HORRY COUNTY, S.C. (WPDE) — Like many eight year olds, Brooklynn Reiter spends her time drawing, playing music, and cheering on her Oakland Raiders.

“Because my dad likes them. And me and my dad watch them,” Brooklynn said.

Now, she’ll add another activity to that list: being a 2019 ambassador for the Pediatric Hydrocephalus Foundation.

Hydrocephalus is a rare brain condition, affecting around one in every 500 babies.

“The fluid around your brain doesn’t drain on its own,” father John Reiter explained.

Brooklynn has undergone one surgery every year to clear the fluid.

“It felt weird at first. But whenever you fall asleep. It doesn’t feel that weird,” Brooklynn said.

As a parent, her father says its tough to see his daughter go through something so painful.

“Its scary. You don’t really know whats going to happen from one day to the next,” John Reiter said. “The shunts on average have a 50% success rate. They either work or they don’t,”

So far, Brooklynn’s shunts have been successful.

Now, her goal is to raise awareness about the rare condition.

“Some people don’t know what the word means and they don’t know how to say it,” Brooklynn said.

Her motto echoes her favorite team.

“Just win baby.”

Source:

8-Year-Old Brooklynn Reiter From South Carolina Selected as 2019 National Ambassador of Hydrocephalus Awareness for Incurable Brain Condition

First time we ever heard the word hydrocephalus was when I was 20+ weeks pregnant at a ultrasound. She was born on 12-31-10 and had her first ETV surgery at 4 days old.

After about a month she was back in surgery for another ETV attempt due to the first one closing. A month later she was in surgery again to place a shunt.

She has had 4 shunt revisions since then. The latest being just this past November 4th, you can find a more in depth post about that on my Facebook page.

Brooklynn has also had surgery to correct the nerves behind her eyes due to the pressure. So, she has had a total of 8 surgeries due to hydrocephalus.

She was also diagnosed with IS as a baby but has since been seizure free.

Before his first birthday, Owen Rush had undergone five surgeries for an incurable brain condition.

The 4-year-old Chesnee boy will raise awareness of the condition he’s battled since birth in a national campaign.

Owen will serve as the 2014 “National Face of Hydrocephalus Awareness” for the Pediatric Hydrocephalus Foundation. Owen will represent male children, while a 4-year-old New Jersey child will represent girls.

He will be featured in ad campaigns, promotional materials and literature for National Hydrocephalus Awareness Month in September. He and his family also will travel to Washington, D.C. for “National Hydrocephalus Awareness Day on Capitol Hill” in August.

Hydrocephalus affects hundreds of thousands of Americans of all ages, according to the Hydrocephalus Association. The condition occurs when excess cerebrospinal fluid surrounds the brain and spinal cord. The excess fluid can harm brain tissue and can be fatal. Hydrocephalus occurs at birth or may develop later in life.

Owen’s parents, James and Stacie Rush, learned Owen, their second child, had the condition when Stacie was 20 weeks pregnant.

“We didn’t know anything about hydrocephalus,” James said.

The couple was faced with many unknowns and asked many questions. Why did Owen have it? How did he get it? What would happen after his birth?

Stacie said they were uncertain what potential challenges awaited their son.

Abortion was not an option.

“We just continued with the pregnancy,” Stacie said.

She cried when fears set in. She wondered if she had unknowingly passed on genes that caused Owen’s hydrocephalus. Testing revealed she had not.

Owen — their “miracle” — was born Dec. 17, 2009. After five days in a neonatal intensive care unit, Owen spent a couple of weeks at home before his first shunt was implanted.

The shunt malfunctioned on Mother’s Day 2010, then again on Father’s Day, requiring emergency surgeries. A different shunt was implanted in another area of Owen’s brain later that year. Surgery to repair his skull was performed Thanksgiving.

Fortunately, there have been no more emergency complications with Owen’s shunt. But he began having seizures around 10 months old – as many as 40 a day.

Surgeons implanted a medical device this past August in the hopes to help treat Owen’s epilepsy and improve his quality of life. He continues to have about 15 seizures each day.

“Though we’ve not seen any change in his seizures, he is more cognitively aware,” Stacie said.

Owen cannot tell you if he’s hungry, cold or needs his diaper changed. Yet, he happily runs to give you a hug and announce he loves you. There’s almost always a smile on his face, even when he’s not well.

Owen may cry when nurses draw his blood, then he wants to hug them.

“He’s so loving,” Stacie said.

And at the emergency room, the parents are told that Owen appears fine. James said they explain that’s just the way Owen is—he gets sick and turns around for a hug.

Owen’s grandfather, Charlie Drake, called him a “trooper.”

Stacie said Owen isn’t saddened about his limitations.

“He has no conception of fear,” she said.

“He’s my bionic boy,” she said with a smile as Owen walked through the living room.

Stacie took the photo of Owen that was randomly selected by the Pediatric Hydrocephalus Foundation.

Owen was in the backyard wearing his big brother, Drake’s hat, when she snapped the shot with her cellphone. Owen also has a little sister named Charlee-Kate who looks out for her big brother and warns her parents when he’s having a seizure.

Stacie, a respiratory therapist, works weekends, while James, a deputy with the Spartanburg County Sheriff’s Office, works nights.

