Category Archives: Life After Cancer

Where Does The Time Go?

1 Dec

Three years ago, I could still feel the sting in my left armpit every time I lifted my arm past shoulder height. With one eye closed, anxiety and denial flooded through me as I opened the mailbox and waited for the white BC Cancer Agency envelope, announcing the start of chemotherapy, to appear.

As Christmas carols played in every Starbucks in Vancouver, time slowed as I hovered in the doorway between my past life as a professional, suit-wearing, laptop-slinging headhunter and my interim reality as a bald, scrawny, fatigued cancer patient. Then, throughout the first few months of 2010, there were days when the engine of time seemed to sputter and then die completely as each moment of chemo-induced joint pain felt like a merciless life sentence.

When I think back on those endless hours, knit together by boredom, pain, fear, and anxiety, it’s hard to believe I have arrived in a place where I’m so deep into my new life that I can barely snag a moment of peace and quiet contemplation. On the busiest of days, I try to remember my silent negotiations as I recovered from surgeries, and swore I would never again let stress become my dictator.

Yet here I am…neck deep into an exciting and terrifying chapter where the fear about how to pull off a Big Hairy Audacious Dream sometimes shakes me awake in the night and then pokes at me whenever I attempt to sleep again.

But, there is a gigantic upside to this fear. The dream engine is working in overdrive and soon, 12 other cancer survivors, including two of my fellow Facing Cancer Bloggers, will have the chance to travel to New Delhi, India for a 2-week volunteer program. My hope is that the stories of these 12 will make an impact on all of you and on people around the world. Their stories are about how to pick up the pieces of your life after treatment ends. But, these stories are also about our global village and how we are more the same than we are different.

There is a huge amount of work to be done, in order to make this trip a reality and we have just over 2 months to do it. Will you help us make this happen by visiting the latest post on my website and leaving your comment for Sir Richard Branson?: The #Delhi2013 Mob on Richard Branson Continues. Share Your Voice To Shape History.

Yes, you heard me right, Richard Branson – billionaire, philanthropic visonary, and leader of all things Virgin. After our successful social media mob last Tuesday, we are now trying to get to 200 comments by Tuesday because then we plan to take this story to the media. We want Virgin Atlantic to donate round trip flights to New Delhi for our #Delhi2013 Dozen and we need your help to pull this off.

This trip is a pilot program to see if an international volunteer experience helps other cancer survivors heal the way it helped me. If we’re successful, we hope that means plenty more adventures ahead for people just like you.

I continue to be so grateful to all of you and to the support of this community. You have held me up through some of my darkest times and I hope each of you finds the support you need through the tough days in your world. When the time comes for your fresh chapter, we’ll be right there beside you too.

Posted in Life After Cancer | 1 Comment

Nothing is “Unthinkable”

4 Sep

Today, I had the opportunity to share a guest blog post on A Fresh Chapter that brought me to tears. Here’s a short excerpt:

Your post about “What’s Next?” got me thinking about our situation. How do we pick up the pieces of our lives and move forward, knowing we both have incurable cancer?

What I have learned is this: no one ever knows what life will present them with. Nothing is “unthinkable”. But, by investing one’s whole being in learning to live in the present, we have the ability to replace fear with hope, love, and generosity to others. We can also cultivate a deep appreciation for the gifts of life – nature, art, music. Having all of our senses piqued to possibilities is what will see us through.

To read the full post by Karen Sutherland, CLICK HERE.

Posted in Coping with Cancer, Life After Cancer | Leave a comment

So, Now What?

31 Jul

Returning from an epic trip and finishing cancer treatment can both evoke the powerful (and often difficult to answer) question, Now What?

If you are rounding the final lap of treatment and about to step out the doors of the Cancer Agency for the last time (at least until your first follow-up appointment), perhaps you are faced with questions like:

  • Am I ready to go back to work?
  • Why do I feel so disengaged from conversations with my friends and family?
  • What if the cancer comes back and I have to face treatment AGAIN, or worse, what if it comes back and it’s not treatable?

Here is excerpt from one of my January 2011 posts, Picking Up the Pieces, when I was navigating through a field of emotional land mines, searching for what the hell was supposed to come next:

For me, the transition from healthy person to cancer patient in October of 2009 grabbed me by the neck and throttled me. I reeled from my emotions, but the shock and fear made sense to me (even seemed like the appropriate, socially acceptable response). What I did not see coming was the overwhelming transition that I am now faced with. The transition from patient back to healthy person.

