Showing posts with label cancer. Show all posts
Showing posts with label cancer. Show all posts

Epigenetics Research Brings New Strategy to Cancer Research

Posted by admin on 12/16/12

By Doug Bintzler

The epigenome is an extension of the genome. Epigenetic mechanisms cause specific genes in certain cells to become inaccessible, thus causing these genes to be silenced. Cells become increasingly specialized, or differentiated, into a specialized cell during development. For example, liver cells and lung cells carry the same DNA. However, only certain genes are active in liver cells while other genes are active in lung cells. This is the result of cell differentiation. What typically happens during cellular development is regions of DNA become methylated and wrap around protein molecules called histones. Genes bound to histones are silenced. This determines how a cell will differentiate.

Changes in the Epigenome

Environmental influences can impact the epigenome. Ultraviolet light and chemicals associated with tobacco are two examples. These influences can affect factors in the epigenome as well as cause mutation. Mutation has often been thought of as the primary causative agent of many cancers. However, mutation in the region of a silenced gene should not cause cancer. A silenced gene does nothing so it is as if it is not even there. Changes to factors in the epigenome can loosen the DNA bound to histones. This can cause the silenced genes to become active. Cells that loose this control may go into a stage of rapid division, eventually developing into cancer.

New Treatments for Damage Caused by Changes in the Epigenome

Typical treatments for patients with cancer include radiation therapy and chemotherapy. Although these traditional forms of treatment are sometimes successful, cancer remission does not always happen. Plus, these treatments attack both cancerous and healthy cells. This makes them very taxing on the recipient with no guarantee of remission. In many cases these therapies are the best means of treatment. Fortunately the treatments and how they are administered are continually improving.

The problem with genetic mutations that cause cancer is that the mutation is not reversible. People who survive cancer may still carry the genetic cause. If this is the case, then they may pass the cause on to the next generation. This is one reason doctors evaluate the family's medical history. Unlike mutation, epigenetic change is reversible. Some forms of treatment currently in clinical trials use drugs to repair cancerous cells instead of destroying them. Unfortunately, much like radiation and chemotherapy, these drugs are known to cause damage to healthy cells when high doses are used. However, some success has been seen when they are administered in low dosages. Azacitidine and decitabine are currently being used in studies at John Hopkins. Studies being conducted at the University of Texas MD Anderson Cancer Center are using similar treatments with Leukemia patients with varying degrees of success.

Epigenetic research is a field that helps science understand more about the complex relationship between DNA, histones and cell differentiation. It provides a new direction for the potential treatment of patients afflicted with cancer.

Doug Bintzler is the Laboratory Director for DNA Analysis, LLC. They provide automated DNA sequencing and fragment analysis services. Reprints of this article and other education resources are available at http://www.agctsequencing.com
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Progress!

Posted by admin on 8/6/10

I just have to make note of my Hair Tracker progress. What a difference a month makes. Although Cody has been retired for quite some time, her work is truly done.

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Cleaning Cancer Out Of My Apartment: An Initiative

Posted by admin on 7/11/10


In continuing to make this remission thing more official, I recently un-medicalized my apartment. No government leaflets about "Cancer and Me." No excess pill bottles. No patient binder. What we've affectionately dubbed the Apothecary Table has been eradicated.



Part symbolic measure, part need to clean my dusty apartment, the moment I cleared this table I knew it meant something. In fact, I deemed it so meaningful I decided to put everything back on the table to take a picture so I could share the "before" and "after" with you all. 



And since I am a self-proclaimed pack rat, I didn't feel like I could just throw all this stuff away. It's  been banished to a box simply labeled "DO NOT OPEN." Enough said.




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The Cancer Dancer dances on this June!

Posted by admin on 5/25/10

 In the Looking postcard
   Join Zephyr Dance for our 20th Anniversary Concert

in the looking
June 24, 25 and 26 at 8:00pm
Epiphany Episcopal Church
201 S. Ashland in Chicago (map)
Tickets are $20 for adults,
$15 for students and seniors
For tickets and information, visit our website

...And don't forget to sign our birthday card!
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Welcome back...

