Writing by Yvonne Watterson

~ considering the lilies & lessons from the field ©

Writing by Yvonne Watterson

Monthly Archives: October 2012

women . . . booby-trapped in October

27 Saturday Oct 2012

Posted by Editor in Breast Cancer Awareness Month, Memoir

≈ 11 Comments

Tags

Advocacy, BCAction, Belfast says No, Breast Cancer Awareness Month, Choice, Critical Questions to Ask Before Buying PInk Ribbon Products, Culture of Cancer, DIEP, Incendiary devices, Memoir, Michelle Bachelett, Murdouch, October, pink pasta, Pink Ribbon Culture, Rape, Reconstruction, Republican, Romney, Safeway Breast Cancer Awareness, Sexism, Sexual Discrimination in the Workplace, The Daily Show, Treatment, UN Women, women's rights

boo·by trap 

Meaning: A practical joke. Also a concealed and possibly lethal trap.
Noun: A thing designed to catch the unwary, in particular
Verb: Place a booby trap in or on (an object or area): “the area was booby-trapped.”
Synonyms: snare, trick into doing something
 

“Thirty days hath September, April, June, and November . . .”  the rhyme reminds me, as it has done countless times before, that October has thirty-one days. Thirty one days to make us all abundantly aware of breast cancer, breasts and being a woman in America in 2012. Just ask any of the white, male, well-fed politicians whose offensive nonsense has taken up entirely too much of the media’s time in recent days.  As foreign to me as the patricians of ancient Rome, they stare down the TV cameras and look right into my living room, spewing about women and rape and gifts from God (in the same sentence). Maddeningly one-dimensional, like 1950’s made-for-TV fathers, they are fast becoming media darlings, exploiting every opportunity to make a point that resonates with “the base,” getting the  word out about what they really think about rape, choice, discrimination of women in the workplace, religion. Romney. Murdouch. Ryan. Men who interview them. I am so tired of you. All of you. Your perversion of logic, your ignorance about women.

I imagine former Chilean President,  Michelle Bachelett, is weary too. In her impassioned plea at the 20th anniversary gala at the Center for Reproductive Rights, she reminded a room full of like-minded women that:

We can all remember a time when women’s sexual and reproductive rights were not considered human rights … We continue to encounter backlash and opposition.That’s why our work is so crucial, to draw the line and hold the line on women’s rights. It must be reinforced: women’s rights are not a bargaining chip. Women’s rights are not up for negotiation. Women’s rights are fundamental to global development, and to international peace and security. Yet an estimated 222 million women in the developing world who want to plan and space their pregnancies still have no access to modern contraception. This leads to more than 9,000 unintended pregnancies every hour . . . these are women now placed at risk of unintended pregnancy and abortion, because they have no reproductive options.

No woman should pay with her life for a lack of options. But every year, 47,000 women die from unsafe abortions. Complications of pregnancy and childbirth are the number one killer of young women aged 15 to 19 worldwide.

It is unacceptable that we continue to talk about deaths we can prevent. What is really at stake here is the right to life: a woman’s right to life, and all the other human rights to which every woman is entitled.

Women must enjoy full and equal rights – to sexual and reproductive health, to education, to be equal participants and leaders in their economies and societies, and to be free from violence and discrimination. Until all women can enjoy all rights, including reproductive rights, we will draw the line & hold the line. Reproductive rights are absolutely fundamental to gender equality and women’s empowerment.

Women’s empowerment? Gender equality? Who did we think we were fooling when we told women they had come a long way, baby. As a mother and an immigrant woman who traded in the country of her birth for the dream of America, I can barely believe the words that fly at lightning speed from the lips of men who would be our leaders. I  have lost patience with cable news networks, mean-spirited campaign ads, and political punditry. I am stunned by the sexism – subtle and not so much – that has maintained a level of “acceptability.”  Watching The Daily Show is as important as a work-out, and I feel sluggish when I miss it. Jon Stewart’s take on the media suggests that he and his writers take me seriously. Smart and funny, The Daily Show “satirizes spin, punctures pretense and belittles bombast,” and then the “real” news networks talk about it.

