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Gigi’s Playhouse

Ryan Degnan smiles big while playing at GiGi's. Photo by Julianne Mosher

A group of Long Islanders saw a need for a safe space for people with Down syndrome and, despite COVID-19, they made it happen.

Founded in 2003, GiGi’s Playhouse is an international network of achievement centers, providing free therapeutic and educational programs for people of all ages. This month, the nonprofit’s 52nd location — and Long Island’s first — will open in Patchogue. 

But families from across both North and South shores helped bring this safe space to life. 

Mike Cirigliano, board president. Photo by Julianne Mosher

Mike Cirigliano, board president and owner of Cirigliano Agency, said that GiGi’s Playhouse Long Island will help fill a void for families of loved ones with Down syndrome. Over the course of several years, the group tried to find the perfect site, scouting locations across Long Island. They eventually settled on 100 Austin St. (in Patchogue), where they took over three of the four units inside the building. 

Located right off Sunrise Highway, he said the spot is easy for families to get to whether they come from Nassau County or the Hamptons. 

“There is a true need for this on Long Island,” he said. “This is where people can come — a place where parents who need a place to go with their child can come play, hang out.”

But it’s not just a place to chill. Board member Karyn Degnan said it will offer programs for people with a prenatal diagnosis to those adults with Down syndrome.

“Moms and dads can go to this common place to talk and share their stories,” she said. “They can grow with the center.”

The new facility offers everything from fine motor skills to speech and socialization programs, to tutoring, exercise classes and even a kitchen where young adults can learn how to cook.

The Degnan family. Photo by Julianne Mosher

Degnan, a Centereach mom of three, said two of her children have Down syndrome: Sal, who’s 11 and daughter Ryan, who’s 5.

“As my kids grow, they have a teen center there — a place where people can go as they grow into their young adulthood life,” she said. “It’s a place where they can feel like they belong.”

Cirigliano said that although the fundraising aspect and search for a spot has been years in the making, they officially signed the lease in early February. Over the last month, the group of 50-plus volunteers helped turn the office spaces into a vibrant, exciting place.

“What’s really cool is I brought my kids with me so they can see the before and after,” Degnan added. “After we were done with the construction, I could feel their positive energy and their love for it. When they were able to witness it being all done, there was this happiness that was beaming from them.”

She said her 11-year-old can’t wait to hang out there with his friends. 

Derek DeProspo plays on a toy car inside GiGi’s Playhouse. Photo by Julianne Mosher

One of those friends is Derek DeProspo, an 8-year-old from Selden who also has Down syndrome. His grandmother, Elizabeth Rahne of Selden, is GiGi’s new program director.

“It’s an incredible organization and has incredible mission,” she said. “It’s giving parents and families the support they need to help their children become the best they can be.”

Rahne said groups like the ones at GiGi’s Playhouse are important for new parents.

“It’s an overwhelming diagnosis,” she said. “You don’t know how much they’re going to progress or what they’ll able to accomplish.”

But Derek runs and plays with the kids inside the center — an inclusive space where kids who are neurotypical, on the autism spectrum or who have Down syndrome can play, dance, create and socialize with no judgment or fear. 

“I’m so proud of what he’s able to do now,” she said. “I think people need to hear the story that our children do have some difficulties, but they can accomplish so much more than people think. We need to celebrate their uniqueness.”

Angelique Sternberger, of Port Jefferson Station, lost her 3-year-old son, DJ, eight years ago. 

“When DJ was born, the doctors came to us and told us he had Down syndrome,” she said. “They always focus on the worst things possible, but it’s all about what these children can do.”

She joined GiGi’s Playhouse in 2017 in memory of him and is now the board secretary. 

Port Jefferson Station’s Angelique Sternberger with her late son, DJ. Photo from Angelique Sternberger

“It’s helpful to have a place where you can go if you need some assistance,” she said. “I wish I had a GiGi’s Playhouse when DJ was born.”

This April, DJ would be turning 12 and, looking back, Sternberger thinks he would be thrilled to know what his mom has helped accomplish.“I’m sure he would love it here,” she said. “He was such a social child …  he was the mayor of his school, and he would love being able to interact with other kids.”

Run solely on donations and fundraisers, GiGi’s Playhouse is 99% volunteer based. The only paid employee is the site manager, who opens and closes every day. 

Cirigliano said that people who want to donate can do so online at gigisplayhouse.org. He said that they will be highlighting donors on their front door every month to say “thank you” for making this all possible. 

And the opening comes at a special time for the Down syndrome community: March 21 is World Down Syndrome Day, and the Long Island chapter of GiGi’s Playhouse is officially opening its doors one day before. From 10 a.m. until 10:30 a.m. on March 20, a virtual grand opening will be streamed through Facebook and online.

Everyone is welcome at GiGi’s Playhouse in Patchogue. Photo by Julianne Mosher

Due to COVID-19, families who want to start using the achievement center’s services must schedule an appointment online. 

