Stories about: Children’s Hospital Boston Down Syndrome Program

Are medical communities the new marketing demographic?

Have you heard about the bald Barbie movement? It’s a grassroots, digital campaign asking Mattel to make a version of the doll without her trademark golden locks to benefit children with illness. According to the group’s Facebook page, which has gained more than 130,000 fans in less than a month, bald Barbie would let “children suffering cancer, alopecia and any other illness that causes them to lose their hair, feel just as beautiful as the dolls they play with.”

Regardless of how people feel about the plastic fashion icon—she’s been around for more than half a century but still seems to be a very polarizing figure; often because of her figure—the online support for bald Barbie is undeniable. Many people seem ready to overlook any issues they may have had with Barbie’s build and stereotyped past in order to focus on her potential as a cancer survival spokes doll. Here’s just a slight sample of the thousands of messages her online fans are sharing with each other:

I will keep posting all the great things about this Bald Barbie God Bless the work you are doing

I’ve forwarded it and wish I could do more. How can I help from Brazil?

Amazing idea! I re-posted a messages about a week ago that said…why don’t they make a hairless Barbie named hope dressed in pink with all proceeds going to help to cure cancer. I had no idea it was actually a work in progress! I 100% support this. I think it would make children fighting this feel good. Anything to help. And why not make dolls with other problems?! Spreading information and helping the cause or even a cure for the cause…what a Wonderful idea!

And it’s not just parents online that like the idea. Cori Liptak, PhD, a psychologist in the Pediatric Psychosocial Oncology Program at Dana-Farber/Children’s Hospital Cancer Center was recently interviewed about her support for the doll.

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Let’s get real about Down syndrome

by Brian Skotko, physician in Children’s Hospital Boston Down Syndrome Program

Brian Skotko, MD, MPP

In mere months, pregnant American women might be able to learn if their fetuses have Down syndrome with a simple blood test. The test will be perfectly safe, eliminating the small, but real, chance of miscarriage that comes with our current diagnostic options. If these tests do become a routine part of obstetric care, thousands of expectant parents will be receiving a phone call from their healthcare provider each year with this message: your fetus has Down syndrome.

That will be a panicked moment, according to women studied in previous research. But, what should healthcare professionals say about Down syndrome? What does it really mean to have Down syndrome? Six years ago, Sue Levine, Dr. Rick Goldstein, and I set out to find the answer to that question. Rather than let Rahm Emmanuel or GQ Magazine have the final word on what life is like with Down syndrome, we spoke to the people who truly understand.

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