Planning an Inclusive Playground

Planning a playground requires consideration for children of all abilities. The Americans with Disabilities Act (ADA) requires all playgrounds to be brought into compliance. Since the ADA requirements have come out, the American Society for Testing and Materials (ASTM) have provided written guidelines for accessibility compliance. ASTM F1487-05 Standard is a document that provides specific playground/play equipment accessibility guidance.

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The Architectural and Transportation Barriers Compliance Board has also authored a guideline that is the standard of practice for determining compliance with the ADA.

Legally, the ADA requires that “each service, program, or activity conducted by a public entity when viewed in its entirety, be readily accessible to, and usable by, individuals with disabilities.” This law covers “both indoor and outdoor areas where human constructed improvements, structures, equipment or property have been added to the natural environment.”

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Accessibility law only requires that comparable experiences must be provided for all. If there are several slides and two or more swings, it is considered accessible if children with disabilities can use one of the slides and one of the swings. To learn more about the difference between accessibility and inclusivity, click here.

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Aside from the regulations put forth that determine how to design an accessible playground for children of varying mobilities, there are many actions a planner should take to ensure their structure is truly inclusive. Inclusivity on a playground can be witnessed when children of all abilities can play together and participate equally- not separately and on their own. A well-designed playground incorporates the aspects of inclusive play to blend seamlessly.

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To learn more about inclusive play structures, visit playlsi.com

To find an inclusive playground near you, click here.

Inclusivity Versus Accessibility

Though inclusivity and accessibility are concepts used interchangeably, there are in fact many differences between the two ideas. Landscape Structures proudly boasts of inclusive design in their products- but what is the difference?

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Understanding what makes accessibility and inclusivity different comes down to considering the user of the design.

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Accessibility matches the need of a user in a singular context. Accessible design is specific in that it considers a single context, problem, user, and experience. A resource may be inaccessible to one group in the way that it is accessible to another. It removes a roadblock from one group’s path.

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Inclusivity creates an environment or experience designed so that it is usable by people of a variety of abilities, in many scenarios, alongside differently abled people. Inclusivity provides the tools for a user to choose the experience that best fits their situation and ability.

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Landscape Structures believes in creating play experiences for children of all physical and mental abilities, in all aspects of physical, social and sensory play. Inclusive play is an open invitation for children to learn alongside those both similar and different from them- shaping the next generation of leaders and thinkers for the better.

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To learn more about inclusive design or find an inclusive playground near you, visit our website.

Spreading global awareness about Sensory Processing Disorder

STAR Institute for Sensory Processing Disorder

October is Sensory Awareness Month, and we’re already focusing on next month because we want to help spread global awareness about this disorder.

On Oct. 6-7, our partners at the STAR Institute for Sensory Processing Disorder will host their 20th Annual International 3S Symposium in Denver, Colo. The Symposium will highlight 20 years of research accomplishments with though-provoking research and strategy presentations by clinical experts.

The Symposium is great for any individuals–occupational or physical therapists, special education teachers, early intervention specialists, parents and more–seeking a better understanding of Sensory Processing Disorder. And in addition to the two-day Symposium, the STAR Institute is hosting a pre-symposium workshop for parents focused on relationships and SPD across the lifespan.

Learn more and register for the 3S Symposium and pre-symposium workshop here. And watch our short video below to learn more about the history of the STAR Institute.

Join us in Denver on June 8

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Join us, our playground consultants in Colorado, Rocky Mountain Recreation, and the STAR Institute for a one-day workshop, Play for ALL: Advocating for Excellence in Play Spaces, on Thursday, June 8. During the educational workshop, you’ll learn from Dr. Lucy Jane Miller, founder of the SPD Foundation and STAR Institute, as well as experts in the fields of landscape architecture, parks and recreation, and others.

The workshop will share evidence-based practices through presentations, round table discussions and expert panels in an effort to help you create more fun and functional inclusive play environments for users of all ages and abilities. Even more, you’ll learn how to build collaborative partnerships and put together a plan of action to make a difference in your community.

Space is limited! Register for the workshop today!

  • Date: Thursday, June 8
  • Time: 8 a.m. to 5 p.m.
  • Location: Marriott Tech Center, 4900 Syracuse St., Denver, CO 80237

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Celebrating Sensory Awareness Month

National Sensory Awareness Month | October 2015

October is National Sensory Awareness Month… a time for us to help spread awareness of sensory processing disorder (SPD). SPD, which affects both children and adults, is a condition that exists when sensory signals don’t get organized into appropriate responses. The causes of SPD are among the subjects that researchers at the SPD Foundation have been studying, and treatment often includes natural setting therapy like at home, school or the playground.

The benefits of sensory-stimulating playground activities—those that engage all their senses—affect children of all abilities. The more they engage all of their senses, the better they make sense of the world around them and their relationship to it. See our infographic below of five ways that children benefit from sensory play.

5 Key Benefits of Sensory Play | Landscape Structures Inc.

Supporting inclusive play

Last week, we were honored at the Sensory Processing Disorder (SPD) Foundation’s 1st Annual Banquet of Champions. Held at the Inverness Hotel and Conference Center in Englewood, Colo., the event brought together people to help raise funds for research towards understanding behavioral and brain differences in children with SPD. Additionally, the Foundation celebrated individuals and organizations that have supported the SPD Foundation.

Proud to be recognized by the SPD Foundation for our commitment to inclusive play.

We were presented the Champion of Partnership award for partnering with the SPD Foundation to bring “The World’s Best Sensory Playground” to the STAR Center. The inclusive and sensory-stimulating playground equipment is used as a therapy tool for kids receiving treatment at the STAR Center.