Posted by admin on 5/19/10

Behold my calloused, filthy gems:

I've been extra cautious about the welfare of my feet throughout treatment. They've been heavily guarded by the ever-durable Target sock (perfect thickness and warmth for a marley floor) for fear that I'd manage to slice my foot open while doing some treacherous pas de bourrées.

But the weather's getting warmer, and unless I can shuffle around in my dingy old J. Crew flip flops something is truly missing from my spring/summer self. Plus, Zephyr's annual Illinois Wesleyan Tour de Dance Appreciation class is upon us. And my turquoise socks ARE NOT considered nice rehearsal attire in any sense of the word. (Check out the neglected ones heaped in the corner...)

Oh bare feet, I've missed you so very much.
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In the name of millimeters...

Posted by admin on 4/8/10

Four more treatments to go...the end is in sight. Not quite plain view, but that point when you're driving southbound on the Edens and you get that first shadowy glimpse of the Sears Tower. I've certainly taken better care of myself this time around. (Translation: not drinking so much that my veins disappear. Even Chemo Girl gets to have a little fun!)

Another test is upon us. Tomorrow I visit the friendly radiology department at NorthShore for a CT Scan. Though February's PET Scan showed that there is no more abnormal uptake (the cancer is not active/spreading), my lymph nodes were still enlarged. And by enlarged I mean centimeters. These nodes have been seriously cramping my lung capacity's style for far too long, so I'm really excited to see the results of tomorrow's photo shoot.  Not only am I excited, I'm sure that they've shrunk. Considering my sizable knowledge of the medical field,  here are several reasons why I might be the most optimistic (or delusional?) girl you know:

On Monday, I was doing a pretty intense pectoral muscle stretch during rehearsal and discovered that I was able to breathe easily in the position for the first time IN THREE YEARS. The reason that was my first foray into that particular stretch in awhile is because during Zephyr's usual Monday yoga routine I typically feel like falling down. Recently, however, I'd compare my energy level to that of the Grinch when he lifts the sleigh over his head. Serious power! So not only does my strength and energy level continue to dramatically rise, but I actually feel like I can understand the clues my body gives me.

Time to drink a really awful concoction no milkshake will mask in the name of measurement. Millimeters and such....
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A Wedding of Wigs and Wicks

Posted by admin on 4/2/10

So I'm hoping that you are all very slow readers. I've been immersed in wedding hoopla and can't seem to jump back in to writing about cancer. Go figure! But really, who am I helping by looking at the 37th blog filled with inspiration boards and DIY projects for a glamorous backyard shindig?

Last weekend, I was unbelievably thrilled to partake in one of my oldest and dearest friend's wedding. I was super honored that Jessie asked me to be her maid of honor and spent the last nine months obsessively asking how I could help with the planning. So when this business popped up in December, I had plenty of concerns. I wanted to participate in the same capacity but was unsure of how I would feel and (yes, I'll admit it) look. It's a moot point. Who's looking at the maid of honor? Well, I wanted to keep it that way and opted to bring along my new friend Cody for a bit of support.


I will say this: I've worn "Cody" (the blonde-choppy counterpart to my otherwise scantily clad head) maybe 7-8 times, and I still can't decide if I'm sold. For the record, Jerome Krause names their wigs, not me. I'm not sure whether anyone was fooled, but she stayed intact all night. Even through my own personal rendition of "Thriller."

(If it weren't my 4th day after chemo I swear I'd crop out the lower 
right corner of this pic. You get the idea regardless.)

 Bottom line, we all had an amazing and sentimental weekend. Certainly I could have gone without splitting my dress up the back, but I blamed the steroids and some dance floor lunges and moved on. 

In terms of feeling up to the trip, I am positive that the excitement leading up to last weekend helped me fly through the usual chemo side effects. Amidst concerns about my weakened immune system, I was prescribed a 3-day neupogen injection to boost my white count while we navigated one too many germy airports. I was nervous that the brief treatment would be painful, but I made it through with just a bit of jaw pain.

In conclusion, (it feels like time to be conclusive)...

