TOWN OF VERNON — This Friday, 7-year-old Westmoreland Elementary student Elyse Clough plans to address Congress, hoping to educate lawmakers on hydrocephalus and to seek their help in fighting it.

Elyse and her family left this morning for Washington, DC despite her emergency surgery last Saturday.

“She made it through, and she’s a real fighter,” Elyse’s father, Tom Clough, said. “And now we’re definitely heading out to speak on hydrocephalus.”

Elyse, who aspires to be a pediatrician, has been named National Ambassador of Hydrocephalus Awareness for 2016 by the Pediatric Hydrocephalus Foundation. On Friday she will join her parents and 23 other members of Research, Educate, and Cure Hydrocephalus, a DeWitt-based support group, to advocate for hydrocephalus research.

Hydrocephalus is a medical condition caused when an excess of fluid causes swelling and pressure on the brain. It has no known cure, and the only treatment is a shunt implant. A shunt is a soft silicone implant placed in the brain, then directed under the skin to the abdomen where excess fluid is drained and re-absorbed into the body.

Elyse received her seventh shunt after a seizure Friday evening.

“I was saying good night to my son, and as I passed her room I saw her hand shaking. I knew she was having a seizure, and we drove to Upstate University Hosptal (in Syracuse). We stayed there until Sunday afternoon,” Elyse’s father, Tom, said.

Elyse suffered the seizure at 10:30 that evening, and she underwent surgery 8:25 a.m. Saturday morning. After doctors confirmed the shunt was not infected and that Elyse was healthy she was released and sent home.

“The doctors ran some tests to be sure she is eating and drinking, that her eyes are clear and she is walking and using the bathroom,” Tom Clough said. “Because of the number of sick people in a hospital the risk of infection is lower at our home.”

On Friday morning Tyler Side, 11, of Washington state, will join her to represent boys battling hydrocephalus. They will then make a number of public and social media appearances during September, which PHF has designated as National Hydrocephalus Awareness Month.

But first she will enjoy some time visiting Washington and Virginia Beach.

“I am ready to stand before the people in suits and talk,” Elyse said. “Then I will go to the beach with my pail and shovel and play.”

Request for help

Elyse and other members of the delegation will stand before the country’s legislative branch to help advocate for continued education and research for her condition. Their goal is to have Bill H.R. 2313 passed into law.

If passed the Public Health Services Act would require the Centers for Disease Control and Prevention to expand its tracking of the epidemiology — the patterns, causes and effects — of hydrocephalus and use the information as part of a national database to spur research on the condition.

“We hope to accomplish more than we did last year,” Elyse’s mother, Kim Clough, said. “We’ve had good success with (U.S. Senator Charles) Schumer’s office, but we need to get this passed in the House of Representatives first before the Senate will consider it. We met with a representative’s staffer and all he did was stare at his pen and ignore what we said.”

An ongoing battle

PHF, which has chapters in 30 states, provides supports to families and also advocates with the medical and legal communities to help find a cure. Since 2010 they have given $375,000 in grants and donations towards research and education on the condition.

Research is needed because the relief provided by shunts is compromised by their frequent failure rate. Children have a shunt failure rate between 25 and 40 percent. Replacing a shunt is a complicated and potentially dangerous process. Elyse most recently had a shunt replaced in February.

“There are 40,000 shunt replacements a year, one every 15 minutes,” Tom Clough said.

Endoscopic third ventriculostomy, a shunt-free procedure where an incision at the bottom of enlarged ventricles allows fluid to drain, only works in two-thirds of patients.

Despite its myriad disorders hydrocephalus has a high survival rate. Several of the estimated 125,000 people suffering from have reached middle-age and older. “Some of these people will be coming with us this week,” Tom Clough said.

The Clough family remains proactive in supporting Elyse. Older brother Nathan supports his sister in school, and saves his allowance to help fund a cure. Tom Clough has organized the second fun run to raise money for Elyse. Information on the run and REACH’s mission may be found at www.reachorg.org

Hydrocephalus has over 180 different causes. They include birth defects, traumatic brain injury, infection, and overproduction or under-absorption of brain fluid. Symptoms include headaches, nausea and vomiting and sensitivity to light and flu-like pains. Elyse developed hydrocephalus after she was born premature, at 24 weeks.

