Secret Surgery

Scan any well-stocked newsstand, and you’ll no doubt find a bounty of women’s magazines touting tips for achieving bouncy hair, kissable lips and a cellulite-free derriere.

What you won’t see are headlines hyping haute , artful colostomy pouches or flirty tracheostomy covers. Meanwhile, there are countless women dealing with the daily challenge of feeling beautiful while tethered to a device that’s necessary to stay alive, but often unlovely to look at.

In decades past, people with external were sentenced to life of voluminous “clown clothes” (as one ileostomy wearer puts it) and counseled to hide their conditions as best they could. But in this golden age of Internet community, designers and patients are taking matters into their own hands to create clothing and accessories that help women feel gorgeous in their own skin — and spark conversation about a previously .

The secret surgery

Secret Surgery

Secret Surgery

In 1990, Leah Humphries went to sleep as a carefree young woman and woke up with a hole punched in her gut and a pouch strapped to it. The 22-year-old art student had been diagnosed with Crohn’s disease 20 months earlier and checked into the hospital for she hoped would bring some relief. The disease ended up being more severe than anyone had anticipated, and the surgeons re-routed her out through an angry red opening — a permanent “” — on her abdomen. While the ileostomy may have saved her body, it crushed her soul.

For a year, Humphries spiraled into sadness. She’d always been a free-spirited, active, pretty girl, yet she suddenly found herself keeping company with other many decades her senior. They were content to while away afternoons shooting the breeze, tented in loose, flowing clothes calculated to conceal the existence of a pouch full of their waste and never talking about the more private aspects of their condition.

It was called the “secret surgery” for a reason. Many at the time were unwilling to discuss the social issues surrounding the mechanics of their device (which have improved radically since then), and the prevailing image was, as Humphries said, “Grandpa had the bag, and you kept him in the corner, and he smelled.”

Read the full article Physically challenged and fashionable

About Robert Hill

I founded IDEAS Intestinal Disease Education and Awareness Society, from my home base in Vancouver, British Columbia. Intestinal Disease Education and Awareness Society IDEAS is established to raise public awareness of intestinal diseases in order to help remove the stigmas associated with these illnesses. The programs of IDEAS help children, youth and young adults learn to live full lives, find acceptance and gain confidence.

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