Wall of Hope Wall of Hope

Diane’s Story

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As told to the Lethbridge Herald

The very moment after the surgeon told her she had breast cancer, everything in the room lost its clarity for Diane Gallant.

Sights and sounds morphed into slow motion as the physician’s mouth continued to move, but no longer made sense. Blood pounded in her head like a tribal drum. Her first clear thought, she remembers, was to call upon God to help her. Her second was to wonder, “why me?”

The day she was diagnosed – in June 2006 – was the same day Diane and her husband Wayne took possession of their new home west of Lethbridge. Wayne had just purchased Mountview Dodge – now Lethbridge Dodge – and the couple was moving from Cochrane after 20 years there, coming back to Lethbridge where they had both been raised.

They were excited to be embarking on this new phase of their lives. Son Russell, 24, was about to begin law school but decided to take a year off and help his dad at the dealership. Daughter Jeni, an education student who wants to teach French immersion, was only too happy to move to the University of Lethbridge. Everything was falling into place.

But first there was this business of a lump in her breast to be taken care of.

“We drove down here to do a walk-through of the house, then we had to race back to Calgary for a doctor’s appointment at 2 p.m.,” she recalls.

She wasn’t worried at all. There was no history. And she’d taken very good care of herself. She expected nothing; and then the doctor dropped the “C” bomb.

“Why me? I thought, I’ve done everything right in life. I always wear my seatbelt, I wear my helmets, I eat pretty well. My mother has 10 sisters, all between the ages of 58 and 78, and not one of them has had breast cancer. Not one. I answered all the questions – I had my kids at the right age, I nursed both of them, I took the pill but only for a short time. Why the hell me?

“And then I thought, OK, it’s me. Thank God it’s me, and not my daughter or my mother.”

Diane had found the lump on her right breast that Mother’s Day, while she was away at a horse competition with Jeni. Until that day, she’d gone dutifully for an annual mammogram since she was 40, and they’d always been clear. Now, within a few days and after numerous tests, she learned the lump that got her attention was merely a cyst, but the cyst had served as a beacon that led to the discovery of cancerous tissue beneath.

As the news began to sink in, Diane and her family were faced with a couple of days to discuss her options. Would it be lumpectomy or mastectomy? She had three surgeries in six weeks, followed by several months of intense chemotherapy.

It was during her chemotherapy that Diane learned about the Canadian Breast Cancer Foundation in a way that proved to be life-changing. She read a newspaper article about the cancer drug Herceptin, which she knew was one of her medications. The article extolled its the virtues and called upon the Alberta government to join other provinces in adding it to the provincial drug list. The cost per patient, she learned, was $40,000.

“I took the article with me to the doctor. No one had asked me if I had insurance, or how I would pay for this medication, so I asked him who was going to pay for it. He told me that coincidentally, the government had announced that day it would cover Herceptin, but he said even if they weren’t going to, the Canadian  Breast Cancer Foundation would pay for it.

“There’s where my determination comes from. I decided to run in the Canadian Breast Cancer Foundation CIBC Run for the Cure, and I said to my husband if I could get 500 people to sponsor me for $20 each, that would be $10,000.”

By the time the run happened Sunday, Diane had raised more than $12,000 along with her team, Jugs and Jocks, and earned the Ford Determination Award for raising the most money. That determination is growing, and Diane intends to make the run an annual event.

“I learned three things through this,” she says. “Number one, I am a lot stronger than I thought I was. Than I ever knew I was. Number two, I don’t have control as much as I thought I did, and I’ve learned what I do have control of and don’t worry about the rest. And third, there’s just a lot of stuff in life that doesn’t really matter.”

My Journey Begins

I am 48 years old and was diagnosed last December.  At first I was told don’t worry its probably nothing, but nothing turned into 8 chemo treatments, 16 radiation treatments and a mastectomy which I had just two short weeks ago.  I got the results of my pathology reports last Friday and I am happy to report all came back negative.  This is a poem I wrote the night before the first stage of my treatments.