Along with the risk of seizure, Elyse takes medication for her underdeveloped lungs (caused by her premature birth) and undergoes physical therapy, occupational therapy and speech therapy. She has trouble feeding herself anything besides finger foods. And she’s endured six shunt operations.

“This child could take up all of our time, but it is what it is,” Kim Clough said. “We know there has to be a better solution. If we can get political help then we will be closer to that solution.”

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I spent time with 6th year old Elyse Clough and her family to see how hydrocephalus impacts their family. Elyse has had 6 brain surgeries since birth, tonight you hear Elyse’s story.

“She was only 24 weeks along when she was born. She weighted a pound and seven ounces. Two weeks after she was born we found out that she had a massive brain bleed and so she essentially had a stroke. And as a result of that, that was how she developed hydrocephalus,” said mom Kim Clough.

Having an incurable brain condition isn’t stopping Elyse from having the time of her life. She enjoys playing games with her big brother and has big plans for the future.

“And this is lamby, yea, a doctor,” Elyse Clough said.

Sometimes though Elyse can’t have fun like every other little kid. Sometimes her shunt, that keeps her alive, shuts down and overflows with fluid…sending Elsye to the hospital for emergency surgery and leaving the family at a standstill.

“Quiet, boring, lonely,” Nathan Clough said.

“She knows that when she has a seizure that she needs to go to the hospital. She knows that when she’s in the hospital she’s going to need surgery and have an incision and she knows after surgery she won’t be able to go to school or see her friends or her cousins for a long time until she heals,” Tom Clough said.

Seeing what Elyse goes through on a daily basis, mom Kim and dad Tom along with other families and supporters created the reach organization. Research, educate and cure hydrocephalus. This gained national attention from the pediatric hydrocephalus foundation to send Elyse to Capitol Hill on August 19th for National Hydrocephalus Awareness Day.

“Are you excited for DC? Yea. What are you going to do down there? You’re the spokesperson for hydrocephalus. Oh, yeah,” said Elyse and brother Nathan.

Elyse was a little camera shy, but her family is very excited for the trip that Elyse is the spokesperson for and to one day find a cure. But, until then they hope to gain support in Washington to create a spinal fluid bank database. For more information head on Elyse and the condition head to www.hydrocephaluskids.org.

Tonight I’m taking you into the life of 6 year old Elyse Clough who’s fighting an incurable brain condition.

Behind Elyse’s smile and long hair are stitches and scars from six brain surgeries. But it doesn’t stop her from being like every other little girl. She loves playing with her big brother Nathan. But some days she can’t play, because she’s sick and her shunt has failed…sending her to get emergency brain surgery.

Her family, along with others, created an organization called REaCH–to research, educate and cure hydrocephalus. This August, the family heads to Washington, D.C to gain support in Congress.

“We try to make money, raise awareness, have a support system for people that have children with Hydrocephalus, we have adults in the group that have Hydrocephalus so it’s been a really good outlet for us to be able to kind of streamline something that’s really bad and make it into something positive and something that has helped a lot of other people,” Kim Clough said.

Tonight at 10 on WFXv and 11 here on WUTR the Clough family shares their in-depth story on Hydrocephalus and Elyse shares her excitement for being a national ambassador.

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TOWN OF VERNON — The battle against the brain condition hydrocephalus has found a champion in six-year-old Westmoreland elementary school student Elyse Clough.

Like her namesake (Clough is based on an old Irish word, an Chloch, which means ‘the stone’), Elyse has been a rock for her family through her efforts to live a full life despite her disability.

Her bravery, and her parents’ commitment to help her and others overcome legal and medical barriers to fighting the condition, have led to her being named National Ambassador of Hydrocephalus Awareness for 2016 by the Pediatric Hydrocephalus Foundation (PHF).

“We had formed the group, REaCH, (Research, Educate, and Cure Hydrocephalus) to provide support for those suffering from hydrocephalus and their families and had been in contact with PHF,” Elyse’s mother, Kim, said. “They knew about us and thought Elyse was a good match.”

Later this year Elyse will make a number of appearances on social media and will speak before the U.S. Congress and House of Representatives in Washington, DC on August 19.

