Monthly Archives: May 2009

Cancer Rates Decline Again* (The asterisk is for fun!)

WASHINGTON (Reuters) – A steady 15-year decline in the U.S. death rate from cancer translates to about 650,000 lives over that time, the American Cancer Society said on Wednesday.

*UNLESS YOU’RE UNDER 40

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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.

The Taking Tree: Late Effects Are Teh Awesome

On March 28th, 2007 I went spontaneously deaf in my left ear. Yes. it apparently can happen just like that. It’s called Sudden Onset Sensory Neural Healing Loss and it happens every day, mostly to old people. Evidently, the cochlea just wakes up and decides to stop working.

It was the general consensus of my entire medical team that this was — for me — in fact a late-effect rearing it’s ugly head after all that Chernobyl-level head radiation I had when I was being treated for brain cancer in 1996. Two weeks of Prednisone plus three months of recovery and I was fine. Thank God.

The experience yielded my first essay, “The Cost Of Living: No Cure For Cancer” which was featured on The Huffington Post. I somehow felt that getting it all down on paper would be karmically cathartic enough to put to rest any remaining fears, apprehensions or frustrations. We all know the saying, “I’ve been through worse” but apparently the best is always yet to come.

Well, it happened again.

February 2nd, 2009. Only this time it’s my other ear. WTF? So thanks “Late Effects Fairy” for keeping me sane and reminding me I am living on borrowed time and trying to make the most of what I’ve got right now. You should leave a dime under my pillow. And so, I’m going back on Prednisone and can only pray it works as well this time as it did last time. So here is my as-to-be-expected ensuing rant.
Life is about choice. Remission is not a cure. Survivorship is all the rage.

Why we fight …

“You’re cured, go home!,” sayeth the Doctor.
“Kiss my ass!”, sayeth the me.

Man, if I had a dime for every time I’ve heard that. Well, actually, I’ve only personally been told that once back in the stone age of 1996 when I was diagnosed with brain cancer at the age of 21. So congratulations me! I have 10¢ — and I can’t even make a phone call anymore. Hell, even gum is 25¢.

However, if I had a dime for every time I heard that from another young adult survivor, well… I’d probably have about $124. Do the math. That’s still a hell of a lot of pissed off people. And a tank of gas in your Escalade.

So, when I was actually told “You’re cured, go home!”, it was March 30th, 1996. I was an aspiring concert pianist and composer at the time just six months shy of my college graduation. At the time, however, this fabulous malignant brain tumor crippled my left hand negating 10 years of classical training and rendering my dreams to be a Hollywood film composer crushed, diced, minced, pureed, ingested, digested, and then crapped out into a martini glass. Many people know this part of my story. If you don’t, welcome to the party.

Apparently “You’re cured, go home!,” rarely takes into consideration what, precisely, your life after cancer will look like. Just a handful of my then-never-to-be-answered personal questions included “Will I be able to play piano again?”, “Will I have children?”, “Will I be alive in 5 years?”, “Who’s going to pay for all this?”, “What about my family?” “How will I ever get life insurance now?”, “How will I reintegrate myself?”, “What the hell does ‘new normal’ mean anyway?”, and the grand daddy of them all, “What now?” Mostly selfish questions but appropriately justified.

My favorite was “Where are all the other people who look like me?” (Cuz, frankly, I’m über sick of all those well-meaning geriatrics in the waiting room staring me down with pity.) “Oh, you poor thing. You’re too young for this”, sayeth the Octogenarian.
“Enjoy your gumming, Agnes or Thaddius or Esther or Pappy”, sayeth the me.

So apparently, from the lack of support I received specifically from the medical community, it seemed that life after cancer must be only about heartbeats and breaths? After all, who cares whether you’re missing a ball, a boob, half your brain, pubic hair, your dignity or perhaps several inches of your colon?

The point is you’re alive, right?

And isn’t that all that really matters?

“We’re trying to save your life, Matthew!”, sayeth the doctors.
“At what cost?”, sayeth the me.

