10 years later

Ten years ago today, I got the call. The call I’d been dreading. The call from my dad to tell me that my mom was dead. I was in my car, in line to drop my #1 son at school. He was still in the car, but I answered the phone because it was my dad calling. Trying to respond to him while cloaking my words in a way as to not upset my 6-year-old was hard. Living the last 10 years without my mom has been even harder.

I’ve written much about my sweet mama and how much I miss her. I’m not sure that there are new ways to say, I’m sad. I miss her. I feel lost sometimes. I worry that I don’t do enough to keep her memory alive. I can’t believe she’s gone. I don’t want to live the rest of my life without her. I’m afraid I don’t mother my kids as well as she mothered me. I’m totally pissed that she’s gone. I was robbed. She was robbed. It still hurts, a lot. It’s better, but it still hurts.

I miss her. So much.

I’ve been torn today, between wallowing in the sadness and doing the kinds of things she respected. Between feeling sorry for myself and being productive. Between having a shitty day and “walking on the sunny side of the street” (the latter was how she bid me farewell every day when I left for school when I was little). How can I walk on the sunny side of the street when the sunshine is gone?

And yet I will try. I will. Because that’s what she would want. img_1199


Angelina’s Diary of a Surgery

I just read Angelina Jolie Pitt’s op-ed in The New York Times about her second preventative surgery: to remove her fallopian tubes and ovaries. Just as she did with her prophylactic bilateral mastectomy two years ago, Jolie Pitt writes articulately and openly about her laparoscopic bilateral salpingo-oophorectomy, using imagery and opinions that those of us who have walked in her shoes immediately understand.

She writes, “The beautiful thing about such moments in life is that there is so much clarity. You know what you live for and what matters. It is polarizing, and it is peaceful.”

So much clarity. Amidst untold chaos and unimaginable confusion, there is clarity.

She recounts her consultation with the GYN surgeon, who had also treated her mother: “I last saw her [the surgeon] the day my mother passed away, and she teared up when she saw me: ‘You look just like her.’ I broke down. But we smiled at each other and agreed we were there to deal with any problem, so ‘let’s get on with it.’”

I had a similar encounter with someone who cared for my own sweet mama during her cancer treatment. The woman who was my mom’s radiation tech is now a nurse in my orthopedist’s office. I knew as soon as I saw her face that she was the kind practitioner who blasted pointed radiation into my mom’s beleaguered body five days a week for weeks on end. When I encountered her in the orthopedist’s office, I was thrown for a moment because she was out of context. But before long we realized who each other was, and she said the same thing to me that Jolie Pitt’s mom’s surgeon said to her: “You look just like her.”

Stupid fucking cancer.

When Jolie Pitt wrote about her mastectomy in May 2013 she cast the spotlight on the issue of femininity being defined by body parts. After her mastectomy she wrote: “I do not feel any less of a woman. I feel empowered that I made a strong choice that in no way diminishes my femininity.” With her latest surgery, Jolie Pitt casts the spotlight on another jarring and difficult result: forced menopause.

Becoming menopausal decades before its natural occurrence is unpleasant, to say the least. The physical and emotional ramifications of forced menopause suck. Really suck. There is no easing into the myriad effects, which can include hot flashes, night sweats, increased sweating, sleep disturbances, mood swings, urinary tract infections, sexual disfunction, memory loss, difficulty concentrating, back pain, joint stiffness, and fatigue. As if that’s not enough, throw in the accelerated aging: loss of elasticity in skin, lack of collagen, hair loss, brittle nails, diminished muscle tone, slower metabolism, and weight gain. Suck. At a time when many women are claiming the best version of themselves (“40 is the new 20!” “I’ve finally come into my own!” et al), early menopause creates instant grannies. Suck. If anyone can shed light on the ugly truths of forced menopause, my money is on Angelina. Yes, she has unlimited financial means and resources unavailable to the average cancerchick, but she also has a platform for educating the masses and she’s gonna use it. Hooray!

At the time of this publishing, there were 321 comments on her story; by the end of the day that number will have climbed. The handful of comments that I scanned were positive, but there are some who chastise her for her choices. I’m always amazed at how ugly people can be with the anonymity that our online world provides. How nice it would be if those cowardly, overly opinionated haters could really digest Jolie Pitt’s reasoning and respect her choice. How nice it would be if they would re-read the last sentence in this segment of her latest essay:

“I did not do this solely because I carry the BRCA1 gene mutation, and I want other women to hear this. A positive BRCA test does not mean a leap to surgery. I have spoken to many doctors, surgeons and naturopaths. There are other options. There is more than one way to deal with any health issue. The most important thing is to learn about the options and choose what is right for you personally.”

Choose what is right for you personally.

What works for you may not be the same thing that works for me, or for your neighbor or your cousin or the woman who works at your favorite Hallmark store. Cancer, like any disease, is an immensely personal issue, and any and all decisions resulting from a diagnosis should be personal.

 


I want my mommy!

October 13. The day my mom died. It’s here again, and 7 years later, it still sucks.

They say time heals all wounds, but I say “heals” is a bit of a stretch. It’s more like time puts a too-small and not-so-sticky band-aid over the gaping wound where your heart used to be. They also say that you never get over such a loss, you just get through it. Whoever “they” are, they got it right that time.