Although this routine is getting pretty old, attending Jessie's wedding/taking a mini-vacation/discussing the sustainability of salt licks(?) in a toast to 120 people briefly made me forget that this business had ever been an issue.
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Ripping off the Band-aid

Posted by admin on 3/18/10

As bewildered as I've been by this whole hair loss/head shaving debacle, it's over. I decided a while ago that sharing this facet of my experience was particularly important. I wonder if I had stumbled across a similar blog posting a few months ago I would have dealt with it differently. Special thanks to Matt's crafty editing work and my fantastic stylist Courtney Engel's serious abilities with clippers. Although it's not featured in this particular video, her work with thinning shears is also incomparable.
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An Inspiring Story

Posted by admin on 3/17/10

This is sportswriter Rick Reilly's tales of spending time with Denver Nugget's coach and current cancer patient George Karl. His treatment sounds much more intense and invasive than mine, and I admire his open attitude and spirit. Thanks for sharing, Matt!

http://sports.espn.go.com/espn/news/story?id=4997277
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Support the American Cancer Society!

Posted by admin on 2/25/10

Help our friend Bryan Kappy raise money for the American Cancer Society. He's taken on the unenviable task of running Chicago's annual Shamrock Shuffle. (The sheer thought makes me hyperventilate.) Go Kappy Go!!!

http://main.acsevents.org/site/TR/DetermiNation/DNFY10Illinois?px=14175880&pg=personal&fr_id=25051&fl=en_US&et=XVj27bXWBgTGUiwvI0fAMA..&s_tafId=469704
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The Adventures of Chemo Girl!

Posted by admin on 2/10/10

Her special power? In moments of sheer exhaustion, Chemo Girl surprises her fiercest foes with sudden bursts of energy: jumping in heels during a rare night out, dancing through the nausea in company class.

Every one of these startling instances is her opportunity to deliver a time bomb to these vicious invaders. Her energetic optimism is just a reminder: your days are numbered, cancer cells.

And she wears a cape.

Stay tuned! Tomorrow Chemo Girl meets her fate at the PET scan...
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But I'm a Leo!

Posted by admin on 1/6/10

...So you can imagine my surprise, bewilderment and confusion when after 26 years of looking to that bold, fierce symbol for any novelty fortune-telling needs my horoscope indicates that my birthday now falls between August 23 and September 22.

Through six months of self-diagnosis, internet "research," useless doctor visits and a skin tone that quickly faded from healthy to ghost-like, cancer never for a second entered my consciousness. Not once. Even as I sat in the hematology lab telling the 85th intern to ask that I DID NOT remember experiencing any fevers recently I was still convinced it was just pneumonia.

The 95% certainty of my doctor that it was Hodgkin's got through to me the next morning. So after a brief three minutes of being scared out of my mind I started fighting cancer.

Because my birthday is July 30.

The idea to post "The Cancer Dancer" came to me not long after receiving that life-altering information. (Catchy title, inspiring story...read: book and movie deals.) I had immediately considered the implications to my dance career: as an artist, an athlete and as an adult who has to make money. My crazy dance life will be back soon, and this will be the chronicle of how it returns.
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Ethan Zohn, winner of Survivor Africa, Talks About Hodgkin’s Lymphoma

Posted by admin on 1/5/10



THIS IS A REPOST FROM THE GREAT FOLKS OVER AT GiveForward.com!

Most reality TV stars have their fifteen minutes of fame and then are never heard from again (unless of course they later appear on the Surreal World). But Not Ethan Zohn. In 2002 Ethan took home $1,000,000 for winning Survivor Africa and instead of wasting his money like so many others, he used it to help start a non-profit called Grass Roots Soccer that fights the spread of HIV/AIDS. Today, the organization has helped educate over 300,000 young people in 15 different countries around the world and has some pretty heavy hitters like Bill and Melinda Gates, Nike and the Ford Foundation backing it.

