Category Archives: Uncategorized

Mind, Body & Spirit – Making the Connection

1 May

I was recently asked about my connection to healing and the role that spirituality played in that process. I thought it was a great question, so let me share some of my views on my personal spirituality and how it plays an important role in my daily life and living.

To begin, I can honestly say that I’ve always possessed a strong feeling of being connected to a divine presence. As young girls, my sister and I rarely (if ever!) missed Sunday School, which we loved attending. Well, I did anyway. And before going to sleep, we always said our ‘Now I lay me down to sleeps’—as a matter of fact, I still do. I also I fondly remember heading off to Bible School during summer break and loving every minute of it. Not to say that we were a particularly religious family, but those early interventions with church and God certainly instilled in me a strong sense of spirituality. I’ve thoroughly enjoyed the hopeful sense of wellbeing that my growing spirituality has on my values and on my belief system.

With thanks to the Chaplin who regularly visited me in hospital during my darker days while undergoing treatment for cancer, it was she who opened my world to many of the complementary therapies that I have continued to use as tools to help my overall sense of wellbeing and healing. I recently read that the results of over 200 studies suggested that prayer of any type or denomination has proven to effectively support a strong sense of wellbeing and healing of the mind, body and spirit. In fact, in one such survey researchers at the University of Michigan believe that involvement in community and religious rituals may promote feelings of hope, serenity and optimism. The researchers also concluded that participating in or attending religious services can extend one’s lifespan about as much as moderate exercise or not smoking. Pretty impressive!

In prior blog posts I’ve referenced the first-hand benefits of my daily prayerful meditation or visualization techniques. I also love sessions of meditation and yoga, sometimes to Buddha Bar tunes. I’m also particularly interested in metaphysical healing; from sacred places on the earth to the metaphysical powers of crystals, and collecting and learning about objects from various religions or religious practices, I enjoy incorporating the uplifting energy I receive from these practices. On a trip to Arizona in February, I found great joy in ticking off another of my “living list places to see and visit” (no bucket list for me, thanks!!). Sedona is definitely a place I want to spend more time—the spiritual energy there was magical. My Arizona agenda was dominated by my long-time passion to visit the Tucson bead, gem and mineral show. And, oh-my, I’ve been in metaphysical bead heaven ever since.

I’ve been collecting beads and gems to design and selling necklaces since I was about nine years old. To this day, designing jewellery and collecting beads, crystals and baubles from around the globe that I can incorporate into jewellery is one of my greatest pastimes and pleasures.

At the bead show, I found myself particularly fascinated by some old Tibetan pendants, prayer beads and prayer boxes. Of course I added a number of these spectacular pieces to my personal collection.

Of course, being addicted to pearls and more recently hand painted Deity pendants from India, I added many “new to me” objects d’art. These photos show some of my new treasures as seen scattered across my workspace in my mini-Indonesian apartment.

And my Tibetan Prayer Boxes, I just can’t seem to put away, so it seems they too have taken up home on my Singaporean step chest. I think you’ll agree, they are very special indeed!

Since I returned home, you can probably imagine that I’ve been enjoying stringing pearls, semi-precious stones and lovely crystals whenever I can find a few hours to myself. For me, the process of creating is meditative and liberating. What activities connect you to your spiritual self?

Posted in Uncategorized | 1 Comment

How far we’ve come. How far we’ll go.

19 Jul

I have just spent a wonderful morning speaking with some members of the media about the 20-year anniversary of the Look Good Feel Better program.  As women, we all love to read our fashion, beauty and lifestyle magazines, and since Look Good Feel Better began in 1992, our media partners have played a crucial role in helping to spread the word about our free programs to Canadian women.  As I looked around the table this morning at the magazine writers and editors who joined us, I saw some faces who have been with us since the program’s beginning, as well as some new faces. In both instances, it’s a sincere pleasure to let people know about the benefits of our Look Good Feel Better program and our facingcancer.ca community. 

