Monthly Archives: October 2011

The Fear of Recurrence: Cancer’s Evil Twin

A month after I was diagnosed with breast cancer, I got a bone scan. I thought the hard part was going to Nuclear Medicine and being injected with a dye that made me so radioactive I couldn’t stand near newborn son for 24 hours. Then my oncologist called.

“We found a spot on your sternum,” he said.

“What is it?” I asked frantically.

“We don’t know yet. Did you have an accident when you were younger? Did you ever fall off your bike? Those kinds of bumps can leave a mark.” My head was spinning: I am thinking about terminal illness, and he’s talking about bicycles?

“No, I never had an accident. How will we know if this is cancer?”

“We wait and see,” he said quietly. “If it is cancer, it will start to hurt.”

I learned something in that moment: I learned to fear. I learned to read every pain, every scan, every checkup for signs my cancer had spread to another part of my body. And when breast cancer metastasizes, there is no cure.

These fears didn’t end with treatment. They persisted for years because the danger did. After I finished radiation, friends and family looked at my stubbly hair and assumed I was all better. I had to remind them through gritted teeth that my oncologist wouldn’t call me cured for ten years.

People think chemo is the worst part of getting cancer, and yes, being bald, bilious, and menopausal was awful. But those physical trials paled in comparison to the mental challenge of managing fear. I would parse every word my oncologist said and obsess over what he meant when he called my cancer aggressive. I would lie awake at night wondering whether the pain in my back came from carrying the stroller or having a tumor. I would read a news story about a celebrity’s death from cancer and wonder if it would happen to me.

This wasn’t hypochondriacism. It was realism.

Friends tried to brush my concerns aside. “You’ll be fine,” they would say. “You shouldn’t worry so much. We could all get hit by a bus tomorrow.” They meant well and they thought they grasped the fleeting nature of life with their freak-accident analogies, but cancer survivors don’t have the luxury of dealing in generalities. We have had been told by medical experts that we have a life threatening illness, and because of the limits of science, we must wait and see if it kills us. Or not.

So we learn to cope with fear. Almost every young survivor I spoke with had the same preferred method of managing terror: vigilance. We become hyperaware of our bodies and we scrutinize the slightest alteration for signs of cancer.

Michelle got cervical cancer when she was 26; it recurred two years later. “I would go into the doctor with a long list of all that was wrong with me and what I had diagnosed it as,” she told me. “My doctor told his medical students I could be an associate professor by now.”

Theresa didn’t wait for her doctor’s opinion either. After her first go-round with leukemia, she did her own self assessments. Once when she threw a party, she started feeling sick, which in turn made her frightened. She excused herself and ran her checklist in private:

First on the list is temperature. 98.8 degrees. This is acceptable. Next, pulse rate. 90. A little high, but sick-sick is 150, so I’ll take it. I check my fingertips: pink. Not anemic. Moving on, I check the skin on my lower shins, which is clear of those red freckles that mean low platelets. I lie on my back and take a deep breath in, and then out, with hands pushed under my left ribcage. No spleen. Nice. Having finished the checklist, I could now feel slightly more certain that my symptoms were unlikely to be those of acute leukemia.

The constant vigilance is exhausting. I felt drained by it, but it also made me tough. Over the years—and the scares and biopsies and bad scan results—I learned something else besides fear. I learned that coping with fear is a muscle, and mine got stronger. I worked it. I exercised it. I came to believe in it. I can face another biopsy because I have done it before.

Don’t get me wrong. I still get nervous waiting for test results and I still monitor my aches and pains. But I take comfort in the passage of time—every year that goes by without incident lowers the chance of recurrence—and I know I can muscle through the fear and still live my life.

Emily Cousins

Emily Cousins is a writer and editor who was diagnosed with breast cancer when she was 32 and nine-months pregnant with her first child. She is currently writing a book about what it’s like for young survivors once cancer treatment is over-when the radiation burns have healed and the hair has started to come back, but everything else is completely out of whack. After almost a decade living in New York City, Cousins now resides in Northern Arizona with her husband, son, and the daughter she was lucky to have post chemo.