I still miss her every single day, in one way or another. Her big, genuine laugh. The way she fretted incessantly. Her habit of always taking my kids’ side, even when they were naughty and unruly. The daily phone call, even when she had nothing much to report. Her ability to worm her way into anyone’s heart. Watching her in the kitchen, and marveling at how she knew how to get everything just right.

The list goes on.

I’ve written a lot in this little blog about how much I miss my sweet mama. I’ve read a lot about losing one’s mother. I’d like to think it helps, that it’s somehow therapeutic to get it out, to empty my heart and head onto the screen. When I come across a particularly interesting or helpful tidbit on the subject of mothers and/or loss, I jot them down. I usually forget to include the attribution, as I did here:

Motherhood isn’t a test but a religion, a covenant entered into, a promise to be kept.

No idea who wrote that or where I came across it, but I like it, and my sweet mama definitely embodies those ideals.

This one was in O Magazine, and again, I neglected to give credit where credit is due. To the author of these wise words, I apologize, but please know that your words moved me enough to pull out my iPhone, tap on the Notes icon, and copy the passage for quiet reflection at a later date:

You never get over what you lost. You always carry it with you, stitched to you like Peter Pan’s shadow. And you never wanted to get over it, because who wanted to forget a time that had been so important? No, the truth was, you wanted to remember it always.

I guess I’d say that it’s impossible to forget something (someone) so important. I do carry her with me, and I will never get over the loss of her. If I’m half as important to my two kids, a fraction as beloved, I will consider my life a great success.

I read a book review a while back about Caroline Kennedy’s book Jacqueline Kennedy: Historic Conversations on Life with John F Kennedy. (Whew, long title.) In the review, Caroline talked about how at age 53, accomplished and well-educated, she still referred to Jackie O as “mummy.” We never get over losing our mothers.

She went on to talk about the qualities she most admired in her mom, which she wanted to highlight in the book: the sense of strength, her passion for reading, and her will to move forward despite the pain that had come her way.

I can relate to that. My mom was amazingly strong, but in a quiet and gentle way. She loved to read and was a middle school English teacher in her life before becoming a full-time mother. And she had seen her share of pain: losing her own mother at age 13, raising her younger sister, losing that sister to pancreatic cancer, then enduring her own protracted and awful cancer battle.

I can relate to everything Caroline Kennedy says. My mom wasn’t as glamorous as Jackie, and I didn’t grow up in Camelot. I do have a brother named John, though; however my mama wouldn’t let anyone call him John-John or Johnny. Our neighbor across the street tried to call him Johnny, but my determined mama nipped that in the bud. She named him John after my dad’s uncle who immigrated from Greece. His name was John and she insisted that he be called John.

When Caroline Kennedy listened to the 8 hours of interviews between Mrs Kennedy and Arthur Schlesinger, which Caroline used to make up the book, she had a strong reaction. She says, “I read them right after mum died and had the sense she was speaking to me again. I could hear her saying what I was reading (smiles).”

What a precious gift. To hear my sweet mama again would be such a treasure. I have to work hard to remember what her voice sounded like. The more time that passes, the harder it gets. The more years that roll by without her, the less I feel like I know her. She seems to be fading from me.

I still call upon her a lot, especially in the kitchen. Just the other day, I was helping my favorite girl in the kitchen. She’s doing an ongoing bake sale to raise money for her class trip to Washington, D.C. and was baking my mom’s pumpkin bread. The house smelled sweet and spicy, the cinnamon, allspice, cloves and nutmeg redolent of fall (even though it was 90 degrees outside). Watching my girl take on a task (raising money for her trip), executing her plan, and carrying on my mom’s fine tradition of expressing her love through food made me proud. And sad. Because I knew how much my mom would love to see my girl doing her thing. She would fret over my girl, telling her to scoop the flour lightly, without packing it down. She’d say, fold the dry ingredients gently into the pumpkin mixture so the bread will come out light and fluffy instead of dense. She’d tell my girl to clean up as she went along, so that there won’t be a giant mess at the end. And she’d scold my girl for wanting to taste the batter; my mom grew up on a farm with chickens and was always leery of eating raw eggs.

I needed my mama that day in the kitchen with my hard-working girl. After the pumpkin bread baked and we let the loaves rest in the pan for 10 minutes, we knew to turn them out onto a rack to cool. But the still-warm bread was so moist it was very soft on the bottom, and I didn’t want the rack to make marks, or even worse, for the bread to stick to the rack. If we turned the loaves upside down, to rest on their tops, would the racks still make marks? What to do? Mom’s recipe didn’t address this important question, and although I’d seen her make pumpkin bread countless times, I couldn’t for the life of me remember what she did with the cooling loaves. And I sure couldn’t just call her up and ask her.

My mom and my girl didn’t get to spend much time together, because cancer stole YaYa from my girl when she was just 3 years old. No fair.

My sweet mama and my favorite girl, at home the day after my girl was born

They didn’t have a lot of time together, but they made the most of it.

