Thursday, September 10, 2009

Peg's stronger this week

She took a half-hour walk by herself two days ago, and this morning our friend Katie took her to Target to buy some comfortable pants.  It's the first trip somewhere besides a doctor's appointment since the surgery.

Peg's been getting in, through herculean effort, 2,600+ calories a day-- mostly protein powder packed smoothies.  For some reason, she won't go for an Ultimate Cheeseburger from Jack in the Box (910 easy calories!)  Her appetite is pretty good; the tough part is having to eat every two hours or so to build her weight back up.  She's up to 126 from her lowest weight of 119.  Her walk is stronger and more confident than it was even two weeks ago.

Next Wednesday is Round Four (of six) for chemo.  Her nickname is chemo-sabi– she's the "paleface" from being inside all day and I'm the "red" man from bicycling in sizzling Sacramento.

Dr. B. eyeballed her yesterday and is really pleased at where she's at in her treatment.  They run a CA-125 chem panel after chemo, so we'll know Peg's new numbers about a week from next Monday.  Stay tuned...


Friday, September 4, 2009

No California State Fair for Peggy




It's been our family tradition since Zoë was a year old– the three of us go to the fair and get our family picture taken in one of the funky old-time photo booths that line the midway. Each little photo strip is lovingly tucked into a pocket and makes its way into our annual newsletter.

Tomorrow I'll take Zoë to the fair without Peg... she's just not up to it.  She was tearful about it tonight.  Another thing to give up.  She said having cancer is like being a sock in a clothes dryer; you're lofted up, then slammed down to the bottom, then the cycle starts all over again.  Only you never know when you're headed to the bottom of the dryer.

So this year our family newsletter will have a photo booth picture taken in front of WalMart.  They have half a dozen booths just outside the entrance. No rides there except for the one we're on.

Tuesday, September 1, 2009

Tears of gratitude and celebration

Yesterday our family doc called to say that Peg's CA-125 levels were down to 33.

This is big, and welcome, news.  

CA-125 is a marker for ovarian cancer. When Peg had her surgery on June 23, her levels were at 125.  Just three weeks ago, before the second chemo, they spiked at  178.  

Now they're at 33... below 20 is considered normal.

We're grateful for all your love and support.  You have nourished us with your presence, food, prayers and phone calls.  Things are heading in the right direction!

Sunday, August 30, 2009

More eloquent words than mine

Our brother-in-law Greg (Peg's older sister's husband) dropped by to read to Peg today and brought this article  from the New Yorker.  Black humor got Peg through the grueling regimen of medical school and psychiatric residency, and she thoroughly enjoyed this (as I hope you will as well).  As far as I'm concerned, black humor is mission-critical--- even if you're not dealing with cancer.  Taking things totally seriously is a recipe for disaster, regardless of the situation.

Today was a good day.  Had a delightful visit with Chandra who we've known since our children were in kindergarten, fun shenanigans  with Greg, and I enjoyed a 25 mile bike ride.  Zoë was at a friend's sleepover birthday party last night and on her arrival home at 2pm did a total carpet face-plant/one-hour snooze.

As Yoda famously said, "Do... or do not.  There is no try." 

Here you go:  

"Cancer Becomes Me," by Marjorie Gross

So I'm sitting in the doctor's office, he walks in, just tell me straight out, "I was right - it's ovarian cancer, so I win. Pay up."  And I say, "Oh, no, you're not gonna hold me to that, are you?" And he says, "Hey, a bet's a bet."  You don't know what it's like to leave a doctor's office knowing you've lost a hundred dollars: suddenly everything's changed.

Well, OK, I've exaggerated a little. What really happens is the doctor walks in and gives you the sympathetic head tilt that right away tells you, "Don't buy in bulk." The degree of tilt corresponds directly with the level of bad news. You know, a little tilt: "We've caught it in time"; sixty-degree angle: "Spread to the lymph nodes"; forty-five-degree angle: "Spread to your clothes." In her book about cancer, Betty Rollin wrote, "First, you cry" However, she didn't mention what you do second, which is "Spend, spend, spend." You're sort of freed up, in a weird way. Suddenly, everything has a lifetime guarantee.

So I had a hysterectomy, and they found a tumor that they said was the size of an orange. (See, for women they use the citrus-fruit comparison; for men it's sporting goods: "Oh, it's the size of a softball," or, in England, a cricket ball.) I languished in the hospital for ten days, on a floor where everybody had cancer, so the sympathy playing field was level. You can't say, "Hey, can you keep it down? I just had my operation." You might get, "So what? I'm on my fifth. “Poor thing” doesn’t really come into play much on this floor. My mother, who also had this disease (yeah, I inherited the cancer gene; my older brother got the blue eyes, but I’m not bitter) – anyway, my mother told me that for some women a hospital stay is a welcome relief. You know, to have someone bringing you food, asking how you are, catering to you every vital sign. See, she wound up in a room with five other women, and they would sit around talking on one bed, and the minute the doctor walked in they would jump into their own beds and re-create the “incoming wounded” scene from ‘M*A*S*H*”, insuring that they would not be sent home early.

Which now leads us quixotically but inevitably to chemotherapy. What can I say about chemotherapy that hasn’t already been said, in a million pop songs? I was prepared for the chemo side effects. I had my bald plans all in place. I decided to eschew wigs – all except the rainbow wig. Once in a while, I’d put that on when I didn’t want to be stared at. Luckily, in my life-style (Lesbeterian) you can be bald and still remain sexually attractive. In fact, the word “sexy” has been thrown my way more times this year than ever before. I’ve had dreams where my hair grows back and I’m profoundly disappointed. The bald thing works on other levels as well. The shortened shower time – in and out in three minutes easy. Shampoo-free travel. Plus, I get to annoy my father for the first time in twenty years. He hates to see me flaunting my baldness. I thought I’d lost the power to disgust him, but it was right there under my follicles all along.