But conquering reality TV and co-founding a global non-profit pale in comparison with Ethan’s most recent challenge – a battle with cancer. Since last April, Ethan has been publicly battling a rare form of Hodgkin’s Lymphoma. Fortunately, Ethan had some great news recently. As reported by People Magazine on December 10, Ethan’s most recent PET scan showed that this Survivor is crushing cancer and for the first time since his diagnosis he has no active cancer cells in his body.

Not only did Ethan beat cancer, but by taking his battle public he has helped others get diagnosed including a 25-year-old GiveForward user who raised $1800 on GiveForward for his Hodgkin’s treatments after reading an article about Ethan in People magazine.

I recently had the opportunity to chat with Ethan about his battle with Hodgkin’s Lymphoma and how young adults are falling through the cracks in the fight against cancer. You can also read the original unedited interview on PlayCity

Ethan Austin: In your battle with Hodgkin’s Disease you’ve managed to keep a positive attitude throughout. How does fighting cancer compare with some of the other things you’ve done in your life like winning Survivor or starting a global non-profit?

EZ: It doesn’t even compare at all. This is by far the most difficult thing I have ever faced. I mean this is the closest I’ve ever come to death. You might look okay on the outside but inside your body, there is a war of the worlds going on. It’s a challenge. But I just got some really good news the other day so I’m feeling okay.

EA: You’ve been very public about your fight. A lot of people with cancer choose to keep the matter private. Is there anything you want to say to other young people out there battling Hodgkin’s?

EZ: I’ve been fortunate enough to have this platform to speak and I hope to be a megaphone for this generation. By being so public my goal has really just been to bring awareness to the issue. Young people in their 20s and 30s are often forgotten in the fight against cancer. There’s been huge improvements in survival rates for older adults and with pediatric cancers but survivor rates for young adults haven’t improved in 30 years. Today, a young adult has the same chance of getting and dying of cancer as they did in the 1970s. Our demographic has fallen through the cracks on every front including clinical, research, financial and pychosocial.

EA: In your opinion, what needs to be done so our generation stops falling through the cracks so to speak?

EZ: We need more money to go to research for treatment. For those with cancer or those who will diagnosed with it, new treatments can literally be a matter of life and death. But improving survival rates is not just about more money for research. It’s also about early detection.

Early detection is one of the biggest keys to surviving cancer, but most young adults are diagnosed with Stage IV when it’s often too late. One of the problems is that our generation thinks we’re invincible. Many students and young professionals either don’t have access to doctors or choose not to see them. Part of the problem also lies with the health care providers. A lot of doctors misdiagnose cancer. They think the patient is too young to have cancer so they don’t diagnose it until its too late. We need to train health care providers to consider cancer as a possibility to ensure earlier diagnosis.

There are other issues that we need to work on as well such as lack of access to clinical trials and the lack of age-appropriate support for young adults with cancer. At treatment, I see older and younger. Diapers and dentures. I feel like I’m the only going through this because I never see anyone like myself. But on the positive side, I think the voice of the young adult with cancer is now being heard. We each have a role to play in supporting research and it’s urgent that everyone continues to support this effort.
EA: Last Question. This one is non-cancer relatated: I’ve heard you appeared on an episode of Discovery Channel’s Pitchmen with the late, great Billy Mays to pitch the EZCrunch Bowl (a bowl that is supposed to keep cereal from getting soggy). Please indulge us. Does this thing really work, or did you just come up with the idea because you wanted to meet the one and only, supremely awesome Billy Mays?

Ha. Yeah it really works. I had the idea back in college in 1994. I was just trying to come up with something fun that makes people happy.

[editors note: Ethan was too modest to plug EZ crunch bowl but I have done an independent investigation and early reports indicate that the bowl is going to be awesome to quite awesome. You can be the first on your block to own this revolutionary cereal-saving device by pre-ordering yours today at EZcrunchbowl.com]
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Cancer, you are STILL my Bitch!

Posted by admin

Yeah, that's right Mr. Cancer! You are still my BITCH!
Pet scan came back clean, no evidence of disease!
I still have a few enlarged nodes in my chest, but they are unchanged from my last 4 PET/CT scans and have 0 uptake.

