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Karen Putz explores The Shame of Wearing (Fashionable) Hearing Aids

Monday, November 16th, 2009
Filed under: Themes, Deaf Jam

Quoting the always-always-always entertaining Karen Putz, writing on her website deafmomworld.com:

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I came across a post this morning, The Shame of Wearing Hearing Aids, and it brought back memories. I was one of those kids who hid a hearing aid under long hair. It wasn’t until I was in college that I finally wore my hair up and my hearing aid perched for all to see. Kinda sad, eh? All those years spent trying to hide something that was basically a part of me—except I didn’t want any part of it.

I decided to raise my kids with a different attitude about their hearing aids. From the start, we went with brightly-colored earmolds with swirls and glitter. I even joined my daughter in getting matching glitter earmolds. I’m pretty sure I saw my audiologist hold back a gulp when I asked for the blue with glitter when she squeezed the earmold goop into my ear.

So far, no one has had the guts to tell me that I look foolish sporting glitter at my age.

Despite my years of preaching about being proud of those two pieces of technology on their ears, my kids had minds of their own … Continue reading this great essay

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Karen Putz is an insightful, talented and entertaining freelance writer. She provides early intervention services to families with deaf and hard of hearing children. She serves as a board member for Hands & Voices (www.handsandvoices.org) and runs Illinois Hands & Voices in her state. She’s also a deaf mom to three deaf and hard of hearing children, and her husband is deaf, too. Learn more at karenputz.com.

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Sparking the ostomy conversation

Friday, October 30th, 2009
Filed under: Campaign Watch

Quoting uncoverostomy.com:

“Uncover Ostomy is an online awareness campaign shaping a positive conversation about the ostomy in social media spaces. We will be sharing positive stories and thought provoking images—dare we say sexy?—to spark this conversation. We invite you to share your comments and ideas on this website, on Facebook, on YouTube, on Twitter and every where else you spend time engaging other people online.”

Uncover_Ostomy_photo_Jessica

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“BE YOU (tiful)”: spotlighting Erin Matson’s MPR essay

Wednesday, October 28th, 2009
Filed under: ThemesThe Skinny on Fat

Quoting Erin Matson’s truly beautiful editorial for minnesota.publicradio.org:

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“I remember flipping through fashion magazines disinterestedly as a girl, never realizing the extent to which Photoshop could be used as a weapon of mass destruction.

We have all come to expect that photos of models are airbrushed in advertisements and fashion magazines. It’s a fact—one that’s all too easy to swallow and throw back up.

Recently, Ralph Lauren fired size-four model Filippa Hamilton, allegedly for being too large. This story is an outrage in itself. She is, by the standards of the World Health Organization, underweight.

What made me want to burst into tears was far worse: A dramatically Photoshopped Ralph Lauren ad that surfaced in Japan after she had been fired.

I know all too well that the modeling and fashion industries love to portray women who struggle with eating disorders or have been digitally altered to dangerously unrealistic standards, and they do it with dramatic glamour.

While I was dying of anorexia during my late teens, I was recruited by modeling agencies three times. One of the times I was hospitalized, a fellow patient climbed on stage at the Mall of America to win a modeling contest while on a day pass, her hospital bracelet flopping off her wrist as she waved to an applauding crowd.

Recently, Self magazine ran a “total body confidence” issue and digitally slenderized singer Kelly Clarkson before putting her on the cover, even though she has said that she’s comfortable with herself just the way she is.

Women and girls are watching, and the results aren’t pretty. Eighty-one percent of 10-year-old girls are afraid of being fat, and an estimated 10 million … CONTINUE READING THIS WONDERFUL ESSAY

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Join the National Organization for Women’s “Love Your Body” campaign

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Crystal Renn chats with TIME Magazine about body image

Wednesday, October 28th, 2009
Filed under: ThemesThe Skinny on FatInterviews

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Six years ago, Crystal Renn was an unknown size-0 model who moved to New York from Clinton, Mississippi, to make it big. She struggled with her weight for years, however, and finally made the bold decision to switch to plus-size modeling. Now a healthy 165 pounds, she is the highest-paid plus-size model in the world, having graced the covers of American Vogue and Harper’s Bazaar and appeared in Dolce & Gabbana ads. The 23-year-old recently talked with TIME Magazine about her new book Hungry, her size-0 modeling days and walking the runway for Jean Paul Gaultier. Here are the highlights:

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Laurie Toby Edison and Debbie Notkin “weigh in” on the now-famous Baby Alex insurance debacle

Sunday, October 25th, 2009
Filed under: ThemesThe Skinny on Fat

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Quoting Laurie Toby Edison and Debbie Notkin, writing on their always-engaging Body Impolitic blog:

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“We’ve been thinking about the story of Alex Lange, which was in the news earlier this month . . . [The Rocky Mountain Health Plans insurance company] didn’t change its mind because it thinks it was wrong: it changed its mind because Alex’s dad works in television.”