Today is the day my journey begins
Don’t know where I’m going but know where I’ve been
The things that I’ve seen and the things I have done
Have let me to know there’s no army of one
We are many strong, our soldiers are great
We stand side by side challenging our fate
For some it’s been lost the battle too long
They strengthen our hearts no memories gone
I’ve been shown my path for all I will fight
To shine for all those darkened by night
So think happy thoughts from this faith has grown
Our soldiers are many we don’t walk alone
My prayers are to all for what has been done
We don’t stand alone there’s no army of one

Each of us will handle what has been given us in different ways.  I was blessed with many angels along the way and have learned so much about myself and life.  My heart is with  all of you

Karen Scott – No longer a future breast cancer survivor but an actual real life survivor

My Journey

Petra 

I was diagnosed Sept 11,2004.  I had a partial mastectomy, full round of chemo and 28 radiation treatments.  It was quite a journey with peaks and valleys and I would not change one thing.  I was so touched by friends and family who truly love me and I will never take that for granted.  My boys were amazing and my dogs..wow without them I know there would have been days that I would not have gotten out of bed.  They literally saved me from myself.

Now I am facing the possibility of going through the “journey” again.  And I am afraid but there must be a reason and I will walk tall and proud, boobs or no boobs, and take one day at a time.

 LIVESTRONG, Petra Kern-Alexander

Joyce’s story by Sharon Schultz

 Joyce

One day, one moment, one word and one young woman’s world is turned upside down. This is my story of my sister Joyce and her incredible journey living with cancer. I am very sure that when my sister was diagnosed with breast cancer over 20 years ago that she could not have dreamed the path she would walk. Joyce was young, her two boys were young and they enjoyed a wonderful family life.  .With that one diagnosis you are in shock.  Suggested treatment was a radical mastectomy and so Joyce’s “treatment of breast cancer” began. After the radical mastectomy and recovery time, Joyce was healthy enough in July of 1985 for reconstructive surgery. What a great feeling it was to be having surgery to make you feel whole again .This elation lasted for some time but Joyce soon found out that all too often we can be struck again and our life will again be changed forever.
 
In 1997 the cancer was found to have spread to the bones. This was hard to take and knowing what was in store I am sure she questioned yet another round of chemotherapy. Joyce has had two stem cell replacements, both difficult procedures for her and of course the biggest treatment of all, on going chemotherapy. To have your body “back” after the reconstruction and then have your appearance once again shaken by chemo is heart wrenching. You live with the feeling of never being quite the same again. Joyce will tell you that cancer is a very lonely disease. There is some comfort when you are at the clinic and you are sitting with others who share your treatment. The loss of hair, the fingernails and toenails that just change, extra weight, or loss of, all of these changes make it difficult to keep going, both physically and mentally. Imagine going through this continually for over 10 years. The nurses at the Tom Baker Cancer Institute in Calgary are in awe of Joyce and her own doctor calls her his star patient. Joyce recently ran into her surgeon of 1984 and he was genuinely elated and amazed…asking Joyce lots of questions.
 
Joyce is one of the strongest people I know and will tell you that having cancer has given her more than it has taken. With her close friends and an incredible husband Nick who has stood by her with great compassion and doesn’t see what the disease has done  physically, Joyce would be the first to tell you how important it is to share your story, your experience and your power of positive thinking with others.
I know that each and every story you hear, touches your heart and every person is touched in some way by Breast Cancer. Whether it is themselves, a friend, co-worker, family member, it is far reaching. I however still swell with pride when I meet someone new to our team who has just recently met Joyce and already has felt that wonderful aura that surrounds her. You can’t help but be drawn in to her desire to fight the disease and spread the message of hope.

There are now over 100 of us who run/walk for this remarkable lady on that Sunday morning in the annual Run for the Cure. We are Joyce’s Angel Network.  We have won the” Friends and Family “category for a number of years. .no small feat when you consider the number of participants in a city the size of Calgary. This year was especially rewarding. We raised close to $50,000!
 
