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SEPTEMBER 2026

DETROIT METRO

meet

Dr. Claudreen Jackson and P.J.

A Mother’s Story of Autism

Your Michigan Law Firm For Special Needs Planning and Advocacy MielderLaw.com • 248-799-2711

September 2026

CONTENTS 6

Meet the Uniquely You Team!

Important Phone Numbers

Your Story Matters!: Meet Dr. Claudreen Jackson and her son Pervis Jr.

Save the Date: Moms Retreat

The Heart of Supported Employment: How a Job Coach Changes Lives

Technology First News: Technology First Reimagines Support to Ease Michigan’s Direct Care Worker Shortage

See What’s Happening at STEP!: STEP Champions Inclusive Employment During National Disability Employment Awareness Month

Making A Difference: D man with D Big Heart and D Plan

Partner Spotlight: Finding Mooseness at North Star Reach Chapters of Change: “Breathe in deeply. And let it all go.”

Advocate Like A Mother: Understanding Present Levels of Performance (PLAAFP)

Healing Haven: The Benefits of Organized Spaces for Children with Autism

Preferred Partners

Uniquely You Detroit Metro

Meet the Uniquely You Team! Publication Staff

Jamie Olson AREA DIRECTOR & PUBLISHER

Christia Woodford CONTENT MANAGER, PUBLISHING ASSISTANT AND LOCAL EVENTS

Christina McGairk EDITOR-IN-CHIEF

Janalee Grainer UNIQUELY YOU - ACCOUNT EXECUTIVE STROLL OAKHURST

Kristin Dillon EVENTS COORDINATOR AND STAFF WRITER

Staff Writers and Contributors

Maria Giancotti

Steve Friess

Melanie Young

Dorene Philpot

Photographer

Ashley Ferrell A. FERRELL PHOTOGRAPHY

September 2026

Erin Drallos

FOOTPRINTS PHOTOGRAPHY

Charlotte Bachelor

Rebecca Parten

Molly David

Jesse Ronne

Chris Butts

Ron Sandison

Dr. Claudreen Jackson

PUBLISHER/ ADVERTISING INQUIRIES

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Jamie Olson 248-882-8448 Jamie.Olson@n2co.com

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Scan to view past digital copies, find resources, share a story or learn more about being involved.

IMPORTANT PHONE NUMBERS 517-241-3740

517-487-5426 877-463-2266 517-882-2800 517-241-3740

269-345-1913 517-241-3740

800-605-6722 517-333-6655 616-732-7358 269-337-3600 800-75-SEALS

Aging, Community Living, and Supports Bureau (ACLS Bureau) www.michigan.gov/mdhhs/adult-child-serv/adults-andseniors/behavioral-and-physical-health-and-agingservices/aging-services Arc Michigan arcmi.org Autism Alliance of Michigan https://autismallianceofmichigan.org/ Autism Support of Michigan https://autism-mi.org/ Behavioral Health and Developmental Disabilities Administration https://www.michigan.gov/mdhhs/keep-mi-healthy/ mentalhealth/procurement/welcome-to-behavioralhealth-and-developmental-disabilities-administration Michigan Foundation for the Blind and Visually Impaired Michigan Developmental Disabilities Council https://www.michigan.gov/mdhhs/keep-mi-healthy/ mentalhealth/developmentaldisability Michigan Rehabilitation Services (MRS) Capital Area Down Syndrome Association www.cadsa.org Deaf and Hard of Hearing Services (DHHS) www.deafhhs.org/ Disability Determination Bureau Easterseals MORC www.easterseals.com/MORC/

911 1-800-327-5966 833-633-5788

517-374-1171 517-241-3740 517-241-3740 517-241-3740

517-241-3740 833-808-7452

800-457-4584 313-446-4444 988 517-241-7004

517-284-7290 1-800-772-1213 1-800-772-1213 833-633-5788 517-203-1200 517-241-5324

Emergency Early On Michigan https://www.1800earlyon.org/directory.php Michigan Department of Education: Office of Special Education https://www.michigan.gov/mde/services/ special-education Michigan Family Forum Michigan Family to Family www.f2fmichigan.org/ Michigan Department of Health and Human Services www.michigan.gov/mdhhs Michigan Family and Social Services Administration (FSSA) www.michigan.gov/mdhhs Michigan State Department of Health www.michigan.gov/mdhhs Michigan Statewide Independent Living Council (MSILC) www.misilc.org/ Medicaid Disability MI Choice Waiver Program National Alliance on Mental Illness Preschool & Out-of-School Time Learning https://www.michigan.gov/mileap/educationpartnerships/out-of-school-time-and-summer-learning Self-Advocates of Michigan (SAM) Social Security Administration (SSA) Social Security Disability Insurance (SSDI) Special Education Questions United Cerebral Palsy Association of Michigan ucp@ucpmichigan.org Vocational Rehabilitation Services (VR)

