Faces of Long Island celebrates the uniqueness of everyday Long Islanders. In their own words, they tell us about their life experiences, challenges and triumphs. Newsday launched this social media journey into the human experience to shine a light on the diverse people of this wonderful place we call home.

‘So far, I’ve made 302 cakes, I want to make 1,000 cakes before my 18th birthday. I’m 15, so I have three more years to go.’

Noah Rabinowitz, Dix Hills

“I used to bake cakes and cookies with my mom when I was younger just for fun. My temple had a program to make food for a soup kitchen, and the main thing they didn’t have was dessert. I wanted to have a leadership role within my community, and I realized that baking was a fun thing to do.

“So far, I’ve made 302 cakes, I want to make 1,000 cakes before my 18th birthday. I’m 15, so I have three more years to go. If I get to my goal, I’ll probably set a higher one.

“I mainly get money for this through donations. I’ve found the best cakes are mixes from Costco or Target — they’re cheap and easy to make. When I go to the store, I usually get the whole shelf. I use my donation money to get whatever I can. I usually bake six cakes every Sunday morning. If I had more funding, I might branch out and try different things.

I mainly bake during the weekends, and I study while the cakes are in the oven.

“At school, I’m in a club called One World, and their main goal is to give back to charity. I talked to my adviser in the club, and she emailed all the teachers in the school about what I’m doing. I got a lot of donations, then my school posted on Facebook, and through that there was a link to my website. That’s when donations really picked up.

“I would say I’ve raised around $300 so far. Once or twice a month, I bake at my temple, and the temple brings the cakes to the soup kitchen. Mainly I bake at home, and me and my mother drop the cakes off Monday mornings before school.

“I go to Half Hollow Hills East. I play soccer and tennis and run track. My favorite subject is probably math because I feel like that comes the easiest to me, and I think social studies is interesting, even though it’s hard.

“I mainly bake during the weekends, and I study while the cakes are in the oven. In my free time, I hang out with my friends. I play video games sometimes, but I don’t really have enough time. In the future, I want to be an entrepreneur like my dad and grandpa.

“The people who work at the soup kitchen are very proud of what I’m doing; they’re very appreciative. I’ve gone to the soup kitchen and volunteered. It feels good. It’s very nice to see all the people come in and have smiles on their faces.”

Find out more about Noah’s work at noahscommunitycakes.com

Interviewed by Barbara Schuler

‘My true calling is to be in the water, guiding young children on how to navigate it safely and find their way to safety.’

Rebecca Weiner, Dix Hills

“I have had a passion for swimming for as long as I can remember. Even as a young child, my parents called me a ‘water baby’ because once I entered the water, I never wanted to come out. Growing up in Dix Hills granted me the opportunity to be surrounded by water frequently. I started swimming at the age of 2, which ignited an enduring adoration and admiration for the water.

“As I grew older, I immersed myself in the world of competitive swimming. I participated in competitive swimming with both the Suffolk Y JCC Sharks and the Half Hollow Hills swim team, dedicating four rigorous yet rewarding hours to daily practice. During that time, I excelled in the 50- and 200-meter freestyle races, attaining notable times of 0.39 seconds and 1.38 seconds. Despite not clinching the title of fastest swimmer, my main focus is centered around teaching safe swimming techniques to others. Swimming is so much more than beating out the clock; it involves understanding the nuances and techniques that make the sport so special.

“Before I knew it, I was fueling my passion for swimming by teaching others how to swim. After graduating from the University at Albany, I utilized my expertise in business, education and my extensive experience in the aquatic industry and competitive swimming history to create Aquafinz Infant Aquatics. The thought of a child drowning compelled me to continuously enhance my knowledge in the aquatic field and obtain new certifications.

Before I knew it, I was fueling my passion for swimming by teaching others how to swim.

“I realized that the corporate world didn’t align with my passion; my true calling is to be in the water, guiding young children on how to navigate it safely and find their way to safety. Interacting with kids comes naturally to me and brings immense joy. Combining this with my love for the water allowed me to independently build a successful swim business. Working with children in the water has been a seamless fusion of my passions.”

Interviewed by Starr Fuentes

‘I hope that I can bring awareness to breast cancer.’

