On Steve Jobs and Living the Life You’re Meant To

There’s a For Sale sign on our lawn.

The listing for our house will officially appear tomorrow, but the sign is on our lawn now.

“How can you make a decision like this so calmly?” a friend asked a couple of weeks ago.

Calm? I’m not calm about anything right now (and evidently I wasn’t entirely prepared for that sign to go up).

I’m not calm about the stuff going on at work, and I’m certainly not calm about the fact that there’s a FOR SALE SIGN on the lawn of the house we’ve lived in for almost 9 years – since before we were married, since before we had our dog, since way before Connor was born.

As far as the stuff that happens next – big move, new house, new job – I’m excited about parts of it and, frankly, in denial about the rest. I’m almost 37 years old and I have spent most of my life living very near my parents. I’ve got really good friends here – pseudo-family kind of friends – I don’t want to leave. Both of those things make me want to barf.

But here’s the thing: I can’t stay here. Oh sure, in the literal sense I could. But in the larger-than-life philosophical sense, I can’t.

Last night as we cleaned and tidied and did the last few things needed for a photographer to come and take pictures of our house, I saw the news that Steve Jobs had died. I was sad; more sad than I would have thought, actually, but I’ve enjoyed revisiting his words of wisdom. Such as:

“When I was 17, I read a quote that went something like: ‘If you live each day as if it was your last, someday you’ll most certainly be right.’ It made an impression on me, and since then, for the past 33 years, I have looked in the mirror every morning and asked myself: ‘If today were the last day of my life, would I want to do what I am about to do today?’ And whenever the answer has been ‘No’ for too many days in a row, I know I need to change something.”

I think this is genius. We always hear, “Live each day as if it were your last,” which is romantic and inspring but totally impractical. If I knew tomorrow would be my last I’d hop on a plane for Hawaii. I’d go out for dinner with my boys and overeat to an insane degree and then have the most decadent dessert on the menu. I’d spend hours sitting by the ocean. I’d write a really, really long letter to my son. Some of those are things I could do today – or any day – but I can’t do them over and over and savour the moments as though they were my last. Life doesn’t work that way.

The brilliance of the above quote by Jobs is the “too many days in a row” part. Ignoring the little voice that says, “no” is how years go by until we realize we haven’t done what we want to do in this lifetime.

I certainly don’t have it all figured out and I’m not entirely sure what I want to do next. I know the general direction, but not the specific vision. According to Mr. Jobs, that’s okay:

“Your time is limited, so don’t waste it living someone else’s life. Don’t be trapped by dogma — which is living with the results of other people’s thinking. Don’t let the noise of others’ opinions drown out your own inner voice. And most important, have the courage to follow your heart and intuition. They somehow already know what you truly want to become. Everything else is secondary.”

So I had my little cry about the For Sale sign. I’m not saying I won’t shed many more tears by the time this process is done and I’ve left my first house and the city I grew up in, but in my heart I know those things are secondary.

House for sale sign

Wanna buy a house?

Linking up with Just Write – The Fourth:

I Believed Once

I believed once.

I thought I could make a difference. I followed my heart and used my voice and put it out there. I worked. Hard. I worked through lunch. I worked late, came home, had dinner, and worked some more.

I wrote. I wrote and wrote and brainstormed because I believed. And because I believed I put my whole heart in to my work.

The path my life has taken over the last five years has made me who I am now. Some of that evolution is on this blog, but so much of it is because of my work – the absolute passion and dedication I put into it, the opportunities I’ve had, and the people I’ve worked with.

My work changed who I knew I could be, but it’s the evolution chronicled here that has changed who I am. It has changed what I believe.

It has changed what I believe I can do.

I believe I’ve done what I can do in my current job, especially because recent changes have taken the work in a different direction. Despite knowing this is what I must do, I do it with a heavy heart. I played a big part in building something bold, and because that something will inevitably change – partly because the organization has changed but also because that’s what things do – I feel as though I’m saying goodbye not only to a job and a team but to a piece of myself. When I pack up my desk the box containing my pictures will also contain the shadow of my contribution, exiting the building with me dressed in both regret that things must change and an attempt at preserving something that meant something to me.

It’s time for me to move on.

We’ve spent the better part of the last month sprucing up our house and on Friday a For Sale sign will appear on our lawn.

On a date in the not-too-distant future I will write a letter to my boss and sign a piece of paper giving my house over to someone else.