Would you like to advertise in Uniquely You! to share valuable information and help support the community? Scan to grab some time to connect & learn more about being involved: https://calendly. com/jamie-mccabe/ special-needs-livingmagazine

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Jamie Olson: Uniquely You! Magazine Area Director jamie.olson@n2co.com 248-882-8448

DISCLAIMER: The articles and opinions expressed in this publication are those of the respective authors and do not necessarily reflect the views of The N2 Company d/b/a Uniquely You (“N2”). Advertisements appearing in this publication are paid placements and are not endorsed or recommended by N2. N2 is not responsible for the statements, opinions, or business practices of any authors, contributors, or advertisers featured herein. Portions of this publication may include content created with the assistance of artificial intelligence (AI) tools by authors or contributors and may not be independently verified by N2. We are proud to feature businesses that share our commitment to showcasing local connections. Please note that businesses profiled may have provided free products and/or services for the review. Uniquely You is for general informational and entertainment purposes only and is not intended to provide medical, therapeutic, educational, or legal advice. Always consult qualified professionals regarding the care and support of individuals with disabilities. NOTE: When community events take place, photographers may be present to take photos for the event, and they may be used in this publication.We are proud to feature businesses that share our commitment to showcasing local connections. Please note that businesses profiled may have provided free products and/ or services for the review. Uniquely You is for general informational and entertainment purposes only and is not intended to provide medical, therapeutic, educational, or legal advice. Always consult qualified professionals regarding the care and support of individuals with disabilities. NOTE: When community events take place, photographers may be present to take photos for the event, and they may be used in this publication.

Uniquely You Detroit Metro

Your Story Matters!

Mom and Dad showing off Pervis Jr. artwork

INSPIRED by Autism

A Mother’s Lifelong Journey of Love, Advocacy, and Acceptance

here are moments in life that forever change the direction of a family’s story. For Claudreen Jackson, that moment came not through a single diagnosis, but through a series of heartbreaking realizations that her youngest son, Pervis Jackson Jr., was experiencing the world differently. What began as a mother’s search for answers would become a 6

September 2026

lifelong journey of advocacy, education, faith, and unwavering love—one that has impacted not only her family but countless others throughout Michigan and beyond. Pervis Jackson Jr. was born in 1975. During his first year of life, he appeared to be developing typically, reaching the milestones expected of a growing child. There was little reason to suspect that anything was wrong. However, by 1976,

Pervis Jr.’s artwork turned into “Swag” See Website https:// pervisjackson.org/

Claudreen noticed dramatic changes in his behavior. The little boy who had once been progressing normally began exhibiting behaviors that became increasingly difficult to understand. As time passed, his condition intensified. He stopped sleeping through the night, often screaming for hours while running throughout the house. The entire family was exhausted as they tried to comfort

Pervis Jr. on his mom’s TV show

him while also protecting him from harming himself. His behavior became aggressive and self-injurious. He scratched, hit, and hurt himself while also becoming physically aggressive toward family members. Household belongings were frequently destroyed or thrown away if they did not meet his expectations or sensory preferences. It became painfully clear that something much deeper was happening. Seeking answers, Claudreen turned to medical professionals. After numerous evaluations, psychiatrists consistently reached the same conclusion: Pervis Jr. had autism. At the time, autism was poorly understood, and the guidance she received was discouraging. Physician after physician told her there was no cure, especially given the severity of his symptoms.

For Claudreen, Accepting that Answer was Impossible She spent years searching for another opinion, believing there had to be someone who could offer hope. Every new appointment carried optimism, only to end with the same heartbreaking conclusion. Eventually, after years of searching, she realized that the greatest gift she could give her son was not finding a cure—it was learning to fully accept him for who he was. That acceptance changed everything. Around the same time, America itself was changing. In 1975, the federal government began closing many large mental institutions as part of a national movement toward community-based care. Looking back, Claudreen believes that had those institutions remained open, Pervis Jr.’s severe behaviors almost certainly would have resulted

in institutionalization. Instead, he remained at home surrounded by the love of his family, even though doing so required extraordinary sacrifice.

