I do.  How do people who do not have such amazing friends and family survive?

“Wise men speak because they have something to say; Fools because they have to say something.” (Plato)

December 24, 2007 at 11:06 pm | In breast cancer | Leave a Comment

Merry Christmas. Count your blessings. I have three blonde blessings sleeping like angels in my room, surely dreaming of sugar plums and Webkinz and American Girls. Life is good.

Each of the girls created mile-long wish lists for Santa.  On Arden’s list, item #2 was: “For mommy to get better.”

‘Nuff said.

“Somewhere, something incredible is waiting to be known.” (Blaise Pascal)

December 21, 2007 at 8:16 am | In breast cancer, cancer, health | Leave a Comment

So, I picked this quote for today because I found it under the category “waiting” in the quotation dictionary. So it applies to my current state–but it also has much broader meaning for me.

The first meaning is, of course, my surgery. Apparently the surgeons were waiting for me to confirm that I’m having my surgery there at the Mayo (as IF I’d go anywhere else!); so when I called to nag on Wednesday to find out when it would be, they were actually waiting on me. Then I find out that one of the nurses has laryngitis and one had a family emergency and is out. The smooth-running organizational miracle that is the Mayo came to a screeching halt, at least for me. So I’m still waiting, quite anxiously. I really need to know. Not as much because I worry about the cancer spreading; I just want to move on with my life. I’m a rip-the-bandaid-off-fast kind of girl, not someone who waits to see if it will fall off on its own. I am ready!

I am also absolutely terrified. Who wouldn’t be, really? I was completely impressed with the plastic surgeon–he showed us some photos of results he’s had and it’s amazing what they can do now–but the fact of the matter is that it’s not like losing a kidney, a body part you never saw in the first place. It’s losing both breasts completely and then slowly, slowly being rebuilt into new, though not “natural” models. And, honestly, the pain worries me. I am a world-class wimp when it comes to pain. And all my life I’ve been very healthy–other than the usual bugs provided generously by my children and students, I have had no chronic diseases. Until this year. It’s hardest to accept dealing with life-long changes and chronic illness. Even the reflux I got this year is difficult to deal with.

The other side of the quote speaks to me because it seems to represent utterly my understanding of the world ever since I learned to read. If for no other reason I’m glad to be a human because I can read. Books represent opportunity, and there’s nothing worse to me than to be disappointed in a story. Also, the quote makes me think about my perception of the world beyond reading–every day is an exciting opportunity to learn something. I’m not talking about differential equations here (as if I even had a clue what those are), I’m talking about everything from facts to events to philosophies. I mentioned in an earlier blog that I don’t “believe in” Dr. Phil and etc.; and it’s not so much that I reject self-help books and that sort of thing–I don’t; it’s that I reject blind acceptance of Oprah’s words as if they were absolute wisdom. A friend of mine said she would love to be Oprah’s girlfriend. And I realized that I would, too! But still and all, I wouldn’t take everything she said as gospel truth. I’d love to be her girlfriend so I could argue, debate, and discuss with her. I love to learn what everyone has to say and then think on it for myself. To examine, think, explore, learn everything that I can. I think that’s why I love teaching and change textbooks every semester–I love reading new essays and ideas and discussing them with my students. I want to have my surgery so I can begin dealing with it by experiencing it.

I was reading the final exam of a student in a colleague’s class (as we do every semester), and I was struck by an essay by a student who wrote that she (maybe it was a he?) believes that people are too afraid of death, and that fear gets in the way of really living. I won’t go into too much detail here, but it really spoke to me. I was awed by the depth and clarity of this student’s thinking (most of UT’s first-year writing students are 18-19 years old and not all that worldly yet–I know I sure wasn’t at that age). I was also taught a lesson–to remember not to let death get in the way of living every day fully. Every day there are multiple incredible things waiting to be known. Life is exciting. Death is, well, it’s something I’ll learn about later. Hopefully, much later!

Carve your blessings in stone, and write your sorrows in sand….and never say never

December 17, 2007 at 8:57 pm | In breast cancer, cancer | Leave a Comment

OK, by now you’ve figured out I love aphorisms. The one above (the part before the ellipsis) I pulled and paraphrased from a Wireless catalog. The rest is my own hard-earned lesson, learned once again recently. Right now I’m getting through my days relying on the fact that my forthcoming mutilation is just a blip on the radar of what has been and will be long, happy life. My blessings are many and so much more important–an amazing husband, fabulous children, tremendous friends and family, and an intact sense of humor. Sorrows, well, they don’t really disappear like words in sand after the tide rushes in, but there’s no need to dwell on them.

