Archive for the ‘Kids’ Category

It could be skin cancer

Friday, December 26th, 2008

I went to the dermatologist on Monday for a suspicious something on my arm. It’s a small, red patch of skin that appears to change in size and color. Seemed time to have it checked out, so off I went with two little boys in tow to an exam room where a nurse numbed and a physician assistant removed a slice of skin for biopsy. Then the PA said, “It could be skin cancer.”

“Cancer?” said 7-year-old Joey. “That would be your second cancer. What was your first one again?”

I told him my first was breast cancer and that he shouldn’t worry since most skin cancers are pretty easy to fix. The PA jumped in, confirming that yes, indeed, skin cancer is usually no big deal. Sometimes, it’s removed with the biopsy alone, she said.

And so that is my hope, that if it is skin cancer that lives on my arm, it’s the kind that is a cinch to eradicate. Well, my hope is that it’s not skin cancer at all because, really, one cancer is enough. No seconds for me, thank you.

Ho, Ho, Ho

Wednesday, December 24th, 2008

For all you Santa-believers out there, the big guy is almost here. Are you ready? We are.

Our tree is up, decorated and sparkling with white lights. A few wrapped gifts sit underneath, tempting two little boys who want to know so badly what’s packaged inside. Our gas fireplace is roaring (even though Florida temps will reach the 70s today), and we have our kids fully confused about how exactly Santa will enter our house without a chimney.

We’re all abuzz here about what the jolly old guy will deliver. Will it be a Wii, Ben 10 toys, a pirate castle? We’re also wondering what will happen if we catch Santa in our house. “What if I wake up and see Santa here?” 7-year-old Joey asked. “He’ll probably just tell you to go back to bed,” was my response. Good enough? I’m not sure.

I’m not really sold on the whole Santa story. I know it’s all in good fun, but I wonder when we’ll be found out, what we’ll say to explain our sketchy stories. Today, it doesn’t matter. Today, it’s all about the countdown to Santa and gifts and family and fun. It’s exciting indeed.

Bump

Friday, December 19th, 2008

Last night while John was reading the boys’ favorite Goosebumps book, 5-year-old Danny curled up in my lap (I love that), tugged at my shirt and asked, “Where’s that thing, where you had that bump?” I knew just what he meant. He wondered where to find the area where a port once poked up from underneath my skin. (My port lived near my collarbone for almost two years so that chemotherapy drugs had easy access to my veins.) I pointed to the area, now marked by a very faint scar about two inches long.

“Oh,” he said, and then returned his attention to the story about a boy who became a wax figure in a museum.

Danny doesn’t have much memory of breast cancer. A “thing” and a “bump” pretty much sum up his recollection of a disease that entered his life when he was just 18 months old. It seemed sad way back then to have a baby and cancer at the same time. Now, it seems a blessing. He doesn’t have a clue really. And that’s just how I think it should be.

Happy Holidays 2008

Friday, December 12th, 2008

Just before Joey turned one, we snapped our very first holiday photo and mailed it off to family and friends. That was, gosh, seven years ago. Six photos followed, and now we have a collection of shots that capture our boys, and sometimes all four of us, at very specific moments in time.

Above is this year’s photo, taken on a whim at Lake Alice on The University of Florida campus. Below, two of my favorites from years past.

Classic Christmas

Sunday, December 7th, 2008

What would the holiday season be without a screaming baby on the lap of Santa? Here, cousin Tori refuses to tell the big guy what she wants for Christmas. Classic.

I love this one too: Danny feeding a happier Tori some of his flavored shaved ice. “She’s had like 11 bites,” he declared, after announcing he was done serving her.

Remembering Danny

Saturday, November 29th, 2008

I wrote this story about a year ago for a local parenting magazine. It’s all about Danny, my now 5-year-old. He is nothing like I describe him in the words that follow—well, except for the whining. Amazing how time changes little people so profoundly. I miss this Danny. And I love the one who sits next to me playing computer games at this very moment.