In this post, I share a quote from the book of the same name, Picking Up The Pieces by Kathy Scalzo and Dr. Sherri Magee. It’s one of the best books I have found for navigating the conflicting emotions that can come along with survivorship.

Ironically, the emotional sh!tstorm I faced when coming out of treatment was the catalyst to making a decision to Jump Off The Cliff (not literally), quit my job, and travel to volunteer in South Africa in April of 2011.

Since then, I’ve become addicted to cliff jumping into big dreams and recently had the chance to chase a Big Hairy Audacious Dream on a volunteer trip around the globe. In the month since I returned to Canada, I’ve reflected a lot on my Adventure of Hope and the 18 months leading up to this point. This redesign of my life has felt right for me, even if it hasn’t been easy. As I wrote in the same post, it started with a face plant into my fears:

So, although my cancer journey will finish, the real work  of picking up the pieces of my life has just begun. The thought of shaping those pieces into a brand new identity scares the crap out of me.

So here’s to all of you out-of-breath swimmers who have the courage to join me as we dive into fear and sadness. You brave dog paddlers who teach me to make no guarantees about how or when we’ll make it to the other side. And, here’s to the friends and family who tirelessly cheer us on from the bleachers. Even if they don’t recognize us in our wet, bedraggled, chest heaving state as we climb out of the pool, we appreciate that they will do their best to love us anyways.

Over the last year, I have learned how monumental the challenges of reinvention and reintegration can feel. Thank God for communities like Facing Cancer and the people who help us make it across the divide and into the next phase of whatever we decide we want life to look like. (I hate the phrase, the “new normal”, but I think you know what I mean).

If you feel scared, sad, or alienated by your fears about what comes after treatment, I promise, you are not alone. Many of us have been there and will continue to wade through the murky pool of questions and fears that, unfortunately, may never entirely disappear.

To manage my own fears and questions, I’ve become a subscriber to the “life is short, I’m going to live the hell out of it while I still can” philosophy.

On that note,  I’m not ready to hang up my Big Hairy Audacious Dreaming shoes. In February 2013, I have big plans to take a group of 8-12 cancer survivors, a researcher, and a videographer to New Delhi, India so we can see just how powerful international volunteering and cultural exchange can be for survivors.

If you feel like you need a big adventure to help you kick off your post-cancer chapter. I would love you to join us. Or, if you have a story about what you did to help move forward after treatment, I would love you to share it. Let’s support each other as we ask the question, “Now What” and then bravely put one foot in front of the other as we step into an unknown, but potentially wonderfully exciting, future.

Posted in Life After Cancer | 2 Comments

Global Connections & Lessons Learned…

10 May

Hola from Peru!

I’m sad to say I’ve been MIA on this wonderful site lately. It’s hard to believe that 4 months ago today, I stepped onto a Cathay Pacific flight and took off for Vietnam (by way of Hong Kong). Since then, access to the Internet and time to write has been a precious commodity as I volunteered my way through Vietnam, India, Rwanda, Tanzania, Spain, and now Peru.

For some of you, I’m sure the idea of getting off the couch and going anywhere feels like a MAJOR undertaking. I feel you. It was only 2 years ago when I was counting down the final 7 days until my double mastectomy and still shaky with post-chemo fatigue. Sometimes it feels like only last week that I was trapped inside my apartment, or more specifically – trapped inside my body. But, now – I promise you – there are days when I forget I even had cancer. Days when I make a brand new friend on the road or explore a new country and feel nothing but gratitude over having my body and my life back.

If you and I have met before, you might know the reason behind my Adventure of Hope. You might know about a little blog post I wrote in August called My Big Hairy Audacious Dream that led to this research trip around the world where I am sussing out opportunities for other cancer survivors to volunteer internationally as a way of picking up the pieces of our post-cancer lives.

We all know cancer sucks! It’s gruelling, both physically and emotionally and often feels like we are running the longest marathon in the world (sometimes with no end in site). My hope for you is that you are nearing the finish line and that you have plenty of support to navigate through the surprisingly difficult (for some of us) transition from patient back into fully functioning human being.

If I have learned anything over these past four months, it’s that we have to seize every opportunity presented to us to do things that make us happy because NONE of us know how much longer we have on this earth.

