FRESNO, Calif. (KMPH) –

Carrie Awbrey, California Chapter Director for the Pediatric Hydrocephalus Foundation, visited Great Day to talk about a perilous condition more commonly known as “water on the brain.”

The mission of the Pediatric Hydrocephalus Foundation is to educate the community by raising the level of awareness about this brain condition.

The PHF will also provide support to the families, friends and children who are diagnosed with Hydrocephalus.

The PHF will raise money for and work with the medical community in searching for a cure and additional treatment options for those with Hydrocephalus.

The PHF, Inc. is a non-profit 501 (c) (3) charitable organization and as such, all contributions are tax deductible to the extent allowed by law.

Additionally, the PHF will advocate on behalf of the members of the Hydrocephalus community and work with policy makers at the State and Federal level to raise awareness and push for more research and support in our fight against Hydrocephalus.

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 Michigan State Chapter Co-Director’s Jason & Carmen Adams and Donna West are featured in the September Issue of The Altum Advocate

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.

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.