Mary Pallotta, Dix Hills

“Just before the pandemic, I missed my annual mammography. I was taking care of my mom, who had a stroke, and she needed me. I learned that I had breast cancer and needed a double mastectomy. I’ve been through a lot in my life. Born with one kidney, I had multiple surgeries and needed to relax, because the anxiety one goes through when being diagnosed with breast cancer, I couldn’t breathe.

“I created the Guardian Brain Foundation over 20 years ago after losing my brother to brain cancer, then my father to sporadic Creutzfeldt-Jakob disease. I’ve seen and been through a lot. I’m so used to being there for other people. I had a very hard time being on the other side.

I hope that other women do their research and realize there are different options that they can take.

“So I did my research, and I found a wonderful team of doctors on Long Island. Dr. Randall Feingold introduced me to Molly Sugarman, a clinical director of the Patient Empowerment Program at NYBRA Plastic Surgery. She helped me through deep breathing, guided imagery and meditation. It was such a gift. It helped me broaden my view.

“I decided to do DIEP Flap Microsurgery, which I’m very happy about. It’s been a long and difficult journey. My surgery was nine and a half hours long. When I woke up in ICU, the nurses said, ‘My God, you are breathing so good!’ They were laughing. I was talking up a storm.

“I started to put all my efforts into my art. Art is my passion, and it’s my healing. I’ve always done oil and acrylic and sculpture but wanted to try something new. I met this wonderful art teacher, Jan Guarino. She does classes online. It was extremely therapeutic for me. One day I might like painting hydrangeas. The next day I’ll be painting scenes from Italy. It depends on my mood. I love painting the water, sailboats and ships. It’s just amazing the watercolor, how it drips, and the colors blend together. It’s kept me busy.

“I can’t believe how many paintings I’ve done. I’ve been able to sell, fund-raise and get commissions for my work. I’m having a wonderful time doing it. I feel exposed, but I’m enjoying it. I love to hear what people say.

“I hope that I can bring awareness to breast cancer. I hope that other women do their research and realize there are different options that they can take. Find a hobby; it really helps healing. Try watercolor. You never know. You might want to stick with it.”

Interviewed by Shoshanna McCollum

‘I’ve become a better father and a better high school principal because of creating a podcast.’

Dix Hills

“During the pandemic, I was introduced to podcasts and fell in love with them because of their on-demand nature. I used to DJ as a kid, and I thought, ‘If I’m going to do it, I don’t want to be one of the 80% of podcasts that don’t make it. What do I have to offer people?’ I had just gone through the college decision process with two daughters. For my little one, the journey was difficult because school didn’t come easily. I had to advocate for her and talk to reps, who were so good to me and very accessible.

“As a parent it was emotional going through the process, truly not knowing if your kid was going to be accepted anywhere. When I had the idea for ‘The College Admissions Process Podcast,’ I realized that if the reps were willing to have these conversations with me, and we can give insight into their schools and into their process while providing advice, that might really help people! I’m now in my second year since launching. There’s been over 151,000 downloads. I’m averaging at least 1,700 per week. I’m also the proud principal of Syosset High School. Kids will stop me in the hall and ask what I think about colleges.

If you have an idea for something that is genuine and there to help people, no matter your audience, it’s worth it.

“The feedback from parents all over the country has been tremendous. Because my daughter has an IEP [individualized education program], I always ask reps, ‘What does your school have to help ensure that students with an IEP in high school continue to be successful while on your campus?’ The episodes will hopefully prompt people to come up with their own higher-order thinking questions so that when they meet with the reps, the conversations are going to be richer. I’m having so much fun! I love helping people and giving back. I think I’ve become a better father and a better principal because of the podcast. The creative part is so motivational to me.

“As a high school principal, you have to be creative in many ways because you’re making a million decisions a day, but until now I’ve never had to create a logo or find an intro! I do all of my own editing. It’s extremely rewarding. If you have an idea for something that is genuine and there to help people, no matter your audience, it’s worth it. Pick a topic that is true to you, that you’re passionate about, but that also gives back.”

‘I’m hoping that I’ll get that lifesaving call to come in and get a kidney.’

Dix Hills

“I was born in Huntington and lived most of my life there. I’m fortunate enough to work as a citizen advocate in the town where I grew up. In November, I started feeling sick. I thought maybe it had to do with stress. Shortly after, I had a terrible nosebleed and started noticing when I would go to bed, I couldn’t lie sleeping on my back. I couldn’t breathe. And as that progressed, my legs started swelling up.