We were especially thrilled to welcome our blogger friend, Katie Evans (The Bald & the Beautiful) who shared how the support she found at both the Look Good Feel Better workshop and here, at facingcancer.ca have coloured her cancer experience.  One of the things that resonated with me about what Katie said was that now that she’s out of treatment and back to work, people around her consider cancer to be “over” or “behind her”.  However, for those of us who have been diagnosed, we know that the period after treatment can be just the beginning of the cancer journey, as we adapt to our “new normal”. 

As we look back over the past 20 years of Look Good Feel Better, we also look forward, as we work to find ways to help women face the persistent challenges that follow us long after the diagnosis is given or the tumours have been removed from our bodies. For me, those challenges include wearing leg braces and using a cane to help me walk as a result of the intense treatments I received, as well as the fear of recurrence (that we all know so well) and grieving the life that might have been had cancer not robbed me of so many choices and chances.  That’s not to say there’s not a wonderful existence after cancer, it may just be that “after cancer” doesn’t exist. Rather, once we hear that diagnosis, our reality is altered and we are forced to move forward on a different path that is inextricably shaped by cancer. The important thing is, to keep moving forward with courage, hope and optimism.

Posted in Diagnosis, Life after cancer, New Normal, Uncategorized | 1 Comment

Dopamine Addicts

7 May

In March I had an opportunity to gather with a group of dynamic, enthusiastic, passionate and determined women, all who have faced the extraordinary challenges that come with cancer and its treatment.  Although we had no formal agenda, my goal for us coming together was to determine if there was benefit to meeting several times a year to connect and talk about the many issues, hurdles and yes, opportunities, that become part of our lives on the cancer journey.

One by one, as the women took their seats around the table, enthusiasm and positive energy flowed.  There were nine of us in attendance and we were a diverse group of women.  Some, like me, were long-term survivors.  Several others had recently finished treatment while two of the women in our group are facing the challenges of familial breast and ovarian cancer.  Interestingly, both of these women are mothers to young daughters, which clearly raises concern for their own futures. 

The constant flow and exchange of Information, suggestions, comments and ideas being put on the table was both electric and infectious.  Theme upon theme, we discussed things like medical and insurance coverage, self image as well as what we all agreed as having profound benefits for all — exercise and being positive.   

In regard to staying positive, beyond sharing a host of resources and places to find new inspiration, we talked about the physical benefits that come with things that make us feel good – endorphins for one.  Just exactly where do endorphins come from? They come from laughing, telling inspirational stories, exercise, just about anything at all that has an uplifting effect. 

I shared one of my strategies I use to call upon my own endorphins, which garnered a few good laughs.  It goes like this:  As ridiculous as it sounds, on those nights when I toss and turn and just can’t get the heck to sleep, more often than not I’ll just lay in the dark and smile myself silly.  And you know what, it really works!  Fellow blogger and feel-good doctor, “Both Sides” told us that endorphins naturally release anothr one of the ‘feel-good’ chemicals our body produces called dopamine. I shared with our group that I had always wanted a T-shirt that spelled out Dopamine Addict across the front, at which point we all laughed uncontrollably, clearly releasing lots of endorphins and, in turn, a hit of dopamine that did its work.  It wasn’t long before we had total agreement to call our newly formed group “Dopamine Addicts”.

The Dopamine Addicts. Top L-R: Donna, Farah, Manuela, Karen, Irma, Patricia. Bottom: Heather, Me, Alex

The Dopamine Addicts. Top L-R: Donna, Farah, Manuela, Karen, Irma, Patricia. Bottom: Heather, Me, Alex

As we neared the end of our time together, we set a goal to meet again soon and we are hoping we can have these productive and insightful gatherings in June, September and early January.

Before we parted ways, our group had established a special bond in just a few short hours.  Much like the women in our Look Good Feel Better workshops, we agreed it felt good to be with other women who could understand some of our fears and anxiety as well as future hurdles that may well present themselves somewhere down the road.  Having had the opportunity to share stories and put some context around our unique experiences gave us a renewed outlook on how it’s better together because, as we all agreed, cancer doesn’t end when treatment does.