Read more about my sweet mama:

6 Years Later

The Spring of My Discontent

Motherless Daughters

Only Just a Dream

Blindsided

I Hate Mother’s Day

 

 

 


Torrents

Cancer steals so much. All the time. Every day. This I know for sure.

A couple of days ago I smacked my head upon this truth and watched helplessly as my dear friend experienced this for himself. His dad died from cancer a decade ago. Ten years, yet the grief was as raw as can be, the loss as crushing as it was a decade ago.

His dad was a handy guy who could fix anything. He made a good living — and supported four kids — with his hands. My friend learned from his dad and is handy too. Although his livelihood isn’t manual, he can fix anything, like his dad. He just doesn’t always believe it until it’s done.

My friend was fixing the spring on our gate (one of the many things he’s helped with around our house). The spring on the outside of the gate had lost some of its tension, and the screws holding it in place had wriggled loose after seven years of use. How many hundreds of times has that gate banged shut as my busy little family comes and goes? When we were building our pool, the gate and the fence came down, to be replaced by temporary, orange plastic fencing (seen behind the slabs of flagstone) that couldn’t contain my dogs. My then 7-year-old chased the escaped dogs across a very busy street, unaccompanied, but that’s a story for another day.
In the process of repairing the spring on the gate, my friend broke his screwdriver. The one that he inherited from his dad. No big deal, it’s part of a set and he has several others the same size. But he was upset–really upset–because along with the screwdriver, he felt like he lost a piece of his dad.

His rational brain knows that the screwdriver isn’t indicative of his dad’s presence or absence. His intellect knows that having the screwdriver doesn’t mean that he still has his dad, or that by not having the screwdriver he no longer has a hold on his dad’s memory. But his irrational side mourned the screwdriver. His emotional brain felt that he’d lost another part of his dad. As the wise poet Ralph Waldo Emerson said, “Sorrow makes us all children again – destroys all differences of intellect.  The wisest know nothing.”

I’m very familiar with the destroying of intellect in times of grief, and I know just how my friend feels. After my mom died, I hung on to all kinds of her stuff: cookbooks, costume jewelry, unfinished embroidery projects, even her ratty old college sweatshirt. My dad has the more personal items — her glasses, her wedding ring, her driver’s license. I desperately wanted a piece of her, any piece, to remain, so I clung to her things in hopes of finding pieces of her.

Guess what? It doesn’t work. The desperation, the clinging, the hoping against hope are all for naught. Once the person you loved with your whole heart is gone, snatched away too soon by illness, there is no holding on to them. I’ve learned this slowly and painfully in the almost seven years that my mom has been dead. Her stuff is just that — stuff. It’s not her. She’s gone and that’s the brutal finality of experiencing the death of a loved one.

I’ve written before about how grief sneaks up on us, and can buckle our knees out of nowhere, even after years have passed. I know that this is what happened to my friend the other day: he was going about his business, engaged in a simple task that took little effort and yet would yield great satisfaction when done. The sun was shining, the workday was done, and a cold beer accompanied him as he unscrewed the rusty, spent screws from my gate. But once the screwdriver broke, so did the dam that most days holds back the torrent of sadness that is life without his dad. How many times has he said he wished his dad were here to help him with a DIY project, or to admire his handiwork upon a project’s completion? Too many times to count. And in the midst of an ordinary task being done on an ordinary day, the torrent rushed through.

“It’s so curious: one can resist tears and ‘behave’ very well in the hardest hours of grief.  But then someone makes you a friendly sign behind a window, or one notices that a flower that was in bud only yesterday has suddenly blossomed, or a letter slips from a drawer… and everything collapses.”  ~Colette


The spring of my discontent

As the spring equinox draws to a close, I can’t help but notice that today is the beginning of the season I dread. Springtime is hard, really hard, and today heralds the beginning of the period of time that hurts my heart. Three events in a short span, one right after another, that bring heartbreak.
An anniversary, a birthday, and Mother’s Day. Bam, bam, bam. Just when I get through one, the next one is right on its heels, waiting to slam into me like a brick wall. But instead of mortar and bricks, this wall is made up of sadness and loss.
Today, the first official day of spring, is my parents’ 47th wedding anniversary. 47 years. Just a few years shy of the big 5-0. I can imagine myself planning a gee-gantic golden celebration: friends, family, neighbors, cake, champagne, confetti. But one thing is missing: the bride.

Mom's photo for her wedding announcement in the newspaper

My mom’s chance to celebrate her golden anniversary was stolen by the vicious beast we call cancer. Stupid cancer.
My parents set a great example for what a successful marriage is all about. Give and take, support, and sacrifice. Good years, lean times. For better, for worse. Most definitely in sickness and in health. While they had a lot of good years together, I sure wish they’d have had more.

Blindsided

So I’m minding my own business on a rainy Saturday morning. On a morning in which the thunderstorm woke up my favorite girl, and her hungry little piggy, at 5 a.m. While that’s not my ideal start to a Saturday, we made the best of it: a huge mug of coffee for me, some hot tea for her, a blanket for each and a snuggle by the blue-green glow of the TV. I didn’t really want to be up that early, and I certainly didn’t want to be watching “Hillbilly Handfishing,” but I’ll take the quality time with my girl.