Understandably fatigued by all of this, I take some solace in knowing that I only need to dodge four more days, and Breast Cancer Awareness Month will be over for another year.  When people show up to work on Thursday, November 1st,  morning, the pink ribbon removed from their lapels, I will breathe a sign of relief. I will, of course, still have breast cancer.

I am an unwilling conscript to this battle against breast cancer. Often, it feels as though I am holding my breath, wondering as I did forty years ago if the bomb scare was just that. A scare. A hoax. Except in my altered reality, the suspicious devices come in the form of tumors and test results and in waiting and worrying, in scheduling more time to spend in waiting rooms. It saps my energy. I have things to do. There is laundry and shopping, not because I am a woman, but because I like my clothes clean and our refrigerator stocked. For eleven months of the year, grocery store reconnaissance missions are completed without incident. No camouflage is necessary; it is easy to blend in. Minimal intelligence required. For the next four days, however, my mission is to navigate the Safeway checkout line without being hijacked by a well-meaning cashier who, dispassionately, will ask me to donate a dollar for breast cancer. If I say yes, she will bellow into the intercom, “I just got a donation for Breast Cancer. Can I get a Woo Hoo?” And, as they scan coupons and fill bags, paper or plastic, with other people’s groceries, a chorus of cashiers and bag-boys will, as automatons, respond, “Woo Hoo!” and I will flee. I will feel slightly guilty that I asked how much of my dollar would support breast cancer research, knowing that my question rendered her uncomfortable. But I will be more concerned that she has not been told how to answer my question except with receipt and a “Have a nice day!” Ironically, the young woman at the cash register is caught in the same trap with me –  woo-hoo!

There are other grocery stores, some with nary a lonely pink ribbon fluttering on the door, but they are few and far between. Even speciality stores are dressed out in pink, in an almost festive observance of breast cancer awareness month – a breast fest. Bizarrely, this brings to mind Loyalist areas in the Northern Ireland of my childhood. Parts remain the same today. In anticipation of “marching” season, Union Jacks and flags bearing a red hand hung out from bedroom windows of council houses, proclaiming allegiance to the Crown. Red, white, and blue bunting stretched from house to house, and pavement curbs were roughly painted in homage to British rule. Slogans spray-painted on otherwise scrubbed gable walls, echoed an imperative “Belfast Says No” that hung above the city’s hall in the 1980s and in our faces.  It was unavoidable even for those of us who wanted to remain anonymous, ordinary people for whom the moral imperative was peace. Boldly marking territory in no uncertain terms,  those banners and badges were divisive, as incendiary as the booby-trapped cars that lay in wait for the part-time police officer who, in a hurry to get home for a birthday celebration, failed to check under his car before turning the key in the ignition.

Perhaps it is over-wrought to compare breast cancer awareness campaigns to shows of loyalist strength that often culminated in sectarian violence. Death even. Personally, I find a legitimate link. The bunting that zig-zagged across the skies of the Shankill Road is not much different from the arch of balloons floating above the “KomenPhoenix2012” Finish Line in downtown Phoenix. I did not participate, much to the chagrin of acquaintances who know I have breast cancer. Why wasn’t I part of Komen’s “circle of promise?” Couldn’t I tap into the power of positive thinking? Why do I have to be so negative about breast cancer? Come on! Can’t you ferret out a silver lining? Make a silk purse out of a sow’s ear? “Imagine a life without breast cancer!” the Susan G. Komen Foundation urges me. Alright. I imagine it every morning when I wake up. I imagined it during a recent unguarded moment in Bed, Bath and Beyond, the sole item on my agenda, a new duvet cover. I had barely crossed the threshold, when I was told to Fight like a Girl:

Even the tic tacs on display were pink, as was the pasta and the over-priced machine used to make it. I did my due diligence and visited the The Pasta Shoppe website, where I learned that 10% of proceeds from the sale of fun-shaped pasta will go directly to the Susan G. Komen Foundation.

