The Pediatric Hydrocephalus Foundation has chosen four-year-old Hailie Mussinan of Woodbridge to be the face of its annual “National Face of Hydrocephalus Awareness.”

A little girl from Woodbridge Township has been chosen as the face of a national campaign to fight pediatric Hydrocephalus.

Hailie Mussinan lives with an incurable and potentially life-threatening brain condition called Hydrocephalus, which causes excess fluid to build up in her brain. She is four years old and has already had multiple brain surgeries to install a shunt in her brain, according to a release from the Pediatric Hydrocephalus Foundation.

She has been chosen to serve as a face of the Pediatric Hydrocephalus Foundation’s annual “National Face of Hydrocephalus Awareness.”

Her face will be featured in a national awareness campaign against the condition, and the Mussinan family will travel to Washington, D.C. for “National Hydrocephalus Awareness Day on Capitol Hill” on August 22, according to the release.

September will also be observed as “National Hydrocephalus Awareness Month” for the sixth year, according to the release.

Two children were chosen. Mussinan and Owen Rush, a four-year-old South Carolina boy, according to the release.

“Together as a family we are blessed to have found, and be apart of, the Pediatric Hydrocephalus Foundation and Hailie is honored to represent all the girls with Hydrocephalus in 2014,” said Melody Mussinan, Hailie’s mother.

For information on the Pediatric Hydrocephalus Foundation, visit HydrocephalusKids.org

Source:

4-Year-Old Hailie Mussinan From New Jersey Selected as 2014
National “Face” of Hydrocephalus Awareness for Incurable Brain

Last year our then 3 year old Hailie started having headaches daily sometimes followed by vomiting. We also noticed her balance was off and her eye would slightly turn in at times. We took Hailie to a pediatrician, an eye doctor, and a neurologist who all assured us that it was most likely sinus related. Although her Mother kept insisting something was seriously wrong!

October 2nd of last year Hailie was scheduled for an outpatient MRI. We were quickly admitted shortly after that and she was diagnosed with Hydrocephalus and a cancerous low grade brain tumor; Pilocytic astrocytoma.

Hailie needed an emergency surgery to put in an external drain to relieve the pressure from the Hydrocephalus. Two days following she had a craniotomy and we are blessed to say the tumor was fully resected! Days following the craniotomy a shunt was placed but not for long.The night before we were to get released she had a seizure and a very high fever.

The shunt was removed and another external drain was put in place. Hailie spent the next few days sleeping naked on ice filled cloths to bring the fever down. She was on a very strong antibiotic for 14 days which was hard on her veins during which IV changes were frequent to treat the shunt infection. Finally she was ready for a new shunt and we were able to go home on Halloween.

She had a total of 5 brain surgeries in 22 days! In the summer of 2013, Hailie had another surgery because her shunt incision was not healing correctly. She has also been diagnosed with some eye issues from the Hydrocephalus and tumor. We are in the process of trying correctional therapy.

Today Hailie is a happy 4 year old who loves to dance and is looking forward to starting school next year!

Affecting one in 500 children, hydrocephalus is a condition in which excessive fluid gathers in the brain, abnormally widening the spaces in the brain and placing potentially harmful pressure on brain tissues.

Many of those affected cannot lead full and productive lives – and untreated, hydrocephalus can be fatal.

In May, Brody’s mother, Madonna Logue Bove, became the Southern New Jersey/ Philadelphia chapter director of the Pediatric Hydrocephalus Foundation. Her goal is to raise awareness of the condition and to raise funds for medical research.

Brody’s story began when he was 18 months old.

“Brody had flulike symptoms. He was vomiting a lot,” Logue Bove said. “The next day his balance was off and his eyes were like bulging out of his head. We took him to the local hospital’s emergency room, where they treated him for dehydration, which has many of the same symptoms as hydrocephalus. Brody didn’t react to the treatment and was admitted. Luckily, someone that was familiar with hydrocephalus was able to examine him and thought there was a need for a CAT scan.”

The scan showed fluid on the brain, and Brody’s doctor wanted to send him to St. Christopher’s Hospital in Philadelphia for immediate surgery. But, he was afraid Brody would not survive the ride.

“I was just freaking out this whole time,” Logue Bove said. “I had no idea what hydrocephalus was. I was so scared.”

Brody’s doctor made some phone calls, and finally found a neurosurgeon in Atlantic City who agreed to perform surgery. An external catheter was put in Brody’s brain to drain the fluid and relieve the pressure on his brain. Brody was taken to St. Christopher’s, where a shunt was put inside his brain with a tube that runs down his neck to his stomach. The shunt diverts the excess fluid to Brody’s stomach, where it can be drained out.

“What makes the condition so bad is that it is a lifelong condition,” Logue Bove said. “As the child grows, a new shunt has to be put in. Right now, if all goes well, Brody won’t need surgery again until he is 8. But there can be many complications. Brody had to have surgery after an infection, and there can be other complications as well. It’s hard because you really never know when something will happen and he will need surgery. Through this whole ordeal, Brody has been a terrific kid. He was so well behaved. He had to be restrained because he tried to pull out the external catheter. But once the shunt was in, he was fine. He just seems to take everything into stride.”

Brody’s condition may have caused some developmental delays, and Logue Bove is going to have him evaluated soon, she said.

“His eating habits were affected, he won’t touch anything soft,” Logue Bove said. “And his speech may be a bit delayed, but doctors said he made a remarkable recovery. Other children with hydrocephalus are far worse off. Doctors don’t know why Brody developed this condition, since he didn’t have it from birth. Children who do have it from birth sometimes have brains that aren’t fully developed and have severe problems. Others get the condition from a brain hemorrhage or tumor.”

Logue Bove got in touch with the Pediatric Hydrocephalus Foundation, and when she learned they needed a director for southern New Jersey, she didn’t hesitate to volunteer for the position.

“There is an extreme lack of awareness, and my goal is to increase knowledge and raise money to help find a cure. I hope to be able to provide support and hope to parents and families dealing with similar situations. There have been no advancements in treatment since the 1960s for this condition, and I hope to help change that. I plan to start some local fundraisers in September.”