WESTHAMPTON, MA (WGGB/WSHM) — As a parent, one of the toughest thing you’d ever go through is hearing your child has a rare condition.

One Westhampton woman has used her diagnosis as a defining moment for the rest of her life.

“My parents, after I was born…were told I would never talk, walk, see, hear. They were advised to put me in a home. Thank God they didn’t,” said Isabella Sacharczyk.

Like many 20 year olds, Sacharczyk is in college studying for her future career, but she also has hydrocephalus.

“Hydrocephalus is water on the brain. It’s an incurable condition where the cerebral spinal fluid doesn’t drain. I have hydrocephalus,” Sacharczyk explained.

After her initial diagnosis, Sacharczyk has proven the doctors wrong each step of the way.

“I graduated from Hampshire Regional and am now in college. I’ve made it my mission in life to become a medical researcher to help find a cure for hydrocephalus,” Sacharczyk noted.

Sacharczyk is instrumental in the organization Pediatric Hydrocephalus Foundation, where she is co-director for the Massachusetts chapter.

One of the groups biggest events is a fundraising walk.

“This past walk, we raised a little over $5,000. We do a walk here and an event in New York. Combined, every year, we have been able to donate about $10,000 to Boston Children’s Hospital,” Sacharczyk said.

Many in Westhampton are supportive of her efforts.

“Outlook Farms is absolutely incredible. They are gracious enough to allow me to put a donation jar near their register. I picked up the jars right before the walk and we had $150 to add to the total we raised for the walk,” Sacharczyk added.

We wanted to help, so on behalf of Western Mass News and Diamond RV, Jacob presented Sacharczyk with a check for $500.

“Every dollar gets us closer to a cure. I feel that we are close,” Sacharczyk said.

CLICK HERE for more information on Sacharczyk’s mission and CLICK HERE to learn more about the Pediatric Hydrocephalus Foundation.

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The PHF is looking for one boy and one girl to serve as our National Spokesperson for our 2019 National Hydrocephalus Awareness Campaign.

These 2 National Ambassasors will be featured in marketing and promotional materials all through the year ending in September 2019 with National Hydrocephalus Awareness Month, (The winners in 2018 received a letter from their Member of Congress and mentioned on the Floor of the House of Representative and entered into the Congressional Record).

The National Ambassadors & their families will also receive a 2 night complimentary stay @ the Embassy Suites Hotel for the 2019 PHF Issues & Action Hydrocephalus Conference on Capitol Hill in Washington. DC on Thursday August 15th & Friday August 16th.

We will randomly selection ONE boy and ONE girl from all entries received. Read the rules carefully!

1) Submit one picture of your nominee*, between the ages of newborn to 19 years old, with their name, D.O.B., and location. *(By submitting a picture, you authorize the PHF to use the picture for promotional purposes).
** Failure to comply with Rule #1 will disqualify that entry.

2) Only one entry per child will be accepted. Siblings with Hydrocephalus can be entered separately.

3) ** PHF Board of Directors & State Chapter Directors are eligible to participate and enter their child.

4) All entries will be featured on the PHF website in a pictorial collage.

EMAIL your entries to mike@hydrocephaluskids.org (Entries sent any other way will NOT be accepted or acknowledged).

Contest ends 12/31 & both winners will be announced on January 2nd, 2019 in the evening via video announcement.

Check out the picture galleries of everyone who has been entered: