2009

“O” My

Wow. How weird was that?

Thanks to everyone here for your support and faithful viewing! 

Overall, I was happy with the show but (I must admit) a bit disappointed with the editing, which made my segment feel a little disjointed. Here’s what I was trying to get across: There were two things Dr. Oz said that stuck with me that fateful day in the surgeon’s office. One was about being the world’s expert on your body. Yes, good. But the second point was about the importance of hearing your doctor say the words “I’m sorry.” I explained how Mary looked the surgeon in the eye and asked  him to say that he was sorry. I explained how the minute he apologized, the energy in the room shifted from confrontational to compassionate. And that hearing him say he was sorry is what allowed me to release my anger and see him as a human being who’d made a mistake. Well, the editors kept point #1 and spliced it together with the tail end of point #2, which didn’t make sense to me. All of a sudden I went from feeling like an expert on my body to releasing my anger. Wha? I know I’m splitting hairs here, but, in a perfect world, I wish there’d been time to get both messages across. But that’s okay…the television experience was a hoot, and we came home  with a suitcase full of neti pots and “O” swag. If anyone missed the show and is feeling left out, check out an awful picture of me and read my sad story here. 

Stranger Than Fiction

Believe it or not, I’m appearing as a guest on The Oprah Show tomorrow, May 12th. The show is a final tribute to Dr. Oz, and I’m on talking (very briefly) about my botched mastectomy. Might as well make lemonade out of that awfulness, right? I know, I know…why the hell haven’t I blogged about this? Especially given that Mary and I flew to Chicago two weeks ago to tape the show!!! Well, because I signed a strongly worded legal document agreeing not to blog, write, or otherwise report on my “O” experience. So, no, you won’t be reading any behind-the-scenes “O” scuttlebutt here. And, hopefully, this post won’t land me in hot water. BUT I wanted to let y’all know in case you wanted to tune in and share in this very surreal experience with me.

Coming Home to Family

Last weekend marked the two-month anniversary of my double mastectomy AND the 135th running of the Kentucky Derby. So, of course, I went to Louisville, to my parents’ house, the house of my adolescence, and the first place that comes to mind when I think of Home. 

Coming home to my family is almost as daunting as coming home to myself. Something about being surrounded by family is both comforting and excruciating. Maybe because, under the lens of their loving scrutiny, there is no place to hide. I eventually relax into their collective embrace but it takes awhile. And, while the end point is freeing, getting there is exhausting.

As the sole homo in a very hetero group, I’ve always felt a bit like the family oddball. Now, I’m not just the homo in the room–I’m the homo with cancer. Great.

I arrive just in time for the annual Derby party. It’s a contained but boisterous gathering of familiar faces, and I’m seduced by the group’s revelry. Wanting to join the fray, I sit in an overstuffed chair next to the television. In less than five minutes I’m back in the kitchen gasping for air. A few minutes later I try again, but this time I stay on the outskirts of the room, near the door. I feel like a child hovering at the edge of a pool, one who wants to join the fun but is deathly afraid of the water. So I skirt the edge, dipping my toe in and yanking it back out, shocked by the intensity of the cold and the potential for drowning.

Of course, my behavior isn’t that unusual. Like I said, I’m a bit of an oddball, and in a crowd, even a familiar one, I’m easily overstimulated and quick to retreat into myself, like a box turtle at a kids birthday party. My immediate family is comfortable with my awkwardness. And they know that my illness has intensified my skittish nature. They help me lick my wounds without ripping things wide open and, for that, I am grateful.

My extended family—god love’em—is a different story. Overflowing with good intentions, they march right up to  my rawness and begin the debridement. I’m not twenty seconds in the door before I’m ushered front and center, told a feel-good-breast-cancer story, and presented with a pink-ribbon-styled lapel pin. Staring at the trinket in my palm, I can’t help but wonder if this trip was a bad idea. “Too vulnerable to exist” is how Audre Lorde described feeling after her mastectomy and I can relate.

Indeed, I have several of you to thank for suggesting I read The Cancer Journals by Audre Lorde. Her reflections upon breast cancer and her mastectomy have resonated deeply with me, including her experience of homecoming:

Going home to the very people and places that I loved most, at the same time as it was welcome and so desirable, also felt intolerable, like there was an unbearable demand about to be made upon me that I would have to meet. And it was to be made by people whom I loved, and to whom I would have to respond. Now I was going to have to begin feeling, dealing, not only with the results of the amputation, the physical effects of the surgery, but also with examining and making my own, the demands and changes inside of me and my life.

Eight weeks post-op and I’ve only begun to feel the traumatic impact of cancer on my mind and body. On a physical level, my chest is slowly thawing. The right side has more sensation than the left, partially because the left was assaulted a second time and partly because the lymph nodes were taken from under the left arm, creating a heavy, thick numbness. I’m still disturbed by the sheer boniness of my chest and its lack of contour, how the outline of every rib is laid bare, and how the distortion of my left rib cage, caused by the curve of my spine, protrudes so that, when I’m wearing certain clothes, I’ll catch a glimpse of it and think it is the rise of my breast. The flash of reality that follows, the sharp pain of loss, is one of the hardest parts of my so-called recovery.