As for never say never, well, I have learned that the hard way. Examples: “I’ll never drive a minivan” (I did, 2001-04); “I’ll never live in the suburbs” (I live so far out in the sticks of NW Tampa now that my urban-hip work friends say I live in “Georgia”); “I’ll never get old and move to Florida,” well, you get the picture. Once upon a time I also said I’d never get plastic surgery. OOPS! That one sure is coming back to bite me!

I had my consult with the general surgeon and the plastic surgeon today. I learned that I am not a good candidate for a lumpectomy, so I’m definitely in for a mastectomy. And, given my family history and my relative youth, having a bilateral mastectomy and reconstruction is a good option. And that’s the way I’m going to go . So in a couple of weeks I’ll be operated on and then the process to replace my breasts will begin. It will take a lot of visits to the Mayo, apparently, even if all goes perfectly during surgery. If all does not, then they may have to go back in later for more cancer-treating surgery.

I will also have a test for the so-called breast cancer genes (BRCA-1 or BRCA-2) and genetic testing; that takes 6-8 weeks to come back. If it’s positive they may also send me to have my ovaries removed as a preventative to getting ovarian cancer. I’ve learned a lot today–hopefully in the next day or so I should know when the surgery will be. I’m beginning to feel like a moldy cheese–you know, it’s still good if you cut off the moldy parts. When my hair starts to fall out during chemo I think I’ll get a new t-shirt that says “bald is the new gray.”

And throughout all of this I feel tempted to just numb myself and look to the future–but I feel like that’s the wrong choice. I should not miss any of this. I’m grateful it’s not lung cancer, that my children are not sick, that, as my daughter said tonight, “I’m sure glad we’re not homeless and in Boston. We’d be freezing to death!” Definitely a blessing.

“In all affairs it’s a healthy thing now and then to hang a question mark on the things you have long taken for granted.” (Bertrand Russell)

December 13, 2007 at 9:00 pm | In breast cancer | Leave a Comment

I am here in the car, Jay driving, on our way back to the Mayo Clinic for a meeting with the oncologist and an MRI to take a final pre-surgical look at what’s going on with me. I’m reading Chapter 8 of Care of The Soul, photocopied and given to me by a colleague who is also a 17-year breast cancer survivor. In one section, the author writes: “If my colon is in pain because of anxiety, then the organ is not just a piece of biologically functioning flesh. It has some link with consciousness and a particular mode of expression” (163). After reading this I felt I had to sit down and write. I have written before about this mind-body connection. I do believe that I must learn to listen to my body, soul, and mind in order to create a positive, present-living existence that actually works for me. Though I have rigorously followed the tradition of those whom I idealized–other academics, superwomen, great thinkers. But, my life simply has not been working. Those rules just don’t work for me, though I have never questioned their legitimacy. I’ve just always tried to make my life work by those rules.

People often say to me, “I don’t know how you do it” referring to my so-far successful career, my almost full-time parenting duties, my sole management of our household, and my very happy marriage. What I usually say is, “I do none of it well.” They perhaps think I am joking, for on the outside I appear to be pretty successful at juggling. But my health has been fading and my heart has slowly been abandoning a career I once loved. The fact is, I cannot do it all. Maybe some can, but I cannot.

I do believe that sickness arises often in part to life’s imbalance. Of course, there are germs and genes to consider, but I think that’s an oversimplification, too easy an answer. Just recently I watched a stomach virus run through my family–it hit Elise immediately but for no more than 24 hours, but then she threw up again 4 days later. Jay it took almost a week to hit, but he was over it in a day. I never got it. My mother in law and father in law caught it after a couple of days, but when it did it felled them so completely I thought for sure they’d be hospitalized. Perhaps my body, feeling pretty satisfied with its recent onslaughts with me, protected me. Why is this? I simply don’t believe that there are any one-size-fits-all answers any more, which is why I don’t believe in Dr. Phil, the South Beach Diet, Parenting Manuals, or How-to-Make-a-Million dollars books. I never believed that there was one right way to teach writing, so why would I believe there was one answer to illness, or to how to live? It’s just too easy.

My father commented on one of my posts here that I should not blame myself for my cancer, that he is sure it is just a broken gene that has been passed along. This is surely true—I can hardly see how it can be mere coincidence that so many in my family could have been stricken with breast cancer at my age. But there’s a larger question here—how did the gene get “broken?” Why do we keep passing it on? What mind-body-soul connection could be made here? Could it really be as simple as a mutated gene?