Susan G. Komen was only 36 years old when she was killed by metastatic breast cancer  In the blink of an eye, just three years, it ravaged her body. The organization subsequently established by her sister, however, has failed to appropriately address the kind of cancer that killed her. Instead, the Komen foundation has relentlessly emphasized early detection and awareness. Sealed it with a pink ribbon, it is just not good enough. Not for me. Not for my daughter. Nor yours.

Surely the men who would be our leaders agree that we have made inadequate progress, that profit  – not people – has been of paramount importance? I have to wonder what Susan G. Komen would say about our progress, or Rachel Carson, who fifty years ago, warned us about pesticides and their link to cancer. Breast cancer killed her too. She would have something to say, I know, about the limited edition pink ribbon tic tacs. While I do not know how much of the tic tac proceeds go towards breast cancer research, I know they contain corn gluten, which is cause for concern. For Susan and for Rachel, and in this 2012 general election, all those women who fought hard for the right to vote, to be taken as seriously as men, Breast Cancer Action urges us to ask these Critical Questions Before You Buy Pink: 

  1. Does any money from this purchase go to support breast cancer programs? How much?
  2. What organization will get the money? What will they do with the funds, and how do these programs turn the tide of the breast cancer epidemic?
  3. Is there a “cap” on the amount the company will donate? Has this maximum donation already been met? Can you tell?
  4. Does this purchase put you or someone you love at risk for exposure to toxins linked to breast cancer? What is the company doing to ensure that its products are not contributing to the breast cancer epidemic?

Further, BCAction’s critical questions for voters help us apply and sustain pressure on policy makers. Breast cancer can no longer be covered up with pink ribbon purchases that manipulate us into feeling good about ourselves. The epidemic has been trivialized, glamorized, feminized. In October, it is more about the boobies and less about the disease. The slogans and the pink wristbands, the trappings of breast cancer are as acceptable as fashion accessories. For thirty-one days, we are told “to save the tatas” and reminded to “feel the boobies.” Baby-talk, sugar and spice and all things nice, the stuff of fairy-tales. Even the President of the United States sports a pink breast cancer awareness bracelet. Truly, it is just not enough.

I may be way off the mark, but somehow I cannot imagine our nation in the grip of a “Feel my Balls” campaign. America seems confounded by sex and gender; thus, guarantees of life, liberty, and the pursuit of happiness for everyone, ring hollow. Somewhere within the ‘Spaghetti Junction’ of stories that spin to advance political agendas and generate massive profits, lies the truth about the way things are and how they appear to be. A glamorous pink ribbon wrapped around an Estee Lauder model seems more socially palatable than a bald and fragile, vomiting cancer patient in the throes of yet another grueling, poisonous chemotherapy treatment.

Confronting the chilling reality of breast cancer is non-negotiable. It is time to ask the questions that will quell the rising tide and to demand answers. This leads me back to those men in the highest offices of the land, men who have failed to speak up, speak out, and mandate meaningful action, beyond the breasts and into research of the cancer that kills. It was a decade ago when BBC News reported that then United States Attorney General, John Ashcroft, asked the United States Department of Justice to shell out $8,000 for drapes to cover up the exposed right breast of The Spirit of Justice statue. The offending art-deco figure was often photographed behind him while he spoke to the media. Was it too life-like? Would a pink ribbon in front of the White House have been more acceptable? Regretfully, I think it might.

Breast cancer is ugly, and it hurts. Awareness campaigns hurt too, especially when they focus on the same old stories of early detection and treatment regimens that have been prescribed for decades –  some combination of surgery, radiation, chemotherapy, hormonal therapy. All about the boobs? Given the devastating toll of the disease, shouldn’t it all about the metastatic breast cancer?

I am supposed to be grateful, having paid – one way or another – over $80,000 – for a brand new breast and the flat stomach left behind after a brilliant surgeon spent almost 8 hours, painstakingly performing a DIEP flap. I have been told how lucky I am more times than I can recall. Offended by the picture? Don’t be. It is less offensive than the disease and the appalling lack of progress in figuring out what causes it or how to stop it in its tracks.  The JP drains, grenade-like, hanging from long rubber tubes that sprouted from either end of a hip-to-hip incision, are less contrived and embarrassing than the pink ribbon earrings that sell for thirty bucks on Ebay.