It’s my hope that this dynamic group of women, some who preferred to be call survivors, while others felt “thrivers” more aptly described their personal situation and outlook, can come together to learn, grow and be stronger by facing cancer together.

Posted in Life after cancer, Support, Uncategorized | 2 Comments

Mind, Body and Spirit

5 Mar

Mind, Body and Spirit.  We hear lots about it – it’s become a motto, a tagline and a mantra for many – but what does it really mean to those of us on the lifelong cancer journey? 

Taking that question to heart, I spent some time recently talking with a doctor friend of mine about the long-term impact of cancer and how it relates to ongoing health care and general well-being.  We discussed a range of topics including how once an individual is diagnosed with cancer, even well beyond active treatment, the focus of health care often revolves around the cancer, and the host of physical challenges it presents. For example, because of the tendency to be particularly cautious about cancer’s side effects and alert to possible recurrence, other regular and routine checks that should take place often don’t.  We also discussed how the need to care not just for the body, but the mind and spirit as well is so vital to ongoing well-being and quality of daily life and living. 

Throughout my cancer journey I’ve have great interest in and good reason to explore the mind-body-spirit connection.  As a result, I am a firm believer in the need to care for the whole person – not just the physical part of the cancer experience. Many of you know from my prior blogs that one of my greatest physical side effects from cancer is the nerve damage resulting from the host of aggressive treatments I received including surgery, chemotherapy and radiation.  I wear braces on my legs and walk with a cane, and despite the daily challenges my disability causes, I am always grateful that I am independent and the very fact that I can even walk at all.  

For me, visualization can be a powerful way to re-energize myself.  I find prayerful meditation can be as calming and relaxing as it is inspiring and uplifting, helping to calm some of my daily stress and anxiety.  I like to call these self-care techniques my daily “Good for Me’s”.  More recently, despite my mobility issues, I’ve created my own approach to a gentle workout routine based on breathing and stretching while listening to chakra balancing music … and I’ve come to love it.  I think I’m addicted to endorphins and dopamine, and it never ceases to surprise me how empowering this special time of self-care and development is, uplifting and motivating me all day long.

One of my favourite books, Molecules of Emotion by Dr. Candace Pert states that our thoughts and emotions impact our health through the mind-body connection.  Dr. Pert’s work suggests that that the body and mind are one. She would also tell us that the body feeds the mind and the mind feeds the body, and that our thoughts and feelings, in addition to our beliefs and attitudes, all impact and shape who we are as well as our biological functioning.  Interesting? You bet!

I also know how empowering self-care can be not only for those is us living with cancer (present and past) but also for our caregivers.  This past year I had the honour of working with the Nakurk Hospice in Kenya to address a vastly diverse group of caregivers for those with cancer.  We talked about how vital self-care was and the many ways in which it can be incorporated into our day-to-day lives.  Simple things like feeling the sun on your face, taking a quiet walk and looking to nature can boost our spirits and recharge our energy bank. So, as I write this blog entry, I’m especially interested to know more about the ways you make time for yourself and your personal self-care. Perhaps, like me, you’ve incorporated some daily rituals to nurture your emotional and spiritual health as well as your physical well-being. I’d love for you to tell me about them in the comments section.

Posted in Uncategorized | 3 Comments

What’s Your Word?

31 Jan

We are only weeks into the New Year but 2012 is already shaping up to be an exciting year for us.  This is the year that we will celebrate the 20th anniversary of  our foundation and the Look Good Feel Better program in Canada.  We are in the early stages of planning the 20th issue of our annual magazine, which has given us a reason to dig through our archives and revisit some of the touching, hopeful and empowering stories that we’ve had the privilege of sharing over the past two decades.