“My coworkers saw me at Town Hall and said, ‘Jonas, you don’t look right. You really need to be checked out.’ So, I finally had blood work done and I got a phone call saying the doctor has my results to go over. I asked him when I should come in and he said, ‘Now.’

I’m going to dialysis three times a week, and that’s keeping me alive.

“I went right to the doctor; he sat me down and said I have one hour to get to the hospital. They had a whole team of doctors come by. It was very overwhelming. My kidney levels were not normal. They did an emergency procedure to put a catheter in my jugular, and they started dialysis right away. I eventually had a biopsy of my kidney which showed that I have FSGS [focal segmental glomerulosclerosis], a rare type of kidney disease. It makes the kidneys deteriorate very rapidly. They said I need to get listed for a kidney transplant.

“A friend of ours recommended going to this organization called Renewal. Their whole mission is to help people like me find a living kidney donor. It’s a simple program. They take samples of a cheek swab and send it to a lab that looks at your blood type and antigens. They’re trying to get someone who’s the best match. You can do it from home. Renewal mails a swab kit and envelope to everybody who wants to donate. It takes five minutes, and you never know, you could be the person who saves a life.

“So, we’re still waiting. My wife’s here with me today and I have a 14-year-old son and an 8-year-old daughter, and I want to be here to help support them and see them grow up. My daughter had a father-daughter dance, and I couldn’t go. I’m going to dialysis three times a week, and that’s keeping me alive. It’s hard. I’m just hoping, relatively soon, we’ll hear some good news, and I’ll get that lifesaving call to come in and get a kidney.”

To learn more about kidney donation or to see if you’re a match, please contact Renewal at 718-431-9831, ext. 209 or email R25727@renewal.org.

Interviewed by Jay Max

‘There are no words to describe the moment your baby girl asks, “Mommy, what does this cancer want with me?”’

Dix Hills

“There are no words to describe the moment your baby girl asks, ‘Mommy, what does this cancer want with me?’ The first four years of Daniela’s life were full of memory-making and milestones, just like those of any other child. But in the fall of 2016, when she was barely 5 years old, everything changed. An ongoing stomachache grew until rounds of MRIs and PET scans finally uncovered a tumor in her hepatic portal vein, which spread to her liver.

“On October 5, 2016, Daniela was diagnosed with a rare form of childhood cancer: rhabdomyosarcoma. It was a word we had never before heard. Doctors gave her two days to live, but she fought like hell for four years.

“After 12 months of grueling chemotherapy, Daniela was finally declared cancer free, and we thought we had beaten the monster threatening our little girl’s life. Three months later, the cancer returned, and far worse than before.

“The next two years were a dizzying procession of hospital stays, chemotherapy, radiation and experimental treatments. Three years from the time she was diagnosed, the doctors declared Daniela cancer free three times. But the disease always came back.

“It was heartbreaking to watch as the poison meant to kill the cancer also took a toll on her little body. Daniela’s intestines became inflamed and painful; she was tired and had difficulty eating. Daniela had gone through nearly every form of treatment options available over the course of four years when doctors told us that there was nothing more that they could do, so the decision was made to change our focus to maintaining a good quality of life for her while she lived with cancer.

“A week before COVID hit on March 2, 2020, Daniela took her last breath in her daddy’s arms. She lost her battle with rhabdomyosarcoma after almost four years of courageous fighting. I have told this story many times, but it never gets any easier. The details are always the same. It’s a story that no child and no family should ever have to endure. In Daniela’s memory, my family and I along with my team are now working toward that end through the nonprofit Daniela Conte Foundation.”

The harsh reality is that the treatments Daniela received – which didn’t work – were developed 40 years ago.

“Daniela had an infectious smile and powerful personality. Even on the most grueling days, she never complained. Through every treatment and every test she had to go through, there was always a light behind those big, brown eyes and a sparkling smile to boot.

“The strength of such a little person could have touched everyone who met her. I can’t tell you how many times Daniela left the hospital and lived life to the fullest the next day. She may have gotten sick in a trash can or two, but she never let the cancer steal her joy.

“She was never going to let the cancer win. Daniela wished for a day where ‘there was no more cancer’ and often spoke about helping other pediatric cancer patients. Before, during and after the diagnosis, Daniela always wanted to help others.

“Today, Daniela’s story continues through the Daniela Conte Foundation. We couldn’t save Daniela, but it is the mission of DCF that her story is a catalyst for change. Through the lives of the children and families we support, Daniela’s legacy lives on.