I’m leaving the work and the people and the organization that changed how I think about what work is.

I’m leaving the first house we owned, and the house I brought my son home to.

I’m leaving the city I grew up in, where my parents – and my son’s grandparents – are six minutes away.

I’m leaving who I used to be in order to find out who I can become.

Who I think I am now.

I believed once.

And I’m choosing to believe again.

Sunrise. A new day in the Canadian Rockies.

 

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Beating Cancer With Love

September is Ovarian Cancer Awareness month. This disease barely registered with me until my mom showed up on my doorstep the day after I got home from my honeymoon and told me she had a tumour the size of a grapefruit. She’s here today to tell her cancer story. 

***

How do you survive a cancer that has a 30% survival rate? It’s been 7 years since my surgery and I have long since been declared free of ovarian cancer, but I’m still not sure of the secret. Truly I think my time had not come. However, in addition to good care I firmly believe positive thinking and a huge dose of support are key.

Just before our oldest daughter’s wedding – first wedding, oldest of four – we were putting the the last details of The Plan in place. The couple wanted a relaxed get together with out of town guests so we planned a buffet at our house after the rehearsal.

I was feeling not so good. Unusually for me I decided to go to the doctor; I didn’t want to be sick for the wedding. If not for that wedding I doubt I’d have made it.

teal ovarian cancer ribbon“How long have you had this growth?” my doctor asked.

“What growth?” was my response.

I’d read about the signs of ovarian cancer but there was no family history so I didn’t think it could happen to me. As it turned out I did have several of the signs.

By the Tuesday before the wedding I’d had blood tests. My CA125 score was really high, six times what it should be. An ultrasound was scheduled. The technician, looking serious, promised to have the result to my doctor by Friday. I told her to wait until after the wedding but it was there that afternoon, which seemed like a bad sign.

An MRI was scheduled for Thursday. My husband and I sneaked away saying we were picking up supplies for Friday’s dinner. By then I knew it was serious but (fortunately) didn’t have time to think. And of course we couldn’t tell anyone. How could we tell the other kids if I didn’t tell the bride? And how could they keep a secret like that? On the other hand for me not talking about it may have carried me through!

The wedding was wonderful, a huge success. I don’t remember much but do have one flash of memory, quoting an Ogden Nash poem during the speech I made on behalf of my husband and me: “To keep your marriage brimming, With love in the loving cup, Whenever you’re wrong admit it, Whenever you’re right, shut up.”

When it was done my marvellous gynaecologist oncologist suggested I do a course of chemotherapy “in case of rogue cells”. She was pretty sure she’d got it all and she would like to declare me cured before she retired. My family said I wasn’t through with life yet. (Remember that positive thinking component?)After that it was reality time. I was at the top of the surgery list and in at the first cancellation. The Universe decided it was to be right after the honeymooners got home.

My city has a terrific treatment facility due to a generous donation. The chemo room is surrounded by windows and trees. And I am truly blessed in my family. One of the kids came each time I went to my day-long chemo treatment. My husband (who had to skip the IV insertion part because of needle phobia) brought lunch. There was never nothing to do or nothing to say.

I had a few days of miserable neuralgia each time but limited nausea because of the timely invention of a good anti-nausea drug. I was bald and puffy from steroids and my energy was low but I never doubted I could make it. I even worked part of the time. What I remember now is the sea of love. That was the most important therapy.

My out of town daughter sent me a lovely journal suggesting I keep a sunshine journal, putting in only things that made me smile. (I am on the 4th one now and still smiling.) She invited me to come on a soul journey after chemo was over, to drive to the mountains for an injection of peace, hope and serenity.

A friend sent me to a wonderful alternative treatment program during the chemotherapy time.

My oldest daughter came with me and also gave me a treasured silver bell charm from her wedding to wear.

My son, who was both working and commuting to Vancouver for classes, came to one chemo treatment, supposedly for an hour and stayed 4 hours, causing him to miss his ferry and his class.

My healer daughter supported me in listening to my body rather than well meant advice and found me a wonderful cancer patient yoga CD which I still use.

People made marvellous soups and dropped them off. People sent plants and flowers. My son-in-law gave me mind-bending crossword puzzles. My husband did the cooking. My cherished colleague said, “go away and heal” and looked after my business. Another friend sent me some wonderful meditation CDs. How could I not get better?