Those Sacrifices Affected Everyone Pervis Jr.’s siblings—Cindy, Stephanie, and Shawn—helped their mother care for their younger brother despite becoming targets of his aggressive behaviors themselves. They experienced firsthand the unpredictability that autism brought into their home while continuing to support both their mother and brother with remarkable love. The greatest daily challenges revolved around safety. Claudreen worked tirelessly to teach self-control, reduce aggressive behaviors, establish bedtime routines, and prevent selfinjury. There were countless sleepless nights and moments Uniquely You Detroit Metro

She realized she could no longer parent Pervis Jr. the same way she had parented her older children. He needed a different kind of mother— one who understood his world instead of expecting him to fit into hers. Accepting that reality was one of the hardest emotional journeys she ever experienced.

She also wants other families to understand something she wishes someone had told her decades ago: having a difficult day is not a sign of failure. Caring for someone with significant disabilities is challenging, and parents should never blame themselves when progress feels slow. Although autism brought immense challenges, it also revealed remarkable strengths.

One of Those Strengths Emerged Through Athletics

when exhaustion threatened to overwhelm the family. Initially, Claudreen resisted the idea of medication. Like many parents, she hoped behavioral strategies alone would be enough. Over time, however, she realized that medication had been developed for individuals exactly like her son—people whose neurological challenges required additional medical support. Accepting medication became another difficult but important step, helping reduce some of his most severe behaviors and allowing the family to achieve goals that once seemed impossible. Reflecting on those years, Claudreen often says one of her greatest lessons was learning to shift her perspective. She stopped asking, “Why is this happening to me?” and instead began asking, “What must life be like for my son?”

She stopped asking, “Why is this happening to me?” and instead began asking, “What must life be like for my son?” 8

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Beacons of Light

“I want to say thank you to all the people who helped me in my journey to acceptance for my son. Special educators, therapists, counselors, caregivers, respite workers, group home workers and others taught me that there are kind, sensitive people who sincerely wanted to help people like P.J. They tolerated his challenging behaviors and came back day after day with a smile. They became my mentors and guides who helped me learn how to be his mother. Thank God there are people like this in the world. You all are still my Beacons of Light.” —Dr. Claudreen Jackson

Pervis Jr. became an accomplished Special Olympics athlete, earning gold medals in both track and ice skating. Ironically, the medals themselves held very little meaning for him. After one competition, he attempted to throw them into the trash because he simply did not value the awards. What mattered to him was participating in the sport itself. Claudreen often reflects that many athletes could learn from his perspective. He competed not for trophies or recognition, but purely for the joy of participating.

Another Unexpected Milestone Came Through Cooking As a teenager, Pervis Jr. loved French fries and expected them every day. One afternoon, while Claudreen was preparing them, he became physically aggressive toward her. Rather than continue rewarding the behavior, she quietly stepped away, refusing to finish cooking. Half an hour later, he appeared carrying a plate of finished fries. The discovery frightened her because she knew she had turned the stove off. Somehow, he had independently turned it back on and completed the cooking himself. While the moment initially caused concern, it also revealed an ability she never imagined he possessed. Today, cooking remains one of his favorite activities, and he continues preparing fries and sausages independently. Academically, Pervis Jr. faced significant cognitive and communication challenges. He attended Burger School in Garden City, which at the time was the only school in Wayne

Pervis Jr. and his big brother Shawn

County specifically serving students with autism. Despite years of education, he never developed functional reading or writing skills and remains largely nonverbal due to both limited motivation for language and a speech impairment. Today, Pervis Jr. is 51 years old. After living with his mother until she was 75 years old, he transitioned into a group home where he receives the support he needs while maintaining treasured visits home one week each month. He still enjoys cooking and skating— activities that continue bringing him joy decades later.

While Caring for Her Son Transformed Her Life, It Also Ignited a Passion for Advocacy That Would Impact Thousands of Families

When Claudreen first sought services in 1976, she was repeatedly turned away. Many agencies that served children with disabilities simply did not serve children with autism. Each rejection deepened her determination to create a better future for families who would come after hers.

