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Team Save Your Skin

Team Save Your Skin is a sports fundraising team – members are Save Your Skin Foundation Champions!

Throughout the year, Team SYS – who are active runners, marathoners and cyclists– compete in various races to support the Save Your Skin Foundation through fundraising and awareness. All money raised through the Team’s fundraising efforts, goes directly to the Save Your Skin Foundation and in turn, directly helps those touched by melanoma through financial support (click here to read a story about why, who and how we help)!

We ask members of Team Save Your Skin to raise an annual minimum of $250 in donations. But, the sky is the limit! If you are interested in joining Team Save Your Skin and helping to support our fundraising goals – please email natalie@saveyourskin.ca today!

We’ll be featuring some of our fundraising All-stars on the Save Your Skin blog and social media platforms so stay tuned! To follow along on social media – use our official hashtag #Run2Win @saveyourskinfdn

Here’s an example of someone already on their way to reaching their fundraising goals!

Rose Westie – Kathy’s sister ran the Sun Mountain 80Km race in Winthrop, Washington! Check our her fundraising page here!

Details:

Team Save Your Skin Registration

To register for Team Save Your Skin – please contact natalie@saveyourskin.ca

Registration Fees are $75.00CAD and include:

o Lululemon Technical Team Shirt (product details below)
o Informational Package that includes an Infographic and ‘Getting Started’ Fundraising Guide
o Reach your annual minimum of $250.00 CAD and receive complimentary access to our annual fundraiser!
o Fundraising Support
o Becoming a part of an amazing community of dedicated SYS Champions!

Want to get the jersey but aren’t interesting in running a fundraising campaign? Contact us here.

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Nigel’s Story

Victoria, B.C.

In June of 2010 I was diagnosed with an ocular melanoma tumor at the back of my right eye. In July of that same year I had brachytherapy. In March 2012, metastases were confirmed in my abdomen and I proceeded to have four infusions of Yervoy (ipilimumab) in the late fall of 2012 and then again in the late fall of 2013.

I also had two radiation treatments to the abdomen in March and April of 2012 and one radiation treatment to the spine in September 2013. I’m alive today. I am here. I can enjoy life.

 

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Mike’s Story

Prince George, B.C.

In 2006, I noticed a mole on my thigh. Back then, I knew nothing of skin cancer. It wasn’t even a consideration. This was just a mole that hadn’t been there before. I went several times to my doctor about it but his answer was always the same, “It’s just a mole, don’t worry about it”. I started to worry at the end of that year when the mole started to bleed while I sat and watched TV. I made an appointment with the doctor again but had to wait a couple weeks to get in. By the time I got in, the bleeding had stopped. When the Dr. looked at it, I heard the same words, “It’s just a mole”. This time however, I held my ground and told them I wanted it removed, no more talk. Two weeks after that I went back to get my stitches out. When the doctor came in I said I was there for my stitches removed and she said, “We have a problem”. It was then that I got my diagnosis that the mole was malignant melanoma.

My 2007 diagnosis led to 3 unsuccessful surgery attempts before I was sent to a larger center for a sentinel node biopsy. Fear abounded as I tried to find out about this condition. No one seemed to know anything about this malignant melanoma. All I got from Drs. and people that I asked was that this was cancer and not a good cancer to have.
After my diagnosis and surgeries, life started to settle back down. I was referred to a cancer doctor that would see me for a checkup every three months. If nothing changed, then after 2 years I would only have to see him every 6 months and if nothing reappeared within 5 years, I would be cancer free.

In May 2009, I had a recurrence as the cancer came back as a tumor in my groin. After the surgery to remove it, I got to see the doctor that was following me. As I sat across the desk from him, he opened my folder, read something, and then he closed the folder and said: “There is nothing I can do anymore, go home and get your affairs in order as there is no chance for survival now that the disease had gone metastatic”.

Needless to say, my family and I were stunned. I felt fine but the doctors were telling me that I was in the last year of my life. I searched everywhere to find out more information on this cancer. Everything I read was all about how not to get it, not what to do if you had it.

My sister sent me a news article about this lady that had started a melanoma foundation so I reached out and contacted Kathy Barnard. She had just gone through a similar whirlwind in her life and was still living and ready to tell her story. She suggested that I get a second opinion with a doctor in another province that she had seen. Then, she went and made arrangements for me to get in to see him.

My wife and I traveled the 900kms to the Cross Cancer Institute. Sitting with Dr. Smylie, he agreed that I was in trouble but then he said the magic words: “I can keep you alive”. That was all I needed to hear and at that point, I enrolled in a clinical trial. In October 2009, I entered into my first clinical study.

Unfortunately I had yet another recurrence in December 2010. They found an 8cm tumor in my lungs. A major surgery in the hospital in Alberta confirmed that the tumor was unresolvable but it did allow the clinical study team to get a biopsy of the tumor. I was closed back up and sent home. At this time I was starting to not be able to breath on my own. I was considered palliative and placed in hospice.

During my final hours, while I lay in the hospice bed breathing straight oxygen, my wife and Dr. Smylie were working feverously to come up with a plan.

Dr. Smylie announced to my family that he had found a new trial that had great promises of working on my tumor to eradicate it but he needed me back in Edmonton. My wife called everywhere and everyone she could, to try and get me across the mountains to Edmonton, but there was no medical transportation that would take me in my condition. With the help of local people in our town, I found myself being picked up out of my bed and placed in the back seat of our truck. My wife jumped in the driver’s seat and raced out into the night to take me to the cancer clinic in Alberta.