I’ll let you in on a secret. I miss my old body and the woman I used to be. I am wary and weary. Trapped.

 

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make metastatic breast cancer matter

23 Tuesday Oct 2012

Posted by Editor in Breast Cancer Awareness Month

≈ 52 Comments

Tags

#BCSM, Advocacy, breast cancer, Breast cancer as family issue, Breast Cancer Awareness Month, Cancer, Culture of Cancer, density, diagnosis, Harvard University, Komen, Liz Scabo, MBC, media, Metastasis, metastatic breast cancer, METAvivor, Phoenix Public Library, Pink Ribbon Culture, pinkwashing, Reconstruction, research funding, Tweetchat, Twitter, USA TODAY

Reposted from March 23, 2012 in support of increasing awareness and support for Metastatic Breast Cancer research. Please visit METAvivor to learn about “The Elephant in the Pink Room.” 

Perhaps it is because my family history is bereft of breast cancer. Perhaps I was lulled into a false sense of security by three mammogram reports that lacked information about the density of my breasts. Whatever the reason, until my own diagnosis, I assumed that breast cancer was what happened to other women in other families.  Such naïveté. Cancer always happens to people who are just like you and me. In fact, the Dr. Susan Love Research Foundation estimates that 70% of the women who have breast cancer, have what is known as a “sporadic occurrence” – no family history.

It is almost twelve months now since I heard the Breast Patient Navigator tell me, as if by rote, but not unkindly, about the malignant tumor at 12 o’clock, 3cm from the nipple of my the right breast. I imagine, in her almost-cozy office, she has had to deliver the same sentence and respond to the same shock all too often. While I wept, she reassured my husband and me with what I now realize was relatively good news. While many of the details are unclear, I distinctly remember her congratulating me on having found the lump all by myself, reassuring me, “what you’re hearing today is not a death sentence.” It isn’t. Not yet.

The day before her pronouncement, I would never have predicted that the day after – and every day since – my life would often resemble the one I led as a graduate student, before motherhood, before the Internet and the iPhone, an artful balance of work and study with frequent visits to the musty basement floor of the old Phoenix Public Library, a library made of bricks and mortar. There, I spent countless hours perusing education periodicals and old newspaper articles on microfiche, taking notes, and making photocopies. Almost twenty years since, and in the interest of full disclosure, the notion of continuing a formal education is wholly unappealing. Thoughts of a PhD fell by the wayside during a summer conference at Harvard some years ago when I realized I have a deep aversion to homework. Nonetheless, I was duly seduced by the aura of Harvard University and readily donned the mantle of “academic” – for all of one day. Reality set in when I failed to complete the required reading and subsequently spent classes avoiding eye contact with the lecturer just in case I was called upon. Clearly, further education was out of the question for me. However, in the past year, the language and politics of breast cancer have forced me to resume the ways of a full-time, often recalcitrant, student with a full-time job.

Until one Monday evening this past March, I thought I had done a decent job on my breast cancer homework. I could talk quite knowledgeably about breast density and mammograms, estrogen and progesterone receptors, and the difference between DCIS and IDC. I had even learned how to decipher a surgical pathology report. Regretfully, I had not been thorough enough. Peeling away the layers of awareness, I felt betrayed, duped even, by a media saturated with stories of breast cancer like mine, of ribbons and races, of celebrities who triumphantly “overcome.” A cold reality emerged from a virtual conversation with a group that meets online every Monday, 9pm ET at #BCSM, The Breast Cancer and Social Media Tweetchat.  It was here at “the intersection of breast cancer and all things social media,” that I learned about metastatic breast cancer, mets, and METAvivor, a volunteer-run non-profit which has coalesced around three sad truths: support for mets patients is lacking; awareness about the disease is strikingly low; and, research devoted to mets is woefully underfunded. 

