A beautiful summer night wouldn’t be complete without lemonade. And the Washingtonville community wouldn’t be itself unless it came out in droves to support a child’s stand.

On the Aug. 24 Date Night of this summer’s season, $642 was raised for the Pediatric Hydrocephalus Foundation through Washingtonville resident Brayden Thew, who served regular and pink lemonade with all of the proceeds going to the foundation that helped save his life. “Brayden was diagnosed at 11 days old with hydrocephalus,” his mom Cassandra said, “an incurable brain condition, and had seven brain surgeries by the time he was five years old. The Pediatric Hydrocephalus Foundation had given us a tight community when we felt so alone and had become like family to us.” So when Brayden held a small lemonade stand on his road this summer and wanted to give the full $12 he had made to the foundation, his mom was floored — and thought about how to grow the idea.

Which is when the community immediately stepped in and the Washingtonville Community Events Team, Betty’s Country Kitchen, J. Hoffman Insurance, and Hudson Heritage Realty all worked to make this idea a reality by suggesting Brayden set up his stand at the last Date Night of the season at Vern Allen Park (and providing the resources to do so), where children and adults played and socialized, and even danced for prizes, as tunes were spun by Washingtonville’s own Jeffrey Blizard of That’s EnterTOONment until the outdoor movie, Despicable Me 3, was played and gallons of lemonade was enjoyed by everyone.

Congratulations to Brayden, his family, and the Washingtonville community for just being itself and supporting a child and a cause. For more information on hydrocephalus, go to http://www.HydrocephalusKids.org.

The closing Date Night of the season will be in September (date to be determined) as a rescheduling of the one evening in July that had been rained out.

CAPTION 1: Brayden Thew serves up the sweet stuff to a customer at last week’s Date Night in Washingtonville. (Photo by Eugenia Moskowitz)

Source:

HORSEHEADS, N.Y. (18 NEWS) – Imagine having more surgeries than you are years old. That’s exactly what 19-year-old Isabella Sacharczyk has gone through, 23 times, in her brain.

“It’s very, very hard, to be honest with you, I didn’t let her sleep by herself until she was 16,” Denise Sacharczyk, Isabella’s mother, said. “I was scared to death that something would happen while she was sleeping.”

Hyrocephalus is the neurological condition Isabella was born with. It’s caused by too much fluid pressing on the brain. She has two medical devices, known as shunts, put into her brain, to drain excess fluids.

October will mark four years Isabella has been surgery free.

“It feels great, because I went a good six years with at least having one surgery a year, and as a little seventh grader, I missed three months of school that year,” Isabella Sacharczyk, said.

Today also marks four years of fundraising for “Bella’s Journey”. Isabella and some of her family flew from their home state, Massachusetts, to fundraise here, in Horseheads, where most of her family resides.

This annual “Bella’s Journey” event is a fundraiser for education and research for Hydrocephalus.

A 60 miles motorcycle ride is the newest addition to this annual event.

“A lot of motorcycles get together for a lot of charity rides like this because there are so many negative things in the world being said about motorcyclists and I think it’s a good thing that all these people, a nice group of people are getting together and doing a charity ride for a common cause,” Olavs Ozolins, road captain at the Finger Lakes New York H.O.G. group, said.

“Just the love of children, you know, whatever we can do to help is great,” Hazel Hall, a member of the Finger Lakes New York H.O.G. group, said. “As we’re out riding, it seems like everybody waves at us, toots at us, you know, it makes us feel real welcomed.”

Isabella is now studying for her doctorates to become a medical researcher.

Source:

HORSEHEADS, N.Y. (WENY) – Raymour and Flanigan is partnering with the Pediatric Hydrocephalus Foundation to host the 4th annual “Bella’s Journey” Fundraiser event.

The event is happening today at Raymour and Flanigan in Horseheads from 12-4 pm. The event is for 19-year-old Bella Sacharczyk, who is living with Pediatric Hydrocephalu also known as, PHF. Bella is a survivor of 23 brain surgeries, her mission is to raise awareness and money to fund research projects for the disease. “Bella’s Journey” has resulted in $25,000 being raised in research grants over the last 3 years. The fundraiser is open to the public and is kid friendly.

There will be food, baked goods, raffles, kids games, a bounce house, music and much more. There is also a new 60 mile Motorcycle ride that has been added to this year’s fundraiser.

If you want to know more about the condition, click here.

Source:

16-Year-Old Madison Fleming From New York Selected as 2018 National Ambassador of Hydrocephalus Awareness for Incurable Brain Condition

Madison was born four weeks early and weighed 4lbs 4oz. Three weeks after Madison was born she was diagnosed with Hydrocephalus caused by a cerebral hemorrhage. After numerous fontanelle taps she had her first shunt placed at 1 month old. Since her first shunt was placed she has had 5 emergency brain surgeries to replace/fix the shunt. Four of those emergency brain surgeries were within 9 months of each other.

Other than the brain surgeries that Madison has gone through she has also faced eye surgeries, learning disabilities, debilitating migraines, and years of physical therapy.

With all the challenges that Madison has faced she has pushed herself to compete in ice hockey, lacrosse, cross country and horseback riding.

3-Year-Old Owen Davidson From Tennessee Selected as 2018 National Ambassador of Hydrocephalus Awareness for Incurable Brain Condition

Owen was born October 20th 2014 along with his twin sister Shelby. When he was born, he was having a hard time breathing. They sent him to East Tennessee Children’s Hospital. The first few days were rough. They diagnosed him with SVT. It’s a heart condition. Then as days passed they told us he had a IVH grade 3 on the left and grade 4 on the right brain bleed. Then they said this word.. (Hydrocephalus).

As parents we didn’t really understand what this was. So we did our research and we were heartbroken because we didn’t know when, why, or how this happened. We wanted answers, but they really couldn’t tell us anything. They did so many taps to keep the fluid off, we lost count. He had to have 2 blood transfusions.

He was too little to have the surgery. So at 1 month of age the VP Shunt was placed. Everything went great, he came home after a 40 day nicu stay. At 15 months he was diagnosed with cerebral palsy. We were heartbroken again. They first said spastic quadriplegic CP. Then changed it to mixed cerebral palsy.

At 18 months of age he had his first revision and, oh my goodness, this was bad. We almost lost him because we couldn’t get anyone to listen to us. All they would stay he doesn’t have the symptom of a shunt malfunction. No tests were done. So we had enough. We took him to the ER at the Vanderbilt children’s hospital.

The scan came back yes his shunt has malfunction and he needs surgery right now. During the surgery while they were removing the other shunt he had another brain bleed. So they had to do a EVD til all the blood was gone. So after 23 days in the picu his vp shunt was placed.

Owen has had other surgeries not hydro related. But Owen is one true fighter. He has a lot of family supporting him in this journey. He has his Mother Crystal, Father Rodney, brother Hunter, sisters Cheyenne and Faith and his twin sister Shelby. We all love him unconditionally. He always keeps a smile on his face. He is a true inspiration.