Joyce was proud also to be on stage at the Calgary Stampede this year where their theme was “Are you tough enough to wear pink? She has participated in three Survivors’ Walks with close to 200 other ladies and two men. She tells me of the emotion and support felt at these events and you can feel her pride as she talks about these in particular. Not many people have fought the battle like Joyce and continue to smile and support each of us at the same time.
 
What began as one woman, and one disease has grown to include not only the one hundred plus individuals that participate together   but the long list of people who sponsor each of us .The power of one. This number has grown significantly since Joyce participated in her first run 12 years ago with one other lady. Joyce would be the first to take the spotlight off of herself and turn that light so that it shines on those who do so much for her in so many ways. From her incredible daughter-in-law Alanna who “manages” our team each year, to the friends who are there always, to walk her dog Billie, decorate her Christmas  tree, bring food to her home when needed,  host a  large fund raiser, shave their own heads, take official group pictures at the run, or accompany her on treatment day. Each person seems to have their thing that they do to help, one simple way of showing your love and support.Joyce also tells me that her father-in-law and his wisdom has played large role in her attitude. His one repeated saying of Joyce was “Never give up.” Rather good advice from a man who lived to be 96.

Joyce would not for one minute want this to be solely about her. It is about her husband Nick, her children, immediate family and those friends who have been there for the past 20 years and are still there. It is about every woman and man battling this disease. It is about finding a cure. It is about Hope. Hope without action however, is like wishful thinking. By all Joyce has done; by virtue of whom she is, we have been inspired into action. This has resulted in tremendous rewards. The power of one appears significant in that when I asked Joyce how much she thinks our team has raised it is not surprising that the number one came up again. . Over $150,000 to date.   All because of this incredible lady and the power of one individual to inspire and encourage us. Joyce would say she is only one in a million of individuals fighting this disease but I just say she is one in a million.

Raising funds for my Grandma

BROOKE 

Hi my name is Brooke Corner and I am 13 years old.  I started raising money for breast cancer 5 years ago when my Grandma was diagnosed with it.  I was not sure how to handle the news about my grandma, I felt sad and scared that she might die.  When grandma was going through her treatments we made every trip to Sunnybrook hospital with her and my grandpa so she could have her radiation treatments, and after chemo treatments we would spend the night with her to make sure she was okay.  Knowing that we could not help grandma in many ways because we were just kids, we were trying to find another way to help.  So my brother came up with a good idea of putting a team together at his school to raise money for the Canadian Breast Cancer Foundation CIBC Run for the Cure.  At the end of the fundraising the school only had a team of nine, and they needed ten to make the team; this is where I came in.  My brother gave me some of his money that he collected so I could run with him.  I think we divided $360.00 between us.  That started my first year being involved with the CIBC Run for the Cure. Being chronically ill myself, the CIBC Run for the Cure day is sometimes difficult for me to run, but in the back of my mind I say to myself if people with breast cancer can go through what they can, then for one day I can run for them. It is now five years later and my grandma is a survivor of breast cancer and I am still running for her.  Last year I raised over $3600.00.  Each year we make it a bigger and bigger fundraising event for our whole family.  My mom and sister make jewelry for me to sell, I go door to door asking for donations and my dad helps with driving me to the locations I need to go to.  My older brother helps by racing with me to see who can get to the door first and who can collect the most.  I always look forward to raising money for breast cancer because I like to help others and hope someday they can find a cure.
 

Chantal and Mom

Mom & Me

Team Lafontaine – A survivor story

My name is Chantal Lafontaine from Ottawa, Ontario and I am almost a one year survivor ( January 2008).  I found a lump on my left breast in January 2006 during my my pregnancy.  I was in my third trimester.  I gave birth to my wonderful baby boy Nickolas on March 15, 2006.  My doctor thought the lump might be an inflamed milk gland.  I had a feeling since my mother was diagnosed and operated on for breast cancer over 18 years ago, that it was cancer.  She is still with us and cancer free!  I had a biopsy in April 2006.  My surgeon called me a week later to confirm it was breast cancer.  I had my lumpectomy on May 19, 2006, which was followed by 8 chemo treatments and 30 radiation sessions that lasted over the fall and winter.  My last treatment was January 2, 2007.