The other side effect is that I’ve lost twenty pounds, which has sent my women friends into spasms of jealousy. I think I even heard “Lucky stiff.” I said, “I think I’m closer to being a stiff than lucky!” But it fell on deaf ears. I suppose it’s a testament to the overall self-esteem of my fellow-women that, after hearing all about the operations, the chemo, and the nausea, the only thing that registers is “Wow, twenty pounds!” and “You look fabulous!” It’s a really good weight-loss system for the terminally lazy. I mean, a StairMaster would have been preferable, but mine wound up as a pants tree.

Then, there are my other friends, who are bugging me to go alternative. So now I’m inundated with articles, books and pamphlets on healers, nutritionists, and visualization (which I know doesn’t work because if it did, Uma Thurman would be running around my house naked asking me what I want for breakfast). I was also given a crystal by a friend who was going through a messy divorce. She was given the crystal by a guy who died of AIDS. As far as I was concerned, this crystal had a terrible resume. As far as the healing power of crystals goes, let me just say that I grew up eating dinner under a crystal chandelier every night, and look what came of that: two cancers, a busted marriage and an autistic little brother. There, in the healing power of crystals. Enjoy.

This is not to say I’m completely devoid of spirituality. I mean, when you’re faced with the dark spectre of death you formulate an afterlife theory in a hurry. I decided to go with reincarnation, mixed with some sort of Heaven-like holding area. Then, of course, we could also just turn to dust and that’s it. I come from a family of dust believers. They believe in dust and money: the tangibles. The thing about death that bugs me the most is that I don’t want to get there before all my friends. I don’t even like to be the first one at the restaurant.

The hardest part of this whole thing is that it has completely ruined my loner lifestyle. I’ve never felt the need to have anyone around constantly. I mean, I never wear anything that zips up in the back, and I hate cowboy boots. And now I get ten times as many phone calls – people wanting to come over and see me. When I’m well, I can go months without seeing someone. Whey the rush to see me nauseated? I especially don’t believe in the hospital visit. People come in, you’re lying there, you can’t do anything, and they start talking about their plans for the night.

I hope with all this negative talk I haven’t painted too bleak a picture and therefore discouraged you from getting cancer. I mean, there are some really good things about it. Like:

(1) You automatically get called courageous. The rest of you people have to save somebody from drowning. We just have to wake up.

(2) You are never called rude again. You can cancel appointments left and right, leave boring dinners after ten minutes and still not become a social pariah.

(3) Everyone returns your calls immediately – having cancer is like being Mike Ovitz. And you’re definitely not put on hold for long.

(4) People don’t ask you to help them move.

(5) If you’re really shameless, you never have to wait in line for anything again. Take off the hat and get whisked to the front.

So it hasn’t been all bad. I’ve done things I never would have done before. I even got to go to Europe with a creamy-white pop star. I used to use the word “someday,” but now I figure someday is for people with better gene pools.


Saturday, August 29, 2009

Keep your hands and feet inside the ride at all times

Round three of chemo has been tough so far emotionally for Peg. We weren't prepared for that aspect, naturally focusing on the physical effects, but it's just as important. 

Friends brought us dinner, company and a fun TV show on DVD tonight. Helped turn things around. 

This is apropos of nothing, but a friend shared it with me this morning and I got a good laugh out of it.  It's a quote from Oscar Wilde: "Be yourself.  Everyone else is already taken."

Wednesday, August 26, 2009

Protein Packin' Peggy


Mahalo to our friend Ted in Maui, who steered us away from the "steak in a  can" stuff from Carnation.  Peg's doing much better with smoothies-- yogurt, almond milk, frozen fruit and protein powder from GNC.

When I brought this stuff back from the store, none of us could believe how huge the package is.  Four  one-cup scoops is 720 calories, 13 servings in a container.  (I didn't Photoshop in the crepe myrtle trees behind my truck-- they're in full bloom and we're really enjoying them).

Peg's rounding out her diet with the wonderful food our friends bring by and has a good appetite.  

Today's chemo went well.  Outpatient for this round, and probably the next two. She got a shot to boost her red cell count, which will help her energy level, which is already better than it was a few days ago.

Peg and I were talking in the car on the way back to the house about how much it means to have so many people keeping her in your thoughts and prayers.  We are truly blessed having you in our lives.

Monday, August 24, 2009

Zoë started 9th grade today


Zoë and I spent a fun two hours yesterday at our neighborhood Starbucks with our friends Bruce (who took this photo), Mary, daughter Julie and Eddie, The World's Officially Cutest Dog.  This was the day before our daughters entered high school.  

Unseasonably cool weather for Sacramento, perfect for reflecting on life and enjoying one of its gifts-- a long and rich history with friends of many years.  Mary spotted Peg when she and Zoë were at a neighborhood coffee shop twelve years ago, when our identically aged squids were tiny... introduced herself, and the rest is history.  So glad Peg had a hankerin' for a mocha that particular day.  Can't imagine not knowing these wonderful folks.

Zoë's doing well with braces and doesn't complain.  I'll be honest-- if I had braces, I'd be whining all the time and you'd be plenty tired of hearing about it.

Wednesday is Peg's halfway point for chemo, third of six.  We'll keep you posted.