[PRESS RELEASE] The Stupid Cancer Show Crosses 200th Broadcast Milestone

THE STUPID CANCER SHOW CROSSES 200TH BROADCAST MILESTONE
***
Celebrates Breast Cancer Awareness Month with special spotlight on Breast Cancer Action

NEW YORK, NY, October 13, 2011 – The Stupid Cancer Show, winner of “Most Innovative Use Of Social Media” at the 3rd Annual CLASSY Awards, celebrates the historic airing of its 200th live broadcast on Monday, October 10th, 2012 at 8pm/ET online at http://stupidcancershow.

The 200th show will celebrate Breast Cancer Awareness Month with a special focus on young adults who have survived breast cancer. Marissa Levesque, cancer survivor, will join for the “Survivor Spotlight” and share her experiences of what it was like to live as a young woman with breast cancer. Two representatives from Breast Cancer Action, the watchdog of the breast cancer movement, will also join the show to discuss their organization and how the community can join together to end the breast cancer epidemic.

A program of the I’m Too Young For This! Cancer Foundation (“i[2]y”), The Stupid Cancer Show was launched in May of 2007 as “The Voice of Young Adult Cancer.” Over four years later, the show has an impressive aggregate listenership exceeding 1.5 million worldwide. Now in its 9th season, the radio program tackles hard hitting issues from politics, health care, civil rights and the environment to social media, entertainment, cancer research and education.

“We could not be happier to have reached this significant milestone in our history and the history of the young adult cancer movement,” said Matthew Zachary, a 15-year pediatric brain cancer survivor and Founder/CEO at i[2]y. “Cancer talk radio has helped to change the lives of young adults living with cancer by addressing issues that are important and often life-critical to them,” added Zachary.

Hosted by Zachary and young adult breast cancer survivor Lisa Bernhard, former Entertainment Correspondent for FOX News, The Stupid Cancer Show has given a voice to millions of underserved children, teenagers and young adults living with, through and beyond cancer. The edginess and irreverent tone of this media platform challenges the status quo and has elevated young adult cancer survivorship to the national spotlight.

“This is a testament to the collective power of social media and social good,” says Bernhard. “It is only due to the support and passion of our growing global community that this program has become an international outlet for causes, issues and topics relevant through the lens of young adult cancer, public health and social welfare.”

The Stupid Cancer Show airs live on Mondays at 8pm/ET online at http://stupidcancershow.com. All episodes are archived and podcasted on iTunes at http://itunes.stupidcancer.com.

About the I’m Too Young For This! Cancer Foundation
The I’m Too Young For This! Cancer Foundation is the nation’s largest support community for the next generation of patients, survivors and caregivers between ages 15-40. Our mission is to empower young adults affected by cancer. A TIME Magazine Best 50 website and FOX News Top 10 Healthcare Blog, we support a global following of friends, fans, readers, listeners and members. Since our launch in 2007, we have helped bring the cause of ‘cancer under 40′ to the national spotlight and rallied a new crop of activists to give a much needed voice to our forgotten population. Visit http://stupidcancer.com for more information.

# # #

Matthew Zachary

Matthew Zachary was a 21-year old college senior and concert pianist en route to film school when he lost use of his left hand. He was diagnosed with pediatric brain cancer, told he’d likely never perform again and given a 50/50 chance of surviving. Sixteen years later, Matthew’s survivorship and dedication to “get busy living” has inspired countless thousands. Today, he is an award-winning recording artist and accredited thought-leader in digital health, social media, youth culture and nonprofit enterprise.

A founding member of the original Google Health Advisory Council, he launched Stupid Cancer in 2007. The organization formed to be a social bullhorn to raise awareness of his own generation of young adults, a largely unknown group in the war on cancer, accounting for 72,000 new diagnosis each year. This age group also represents a population that has not seen any improvements in survival rates and quality of life when compared to other age groups.

As CEO of Stupid Cancer, Matthew has built an extraordinary team of staff members and volunteers who have helped launch a social movement, uniting several industries to address the underserved needs of young adults affected by cancer. He has also flipped the nonprofit business model on its ear by focusing on innovation, enterprise strategies, community wealth and brand partnerships. These efforts empower and retain the organization’s massive following through award-winning click-and-mortar programs and services.

Matthew has a BA in Music, Computer Science and Sociology from Binghamton University and currently lives with his wife and twins in Brooklyn, NY.

