When Carol Jackson took her then 9-month-old daughter, Delaney, to the pediatrician for a regular check-up, she had the suspicion that something might be wrong.

“Before that I kind of knew she wasn’t hitting the milestones,” Carol recently recalled while holding the now nearly 3-year-old Delaney on her lap.

A typical, happy little girl with a bright smile, Delaney wears her blond hair in pigtails and likes to show off her purple tennis shoes. But at 9 months old, the Macomb girl wasn’t developing the motor skills of other children her age and her legs were often shaky.

Delaney’s pediatrician at McDonough District Hospital ordered an MRI brain scan, which showed excessive fluid in the little girl’s brain.

Hydrocephalus, a condition in which excessive fluid builds up in the brain and causes pressure, had been causing Delaney’s delayed motor skill development and shaky legs.

She underwent emergency surgery at St. John’s Hospital in Springfield to drain the fluid and relieve the pressure on her brain. Doctors implanted a plastic shunt in Delaney’s brain to direct away the excess fluid away.

In February 2012, Delaney underwent revision surgery to replace the shunt. In October, Delaney also got an infection from her shunt and spent a month at St. Francis Hospital in Peoria.

“It was all so fast,” Carol says about the time period from the first visit to the pediatrician to the first surgery. “We knew something wasn’t clicking. It was just a whirlwind.”

The facts

According to the Pediatric Hydrocephalus Foundation, the condition affects more than one million Americans — from newborns to senior citizens — and an average of 40,000 shunt surgeries are performed in the U.S. each year.

Little is known about what causes the condition, and there has been almost no advancement in the treatment of Hydrocephalus.

While surgery to implant a shunt is the most effective treatment for Hydrocephalus, the shunts often fail or cause infections, just as it happened with Delaney.

“Hydrocephalus is like the most common brain surgery in children,” Carol said, “but a lot of time within the first year half the shunts fail, and that’s why I think they need to do more research.”

The shunts include a valve that is implanted behind an ear and a tube that extends through the body to direct fluid away from the brain.

Dr. Mary Kathleen Lockard is Delaney’s pediatrician at McDonough District Hospital and has treated others with the condition. She said there are signs and symptoms parents can look for in pediatric Hydrocephalus.
“If there is an enlarged head, or the head is growing more rapidly, that is something to look for,” she said. “We look for developmental delays as well, such as not crawling or sitting up. Those are the big things we look for. Also a loss of motor skill or headaches, but the head size and rate of development would be the biggest things.”

Lockard said it can difficult to determine what causes Hydrocephalus.

“It can be related to something that happened during prenatal development or something after birth,” she said. “In her (Delaney’s) case, we don’t know if it was something that was already there.”

The cause

Today, physical and speech therapy are helping Delaney maintain her motor skills.

But Hydrocephalus is a condition she will live with the rest of her life.

For support and to learn more about the condition, Carol reached out to the Pediatric Hydrocephalus Foundation and became that organization’s Illinois event coordinator. The nonprofit, 501(c) foundation is run by volunteers.

“I wanted do something,” Carol said. “I wanted something positive to come out of all this. I wanted people to be aware of what Hydrocephalus is, because we didn’t really know what it was.”

Carol, who works as a reading specialist with Macomb CUSD #185, hopes to continue raising awareness about Hydrocephalus. She is organizing a 5K fun run and walk for the Pediatric Hydrocephalus Foundation. The event will kick off at 9 a.m. on Saturday, Sept. 14, at the Old Dairy restaurant. All proceeds will go to the foundation. To register for the event, visit www.active.com/donate/phfrunil2013 or email Carol at carol@hydrocephaluskids.org.

Matthew Elicea, one half of the PHF’s “National Face of Hydrocephalus Awareness” winners, was featured in a TV Interview on California’s KGET-TV Channel 17.

“It’s like stabbing you in your head. For migraines it’s horrible, and I went to the emergency room countless times,” Lauryn Freeman said.

Lauryn learned last year that these were more than painful headaches. A Cat scan revealed a large amount of water on her brain, and she was diagnosed with Hydrocephalus.

“I knew what it was, I knew what to expect, I knew how hard it could be so I was devastated,” Lauryn’s mother Rebekah Wright said.

Hydrocephalus, also known as “Water-head” is when spinal fluid that is normally in your head builds up and it’s not able to drain. Treatment for Lauryn meant having surgery to get a shunt put into her head.

“By putting the shunt in place, you can actually set it so the pressure will be where you want it to be at, for that to actually let spinal fluid drain. So the pressure won’t get too high in her head and cause further damage in terms of brain injury or complications such as headaches or vision changes,” Lauryn’s doctor, Pediatric Neurologist Dr. John Flatt said.