Just this week, we were beyond thrilled to hear from an amazing woman we first met when she appeared in the 1998 issue of our magazine.  Dionne Warner is nothing short of a miracle.  She is a seven-time cancer survivor, having had cancer in her breast and brain and two bouts of liver cancer before being diagnosed in 2009 with Stage 4 cancer in her lungs, bones and liver.  Dionne and her husband Graham are known at the cancer care centre where Dionne receives her treatment for dressing up in themed costumes for each of her chemo appointments, often marking their entrance with music, laughter and commotion.  We received the incredible news this week that Dionne’s cancer is in complete remission!  I have no doubt that Dionne’s indomitable spirit and resolute optimism helped propel her to this point. She’s a true personification of what it means to have hope.

We use the word ‘hope’ a lot around our office because we believe that every woman deserves to face cancer with hope, support and optimism. That’s not to discount the bad days or the seriousness of cancer, but we believe, and our report proves, that women are, overall, determined to face cancer with positivity. The women we surveyed told us they just need the supports to help lift them up when the really low lows hit.  In fact, I would have to say that ‘determined’ is the word that I use most often to describe my own cancer experience.  Despite being given just three months to live, I was determined to do everything in my power to turn my grim prognosis on its head and make medical history. I was also determined  to face each day with as much positive spirit as I could muster.  Many days, when my own supply of positive spirit was depleted, I had to borrow some from the many friends and family members who rallied around me, but together we got through the scarring surgeries, the gruelling treatments, the pain and the nausea to the point I am at today – 22 years cancer free!  How truly grateful I am.  

Despite the fact that doctors were able to remove the cancer from my body many years ago, I face the lifelong impact of cancer every day with the same determination that I did back when I was undergoing treatment.  Because my treatments and surgeries were so extreme, I am left with lifelong physical challenges that require me to wear braces on both of my legs and walk with a cane.  Every day when I strap on those prosthesis that enable me to walk, I am reminded of the ‘new normal’ cancer created for me and I am determined to face these challenges head on.

What word best describes your cancer experience?  Has your word changed over the course of your journey? Please share your word in the comments section below.  We might include your comments in the 2012 issue of our magazine, so that you can help other women facing similar challenges.

I’m looking forward to hearing from you as we face cancer together. 

Posted in Life after cancer, New Normal, Uncategorized | 2 Comments

Getting Back to ‘Normal’

29 Aug

Recently, I’ve been revisiting the findings of our 2010 national survey of women with cancer, and thinking about how so much of what women told us mirrors my own experience. It got me to thinking about the things women with cancer want. Of course, there are things we all want — a self-clean bathroom, the perfect pair of jeans, great boots — but a cancer diagnosis changes everything and suddenly and somehow, for awhile anyway, many of the things we once wanted aren’t very important anymore.

In our survey, women told us that more than anything, they didn’t want the people around them to treat them differently just because they had cancer. I remember very well the overwhelming need for life to be as normal as possible (which was virtually impossible at best) during my cancer journey. For me, this meant getting up every morning and attempting to brush on touch of mood-lifting blush, pencil on some eyebrows, spritz on some of my favourite fragrance and, of course, put on my wig, just so I could start my day feeling a little more like myself. It wasn’t that I looked pretty, but somehow investing the time and effort into how I faced the day had a powerful impact on my psyche. Even while I was in the hospital — desperately thin and feeling anxious and weak as I faced more nauseating treatment — I wore my lipstick. I suppose that slash of One Perfect Coral on my lips (my late 1980s go-to shade) was my way of showing people that the ‘old’ me was still there, inside a body that was supposedly mine despite the fact that it looked so drastically different. It was an invitation (a plea?) to all of my visitors to speak to that sassy blonde who carries her lipstick everywhere she goes, even if the blonde hair was nowhere to be seen.