[PRESS RELEASE] The Stupid Cancer Show Wins "Most Innovative Use Of Social Media" At 3rd Annual Classy Awards

THE STUPID CANCER SHOW WINS “MOST INNOVATIVE USE OF SOCIAL MEDIA” AT 3RD ANNUAL CLASSY AWARDS
***
StayClassy and Sponsors Offer More Than $150,000 to CLASSY Award Winners

NEW YORK, NY, October 13, 2011 – The Stupid Cancer Show won “Most Innovative Use Of Social Media” at the 3rd Annual CLASSY Awards, the largest philanthropic awards ceremony in the country which recognizes the most outstanding philanthropic achievements by charities, businesses and individuals nationwide.

With more than 2,000 nominations submitted to StayClassy for consideration, a combination of public votes and a decision by a panel of industry professionals determined The Stupid Cancer Show’s CLASSY Award win.

A program of the I’m Too Young For This! Cancer Foundation (“i[2]y”), The Stupid Cancer Show is an award-winning international live talk radio webcast giving voice to a lost generation of cancer survivors by tackling hard hitting issues from politics, health care and the environment to social media, entertainment and education.

Hosted by young adult survivors Matthew Zachary, i[2]y Founder/CEO and Lisa Bernhard—acclaimed journalist, former Entertainment Correspondent for Fox News and former Deputy Editor of TV Guide—The Stupid Cancer Show airs live Mondays at 8PM/ET at http://stupidcancershow.com. Episodes are also available for download on the show’s site, and as podcasts on iTunes.

“Cancer talk radio has indeed changed the world and we could not be happier to have been recognized by the CLASSY Awards as a leader in social media innovation,” said Zachary, a 15-year pediatric brain cancer survivor. “It is an honor to be recognized for our social entrepreneurship in the name of the more than 70,000 young adults diagnosed with cancer each year.”

About the I’m Too Young For This! Cancer Foundation

The I’m Too Young For This! Cancer Foundation is the nation’s largest support community for the next generation of patients, survivors and caregivers between ages 15-40. Our mission is to empower young adults affected by cancer. A TIME Magazine Best 50 website and FOX News Top 10 Healthcare Blog, we support a global following of friends, fans, readers, listeners and members. Since our launch in 2007, we have helped bring the cause of ‘cancer under 40′ to the national spotlight and rallied a new crop of activists to give a much needed voice to our forgotten population. Visit http://stupidcancer.com for more information.

About StayClassy.org

StayClassy (http://www.stayclassy.org) is the easiest and most affordable way for organizations to raise funds and manage donor relationships online. Based in San Diego, CA, the company develops easy-to-use web-based fundraising software for nonprofit organizations. StayClassy launched its new platform in May 2010, and has over 2,000 customers using its services. It’s free to sign up, making it extremely attractive to small and medium sized organizations on a tight budget. StayClassy is also the host of the Annual CLASSY Awards, a national award show that recognizes outstanding philanthropic achievements throughout the world.

# # #

Matthew Zachary

Matthew Zachary was a 21-year old college senior and concert pianist en route to film school when he lost use of his left hand. He was diagnosed with pediatric brain cancer, told he’d likely never perform again and given a 50/50 chance of surviving. Sixteen years later, Matthew’s survivorship and dedication to “get busy living” has inspired countless thousands. Today, he is an award-winning recording artist and accredited thought-leader in digital health, social media, youth culture and nonprofit enterprise.

A founding member of the original Google Health Advisory Council, he launched Stupid Cancer in 2007. The organization formed to be a social bullhorn to raise awareness of his own generation of young adults, a largely unknown group in the war on cancer, accounting for 72,000 new diagnosis each year. This age group also represents a population that has not seen any improvements in survival rates and quality of life when compared to other age groups.

As CEO of Stupid Cancer, Matthew has built an extraordinary team of staff members and volunteers who have helped launch a social movement, uniting several industries to address the underserved needs of young adults affected by cancer. He has also flipped the nonprofit business model on its ear by focusing on innovation, enterprise strategies, community wealth and brand partnerships. These efforts empower and retain the organization’s massive following through award-winning click-and-mortar programs and services.