I’ve also learned how incredibly LUCKY I am that I was born in Canada and had access to treatment in some of the best medical facilities in the world. I’m sure you don’t feel lucky if you’re on your way to chemo right now, but, I have recently spent time in African countries where people would rather get HIV than cancer because they “know” if they get cancer, they WILL die. I have heard shocking stories about the stigma and secrecy that still enshrouds cancer in the developing world and I have seen women getting chemo infusions as they lie on dirty hospital floors in Vietnam. We are lucky to have access to treatment and to have a community like Facing Cancer to help us navigate through the journey.

If you want to catch up on some of the hi-lights from the last four months and meet some amazing and inspiring people from around the globe, here are a few links:

The Global Cancer World:

New Connections & Beautiful Lessons Learned:

I’m so happy to have some of you along for the ride and would love to stay connected. And IF – you are nearing the end of your treatment and want something to look forward to, let’s talk…

I am hatching a new DREAM to bring a group of 8-10 survivors on a once in a lifetime volunteer trip in early 2013 and I would love to have you along for the ride.

Posted in Life After Cancer | 3 Comments

Joy Rising in New Delhi

2 Apr

When was the last time you witnessed a moment of pure joy?

On Friday last week, I had an unforgettable opportunity to do just that. Rather than trying to tell you what it looked and felt like, I want to show you …

Would you believe me if I told you I took these pictures at a support session for people affected by cancer in New Delhi? I watched a group of 25-30 men, women, and children of all ages shuffle into CanSupport’s cozy and cramped second level daycare (not synonymous with childcare in India). Many of these people had the haunted looks of caregivers and patients still reeling from the devastation of a cancer diagnosis. But, with a little help from an inspiring music therapy outreach group called Resounding Joy, I spent the next hour watching their faces transform. Partway through, one of the therapists invited me to join the circle as the group sang, shook egg shakers, and took turns playing the bongo drums in an experience I can only describe to you as pure joy rising.

Maybe you are wondering how I ended up on the floor of a cancer support session in New Delhi? Well, as part of my Adventure of Hope, I am using some of my free time to investigate the global cancer landscape as well as to seek out opportunities for other survivors to volunteer within cancer outreach in developing countries. Thanks to an introduction from Carolyn Taylor of Global Focus on Cancer, I had the good fortune to meet another soul sister, Harmala Gupta, which led to my time on the floor with some of my cancer sisters and brothers on the other side of the globe.

Harmala is a fellow survivor, the founder of CanSupport, and one of the most inspiring people I have ever had the pleasure of knowing. During our conversation, she shed a little light for me on the landscape of cancer here in India. The numbers and the stigma still surrounding the disease break my heart. In India, an obscene amount of cancers (in the neighbourhood of 80%) are not diagnosed until late stage 3 or stage 4 and often the only option is palliative care. To make a tragic situation even worse, the cancer is often kept a secret from friends, acquaintances, and sometimes even the patient herself. The patient may know she has cancer, but because her caregivers/family won’t ever talk about it with her, she’s trapped in a world where she’s being treated for, or worse yet, dying of a disease that she has to pretend she doesn’t know she has. I cannot imagine a more isolating or terrifying experience.

All I can say is Thank God (literally) for CanSupport. Here is an overview from their website about their much-needed work: “CanSupport has pioneered home care support for people with terminal cancer in New Delhi. It works in collaboration with the Pain & Palliative Care Clinic at the Institute Rotary Cancer Hospital (IRCH) at AIIMS. Under this programme more than 12,000 patients and members of the family have received high quality and appropriate medical, nursing and psychological care. CanSupport also runs a daycare programme for children and adults with cancer, a cancer support group and a telephone helpline for cancer. All its services are free as they are aimed at the most needy.”

My morning with Harmala, Resounding Joy, and the wonderful volunteers of CanSupport has once again left me filled with gratitude and hope. Yes, the cancer situation is a challenging one here in India (and really everywhere around the world), but Harmala and her team are continuing to live out the Mother Teresa quote, “We can’t do great things in this life. We can only do little things great love.” CanSupport and the volunteers of Resounding Joy are proof of how those little things can add up to making a massive difference in the lives of so many and their efforts will inspire me over the weeks and months to come.