Her Advocacy Soon Expanded Throughout Michigan She served on the State Board of Directors for the Autism Society of Michigan and became president of the Wayne County Chapter during the early 1980s. She served on advisory councils for Governors James Blanchard and John Engler and participated on numerous Parent Advisory Committees, including Detroit Special Education and Wayne County Special

Pervis Jr. on his mother’s tv show

Pervis Jackson

Education. Through these leadership roles, she helped shape policies, educate communities, and improve opportunities for individuals with autism across the state. In 2008, after decades of advocating for her own son and countless other families, Dr. Claudreen Jackson founded the Pervis Jackson Jr. Autism Foundation. Named in honor of her son, the Foundation was created to ensure that families facing any disability diagnosis would have access to information, encouragement, and resources that simply did not exist when her own journey began. The Foundation works to increase autism awareness, educate communities, connect families with valuable resources, and promote acceptance of individuals on the autism spectrum. Through community outreach, educational programs, speaking engagements, and family support, the Foundation continues Dr. Jackson’s lifelong mission of helping others navigate the challenges— and celebrate the possibilities—of all disabilities. For Dr. Jackson, the Foundation is more than an organization. It is a promise that no parent should ever feel as alone as she once did, and a tribute to the son who inspired a lifetime of advocacy, compassion, and service.

Her Passion for Advocacy Extended into Writing Claudreen has authored several books that reflect her faith, resilience, and lifelong commitment to encouraging others. Her three books of poetry—Let There Be Light, The Butterfly, and It Had

To Be Grace—offer readers reflections on perseverance, healing, and God’s faithfulness. It Had To Be Grace holds especially deep meaning because it was inspired by her beloved mother, Grace, who passed away in November 2023. Through its pages, Claudreen honors both her mother’s legacy and the grace that has sustained her throughout life’s greatest challenges.

A Promise Fulfilled Behind Claudreen’s writing journey was her husband, Pervis Jackson, a member of the singing group, The Spinners. Although Claudreen had written poetry for years, she was reluctant to publish her work or write the deeply personal story of raising Pervis Jr. because she did not consider it a traditional success story. Pervis encouraged her, pushed her, pulled her, pleaded with her, and even ‘nagged’ her to publish her poems and tell their family’s story. Before his passing in 2008, he convinced her to try. “You don’t know what you can do, but you know what you can try to do.”

“You don’t know what you can do, but you know what you can try to do.” —Pervis Jackson

Uniquely You Detroit Metro

Mother’s Day gift billboard

Claudreen, Pervis Jr. and Pervis

Pervis Jr.’s artwork

PJ’s Hidden Gift P.J. created colorful artwork with magic markers almost every day for more than a year. Claudreen preserved his artwork, and it now appears on the covers of her books Inspired By Autism and The Butterfly, celebrating his creativity. She also authored Inspired By Autism, sharing the lessons learned from raising Pervis Jr. while offering encouragement to other families walking similar paths. Her advocacy continues through her blog, A Spoonful of Comfort, where she writes honestly about autism, caregiving, faith, and hope. Another of her beloved works, The Magic Van, is a children’s book inspired by her years as an Special Education Educator. The story was beautifully illustrated by her own students with disabilities, making it a treasured collaboration born from the creativity and imagination of the children she taught. Today, both The Magic Van and It Had To Be Grace are available through Amazon, 10

September 2026

allowing even more readers to experience the messages of hope found within their pages. Beyond writing, Claudreen has shared her voice through television and radio. She hosts The Claudreen Jackson Show on WHPR TV and the radio program Let Your Light Shine on WMKM Gospel Radio 1440 AM, using both platforms to encourage families, celebrate individuals with disabilities, and inspire communities to embrace inclusion.

At 84, She Was Deeply Humbled to Receive These Honors

Her Decades of Service Have Not Gone Unnoticed

What once felt like overwhelming heartbreak eventually became a calling. Every disappointment fueled greater determination. Every obstacle became an opportunity to advocate. Every unanswered prayer became the foundation for helping another family find hope. For families who know little about autism, Claudreen offers a simple but profound perspective. Autism is not defined by limitations. Every individual experiences it differently. Some communicate through

In 2024, Claudreen received the Lifetime Achievement Award from President Joe Biden in recognition of her extraordinary volunteerism, leadership, and decades of advocacy on behalf of individuals with autism and disabilities. Later that same year, she was awarded an Honorary Doctorate Degree from Grace International Seminary, recognizing both her humanitarian work and her lifelong commitment to serving others.

She never pursued recognition. Every committee she joined, every family she encouraged, every speech she gave, every book she wrote, and every organization she helped build all began with one simple goal—to help her son.