The last thing I expected on this rainy day was to be blindsided by grief. It happened innocently enough, as it tends to after several years of loss. After the sun rose and the handfishing concluded, I was searching through the cupboards in the game room for a small paintbrush to touch up some paint. No paintbrush to be found, but my search did turn up something I didn’t expect to find: a hospice booklet left over from my mom’s cancer “journey.”

For those of you fortunate enough to be uninitiated in grief and loss, you may not understand. For those of you who have been initiated in this dreadful state, you know. You know exactly how grief comes out of nowhere to blindside you.

I remember reading this booklet, in the fall of 2005 when my mom’s cancer “journey” was coming to a really yucky end. The hospice people were wonderful, providing much more than just care for my dying mama. They had care packages for my two young kids and for my niece and nephew. The oldest of YaYa’s 4 grandbabies was 8 when she died, the youngest (who happens to be my favorite girl) was 3. The teddy bears and coloring books given to them by the hospice workers probably didn’t register in the same way the “Gone From My Sight: The Dying Experience” booklet did with me.

Because the whole experience of my mom dying was rather surreal, I don’t recall feeling strange about being handed a booklet with such a title. I don’t recall wondering what The Dying Experience was all about, because we were living it. How ironic to be living The Dying Experience.

I do recall being grateful for the booklet’s upfront, go-at-your-pace approach to grief. This is the one thing I know for sure: no one can dictate another person’s grief, and no can anyone dictate another person’s death experience. As the booklet so aptly describes, “Each person approaches death in their own way, bringing to this last experience their own uniqueness. This is simply a guideline, a road map. Like any map, there are many roads arriving at the same destination, many ways to enter the same city.”

Hmmm, I certainly never likened death to a city, but it sure makes sense. Of course, I never thought I’d be facing thoughts like these, much less the death of my sweet, beloved mama. My own life as a mother had barely started, with a 3-year-old wild animal disguised as a very creative and outside-of-the-box little girl, and a headstrong 6-year-old boy who would astound me in the years to come with the memories he retained of his YaYa. How could my sweet mama be leaving me just as I was starting to learn to navigate this not-always-tranquil motherhood?

How could she be leaving me? “In her own time, in her own way,” as the booklet told me. Reading on, I learned another truth: “Death is as unique as the individual who is experiencing it.”

The booklet goes on to say that there is a shift that occurs within the dying person, which takes them from “a mental processing of death to a true comprehension and belief in their own mortality.”

Another thing I learned the hard way.

I’m certain that my sweet mama knew she was dying. Being told by the gurus at MD Anderson that the clinical-trial drug didn’t work to arrest the cancer that was eating her alive is rather concrete. Being told that the only thing left to do is call hospice is rather concrete as well. She knew. But in her quiet way, she didn’t talk about it. No bitching or moaning, no complaining, no ranting or shaking her fists at the heavens for being dealt such a rotten hand.

Instead, she hugged each doctor (she was really good at that, and I wish I’d inherited that trait; I’m not much of a hugger). She gathered herself and without shedding one tear or divulging her true feelings, she thanked the docs for trying so hard to save her. And she went home to plan her funeral.

For real. She wanted to plan it all–from the psalms read to the hymns sung to the outfit she would wear–so that those of us left behind wouldn’t be stuck trying to figure it all out. At a time when she could have stuck her head in the sand and said to hell with it all, she buckled down and spent her remaining strength on making things easier for her family. That’s the kind of person she was, and it’s a damn shame that she is with us no more. A bright and precious light went out when she died.

I thought I was prepared. I’d had months to wrap my head around it, after all. Watching her go from a vivacious, outgoing Nosey Rosey who never met a stranger to a wisp of herself should have prepared me. Seeing the life slowly fade from her immensely bright soul should have eased the transition from her being the center of our lives to her being gone. Being witness to the slow yet certain creep of cancer’s all-encompassing grasp of all things Barb should have steeled me to the reality I was facing.

And yet, none of those things happened. As Gone From My Sight: The Dying Experience so succinctly explains, “Focus changes from this world to the next, as the dying person loses his/her grounding to Earth.” She lost her ground to Earth, and we lost the glue, the sweetness, the center of our family. There is no preparing for that. There is no transition, no steeling. Although I knew it was happening and had accepted the fact that my beloved mother was dying, I was not prepared.

Just as I was not prepared for the onslaught of grief that hit me today as I came across the hospice booklet. In the middle of a perfectly normal day, while searching through a cupboard for a paintbrush, I was instantly transported back to the awful, wrenching reality of her death. I had no idea the booklet was in that cupboard. More importantly, I had no idea that the magnitude of grief, the bottomless pit of despair, could come back so quickly. In an instant, the swirling eddy of loss surrounded me, as heavy today as it was 6 years ago. As Kate Winslet said as she dedicated her Emmy win for the HBO miniseries “Mildred Pierce” last fall, “It doesn’t matter how old you are or what you do in your life. You never stop needing your mum.”

The last page of  Gone From My Sight: The Dying Experience contains a Henry Van Dyke poem unfamiliar to me. I don’t remember reading it when I received the booklet; my guess is that I didn’t make it that far. But now I have, and I’m glad I did.