Posted in Life After Cancer, Uncategorized | Leave a comment

Sisters From Another Mister…

24 Jan

Hello from Vietnam! In the chaos of getting ready for my Big Hairy Audacious Adventure of Hope, I have fallen a little behind on my blog posts. If you want to catch up, please come visit me at A Fresh Chapter where you can read Hello Fear, Welcome Back; My First Travel Fiasco & It Only Took 24 Hours; and Gooood Morning Vietnam.

But, for today, I want to share with you Friday’s post because my experience at the K Cancer Hospital in Ha Noi is still having a major impact on me…

Peeling yellow paint hangs from the gritty cement walls and I look down just in time to step over a puddle of muddy liquid on the worn landing. As we pass through the congested doorway and onto the third floor, I bite down hard on my lip so my chin won’t drop. The last thing I want is to look like a stereotypical Westerner with pity pooling in my eyes at the site of circumstances far different from my own.

I look to the right and a man, barely more than a boy, lies on a splintered bench that hangs at an awkward slope from its hinges. He stares at a point in the distance as a bottle, hooked on a nail overhead, dispenses what I assume to be chemo drugs down the length of the dirty wall and into his waiting vein. An old man in black plastic sandals scuffs towards the bright fluorescent lights of the communal bathroom. Instead of an IV pole to rest against, he leans heavily on the middle aged woman beside him. His caregiver holds the bottle high in the air, like a flag, as they continue their slow march through the crowd.

Then, a woman with a telltale lopsided chest stops my host, Mrs. Anh Phan of Sympameals. Anh immediately crouches down to remove a notebook from her handwoven bag and it seems that everyone else except this patient disappears from her view. As I hover in the background, I don’t need to speak Vietnamese to understand the patient’s anxious request or Anh’s gentle response. This woman is probably hoping to be one of the “lucky” breast cancer patients who will receive a subsidy from Sympameals. Not only has Mrs. Anh Phan (along with her husband) started an organization that provides 180 meal vouchers everyday to ensure that the most destitute cancer patients at K hospital get access to at least 1 nutritious meal per day. She also, in partnership with the Hanoi International Women’s Club, gives $150 subsidies to 10 breast cancer patients in the greatest need each month. Many of these women have had to leave the fields, and their only source of income, in order to seek treatment. For so many living in rural Vietnam, a lack of awareness and screening options means that breast cancer is often discovered very late. The expense and inconvenience of treatment can often prove too much for their husbands and many of these women are abandoned, with no way to support themselves, and no money to pay for either treatment or food. Sympameals is a grassroots organization that is feeding these women and giving them hope, when they have nowhere else to turn. It is an honour and a privilege to be here today to see the compassion Anh shares with each patient.

When Anh stands, the patient motions for us to follow, The scent of stale rice, musty blankets, and dried sweat presses up against me and I shiver in spite of the humidity of the day. I hurry to keep up as we wind past stretchers laid out in the hallway, past whole families crowded onto benches, and past cubbies stacked with blankets, cooking pots, and wicker baskets.

We stop in front of a young woman who is lying on a faded lounger in the hallway. Two older, cap-wearing fellow patients hover over her like nervous hens; their brows furrowed and their faces filled with concern. Anh sinks down to perch on the side of the stretcher and holds the young patient’s hand. The women looks up at me and I can almost feel the fatigue in the slowness of her movements as she reaches up to tug her hat a little lower to hide her bald head. As she struggles to catch her breath, I watch the chemo drugs drip into her veins and have a flashback to a day 2 years ago when the same drugs dripped into mine. The staccato conversation before me continues until the patient looks from Anh to me and her eyes shift from dark to light. She points to my hair and her features melt into a beautiful smile.

Anh turns to me and says, “I told her that you also had breast cancer and survived it and she will too.”

Too soon, we have to leave, but I crouch down beside the woman and for a moment have the opportunity to hold her hand. It takes everything in me to hold back my tears. In this moment, it does not matter that we speak different languages and come from very different circumstances. In this moment, we are simply two sisters who share the same disease. Our stories may be different, but we are the same.

The time I spent with Anh of Sympameals left me deeply inspired by the difference one person can make. I saw the tears of gratitude from three women who received this month’s subsidy and I felt honoured to meet Anh and further understand the critical work she and her team are doing for cancer patients here in Ha Noi, Vietnam.