I don’t remember much of that trip. But I do vaguely remember sitting on the Drs. examination table and the Dr. saying that I was to receive the strongest version of the new drug. We finished the exam and then headed to the clinical pharmacy where we received 3 weeks of this new drug to take home with us.

Back at home, the oxygen machine had made its way there and I was laid in my own bed. Now, twice a day, I was taking a pill that would hopefully make a difference.
Two weeks later, I removed the oxygen mask and was able to breath on my own. Then it was time for my first checkup in Alberta but this time, rather than sleeping the whole way, I got to sit in the passenger seat. The Dr. was very surprised to see my new condition. They did a CT scan and were quick to show me how much the tumor had shrunk. It appeared that we were on the right track.

That was at the end of April 2011 and today I am still free of the cancer that so badly wanted to take my life. This drug was the very first version of a treatment that has come full circle and is now the approved drug for Melanoma. I was in the very first group of patients to ever receive this drug. There were a lot of really bad side effects from the drug but I stuck with it with the reason being that back then, the only real piece of info we had was that if treatment stopped, the melanoma would come back as it did for so many others in this trial. Without any other options, and not wanting to have to look at death again, I stayed with it until 2 and a half years later when a new trial was presented that I could go on should the melanoma come back.

Today, I’m still cancer free.

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Meloney’s Story

Port Alberni, B.C.

I was first diagnosed in April 2006 with stage 4 metastatic melanoma. I was considered terminal. The origin of my melanoma was a large mole on my back that I’d had most of my life – my family doctor had failed to diagnose it properly. My first clinical trial with the drug Temozolomide failed.

I then entered a Yervoy (ipilimumab) trial in September 2006. In January 2007 test results came back successful enough for me to proceed with surgery. As of April 4, 2007, I had completed surgery and that day now marks my cancer-free anniversary. From August 2007 until February 2012 I re-entered a trial for the maintenance and monitoring phase of my post-cancer treatments.

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One Melanoma Patient’s Need for Community

 I find it comforting to meet or speak with others surviving the melanoma maze. Visiting my cancer centre on a regular basis for all of my appointments and treatments, I sit quietly with my peers awaiting theirs, but I almost eagerly strike up conversation if someone even glances my way. I must startle some of these unknown strangers, likely appearing like some overzealous puppy jumping up to make friends, panting all over the place. I have plenty of wonderful friends already, but I seem to crave new friends. I want cancer friends, I need common ground.

Since my diagnosis and countless consultations with medical professionals of all types, I still find the greatest comfort speaking with others in the same boat as I am. We compare facilities and oncologists, pain levels, side effects, and remedies for improvement of our symptoms.

We are all there for the same reason, and we seem keen to exchange stories and curious questions about clinical trials and treatment options and number of surgeries under our belts. It is a strange language, one I have learned a lot about in the past year, but one that I believe I will never fully understand.

I have happened to have met three people with melanoma, but that’s it. It is not the most common ailment along my traveled path. All cancer cases are personal of course, but I quickly learned that melanoma is even more a mysterious beast.

Melanoma patients are a unique breed, fighting a unique battle, and we need comrades on our side. Talking it out with someone with the same type of metastatic cells not only eases our psychological burden, but it lends hope to the fight. It reinforces in our minds and bodies that we may have other options to explore or other questions to ask our oncologists. There are other people ALIVE coping with what we are coping with, and they may be able to help.

Life raft thrown out! Even if for just one day, that is one day’s worth of hope that I may not have had if I hadn’t spoken with my comrade.

Online resources are a huge help also – when first diagnosed I was banned by my doctor from the internet, but now that I have learned more and I am more comfortable with the way things seem to work, I feel less panic about reading things online about my disease. Even the venting of fellow bloggers is comforting, I feel relief when reading their words and knowing that I am not the only one who is afraid or discouraged or angry.

I can sift through the medical terms and look past the statistics, and every now and then I find a nugget of information that sends me in an entirely different direction, usually uncovering another piece of my puzzle. Whether about melanoma or the likes of a new meditation technique, it gives me the feeling that there is something I can do about my situation, and that there are others who are doing the same.

I remember feeling when I was first diagnosed that I was walking around with a giant digital clock above my head, with large green numbers counting down to my expiry date. I felt I stuck out like a sore thumb, wore that clock around like a black cloud, wondering how to get it away from me. I ducked and dodged and denied until I was blue in the face, now I focus my energy on positive action, namely, writing or talking with anyone willing to show their community flag.

The clock seems to have faded this year later, but it is not gone. That is in part due to those that I have connected with, in person or online, that have said the same things I have felt, or that have experienced the situation I am in. Venting, learning, sharing: all coping mechanisms.

I trust my oncologists, but I gain extra strength when I speak to people who have walked the same steps I am being directed to take. I hear it repeated and think it is a good sign that I am not some entirely solitary being receiving a mystical treatment unknown to anyone outside of the chemical laboratory that mixes up my IV bag of potion.

Every day I push on, hanging out with my family and friends, going to my appointments, resting with my cat, and seeking the additional community that I need in order to properly fulfill my ambition to fight melanoma. I have to fight my individual battle my way, but I am also content to share that fight with others, either gaining from their perspective, or being able to help someone else in some small way. We are all neighbours on this ship, and I think we can paddle together to keep it afloat.

Natalie Richardson – www.impatientpatientmomma.blogspot.ca

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