Since her diagnosis, Lauryn’s mother has started the first Pediatric Hydrocephalus Foundation chapter in Louisiana. She’s currently organizing its first fundraiser, and it will be held March 27th at the Icegators’ playoff game. If you use the code “Ice” you get tickets to the game for 10 dollars, and one dollar from each ticket will be donated to the organization.

9-Year-Old Matthew Elicea From Bakersfield Selected as National “Face” of Hydrocephalus Awareness for Incurable Brain Condition

Bakersfield, CA – When looking quickly at 9-year-old Matthew Elicea, one would see a happy, athletic, & energetic boy. When you look a little closer and see the scars and stitch marks on his head, a different story is being told.

Matthew suffers from an incurable brain condition called Hydrocephalus, and the scars and stitch marks are the result of the multiple brain surgeries to implant the device in his brain, known as a shunt, that keeps him alive.

Occurring in approximately 1 of every 500 births and in over One Million Americans today, (including former Congresswoman Gabrielle Giffords), Hydrocephalus is a condition in which excessive fluid gathers in the brain, abnormally widening spaces in the brain and placing potentially harmful pressure on brain tissues. Because of lack of advancements in treatment, many affected individuals are left unable to lead full and productive lives.

Untreated, Hydrocephalus could be fatal.

Matthew was selected as one of two children to serve as this year’s “National Face of Hydrocephalus Awareness”, for the Pediatric Hydrocephalus Foundation, to help raise the level of awareness and education about Hydrocephalus in the United States. Matthew, whose family lives in Baskersfield, will represent the boys, while 7-month-old Aila Elmore of Indiana will represent the girls.

Debra Shoulet, Matthew’s mom, is ecstatic that her son will be the “Face” of Hydrocephalus Awareness for the Hydrocephalus Community in 2013; “One thing we believe we can do, is provide hope to parents, like us, who are given the heartbreaking news that comes with a diagnosis of hydrocephalus. There is HOPE!!! Miracles do happen! We live with a miracle. And some times those miracles are as small as a smile!”

Matthew will be featured in advertisement campaigns & promotional materials for Hydrocephalus Awareness as we head towards the 5th Annual “National Hydrocephalus Awareness Month” in September.

The Pediatric Hydrocephalus Foundation, an all-volunteer non-profit 501(c) (3) charitable organization, educates the community by creating awareness about Hydrocephalus. PHF, with 30 state chapters, provides support to families, friends and children affected by this incurable brain condition.

PHF assists the medical community by raising funds to search for treatment options, and ultimately, a cure. PHF advocates on behalf of members while working with policy makers at State and Federal levels to push for more research and support in the fight against Hydrocephalus. Donations are tax-deductible.

Since 2010, PHF awarded $170,000 in grants and donations to Hospitals, Neuroscience Institutes and Medical Research Centers for research and education. For information, visit HydrocephalusKids.org.

7-Month-Old Aila Elmore From Gosport Selected as 2013
National “Face” of Hydrocephalus Awareness for Incurable Brain

Gosport, IN – When looking quickly at 7-month-old Aila Elmore, one would see a happy baby girl. When you look a little closer and see the scars and stitch marks on her head, a completely different story is being told.

Aila suffers from an incurable brain condition called Hydrocephalus, and the scars and stitch marks are the result of the brain surgery she has had to install the device in her brain, known as a shunt, that keeps her alive.

Occurring in approximately 1 of every 500 births and currently affecting over One Million Americans today, Hydrocephalus is a condition in which excessive fluid gathers in the brain, abnormally widening spaces in the brain and placing potentially harmful pressure on brain tissues. Because of lack of advancements in treatment, many affected individuals are left unable to lead full and productive lives.

Untreated, Hydrocephalus could be fatal.

Aila was selected as one of the two children to serve as this year’s “National Face of Hydrocephalus Awareness”, for the Pediatric Hydrocephalus Foundation, to help raise the level of awareness and education about Hydrocephalus in the United States. Aila, whose family live in Gosport will represent the girls, while 9-year-old Matthew Elicea of California, will be representing the boys.

Aila will be featured in advertisement campaigns & promotional materials for Hydrocephalus Awareness as we head towards the 5th Annual “National Hydrocephalus Awareness Month” in September.

The Pediatric Hydrocephalus Foundation, an all-volunteer non-profit 501(c) (3) charitable organization, educates the community by creating awareness about Hydrocephalus. PHF, with 30 state chapters, provides support to families, friends and children affected by this incurable brain condition.

PHF assists the medical community by raising funds to search for treatment options, and ultimately, a cure. PHF advocates on behalf of members while working with policy makers at State and Federal levels to push for more research and support in the fight against Hydrocephalus. Donations are tax-deductible.

Since 2010, PHF awarded $170,000 in grants and donations to Hospitals, Neuroscience Institutes and Medical Research Centers for research and education. For information, visit HydrocephalusKids.org.