I never realized until my husband took Joey away for the weekend just how much Danny talks. We spent two whole days together, my 4-year-old and me, and except for the hours when Danny was asleep, we experienced not one minute of silence.

Danny talks while playing, while eating, while splashing in the tub, and while riding in the car. He talks himself to sleep, begins talking the instant his eyes open in the morning and when his brother isn’t home to engage with him, talks at my bedside until I emerge from my slumber. And while much of his verbal discourse is of the story-telling nature, he’s got quite a knack for asking questions—which requires my full presence, my undivided attention, and all sorts of meaningful responses.

“How old are you? What’s your name? What did you look like when you were a baby? How old were you when you were a baby? Are you bigger than Daddy? Is Daddy bigger than you? Are you going the speed limit?”

Boy, can that kid talk.

Danny has just a few jobs at his young age—he’s expected to dress himself, brush his teeth, practice good manners, share, recognize his letters, and minimize his propensity for whining. His biggest job, however, is to talk. It’s his best chance at understanding the world around him. Danny’s incessant questions lead to spirited information gathering and when I’m not too exhausted by his constant chattering, I realize how fun it is to inform someone who so enthusiastically wishes to be informed.

It all came down to me that weekend Danny and I spent together. I was on a solo mission, responsible for the accurate dispensing of facts and figures. What I told Danny may have helped shape his perspective on life. What a job. What an honor.

Danny wasn’t the only one rattling of questions during our one-on-one session. I asked my fair share too—I just couldn’t pass up the opportunity to bond with my youngest guy.

“What did you look like when you were a baby?” I asked Danny. “Like a baby,” he replied. “Tell me more,” I said. “My hair was blond,” he told me. “My eyes were green. I liked to play in the bath. I always liked to play with my toys. I loved my mommy, and I loved to talk.”

Yes, Danny likes to talk. And because I suspect the day will come when I won’t be able to lure more than a few words out of him, I’m going to soak up every syllable that flows from his sweet mouth. I’m going to savor every sound he makes with his raspy little voice, and I’m going to never forget that at this moment in time, I am Danny’s most trusted source of knowledge. I may never again appear so important in his eyes—which, incidentally, are blue—but for now, I’m his go-to girl. And there’s no way I’m letting go of this title.

Boo from my boys

Sunday, November 9th, 2008

We hope you had a Happy Halloween. We sure did. We trick-or-treated, scored lots of candy, and are busy dishing it out with healthy-food bribes. Eat a pear, get some candy. Knock back a nutritious dinner, get some candy. Opt for yogurt instead of cookies, get some candy. Soon the bribes will come to an end, because soon, the candy will be gone. We’re at the bottom of the orange candy bowl already. How are your candy bowls doing?

Inspire me

Friday, October 24th, 2008

This is my Danny. He’s five years old, and he can do four pull-ups. That’s four more than I can do. He inspires me. Who, or what, inspires you?

Circus of Cancer

Saturday, October 18th, 2008

I’ve read her book, The Middle Place, and I tell you: It’s the best. Really, a touching story of her life with cancer, her dad’s life with cancer, and her relationship with one husband, two kids, a mom, brothers, and others. Read it if you can. You’ll laugh. You’ll cry. You’ll be inspired, by the one and only Kelly Corrigan.

Corrigan also has a cool website, called Circus of Cancer. I’m just starting to find my way around this magical place. Want to join me? Click here and you’ll find all sorts of great stuff—photographs of Corrigan during her cancer days, tips on how to help friends with cancer, gifts and free e-cards, and the latest on Corrigan’s writing endeavors. Even her little girl are getting in on the writing gig—check out this picture book, pictured above, written for mommy’s with cancer.

Boo-Boo in my boobie

Saturday, October 11th, 2008

I wrote this essay on December 4, 2006 for Orato.com. It still appears on this site in its original published format. Keep in mind that it’s a two-year-old story. My boys are not four and 18 months anymore. They are seven and five. It has not been two years since my diagnosis. It’s been almost four.