A neophyte to breast cancer country and Twitter, I was a stranger in a strange land by any measure.  Odd, then, to experience such a level of familiarity in the virtual company of The Breast Cancer and Social Media twitter chat, where truth is conveyed at lightning speed in 140 characters or less. That particular Monday, the group was “speaking” with @CJMeta from Metavivor,  Dian “CJ” M. Coreliussen-James  who introduced herself thus:  “Founded an MBC support prog 07. Grew FAST! Knew we could do more as non-profit. And 4 of us founded METAvivor in Jan 09.” Such urgency behind those words. This was an unfamiliar urgency. @MetaCJ then went on to explain that “METAvivor offers support, builds awareness and funds MBC research. 100% volunteer run. Most have MBC.” And then the sentence that leaped from the screen and into my heart:

One of the things we talked about today was this reality: of four founders only two are still living.

Re-tweeted again and again, the message was clear. Metastatic breast cancer is the kind of breast cancer we all fear most, the kind that spreads to distant places on our boides, usually the bones, the liver, or the brain. It was beginning to dawn on me that the lump in my breast was not the thing that could kill me; a lump could be survived. But the breast cancer that metastasizes, the cancer that spreads to distant organs is not considered survivable.  METAvivor is committed to helping change what continues to be this tragic inevitability.

At the risk of oversimplifying a complex issue, I wonder if we could figure out what causes the spread, then couldn’t we figure out breast cancer?  Figuring this out requires research, so surely metastasis research is well funded? No. During the Tweetchat, CJ explained that a mere 2% of US Breast Cancer dollars support metastatic breast cancer research. Two percent.  How could that be? Could it be that we have grown content, as a country, with detecting lumps and accepting as acceptable the race toward cure before cause. The Tweetchat left me knowing, in no uncertain terms, not only are there many types of cancer, but also that American culture is paralyzed in a paradigm that sees one type of cancer, mine, as more “socially acceptable,” more worthy of media attention and research than others. With that in mind, I posted a comment at the MBCNBuzz website in response to a powerful letter to the Editor of US Weekly. “I am so tired hearing of celebrities putting a happy face on for cancer.” Buried in over 30 responses, I found this comment by someone I know only as Kelly K:

“With no family history, no positive genes, I was dxed with stage III lobular triple positive breast cancer at 29 and mets at 30. That year my oncologist practice selected me to be honored at a Komen luncheon. I spent a few hours one day being interviewed for a video they do about the honorees breast cancer story. My onc selected me bc when I found out I had mets, everyone I knew from working in a hospital and covering oncology at times, had died quickly it seemed. She said because the ones doing well just go about living their lives. I wanted to show people that was true. Komen edited out every reference to my mets in the video. If that isn’t pink washing I don’t know what qualifies. That experience was March 2003. I’m still here with mets to stomach, ovaries, pleural lining now with effusion, adrenal gland and countless lymph nodes. Just started seventh chemo regime yesterday. But you know what I’m still here, still living my life as a mom to a wonderful 11 yo son, wife, daughter and friend.”

I can only tell her I am sorry and pledge to Kelly that I will do my part to  “edit in” her story and the stories of those who live with mets. I am still dismayed by Komen’s treatment of her, that they apparently wanted to hide from view the offensive disease that has spread to her stomach, ovaries, adrenal gland, and lymph nodes. Why would the organization that is virtually synonymous with breast cancer choose to erase rather than confront the very thing they say they are committed to curing? It is chilling to consider the answer to that question as it is to know that Kelly was, this March, beginning her seventh chemotherapy regime, not knowing if the right research is being funded right now to figure out what caused breast cancer to metastasize to other places on her young body.

It is maddening and unacceptable to have made so little progress towards eradicating this scourge of our time. Research should be targeted, differentiated, and funded appropriately. According to METAvivor’s website, 90% of cancer deaths result from Stage IV cancer, but only 2% of research funding is devoted to StageIV.* The website goes on to explain that this is not a “rare” disease; 30% of breast cancer patients will progress to stage IV. In light of this, METAVivor has an urgent request: “30% for 30%”: We believe that since 30% of breast cancer patients metastasize, 30% of breast cancer research funds should go toward MBC research.” Surely the time has come, especially in this election year, for us to exert pressure on those who can to make decisions that will affect the flow of money and the right kind of attention, the research that would matter to those with Stage IV cancer and those at risk of Metastatic Breast Cancer.  