Autism Did Not Just Shape Pervis Jr.’s Life. It Transformed Hers

Claudreen and her mother Grace at her 94th birthday

Spinners meeting President Clinton at the White House

Claudreen receiving her honorary Doctorate degree

words, others through actions. Some struggle with behavior, while others quietly navigate sensory challenges. Progress cannot be measured by comparing one person to another. Instead, success is found in celebrating every achievement, no matter how small it may seem to the outside world. Most importantly, she encourages parents to accept the child they have rather than mourning the child they expected. She reminds caregivers that difficult days are not evidence of failure and that asking for help is a sign of strength, not weakness. Today, Claudreen Jackson’s legacy reaches far beyond her own family. Through decades of advocacy, leadership, writing, broadcasting, and service, she has helped reshape how autism is understood throughout her community. Her work has touched countless lives, offering encouragement to parents who once felt alone and helping build a future where families have access to resources that simply did not exist when her own journey began. Her life stands as a testament that purpose is often born through

perseverance. What began with one mother’s determination to help her son has grown into a legacy of compassion, faith, and hope that continues to inspire generations. As the title of her book so beautifully declares, Claudreen Jackson truly is

Inspired By Autism —and through her unwavering love for Pervis Jackson Jr., she has inspired countless others to see beyond a diagnosis and recognize the extraordinary value, dignity, and potential within every individual.

About the Pervis Jackson Jr. Autism Foundation Mission To educate, advocate, and inspire while supporting individuals with autism and their families through awareness, community partnerships, and resources. Focus Areas: • Autism education and awareness • Family support and advocacy • Community outreach • Resource connections • Public speaking and education • Promoting inclusion and acceptance Website: https://pervisjackson.org

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The Heart of Supported Employment

How a Job Coach

CHANGES LIVES

Through Supported Employment

velina Arnold has been a job coach at Judson Center’s Supported Employment program for nearly twenty years. She started because she believed in the work — helping people with disabilities find and keep employment, build routines, and stay connected to places where they could belong. What she did not fully expect was how much the work would become part of her own life, too. Over the years, she has shown up to work sites across the area, restaurants, offices, and retail stores, meeting clients where they are and helping them succeed at their jobs. Some of those relationships have stretched on for years, even decades. Somewhere in that accumulation of ordinary mornings, the job became something she could not imagine walking away from. “It’s rewarding,” she said. And after nearly twenty years, she still means it. Matt Staines has been working at Chili’s for more than twenty years. For a significant stretch of that time, Evelina has been with him for quite some time as his job coach. For much of Matt’s time at Chili’s, Evelina has been there to support him every step of the way. When she arrives, her priority is making sure Matt is set up for success before he starts his shift. She checks that he has everything he needs, his supplies in place, and his workspace ready. Once everything is good to go, Matt is ready to take it from there, with Evelina in his corner if anything comes up. Matt has a way of making the people around him feel at ease. He moves through his shift with quiet confidence,

September 2026

working steadily, engaging with the people around him, and bringing warmth to the room. It is the kind of presence that makes a workplace feel a little lighter. On harder days, when other clients require more attention or problem-solving, she says Matt has a way of keeping her grounded. He is reliable, consistent, and genuinely easy to be around. “He is one of the most gracious people that I know,” she said. “He makes my job easy.”

When life feels overwhelming, structure helps.

Helping Others Thrive at Work The impact of a Job Coach is not always easy to see from the outside. Most days are made up of small, consistent moments: checking in with a client, offering encouragement, helping someone navigate a challenge at work, or celebrating a success that others might overlook. The work isn’t about grand gestures; it’s about showing up, day after day, and helping people build confidence, independence, and meaningful employment. “I can fluff up my pillow extra fluffy,” she said, “because I know I helped someone today.” That sense of purpose has guided her through nearly two decades as a Job Coach. Seeing individuals gain skills, achieve goals, and succeed in the workplace is what keeps her coming back. And she’s not alone; many of her colleagues have dedicated years, even decades, to this work. To her, that longevity reflects the lasting impact they have on the lives of the people they support.