Two years ago, I told my two little boys—then four and 18 months—that I had cancer. I told them cancer meant I had a boo-boo in my boobie. I told them doctors would take it out, I would take medicine, my hair would fall out, and I would get better. They heard my words, translated them into their own meanings, and have been caring for me ever since that November day in 2004 when my life suddenly appeared anything but a guarantee.

My breasts have been abundantly front and center in my life for dozens of years. First they were too big—34 DDD—and I tried valiantly to disguise the bulk on my chest with large shirts, harness-type bras, and rounded shoulders to shelter others from my most obvious feature. Then came a breast reduction surgery to remove four pounds of dense tissue and to augment my waning self-confidence. Cute bras, tight shirts, and better posture became staples in my life. My breasts made me happy—finally—despite surgery scars, occasional numbness, and an eventual inability to breastfeed my babies.

My small, perky breasts made me happy for eight years. Then I found a lump in the left one—a hard, pea-sized lump that presented itself right beneath my fingertips one day while I was in the shower. It became my obsession for the days leading up to my official clinical examination. I touched it and maneuvered it and examined it until I was sure it was growing with each moment.

And so was born the boo-boo in my boobie—the boo-boo my family and friends and doctors predicted was nothing to worry about. The boo-boo that was in fact cancer—housed in a tumor 1.1 centimeters in size, which had not yet spread to my lymph nodes and was considered stage I.

I found my lump early, and my prognosis was good—in some ways. In other ways, I faced a not-so-good prognosis. I was young—34 years old—and tumors found in young women are typically aggressive. My tumor also contained too much of a certain protein that made it wildly aggressive. So for the 24 months that have followed my diagnosis, I have been receiving intensive treatment for a mass that appears treatable and at the same time threatens to take my life.

A lumpectomy took my tumor and four lymph nodes. Four doses of chemotherapy—given every two weeks in a dose-dense fashion— took my hair and my energy and my overall sense of wellness. It landed me in the hospital twice due to fever and a suppressed immune system and was cause for a blood transfusion during one hospital stay. Radiation took hours of my day—five days per week for seven weeks—and left me with temporary burns and ten tiny permanent blue tattoos. And then one year of targeted drug therapy took me back to the chemo room for every-three week infusions of a new wonder drug intended to block that same protein that made my tumor so deadly.

This whole journey, complete with stops for physical therapy, counseling, and treatment with an anti-depressant, is winding down. With surgery and treatment behind me, I have just one final counseling session remaining. And when the session ends and my case is closed, I will begin a new version of my life—free of constant medical intervention and with just a touch of monitoring.

I will visit my medical oncologist every three months for the next five years—when, if cancer has not returned, it will be safe to say I am in remission. For five years, I will also see my radiation oncologist every six months. For the rest of my life, I will receive a mammogram and ultrasound every six months, will report for a breast MRI once every year, and will conduct my own breast self-exams every month. And while there is no comprehensive blood test or can available to offer me peace of mind that cancer is not taking up residence in my body again, I will closely monitor every bit of pain and discomfort, every bump and lump that gives me reason to worry. And I will pursue it all—with a vengeance—so I can catch anything that creeps up on me with enough time to conquer it.

If cancer must enter my world, I will only allow it to stay for a short time-because I have a lifetime of joy and happiness ahead of me, and I cannot be distracted for long. I have two little boys—now almost six and three and a half—whose lives I must witness. They are the boys who propelled me through my darkest days and have touched me deeply with their unwavering love and concern and simple wisdom.

When radiation zapped every bit of energy I possessed and caused me to unintentionally fall asleep in my living room recliner, Joey—my oldest—would ask me when I opened my eyes, “Mommy, did you have a nice rest?” One day when I felt terribly ill, he said, “Mommy, you go to your bed and I’ll bring you a banana.” He worried that my port—or stone, as he called it—might hurt me and when I told him it did not hurt, he replied, “Won’t you be so happy when you can be on your own without cancer?”