“The harsh reality is that the treatments Daniela received – which didn’t work – were developed 40 years ago. These are toxic treatments, and the children who do survive suffer long-term effects.

“Private foundations like DCF are the ones supporting the doctors and research that are working on these cancers. Cancer is the number one disease killer of children, and that has to change.

“Even where kids survive, by the time they’re 45, they’re at a high risk for hearing loss, infertility, and a litany of other issues. There’s also a good chance the cancer might come back or that they will get a secondary cancer.”

As parents, we plan for vacations and college, but nobody plans for cancer.

“The Daniela Conte Foundation was formed just three years ago, but we’ve made great strides thanks to an incredibly passionate and talented team. In 2022 alone, we helped 150 families and provided more than $75,000 in financial and memorial assistance.

“Ninety-five cents of every dollar raised by DCF has gone directly to cancer families and research. As parents, we plan for vacations and college, but nobody plans for cancer. Our own family would have been completely lost without the financial support of private foundations, and now I’m proud to give back.

“There hasn’t been one new drug developed for the type of cancer Daniela had in more than a decade. That’s a pillar of the DCF mission: to bring more awareness. I don’t want another family going through this. We’ve seen a lot of pink in October, but we don’t see a lot of gold. Gold is the color we use for September, Pediatric Cancer Awareness Month.

“Before Daniela’s diagnosis, we, like many other families, didn’t even know there was a month or color. We’re working to change that too. Through increased awareness, we can change the narrative of pediatric cancer.

“One of our most meaningful events at DCF is the annual March blood drives held every year in Daniela’s memory. Daniela went through many blood transfusions and platelets because the chemo destroys your good and your bad cells. We had close to 78 blood donors come out this March to donate blood, and that translates to over 200 lives saved. In the last three years we have collected over 225 units of blood, which helped save 675 patient lives.

“This year, DCF will proudly host its third annual Butterfly 5K Run/Walk on Saturday, April 22, at Sunken Meadow Park. Anyone can participate; you don’t have to live on Long Island. We have virtual participants joining us from all over the country.

“We’ll have a fun run, games, prizes, giveaways. It’s one of our biggest events, and the money we raise will continue to help families and fund pediatric cancer research. This year we will also honor children and young adult survivors in the community with special medals. Those who wish to sign up and participate can get more information at 5k.danielacontefoundation.org.”

Interviewed by Tracey Cheek

‘I want open communication around our feelings. This film is a way to hopefully open your mind and get a conversation going.’

Dix Hills

“Last year, I lost a lifelong friend unexpectedly and went through an immense amount of grief. A few months after losing him, I lost my closest uncle. These emotions served as the inspiration for the short film I wrote and directed, ‘Speak to Me.’

“It’s a short film about mental health struggles for men. My friend who passed away inspired it. I have a big group of friends, and we didn’t know Barry was dealing with as much as he was. He was healthy, in shape, and yet we still lost him suddenly. They said they found him unresponsive.

“It was my son’s birthday, and I got the phone call. More than half of my friend group was together when I got that call. They looked over at me and saw that I was crying. I was blessed to have a support system with me on that day and for the months that followed. My group of friends, wife and family are all nonjudgmental and allow me to be vulnerable with them.

My father would tell me to ‘be a man,’ and that statement could be damaging to a young boy.

“My friends and I joke around all the time, but we also have deep conversations and uplift each other. We’re always there for each other. A few months after Barry passed, my uncle passed away. He was my biggest cheerleader.

“I wrote the script a month later and sent it to my friend, who became its producer and co-director. I used the creative process as my therapy. Barry had a clothing line and was working to release Olive Forever.

“He will live through my art. His living on Earth inspired and ignited my fire. He was an inspiration, and he passed away as a legend. The film dives into the mental health struggles men deal with, including shocking statistics on the amount of Black men who see mental problems as a personal weakness. I see this in my own community and with how I grew up from generations past.

“My father would tell me to ‘be a man,’ and that statement could be damaging to a young boy. Our ancestors dealt with traumas, and these stigmas around mental health should be broken. I have three awesome kids. I want them to know it’s all right to cry and to use their words to tell me how they’re feeling. I want open communication around our feelings. This film is a way to hopefully open your mind and get a conversation going. Mental health is for everyone.”