There’s certainly no dearth of sadness, of mind-body separation, in my bloodline. Running alongside the premature gray gene are tendencies toward addiction, toward mental illness, toward destructive perfectionism. Could the gene be a broken attempt to evolve with the people it inhabited? What would “fix” the gene that science cannot address?
Maybe I wonder about this because I want to imagine that I can work on changing, or un-mutating those genes, through my actions. I mentioned before how I feared that I had handed my daughters a deadly cancer gene. But more importantly, really, is what I hand them every day. I am teaching them that what it means to be a woman is to be overextended, overcommitted, and still undervalued in many of the arenas in which she lives. It means finding what might be someone else’s way to a fulfilling life, rather than one’s own. I haven’t been creative in trying to solve the issues that face me. I have not only ignored my body, I’ve ignored my spirit.

Another reading from my colleague spoke of cancer as a gift. Also, a comment here by Trudi Buscemi spoke of my cancer as an opportunity, and a gift that would change my life. I find myself agreeing. This is better than a midlife crisis (I never wanted a red sportscar anyway). It has been an opportunity to see the beauty of the human spirit in others; to reevaluate how I can live my life in the right now (instead of in the constant forward-looking fashion that academia dictates); and how I can live a life that will feed my soul and bring something forth that will positively affect the world. And though it’s a time of destruction of part of my body, I think it’s also an opportunity to recreate the rules I choose to live by.

Next time: Whose dream is it, anyway?

“Why do you hasten to remove anything which hurts your eye, while if something affects your soul you postpone the cure until next year?” ~Horace

December 11, 2007 at 2:18 am | In breast cancer | Leave a Comment

I was searching for an appropos quote about the body-mind-soul connection. I have been thinking a lot about that lately. And I have also been thinking about how quick we are to ignore our soul’s aches and needs, while never giving a second thought to how we labor over our bodies’ appearance. A friend and I were talking today about how outward-looking we tend to be. We look to the sky for God, to others for approval, to money for happiness. Why don’t we look inward for these things? Why don’t we protect our souls the way we protect our hair follicles, skin cells, cuticles, and tooth enamel?

After all, I tend to think that when we neglect our spirits, they find a way to be heard. This semester has been an especially diffifult one in terms of my health. Since I had my children I and then returned to full-time work almost five years ago, I have struggled mightily to find some sort of balance between the demands of work (where there’s never a limit to the number of committees needing my help, students needing my attention, and articles to be researched and written), home (don’t even get me started), and family. I have forgotten or missed dental appointments, hours of necessary sleep, and cut corners in every facet of my life in order to try to be everything to everyone all the time. Oh, my soul probably tried to tug at my sleeve for attention, but when I didn’t listen, my body started dropping hints. First, the headaches and sore throats that turned out to be reflux; then, the stumbling-over pain of ovarian cysts. And in between, appointments with two doctors, 2 MRIs, x-rays, and a sonogram. Eventually, I just had to take out the time to find out what was wrong. And then…the LUMP. And about a hundred
MORE tests.

I think that we (or at least I) tend to think of the body as discrete sets of systems–the brain, the digestive system, the reproductive system, and so on. When one acts up, we go see a specialist–psychiatrist, ENT, opthamologist, priest. The truth, I think, is that that they’re all interdependent and all require some sort of balance. And balance, perhaps, is achieved through listening quietly to our spirits for guidance–from God, from the cosmos, wherever. The point is, the answer isn’t on Oprah and it isn’t in our role models, who probably have problems of their own. the answer is most likely within us somewhere.

I have had a couple of those moments of peaceful conversation within my soul. For me, they were moments when I felt God spoke to, through, from within me. The first was shortly after I found out I was pregnant with my elder daughter. I have spent much of my academic research life interested in questions of power–who has it, who doesn’t, what people who don’t have power do to make their way in the world–and then, in a casual moment, I realized what true power is–it was right there within me. What can be more powerful than holding life within the body? What can be more miraculous than that? As my friend and I talked about this today, we brought the comparison of the celebration of the Christ child to the reverence we hold for new life in general, and she commented that if all the world for just one moment could feel the this power, which is manifested, paradoxically, through the complete surrender of personal power to the potential of new life, then we might remember what really matters for just one moment.

So I am promising myself to do a better job of balancing my life once I get through this cancer thing. This time, I’m going to count myself into the balance and figure out what works for me–not based on what anyone chooses to do, but on what feeds and nurtures my spirit, as well as my body and mind. Otherwise, I won’t be around long enough to be much of a mom, wife, teacher, daughter, friend…to anyone!