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A Legacy of Support There is a reason Matt Staines has stayed at Chili’s for more than twenty years. The support around him never wavered, giving him the stability to grow into the role he holds today. That is what Evelina sees when she thinks about the broader purpose of supported employment. Not the placement itself, but what comes after it: the slow, steady accumulation of ordinary days that eventually becomes something a person can call their own. A career. A routine. A sense of belonging that builds quietly, day by day, through consistency and care. Judson Center has been walking alongside individuals and families for over a hundred years, and that legacy is something Evelina carries with her. Knowing she is part of an organization with such a long history of service gives her work a deeper sense of purpose, a reminder that every small moment of support is part of something larger. “I think about the fact that we’ve been here over a hundred years helping people,” she said. “It really warms my heart.” After nearly twenty years as a Job Coach, Evelina knows that lasting impact isn’t measured in a single day— it’s built over years of showing up, believing in people, and helping them succeed. Learn More About How Judson Center Can Help! Connect with our Disability Program at judsoncenter.org/disability Uniquely You Detroit Metro

Technology First News

TECHNOLOGY FIRST

Reimagines Support to Ease Michigan’s Direct Care Worker Shortage

cross Michigan, people with intellectual disabilities and their families who depend on daily support are facing an urgent crisis: there are not enough direct care workers to meet the need. Direct care workers are essential to helping people with intellectual disabilities complete daily activities, get to work, live safely, and participate in their communities. Michigan has approximately 190,000 direct care workers, however, estimates show the state needs at least 36,000 more to meet current demand. High turnover and unfilled positions are putting pressure on provider agencies, families, and the people who rely on support every day. Michigan is proud of its strong history of moving people with intellectual disabilities out of institutions and into community life. However, continued progress depends on having a robust, stable workforce. As the workforce shortage grows, Michigan needs a broader support model that uses every available tool to help people live safely and independently in the community. Technology First is such a model. Technology First asks a simple question at the beginning of support planning: Can technology help this person live more independently? It does not mean technology replaces people. It means enabling technology and remote support are considered as part of the full range of support options, alongside family, community resources, and direct care staff. Remote support allows trained staff in another location to respond to alerts or to a person’s request for assistance. It can be a sensor alerting staff that someone may need help. It could

September 2026

Empowering And Enriching The Lives Of People With Disabilities. Springhill Pooled Accounts Trust is a trusted advocate in the special needs community. As professional trust administrators, we manage your assets, distribute funds for discretionary expenses, and help maintain your public benefits eligibility. We take the time to understand beneficiaries' specific needs to determine if our trust is the best option for their long-term goals. also be a person using a device to connect with support when they have a need. Importantly, remote support is not about watching people on camera. In most cases, it is less intrusive than having someone physically present at all times. It gives individuals more privacy, more choice, and more control while ensuring help is available when needed. For example, a person who does not need a direct care worker physically present overnight may be able to use sensors, emergency buttons, and two-way communication to access help if needed. Another person may use medication reminders, smart home tools, or task prompts to complete routines with more independence. In these situations, remote support complements existing services. It allows in-person direct care workers to focus their time on individuals with more complex needs that require hands-on assistance. This shift to incorporating remote support also elevates the role of direct care workers. Instead of having to provide every reminder and every prompt in person, workers can become coaches, teachers, advocates, and skilled partners in independence. Remote support and enabling technology can create new career ladders, new technical skills, and opportunities for workers to strengthen their relationships with those they serve. Michigan, however, remains behind many states in making these options broadly available and fundable through the Medicaid system. The Michigan Technology First Task Force has been working to develop a blueprint for integrating enabling technology and remote support into Michigan’s system of care for individuals with intellectual disabilities. To make Technology First successful, Michigan will need thoughtful policy changes, sustainable funding, strong training, and reliable backup plans. Families and individuals served will need to know that technology will not be used to cut essential services, but to expand options. Direct care workers will need to know that technology is not a threat to their work, but a tool that can strengthen their role and help them focus where their skills are needed most. The state must continue to value and invest in direct care workers. At the same time, it must modernize the way support is delivered. Technology First offers Michigan a practical and forwardlooking solution. By introducing remote support options that complement existing services, Michigan can help people with disabilities live with greater independence while freeing direct caregivers to support those with the highest needs. It is a reimagining of care that meets the moment so more people with intellectual disabilities can receive the supports they need to maximize independence.