Elyse will join her parents and 23 other members of REaCH. Her counterpart, Tyler Side, 11, of Washington State, whom PHF has chosen to represent boys battling hydrocephalus, will join her there. They will stand before the country’s legislative branch to help advocate for continued education and research for her condition.

“It’s been a big deal to her to be chosen,” Kim Clough said.

Her work will continue into September, which PHF has designated as National hydrocephalus Awareness Month for the eighth year.

PHF, which has chapters in 30 states, provides supports to families and also advocates with the medical and legal communities to help find a cure. Since 2010 they have awarded $375,000 in grants and donations towards research and education on the condition.

Hydrocephalus (a combination of the Greek words hydro, or ‘water,’ and kephalos, or ‘head’) is a condition in which an abnormal amount of cerebrospinal fluid accumulates in the brain’s ventricles. The excess fluid causes swelling on the brain.

The ventricles are inter-connected spaces in the brain that produce cerebrospinal fluid; the fluid cushions the brain, helps prevent infection and eases blood flow in the brain.

“The problem is that the fluid will not drain, and there is increased swelling in the brain and other issues,” Elyse’s father, Tom, said.

Hydrocephalus has over 180 different causes. They include birth defects, traumatic brain injury, infection, and overproduction or under absorption of brain fluid. Elyse’s began when she was born premature, at 24 weeks.

“She can be fine one minute and then start having a seizure, and she’s in an ambulance,” Kim Clough said. “Life can change in a minute.”

Along with the risk of seizure, Elyse takes medication for her underdeveloped lungs (caused by her premature birth) and undergoes physical therapy, occupational therapy and speech therapy. She has trouble feeding herself anything besides finger foods. And she’s endured six shunt operations.

Hydrocephalus has no known cure, and the only universally reliable treatment is a shunt implant. (Endoscopic third ventriculostomy, a shunt-free procedure where an incision at the bottom of enlarged ventricles allows fluid to drain only works in two-thirds of patients). A shunt is a soft silicone implant placed in the ventricle, then tunneled under the skin to the abdomen where excess fluid is drained and re-absorbed into the body.

The relief provided by shunts is compromised by their frequent failure rate. Children have a shunt failure rate between 25 and 40 percent. Replacing a shunt is a complicated and potentially dangerous process.

“Every time Elyse, or anyone, has a shunt replaced they require a battery of tests,” Tom Clough said. “They include a CTE scan and several x-rays. Elyse is forced to absorb more radiation than she should have to.”

CTE stands for chronic traumatic encephalopathy, the brain condition recently brought into national attention because of its prevalence among former professional football players.

Elyse is also beginning to deal with the emotional impact of her condition.

“She is becoming more aware of what is happening with her, and she gets nervous sometimes,” Tom Clough said.

Elyse’s state of mind is helped by the presence of her eight-year-old brother, Nathan, who proudly wears a PHF pin on his backpack.

“I’m a sound sleeper, and I missed the ambulance the last time Elyse had a shunt put in (on Feb. 10),” he said. “I stayed with my grandmother the next day, and after I went to school I kept wanting to leave school and check on my sister.”

Nathan’s constant interaction with Elyse has helped her improve her daily living skills.

“She’s very reliant on her brother,” Kim Clough said.

Kim and Tom have joined Elyse in her fight. They formed REaCH in 2010; Kim serves as president and Tom is the group’s treasurer. The group meets once a month at the library in the town of DeWitt near Syracuse.

“It’s important to have the support of those enduring the same challenges that you’re going through,” Kim Clough said.

The Cloughs’ burden is eased by their flexible work schedule. Kim is part-owner of Colonial Pharmacy in Whitestown, where Tom works as an accountant.

“We are able to work around her needs, which is good because she always needs someone with her,” Kim Clough said. “She always comes first.”

Those suffering from hydrocephalus and their families may take solace that the condition, like juvenile diabetes, is not necessarily fatal if properly treated.

“We have all sorts of people of all ages at our meetings,” Kim Clough said. “They won’t let hydrocephalus stop them from living their lives.”

Count Elyse among them. Despite her pain she is planning on living a fulfilling life.

“They asked me in school what I wanted to be when I grow up, and I told them I wanted to be a pediatrician,” she said.

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