To all of my breast cancer sisters who may not have the means or opportunity to travel around the world, but want to give back in a tangible way, here is something we can all do. Consider joining SympaMeals on Facebook and making a contribution to your sisters on the other side of the world. Your sisters who know nothing about a world of pink ribbons and the over commercialization of breast cancer. Your sisters who simply need food to eat and money to move forward from a disease that still has stigma and disfigurement attached to it.

It’s currently 4:30am and although I wanted to post this last night, the Internet was down and I still have no access to Facebook. Ahh the joys of technology and travel.

Today, I will take a 16 hour train to Da Nang to celebrate Lunar New Year with my host family and then on to Ho Chi Minh City where I will spend time in a pediactric oncology hospital as well as meet with people working in the breast cancer world. A huge thank you to GeoVisions for helping make my experience in Vietnam memorable and moving. And, an even bigger thank you to CLOUDInc, GO Overseas and to all of you.  I am so grateful to almost be at 50% of my fundraising goal because of your generosity. Your contributions have made it possible for me to crouch down in a hospital and connect with a breast cancer sister on the other side of the world and hopefully, even if only for a fleeting moment, help her feel less alone.

Posted in Coping with Cancer, Life After Cancer | Leave a comment

Resolutions Schmesolutions…

3 Jan

It’s Day 3 of 2012 and already the 2-day hangovers have dissipated, the Christmas lights are  disappearing from the houses on my friend’s street, and everyone is slipping back into the busyness of life.

How’s it going with those New Year’s Resolutions of yours? Is 2012 the year you will end your long term relationship with Suzy Saddlebags & Paula Paunch? The 12 months where you will drink green tea every single day or finally admit to yourself that using a glass of Shiraz to suppress your anxiety about your job, your boyfriend, or your budget is not a great strategy (ahh, when will I ever learn…)?

I’ve always sucked at keeping New Year’s Resolutions, so I gave up making them years ago. I don’t know about you, but as soon as someone tells me I HAVE to do ____________, I lose interest (even if the person bossing me around is me).

But last year, a little article by Martha Beck shifted my perspective on resolutions and quite literally changed my life. Sounds dramatic, doesn’t it? But, if you have been around for awhile, you know how choosing my three words for 2011: healthy, loved, and inspired led me down the garden path (or whatever path it was) to a brand new life. If you read my Hell Yes post, you know how thinking about what would INSPIRE me led to a volunteer trip in Africa and put the wheels in motion for my upcoming (equal parts terrifying and exciting) Adventure of Hope.

With the start of a New Year, I have thought a lot about what bright and shiny word I want to choose for 2012. You see, late last year, I thought my word might be FREEDOM. But, here’s the thing…you should be careful what you wish for. I have never felt more FREE in my life. With no home, job, boyfriend, or family of my own, I have absolutely zero attachments. Are there perks that come with this freedom? Absolutely. But, do I want to live with this kind of zero-attachments-freedom forever? Absolutely not.

So instead, I’ve decided that in 2012, I want to cultivate CONNECTION. I know – pass the patchouli and let’s all sing “Kumbaya”. But, in all seriousness…one week from today, I will search in the bottom of my new rolling duffle bag (who knew trying to wear a travel backpack post mastectomy and reconstruction would be such a painful idea) for my Big Girl Panties and then board a flight to Hong Kong, en route to Vietnam. Then, you and I will spend the next six months traveling around the world, volunteering on almost every continent.

So, how does my big word for 2012 fit in? Well, I believe that this trip is about more than “just” international volunteering and more than “just” cancer survivorship; it’s about CONNECTION. It’s about moments like when I was there to bathe and care for a scared little boy in the Townships of Cape Town and he was there to remind me of how far I’d come since my double mastectomy. It’s about having the opportunity to share stories about these global connections with you. Stories about the resilience of the human spirit and about families who come from the most meagre of circumstances but still have hope for a better tomorrow. And just maybe, this trip is a reminder for me (and hopefully for you) that the past does not define us. Whether our story used to be cancer, a failed relationship, or a lost job, it’s never too late to write a new one.

I’m still working on my other two words, but hell, it’s only January 3rd and I have fundraising goals to hit (38% and climbing thanks to your support – Woohoo!), a spreadsheet to keep updating as you help me get back “in the black”, and a few great prizes to give away to anyone who contributes between now and midnight PST on January 9th. Besides, my first 12-hour flight next week should give me plenty of time to decide on the next two words.