I am standing upon the seashore. A ship at my side spreads her white sails to the morning breeze and starts for the blue ocean. She is an object of beauty and strength. I stand and watch her until at length she hangs like a speck of white cloud just where the sea and sky come to mingle with each other.

Then someone at my side says: “There, she is gone!”

“Gone where?”

Gone from my sight. That is all. She is just as large in mast and hull and spar as she was when she left my side and she is just as able to bear the load of living freight to her destined port.

Her diminished size is in me, not in her. And just at the moment when someone at my side says: “There, she is gone!” There are other eyes watching her coming, and other voices ready to take up the glad shout: “Here she comes!”

And that is dying.

 

 


6 years later…

Today is National Metastatic Breast Cancer Awareness Day. Congress said so, and in making such a proclamation, let’s hope we get some action. Action beyond pink ribbons and promotional tie-ins like toilet paper and cups of yogurt. The estimate is that some 160,000 women are dealing with metastatic breast cancer, but I suspect the number is much higher. Metastatic means the cancer has spread. Stage IV. There is no Stage V. Every BC patient’s worst nightmare. Because being diagnosed at all, regardless of stage, isn’t nightmare enough.

I’ll save the mets post for another day, because there’s another commemoration taking place today, and I won’t be able to rest until I get this post out of my head.

Or so I thought.

I sat down at my computer to mark this important day, but I got nothing. I am stuck. The enormity of the topic overwhelms me. I want to write just the right thing, but in my quest for perfection I’m struck down, unable to convey the importance that screams to get out.

It’s not often that I’m at a loss for words, particularly on this little blog. I rarely have trouble thinking of what to write, and most days the topic guides me. Sometimes a topic pops into my head and I have an overwhelming urge to write. My fingers on the keyboard can hardly keep up with my thoughts as they tumble out of my head.

But today, I’ve got nothing.

And rather than make myself crazy on this day, this important yet heartbreaking day, I’m going to re-run the post from last year. I added a few more pictures, because this time last year I was brand-new to blogging and hadn’t quite figured out how to manage the images in my posts. But more importantly, I added a few more pictures because I need to remember what she looked like.

My heart is heavy as grief once again rears its ugly head and reminds me that she is gone, forever. 
It’s been exactly 5 years since my mom died. Lots of people have written about loss & grief, and most of them have done it more eloquently than I. If you knew her, you loved her. Plain & simple. She was one of those people. She never met a stranger and could talk to anyone. The stories are endless, and if I think really hard I can conjure up the sound of her laugh. I have to work hard to remember her voice, though, because her “sick” voice is the freshest one. I also have to think back to how she looked, pre-cancer, before the dreaded disease ravaged her body yet was unable to extinguish her effervescent personality.

My mom was an incredible cook. She grew up on a farm and lost her own mom at age 13, so she assumed more responsibility than a middle-schooler should. She taught me a lot in the kitchen, although I’ll never match her skill with pie crust. I try every year at Thanksgiving and Christmas, and end up exhausted, frustrated and having used a month’s worth of curse words. One year at Christmas she gave coupons for a homemade pie, and those were highly prized gifts for sure.

She was a “white” woman who married into a Greek family. “White” means anyone who’s not Greek. Sometimes the Greeks aren’t happy about “whites” joining a family, because they want their kids to marry other Greeks. My mom didn’t let that stop her. She ingratiated herself into the lives of the Greek women and learned their culinary secrets. It wasn’t long before she was the best cook in the bunch. Not bad for a “white” girl.

My sweet mama was the quintessential suburban at-home mom: PTA president, Girl Scout leader, queen of homemade Halloween costumes. She put a homemade meal on the table every night for dinner, and I was halfway through elementary school before I realized that the homemade cinnamon roll that was my lunchbox treat was a rarity.

She had a love of learning that I see echoed in my own kids. I’m sure she flourished at college, probably thrilled to be responsible only for herself for the first time in years. She was president of her sorority and got this fancy necklace to wear during her reign. The look of pure happiness on her face makes me smile all these years later. In her typical over-achieving way, she graduated college in 3 years, then became an English teacher before she became a mom. My whole childhood, she had us look up words in the dictionary to learn how to spell. I won the spelling bee in 4th grade, and to this day am proud of being a good speller. She instilled a love of words and reading that I’ll carry with me my entire life.

When Trevor graduated from business school in 2004, she was as proud of him as if he were her own child. In fact, once he married into her family, she considered him a son. Not a son-in-law, but a son. She was sick at the time this photo was taken, but hid it well. She didn’t want anything to interfere with his big day.

She had a lot of success in life, but her greatest achievement was being YaYa. She loved her grandbabies to the max, and when she knew she was losing her battle against cancer, she spoke of her sadness in not being able to watch them grow up. She’s missed out on a lot. But loss is a 2-way street, and the 4 kids who were lucky enough to have her as their YaYa, albeit way too briefly, have missed out as well. As each year passes, and her grandbabies grow up, they change and take on new interests and habits. She would have loved every minute of it. Something tells me she would have been quite adept at navigating whatever stage those little darlins are in.

Here they are on the day of her funeral.

Andrew was 8, Payton and his cousin Megan were 6, Macy was 3 when YaYa died. She was 67. Way too young, all the way around.