Dr. Miller created an inclusive playground with many sensory-rich activities at the STAR Center.

We’re proud to work with the SPD Foundation and support their research in sensory processing disorders, and honored by this recognition. Learn more about the SPD Foundation and the STAR Center, and go here to read more about our commitment to inclusive play.

Meet the professional: Dr. Lucy Jane Miller

Dr. Lucy Jane Miller, founder of the SPD Foundation and STAR CenterWe are so honored to work with clients around the world, and we’re constantly learning about their fun and unique projects, obstacles they’ve faced and the innovative solutions they’ve created to overcome challenges. That’s why we’ve created this new feature that spotlights professionals. This week, meet Dr. Lucy Jane Miller, founder of the Sensory Processing Disorder (SPD) Foundation and the STAR Center. Below, you’ll learn how she came to begin her career, and what lead her to start the SPD Foundation.

When I was 16-years-old, I stopped seeing things the way other people do. Literally.

Without contact lenses in my eyes, objects were growing blurrier and blurrier. With contacts in, I could see but my eyes ached until, after several hours, I could hardly bear the pain. Only a few months earlier, I’d been thinking about where to go to college, what to do for the summer and all the other things typical 16-year-old girls think about. Then this one big sensory piece started to fail—my sense of sight—and my whole world shifted. My parents took me to a local ophthalmologist but he brushed aside my complaints. “There’s nothing the matter with her eyes,” he told us. “It’s all in her head.”

I was in college before we solved the mystery of my fading vision. By then, wearing contact lenses for more than a few minutes had become agony and even enormous shapes were fuzzy without them. It was my alarmed freshman roommate who insisted I see a doctor at the school clinic, triggering a series of referrals that finally brought answers and help. I was diagnosed with advanced kerateconus, a disease that distorts the corneas and—without treatment—eventually, leads to blindness.

The diagnosis was grave but it also came as a relief. My vision problems weren’t all in my head after all! The symptoms were real and they had a name. I finally knew what I was fighting and could make a plan for fighting it.

The year was 1971 and the cure for the disease was corneal transplants in both eyes, a procedure only two doctors in the U.S. were qualified to perform. I went on a waiting list for donor corneas, doubling up on classes so I could finish college before my surgery, learning Braille and practicing with a white cane, just in case the cure didn’t work and I lost what was left of my eyesight. A few weeks before graduation, I reached the top of the list for my first transplant. During the two-hour surgery, the old bad right cornea was removed and a new donated cornea was stitched to my eyeball with 16 sutures that would jab my eye and eyelid like teensy relentless needles for the three months after surgery when both my eyes had to be patched.

The operation was a total success, but I felt lost in my carefully maintained darkness. The endless stream of doctors, fellows, residents and medical students who gazed admiringly at my eye murmured, “beautiful, beautiful,” but I didn’t feel beautiful at all. I couldn’t see. I made a mess when I tried to eat. I couldn’t perform basic personal hygiene tasks and, after a lifetime seeing people when I talked, it didn’t feel like communication when I talked in the dark. What’s more, the admiring medical people who visited seemed to care only about my beautiful new eye. I felt reduced to a single sensory organ—an eyeball.

Then a new person entered my life. She was a young occupational therapy student doing her internship and she had been assigned to teach me how to feed, dress and take care of myself. She was about my age and showed no interest in my eyeball at all. Instead, she talked to me, Lucy Jane Miller, and listened to what I said. She always wanted to know how I—not my eye—was doing and she told me little things about her life so we had a real relationship even though I couldn’t see her. I silently called her “Angel” and imagined her with long blonde hair, blue eyes, a perfect Olympian body, and a halo, of course. I learned to identify her footsteps and detect her scent so I could say, “Hi, Angel!” just as she came into my room.

Then came the day when Angel chanced into the room when my patches were being changed and I finally glimpsed my rescuer with my eyes as well as with my other senses. The sight astonished me. Angel was a polio survivor. Half her face and body had been paralyzed and left sagging by the disease. In my darkness, Angel was beautiful because I could only “see” the beauty that was inside.

In the fog of recuperation, my future came into focus. While still in my eye patches, I applied to occupational therapy school. Two days after the last stitches were removed following my second transplant, I started graduate school.

One of the first books I read with my new good eyes was the work of a pioneering occupational therapist and neuroscientist named A. Jean Ayres. In Sensory Integration and Learning Disabilities, Dr. Ayres wrote in detail about the behavioral, social and emotional issues that arise when a child’s sensory foundation is not firmly established early in life. She stressed the importance of early diagnosis of sensory disorders and described in detail how occupational therapy (OT) could and was helping children. Fresh as I was from my own darkness, Dr. Ayres’ words resonated instantly.

Demoralized and disabled by the long-term repercussions of a doctor’s proclamation that my symptoms were all in my head, I knew how critical accurate and early diagnosis was. Barely out of my teens, I had known the humiliation of being unable to perform normal, everyday routines like other people my age. Grateful for Angel’s care, I was a firm believer in how dramatically OT could address sensory issues and improve a person’s life. Before first semester ended, I decided to spend my life promoting the understanding, accurate diagnosis and effective treatment of the sensory-based disorders that Dr. Ayres described.

From Sensational Kids: Hope and Help for Children with Sensory Processing Disorder (SPD)

Learn more about Dr. Miller and the research, education and treatment she provides to help individuals struggling with SPD. Then read about our partnership with the SPD Foundation and the STAR Center, including its sensory playground.

Dr. Miller created an inclusive playground with many sensory-rich activities at the STAR Center.

Dr. Miller created an inclusive playground with many sensory-rich activities at the STAR Center.