That's why I'm like "Fuck-a-bunch-a-cancer"!
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Breast Cancer Awareness Month?

Posted by admin on 10/8/09

Breast Cancer Awareness Month? That's right. October is Breast Cancer Awareness Month.
You show me someone who has NOT heard of Breast Cancer and I will show you the most ignorant son-of-a-bitch to walk the earth!
Where's my Lymphoma Month?
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Sad...

Posted by admin on 10/2/09

Yesterday one of my Hodge Friends lost her 13 year battle.
Adrienne, you will be missed.

The photo below was taken in Boston a year or so ago.
Adrienne is on the far left.


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My blog was mentioned in Newsweek!

Posted by admin on 7/31/09


The other day, Newsweek did a story on young folks with cancer. They talked about how we use humor to get through the whole cancer thing. In the article, they mentioned a few humorous cancer blogs, mine was one of them.

Below is the article.


A Malignant Melanoma Walks Into a Bar...
Cancer kills more young people than any other disease, and survival rates have not improved in more than 30 years for people in their 20s and 30s. How some patients are using humor to fight back.


Crammed inside a subway car in Manhattan—feeling remarkably generous, as I often do these days—I smiled at a young woman with a fancy black ponytail hairdo who was intensely staring at me. She didn't smile back. She said: "This is the second time you stepped on my shoe."

It was quite possible that I stepped on her foot. I'm a little clumsy nowadays. Almost three years ago, at age 29, I was diagnosed with stage III colon cancer The chemotherapy treatment that followed left me, among other keepsakes, with neuropathy in my feet, numbness and tingling similar to what advanced diabetes patients experience. One day I walked two blocks barefoot before I noticed my missing sandal.

"I'm sorry," I said, then whispered, "I know this will sound strange, but I can't feel my feet."


She rolled her eyes.

It was funny. In this crowded train, nobody was paying attention to my cancer, and it all seemed surreal again: my numb feet, my uncertain life expectancy, the loneliness, all coupled with gratitude for being alive, even if it means sharing a world with this bitch on the 1 train.

Cancer. Hilarious. I later typed these words into Google and found Kaylin Andres, a 24-year-old San Francisco fashion designer who was diagnosed with Ewing's sarcoma, a rare form of bone cancer normally fond in children, last September. She uses her blog, Cancer Is Hilarious, to document her experience in a way young people could relate. Thank God for cancer humor. I need something other than yet another study that offered grim survival rates or scary-sounding side effects.

Cancer Is Hilarious is just one of the hundreds of blogs combining realistic cancer confessions with humor: Making Cancer My Bitch. My Blood Hates Me. What’s Up Your Butt?Kiss My Bald Head. I’m Not an Asshole. Surgically Speaking. I’ve Still Got Both My Nuts. Virtually all of them are written by cancer patients younger than 40. The blogs are just one way younger patients are addressing the absurdity of life with cancer with humor, rather than pink-ribboned, glassy-eyed earnestness.

About 70,000 people between the ages of 18 and 40 are diagnosed with cancer every year, representing about 6 percent of all new cancer cases. About 10,000 young adults die from cancer annually, more than from any other disease. This is not the best statistic to stumble on when you are looking online for hope, as I did in September 2006 after my doctor told me he found a growth in my colon. There I was—nonsmoker, athlete, young—diagnosed with colon cancer, the disease that more commonly afflicts overweight, elderly men. And all I could think was: how inconvenient. I was a travel writer and had just scheduled trips to Rome and Cologne for the following week. Bummer. I would have to reschedule those flights.

Then I did what anyone of my generation would do: I Googled "colon cancer." Within seconds, I found out that my cancer stage, advanced stage IIIC, gave me a 44 percent chance to survive five years. I swore I would never use the Internet to research colon cancer again. (That promise lasted all of five days)

At the same time, I started receiving books, stacks of self-help volumes from well-meaning people. Books claiming that cancer was hate materialized in the body of people who don't love enough. Books promising you can cure cancer by drinking wheat-grass juice. It made me want to throw up, even before my chemotherapy regimen started and I became a vomiting expert. I didn't need more things to make me feel guilty and excluded. I already felt like an outsider. I was by far the youngest patient in the oncology ward. I was too cynical to believe herbal remedies were going to cure me but unwilling to venture onto medical Web sites, where the depressing prognosis stats were lurking, ready to scare the hell out of me.

