A CULTURAL NOTE
Do you ever keep up with health and beauty trends?  Well, here's the latest, from CNN:
"We're not usually the type to follow every beauty trend, but this spring we found one we just adore: "Looking imperfect is in," says Eva Scrivo, a New York City salon owner and author of Eva Scrivo on Beauty, "because it shows off what makes us individuals, and unique."
And, she points out, when you work with -- not against -- your own features, you get better (read: more beautiful) results. Here are the freshest ways to look amazing with the skin and hair you're in."

Well, for those of us with Moebius or other physical differences, that's good to know! 
The truth of course is that no one has a "perfect" body; or, put even better, everyone has beauty within them.  But anyway, here's an example of what you can do with your natural body, according to the article:
"What's hot: Freckles for all ages. Just take a look at all the A-list beauties -- Julianne Moore, Sienna Miller, Giselle Bündchen -- who show off their sweet spots. "Freckles make you look youthful -- in a good way," says New York City-based makeup artist Suzanne Katz, who wears her own freckles (compliments of her Irish genes) proudly.
Play yours up: Go for tinted moisturizer instead of a full-coverage foundation, Katz says. Dab it on to even out your tone, while letting your lovely freckles show through. Then, dust a peach-colored blush across your cheekbones. "There's something about the shade that looks so fresh on freckle-dotted skin," Katz says. For extra oomph, top with a little glistening highlighter. It gives a glow and acts like a spotlight on cheeks."

INSPIRATIONAL STORY OF THE DAY
This young man doesn't have Moebius--he has a different, very life-threatening, condition.  But look at how he and his family battle through things.  His story also also shows how we need to continue to fight for bring awareness for all those with physical differences--because life is precious for all.  Read on to see why this is so:
"If medical books told the story, Lane Hauber wouldn't be alive.
When he was born three years ago, he would have never made it home from the hospital.
Lane was diagnosed with Trisomy 18, a rare genetic disorder that is supposed to be fatal — incompatible with life.
The three-year-old daughter of Republican presidential candidate Rick Santorum has been in the news in recent days; she suffers from the same disease.
Lane's mom, Alisha Hauber, remembers researching Trisomy 18 for days after her newborn son was diagnosed. "I didn't have the hope in the beginning, because all I heard was that he was going to die," she told News 8, holding her son in their Springtown home.
Moments later, Lane was playing with his 10-month-old sister Taylon. She's about the same size, but quickly passing her brother developmentally.
Lane cannot talk or walk, but he recognizes family members and interacts with playful movements.
His dad, Alex, takes pride in the way Lane defies the odds. Ninety-eight percent of Trisomy 18 infants never leave the hospital.
Lane has already battled back from cardiac arrest four times. Alex remembers one occasion when Lane went into cardiac arrest in the hospital and was on a ventilator for three days.
Then, doctors decided he might be able to breathe on his own.
"It happened that the doctor walked in at the moment they pulled the ventilator, and he was perfectly fine," Alex recalled. "Me and Alisha were both like, 'Ha ha ha! Yes! Right in your face!"
The Haubers are still fighting for their son. Trisomy 18 survivors have to overcome several other associated health issues involving the heart and lungs.
Lane has two holes in heart, and requires oxygen to survive.
Heart surgery could save him, but Trisomy 18 complicates the process, because surgeons calculate the cost versus life expectancy.
Several doctors at Fort Worth's Cook Children's Medical Center have made it their mission to help Lane, but that's not a risk most doctors are willing to take.
Lane's cardiologist, Dr. Benjamin Siu, died earlier this month in a bicycle accident. The Haubers said he was Lane's biggest advocate who made countless phone calls trying to find a surgeon.
Dr. Mary Kukolich, Lane's geneticist, is also supportive, but she doesn't want to give Trisomy 18 families false hope. In more than 30 years of medicine, she's seen fewer than a handful of patients live to adulthood.
"I think care and comfort is the best way to help these children," Dr. Kukolich said. "Most of them would die during the surgery, and that's a lot of pain and a lot of stress."
The Haubers believe Lane can not only survive, but thrive. So they continue the fight. While Lane may never escape the everyday life of syringes and tubes, his life matters to his parents — no matter how long it lasts.
Alex says he refuses to let his son die. "God will make that decision when that day comes. Until then, we fight for our children," he said.
Alisha looks at her son as she talks about his possible surgery. She doesn't blame doctors for being cautious, but she wants someone to break new ground.
"It's just not fair that I don't have a choice, because he wants to be here," she said.
The Haubers say Lane has a story, and they want the world to hear it. While he's alive, Alisha says, he has a lesson to teach.
"Don't take anything for granted. Find joy in the simple things. You never know how long you are going to be here," she said, adding: "And fight for the people you love."
The Haubers have formed the Trisomy Advocacy Group to help other families with newly-diagnosed loved ones."

"When you know what you want, and want it bad enough, you
will find a way to get it." -Jim Rohn