For now – I’m passing the floor over to you. What will your word for 2012 be?

* I have shared this post directly from my blog, A Fresh Chapter, and have not modified it for Facing Cancer because I believe that regardless or where we are in life, we have the ability to think about how we want to feel. Maybe some of you who are trudging through the midst of treatment can’t even begin to think of a positive word for 2012. I can relate – I’ve been there. What I will say is that one of the words that pulled me through the hardest days of treatment was the word healthy. I vowed to do everything in my power to get back to a place of feeling and being healthy. Some days, a walk to the corner store was all I could manage, but eventually I could get through a Hatha Yoga class, or even a long walk on the sea wall. I know it’s a one day at a time battle and I hope that one day, very soon, I will have the chance to support you as you write the post-cancer chapter of your life.

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Raising The Stakes & Going “All In”…

14 Dec

Can you think of a moment in your life when you made the decision to go “all in”? When you pushed your chips into the middle of the table and took a giant leap of faith into your future? Maybe the moment you put down your Visa card and picked up a diamond ring. The day you signed the bold blank line on your first mortgage. Or the moment you threw away your final birth control pill package and decided to open yourself up to the possibility of someone eventually calling you Mom.

Were you terrified before you took the leap? Did you consider, even for just one second, opting out? Out of the “till death do us part” commitment, the massive mortgage payments, or the dirty diapers and Fisher Price toys because the voice of your Inner Critic got the best of you? Maybe you came up with a lengthy mental list of all the ways you might fail. How you might lose your job and default on your mortgage; marry the wrong person; or become a terrible parent.

Even with all of those looming doubts, did you jump anyway?

You would think Jumping off a Cliff would get easier if you have leaped once before and you know you have an important reason to keep Stepping Into The Fear.

But, it doesn’t.

The fear is still there. Breathing its smelly morning breath in your face. Daring you to back away from the edge.

But, today I’m raising the stakes and going “all in” while I repeat one of my favourite quotes over and over in my mind:

Courage is not the absence of fear, but rather the judgement that something else is more important than fear.  ~Ambrose Redmoon

So, with the support of Go Overseas and CLOUDInc, my Adventure of Hope is about to begin. I’m about to travel to almost every continent to partner with 5-10 different volunteer organizations. I’m about to open myself up to opportunities ranging from working with cancer survivors in Vietnam, to teaching women basic business skills in India, to helping with a building or wildlife conservation project in Costa Rica. These experiences will provide the framework for “our” not for profit by introducing me to some of the safest, most ethical, and easiest to work with volunteer organizations in the industry. This insight means I can help fellow survivors get set up with their own Adventures of Hope.

So, (gulp), here’s my tentative itinerary:

  • Jan 10 – Feb 10th – GeoVisions in Vietnam
  • Feb 11 – March 3rd – CCS in New Delhi, India
  • March 15 – March 29 – GVN in Rwanda
  • April 1 – 15 – Tanzania or Kenya
  • April 20 – 28 – Pueblos Ingles in Spain
  • May – Peru
  • June – Costa Rica

In case this all seems like a great big game of let’s pretend (which I get it – sometimes it even feels that way to me), I have exciting news. The first two volunteer partners: Cross Cultural Solutions and Global Volunteer Network have committed to the project!

1. Cross Cultural Solutions

February 11 – March 3rd - Cross Cultural Solutions in New Delhi. It was because of my life-changing experience with CCS in Cape Town that I came up with My Big Hairy Audacious Dream of creating an organization to help other cancer survivors volunteer internationally. Does traveling to a city of 15 million people make me nervous? Absolutely. But in a city with an illiteracy rate of 48% among women, there are plenty of opportunities for me to work on community led projects that make a difference locally and I know I will be in great hands with CCS.

2. Global Volunteer Network

March 15 – 29th - Global Volunteer Network in Rwanda. As soon as I connected with Erin Cassidy the CEO of GVN, I knew I had found a kindred spirit. She suggested GVN’s program in Rwanda because of its connection to survivorship. Surviving genocide and surviving cancer are two very different challenges. But, what a powerful opportunity for cancer survivors to support people who have seen the absolute worst and made it to the other side. As soon as I saw this picture on the GVN website, I knew I had to go to Rwanda.