I’m not sure Joey has ever really understood the magnitude of cancer. Still, he sensed I needed him during my battle with this mysterious condition. He assured me the day he and his daddy shaved my head prior to my chemotherapy fallout that I should not cry. “It’s only a haircut, mommy,” he said. “You are not going to die.”

He was right. It was only a haircut. And Danny—my youngest—may not even remember that my hair, now dark and curly, was once blond and straight. He has just recently started catching on to the series of cancer events unfolding in our household. A few months ago, he asked, “Why you keep doing that?”

“Doing what?” I asked him.

He replied: “Going to the doctor.”

I told him I go to the doctor so I can stay healthy.

Two years ago, I told my two little boys I had cancer. I told them cancer meant I had a boo-boo in my boobie. I told them doctors would take it out, I would take medicine, my hair would fall out, and I would get better.

This is exactly how it happened.

I hate tumors

Monday, October 6th, 2008

There’s nothing fair about the way it happened, the way Amy died just 15 months after a breast cancer diagnosis seemingly similar to mine. She heard the same string of chilling words—you have cancer—as I did, just months after a doctor hurled them at me, over the phone, a day before Thanksgiving. Both in our early 30s with husbands and small children, Amy and I felt like two peas in a pod, situated in what we believed were almost identical positions. We were both young, both with early stage breast cancer. We both knew our cancers, while caught early, were considered aggressive because of our age—young women tend to have aggressive forms of the disease—but we also knew we had a high likelihood of survival, about 93% for at least five years.

Amy and I had common hopes, fears, and worries, and on several occasions we cried tears we were sure flowed from the same well. We also shared an instant urge to reach others with our breast cancer stories. Amy welcomed local newspaper reporters into her world and allowed them to capture through words and photographs her most intimate cancer moments. I began authoring my own breast cancer blog and then ventured into the world of freelance writing. We both wanted to make our experiences matter. And judging by the flood of reaction we received from our combined efforts, it’s clear we did.

Amy and I shared victories—we both managed to escape the threat of lymph node involvement—and we shared cards and e-mails. Thank you for holding my hand through this journey—it would have been pretty lonely without you, Amy wrote in one e-mail.

Amy and I also shared care packages, family photos, even hats. If misery loves company, then Amy and I were in love. And in celebration of our love, we basked in the glory of our most important similarity—our cancers had not spread. This was key to our survival. Or so we thought.

A mutual friend—her high school buddy and my college roommate—matched Amy and me. Ericha was one of a few close friends who after my diagnosis offered to hop on a plane and come to my rescue in Florida. I never accepted her offer—I was sure I could handle cancer all on my own—and so she stayed in Ohio where Amy, also an Ohio girl, welcomed her assistance. It worked out well this way.

Ericha helped Amy as she recovered from surgery, reconstruction, chemotherapy, and countless physical and emotional twists. She watched Amy’s kids—ages four and one at the time—and cleaned her house and drove her to appointments and selflessly assumed some of the burden drowning this young wife and mother who continued working as a nurse while managing a life with cancer.

“I quit my job,” Amy told me just after she announced her cancer had returned. She said she should have quit after her first diagnosis. She should have taken better care of herself. She should have played with her children, spent time with her husband, given up the chore of work. She would do it right this time, she said. She would crush cancer. She was sure if it.

I wrote and published a post about Amy on The Cancer Blog just after she told me how cancer had shown up in her brain and lungs, just five months after her chemotherapy for breast cancer ended. I wrote about my shattered hope, my fear this would happen to me, my complete and total sadness. And then Amy left a comment on my post. She wrote:

Jacki, I am not giving up. I will beat this again. Don’t you give up yet. I have Luke and Ella and they alone are worth fighting for. Just everyone send me your prayers and positive vibes. Quoting the cancer crusade couple, “Setbacks are a chance to pause and review the lesson of life.”

Amy, the one staring down death—doctors said she had two to 12 months to live—was comforting me. Amy, with her spunk and spirit, convinced me she would annihilate this evil disease. I believed her.