‘Normal’ for me also meant getting away for an evening or even just for an hour to enjoy a refreshing adult beverage with my best girlfriends. (That’s me in 1989, taking a break from treatment to attend Flare magazine’s anniversary party.) While it was often a physical struggle for me to get there, I knew that sharing a few laughs would allow me to feel as though I were still engaged in LIVING! And much like the women we surveyed, I craved those moments when I was just ‘me’ not ‘Sherry dying of cancer’. As one of our survey respondents said, “I was cancer girl. It always set me apart.”

But it’s not fair to fault our well-meaning friends and family for acting differently. Most of what we hear about cancer is about the bad news and the struggle so they may be expecting the worse. The people close to you have probably never seen you so unsure of yourself and vulnerable, to say the least. When you think about it, they’re probably feeling pretty scared and vulnerable, too, and they can’t find the right words to convey what they really feel. They might need you to tell them it’s okay to feel the way they’re feeling, but remind them that you’re still you and that hasn’t changed. Sometimes, people need the person with cancer to acknowledge the myriad of emotions that come along with the diagnosis. By putting it out there, you make it okay for them to talk to you about it the way they would talk to you about how your day was, your job or the weather. Tell people what you need to get over each hurdle, whether it’s for them to grab you some groceries on the way over or to take you out for a dirty martini at your favourite old haunt.

And one day, when you aren’t even paying attention, you’ll again start wishing for things like a pair of jeans that fit like a glove and a great new pair of boots … maybe even a new lipstick. You know, the ‘normal’ things in life.

Posted in Life after cancer, New Normal, Uncategorized | 1 Comment

Who Runs the World? Girls.

14 Jul

Over the past couple of weeks I have had the good fortune to do some travelling. First, a work-related trip to the west coast to meet one of our wonderful facingcancer.ca bloggers, Terri, and to meet with and recognize our oh-so dedicated Look Good Feel Better expert volunteers in Victoria and Vancouver; and then it was onto an adventure that took me to Kenya, India and Thailand where I got to spend some time with my delightful goddaughter, Ocea, who is 11 years old. 

After spending time with Ocea, who gave me some insights to the pre-teen world, I am amazed at how different life is for girls who are growing up today. The internet, social media, TV and music open the world to girls in a way that just wasn’t possible when I was her age.  And while there are some negatives to this, I also believe it is making the next generation of women worldly and more aware than in previous generations.  More young people are fundraising and volunteering for causes close to their hearts, and advocacy groups are teaching young girls ways to help other little girls in developing countries.  For Ocea and her peers, the world is definitely a much smaller place than when I was a girl.

At the CCTFA Foundation, we were recently touched by a young girl who, at the age of 10, is already working to make a difference for others. Several months back, a letter arrived at our offices, addressed to the Look Good Feel Better program.  There was no return address on the envelope and inside we found a sealed plastic bag full of hair and a handwritten note that said, simply:

Tamara Card

We have no way of knowing who Tamara is, or how her life was touched by cancer.  But we do know that her compassionate gesture of kindness touched all of us at the Foundation.  I could hardly wait to share Tamara’s story with our friends and long-time supporters at Jon Renau, who supply wigs for our Look Good Feel Better workshops. They, too, were inspired by the caring act of goodwill demonstrated by this special young girl. In Tamara’s honour, Jon Reneau launched a new line of wigs in May called, of course, “Tamara”. The Tamara wig has a Smartlace cap, which provides the most natural-looking hairline and is available at boutiques across Canada. (Visit our site for availability and information.) For each wig sold, Jon Renau is making a generous donation to Look Good Feel Better to help realize Tamara’s wish of helping women face cancer with confidence.

Tamara’s act of kindness is helping more women than she could have possibly imagined when she mailed us her ponytail. If you would like to help ‘pay it forward’, you can make a financial contribution in Tamara’s name.

In closing, on behalf of all of us at the Foundation, Tamara, you’ve inspired us and for that, we thank you. You are making a huge difference in helping women faced with the appearance-related challenges of cancer treatment look and feel more like themselves again. As the formidable Beyoncé says, girls run the world.