Out of meditation came a couple of lullabies that appeared in my head for (then nonexistent) grandchildren. That was when I knew it was going to be okay for sure. I don’t know how to write music down. I had to be here to sing them myself.

Grandmother and newborn grandchild

Grandma and Connor when he was a couple of hours old

***

I will be forever grateful that my mom’s cancer was caught in time for her to be treated and fully recover. Please make sure you know the symptoms. Your grandchildren will be grateful.  

PS The colour of my blog – similar to ovarian cancer teal – is a total coincidence, and one I only caught today. I think it was meant to be.

Construction-Zone Craziness

When we initially started talking about buying our first house, my husband thought it sounded dreamy to buy a fixer-upper we could work on ourselves.

I told him he was crazy.

This was almost 10 years ago, mind you. Before dog, before kid, before we were married, even. I think it’s safe to say life was simpler at the time, and yet I couldn’t imagine diving into a reno and trying to live in the house at the same time. Thanks but no thanks. No way, Jose. Not a chance.

In the end, somewhat ironically, we bought a house in a new development. We picked the colours, the countertops, the cabinets. We watched the walls go up and the windows go in. When it was done, we moved in knowing we didn’t have to do anything. We didn’t even have to change a lightbulb.

Fast forward 9 1/2 years and we’re living in what feels like a construction zone. We’re sprucing things up and fixing things that need to be fixed after inhabiting this space for this many years, more recently with a precocious child who likes to make holes in things and draw on walls. (Magic Erasers are my new best friend.) It’s not a massive undertaking, but it’s starting to feel like it.

We started some of this work in June and then promptly abandoned it (long story), so we’ve been living with spackle-filled holes above our shower and a few other things as part of the scenery ever since. But about three weeks ago we started again in earnest. More holes have been patched, sanded and painted. A wonky skylight no longer looks as though it might share the next heavy rainfall with us. Furniture has been pulled into the middle of the room so we can tackle walls and baseboards.

It’s no large-scale kitchen reno, but it still feels like a construction zone with paint brushes in the kitchen sink and a layer of dust on everything thanks to post-spackle sanding.

Today my husband boldly climbed up to the skylight in our ensuite and fixed the seal around it. Which, understandably, involved the creation of a really big mess. He cleaned it up fairly well, but it will have to be sanded and painted tomorrow so there’s no point getting picky about things tonight. Still, I had to do some sleuthing before bed to figure out where my toothbrush went.

As I brushed I noticed the debris around the sink – pieces of wall and putty and dust and goodness knows what else. Then getting into bed I saw that our duvet was covered in grit. Well, shake it off. Literally. I picked it up, gave it a shake and dumped the grit on the floor.

The mess is temporary, but it’s driving me batty.

I realize this is all a big whine about something insignificant. Something I should be (and am) grateful we’re able to do. In fact, I’m especially grateful for all the work my husband is doing right now – that he’s able to do it all himself and working hard to get it done quickly is not something I take for granted. So yes, this is what you might call a first world problem.

But here’s the thing: I don’t do well in this environment. I get squirrelly enough with clutter – I create my fair share of it, but it makes me crazy. So this is all a bit much.

Every night around 7:00 my husband and I start to get snippy. The cranky cues are subtle – a short fuse when it comes to noisy toys, less patience for repeated requests for a TV show we both hate, and the undercurrent of Oh-God-we’re-never-going-to-get-this-done-and-I-can’t-take-it-anymore in our conversations.

I know – am aware with every fibre of my being – that I could very quickly become a nightmare to live with right now. But I’m determined not to go back there. I am trusting this process to get us where we want to go and in doing so I’m focused on finding a way to live with it – a not insignificant effort that will involve more mood control than I’m usually able to muster.

This is important though and, yes, temporary. So until we’re done I will find a way to overcome the craziness and just be.

Every MONDAY join us…
Write, post, link-up, share your story and your voice.
Be part of carrying the weight of confidence and share our mission
to empower, inspire, and remind women, parents and children
that the time has come to celebrate ourselves!

Next week’s prompt: “I knew I had to….”

(Remember you can also write on a topic of your choice.)

 

Also linked up with Just Write.

Because I am a Survivor – Guest Post by The Empress

My guest poster today is someone many of us know and love. I don’t know when I first met The Empress – she was always just there. And that’s my experience of her now – she’s there, popping into posts when you need some love, offering to help someone, and keeping her PPD radar going so no suffering mother has to do it alone. She’s just always there.