Amy lived for only five weeks after she wrote these words. Ericha called me with the news of her death just as I was leaving my house one Saturday morning to run in a race. I stopped in my tracks when Ericha told me—Amy passed yesterday—and I felt nothing but shock and sorrow for the duration of the run I struggled to finish. I finished for Amy, though. If she could fight cancer—twice—then I could surely pound out a few miles in honor of a friend whose face I never did see.

Amy and I talked about meeting at the beach with our families one day after we’d survived cancer for a few years. We dreamed of going on the Oprah show and proudly announcing our survivorship. We talked about a lot in our short 15-month friendship. What we didn’t talk about was that our situations really were very different. Perhaps we weren’t aware of it at the time. Perhaps we subconsciously chose to find common ground in the midst of our harrowing journeys, to ignore the fact that we were not traveling the same path at all.

Amy had a family history of breast cancer. I did not. Just after Amy completed her chemotherapy, her mother was diagnosed with the same disease that now has affected four generations in her family. Additionally, Amy’s tumor was slightly larger than mine, she received a different chemotherapy protocol than I received, she was not eligible for a year-long drug treatment I accepted to keep cancer at bay and because she had chosen the radical route of removing both of her breasts—I had a lumpectomy—Amy was not a top candidate for the radiation therapy that zapped me five days per week for seven weeks. She wondered if she should have demanded this treatment. She wondered if it would have made a difference in her survival.

The final and perhaps most significant difference in our diseases is that while Amy’s cancer, like mine, had not spread to her lymph nodes, it had found a way to penetrate her bloodstream and was spreading in a secret, silent, and deadly fashion. My oncologist, who dried my tears when I sobbed about the unfairness of Amy’s death, said some young women have a very aggressive disease right away. Amy was one of these women. I, apparently, am not.

There’s nothing fair about the way it happened, how Amy died just 15 months after a breast cancer diagnosis I have now survived for almost four years, how Amy died so quickly and I didn’t, how there is no cure for this mysterious disease that strikes far too many women and some men too.

Amy’s husband sent me an e-mail just after she died. He wrote:

You were a great inspiration to Amy. Your quote ” Fight the Good Fight” was front and center on our fridge. Please don’t let this news get you down, Amy would want your chin up, would want you to keep fighting. Thanks for all your support.

My chin is up. I am fighting. And Amy—thank you for your support.

Making Strides Against Breast Cancer

Sunday, October 5th, 2008

Yesterday, I ran a few miles, turned over a couple thousand dollars, and made some strides against breast cancer. My sincere thanks to those who contributed to my cause and came along with me on my run—see your name on my body? It’s there, somewhere.

Special thanks go to my three guys and my mom who keep life happy; Tracy, my sister, best friend, and running partner; Jack, my other best friend and photographer; Miriam, my friend and neighbor who joined us today, sporting a pink ribbon on her face and pink braces on her teeth; and Ms. Griffith, Joey’s teacher who walked and ran for me too.

Just one story can change a life

Saturday, October 4th, 2008

Michelle is 41 years old.
She has stage IV breast cancer.
This is her story.
It might change your life.

Growing old

Monday, September 29th, 2008

This boy was three years old when I was diagnosed with breast cancer. I was 34. Now, he is seven. I am 38. What a pleasure it is to grow old with this guy, who often recalls my cancer moments.

“Did you almost die from cancer?” Joey asks periodically.

“No, I did not,” I always tell him.

“Remember when you didn’t have any hair?” he’ll sometimes say.

“How could I forget,” I tell him, just before we reminisce about how he helped shave my head, how I cried, how he told me it was just a haircut.

Three years old, he was. And he remembers. So do I.

Sunday Silly

Monday, September 29th, 2008

On Sunday, we were silly. It was John’s idea. A family pyramid—yes, that’s what we’ll do, he decided. Not my favorite idea at first. I mean, it was nearly 90 degrees outside. I was freshly showered after a double workout—bike ride and run—and kneeling on the ground with one 75-pound boy and another 45-pound boy on my back didn’t emerge as my top-ranked activity (strolling the landscape and watching my guys run wild in the grass were my picks).

