BAKERSFIELD, Calif. (KERO) — A Bakersfield family is going viral — their baby with Moebius syndrome is sparking support across the country. Their story is educating others while showing what life with ...

Sharing personal stories of individuals with Moebius Syndrome and their families can help us to better understand the challenges they face and how advocacy, education, and support can make a ...

Add Yahoo as a preferred source to see more of our stories on Google. Welsh 4-year-old Eva Hadley has been diagnosed with Moebius syndrome, which affects two to 20 newborns out of 1 million. A ...

DIX HILLS, Long Island (WABC) -- A school community in Long Island raised nearly $1,000 to celebrate a kindergartner who suffers from a rare disorder. Faculty, students and families of the Half Hallow ...

Moebius Syndrome Awareness Day is January 24. I'm a psychology professor who has and studies Moebius syndrome. Here are seven reasons why people with Moebius syndrome like myself seek understanding on ...

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. THE BRONX, N.Y. (PIX11) — Luis Velazquez is ...

Nine-month-old Hazel has a rare neurological condition called Moebius syndrome which is a form of facial and eye paralysis. Hazel has had multiple brain surgeries as she lives with another ...

Addison “Addie” Garvey is a Melville 10-year-old who enjoys dance and cheerleading, loves to read and write and plays drums in a band. She thrives in her fourth-grade class at Sunquam Elementary ...

Alex Barker wasn’t expecting Erin Smith to smile when they met in 2015 after almost two years of getting to know each other online. He knew he wouldn’t either. Not because he wasn’t sure he would find ...

Add Yahoo as a preferred source to see more of our stories on Google. A newborn in Minnesota has been a fighter since before she entered the world. Little Hazel has hydrocephalus, a condition that ...

A 4-year-old Welsh girl can’t smile, frown, raise her eyebrows or even blink — thanks to a very rare cranial nerve condition without a cure. Eva’s grandfather, Jonathan Watkins, will run the Milton ...