I met Alexandra in San Diego while at BlogHer ’11 and she was every bit as lovely as I had expected. I invited her to guest post here because I knew she’d have something authentic and beautiful to say, and she didn’t disappoint.

***

I have been excited about guest posting at Robin’s site, and I’m so grateful she’s invited me. Thank you, Robin.

I am a PPD survivor. I have, and will always have, the PPD Survivor button up on my site.

My PPD story is a very big part of who I am, but it’s not entirely who I am, as it once was.

My life, when it was in the throes of PPD, was one I never imagined I’d find my way out of. I hoped, I prayed, but never believed I’d be lucky enough to climb out of the dark tunnel that had become my days.

Therapy worked, for the lucky ones. Medication worked, for the lucky ones. But for someone for whom PPD had come to consume every second of every day and every night — like it had for me – I knew I would not be a survivor.

I was barely hanging on by my fingernails.

Even to talk about what my life was like then makes my eyes brim with tears.

If I had to describe what living with PPD feels like to someone who has no experience in this kind of surreal environment, I’d tell them this: picture a churning, dark ocean with ten foot high crashing waves, battering with tremendous force at whatever they slapped. Then see yourself bobbing, right in the center of this storm, alone, arms flailing, growing weaker and losing hope of survival by the minute, with your head barely above the water, despite your struggle to stay afloat.

You just want to stop fighting, and let yourself sink down. To the sweet, quiet bottom. To surrender. You think how peaceful it would feel to just slowly stop trying to keep your head above the water.

But you can’t give in to this thought. You have the responsibility of your baby, who only wants you.

I have pictures of my newborn from this time, but none of me. The haunted face I saw on myself, of this first time mother, was something I couldn’t look at, so I threw out the pictures. Others didn’t see what I saw in those photos: fear, panic, anxiety, depression. Defeat. Disappointment.

I couldn’t sleep. I’d lay awake, thinking about how I needed to sleep.

I couldn’t eat. I’d sit at the table, pushing my food from one corner of the plate to the other — my anxiety not allowing me to swallow.

I couldn’t speak. My unhappiness had such a grip on me that I couldn’t put three words together. How was I supposed to conduct chit chat at the moms’ groups?

I couldn’t smile.

Of all the things PPD did to me, this one, THIS ONE, makes me want to kick its ass.

PPD wouldn’t let me smile for my baby.

I knew I had to see my doctor, who, after our appointment, agreed that something was wrong and started me on a prescription. She also referred me for talk therapy.

These things may have taken the edge off, reduced the crisis.

But I know the real reason for my survival: the kindness of a stranger.

I decided to call the hospital where I delivered to ask if they had any PPD support groups.

I wanted to jump through the phone and kiss the nurse when she answered “yes.” “Yes,” she said, and then continued with the beautiful words, “they meet right here, every Wednesday morning at 9 a.m.”

I would be with people I wouldn’t have to pretend with. I would be with people who understood. All I had to do was hang on until Wednesday, but Wednesday was too far away. I needed something now. I confided to the nurse that my days were made up of minute-to-minute survival. She gave me the phone number of the nurse who facilitated the PPD group.

Her name was Marty, short for Martha, and I called her. I remember her giggly laughter on the phone. I had said something that made her laugh. I surprised myself by smiling. I told her I couldn’t make it until Wednesday.

She said she’d be over in 40 minutes.

She made the drive to my home, sat on the sofa with me and listened, even though there were no words to listen to, only sobs.

She listened until my husband came home from work, with her arm around me, and then she talked with him, about me.

Marty promised me she’d come over every day until my first PPD meeting in two days.

And she was true to her word.

Marty saved my life. She gave me hope, she gave me time, she gave me herself.

Marty is why I will never take the PPD Survivor button on my site down, even though my story is 17 years old.

Because there may be someone, someday, who clicks over, desperately looking for hope.

And I want them to see that we can kick PPD in the ass.

With the help I needed and the kindness of a woman, I survived. I survived something so mentally brutal that I at one time thought it would never end.

It can end. Never give up trying to find a way for it to end.

And if you are a PPD survivor? Please extend your hand to those still trying to climb their way out of the dark tunnel.

Good Day, Regular People
***

I related so much to her description of PPD, and know exactly how it would be that one person coming and sitting with you might make all the difference. Just so you’re not alone.

Because, of course, none of us ever is. Right, Alexandra? Thank you so very much for being here today.