Life isn’t the same without her. While the pain of loss has lessened over the years, it’s still there, and I suspect it never goes away. No one in your life loves you the way a mother does. And no matter how old I become, I will always miss my mother’s love. Oliver Wendell Holmes said that “mothers carry the key of our souls in their bosoms.” That certainly was the case with my mom.

Milestones are hard when you’ve lost someone so dear. Every year, the week or so leading up to the anniversary of her death has been miserable. I find myself transported back to the time of  illness and all of the unpleasantness that entailed. Taking care of her was both the hardest thing ever and the greatest honor. I went into it knowing it would be hard, but having no idea how brutal. Balancing that with taking care of my young family was grueling, no doubt. But I wanted to come out of it with no regrets, and I’m happy to say that I did.

This year, however, was different. I wasn’t dreading the date. Maybe because I’ve got a lot on my mind and a lot on my plate. Maybe because as I get ever closer to regaining my “normal” life after my own cancer battle, I have a new perspective. Maybe I’m just getting absent-minded in my old age.

For a while after she died, I looked for her in crowds: at the grocery store, at a baseball game, at any random gathering. I knew, of course, that she wasn’t there. At least my rational brain knew that, but I looked anyway. I don’t know when it was that I stopped looking, but at some point, I started to see her. Not really her, but glimpses of people or expressions on faces that recalled her: the woman at the gym who looks a lot like her from the back. The resemblance in my niece to my mom’s photos as a child. My aunt’s hands, which look just like my mom’s.

This year, today, on the anniversary of her death, I wasn’t looking for her, but she was there. Today in my much-anticipated first tennis match since my mastectomy, my opponents’ names were Barbara and Ann. Guess what my mom’s name was? Yep, you got it — Barbara Ann.


This may get me in trouble

I’ll probably get in trouble for this. Or at least be on the receiving end of a cacophony of “You shouldn’t have done that” and “Did you have to?” and “That really wasn’t necessary.” But that’s ok; I rather like living my life on the edge. I’ve been known to stir the pot, to not let sleeping dogs lie, and to eschew the leaving of well enough alone.

So here I go.

This post is all about Ed.

He’s going to hate it.

See, Ed is not one for calling a lot of attention to himself. Or any attention, really. But sometimes, like ripping off a Band-Aid, it’s gotta be done.

He deserves it. It’s his birthday, so today it will be all about him.

Ed’s been our best family friend for a long, long time. In fact, it’s been so long, he’s dropped the “friend” and moved right on into “family.” Sometimes family has nothing to do with blood and genes and trees, and everything to do with the contents of one’s hearts and the meshing of like-minded souls. Assuming souls have minds, that is. I don’t think they operate on auto-pilot, do they?

I met Ed while toiling away in the publishing biz many moons ago in Austin. He and Trevor were in grad school at UT (Hook ‘Em!) at the same time, but we didn’t know each other during school; he was reading thick, musty books in the history department while Trevor built up his brain and hung with the geek squad in the computer science world. I hate to think of the years we wasted not knowing each other during that time, but our livers certainly breathe a sigh of relief. There was a fair bit of drinking going on in those days (as opposed to now, when kids’ schedules, middle age, and the threat of recurring cancer tempers my tippling). We did make up for some lost time, though, once we met; happy hours at Trudy’s with multiple Mexican Martinis and extra olives, watermelon margaritas at Maneul’s on South Congress, beers on the roof deck at Waterloo Ice House; and the infamous wine tasting club run by our resident oenophile Anthony King. I hope I never forget the carefree youthful nights spent lifting a glass, enjoying our youth & freedom. None of us will ever forget Trevor puking in the rose bushes at one of the Hess brothers’ houses, then coming back for more. Good times.

But back to work…Ed wrote and I edited. His hair was long back then (mine was too), and he labored over every word, every sentence, every TEKS standard (see how far we go back — long before the TAKS and now the STAR state standardized tests for public schools). I learned real quick that he was smart. Really smart. And he really cared about his work. He had such a high standard for himself that sometimes, just once in a while and not really very often (!), he made me wait for his work. I really don’t like waiting.

See, there was a progression to creation of a textbook, and we were both cogs in the wheel. Schedules were made, which we had to follow. Deadlines were enforced, because if our book wasn’t ready to go to print–back in the day before e-books and widespread Internet use — another publisher would get our spot and the book would be delayed. And we would all be fired. So I learned pretty quick with Ed that some tough love was necessary. I schooled him in the “good enough is good enough” principle that editors must embrace in order to keep the line moving. Oh, how that boy labored over every word, every sentence, every standard. There were days when I was a hair’s breath away from snatching the copy right out of his hands so that I could get my red pen all over it and keep the line moving.

It’s probably no surprise that Ed left publishing and took a rather circuitous route to teaching. A heart-wrenching detour to care for an ailing parent, work for an educational non-profit that trained teachers, a foray into self-employment in the handyman biz, a little time off to determine the color of his parachute (tricky when you’re a little bit color-blind), and finally, he was home.