Call me a good sport, though. I complied with the pyramid idea. And here I am, with my three loves. And while the group arrangement was a tad painful at the time of dismount (see below), it was, yes, fun—especially now as I look back on what was captured on film.

On Sunday, we were silly. So glad we were.

A Great Gator and a Shining Star

Saturday, September 27th, 2008

Last week, Joey was crowned Greatest Gator in his second-grade class. One child gets this honor each week, a boy or girl who practices good behavior all week, works hard, and generally goes with the flow of all things school-related. Joey was this boy on September 19 and for the whole week following, he was the man. We made a photo collage he took to school and displayed for all to see. He wrote a page in the Greatest Gator journal, about how happy he was to have emerged victorious. He completed a special questionnaire, won the gift of a pencil and pencil gripper—pencil grippers are, like, all the rage in second grade—and was lucky enough to have a stuffed alligator sit on his desk for five whole days. Now, Joey’s reign is complete—his pal Lauryn is the new Greatest Gator.

Things are still exciting here in our household, though, because yesterday, Danny came home wearing a Shining Star construction paper hat. Second grade has Greatest Gators. Kindergarten has Shining Stars. And this week, Danny is it. He too was awarded a pencil—with a heart-shaped eraser, no gripper—and he brought home his own borrowed journal (he dictated and I wrote all about his family and what he likes to do). He gets to take in photos on Monday, which will be displayed for his week-long tenure, and he’s borrowing two books we’ll read at home and then return. He’s a proud boy. Yesterday, after I scolded him for doing something disruptive, he asked if I was still happy he’s a shining star. You bet I am.

I’m happy my guys are off to a good start this school year. I’m thankful they model their good behavior at school and save their bad choices for home. I’m proud, simply proud to be the momma of a Great Gator and a Shining Star.

Thankful for slow

Wednesday, September 24th, 2008

Here’s how my typical day flows: Wake up at 6:15 AM and do everything it takes to get two little boys ready for school and out the door. Drive two little boys to school, walk them to their kindergarten and second-grade classrooms, depart school. Exercise. Shower. Dress. Eat big fruit salad. Write—for hours. Eat lunch. Head back to school, get boys, return home. Unpack backpacks and lunch boxes, manage homework and fights, sneak in more writing work, pack lunches, prep dinner, fold laundry, and whatever else comes my way—Wednesdays are library days, grocery stops are frequent, sometimes a movie, maybe a play date, a game of Sorry or Stratego here and there, a round of role playing with Danny (he’s loves to play toy store: He sells his toys; I buy them). We like to go outside too—and I suspect our outdoor adventures will ramp up a bit with this great cooler weather we’re having in Florida.

I am thankful for my schedule. Mornings are for me. They’re quiet—no they’re silent, and I love that. Afternoons are crazier, but it’s a nice balance. Overall, my schedule is slow. It’s not rushed. It’s not hectic. It’s not stressful. After yesterday, I realize how fortunate I am.

My yesterday started with at 5:15 AM workout because I knew a busy day faced me, and I just can’t miss my workout—it’s a mental health thing. Then I chaperoned Joey’s school field trip at Camp Crystal, where we hiked and marveled at nature, enjoyed a hayride, visited a museum, and ate lunch. Then we drove back, got Joey some more lunch—he didn’t touch the one provided at camp—and picked up Danny from school. Then home, where I changed into running gear, dumped the boys into John’s capable hands (he happened to be home from work yesterday, thank goodness) and all but raced out the door to meet a photographer at the University of Florida for a photo shoot—I’m going to be featured on the front page of UF’s website beginning October 1 (check out ufl.edu and you’ll see me as one of three spotlight people in the top banner). Photos took one hour, and then I met Tracy for a run on campus. Three miles and 30 minutes later, I was headed home. Arrival time: 5:15 PM—a whole 12 hours after I first starting doing lunges and squats in my garage. The night continued with the usual—showers, brush teeth, read book, lights out.