So, somehow, in the next 30 days, I need to:

  • Book my flights;
  • Confirm at least 4-6 more Volunteer Providers/Sponsors;
  • Raise approximately $18,000 through personal donations and corporate sponsorship (the donation link just went live on A Fresh Chapter;
  • Purchase/learn how to use a basic HD video camera so I can take footage along the way. (Won’t it feel more like you’re coming if I can upload a few clips?)

Yes, I am overwhelmed and scared sh!tless about how to pull all of this off over a busy, holiday season. But, I’m choosing to believe that if I work hard enough and keep connecting with amazing partners like CLOUDInc, GO Overseas, CCS, GeoVisions, & GVN, this dream IS possible.

Sure, there will be times when I wake up at 3am and I can’t get back to sleep because I’m worried I’ve “bitten off more than I can chew”. But, I will remember that this is about so much more than a trip around the world. I will remember that it’s about providing opportunities for cancer warriors to start A Fresh Chapter in their lives and supporting them as they move through the often difficult transition from patient to survivor. And just maybe, I will take deep breaths for long enough to remember one of Oprah’s favourite quotes that I’ve adopted as my own,

“God can dream a bigger dream for you than you could ever dream for yourself.”

**If you or anyone you know is interested in finding out more about joining this Adventure of Hope, please contact me.

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If You’re Feeling A Little Low on the Ho-Ho-Ho

11 Dec

Maybe you can relate to that first moment of awareness. When you open one eye and search your dark bedroom for clues. You wonder why it’s so quiet. Did you forget to set your alarm? A rush of panic whistles into your gut. Then you remember…it’s Saturday.

You grin and burrow under your duvet as you leaf through the memory of your dream. You pick up the cell phone on your nightstand to call your lover, just so you can hear his scratchy morning voice. But as you continue your ascent into alertness, a bulldozer of pain grinds you under its thick tread. You remember that you can’t call. It’s over. Your stomach pulses, tears slip down to pool in your ears and you lie there, immobilized, as you try to process the reality of another day without him.

This is the beginning of a post called Escape that I wrote almost a year ago. If you click the link, you can read about how I almost car-jacked a woman a couple of years ago (If you remember the days pre-chemo and how distracted you felt, maybe you can relate?) But, for now I’ll let you in on a little secret. With my fingers shaking over the keys and tears streaming down to drip off my chin, I could barely write that post. Although I made it sound like I was remembering the lead up to my first round of chemo (and yes that was also a really tough time), I didn’t tell you the real reason for the emotion behind my words that day. I didn’t tell you that my heart was in shreds because the biggest love of my life had recently exited stage right.

I don’t know what it is about the holiday season and its New Year aftermath, but I have often found myself either knee-deep in moony, over the top, brand new love or devastated by no-appetite-for-days, finally fit into my skinniest jeans, heart break.

This year, for once, I am neither in the midst of falling in love or picking up the pieces after a heartbreak, but as I recently sat with a friend while she grieved the end of a relationship and the loss of the dream she had for her future, I could relate so closely with her pain.

You see – the holidays tend to bring out the lonely for even the most sporadic attendees of the Lonely Hearts Club. And I don’t think I’m just talking about singletons. From what I remember, it can sometimes get pretty lonely even inside the bicycle-built-for-two world of coupledom.

I would be lying if I didn’t admit to catching a touch of the lonely and homesick bug since my recent return to Vancouver. Sounds strange, doesn’t it? Homesick in my own hometown? But, as I surf from couch to spare bed to couch again, I am faced with constant reminders of  how different my life has become from what I once envisioned.

You see, I was the girl who wanted Santa Claus to bring me my Prince Charming as soon as possible, so I could marry him young and have 3 or 4 rug-rats of my own by the wise old age of 30. Instead, here I am at 32. Fake breasted, scarred up, homeless, childless, and relationship less. All of the Norman Rockwell-esque commercials of the season with their candy canes, stockings, fireplaces, and children in footed pajamas reminding me of what my life is not.

But, here’s the thing…

Yes, I have my days where I need to throw myself a 30 minute pity-party and feel the hell out of the sadness until it passes. But most days, I remind myself (hourly if necessary) to cherish the life I have instead of wishing for the one I don’t.