That's when I found Planet Cancer, the most popular cancer humor Web site. It was founded in 1995 by Robin Blue, Paul Cox, and Heidi Schultz Adams, Texans and cancer survivors then in their 20s. They coined the term "cancertainment" to describe the growing subculture of young cancer patients seeking both more information and a space to indulge in inside jokes like "What's one of the top reasons to date a cancer chick? Recreational drugs are paid for by insurance."

According to Kairol Rosenthal, author of Everything Changes: The Insider's Guide to Cancer In Your 20's and 30's, the traditional cancer support system is set up to deal with older patients. Young people want to talk about different issues that the typical cancer patient might consider taboo: How do I have sex with a colostomy bag? How do I masturbate in a hospital? Will I have to choose between chemo and grad school? Rosenthal, a slim brunette with a posture of a dancer, was diagnosed with thyroid cancer nine years ago, when she was a modern dance choreographer. Unable to take radiation treatment, she currently has two tumors resting on her jugular vein, although they haven't been growing. Now 36 years old, the Chicago resident doesn't believe in the benefits of thinking positive. "I believe in the power of realistic thinking," she said. "And the reality is, you know, this sucks."

This is a sharp departure from the cancer survivorship rhetoric of the last 20 years. For members of an earlier generation, curing oneself of cancer was often associated with turning inward to positive thinking and spirituality and away from anything resembling cynicism and irony. Experts nowadays say that the power of positive thinking might be overrated (thankfully). Jimmie Holland, a psychiatrist at the Memorial Sloan-Kettering Cancer Center in New York and the author of The Human Side of Cancer, confirms that patients often feel that being sad, scared, upset or angry is unacceptable and that emotions can somehow make their tumors grow. "For most patients, cancer is the most difficult and frightening experience they have ever encountered," she writes, and she argues that the emphasis on positive attitude invalidates people's natural and understandable reactions to a deadly disease. "Many negative, pessimistic people survive cancer, while others who believe positive attitudes will cure it do not. I do not believe for an instant that people whose cancer progresses have a weaker spirit or character than anyone else."


Despite their cynicism, young cancer patients are some of the most vocal cancer activists out there, precisely because they don't feel like they need to whisper after they lose a breast, a testicle, or sex drive. They start foundations, write books and blogs, launch clubs, and use technology to spread the news. Garland Harwood, a 29-year-old public-relations manager, combined both advocacy and humor when he planned a fundraising event on behalf of the American Cancer Society of Brooklyn, N.Y., which helped when he was diagnosed with sarcoma four years ago. Leery of the usual cancer fundraising event, where clichés are recited and pictures of deceased patients put up in a heart-wrenching slideshow, Harwood instead launched "Comedy for Cancer," a fundraising event in Brooklyn, featuring the stand-up comedian and Hodgkin's lymphoma survivor Nick Ross.

Ross, 27, first got the idea to create a stand-up show about cancer last year, when a man sitting on next to him on the bus asked: "Did you shave your head because you're losing your hair?" Ross, briefly appalled by the incongruity of the question, decided to be brutally honest: "No, man. I am on chemotherapy." Hoping to reconcile with a bald cancer patient, the man offered: "I am in AA." The man's friend chimed in, "I'm addicted to porn." Ross compiled this and other absurd moments in his life as a marginalized citizen in his 35-minute stand-up show, excerpts of which he performed at the fundraiser.

"Comedy for Cancer" was a huge success and resonated especially well with the "Brooklyn hipster crowd," says Harwood. Only one person in the audience, a cancer patient, said later it was "just too much." Cancer was traumatic for her, and joking about it made it worse.

The reality of cancer among young patients obviously isn't funny at all. As a group, we often fall into a no-man's land between pediatric oncology and adult oncology, with few traditional outlets able to cater to our needs. Young adults are the largest underinsured group. We face threats not just to our lives but our fertility, dating prospects, and financial stability. Often, we're long misdiagnosed as "too young for cancer," and by the time the disease is identified, it's too late for an effective treatment.