As for me, what will I do? Someone once said that the little difference each of us makes can make all the difference in the world to someone else. So I will keep doing my homework until I master Twitter.  I will keep doing my homework to learn how I can help change the conversation about cancer in America – sooner not later.  Now, it would be less than true if I didn’t say I’m scared. Really scared. Most days. I am afraid that the cancer that was removed along with my breast, will reappear in my bones or my brain or my liver. That it will sneakily take up residence in a vital organ. So every little headache is a warning bell, every twinge in my left hip is a harbinger of disease. The series of appointments with oncologists, plastic surgeons, breast surgeons is unsettling. Scribbled in a planner, the dates remind me that my life has been forever altered by breast cancer. I suppose I am doing just fine. I’ve even been told I look just like myself, that God would never give me more than I can handle, and admonished to put my “big girl pants on.” The thing is that those tests and scans shocked me once, and I have prepared a little space inside to be shocked once again.

I should know that living in fear is no way to live.  Growing up in Northern Ireland during the Troubles, I learned early on that you can’t not go outside for fear of being blown up by terrorists. You can’t succumb to that fear otherwise you’ll never go outside. So I will continue my education about this cancer that has changed my life. I will continue to reach out to people like the bold and brilliant Dr. Attai, Jody Schroger, and Alicia Stales who moderatethe #BCSM Tweetchat.

Today, it is no surprise to read about what Liz Scabo describes as a  social movement in USA TODAY. The weekly Tweetchat has often been my soft place to fall when I have been unable to find answers anywhere else. So, as Breast Cancer Awareness Month winds down and the pink ribbon products make way for Thanksgiving decor and Christmas decorations, I will do what I can to increase awareness for and traffic to METAVivor where others can learn more about Kelly’s disease, the disease Komen apparently didn’t want anyone else to see at their luncheon. Between all those who blog and tweet, I’m convinced we can create an online revolution that will thrust metastatic cancer into the forefront of a conversation that should be taking place on the national stage. Very soon.

Metastatic breast cancer matters. 

 ** For general information about METAVivor, please contact “CJ” (Dian) Corneliussen-James at cj77@comcast.net

* See CJ’s comment below

 

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blog action … deferred action

15 Monday Oct 2012

Posted by Editor in Memoir

≈ 5 Comments

Tags

Anna Quindlen, Blog Action Day, Dr. Martin Luther King, DREAM Act, Fund for DREAMers, integrated education Northern Ireland, Memoir, Proposition 300, The Power of We, United States Department of Homeland Security

Blog Action Day is a global effort designed to promote discussion around a single issue that affects each of us.  Since 2007, this annual event has inspired positive conversation in the blogosphere, with writers exploring universal topics related to our environment, poverty, climate change, water, and food. This year’s theme, The Power of We, provides an opportunity to define and celebrate the concept of community. How will we make our mark on the world? What will we do to make sure our children’s dreams come true? Everything in our power. 

I am reminded of a former student who graduated recently with an undergraduate degree in Psychology. Like me, she is an immigrant. Unlike me, she must wait a little longer before the dream of America will wrap her in its arms. She tells me she remembers her journey here. She was nine years old when she walked for hours through the desert, carrying her little brother much of the way. She remembers her family being reunited with her father after the exhausting crossing, “Finally, we could throw our arms around him and hug him tight. I just remember his arms weren’t long enough to reach around all of us.”

In the weeks, months, and years that followed, she did everything right. She quickly learned English and played by the rules, every day pledging allegiance to the United States flag at a school where she was often the recipient of certificates for “good citizenship.” She believed everything her teachers told her.  She showed up to school every day, ready to learn and eager to contribute to the only community she had ever known, the only country she had ever called “home.” By the time our paths crossed, she was a teenager, an aspiring nurse. Still without a path to citizenship, disparaged as “an illegal,” her immigrant spirit remained intact and undaunted. Along with approximately 65,000 immigrant children who graduate from high school in the United States every year, she lacked the nine digits of a social security number required for a driver’s license, employment, the military, or a college education. Many of us feared that the pursuit of happiness would remain only a dream for these children who had taken their first steps on American soil, and placed their hands on their hearts every day to pledge allegiance to the only country they have ever known. But somehow, the undocumented children who had become more than collateral damage in this war over immigration, understood Anna Quindlen’s assertion that,