Interviewed by Melanie Gulbas

‘My artwork is about human nature, judgments and the ability to see past the facade to what lies deeper beneath the surface.’

Dix Hills

“My artwork is about human nature, judgments and the ability to see past the facade to what lies deeper beneath the surface. I’ve been making art since I was a child and discovered natural clay at Garvies Point. I studied the arts in high school and college. I began as a painter, but I gravitated toward sculpture because I see the world more three-dimensionally.

“In order to support myself, I worked as a set designer and producer for theater, television, exhibitions and film as a member of the United Scenic Artists union. I created scenery for films such as ‘Noah’ and ‘Men in Black III.’ I also designed and sculpted animated displays for Saks Fifth Avenue, Lord & Taylor, FAO Schwarz and Gucci. In 2016, I opened a not-for-profit art space to share and expand the appreciation of the Arts on Long Island.

“Currently, I am concentrating on my own artwork and my exploration of materials. I use photography to capture images as elements that inform my work. I have always been interested in societal issues and focus on people who are either attention seekers or who keep to the shadows, the extreme sides of the seen and unseen of society.

My ultimate goal is to get my work seen by a larger audience so I can raise awareness and share its message of compassion.

“One of my muses was a tattoo artist named Diablo who I met in Long Island City. He has horn implants and is covered with tattoos. He looks threatening, but he’s a lovely man. Another sculpture created with papier-mâché titled ‘Love Birds’ reflects a man bonded to the pigeons of Washington Square Park. ‘For Sale, Baby Shoes Never Worn’ depicts a heavily pregnant woman hungrily eating soup while wearing baby shoes around her neck. She was photographed in Los Angeles on Skid Row.

“These are the people who most need society’s attention and help. I also created a series of artwork focusing on Kings Park’s defunct psychiatric center, which led to strong responses from the community it affected. My latest series, ‘Rooted in Humanity,’ was inspired by a trip to Bayard Arboretum and root formations. My ultimate goal is to get my work seen by a larger audience so I can raise awareness and share its message of compassion.”

Interviewed by Meagan Meehan

‘Bringing them up alone was difficult; we didn’t have as much as some people we knew, but we made it through and we did it well.’

Dix Hills

“I moved back to Long Island in 1986 with my kids after my divorce, when my son Scott was 4 and my daughter was 6. We were part of a military family, and we had moved around a lot, and I don’t talk about that much, as our lives were so private before Scott’s murder.

“I was born and raised in New York, moving to Roslyn when I was 9 after my family moved there from Queens. By the time I was a teen, I already knew I wanted to go far away to college so I could truly see who I really was. I went to the University of Arizona, and the experience was amazing.

“From ’76 to ’86, I lived as a military wife. I was an elementary school teacher, and I taught in Germany and in four different U.S. states. My kids were born in the South in two different states.

“When I returned to Long Island with the kids, we moved in with my parents for a while until I could afford to find a place of our own, and we moved to Dix Hills. I worked; I had to work, I had no choice, it was tough and I did the best I could.

“Bringing them up alone was difficult; we didn’t have as much as some people we knew, but we made it through and we did it well. To this day, when I walk down the stairs, I feel thankful to be living in a house that’s mine. Before this, I never did, whether it was post housing or renting or my parents’ house.

“The things that you overcome or survive are amazing. I watched my kids flourish here, with both my kids going away to college. Before that, they both went to sleepaway camp. My daughter went to camp first when Scott was 6, and after the hubbub we made about how great camp was, Scott said he wanted to go the next year.

“My dad told me, ‘He’s never getting on the bus,’ but Scott never looked back, and at age 7 was the youngest kid there. He ended up going for 28 years. It was really nice when he became a CIT [counselor in training], so I didn’t have to pay for him to go anymore! He eventually became a counselor and a staff member.

My husband said, “The name is Marjory Stoneman Douglas High School,” and I said, “OK, so?” But he said, “No, no, no, there was a shooting at the school.”

“After college, Scott stayed in Florida. My parents had also moved there, and it’s where my dad passed, just nine months before Scott. My parents would rely on the kids, especially Scott, who would go to brunch with them every weekend, and then when my dad passed, he’d go with his grandma. He was there for them.

“When they were sick, I’d tell him he needed to get them groceries, and Scott would do it in a heartbeat. My daughter ended up in Connecticut, so it was just my husband and me left here on Long Island.