I say so-called because I don’t know what it means to “recover” from cancer. One recovers from the flu or a bad head cold. Recovery implies a sense of normalcy that feels beyond my grasp. But, then again, a certain sense of normalcy has always felt beyond my reach, so maybe this is just to be expected.

The Accidental Vegan

Seems I am always hungry these days.

After being a happy-go-lucky vegetarian for twenty years, on the heels of my breast cancer diagnosis and with the encouragement of several trusted sources, I’ve sworn off dairy, wheat, and sugar. And, given that my cancer is estrogen sensitive, soy may be next. (Even though soy lattés are the only thing saving my sanity at the moment, so you may have to pry them from my cold, dead hands.)

What do I eat? Mostly veggies, nuts, beans, rice, steel cut oats, and a few quixotic grains, such as quinoa.

Of course, I’m hoping to expand that list (soon). Any given day will find me wandering the aisles of my local health food store with a wild look in my eye. I skip sections I used to drool over, like the cheeses and baked goods. Instead, I hover dutifully in the produce aisle and fill my cart with purple kale, lush broccoli, and stumpy carrots. Then I take my greenery for a spin. We ride up and down every aisle hunting for something that will satisfy my gnawing hunger. Last week I discovered a bulk bin full of date bars sprinkled with coconut, and I felt like I’d won the lottery. Sure, they look like cat turds coated in litter, but I devoured them anyway. That’s how desperate I am. Besides, I’m cranky. I’ve got a caffeine headache. And I’m never in the mood to cook anymore. 

My predicament is made doubly painful by the fact that I love food. (And, by food, I mean anything that contain sugar, wheat, and dairy.) And, when I say love, I mean LOVE. Food is my hobby. I love to think about it, shop for it, and–once upon a time–cook it. For years I meticulously planned my afternoon outings according to what errand might take me within arm’s distance of a brownie or overpriced coffee drink. Mary laughs because I won’t even go on a dog walk without at least $2 in my pocket  in case I stumble across a bakery. If you’d told me six months ago that I’d soon give up every food I held dear, I would have laughed–hard. But then I got breast cancer and things changed. I changed. Funny how once you hear the doctor say, “it’s cancer,” you can’t help but stare at the food perched on the end of your fork and think “did you do this to me?”

Yes, trying to regain control of one’s life with a knife and fork is a cancer cliche. Whatever. Shortly after my diagnosis, I spoke with several breast cancer survivors. Our conversations meandered down the usual paths of diagnostics, surgeries, and treatment protocols. And, near the end of each chat, I’d ask about lifestyle changes. As in, “so, did you change your diet?” Without fail, every woman admitted that, yes, in the throes of the initial scare, she’d raced out to buy “The Juicer.” Then she’d guiltily confess that, after securing a clean bill of health from her oncologist, she ran straight back to her old ways of eating. Sayonara juicer (aka sucker). Once a symbol of health and salvation, the treasured juicer became just another discarded souvenir of her visit to Cancerland…a trip she’d rather forget. Besides, what better way to forget your troubles than with a triple fudge sundae?

Call me a control freak. Call me self-punishing. But I don’t want to forget my trip to Cancerland. How can I forget when I’m tossing back 20 milligrams of Tamoxifen every morning and wondering if the drug will make my uterus implode. Plus, HELLO, if something is going to have an impact on your body wouldn’t it be food…the stuff you’re gobbling by the pound instead of by the milligram? And so I trudge on…steering my cart through a world of temptation, listening to my stomach growl, and, eventually, heading for the cat turds.

 

 

 

 

Now what?

Life is so weird. Last week, after giving me a get-out-of-chemo-free card, my oncologist wrote me a prescription for Tamoxifen and told me to come back in six months. That was it. End of story. As in, don’t let the door hit you on your way out. Mary and I were giddy as we left his office. We drove home chatty with our good fortune, called our families to share the good news, and took ourselves to a celebratory dinner. Then came Thursday morning. With no doctor’s appointments, no medical errands, no looming surgery to fret about, I vacillated between a profound sense of relief and a disturbing sense of “now what?”  

Mary and I both felt the shift and quickly landed on metaphors as different as our personalities. I pictured Dorothy in the Wizard of Oz. I felt as though I’d spent the last 10 weeks tossed about in the eye of a tornado. My life turned upside down, shaken, rearranged. Then, a week ago Wednesday, the wind stopped howling, my world stopped spinning, and I dropped back to earth. Now, I’m struggling to get up and dust myself off, but I can’t get my bearings. I’m home, but I’m lost.

Mary, the media scholar, said it was as though her brain was no longer stuck on the “cancer channel.” As if someone had finally handed her the long-lost remote, giving her the freedom to choose her programming again. This past week, as I watched her get sucked back into her hectic work life, a part of me is jealous (something I thought I’d never say) because it feels like she can switch back to her “regularly scheduled programming.” I, on the other hand, have no idea what that looks like anymore.