immigration is never about today; it is always about tomorrow

~ the kind of tomorrow that Dr. Martin Luther King envisioned when he described his dream of an America with a place at the table for children of every race and room at the inn for every needy child. The kind of tomorrow I dreamed about as a little girl in Northern Ireland, a tomorrow where Catholics and Protestants would attend the same schools. The kind of tomorrow that belongs to the young people who were brought here as infants by parents who had dreams of a better life for them. For them, immigration is an exercise in hope. It is a story of deferred gratification, deferred dreams.

They continue to wait, the DREAM (Development Relief and Education for Alien Minors) Act still maddeningly elusive. The DREAM Act makes sense to reasonable people, its purpose to help young people who meet the following requirements so they may enlist in the military or go to college and finally have a path to citizenship:

  • must have entered the United States before the age of 16
  • must have been present in the United States for at least five (5) consecutive years prior to enactment of the bill
  • must have graduated from a United States high school, or have obtained a GED, or have been accepted into an institution of higher education (i.e. college/university)
  • must be between the ages of 12 and 35
  • must have good moral character

 

The DREAM Act would allow those young immigrants who live quietly among us, often in fear, to give back to America. It makes sense to protect our investment in their education through sensible legislation, and finally, we took a giant step forward, when on June 15, 2012, President Obama announced that the U.S. Department of Homeland Security would not deport certain DREAM Act–eligible undocumented youth. Under a directive from the secretary of DHS, these young people will be given temporary relief called “deferred action.” More information is available in this FAQ created jointly by NILC and United We Dream.

It is a cumbersome process, however, and the application fee is $465 – a hefty sum for young people who cannot work, and it will undoubtedly deter some of them from applying to the deferred action program. A national fundraising effort is underway to support those DREAMers – like my former student – who need financial assistance. The “Fund for DREAMers” hopes to raise funds to help offset the application fee for as many as one million undocumented young people who meet those qualifications listed above.

To learn more or to make a donation – to exert the power of we – please visit http://bit.ly/Fund4Dreamers.

 

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breast cancer … not worth debating?

06 Saturday Oct 2012

Posted by Editor in Uncategorized

≈ 9 Comments

Tags

Advocacy, American Cancer Society, breast cancer, Breast Cancer Action, Candy Crowley, Culture of Cancer, Jim Lehrer, Mammograms, Nancy Brinker, National Breast Cancer Awareness Month, Phoenix Race for a Cure, Pink Ribbon Culture, pinkwashing, Presidential debate, Think before you pink, Treatment, United States, White House

It is Breast Cancer Awareness Month. President Obama proclaimed it so on October 1, 2012. For added emphasis, the North Portico of the White House was illuminated pink for one evening. Basking in a ubiquitous pink glow, America’s most famous house reconfirms the power of the organization that bears the name of Nancy Brinker’s dead sister, Susan G. Komen, to deliver what Brinker once described as “conventional messages in unconventional ways in unexpected environments.” Given this logic, perhaps the presidential debate was “too conventional” a venue to raise the question of breast cancer. On top of that, there was that whole issue of the altitude in Denver . . .

Incomprehensibly, it did not occur to Jim Lehrer, the veteran newsman who has moderated eleven nationally televised presidential debates, to ask a single question about breast cancer (or any cancer), and neither the incumbent President of the United States nor his Republican opponent broached the subject. There were opportunities, especially during lengthy and detailed exchanges about the deficit, the tax code, and healthcare, but not one of these men seized a prime-time opportunity to take a TV  audience of over 67 million beyond “awareness” of a disease that, according to the American Cancer Society will kill approximately 40,000 women and 400 men in 2012. Clearly, breast cancer constitutes a substantive issue worthy of debate, but not this past Wednesday. Instead, the pundits are still hammering away about how Romney deftly injected an un-funny promise to de-fund Big Bird and how Obama’s performance lacked luster. Admittedly, I was positively willing him to make eye contact with his challenger, to question some of Romney’s “revisions,” but President Obama often appeared to be just going through the motions. More troubling than any of this, however, is that if neither candidate is willing to get specific about breast cancer in the month before the general election – during the most “aware” month of the year – then what’s in store for us over the next four years? More awareness? More pink?

