Make a Wish

By Martin Lenkowsky

IMG_4404

When 14-year-old Coral Springs resident Gilon Kravatsky traveled to New York in May to

see the world-renowned New York Philharmonic Orchestra perform Gustav Holst’s orchestral suite, The Planets, at Lincoln Center, he not only had a backstage pass; he got to take out his French horn and rehearse with them as well.

 

Plus, there’s a lot more to this story. Gilon – along with his family – were invited guests of the orchestra, courtesy of Make-A-Wish Southern Florida. Gilon, who will be entering Douglas High School in the fall, suffers from Chrohn’s disease, a severe inflammatory disease affecting the bowels.

“His wish was to hear and play with the New York Philharmonic,” said his dad, Steven Kravatsky. “He came up with it on his own. What they actually arranged was for him to play with them.”

His father was surprised when Make-A-Wish liaisons told them they’d sponsor a trip for Gilon. He says he – like many people – had been under the mistaken impression that Make-A-Wish only grants wishes to terminally ill children. “It also includes chronic diseases,” Steven said. Not only did the organization send Gilon to New York, they also sent his dad, his mom, Michelle, along with his three siblings, Ari, 22, Rachel, 20, and Yaacov, 6.

“It was a family-oriented experience,” Steven said, adding Make-A-Wish also paid for the family’s side trips to New York’s Museum of Natural History, the Statue of Liberty and Ellis Island. “All the things Gilon wanted to see,” said Steven.

When the Kravatskys traveled to Lincoln Center they were escorted by chaperones and transported by limousine. The orchestra treated them well, Steven said. “They were a very laid back bunch,” he said. “They made it a special experience for him.”

Gilon had the honor of having lunch with orchestra members. “He met with the conductor and the trombone player, who’s one of the foremost in the world,” said his dad. “They were so nice to him.”

Before they departed South Florida for New York, Gilon received an email from the principal French horn player, containing the sheet music for one of the pieces for The Planets. To prepare, Gilon practiced it with his older brother, Ari, who plays the bassoon. The day prior to the orchestra’s performance, Gilon rehearsed the piece with the band.

And how does Gilon describe his experience? “It was amazing,” he said, “just getting to talk to the players, sit next to them and have lunch with them. Some of the pieces they played were so insane. The way the played them was amazing.”

Gilon switched to the French horn from trumpet in the fifth grade. “If you want to get a music scholarship, there’s a lot less French horn than trumpet or clarinet players,” he said.

As expected, Gilon loved the Big Apple. “There’s a big difference from South Florida,” he said.

One of the people instrumental in getting Gilon his wish was Fran Garfunkel, a volunteer “wish granter” with Make-A-Wish. “I do have a ‘wish partner,’ Martha Carmen, who worked for Gilon’s doctor and recommended him to be a wish child. He met all the qualifications,” Garfunkel said.

She confirmed a wish child no longer has to carry a terminal diagnosis. “That was eons ago,” Garfunkel said. “Make-A-Wish grants wishes to children with life-threatening illnesses. We’re not just granting wishes to terminally ill children. A majority do survive and go into remission.”

Gilon’s first choice was actually the Chicago Philharmonic, but that didn’t work out. Garfunkel said she suggested the New York Philharmonic. “I had a gut instinct they were going to do it,” she said, “and the New York Philharmonic said, ‘bring him on.’”

According to Steven Kravatsky, Gilon’s condition appears to be stable with the infusion treatments he gets for three hours every six weeks. “That’s how his meds are administered,” his dad said. “You’d never know it looking at him. You wouldn’t know he’s sick.”

In fact, Gilon and brother Ari are driving up to Maine in the middle of July for a camping trip. While there, they plan to go rock climbing and white water rafting.

 

 

Fight Against Cancer – Sports Team Rally For Young Parklander

Fight Against Cancer

ADAM-FULL1January 20th was officially Adam Fiorello Day in Parkland, Mayor Michael Udine proclaimed. The young Parkland resident, who turned 22 just the day before, is in a fight for his survival. He was diagnosed in December 2013 with alveolar rhabdomyosarcoma, a cancer affecting the soft tissues in the muscles and connective tissue.
The rarity of Adam’s disease cannot be overstated. According to his mother, Heidi Fiorello, a registered nurse, “roughly 200 to 300 children per year contract it and it can affect all children, mostly younger between three to nine years old. The subtype of Adam’s disease affects 50 to 60 children, but he got it before his 20th birthday.”
Adam was first affected in his right ear behind the sinus cavity. His mother describes his ordeal: “He went through 54 weeks of chemotherapy and had hand-neck radiation. At 6-foot-3-inches and 250 pounds, he went down to 175 pounds and couldn’t swallow his own saliva and had a feeding tube.”
January 20th, says his mother, “was a day to celebrate Adam and his courage and then to acknowledge his pro-activity in helping others and speaking to groups. He will know that there is still hope for a miracle and not to give up.”
ADAM-FULLHaving visited Adam in the hospital, local sports teams have rallied around him, including Miami FC soccer coach Alessandro Nesta and Chicago Cubs baseball player Anthony Rizzo and other people at the local event. He was introduced at a Miami Heat basketball game and honored with a jersey in his name in February.
“The city of Parkland honored me, and a whole bunch of people showed up to support me,” Adam says. “Every day is difficult. I have bad days and good days. A bunch of stuff is affecting me. My motto is to never give up. This is God’s plan.”
Last July, Adam suffered a mini-stroke and the family had to move again from Parkland to New York City for treatment at Memorial Sloan-Kettering Cancer Center with his family and older brother Nicholas, 24, by his side. The cancer has spread to his brain, and doctors predict he will decline quickly. There are no known survivors. But doctors can be proved wrong with the strength and support of his immediate family and many fans on Facebook supporting Team Adam-Parkland and events to rally behind the cause.
“Cycle for Survival.org” events are scheduled in cities around the U.S. for rare pediatric cancers. One event will take place from 11am to 3pm on March 13th at Pine Trails Amphitheater in Parkland. Adam may possibly speak at the event.