“My husband is the greatest guy in the whole wide world by the way, I got so lucky. He adopted the kids when they were in their 20s; Scott adored him. Scott became a teacher in Florida, but before that he volunteered to teach in South Africa for two months.

“He went with two suitcases, with what he thought he needed to bring, but when he came back, all he had with him was his favorite pillow in a backpack. I thought at first maybe the airline had lost his suitcases, but when I asked, he put his hand up and just said, ‘Ma, you don’t understand. I left my stuff; they need it way more than I do.’ That’s Scott!

“He got a job teaching geography at Marjory Stoneman Douglas High School [in Parkland, Florida] in August of 2017. It was really his excuse to go back to camp, I like to say, as he never stopped loving summer camp. We joked that he needed to go into teaching because you can’t just be a counselor at summer camp for three months and get by on that. But seriously, he loved teaching there. They let him teach the way he would liked to have been taught when he was in school.

“On Feb. 14, 2018, I had taken my husband to the doctor early that morning, at 8 a.m., and after bringing him home, I went to work. Around 2:22 p.m., I got a call from him. He asked what school Scott worked at, and I wasn’t sure; I just knew it had a lot of names. I told him, ‘I’m busy. I’ll talk to you later.’ But then he called me back. My husband said, ‘The name is Marjory Stoneman Douglas High School,’ and I said, ‘OK, so?’ But he said, ‘No, no, no, there was a shooting at the school.’

One of the police officers bent over and said, “You know, your son was definitely a hero.” Then two other officers said, “But he didn’t make it.”

“He told me to come home, but I said no because, and it’s my philosophy, you don’t worry until there’s something to worry about. But then he called me again and said, ‘I think you need to come home,’ because he had heard on TV that a geography teacher was shot. So I went home, and I went fast.

“I told my husband Scott was OK, he was probably in the hospital, and we knew we had to go down there. There weren’t seats available on any plane due to a sports tournament, so we chartered one, even though we couldn’t afford it, we didn’t care. I just put it on a credit card.

“We got down there about 8:45 p.m., and we were whisked off to a command center. We know today that they knew at 2:30 p.m. who had been murdered, but we weren’t told until 1:50 a.m. That’s when they called us in.

“One of the police officers bent over, and said, ’You know, your son was definitely a hero.’ Then two other officers said, ‘But he didn’t make it.’ That’s how we found out it was Scott. I know now that Scott did what he would have wanted someone to do for him. He opened a [classroom] door and saved kids. I think he didn’t stop to think about it; it was instinctual.

“After we were escorted out and got back to the hotel, at about 4:20 a.m., my phone rang. It was a voice going, ‘I’m just letting you know that we’re going to be doing an autopsy.’ I pulled the religion card for the first time in my life and explained, ’You can’t. YOU CAN’T,’ based on my beliefs and ‘What can I do to stop this?’ But the voice said, and I quote, ‘Lady, you can get a court order, you can bring it in, nobody will see it until Monday. Your son will be on ice until then. The judge will not grant it, and we’re going to do that autopsy anyway.’

“This was because it was a criminal investigation, but we didn’t know that at the time. I still don’t know who it was that spoke to me like that during that call, but believe me, I am going to find out. I would like to face-to-face with that person and tell him, ‘Please, don’t ever do that to anybody else,’ and that, ‘I’m scarred from what you did to me.’ I understand, Scott was just another person to him, but I don’t want another person, any other person, to ever hear those same words.

I said I will never mourn my son’s death; I will celebrate his life.

“Scott was shot six times, or as the medical examiner explained, it was actually four times, but because the bullets went in, and then went out…we had everything explained to us ad nauseam.

“I never got to say goodbye to Scott. That is the one thing I will never get past. When we had his funeral, I had to bury him in his cap, because the cap would cover the scar on the back of his head where they had cut.

“I haven’t exactly figured out how I’m going to do it, but I want to be able to show the public what an AR-15 does to you. Scott gives me permission, I believe that. I want to publicly show his autopsy pictures. I want to show what it looked like when Scott was murdered.

“When the medical examiner talked about our loved ones and what happened to them, what a bullet does when it goes in … One of the victims was shot and only hurt, and when he put his hand up as the murderer came back, begging, ‘Please don’t,’ the murderer shot this kid through his hand. The bullet went into his skull, and the medical examiner said after that the only thing holding his head together was his scalp.