Pooped, I was, by the end of yesterday. So tired, I couldn’t even stop on the way home from campus to put gas in my car, a mistake I realized this morning while racing to do my school drop-off after waking much too late and starting the day off in a rush.

I didn’t like yesterday. I mean, I liked the individual events of the day, I just didn’t like the rush of it all, which makes me so thankful for today.

Controlled.

Even.

Steady.

Slow.

Just how I like it.

Photo courtesy of antkris on flickr

To have hair

Sunday, September 21st, 2008

It was a shot in the dark when I asked my two little boys last night on they way home from our dinner out: “Who wants to do mommy’s hair when we get home?” Who knew both boys would shoot a hand in the air, like they eagerly wanted to answer a teacher’s question at school, and simultaneously repeat, “Me,” “Me,” “Me,” Me,” until I happily informed them they both could do my hair.

I love to have my hair done. And since I’m not sure my growing boys will want to play beauty shop for much longer, I’m capitalizing on this game while I can. I’m all-willing to let them do as they please, too. Spray bottles full of water? Sure. Yanking and pulling as they fumble a rubber band around clumps of my hair? Yep. A delayed bedtime so they can turn my hair into a tangle of knots? Of course.

“Mommy, your hair is so long,” Joey told me as his bedtime hour slipped away and he soaked my hair with blasts of water—it’s easier to brush this way, he tells me. “I remember when it was, like, one inch long,” he continued.

“Yeah, me too,” I told him, realizing I like this hair playtime for many reasons. One, it’s relaxing. Two, it gives me time with my boys. Three, it gives them time with me. Four: It means I have hair.

Gosh, is it nice to have hair—to have someone tear a brush through it and twist it into all sorts of unrecognizable styles, to pull it back into a ponytail, to have the pleasure of complaining about what this crappy Florida humidity does to my chemotherapy-acquired waves, to have an appointment on Thursday to get it cut because it’s too long.

Yes, my hair is long. Too long even.

Gosh, is it nice to have hair.

Flashes of Hope

Friday, September 19th, 2008

This little boy has cancer. So do the other kids featured in Parade magazine’s Changing Faces of Cancer feature. It’s all part of Flashes of Hope, a non-profit organization dedicated to creating powerful, uplifting portraits of kids battling cancer and other life-threatening diseases.

Powerful and uplifting they are. Check them out right here.

Pretty good day

Friday, September 12th, 2008

Did a radio show yesterday with Dr. Fitness and The Fat Guy, two guys in Atlanta who strive to make healthy living fun for everyone. We talked breast cancer—I told them how I found my lump, how I coped through treatment, how I started this blog, how I lost my hair. Check me out here. Don’t expect me to belt out any songs on this radio clip. That’s what Danny imagined I’d be doing when I told him the other day about my upcoming appearance.

“When are we going to hear your song?” 5-year-old Danny asked this morning on the way to school, just after I’d turned on some tunes.

“My song?” I asked.

“When are you going to sing on the radio?” he responded with impatience. Sensing my cluelessness, he declared: “You said you were going to be on the radio.”

“Oh, I was on the radio,” I explained. “But I just answered questions.”

“That’s all you did?” chimed in Joey. “About what?”

“About breast cancer,” I told both boys. “I talked about how Joey shaved my head and told me not to cry because it was only a haircut and I wouldn’t die.” I could see Joey smiling as I peeked at him through the mirror.

“You were right,” I told Joey. “It was just a haircut. My hair grew back, and I didn’t die.”

“And you look pretty,” Joey said. “And I like you’re hair better now.”

I told Joey he made my day.

“I thought your day was made by my goodness,” he said.

I asked for clarification.

“I thought your day was already made because I’m being so good,” said my 7-year-old guy.

OK, I get it. You see, Joey gets quite a lot of coaching in the mornings to stay on track and get out the door for school. This morning, he did well. So yes, he had essentially already made my day. And then he made it better.

Today, Joey was good. And he told me I’m pretty. And I don’t think I could have asked for anything more at 7:15 AM on a Friday morning.

A pretty good day, it is.