Ed has a job that not many people would take on: he teaches kids who’ve been sent to the alternative school. Reasons for being sent there vary from fighting to drug use to crimes both petty and serious. The classes are small in number but large in ramifications. Several years ago, when Ed was contemplating whether to enter the teaching profession, I told him that he would be the kind of teacher who made a difference in kids’ lives. It sounds hokey but it’s true: he’s the sort of teacher who kids will remember always, and they’ll look back and say, “Man, Mr C really cared.” It’s true, and he does. He guides kids that a lot of people would cast aside as lost causes. He listens and becomes the sole person who cares. It’s no surprise to me that kids who pass through his class come back to visit, bring him a homemade Christmas treat, and mail him an invitation to their graduation ceremonies.

Those kids are not the only people who benefit from Ed’s unique brand of caring. After enduring the rigors and heartache of watching his dad die of pancreatic cancer, he became my sherpa when my mom got sick. I’ll always remember him telling me that if I thought it was bad now, it was gonna get worse. A lot worse. He was right. It was awful.

My mom knew Ed well, and when she moved in with me after retiring and moving away from Houston, it was Ed — not me — who she wanted as her caregiver for the icky parts of her cancer battle. She wanted him to sit through the class at MD Anderson on how to care for a PICC line, not me. I didn’t know it at the time, but she was trying to shield me from the routine horrors that make up a cancer patient’s life. When she was too frail and weak to step into my deep bathtub, it was Ed she asked for help. She would rather have had him see her in that state, to spare me from the eternal impression of being able to count each rib in her battle-weary, wasted body. It was Ed who she requested, not me. He made many food runs in the maddening game of “What can we get her to eat?” only to see her take 2 bites and be done. So much for that. But he never got frustrated, he never pressured her to eat. It was Ed who bore the brunt of the fallout from her radiated bowels. And that’s all I’m going to say about that.

It takes a special kind of person to volunteer for such service, but that’s just the kind of person he is. My mom knew it, and so do I. Ed’s the kind of guy who sets up the ladder and willingly allows grafitti in his garage. No project is too big, no mess too messy.

He’s the kind of guy who doesn’t freak when a little kid pukes on his brand-new couch, which Macy (right) did just after this photo was taken at Ed’s house in DC.

He’s the kind of guy who gives a little kid his watch to wear while patience runs short and naptime runs on by during sight-seeing in DC. He knows how to make a little kid feel like the most important person in the world. 

He knows how to keep a little kid quiet during a long, boring grad-school graduation ceremony, and he thinks anytime is the right time for a junky snack.

He digs the deepest sand-pit every year at Salisbury Beach every year, even when he’d rather be reading his book, and waves off the old-man critics who pass by and warn of the pit’s collapse and threat of said pit swallowing little kids whole. He knows what he’s doing.

He’s the creator of Halloween costumes too far-out for my brain to imagine.

He knew Maddy, the best dog on Earth. Ever. In the history of dogs. He loved her with his whole heart, and finally gave in to my years-long pestering that he needed a dog of his own. Not once, but twice. And he let my kids name both dogs. Hence, a female chocolate lab named Snoopy, and a wily basenji-mix named Sugar.

We have Ed to thank for the Red Sox fever that exists in our lives. A native Mass-hole, Ed is a Sox fan for life, and he taught Payton the joys and heartbreak that is Red Sox nation. When Payton was four years old, at his first trip to Fenway, Ed showed his devious side when he made Pay think that Nomar Garciaparra hit a foul ball right into Payton’s lap. Eight years later, I think Pay still believes it really happened.

When Macy came along, a new bond was forged, and the strength of that bond sometimes startles and always amazes me. Mrs Dally, Macy’s first-grade teacher, told me in confidence one day that I might want to be careful because Macy told the class, during an exercise about friends, that her best friend is a 42-year-old man. In the case of anyone but Ed, this might raise a few eyebrows. But spend two minutes with him and you get it. In third grade, Macy filled out the “getting to know you” questionnaire from the teacher on the first day of school. For the question about  her best friend’s favorite activity, Macy wrote: landscaping. Those two are tight. 

Happy birthday, Ed. May the day be as fantastic, wonderful, and all-out-awesome as you are.


6 years later…

Today is National Metastatic Breast Cancer Awareness Day. Congress said so, and in making such a proclamation, let’s hope we get some action. Action beyond pink ribbons and promotional tie-ins like toilet paper and cups of yogurt. The estimate is that some 160,000 women are dealing with metastatic breast cancer, but I suspect the number is much higher. Metastatic means the cancer has spread. Stage IV. There is no Stage V. Every BC patient’s worst nightmare. Because being diagnosed at all, regardless of stage, isn’t nightmare enough.

I’ll save the mets post for another day, because there’s another commemoration taking place today, and I won’t be able to rest until I get this post out of my head.

Or so I thought.

I sat down at my computer to mark this important day, but I got nothing. I am stuck. The enormity of the topic overwhelms me. I want to write just the right thing, but in my quest for perfection I’m struck down, unable to convey the importance that screams to get out.

It’s not often that I’m at a loss for words, particularly on this little blog. I rarely have trouble thinking of what to write, and most days the topic guides me. Sometimes a topic pops into my head and I have an overwhelming urge to write. My fingers on the keyboard can hardly keep up with my thoughts as they tumble out of my head.

