Hawaii Governor Proclaims September 21st Hydrocephalus Awareness Day in Hawaii
September 21, 2013 by PHF
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As part of the PHF’s Hydrocephalus Awareness Over America (HAOA) campaign, today, Saturday, September 21st is the 1st ever Hydrocephalus Awareness Day in Hawaii!!
Congratulations to PHF State Chapter Director’s Shaula Tualaulelei & Amanda Klebe in getting this done, and to Governor Abercrombie for his participation:
** PHF IN THE NEWS ** PHF Michigan State Chapter Co-Director’s Featured in the September Issue of The Altum Advocate
September 9, 2013 by PHF
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PHF Michigan State Chapter Co-Director’s Jason & Carmen Adams and Donna West are featured in the September Issue of The Altum Advocate
PHF in the News: Hickenlooper recognizes brain-swelling condition
September 6, 2013 by PHF
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Durangoan, whose son has hydrocephalus, pressed for Colo. representatives’ support
The proclamation by Gov. John Hickenlooper designating September as Hydrocephalus Awareness Month came through the effort of a Durango woman whose son has the condition.
Christina Brown drafted a proclamation in mid-July and sent it to the governor’s office. She learned a month later it had Hickenlooper’s signature.
Brown’s son, 3½-year-old Jaden, has hydrocephalus, a swelling of the brain caused by an accumulation of the fluid that surrounds the brain and spinal cord, a condition found in one in 500 births.
About 1 million adults and children in the United States have hydrocephalus.
Brown said she found support from the region’s representatives in Washington, D.C., when she visited Capitol Hill with 140 members of the national Pediatric Hydrocephalus Foundation last week. The contingent represented the country from coast to coast.
Brown is the founder and director of the Colorado chapter of the Pediatric Hydrocephalus Foundation. She can be reached at christina@hydrocephaluskids.org.
She said U.S. Sens. Mark Udall and Michael Bennet and U.S. Rep. Scott Tipton appeared receptive when she urged them to support efforts to fund hydrocephalus education and research.
Brown said Jaden is doing very well and is receiving speech, physical and occupational therapy.
Contact Christina Brown at christina@hydrocephaluskids.org for more information.
PHF in the News: Walk for the Pediatric Hydrocephalus Foundation This Weekend
September 5, 2013 by PHF
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The walk begins at 11 a.m. Saturday at Roosevelt Park in Edison.
The Pediatric Hydrocephalus Foundation will once again lace up their walking sneakers on Saturday for the 7th Annual Walk & Family Fun Day.
The day will begin at 11 a.m. Saturday, Sept. 7 at Roosevelt Park in Edison, and is free.
Donations will be accepted to benefit the Pediatric Hydrocephalus Foundation, a nonprofit organization founded by Woodbridge residents that raises awareness of the brain condition and money for a cure.
The day will include face painting, music, refreshments, “Jedi Knight Training” and appearances by characters from Star Wars, according to a press release from the organization.
Registration for the walk open at 10 a.m.
Contact Kimberly Illions at 732-634-1283 or kim@hydrocephaluskids.org for more information.
PHF in the News: Woman to raise funds for brain condition with golf tournament
July 5, 2013 by PHF
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MIDDLEFIELD >> Samantha Pacelli has worked year round to put on a special fundraising event through the state’s Pediatric Hydrocephalus Foundation chapter in hopes of finding a cure for those affected by the brain condition.
On Tuesday, July 9, community members can help in the cause when Lyman Orchards hosts the second annual Hydrocephalus Awarness Golf Tournament. The PHF is an all-volunteer, nonprofit charitable organization that aims to raise awareness and provide assistance against the illness.
Pacelli, the state director for the PHF, feels the event will hold a special meaning for her 3-year-old son, Luca, who has hydrocephalus. She couldn’t get through her opening speech at last year’s event without showing any emotion, she said, but hopes it’ll be a smoother process this year.
“Raising awareness is my number one goal,” said Pacelli. “Thinking about it now, I get all teared up. I’m a very emotional person, so it’s overwhelming.”
Around 140 people came out in support last year, but with the backing of Lyman Orchards, Pacelli anticipates a bigger turnout this year.
“The crew has been very supportive of the efforts,” Pacelli said.
The Hydrocephalus Awareness Golf Tournament also includes a luncheon with a raffle drawing after the golfing session. Registration begins at 8 a.m. at Lyman Orchards with a shotgun start set for 9 a.m. The cost is $165 per player and includes the luncheon, while registration for the luncheon itself costs $50.
Contact Samantha Pacelli at 203-710-1031 or hydrocephhope@aol.com for more information.