You see, there’s this thing. It’s not really anything. Just an afterthought. It’s a meaningless term. Barely mentioned. Harmless, actually.

It’s called quality of life.

Apparently the ‘Aha! Moment’ is that there’s more to the ‘cure’ than just toxic medicine and a placental discharge back into the real world. When your clinical cancerverse runs out and the most frantically panicked day of your treatment is your last day, life does not just magically start anew. There’s no magic fairy with a bad 1940s hairstyle to sprinkle pixie dust on you and poof that whole “crying in the shower” thing mystically transmogrifies into a perfectly holistic serenity of “nothing will ever bother me again and all my cares are footloose and fancy free.”

No, life after cancer is just as — if not more important than — life with and through your diagnosis, surgery, radiation, chemo, bone marrow transplants, platelet infusions, port surgeries and stem cell fabulousness.

Ah, smell that metallic taste in your mouth.

And cancer isn’t just about babies, boomers and seniors anymore. It’s about young adults too, a population for whom there has been zero improvement in survival rates in 30 years. What makes it worse for young adults is that we actually hope to have a good 60 or 70 years of life left to live and dealing with this crap kind of cramps our style big time.

And don’t get me started on the “Can’t we all just get along?” bent.

No, we can’t. Not at least until we have a fundamental understanding that we will never be able to truly and directly relate to one another’s uniquely generational and individual experiences outside of the whole fear thing. With 99.9% of the focus in this country on the 94% of people who get cancer (10,000 children and 1.4M adults over 40), how is it fair to ask us to get along when we’ve been ignored?

Personally, I didn’t want to then and I still don’t want to now have my survivorship associated with anything that even remotely stinks of children, boomers or seniors. I like our little niche club. It’s like Fight Club with chemo — only we are allowed to talk about Chemo Club and tag/share/tweet/blog/digg our bitterness, angst, anger, frustration and countercultural resentment right back out to the world.

The young adult cancer movement is just awesome.

Permission to rebel. Speak our mind and finally have a voice…

“This is what matters to us!”

Some say I was given a gift. I often see it that way. The gift of surviving cancer. In fact, I once heard someone say that they don’t consider their cancer experience a gift because they’d “never want to give it to someone else as a present.” Isn’t that why they have gift receipts? Could you just imagine a gift receipt for some cancer?

Me: “I’d like to return this.”
Apple Store: “Is something wrong with it?”
Me: “Uhm, yeah. It’s cancer.”
Apple Store: “Did it not work with your operating system?”
Me: “Dude, it’s cancer. I want a refund.”
Apple Store: “How much RAM do you have installed?”
Me: “English dude, it’s cancer. I want a refund.”
Apple Store: “Sorry but we only do exchanges.”
Me: “Jeez. OK. What does that mean?”
Apple Store: “You can get something of equal or lesser value.”
Me: “F@ck me! Fine. I’ll take diphtheria.”
Apple Store: “I’m sorry sir we’re out of that.”
Me: “Can you suggest something semi-nonlethal?”
Apple Store: “We have iAbetes and eBola, our top sellers.”
Me: “Actually, I’m just going to leave now.”
Apple Store: “Have a good day sir.”

I digress. My “gift”, like that of so many others, is one that has a tendency to keep on giving. And giving. And giving. In fact, it’s been so incredibly generous, that I can safely say that each and every year since I was “cured”, cancer’s gift has yielded way too many fond memories of said generosity. Thankfully, I should strenuously point out, none of which to date have involved a recurrence.

The issue I can’t help but continue to shove down society’s throat is plain and simple. There’s more to curing cancer than just research. Research. Research. Research. Marcia. Marcia. Marcia. See you on the see-saw Cindy!

While everyone is relaying, racing, training, frolicking and crocheting for the cure, millions of Americans (and in particular hundreds of thousands of young adults) actually don’t die and are faced with the challenge of rebuilding their lives, starting over, often from scratch without any help.

And that is not OK — especially for young adults.

Where is the awareness for “what’s next?”