But today, I’ve got nothing.

And rather than make myself crazy on this day, this important yet heartbreaking day, I’m going to re-run the post from last year. I added a few more pictures, because this time last year I was brand-new to blogging and hadn’t quite figured out how to manage the images in my posts. But more importantly, I added a few more pictures because I need to remember what she looked like.

My heart is heavy as grief once again rears its ugly head and reminds me that she is gone, forever. 
It’s been exactly 5 years since my mom died. Lots of people have written about loss & grief, and most of them have done it more eloquently than I. If you knew her, you loved her. Plain & simple. She was one of those people. She never met a stranger and could talk to anyone. The stories are endless, and if I think really hard I can conjure up the sound of her laugh. I have to work hard to remember her voice, though, because her “sick” voice is the freshest one. I also have to think back to how she looked, pre-cancer, before the dreaded disease ravaged her body yet was unable to extinguish her effervescent personality.

My mom was an incredible cook. She grew up on a farm and lost her own mom at age 13, so she assumed more responsibility than a middle-schooler should. She taught me a lot in the kitchen, although I’ll never match her skill with pie crust. I try every year at Thanksgiving and Christmas, and end up exhausted, frustrated and having used a month’s worth of curse words. One year at Christmas she gave coupons for a homemade pie, and those were highly prized gifts for sure.

She was a “white” woman who married into a Greek family. “White” means anyone who’s not Greek. Sometimes the Greeks aren’t happy about “whites” joining a family, because they want their kids to marry other Greeks. My mom didn’t let that stop her. She ingratiated herself into the lives of the Greek women and learned their culinary secrets. It wasn’t long before she was the best cook in the bunch. Not bad for a “white” girl.

My sweet mama was the quintessential suburban at-home mom: PTA president, Girl Scout leader, queen of homemade Halloween costumes. She put a homemade meal on the table every night for dinner, and I was halfway through elementary school before I realized that the homemade cinnamon roll that was my lunchbox treat was a rarity.

She had a love of learning that I see echoed in my own kids. I’m sure she flourished at college, probably thrilled to be responsible only for herself for the first time in years. She was president of her sorority and got this fancy necklace to wear during her reign. The look of pure happiness on her face makes me smile all these years later. In her typical over-achieving way, she graduated college in 3 years, then became an English teacher before she became a mom. My whole childhood, she had us look up words in the dictionary to learn how to spell. I won the spelling bee in 4th grade, and to this day am proud of being a good speller. She instilled a love of words and reading that I’ll carry with me my entire life.

When Trevor graduated from business school in 2004, she was as proud of him as if he were her own child. In fact, once he married into her family, she considered him a son. Not a son-in-law, but a son. She was sick at the time this photo was taken, but hid it well. She didn’t want anything to interfere with his big day.

She had a lot of success in life, but her greatest achievement was being YaYa. She loved her grandbabies to the max, and when she knew she was losing her battle against cancer, she spoke of her sadness in not being able to watch them grow up. She’s missed out on a lot. But loss is a 2-way street, and the 4 kids who were lucky enough to have her as their YaYa, albeit way too briefly, have missed out as well. As each year passes, and her grandbabies grow up, they change and take on new interests and habits. She would have loved every minute of it. Something tells me she would have been quite adept at navigating whatever stage those little darlins are in.

Here they are on the day of her funeral.

Andrew was 8, Payton and his cousin Megan were 6, Macy was 3 when YaYa died. She was 67. Way too young, all the way around.

Life isn’t the same without her. While the pain of loss has lessened over the years, it’s still there, and I suspect it never goes away. No one in your life loves you the way a mother does. And no matter how old I become, I will always miss my mother’s love. Oliver Wendell Holmes said that “mothers carry the key of our souls in their bosoms.” That certainly was the case with my mom.

Milestones are hard when you’ve lost someone so dear. Every year, the week or so leading up to the anniversary of her death has been miserable. I find myself transported back to the time of  illness and all of the unpleasantness that entailed. Taking care of her was both the hardest thing ever and the greatest honor. I went into it knowing it would be hard, but having no idea how brutal. Balancing that with taking care of my young family was grueling, no doubt. But I wanted to come out of it with no regrets, and I’m happy to say that I did.

This year, however, was different. I wasn’t dreading the date. Maybe because I’ve got a lot on my mind and a lot on my plate. Maybe because as I get ever closer to regaining my “normal” life after my own cancer battle, I have a new perspective. Maybe I’m just getting absent-minded in my old age.

For a while after she died, I looked for her in crowds: at the grocery store, at a baseball game, at any random gathering. I knew, of course, that she wasn’t there. At least my rational brain knew that, but I looked anyway. I don’t know when it was that I stopped looking, but at some point, I started to see her. Not really her, but glimpses of people or expressions on faces that recalled her: the woman at the gym who looks a lot like her from the back. The resemblance in my niece to my mom’s photos as a child. My aunt’s hands, which look just like my mom’s.

This year, today, on the anniversary of her death, I wasn’t looking for her, but she was there. Today in my much-anticipated first tennis match since my mastectomy, my opponents’ names were Barbara and Ann. Guess what my mom’s name was? Yep, you got it — Barbara Ann.