A typical day starts with a flurry of activity – assembling book bags and deciding who will take which kids where.

Drake attends Chesnee Elementary School, while Owen is at McCarthy Teszler School.

Owen has about 10 doctors. The family is often rushing to appointments and therapy sessions. When she has spare time, Stacie prepares for the next day.

The couple has learned to take one day at a time and not take small things for granted.

James said they wish hydrocephalus received more funding that would advance treatments.

Owen could die if his shunt malfunctions.

Michael Illions, vice president of the Pediatric Hydrocephalus Foundation (PHF), has a son, Cole, who was the inspiration for the foundation. Illions said in a phone interview that Cole, 8, has had 13 surgeries related to hydrocephalus. Hydrocephalus and the surgeries to treat it have left Cole unable to speak and caused other developmental delays.

“It’s been heartbreaking and difficult,” Illions said.

Cole, he said, excels in math, electronics and reads. He’s able to communicate by typing his thoughts.

Illions said a lack of advancements in treatment has left many affected individuals unable to lead full, productive lives.

Illions said that although someone with hydrocephalus may not appear sick, they have a potentially fatal condition.

He said hydrocephalus has not received the same level of attention as other conditions.

Hydrocephalus is often treated with a shunt system that’s surgically inserted to divert the flow of excess cerebrospinal fluid to another area of the body where it’s absorbed, according to the National Institute of Neurological Disorders and Stroke.

Illions and others want to see a cure.

“While the shunt itself is a life-saving device, it has its own problems,” Illions said.

He said shunts are subject to failure and there’s a window of time to correct that failure.

“It’s like a ticking time bomb when the shunt fails,” he said.

Hydrocephalus affects an estimated one to two of every 1,000 babies born in the United States.

PHF is an all-volunteer nonprofit that provides education and increases awareness of hydrocephalus with 34 state chapters. In addition to providing support to families, the organization also advocates for those with the incurable brain condition and raises funds for research in hopes there will be a cure. According to numbers provided by PHF, it has awarded $225,000 to hospitals, neuroscience institutes and medical research centers for research and education since 2010.

Illions said the face for PHF’s awareness campaign is randomly selected.

The foundation received 160 entries from around the world, including Africa, the United Kingdom, Pakistan, India, Australia and the Philippines. About 40 states also were represented.

Illions expects a “huge turnout” at this year’s annual retreat in Washington, D.C. He said more than 100 people have registered so far.

Owen’s photograph and his story are featured on the foundation’s website at www.hydrocephaluskids.org.

Owen has inspired the Rush family more than they thought imaginable.

“He’s definitely taught us patience and so much,” Stacie said.

James said they have more gratitude for everyday things.

“Simple things for us are accomplishments for him,” James said.

What some consider a big deal, is not so big after all, James said.

Stacie’s mother, Sandra, said God has helped the family through it all.

“There are strengths that you don’t know you’ve got,” Sandra said.

“Exactly — until you’re faced with it,” Stacie added.

Source:

4-Year-Old Owen Rush From South Carolina Selected as 2014
National “Face” of Hydrocephalus Awareness for Incurable Brain

Owen was diagnosed with hydrocephalus in utero at 20 weeks. We were well prepared for his arrival the week before Christmas, though nervous but exited as well. Our miracle was born at 37 weeks on December 17, 2009 with an OR full of staff and no complications. He stayed in NICU for 5 days with a small amount of feeding issues. He was discharged a few days before Christmas and we spent the rest of holidays with our family.

He had his initial VP shunt placed on January 5th and we came home 4 days later. He had his first emergency shunt malfunction on Mother’s Day 2010, his second shunt malfunction was a few weeks later on Father’s Day. Few weeks later he was back in for another shunt revision. This time they changed the shunt location and type, it was placed on the top right side of his head and programmable. All things were well until Thanksgiving 2010 he had a skull repair on his old shunt site, they used a plate and screws to fix the bone that wouldn’t seal up.

All these surgeries before our miracle turned 1 years old. He had his first seizure at 10 months old. since then hes tried 10 different medications an still having seizures on a daily basis. We traveled to Le Bonheur’s Children’s hospital in Memphis Tennessee in October 2012 and the team confirm he wasn’t a good candidate for any type of Epilepsy surgery, and were told how severe his developmental delay was after being through an intense evaluation, which we already knew and was shortly diagnosed with Autism.

We then traveled to Duke Hospital in NC for a Vagal Nerve Stimulator in August 2013 in hopes to improve his epilepsy and overall quality of life. He can’t feed himself, dress himself, he’s not toilet trained, nor can he tell you If he’s in pain or say I love you yet! He has been in Occupational, Physical and Speech Therapy since he was 4 months old.

He started school when he turned 3 to a school for the most disabled children in our county. Owen has adapted very well with the routine and friends, and is most importantly loved unconditional by all the staff at his school. Despite Owen’s disabilities he never stops smiling or wanting hugs.

We are pleased to announce that 2 more Members of Congress have joined the Congressional Pediatric & Adult Hydrocephalus Caucus. They are South Carolina Congressman Joe Wilson & Congressman Mick Mulvaney, also of South Carolina.