Jill Harrison, a 26-year-old director-playwright, was misdiagnosed by her general practitioner for months after "getting the flu over and over" five years ago. She had lung cancer, an unlikely scenario for a 21-year-old nonsmoker with no family history of lung cancer. After a successful surgery and no reoccurrence of cancer so far, Harrison is grateful her generation and many of her friends were comfortable with "putting it all out there." Humor and openness, she said, saved her life. She has just finished writing a play called In Search of Hope. It starts with the main character, Hope, walking into a radiation room insisting that she be allowed to bring in her iPod to drown out the radio, playing Tony Bennett's "Put On a Happy Face."

But Harrison looks for meaning behind all the humor and sarcasm. To her generation, she says, "everything is funny." She argues that while funny cancer blogs create an instant community, they fail to truly connect people. "It's just another version of not talking about it," she says. She found the right mix of support and cancertainment through the foundation I'm Too Young For This! "They are a rocking young-adult support group because they are all about inspiring connections and talking about 'it,' " she says.

The I’m Too Young For This! Web site functions as an aggregator of all organizations and blogs by young patients. It uses the arts and social media to organize, mobilize and activate young adults, destigmatize cancer as a death sentence, and make it easy to talk openly. They sell "Stupid Cancer" merchandise (WHITE BLOOD CELLS ARE FOR LOSERS T shirt, anyone?) and organize Stupid Cancer Happy Hours. "There are huge generational disconnects with the old-school, big-box cancer societies," said Matthew Zachary, the founder and CEO of the I'm Too Young For This Cancer Foundation. "We're trying to be more hip and more relevant whereas those other charities come across as stodgy and out of touch."

As a part of the foundation's outreach effort, Zachary, 35, a survivor of pediatric brain cancer diagnosed in college, has been producing and co-hosting The Stupid Cancer Show out of the foundation's office in New York. With more than 18,000 live listeners each week, the internationally syndicated live talk-radio broadcast has become the voice of young adults with cancer. For the last two years, every Monday night he has been interviewing doctors who often have the "personality of oatmeal," mobilizing cancer patients to "kick cancer's ass," and being the cancertainer that he is, offering endless cancer jokes.

It's not always easy to poke fun at cancer. Zachary's friend, Susan Cross, 38, had just died of brain cancer the week before that day's show. During the broadcast, he asked everyone who was listening—PEOPLE at home, hospitals, and at work—FOR a brief moment of silence. One young adult dies of cancer every hour, he said. "Do I ever get numb?" he asks his audience. "I do, honestly."

So do I. Though I have been cancer-free since I finished chemo more than two years ago, I will always remain a cancer girl—THE affectionate nickname bestowed on me by friends. Last year, a genetic test reveled that my mother and I are carriers of the Lynch syndrome, an inherited gene mutation that causes not only significant risk of colorectal cancer (check), but also cancers of the uterus, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin. So, aside from breast and lung cancers, I'm well suited for a BINGO on my oncology scorecard. My doctors try to be one step ahead by giving me annual colonoscopies, semiannual stomach endoscopies, annual PET scans, twice yearly blood work, annual skin checkups, twice yearly gynecologic smears and ultrasounds, and something else I'm probably forgetting. Chances are, on any given day, I'm either scheduling or rescheduling a doctor's appointment, waiting in a specialists' office or having a scope put in one of my body cavities.


Still, I have always joked about cancer, often to put other people at ease. At times, making jokes feels just as thin, forced, and fake as those HANG IN THERE kitten posters. But often, the reality is so overwhelming that all I can do is laugh.