It’s like Christmas….you know…..it’s not really about the presents.

Is this the most amazing group of people, or what?

December 8, 2007 at 2:49 am | In breast cancer | Leave a Comment

All my thanks and appreciation to my Digital Rhetorics class–and BRAVO for putting Digital Rhetoric in action with this video and piling on the pathos ;) I miss you guys and I can’t wait to see you all graduate!! Just think, you will all be famous and known nationwide for your rhetorical skills at each of your professions, and *I* will be going on Oprah to talk about each of you :)

Have a wonderful Christmas/Holiday season/New Year. THANK YOU. You made my day!

Dr. SG

Out, damn spot! Out, I say! –Lady Macbeth

December 7, 2007 at 2:20 am | In breast cancer | Leave a Comment

Today we were back in Jacksonville for more tests (chest x-ray, EKG, urine, blood, etc.) and to meet with the nurse educator. I was fine, really fine, and ready to get the show on the road. I was handed a new schedule (back next week for MRI and then to meet with the oncologist, plastic surgeon, and general surgeon after that) and discovered that I won’t know when my surgery will be until the 17th at least, and it can be anywhere from a few days to a few weeks after that date. Since we’re getting frightfully close to Christmas, it may well not be until after the new year until I have the surgery. Between now and then I have lots to look over and think over.

Ever since I found out that this was probably cancer I have been desperate to have the surgery and just get these poisonous cells out of my body. Like Lady Macbeth, I just want them OUT! I’ve also had so many questions in my mind, like: what did I do to deserve this? Is this some cosmic payback for throwing that dictionary at my sister in 1977? I realize that, of course, it’s most likely a genetic thing in my case, but still–I have imaginary blood on my hands, as it were–guilt for not eating well enough all these years (though I eat so little red meat and a generally healthy diet, except of course for all that ice cream), for not exercising enough in my 30s, that sort of thing. Although as a professor I live in the world of ideas, the intellectual life, my body is calling attention to itself and calling me to account now. What good is a brain without a body to move it around from place to place?

But the other side of the coin is that proceeding with the surgery makes it all too real. As the nurse educator kindly explained procedures and options and showed me line-drawings of them, I found myself breaking down. Those who know me will have just fallen out of their chairs in shock, so we can wait for them to get up again and keep reading . . . .

I am not A Cryer. In fact, I’ve always had very little patience with Cryers, suspecting them of using tears to manipulate people. I come from a long line of Episcopalian robots who don’t cry (see the video clip, it’s one of my favorites). When I sobbed at my grandfather’s funeral a few years ago (in Richmond, VA, home of the WASP), everyone looked at me like I had utterly lost control and I am surprised no one dragged me off in a straightjacket.

But the fact is I found myself with weepy eyes, reaching out for Jay’s hand and then clutching it in sheer terror. I am going to have part of my body cut away. Then I’m going to have to recover. Then more drugs and/or radiation will assault me and I will have to recover from that. So I’m terrified of proceeding, but also terrified of not doing so. Those cells are inside my body right now, and my best–my only–chance of surviving this for any meaningful length of time is to get them out relatively fast. My academic schedule is inflexible–I can’t exactly ask the University to push back Spring ‘08 semester by a few weeks to accommodate me–and Christmas is pretty much gonna arrive on 12/25, like it or not. And my body will continue to destroy itself, bit by bit, if I don’t let them do something pretty soon.

So, pretty much, today was Feel Sorry for Myself day. I wallowed, I sobbed, I gazed off into the distance, a thoughtful and I hope attractive look of introspection on my face. Tomorrow, I will gird my loins and be ready. I have to. When we got home tonight Elise threw up again.

This Little Light of Mine

December 5, 2007 at 1:03 am | In breast cancer | Leave a Comment
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This morning on the way to work I heard a news reporter conducting a mock-caucus in Iowa. One of the women being polled was talking about how much she resents taking care of others via paying taxes, and said that she works really hard and makes a lot of money off her own hard work. Then she said something that nearly stopped my heart: “I’m sick of paying for other people’s children to eat hot lunch at school.”

How do we respond to that? That kind of comment shows an ignorance of the most basic codes of religious and social norms–that people thrive best in communities, and that we care for others as we would want to be cared for; that children who have been born into poverty–at no fault of their own–have a right to a fair chance at success in the world, and giving them a 50-cent lunch is hardly a cause for resentment. We all depend on one another. Some day that woman, who is single and has no kids, will be dependent on a nursing home employee–perhaps one of those very children whose lunch her tax dollars paid for–I wonder how she will be treated? Will that worker treat her the way he’d treat his own grandmother? Or will he, having been raised in a world where it’s every-person-for-him/her-self, treat her the way she would have treated him?