The next debate, a town-hall, is designed to allow audience members to question the candidates directly about domestic issues and foreign policy. Perhaps this format will bring some questions – and answers – about the health crisis that is breast cancer, for which the greatest factor is being a woman. Maybe the fact that a woman is moderating will jog the candidates’ memories. Unfortunately, award-winning CNN political correspondent, Candy Crowley, will not be positioned, as Lehrer, to fire tough questions from the moderator’s chair which she is well capable of doing; rather, she will ask follow-up questions. Of Jim Lehrer’s performance as moderator, she told Politico, that she was not really paying attention to him; instead, she was “writing down where I saw holes in their arguments thinking, ‘Oh, this would be a good follow up.” Well, Candy, I want to hear more about breast cancer and women’s health from these men who would be President. I hope you find a way to follow-up and facilitate a debate where flat-out lies are challenged and holes in arguments are filled with explanations.

It is impossible to ignore the business of breast cancer, especially in October. For the better part of three decades, an elusive cure has been all wrapped up in a cute pink ribbon that I once regarded with a stunning mixture of indifference and denial.  Breast cancer was the thing that happened to other people, to celebrities who grace the pages of magazines, to women who didn’t show up for their mammograms. Until it happened to me, I had been duped and distracted by the feminine, glamorous, sugar-and-spice, often overtly sexual trappings of breast cancer awareness, so far removed from the ravages of a disease that kills. Only in “cancer country,” would we welcome a “Pink Light District”

Now, I wish I could disappear for October.  Even my state’s newspaper, The Arizona Republic’s saw fit to perpetuate across six pages the myth that breast cancer is literally for the girls. Where else would we find pink feather boas and ribbons and tiaras than in a little girl’s fairy tale whose time has come and gone? If my breast cancer had a color, it would be white, the same white as the dense tissue that concealed it from three mammograms. But nobody told me to ask about tissue density. Every October, Nancy Brinker’s conventional messages failed to remind me when I made a pink purchase or walked in the Race for a Cure that, free or not, standard mammography will not detect cancer in dense breast tissue. Thus, detection will come too late for some women and men.  The time has come for a little less pink and a little more black and white about tissue density or the men who get breast cancer, or the unacceptable numbers of people who still die from breast cancer that spreads to the bone, the liver, the brain, people like Susan G. Komen.

Breast Cancer Action should not be the only group screaming “It’s an epidemic stupid!”  so let’s get it on the agenda. To help voters make the right decisions this general election, the Breast Cancer Action website suggests these critical questions about the candidates who want your votes:

  1. Does your candidate think more mammograms are the only solutions to the breast cancer epidemic?
  2. Does your candidate believe that women can prevent breast cancer through healthy lifestyle choices?
  3. Does your candidate think access to healthcare fully solves the fact that women of color are more likely to die of breast cancer than white women?
  4. Is your candidate beholden to corporate donors whose practices or products are linked to an increased risk of developing breast cancer?
  5. Does your candidate engage in ‘political pinkwashing’ by promoting empty “feel good” activities that win votes and get media attention but do nothing to address and end the epidemic?

Did you answer “yes” to any of the above? Are you less convinced now about your candidate’s willingness to act decisively and differently on the issue of breast cancer?  There are things you can do to help. Think Before you Pink, and urge your representative to fully endorse the 2012 Breast Cancer Action Mandate for Government Action.

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Yvonne hails from Antrim, Northern Ireland, and has lived in the desert southwest of the United States for almost thirty years. Married, with a daughter who is navigating her path through the "teen tunnel," and a haughty cat, Atticus, she has spent the better part of the last three decades in the classroom as a student, teacher, and administrator. Her mid-life crisis came as a sneaky Stage II invasive breast cancer diagnosis which subsequently sent her to the blogosphere where she found a virtual home away from home . . .
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