 I have been doing exremely well.  I am back at work.  My husband and I are enjoying our beautiful boy and living life to the fullest.  I would like to take this opportunity to thank my medical team.  It’s all because of them that I am here today.  Thank you to my family doctor, my surgeon, my oncologists and the many, many nurses and staff at the Ottawa Hospital Regional Cancer Centre.  What amazing people.  They have dedicated their lives to helping people just like me.

 I created Team Lafontaine this year for the Canadian Breast Cancer Foundation CIBC Run for the Cure.  There were a total of 11 in our group and we raised over $2,000.  My family and friends were so supportive when I was going through my experience and were all very generous in supporting our Team this year.  I had run the race a few years back in support of my mother and a few other women I had lost to this horrible disease.  I can’t wait for the run next year, my Team will be bigger and we will raise lots more for the Foundation to find a cure!

Thank you very much

Chantal Lafontaine

Team Kalan Porter – Edmonton

Run Day 2007 – Thanks Everyone!

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Running for Hope in Edmonton

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This year, I ran for the Cure… not because someone close to me has been directly affected, not because I have lost someone I love… but for the exact opposite reason. I am twenty two years old, and I run because I know how LUCKY I am to basically be untouched by this horrific disease. I run for the cure because I HOPE that if we all work together, one dollar and one step at a time, that we will find a cure for breast cancer before someone I love is handed this diagnosis. The facts are straight: 1 in 9 women will be diagnosed, and out of every 100 breast cancer diagnoses, 1 of those will be men. So, this year, and every year until we find a cure, I run for everyone… for all the women, all the men… all the little boys and girls… so that not one more person has to be diagnosed with breast cancer. I run for you, and I run for me. I can only HOPE and do what I can that together, we can create a future without breast cancer.
Amy McCrea
 Edmonton, AB

Kalan Porter touched by breast cancer

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I grew up on a ranch in Southern Alberta, I had a near perfect childhood, with my sisters, cousins and I having our own private wilderness to explore. When I was around 5 my mom started taking me kicking and screaming to every type of music lesson Medicine Hat had to offer. Mom was a bit of a stage mom, supportive but insistent that I practice…she always said one day I would thank her for it. I spent my teen years planning on a music career, with my mom as coach, counselor, chauffeur and short order cook. Just before I was to leave to study music at McGill, a show named Idol came along and changed my life.

After Idol I was on top of the world with an album, videos and a tour. Then on February 21, 2006 my world changed again; I got a call from my mom saying she had breast cancer. The first thing I did when I got off the phone was google cancer life expectancy. I began to learn everything I could about breast cancer. Being I young single guy I thought I knew everything there was to know about breasts, apparently I was wrong.

I kept trying to focus on the music and my career but all I wanted to do was go home. One night after staring at an old holiday photo of my whole family in matching Christmas sweaters I decided it was time to go home. Once I got home breast cancer became real; I saw my mom bald for the first time and she didn’t look like Demi Moore, I saw my dad cry for the first time and I experienced real fear for the first time when I got a glimpse of life without my parents. I spent time at the hospital with my mom, helping around the house and letting her know when her wig had shifted a bit.

After 4 months of surgery and chemo Mom started to get better. Once she began nagging me again I knew it was time to head back to Toronto.

This summer I have a new album and tour, and thanks to the treatment and care my Mom received she is here to enjoy them with me.

I have made a personal commitment to work with the Canadian Breast Cancer Foundation on an on going basis, and on September 30, 2007 I will be participating in the Canadian Breast Cancer Foundation CIBC Run for the Cure.. Thanks to the work of the Foundation there is hope, Hope is what the Foundation has given my family.