We live in a society of extremely generous individuals who want to help. They want to make a difference. But it’s often just too easy to drink the wrong Kool-aid and find out your good intentions have been subverted by clever branding, peer pressure and colorful marketing strategies that make unicorn promises.

I’ve been saying this for 10 years but “Do you know where your money goes?”

What is the transparency and accountability policy of your favorite charity? Have you ever asked to see it? Or their tax returns? Have you ever visited Charity Navigator’s website and seen what one of America’s #1 nonprofit watchdog groups has to say? How do you know you are actually making a difference? It’s rhetorical I suppose.

It took 20 years for the word “survivorship” to enter the mainstream of our pseudo-collective consciousness as a survivor community. So the basic concept of “what’s next” is beginning to penetrate, thanks, in part, to the Lance Armstrong Foundation along with emphatic passion and commitment of the young adult movement.

But for the overwhelming majority of Americans — and I suppose you truly can’t fault them for this — cancer is still the most feared subject in the country, according to a recent survey by the Tower Cancer Foundation. We fear cancer more than terrorism. That’s how bad it is, the irony being that, on the whole, while a pejorative experience, it is a largely survivable experience, unless, of course you’re between 15 and 39.

There was a time when we feared HIV just as much. But it’s not a death sentence in this country anymore. When did that change? Was there a tipping point? An exact moment when the rift tripped? And, more importantly, will we ever get to that same place with cancer? I don’t think it’s a question of if, but when.

My job here isn’t to scare people to death with the notion of recurrence, secondary cancers, late effects, post-traumatic stress, etc… but they are grounding realities that are instilled within the very nature of survivorship, inconvenient truths that cling to the inner digestive walls of our psychology. Cancer may actually be a gift. It may give us perspective, a new philosophy, dogmatic reassessment or even grounding purpose.. but it does take. And sometimes what it takes cannot be replaced. Reminders of it’s influence, no matter how subtle, influence how we choose to live our lives… as victims or survivors. As sufferers or warriors. As fighters or champions.

Challenge is opportunity and, while we’re light years from where we came, we still have quite a ways to go. We’re not where we were but where not where we’d like to be. The very fact that we are in a position to challenge cancer ‘progress’, ask hard questions, take on the establishment and hold accountable the government, the insurance industry and major cancer charities is itself a social statement of progress.

In fact, if you’d have told me when I was diagnosed that 13 years later there’d be two cancer talk radio shows — one just about young adults — I’d have told you to go jump off a bridge. If you’d have told me that there would be a cancer revolution from the youth culture, I’d have thought you were nuts.

If you had told me that “the next me” wouldn’t have to go through the same crap as I did”, I’d have asked you to just leave the room.

Yet here we are. And isn’t that what cancer advocacy is? Ensuring that the next “you” doesn’t have to go through the same crap you did? See, the taking tree does give. Whatever cancer has taken away from me in part or in full has been replaced with passion, energy, commitment and responsibility to roll up the sleeves and give back. This is the virus we want to spread.

The disease of social consciousness, personal accountability, self-sacrifice, altruism and both individual and community reward.

One in 50 Americans between 18 and 40 and one in 100 American college students is a cancer survivor. Chew on that. They are all around us but you’d never know because we look just like you. It is important to recognize that we have made incredible strides for the majority of people who are affected by cancer each year. But for young adults, we are only just now getting our comeuppance and a global voice to share our own generational grievances, public health disparities and too-often ignored unique survival issues.

After all, at the end of the day, the message is “Shit happens but this is how I am going to get busy living, dammit.” We want cancer to be a speed bump so we can get back to our derailed plans. How dare this get in my way? Seriously.

The taking tree has got nothing on me. On you.

On anyone.

So if and when you hear the words “You’re cured, go home.” or “Now get on with the rest of your life.” or “What have you got to complain about, you’re alive!” or “There are people worse off who didn’t go through what you want through.”, just remember the young adult social movement has your back like no one else. The rest of the world doesn’t have to get it, but we do.

So take my ball, boob, brain, hair, hearing, colon and dignity.

I will find something equal if not more fabulous to replace it with.