At the Mercury Bar in New York's Hell's Kitchen, a fitting neighborhood for cancer survivors' bash, cancer patients and survivors below the age of 40 got together in May for a regular happy hour organized by I'm Too Young For This! "Chemo shooters" and "cancertinis" (basic shots and martinis, rebranded) were being served, and with cocktail in hand, nobody looked particularly sick—OR at least not the way "an amateur" would imagine a stereotypical cancer patient to look like. The invitation promised the event would attract people "who don't care whether you have one boob, one ball, two ports or even a hyperactive platelet count," and between the three dozen people who attended, my informal survey added up to at least 50 breasts and approximately as many testicles. People introduced themselves and their friends as efficiently as one would expect from the text-message and Twitter generation: Jennifer, ovarian, five years ago. Scott, testicular, three years in July.

Some attendees, such as Lindsey Brass, 29, went through relapses. Brass, a leukemia patient diagnosed at the age of 24 and relapsed by 25, finished law school last year just months after finishing chemo. At the bar, she mingled with other patients whom she met at previous events months ago and hadn't seen since. "People have been telling me 'We haven't seen you forever. Wow, you are alive!' " she said. "It is kind of a sick thing to say if you think about it." She laughed. Mortality jokes got progressively funnier as the night went on. It was hilarious. Really. You had to be there.
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Please help me promote my funny cancer shirts!

Posted by admin

I am looking for Bloggers to place my FunnyCancerShirts.com banner into the sidebar of their Cancer blogs. The site is getting a lot of exposure, sales have been great. You can feel all warm and bubbly knowing that a portion of each sale will be donated to a different cancer charity. The more shirts I sell, the more money I donate. Anything you could do to help with this would be GREAT!

Thanks in advance,
Ryan




Cut and paste the info from the text box below to add this animated banner to your page. Perfect size for the sidebar of your blog!

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Hodgkin's Lymphoma gains notable corporate sponsors!

Posted by admin on 7/26/09

Below is a re post from a friend and fellow Hodgkin's ass kicker, Dwayne. Be sure to check out his blog, http://www.journalofaprizefighter.com
He is MUCH better at writing than I am...


Many people in the Hodgkin's community are unaware that we have several influential voices in corporate America.

Taco Bell President - Greg Creed and Honeywell International - Senior-Vice President Adriane Brown, are emerging as strong advocates for Hodgkin's research. Taco Bell is a household name and diversified manufacturer, Honeywell, is one of the top 50 largest companies in the country.

These two powerful executives reside on the Board of Directors for the Alese Coco - Fight 2 Win Foundation. This New York based foundation is dedicated strictly to Hodgkin's research. Alese was also my friend and we often conversed while she was being treated at Sloan-Kettering.
On July 1, 2009, Greg Creed and Taco Bell facilitated the taping of the first ever Public Service Announcement for Hodgkin's Lymphoma, which was taped at Paramount Studios in Hollywood, California. The PSA was directed by the Russo Brothers who directed Arrested Development and the motion picture, You, Me & Dupree.

I spoke to Paul Coco (Alese's father) last week and he described the PSA as: "Both challenging and gripping. It will bring much needed attention to a lymphoma that receives far too little consideration from pharmaceutical companies for research." He continued: "The fact is that Hodgkin's has somewhere between 25% - 40% recurrence rate and nearly half of all stem cell transplants fail, and that's unacceptable. We're striving for complete cure."

The 30 second spot will begin airing nationally on several major networks beginning this September.

I will keep you posted on details as they became available.

The foundation's website is www.fight2win.org
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Curb Your Enthusiasm!

Posted by admin


Curb Your Enthusiasm has got to be one of my favorite shows of all time.
Recently, I started to re watch them. Will the new season ever start?

Anyway, in episode 34 of season 4 titled "The Weatherman", there is an ongoing joke about Hodgkin's Lymphoma.

When this originally aired, I gave it no thought, because I did not know I had the Hodge.

Anyway, give it a watch, hysterical!

"The good Hodgkins"
When Dr. Funkhouser's receptionist (Alyson Lyon) tell Larry that the Doctor "is not himself lately" because his uncle has Hodgkins disease, Larry says, "but it's the good Hodgkins." Hodgkin's disease is a type of lymphoma, a cancer that can occur in the lymph system. There are two types of lymphoma: Hodgkin's disease and non-Hodgkin's lymphoma.
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