A Nebraska teacher is asking for help raising money for research as her 3-year-old niece in Wisconsin faces a rare and fatal diagnosis.It’s called Sanfilippo Syndrome Type B and there is no cure. Her family says it’s comparable to childhood Alzheimer’s. Olivia Stoop’s aunt says the girl was diagnosed after a doctor saw a picture of her. A young family full of joy had their world flipped upside down in March. “Actually, how they explain it is like childhood Alzheimer’s,” said Olivia’s aunt, Traci Stoop. Stoop says her brother and sister-in-law in Wisconsin noticed something was wrong with her niece and goddaughter Olivia or “Liv.””She was having chronic sinus infections and a distended belly and was really just overall having a lot of issues with her health,” Stoop said.Stoop says the family wasn’t sure where to turn. But thanks to a post on social media, a doctor here in the metro was able to point the family in the right direction. “And actually contacted the family because she had noticed the signs and symptoms of Sanfilippo by a photo,” said Stoop. Less than 24 hours later, Olivia was diagnosed with Sanfilippo Syndrome Type B, a genetic degenerative brain disorder in children caused by a single missing enzyme.It is fatal, and there is no FDA-approved treatment or cure.Our sister station in Milwaukee spoke with Olivia’s parents. “So she will slowly lose her speech. So slowly lose her ability to walk, her ability to eat,” said Olivia’s mother, Erin Stoop. Olivia will also likely suffer severe dementia and seizures. Doctors believe she won’t live beyond her teenage years. “No mom wants to hear, you know, ‘your child is going to die and there’s nothing you can do.’ You just have to take her home and love her. It’s not OK,” said Erin Stoop. The family says they want to raise a million dollars and put it toward a clinical trial investigating this rare condition hoping that it could save Liv. “We’re going to take this on. We’re going to fight for her. She deserves it. Those other children deserve it,” Erin Stoop said. There is a website where you can read more and donate. You can find that here. Watch the video above for the full story.
A Nebraska teacher is asking for help raising money for research as her 3-year-old niece in Wisconsin faces a rare and fatal diagnosis.
It’s called Sanfilippo Syndrome Type B and there is no cure. Her family says it’s comparable to childhood Alzheimer’s.
Olivia Stoop’s aunt says the girl was diagnosed after a doctor saw a picture of her.
A young family full of joy had their world flipped upside down in March.
“Actually, how they explain it is like childhood Alzheimer’s,” said Olivia’s aunt, Traci Stoop.
Stoop says her brother and sister-in-law in Wisconsin noticed something was wrong with her niece and goddaughter Olivia or “Liv.”
“She was having chronic sinus infections and a distended belly and was really just overall having a lot of issues with her health,” Stoop said.
Stoop says the family wasn’t sure where to turn.
But thanks to a post on social media, a doctor here in the metro was able to point the family in the right direction.
“And actually contacted the family because she had noticed the signs and symptoms of Sanfilippo by a photo,” said Stoop.
Less than 24 hours later, Olivia was diagnosed with Sanfilippo Syndrome Type B, a genetic degenerative brain disorder in children caused by a single missing enzyme.
It is fatal, and there is no FDA-approved treatment or cure.
Our sister station in Milwaukee spoke with Olivia’s parents.
“So she will slowly lose her speech. So slowly lose her ability to walk, her ability to eat,” said Olivia’s mother, Erin Stoop.
Olivia will also likely suffer severe dementia and seizures. Doctors believe she won’t live beyond her teenage years.
“No mom wants to hear, you know, ‘your child is going to die and there’s nothing you can do.’ You just have to take her home and love her. It’s not OK,” said Erin Stoop.
The family says they want to raise a million dollars and put it toward a clinical trial investigating this rare condition hoping that it could save Liv.
“We’re going to take this on. We’re going to fight for her. She deserves it. Those other children deserve it,” Erin Stoop said.
There is a website where you can read more and donate. You can find that here.
Watch the video above for the full story.