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Partner Spotlight

FINDING MOOSENESS AT NORTH STAR REACH

HOW FAMILY CAMP HELPS FAMILIES LIVING WITH SERIOUS ILLNESS REDISCOVER JOY, CONNECTION, AND HOPE BY J. J. L E WI S , C E O, N O RT H S TA R R E AC H

Like many caregivers arriving at North Star Reach for their first Family Camp Weekend, mixed feelings accompany the anticipation including hope, uncertainty, exhaustion, and perhaps a little skepticism. After all, what could a weekend at camp really do? “We didn’t know what to expect but it didn’t take long to make connections and feel like we fit in and were at “home.” It was so nice to “belong” in a community where the other moms/parents/siblings just “get it.” There was an instant bond when the parents had time to meet and form relationships with one another, sharing our stories and experiences. They were all so similar yet different, 18

September 2026

and so many moments with other parents nodding their heads and saying “yes, me too” and the emotions that came up simply because we weren’t alone in what our families have been through,” Ethan’s mom explained. For years, their family had been navigating a reality familiar to far too many families raising children with serious health challenges. Surgeries, hospital stays, new diagnoses, and constant appointments make for endless uncertainty. Life had become less about making memories and more about simply making it through the next day. Their child’s diagnosis added another layer of complexity and

isolation. Friendships became harder to maintain. Family outings have become more difficult to plan. The world around them seemed to keep moving forward while they remained focused on medical needs, therapies, and survival. “It often felt like the world had moved on while we were still in the trenches,” another parent shared If you’ve never walked that road, it’s difficult to understand. If you have, you don’t need an explanation. And that’s exactly what families discover when they arrive at North Star Reach. For one weekend, they are surrounded by people who simply get it. No explanations required.

No awkward conversations. No need to justify medications, accommodations, hospital appointments, or the countless ways serious illness changes a family’s life. Everyone understands because everyone has lived some version of the same story. That understanding is where healing begins.

When Serious Illness Becomes a Family Diagnosis When a child is diagnosed with a serious medical condition, the diagnosis affects far more than one person. Parents become caregivers, advocates, nurses, schedulers, researchers, and protectors. Siblings often become the quiet heroes of the family, adapting to changing plans, missed events, and attention that naturally shifts toward medical needs. Family routines change. Vacations have disappeared. Even simple moments together become harder to find. While the financial burden can be significant, the emotional cost is often even greater. Research consistently shows that children living with chronic or life-threatening illnesses experience higher rates of stress, anxiety, depression, and social isolation. Parents carry the weight of constant caregiving, while siblings often sacrifice parts of their own childhood. The isolation can be overwhelming. The stress can be relentless, and the opportunity to simply be a family can feel increasingly rare. That’s why Family Camp Weekends exist. Not because families need another program. Because they need each other.

Where Medicine Meets Magic Nestled among 105 wooded acres and bordered by two peaceful lakes in Pinckney, Michigan, North Star Reach offers something many families haven’t experienced in years: the freedom to stop worrying. As Michigan’s only fully accessible, medically supported camp serving children with serious health challenges and their families at no cost to the family, North Star Reach exists to ensure that a diagnosis never defines a childhood. Every campfire, canoe ride, fishing trip, arts and crafts session, song, and friendship formed represents

another step toward confidence, independence, and belonging. Founded to serve children who are often unable to attend traditional camps because of chronic or life-threatening illnesses, North Star Reach has become a beacon of hope for families throughout Michigan, Indiana, Ohio, Illinois, Wisconsin, Ontario, and beyond. The camp is part of the internationally recognized SeriousFun Children’s Network, founded by actor and philanthropist Paul Newman. Alongside camps around the world, North Star Reach shares a simple but powerful mission: providing safe, medically supported camp experiences that empower children with serious illnesses to discover confidence, resilience, and lifelong friendships. What makes North Star Reach extraordinary is its commitment to combining the timeless traditions of camp with exceptional medical care. At the heart of campus sits The Observatory, a state-of-the-art health center staffed around the clock by volunteer physicians, nurses, child life specialists, pharmacists, respiratory therapists, and healthcare professionals from leading hospitals and medical centers throughout Michigan and the Great Lakes region. Children requiring chemotherapy, dialysis, ventilators, feeding tubes, central lines, specialized medications, and other complex medical care can safely spend their days boating, casting fishing lines, trying archery, singing around campfires, creating art, performing in talent shows, and making memories that simply aren’t possible in most traditional camp settings.

Medical care never overshadows childhood. Instead, it makes childhood possible. For parents and caregivers, the impact is equally profound. Entrusting a medically fragile child to someone else is often one of the greatest challenges families face. North Star Reach’s experienced medical team provides families with peace of mind, allowing many parents to experience their first true respite in years while knowing their child is safe, supported, and thriving. For the first time in

months—sometimes years—they can simply breathe.

