PHF In The News: Westhampton mother, daughter raise money for medical research
September 23, 2016 by PHF
Filed under Uncategorized
Comments Off on PHF In The News: Westhampton mother, daughter raise money for medical research
WESTHAMPTON — When Isabella Sacharczyk was about a month old, she was diagnosed with hydrocephalus, an incurable condition known as “water on the brain.” Doctors told her parents she would not be able to walk, talk, hear or see, and recommended that Isabella be put in a home for children with those disabilities.
“We chose not to,” her mother Denise Sacharczyk said. “We were going to do whatever we had to do to give her the best quality of life.”
Today, 18-year-old Isabella is a senior at Hampshire Regional High School. She is ranked 16th in her class with a 3.95 grade point average and aspires to become a medical researcher.
To raise awareness and money for hydrocephalus research, Isabella and her mother are hosting a fundraising walk at Hampshire Regional High School from 10 a.m. to 1 p.m. Saturday through the nonprofit Pediatric Hydrocephalus Foundation.
After searching for a support group, about three years ago, Isabella and Denise became involved with the organization, and now head the Massachusetts state chapter. Last year, the mother and daughter hosted their first walk at the high school. About 80 people attended and the event raised about $6,000.
The cause of hydrocephalus can vary person to person.
Isabella’s hydrocephalus was due to damage from E. coli meningitis and a related stroke.
A shunt is surgically placed to drain fluid from the brain and release pressure. Isabella has two of the devices which move fluid from one part of the body to another.
“Pretty much the shunt saves her life,” Denise said. “Without it she would die.”
Isabella has had 23 brain surgeries due to malfunctions or complications related to the shunt, with six of those surgeries were in 2011.
“One in three shunts don’t make it six months,” before malfunctioning, Isabella said. “So the odds aren’t great.”
After one surgery in 2013, Isabella had to learn how to walk again.
“She could be perfectly fine today and tomorrow she could be in the emergency room,” her mother said.
Isabella has trouble with fine motor skills, walks with a cane and experiences headaches on a daily basis. She cannot take notes in school and her memory is not great, but she spends hours studying at home, using notes provided by her teachers.
For exercise, Isabella rides a tricycle, though she joked that she “managed to fall off.” Her mother bought a matching one to go on rides with her daughter.
“I don’t let my condition hold me back,” Isabella said.
The “Funding a Cure for Hydrocephalus” walk on Saturday will feature a bounce house, music, concession stands and a raffle. Students can volunteer at the event for community service hours.
To register or donate, visit active.com/donate/phfwalkma2016.
PHF Sponsors Hydrocephalus Awareness Day On Capitol Hill
September 4, 2011 by PHF
Filed under Uncategorized
The Pediatric Hydrocephalus Foundation will be hosting a Hydrocephalus Awareness Day on Capitol Hill event on Friday, September 23rd, thanks to the Congressional Pediatric & Adult Hydrocephalus Caucus, chaired by Congressman Leonard Lance- (NJ), and Congressman Tim Walz- (MN). Parents of children with Hydrocephalus, teens and adults with Hydrocephalus, and members of the Medical Community will make presentations and tell their stories to Members of Congress and their staff. The Hydrocephalus Awareness event on Washington, DC is the first of it’s kind for the Hydrocephalus Community and the PHF is proud to be able to organize it. Immediately following the event, we will be walking the Halls of Congress and meeting with our individual Congressional Representatives for one on one discussions. For more information please email mike@hydrocephaluskids.org.