This is Brave: Cassie Beisel

This is Brave: Cassie Beisel
For me, change happened on January 24th, 2011. I will never forget those words, “You have cancer.” “How is this even possible?” I thought to myself. As an avid outdoor enthusiast and rock climber, I was in the best shape of my life. How could I have cancer? As I would come to find out, the answer to that question was easy. As an outdoor enthusiast and someone with misinformation about base tans, I often spent many spring seasons prepping my skin in a tanning bed as a preventative measure to burning. [gallery size="full" columns="2" ids="eyJ1cmwiOiJodHRwOlwvXC9jb29saWJhci5sb2NhbFwvd3AtY29udGVudFwvdXBsb2Fkc1wvMjAxOVwvMDRcL0Jpa2luZy5qcGciLCJ0aXRsZSI6IkJpa2luZyIsImNhcHRpb24iOiIiLCJhbHQiOiIiLCJkZXNjcmlwdGlvbiI6IiJ9,eyJ1cmwiOiJodHRwOlwvXC9jb29saWJhci5sb2NhbFwvd3AtY29udGVudFwvdXBsb2Fkc1wvMjAxOVwvMDRcL091dGRvb3JzLmpwZyIsInRpdGxlIjoiT3V0ZG9vcnMiLCJjYXB0aW9uIjoiIiwiYWx0IjoiIiwiZGVzY3JpcHRpb24iOiIifQ=="] With the presentation of a swollen lymph node in my right arm and no primary mole, it took my doctors a month to realize that this was stage 3B melanoma and not breast cancer. I was 32 and had no clue what melanoma was but based on the doctor’s reactions, I knew that treating this was something of urgency. Not knowing what to ask my doctors and perhaps feeling a bit naive for not know what melanoma was, I immediately took to the web, where I came across the Melanoma Research Foundation’s (MRF) website. It was here where I found an abundance of educational resources about melanoma helping me to better understand my diagnosis and treatment options. I underwent a full lymph node dissection, finding melanoma in three out of 36 lymph nodes and completed a year of interferon. The MRF played such an important role in my journey from diagnosis to recovery. Six months after my treatment ended, I dedicated my time to fundraising for them as a volunteer. I would ride 100 miles to raise funds to help other young adults like me; hoping to make their journey a little easier through funding life-saving research. It was three days after my ride that I would land in the hospital with acute leukemia. After a bone marrow transplant and two years of recovery, it was time for me to return to the workforce. As a young adult with two cancers and four year’s out of the workforce, I knew that returning to my everyday life in the hospitality business would be challenging for me. I just couldn’t go back to where I’d come from. My melanoma diagnosis had changed everything for me. In 2014, I joined the Melanoma Research Foundation. Currently, I lead the organization's advocacy efforts to mobilize advances in policy and federal funding. I also represent and engage the interest of the melanoma community and focus on partnering with industries seeking to amplify our voice. [gallery columns="2" size="full" ids="eyJ1cmwiOiJodHRwOlwvXC9jb29saWJhci5sb2NhbFwvd3AtY29udGVudFwvdXBsb2Fkc1wvMjAxOVwvMDRcL2dldC1uYWtlZC1jYW1wYWlnbi5qcGciLCJ0aXRsZSI6ImdldCBuYWtlZCBjYW1wYWlnbiIsImNhcHRpb24iOiIiLCJhbHQiOiIiLCJkZXNjcmlwdGlvbiI6IiJ9,eyJ1cmwiOiJodHRwOlwvXC9jb29saWJhci5sb2NhbFwvd3AtY29udGVudFwvdXBsb2Fkc1wvMjAxOVwvMDRcL2hpbGwtZGF5LW1lbGFub21hLmpwZyIsInRpdGxlIjoiaGlsbCBkYXkgbWVsYW5vbWEiLCJjYXB0aW9uIjoiIiwiYWx0IjoiIiwiZGVzY3JpcHRpb24iOiIifQ=="] My journey with skin cancer hasn’t ended, recently I had my Moh’s surgery to remove my third squamous cell carcinoma (the second most common form of skin cancer). I still live with the fear of a melanoma recurrence daily. Melanoma is not “just skin cancer,” no skin cancer is “just skin cancer.” It is a big deal and it impacts the lives of millions across the globe and contributes to over tens of thousands of deaths each year. I am honored to have survived and been able to devote my career to helping those who have been impacted by this disease.
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