Matthew has a BA in Music, Computer Science and Sociology from Binghamton University and currently lives with his wife and twins in Brooklyn, NY.

Life after Treatment Can Be Almost As Hard as the Chemo

I remember the sensation clearly. I felt sheepish walking into the room full of young cancer survivors. We had come to the Post Treatment Resource Program at Memorial Sloan Kettering to talk about life after cancer, but I wondered if I really belonged here. I had been diagnosed with breast cancer at the age of thirty-two, but that was over two years ago. I imagined the other people in the room where more recent graduates of the cancer experience, and they might wonder what this old-timer was doing here. Why did I still need a cancer support group? Shouldn’t I be over it by now?

The truth is I wasn’t close to being over cancer. In the first years after treatment, cancer still made its presence known in my marriage, my work life, and my trouble seeing past the next scan.

It turns out I wasn’t alone, and that’s why the room at Sloan Kettering was crowded with survivors who were two, three, even four years out of treatment.

Experts are beginning to recognize that the shock of cancer doesn’t end when we graduate out of the port. Page Tolbert, a former social worker at the Post Treatment Resource Program at Memorial Sloan Kettering, explains, “People think of getting a cancer diagnosis as a crisis. Sometimes the treatment itself is a crisis. But people don’t often acknowledge that the end of treatment can be a crisis as well.”

Tolbert’s insights were confirmed in a recent study featured in the Wall Street Journal this week. A survey of 1,032 breast cancer patients released by the Cancer Support Community revealed the persistence of cancer’s impact long after treatment ends. Almost 90 percent of those surveyed said they had a least one physical, psychological, or social problem, even though they average about 5.6 years since diagnosis.

A young survivor featured in the piece, Carie Capossela said, “The second-hardest phase—after the initial diagnosis—is the minute your treatment ends. The reality sets in that you have to live with this the rest of your life and the safety net is gone. That’s when you really freak out.”

The survey included women of all ages, but oncology social workers have noticed that the long shadow cast by cancer is especially jarring for young adults—of both genders and all diagnoses.

Young survivors tend to summon all our strength to sprint through treatment. We are in such a hurry to regain our “normal” lives as soon as the stubble grows back on our heads that we are caught off guard by the intensity of emotions that hit us as soon as we slow down.

One survivors I spoke to who got breast cancer at 27, explained, “I underestimated life after treatment and thought things were going to be just like they were before my cancer, but I’m finding out it’s a lot tougher than I expected.”

The expectations that were suspended while we were sick are reactivated: time to get back to work, time to date again, time to stop being afraid, time to move on. There is a prevailing idea that cancer survivors should be happy to be alive and embrace life. It is true, most of us are deeply grateful. But we are also swamped by the conflicting feelings that cancer leaves in its wake. One survivor described it in an essay in the New York Times:

I am doing my best these days to stick to the script in which the cancer patient ‘bounces back’ after successful treatment–not only bounces back but is returned to her family and friends in an improved version, a person flooded with gratitude and a refreshed love for life–but I am not doing so with much conviction. I have learned that just as you are beginning to realize you have had this dreadful disease, everyone else is starting to forget it. It is like arriving at the end of an awful trip, craving the embrace of your loved ones and finding they have all gone somewhere else. The party, if you could call it that, is over.

There is no way to avoid the pain and confusion that descends at the end of treatment. Yet knowing you are not alone can help you cope. Almost all the survivors I have spoken to said the best remedy was connecting with other young survivors.

One survivor of nasal cancer described it like this: “After treatment, you feel like you are an alien. Then you see another survivor, and you think, ‘Oh, that is one of my own.’”

That’s what I felt like when I found the post-treatment group at Sloan Kettering. You can find it here at i2y.

Emily Cousins

Emily Cousins is a writer and editor who was diagnosed with breast cancer when she was 32 and nine-months pregnant with her first child. She is currently writing a book about what it’s like for young survivors once cancer treatment is over-when the radiation burns have healed and the hair has started to come back, but everything else is completely out of whack. After almost a decade living in New York City, Cousins now resides in Northern Arizona with her husband, son, and the daughter she was lucky to have post chemo.

Think Different.