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*If you’re unfamiliar with the story, here’s a blurb/video that explains the details. And click here to read Laurie and Debbie’s full post.

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SECOND GLANCE: another look at Aimee Mullins

Tuesday, October 20th, 2009
Filed under: Uncategorized

World-record-setting Paralympian sprinter Aimee Mullins, as you know from our last post, is a bilateral amputee—i.e. both of her legs were amputated below the knee. She learned to walk on prosthetics, then to run.

Aimee said some truly tremendous things during her TED Talk.

But this quote in particular, this hilarious and delicious nugget of a sound byte, is so off-the-wall funny that it bears repeating…

“From an identity standpoint, what does it mean to have a disability?
Pamela Anderson has more prosthetic in her body than I do.
Nobody calls
her disabled.”

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Aimee_Mullins_running_on_beach_photo_by_Howard_Schatz

Another time, being interviewed by Mavian Arocha for Aventura Magazine, Aimee was asked “What quality do you lack that you wish you could attain and embrace?” Not missing a beat, Aimee ran with the generic line of questioning and dryly responded: “Besides being able to bend my ankles? Jeez, this is hard.”

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TED Talk: Aimee Mullins and her 12 pairs of legs

Tuesday, October 20th, 2009
Filed under: Irked Videos

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In this wonderful TED video, filmed in February ‘09, Aimee Mullins talks about her prosthetic legs—she’s got a dozen amazing pairs—and the superpowers they grant her: speed, beauty, an extra 6 inches of height … Quite simply, she redefines what the body can be. [via]

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What to watch next:
TED98 – Aimee Mullins on running

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Visit AimeeMullins.com

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Support Hal Newman’s 250km “Fat Man On Trek to Conquer Cancer” bike ride

Monday, October 19th, 2009
Filed under: ThemesTumour HumourCampaign Watch

Quoting Hal Newman, current managing editor at BigMedicine.ca, former firefighter and paramedic with 3+ decades of experience in emergency services who “reinvented” himself after leaving the streets by becoming a Network Accelerant:

Hal_Newman_cancer_fundraiser_pullout_quote: Text: "I am committed to raising as much money as I can, with $2500 set as the minimum. I am looking for corporate sponsors willing to match the donations made by individual donors. I am hoping to find others who would like to join me on the ride and in the fight against cancer."

If you had to pick someone who would be the least likely to become addicted to road cycling more than 30 km each and every day at speed you need not look any further than me. So, it’s a bit surreal to think that come July 2010, I will be joining thousands of other cyclists riding the 250 km [in two days] from Montreal to Quebec City to raise funds to support the fight against cancer. I’m riding for Abraham, Rose, Mimi, David, Susan, Gil, Mario and many many others who fought cancer right up until their dying breaths. We say the words carefully. Sometimes in a hushed whisper. Sometimes spat out like a foul taste in our mouths. “Cancer” … “The Big CA.” So many family members and friends and colleagues who have waged pitched battles against cancer. Occasionally there are wins—and we celebrate those in grand style although truth be told, once cancer stages a home invasion it never really leaves. Even when it’s gone for good, we all wonder if cancer will find another way to come back into our lives. More often than not there are losses. And we mark those with sorrow and tears and a lasting hatred of a disease that shows no mercy and knows no boundaries. I spent a good chunk of my career as a paramedic/ firefighter. Cancer has become inexorably linked with those who are on the frontlines of emergency services. I’ve gone to the hospital to pick-up a friend/ colleague after his first round of chemo and I’ll always remember his reaction to being able to walk, albeit weakly, out the door under his own power. It was a cold, crisp day and yet he had his window down for the ride home so he could take in the sunshine and the wind. His cancer was beaten back and he’s still a part of our lives. I’m riding for Norm and Don and not enough others who have found a way to beat cancer. Norm Rooker, my brother-of-another-mother, wrote about learning he had bladder cancer . . .

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Continue reading Hal’s stunningly beautiful essay

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DONATE, DONATE, DONATE

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URGENT APPEAL: Julia Barry’s “In Her Image” outreach project needs our help!

Friday, August 21st, 2009
Filed under: Campaign Watch

Julia_Barry_urgent_appeal_title_graphic - Text: "Julia Barry: 'I’m writing with my chutzpah pen to ask you to vote!'"

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“Orgesticulanismus,” a mersmerizingly marvelous short-movie by Mathieu Labaye

Tuesday, February 10th, 2009
Filed under: ThemesWheelchairman of the BoardIrked Videos

Irked Magazine proudly presents Mathieu Labaye’s remarkable short-movie “Orgesticulanismus”—a movie that’s difficult to pronounce, but impossible to forget. This is an extraordinary, poignant tribute to his father, Benoît Labaye, who was diagnosed with multiple sclerosis at 29 years old. Benoît Labaye had been confined to a wheelchair since age 40 and died at 55 years old on April 22, 2006, as a result of pneumonia.


CLICK HERE to watch Orgesticulanismus.

Story courtesy of Élaine Hébert’s CitizenShift/ParoleCitoyenne blog

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