Posted in Uncategorized | Leave a comment

The Lessons Cancer Teaches Us

7 Jun

In my work, I am fortunate to meet inspiring people every day and I find that every encounter leaves me with a “take away”. Whether it’s something simple, or something more profound, I believe we are meant to learn from each other and our unique experiences. Alex Ginty says this is why she is so passionate about telling the story of her cancer journey: so others can get the lessons without having the cancer.

Recently, we received news from one of our dedicated board members that her father was diagnosed with cancer. Despite being told by doctors that his cancer is terminal, he is as determined as ever to live life to the fullest and put every effort into the fight against cancer. He has agreed to share his profound insights with all of us so that we may learn from his situation and look at life a little differently. Here is a letter he has written recently to the many friends and family inquiring about his wellbeing. May you be as inspired by his words as I am.

Dearest friends and family,

So the latest update. I am reminded of the film Forrest Gump, in which Tom Hanks says, “My momma always said, ‘Life was like a box of chocolates. You never know what you’re gonna get’.” After much debate amongst the experts the conclusion is I have terminal cancer.

I am seeing the oncologist on Tuesday next week. It turns out that chemo is kind of useless. Why is it offered? As one doctor said, “people want you to do something!” I am going just to hear what he has to say. If I hear something fantastic then okay we will consider, but it is doubtful. Today Marion, Peter and I are off to see a doctor who specializes in helping strengthen your own immune system. Can’t hurt right?

So where exactly does that leave me? Turns out that there is a whole study on people who were given six months or less to live. A percentage have eradicated their cancer altogether or managed to control it for years. Just so. No medicine or treatments, just their will. I intend to give it a go. If I am right and if what everybody keeps telling me is right, then I can beat this.

I intend to live my life the same way as I have always lived it. A few changes; I will stop worrying about what might happen. The other night I ate oysters and Marion said, “Gosh you haven’t eaten oysters for such a long time – how come?” to which I replied, “I didn’t want to get sick!” We all laughed.

I certainly will not get involved in other people’s problems unless I am specifically asked. You know we feel we have to rush in with an opinion to help them see their foolish ways. I have learned that most people enjoy their problems because they don’t do anything about it, they just complain. I heard the other day of a young woman who has become ill because of the fact that her basement is being altered. She got hives and headaches. I wonder what I should get when considering my situation?

I have to see every day as an opportunity to love my kids, my wife, my extended family. There is no room for petty, trivial arguments that consume our daily lives. There is no refund on the last twenty-five years so I have to live the next years with an openness, a balance and with enjoyment. I will not look at the weather and complain, because the alternative is not to look at the weather at all. I will not shout at the traffic anymore, or get impatient because the fool (see there I go again) drives too slow or too fast.

People often ask if you had six months to live, what would you change? Too late then! Perhaps you should realize that you have a life to live now and that every day is important. Why wait until you realize what you have lost before you start to appreciate what you have?

What can you do? Nothing! You can just be as normal as you always have. Your genuine warmth and words of support have been a great comfort to me. Some people have said, “We are all terminal!” and that’s where the box of chocolates comes in. I am sure they are just trying to say something which is helpful. I am sure we are all terminal only not everyone faces a predicted expired date. You can’t say anything that changes my situation. You can just be there like you always have.

I am quite content. I really am. I feel very calm and I will fight on not because I suddenly discovered the need to fight. I have always been a fighter. I have always had an opinion. I will now use that argumentative strength and opinion for me.

Posted in Uncategorized | 2 Comments

The “Tell Her” Movement Facebook and Twitter Party

4 May

The "Tell Her" Movement Facebook and Twitter Party

Join us on Thursday, May 5, 2011 9:00PM EST for a chance to win a Kobo eReader ($149 value) or 1 of 5 $25 Kobo Gift Cards. Participating is easy – use your Facebook or Twitter account and join in on the discussion. Check out our Party Page for more information.