Perhaps a Snuggie.

After all, if cancer is the worst thing that has ever happened, just think, “Been there. Done that. What could possibly be worse? Bring it on.”

Then again, if it’s a gift, just don’t re-gift it.

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.

Cancer From 30,000 Feet: Are We There Yet?

Cancer From 30,000 Feet
Are We There Yet?

By Matthew Zachary

Life is about choice. Remission is not a cure. Survivorship is all the rage.

Why we fight…

Seeing as how I’m writing this on an airplane, the title may not actually be as clever as it seems. However, with a little foresight, I am hoping that by the time I finish this piece, it will be euphemistic and metaphorical.

I have chosen a life whereby not a single moment passes that I do not think, eat, sleep and breathe cancer advocacy, which, by my own personal definition, means “ensuring that the next ‘you’ doesn’t have to go through the same crap that I did” as a 13-year survivor pediatric brain cancer. I suppose you can take cancer out of that equation entirely in such that my aphorism would be universally applicable to nearly anything, I suppose; civil rights, gay rights, poverty, education…

But let’s say for a moment that we could peer down 30,000 feet to our society as a whole; and I’m not just talking about Americans. All humans. Are we a decent people? By and large, do we not all just want to live productive lives and contribute to the common good? Idealistic as it may sound, it’s unfortunate that a small percentage of bad apples continue to ruin it for the rest of us. Thus we have the hyperbole of human nature and perhaps the reason why change happens so slowly and only from within.

Cancer is only about 100 years old in terms of a recognized disease that the nation felt worthy of focusing resources on. The American Cancer Society was originally founded in 1913 by 15 businessmen and physicians in NYC under the name The American Society For The Control Of Cancer. Then came The National Cancer Institute established in 1937 as part of the New Deal’s National Cancer Institute Act.

In 1949, today’s Leukemia & Lymphoma Society was founded in NYC as the Robert Roesler de Villiers Foundation. Nearly 35 years later, the Susan G. Komen Breast Cancer Research Foundation was formed in 1982 and, more recently, The Lance Armstrong Foundation took its place as a game-changing institution. Considering LAF was founded in 1997, it would seem that, from 30,000 feet, it is taking less and less time to gain effectiveness with the right strategic plan and vision.

And let’s not forget that the “War on Cancer” – a campaign term I have grown to intensely dislike and disavow – is a mere 35 years old. (I’m 35 years old). And now we have the “War On Cancer II: The Cancer Strikes Back”. So, as far as all these ‘big gun initiatives’ are concerned, we’ve had a whole lot of smart people working on this cancer thing for quite some time. For over 100 years. That’s a lot of time, talent and treasure.

But what is 100 years in the scheme of things?

After all, from the perspective of an evolutionary biologist, cancer has been around for millions, perhaps billions of years. It is, after all, a naturally occurring physiological process. By simple definition alone, cancer is simply, “any malignant growth or tumor caused by abnormal and uncontrolled cell division.”

The rub is, our homo sapien immune systems used to be able to deal with cancer cells much like it deals with cuts, bruises, broken bones and the sniffles. You get hurt. You get better. But for some reason, in spite of medical advances, the wildfire increase of cancer incidence during the 20th century–that ironically coincides with modern industrialization, agribusiness, technology-induced creature comforts and the McRib– has shown that our immune systems aren’t doing such a good job anymore.

Our bodies can’t inherently fight the cancer cells the way we used to before. Perhaps our immune systems aren’t doing so well anymore because we are, in fact, living longer than we are genetically predisposed to. Or, perhaps that we have to fortify our bread, juice and milk with vitamins they should normally contain but don’t because of our nutrition-deprived soil?

So what do we do to fight cancer in 2009? What elixir do we offer to bolster our immune systems? We poison ourselves–to the point of near death in many cases such as my own–with the hope of killing the cancer cells (which ironically lack immune systems of their own) along with everything else inside us that technically grows back (stomach lining, hair, sperm, dignity). The goal? Cure.