“Every day is a new beginning. Treat it that way. Stay away from what might have been, and look at what can be.”
~ Marsha Petrie Sue

I remind myself of the wonderful trade-offs to being homeless, rootless, and single. Trade-offs like the freedom to set off on an amazing adventure; the time and space to make my Big Hairy Audacious Dream of creating a not for profit to help other cancer survivors volunteer internationally come true; and the courage to believe that with your support, I can put together a round the world volunteer trip (and somehow raise the funds for it) in the next 33 days (yes – stay tuned  to learn more).

So, if you find yourself feeling low on the ho-ho-ho this holiday season, I hope this post helps you feel just a little less alone. Who knows? Maybe this coming year will bring us both closer to a place where we appreciate what is instead of wishing for what isn’t. God knows it’s a constant work in progress for me…

Posted in Coping with Cancer, Life After Cancer | Leave a comment

Baring It All & Finding A Little Light…

1 Dec

Below is a post I shared on my personal blog, A Fresh Chapter, earlier this week.

High heels, beautiful dresses, topless women, massive scars, empty kleenex boxes, and dim lighting. I know what you’re thinking…a strip club gone terribly wrong? Nope. I’m referring to the opening night of Breast Fest 2011 and a screening of Patricia Zagarella’s powerful new documentary, “Baring It All” featuring renowned photographer David Jay of the SCAR Project and a few brave women who let us into their lives and under their shirts to show the world what we survivors already know – that breast cancer is about SO much more than just a pink ribbon.

If you haven’t heard of Breast Fest yet, here’s a synopsis from Rethink Breast Cancer‘s site: “This annual festival uses films, panels, workshops and speakers to connect people to the breast cancer cause, inspire dialogue, facilitate learning and foster community. Breast Fest is the world’s first film festival dedicated to breast cancer awareness and is an initiative of Rethink Breast Cancer.”

On a side note, I bet you’ve heard of Rethink because you probably saw this clever and drool worthy (for the ladies anyways) video when it made its round on Facebook in the month of October: My Man Reminder

This year was my first Breast Fest and I knew from the moment I arrived at the Royal Ontario Museum in Toronto that I had come home. Right away, I saw the familiar faces of fellow bloggers, old friends from past survivor conferences and plenty of strangers to turn into friends. Some of us traded dark jokes about how to dress up for opening night without looking like a man because of a trademark post chemo crew cut or a newly flattened chest. Although my hair has finally come in (in all of its thin glory), my passport photo reminds me of how recently I looked like “Mr.” Terri Wingham.

“So, you must be a year or so out,” she says to me as she tugs at a strand of her spiky hair.

“Yes, chemo ended in March of 2010,” I say. She nods. We move on to talking about the film. Where she’s from. How many festivals she has attended.

I exhale. Relieved. I can tell she is too. Tonight, neither of have to see the slight sideways tilt of a head or hear someone say, “Wow, you had Breast Cancer? But, you’re SOOO young”.

Here, we all get it. We have faced the worst and made it to the other side. In the safety of a dark theatre, we can pass each other Kleenex because we know sometimes the reality of watching one of our sisters onscreen, fighting for her life, stirs the bubbling pot of fear in our bellies. Why did the cancer come back for her? What if it’s me next? Here, we can drop our masks of bravery and honestly admit the thoughts that sometimes keep us awake at night. But, we can also slip right back into laughter when the lights come on and someone cracks a joke about her red rimmed eyes and the snot smeared on the sleeve of her dress.

Not bad for a Friday night. I could tell you about the rest of the weekend and all of the fantastic films and shorts I got to see, but instead I’ll share the number one hi-light for me. The best part of Breast Fest was the chance to connect with my sisters from across the country and the dedicated and wonderful Rethink Team. To find reasons to laugh until our stomachs hurt. To trade stories about so much more than just breast cancer.  To continue to find light in a dark and sometimes incredibly difficult subject.

So, thank you Rethink for hosting such a great event and thank you to the Canadian Breast Cancer Foundation for helping subsidize travel for 30+ of us to get there. You gave us the chance to connect, laugh, and remember that we are not alone.

I will leave you with a few quotes on light that I’m loving today:

Dare to reach out your hand into the darkness, to pull another hand into the light.  ~Norman B. Rice

You can’t have a light without a dark to stick it in.  ~Arlo Guthrie

The hero is the one who kindles a great light in the world, who sets up blazing torches in the dark streets of life for men to see by.  The saint is the man who walks through the dark paths of the world, himself a light.  ~Felix Adler

Posted in Coping with Cancer, Life After Cancer | Leave a comment