Then, later today, I went to my daughter’s school to watch her Pep Squad practice. A friend whose daughter is in my Arden’s class handed me an envelope. Inside was an amazingly thoughtful card and a magnet that said “Just when the caterpillar thought the world was over, it became a butterfly.” It was all I could take not to cry right then and there. But the best part? There was a note inside that said that she and another friend of ours would like to coordinate help for me during my treatment. They have offered to get meals delivered, cleaning services, errands, well….all the things I will probably feel too cruddy to do for a while! Now, these are not two bored women with nothing better to do, nor are they seeking anything in doing this for me. In fact, they are incredibly busy people with responsiblities and families of their own, as are all the friends who have reached out and offered help. I have always known how fortunate I am to know them. . . yet I am overwhelmed by this amazing generosity. How very blessed my life is!

In addition to that, people at work have gone out of their way to offer support, prayers, practical help, and humor when I need it most. One friend’s mother heard of my situation and send me a little framed print that says “believe.” And I can’t wait to write her a note thanking her and assuring her that, indeed, I do believe! I certainly do!

It would take the rest of my life to repay the many kindnesses and supportive words people have offered me. How truly lucky I am to have such an amazing family and friends. The vast gulf between the comment I heard on the radio this morning and the loving expressions I have been offered this afternoon and at other times actually brings me to pity that woman who resents paying toward school lunches. Who will love her, and care for her, when she needs it most? Her bankers? I doubt it.

And for the title of this post: I have been getting our Christmas decorations up, and pulled out my reindeer lights. It’s a string of lights that’s old and was cheap when I got it. One of the bulbs has gone out and I can’t find any to replace it. On this string, if one light quits, they all quit. I ended up pulling the plastic reindeer off the light string and placing them over other light bulbs on the tree. They’re all there. And I think life is like the lights on the string–the world falls apart when not everyone works for each other. We all have to care for each other. No one knows that better than I do.

Our finest gifts we bring (pa rum pa pum pum)

December 3, 2007 at 12:30 pm | In breast cancer, cancer | 1 Comment
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Saturday my husband’s sister bravely flew in with her three children–the eldest is five–for a 2-week visit. My inlaws live just an hour and a half or so south of us. While it is wonderful to see them–I can’t believe how those kids have grown!–they brought us a bug–a nasty stomach bug that kept my five year old up all night last night, and I imagine the rest of us will get it as well. Oh, the joys of holiday giving!! The upside is that our visitors totally took my mind off my situation and seeing the four of them is worth the throwing up, as we really don’t get to see them nearly enough, and my 5 year old and her 5 year old cousin get along like a house on fire. (Ask me again if it was worth it if *I* actually get sick.)

Yesterday we told my 8-year-old daughter, Arden, about my cancer. I didn’t go into any great detail (5-year survivial rates, that sort of thing) but I did tell her that I have cancer and will be in and out of the hospital for a while. Though she was upset just a little, I think more than anything she was relieved–she has known for some time that things aren’t right. I told her that if she had any questions at all she could ask, and that it is perfectly okay to be upset or to have sad, weird, or unusual feelings. I’ve been trying like crazy to keep her routine, but let’s face it, as my mother in law said, there’s nothing “normal” about what’s going on with me.

If you’ve ever done any research on the statistics about who gets breast cancer, you know that paternal relatives aren’t supposed to “count” in raising your risk. Well, I’m living proof that they do count. My father’s mother, her sister, and her niece all had breast cancer, and all first got it around my age. Now here I am with it. Thanks for the genes, Dad!

Which brings me to my real point today. What really jars me is not losing my breasts or even my hair (about which I confess I am vain), but what I have given my children. I am the mother of girls. In the past, it’s been a wondrous experience watching them grow and to be able to see the little inherited traits in each of them–Elise’s left-handedness is mine; Arden’s eye shape is definitely mine, though the color is either my Great-Aunt Grace’s or my mother in law’s (beautiful blue-green). But breast cancer genes? Who wants those? I suppose I can pin my hopes on the possibility that they will have a cure in 30-35 years when the gene rears its ugly head in them; but I am guessing my grandmother (who had sons) had those same hopes for me. It’s a terrible, terrible feeling to know that I have probably passed this deadly gene onto my children. And it offers me little solace to know that I am the canary in the coal mine for my younger sister, who is now on red alert.

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