“People need to see what it does. They need to see. I need to get to Congress and show them what these weapons do. That’s the only way we’ll ever get the assault rifle ban back. I don’t want to take everybody’s guns away, I just want them to be owned legally, and that they go through the necessary steps to own them, like learning how to use them. But an assault weapon? I mean, if you shoot a deer with it, it’s demolished. In my mind, I can’t understand how this is not common sense, so I realize this must be show and tell.

“At his funeral, I had to speak; whoever thinks they’re going to bury their son? I said I will never mourn my son’s death, I will celebrate his life. That’s what I do.

“Some people I’ve met ask me, ‘How do you do it?’ Well, my experiences, really starting once I got to college, are what made me what I am, that’s what makes you who you are. It makes you have choices: Who do I want to be? Do I want to live hiding under the covers because my son was murdered? Or do I want to make sure nobody else has to go through the hell I went through, and I am still going through?

People talk about my son being a hero, but he was a hero in life.

“Two or three days after the murder, we wanted to do something to honor Scott and his legacy, so we started the Scott J. Beigel Memorial Fund. Based on Scott’s loves, we took what happened. The mission is to send at-risk, underserved children touched by gun violence to summer sleepaway camp, because that was Scott’s love, sleepaway camp.

“Our first year, we sent 54 campers to camp. The second year was the pandemic, so we gave a $25,000 grant to a camp that did virtual camp for 400 children. The third year, we gave out 154 camperships. And then this past year, we gave out 212 camperships after raising $283,600.

“I’ve been told I should write a book, but I’m not doing that, even though I feel like I’ve lived four lifetimes. Every once in a while, I wake up and ask myself, ‘Do I have to do life again?’ But when I visit those kids at the camp in the summer, I look at my husband and say, ‘This is why we do it.’ When I see those kids, and I know where they came from, and they look at me and say things like, ‘Will you send me back again next year?’ or ‘I don’t want camp to be over.’ Because that kid doesn’t know who’s picking her up, or they’re going back to a homeless shelter. That’s what it’s all about.

“I was brought up to care. My daughter was brought up to care. Scott was brought up to care. People talk about my son being a hero that day, but he was a hero in life. How could he have ever looked in the mirror again if he hadn’t done what he did? How could he have done any different? In my mind, there’s no other way he could have done it. What was he going to do, close the door and save himself?

“I believe there is a piece of Scott’s heart in every child we send to camp. Those are not just words; I truly believe that. Every kid we send to camp, that’s a piece of my son alive again. It might sound hokey, but I’ve decided I’m going to believe that. That’s how Scott continues.”

Interviewed by Ian J. Stark

‘We saw that theater and the arts are key to getting people’s attention and reflecting humanity.’

Dix Hills

“The first year we did Stage the Change, a one-day conference that encourages theatre students to get involved in global issues, I dedicated it to my mother who was a Holocaust survivor. There were so many people that made a difference and brought her to the U.S. Her story made me understand the importance of making a difference. Through teaching at Hauppauge High School, I saw how theatre is a wonderful vehicle for doing this. My students became really turned on by writing work about issues that were important to them. We saw that theatre and the arts are key to getting people’s attention and reflecting humanity.

“Theatre allows us to stand in front of people and enlighten others. My students’ writing gave them a seat at the grown-up table; adults were talking to my students about things that were important in their world. Stage the Change began in my classroom nine years ago and became an annual movement. It originally had 200 students. In 2019 we had 850 students from schools in New York, Connecticut and New Jersey. Students get to meet others with similar interests and problems from a diverse group. It’s important to me that this event bridges Long Island, because we’re all in our own pockets here. It’s about listening to one another and understanding our similarities and differences. Over the years we’ve had many theatre greats speak.

“This year, on November 18, we’re at the Tilles Center with Brian Stokes Mitchell as our keynote because he used the arts platform to make a difference. I’ve always known that I’m driven, but until Stage the Change, I never realized how much. When something is a fire within me, I’ve learned that I can’t stop it. This is a monumental thing, and every year at some point in the process I think to myself, ‘Why do I do this?’ It’s a ton of work! Then I get to see the magic when kids literally grow in one day; they’re so excited to create and be engaged like global citizens. I walk away with a sense that we can do even more. There are so many ways that we can inspire kids to do the right thing. If I can make a difference by inspiring kids to learn about each other and to be even that much more present and human, that’s great.”