We want to be cured. We want to know that we are cancer free and that, God willing, we won’t have to deal with this again in our lifetime. Sounds marvelous. But from 30,000 feet, remission from cancer doesn’t sound like a cure. Cures last forever, don’t they? Like the measles vaccine. One shot. No measles. Forever. Isn’t that why it’s called a “cure”?

After all, you can always get cancer again, right? (As I wrote that sentence I realize I’m preaching to the choir since this is being published by MSKCC) Many survivors are actually hyper-predisposed to relapse and secondary recurrence *because* of their initial treatment. Now *that’s* the gift that keeps on giving! But that ain’t ‘cure’ for me.

That’s ‘cure… for now.’

And ‘cure… for now’ is scary. It’s not hopeful. It’s not optimistic. It’s the Boogeyman reality check that few want to acknowledge. But we want to sell hope, not reality. We want to sell ‘cure’ to the masses. It’s sexy. It’s positive. It’s delusional. But it works.

And it raises billions every year.

And it’s attached to a broken healthcare and insurance system governed by profit instead of ethics that is consciously disenfranchising millions of Americans in the fight of their lives every single day.

And this is not OK.

So while the majority of society still continues to blissfully believe not just that cancer is contagious but that it is one single disease (like the measles), it’s no wonder we keep pushing ‘cure’ – because the truth is scary: that there is no cure to cancer in the sense of a magic bullet, fairy dust gelatin capsule just like there has been and will continue to be no cure to diabetes, HIV or any similar chronic condition. Bottom line: so long as you can get it again, it ain’t a cure. Remission is not an excuse for a cure.

So, again, from 30,000 feet, what’s the deal?

The current mission of today’s National Cancer Institute is to “eliminate death and suffering” with regard to cancer. I can live with that.

1. Get cancer.
2. Try not to die.
3. Focus on quality of life, not quantity.

From a death sentence to a life sentence, so cancer now becomes a chronic condition.

They’ve even gone so far as to explore the elimination of the word “prevention”. After all, how can you actually prevent cancer when infants are born with brain cancer and leukemia? How can you prevent cancer when chain smokers live to 100 and athletes in peak physical condition like John Lester, Lance Armstrong and Eric Shanteau and get struck in the prime of their lives for no apparent reason?

Who is doing this math, people?

So to keep up with a time of smarter consumers, we’re now seeing a semantic public health shift from “prevention” to “risk reduction”.

Reduce your risk of getting cancer! Yee Hah!

And voila! A new fear is born.

You can’t prevent it, people! The Boogeyman is coming for you because risk reduction is a game of chance. It’s the ultimate poker match.

Outside of the obvious – don’t smoke, eat right, exercise – how is that any different than reducing your risk for anything outside of pregnancy, gambling and car accidents?

And there is fault with this logic too. We can only reduce the risk of factors we actually have control over. We have no control of various sources of key influence that we already know significantly contribute to our overall well being.

We don’t have control over the water supply. (Move to Montana, perhaps?) We can only do so much to trust our low-mercury fish actually has low mercury. (Organic vegan lifestyle, anyone?) The very air we breathe is laced with all sorts of fabulous multisyllabic chemicals. (Montana, again?)

From 30,000 feet, instead of treating symptoms and racing for the ‘cure’, shouldn’t we be racing for the ’cause’? In lieu of continuing to put band-aids on a leaky faucet, shouldn’t we try to understand what caused the faucet to leak in the first place? Shouldn’t risk reduction be a shared responsibility between individuals and business? What good is juicing kale if you live in Los Angeles and breathe that delicious brown smog for breakfast?

I am a cancer advocate. I am trying to make the next “me” not have to go through the same agony I went through as a 21-year-old college student diagnosed with brain cancer in the prime of his life. The next generation of cancer survivors deserve better than what we’ve been handed – more cancer incidence and a broken healthcare system compounded by a profit based dystopian medical insurance oligarchy.

Solutions to problems always begin with dialogue. Mine started 13 years ago and counting. I am still here. You are still here. This is why we fight. Forget the cure. Survivorship is all that matters. 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.

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