RIP Steve Jobs. Your products gave us the tools to express ourselves. Your vision inspired us to dream big. Your eye for design shaped our creative imaginations. Your acceptance of nothing but perfection fueled our entrepreneurial spirits. Your ethos for what workplace culture should be molded our leadership skills. The depth of your footprint has altered the course of global civilization. Your legacy will endure forever. Thank you for thinking differently. Stupid cancer.

 

Matthew Zachary

Matthew Zachary was a 21-year old college senior and concert pianist en route to film school when he lost use of his left hand. He was diagnosed with pediatric brain cancer, told he’d likely never perform again and given a 50/50 chance of surviving. Sixteen years later, Matthew’s survivorship and dedication to “get busy living” has inspired countless thousands. Today, he is an award-winning recording artist and accredited thought-leader in digital health, social media, youth culture and nonprofit enterprise.

A founding member of the original Google Health Advisory Council, he launched Stupid Cancer in 2007. The organization formed to be a social bullhorn to raise awareness of his own generation of young adults, a largely unknown group in the war on cancer, accounting for 72,000 new diagnosis each year. This age group also represents a population that has not seen any improvements in survival rates and quality of life when compared to other age groups.

As CEO of Stupid Cancer, Matthew has built an extraordinary team of staff members and volunteers who have helped launch a social movement, uniting several industries to address the underserved needs of young adults affected by cancer. He has also flipped the nonprofit business model on its ear by focusing on innovation, enterprise strategies, community wealth and brand partnerships. These efforts empower and retain the organization’s massive following through award-winning click-and-mortar programs and services.

Matthew has a BA in Music, Computer Science and Sociology from Binghamton University and currently lives with his wife and twins in Brooklyn, NY.

Train of Thought

A conductor on my train ride home yesterday evening hit on me. It took me by complete surprise. Cancer patients generally are not the target of smooth dudes, but I guess my hat looked like it was meant to provide warmth, given the cool temperature. He called me, “beautiful.”

My immediate reaction was the thought: “No, I’m not. I have cancer.” I wanted to take off my hat and say, “Look at me. I’m not beautiful. I am broken.”

Instead I politely thanked him for the compliment and asked a fellow commuter to move his backpack, so I could sit down to rest. As the train rolled along, I thought about that initial reaction, and tears streamed down my face. Since my diagnosis, I know my family, friends, and colleagues have continued to think of me as, well, me. But outside that circle, I have either been “someone who has cancer” or a patient. Not just another human being.
Despite the caring nature of my oncologists, especially Dr. Sharma, I can’t help but view myself differently than before my diagnosis. My frequent doctor appointments, blood draws, injections, and daily medications are a constant reminder that I am a patient.

I am a white blood cell count. I am an IgG or INR/PT level. I am a body weight used to calculate a dosage. I am a health insurance member ID number. I am a PCR remission test result. I am a data point in the APL remission rate.

Softly, in the back of my mind, there’s a phrase on constant replay: “I have cancer. I have cancer. I have cancer.”

But this train conductor, who very well might have forgotten his glasses at home, has really low standards, or makes the same comments to every woman who boards the train, didn’t see me as a cancer patient. He saw me as just another human being. It was so incredibly refreshing to have that validation, to have an external voice silence that internal mantra.

And as I continued to cry on that brightly lit train, it occurred to me that those sitting around me also weren’t viewing me as a cancer patient. They had concluded I was a complete basket case. This realization was equally refreshing. My tears shifted from those of sadness to those of relief.

The medical appointments will dissipate, and as I pass more remission tests, I will break free from this emotionally abusive relationship with cancer. Its hold on me is already beginning to loosen. I know I must tell that voice in the back of my mind to stuff it. I may have this going on, but I’m still a mother, a wife, a daughter, a sister, a friend, an employee. That list has got to be long enough to qualify me as just another human being.

Shelley Nolden

Shelley Nolden is a mother, a wife, a financial analyst, and a writer. In March 2011, an obstetrician informed her husband and her that their five-month-old unborn baby girl had no heartbeat. A week later, Shelley was diagnosed with acute myelogenous leukemia (AML), subtype 3 (APL). Shelley is currently in remission and receiving treatments to maintain that status. Like the rest of the Cancer Club, Shelley is trying to adjust to her new reality while keeping a positive mindset. Read more at www.shelleynolden.blogspot.com.

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