“Children with Down syndrome like to follow their peers,” Sternberger said. “We want them to be able to socialize. So, come to GiGi’s and we’ll be there with open arms.”

GiGi’s Playhouse will be open Tuesdays through Saturdays. To view the hours of operation, visit gigisplayhouse.org/longisland.

The cover of Kim Marino's first book.

Reviewed by Melissa Arnold

Above, a little girl enjoys reading ‘Sloths Are Slow.’

As a mother of four busy children and a full-time speech pathologist, Kimberly Marino of Miller Place is constantly thinking about kids. In particular, she’s passionate about engaging children in conversation, interaction and learning. In May, she published her first children’s book, “Sloths Are Slow.” 

Marino has crafted an entertaining and accessible rhyming story about a sloth named Lento (which means “slow” in Spanish) and his rain forest friends. Along the way, readers will learn some interesting facts about sloths while practicing counting, gestures, following directions and more. 

The book is visually stunning as well, featuring artwork by Mariya Stoyanova. It is the perfect pick for sneaking some developmental skills into story time.

Were you a creative child? Did you always want to be a writer?

I never really thought much about writing as a kid, but I was always creative. I liked to draw. My mind is always working and I’m always coming up with ideas. My friend and I actually invented a language game for kids that we were able to sell, so there is definitely a creative spark inside of me.

What did you study in college, and where did you end up working?

I went to school for elementary education at a small school in Pennsylvania called Lock Haven University, and then I got a master’s in speech from Hofstra. I now provide speech services through a company called Metro Therapy. I also work with children from birth through age 3 through Suffolk County Early Intervention.

The cover of Kim Marino’s first book.

What inspired you to write a children’s book?

I’ve had the idea in the back of my head for a long time. Being a speech pathologist means I’m always thinking about language and helping kids develop their language acquisition skills. When my kids were little, they loved a Sesame Street book called “There’s a Monster at the End of This Book.” The main character was [the furry blue Muppet] Grover, and it was very interactive. I knew I wanted to do something like that, to teach parents how to read a book with their kids in an interactive, engaging way. You can learn to be interactive not just with this book, but with any book. There really aren’t a lot of tools out there that teach those skills. I’ve gotten a lot of great feedback from parents who tell me their kids are more excited about listening to the story because of its interactive features.

Did you have any reservations about writing the book?

Honestly, no. Once the idea was in my head, I said to myself, “I’m going to do this.” And that was it.

Why sloths?

My daughter, Katie, has always had a deep passion for all creatures, down to the tiniest bugs. She’s really into sloths, and is always sharing random facts about sloths with me. I thought it was interesting and would make for a fun story.

What was the publishing process like for you?

I started by hiring an illustrator to create the pictures that would go along with the text. My sister-in-law is a graphic artist and editor, basically a jack of all trades, so she was able to help me get the book published on Amazon. It was an easy process for me, but only because I had her help — I wouldn’t have known where to start without her! Getting the first copy was super exciting. I couldn’t believe it. When I started to write the story, I didn’t know what Lento would look like. To see him and the story brought to life in such a beautiful way was amazing to me.

What is the target age for this book?

I would encourage parents to introduce the book when their child is 1 year old by reading it to them and performing the interactive parts themselves. That’s how they learn — by watching you model behavior. But the target audience is for kids ages 3 to 6. 

What is GiGi’s Playhouse of Long Island, and what is your connection to the organization? 

Working as a speech pathologist has put me in touch with a lot of people that have Down syndrome, and you’ll often hear their families refer to themselves as “the lucky few.” There’s nothing down about having Down syndrome, and I wanted to be able to support and give back to the local Down syndrome community with this book. 

A few local moms are in the process of forming a Long Island chapter of GiGi’s Playhouse, a free center that provides speech, language, arts and life skills classes to help people with Down syndrome achieve their goals and function as typically as possible. The centers are run by volunteers who are passionate about the Down’s community, and a portion of the proceeds from “Sloths Are Slow” will go to the national GiGi’s Playhouse organization to support the upcoming Long Island center. They’re looking to open in the spring of 2020.

You dedicate this book to Thomas Scully. Tell us about him.

My friend, Debbie Scully, unfortunately, lost her son Thomas to brain cancer several years ago. I never met him, but the Miller Place community has worked so hard to honor his memory and legacy. Mentioning Thomas and the foundation in the back of the book is just my small way of showing my support for the family. You can learn more about Thomas and the foundation at www.thomasscullyfoundation.org.

What’s next for you? 

I actually have another book in the works called “Cows Don’t Belong in Houses,” inspired by a funny conversation with one of my young clients named Jackson. In his honor, I would want proceeds from that book to benefit cleft palate organizations. I’m also thinking about writing stories based on the other characters you meet in “Sloths Are Slow.”