RSVP now

Posted in Uncategorized | 3 Comments

Women Spoke, We Listened

21 Mar

Last week my colleagues of the CCTFA Foundation and I joined many friends, supporters and members of the media for a breakfast event to mark the official launch of this website and the report that inspired it, Lives affected by cancer…800 women speak.  It marked the culmination of a lot of hard work that began, really, when we launched Look Good Feel Better in 1992.

Since that time, more than 110,000 women have benefitted from our workshop, and over the years they have told us many things about the impact of cancer on their bodies, their lives and the lives of their loved ones.  For nearly two decades, we have been listening and collecting their stories of courage and inspiration in our hearts and in our heads. We learned a lot from these women and in 2010 we broadened the mission of our Foundation to encompass the psychosocial needs of lives affected by cancer, which, quite simply, encompasses everything ‘else’ a woman many be going through with cancer, beyond the medical care of the disease.  In an effort to learn even more about the social and emotional impacts of the disease, and to look at ways that we as a Foundation could help women address some of these psychosocial needs, we conducted a Canada-wide survey to hear first-hand what they had to share about life after a cancer diagnosis. 

 
The resulting report, Lives affected by cancer…800 women speak reveals that even after cancer and its treatment, may women struggle to return to their “normal” life, or perhaps more appropriately worded, their “new normal”.  Whether our body has been changed physically as a result of cancer, we are grieving the loss of life as we once knew it, or dealing with issues of fatigue that can take months or sometimes years to go away, like it or not, many of us have a changed reality.  As one survey respondent told us, “You can’t just close the door and walk out.  You’ll never be who you were.”

For me, although I’ve been cancer free for more than 21 years, the impact of the disease is still very much a part of my daily life, and always will be.  My treatments and surgeries left me with nerve damage that requires me to wear braces on both legs to walk, and I use a cane to support me as my balance is now poor.  Mind you, my cane is studded in rhinestones!  But the lingering effect of nerve damage has meant that my quality of life is different from what it may have been. And while physically I cannot do some of the things I used to, as a result of my cancer journey I am emotionally and spiritually rich in life appreciation as a result of my new normal.

There are many women who will tell you they have emerged ‘stronger and better than ever’ after cancer, finding that the experience of looking into the face of the disease forces them to find inner strength and draw on reserves they didn’t know they possessed.  One of our Look Good Feel Better Ambassadors and models, Line, recently realized a dream of hers and opened a body clinic, Nueeva, in Brossard Quebec with her daughter. With her breast cancer gone and her treatments now complete, she finds she has more confidence that ever before. “I went through all of this, imagine what I can do today,” she says. “I found out that I am very strong.”  Our beloved blogger Dr. Alex Ginty also tries to focus on the things she has learned from cancer, using her experience to relate to the fear and anxiety her patients sometimes feel, and sharing some of the tips she used to get through the darker days of her journey. She eloquently shares some of what cancer has taught her in her poetry on her blog, Both Sides.

Of course not everyone finds the ‘silver lining’ to cancer.  And no one should ever feel pressured or guilty to move on.  Healing takes time, and the fact is, cancer does change you, even if that change may be in your outlook on life, or through the newfound inner-strength and wisdom you’ve unleashed within.  And no matter what, we know that the need for support does not end with the last treatment, or when we ring the chemo bell.  Though our hair, brows and lashes will grow back and many of us do return to work, for many women faced there are bound to be hurdles throughout the cancer journey.  For many of us, healing and well-being becomes a life-long quest – it has for me. 

I would like to personally encourage every woman who has had cancer not to be afraid to acknowledge that you still may need help, that some days are harder than others, or that you are scared that cancer may rear its ugly head again. If you need or are seeking support or resources to help you on this next stage of your journey, please visit the Resources page of our website for a list of places and programs that may be of help to you.  

I’d love to hear from you. You can send me a note on this site, or at thecancerjourney@cctfafoundation.ca

Posted in New Normal, Uncategorized | Tagged , | Leave a comment