A Weekend Where Families Can Be Families Again Family Camp Weekends were created because serious illness affects every member of the family—not just the child with a diagnosis. Parents, siblings, grandparents, caregivers, and children experience camp together. They paddle across the lake. They aim for the bullseye at archery. They laugh through arts and crafts. They gather around campfires. They sing songs. They explore nature. They cheer each other on. Every detail has been thoughtfully designed so families can stop worrying about logistics and focus on something they often have too little time to Simply being together. For some children, it’s the first time they’ve tried a new activity without fear. For some parents, it’s the first time they’ve relaxed in months. For some siblings, it’s the first time they’ve met other children who truly understand what life at home looks like, and for many families, it becomes the first time in years they’ve felt genuinely seen. Because camp sessions bring together children and families navigating similar medical journeys, friendships form naturally. Many campers describe it as the first time they’ve ever met someone just like themselves. Instead of feeling different because of medications, medical equipment, or physical limitations, they become part of a community where everyone belongs. One mother described it this way. “Truly feeling seen and heard, without having to explain every painful detail is a remarkable feeling that I didn’t even know I was craving until I experienced it.” Sometimes healing begins with medicine. Sometimes it begins with belonging and the moment they knew they belonged. Back at Family Camp, Ethan’s family was beginning to settle in. There were activities. There were camp songs. There were smiles from people they had just met. But then something happened. Ethan traveled around camp in an all-terrain wheelchair. Uniquely You Detroit Metro

always placed at the center of every decision. Excellence, safety, inclusion, collaboration, and joy serve as the foundation for everything the camp does. Those values are reflected not only in the experiences offered to campers but also in the dedication of hundreds of volunteers, medical professionals, donors, foundations, and community partners who make the mission possible.

North Star Reach is free for everyone

He and his brothers discovered that their family wasn’t the only one with a sibling in a wheelchair or that cannot speak or eat normal food or walk or play sports or swim on their own. By the time the family participated in North Star Reach’s famous No Hands Spaghetti Dinner, something had changed. They weren’t visitors anymore. They weren’t outsiders, they belonged, and that feeling of belonging is something we have a name for.

The Magic of Mooseness At North Star Reach, we call it Mooseness. It’s difficult to define and impossible to manufacture. Mooseness is the feeling that happens when children discover confidence they didn’t know they possessed. It’s the joy of hearing laughter echo across the lake. It’s watching parents connect with people who truly understand their journey. It’s seeing a sibling feel celebrated. It’s finding community after years of isolation. It’s belonging. Over the last decade, thousands of children, families, volunteers, donors, physicians, nurses, child life specialists, and community members have experienced Mooseness. Some arrive as campers. Some arrive as volunteers. Some arrive as donors or supporters. Many return year after year because once you’ve experienced Mooseness, you want others to experience it too. 20

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Volunteers often describe their experience as just as life-changing as the families they serve. Healthcare professionals accustomed to seeing children inside hospitals witness them becoming artists, comedians, swimmers, adventurers, performers, explorers, and confident young people whose illnesses no longer define them. Donors see generosity transformed into opportunity. Community partners become lifelong advocates. That’s how a camp becomes a community. That’s how a community becomes a family. That’s how a family becomes a Campily.

More Than a Week at Camp While many people know North Star Reach for its summer camps and Family Camp Weekends, the organization’s mission extends far beyond a single week on the calendar. Throughout the year, North Star Reach offers family camps, seasonal programs,”Camp Beyond the Cabin” at children’s hospitals, and special events that keep campers and families connected long after the cabins empty and the campfires fade. These yearround opportunities strengthen friendships, expand support networks, and remind families they never have to navigate their journey alone. The camp’s guiding values are evident in every aspect of its programming. Children and families remain the organization’s North Star,

Everything North Star Reach provides is made possible through the generosity of others. Families never receive a bill. Every memory is completely free of charge. Because financial circumstances should never determine whether a child gets to experience the joy of childhood. Volunteers are equally essential to fulfilling that promise. From cabin counselors and activity leaders to physicians, nurses, event volunteers, and maintenance teams, individuals donate thousands of hours each year to create unforgettable experiences. Their commitment allows North Star Reach to maximize every donated dollar while building a welcoming community rooted in compassion, service, and hope.

Celebrating a Decade of Mooseness This year marks a special milestone for North Star Reach as the organization celebrates its tenth anniversary— affectionately known as the Year of Mooseness. Over the past decade, thousands of children and families have discovered confidence they never knew they possessed. Volunteers have found purpose. Healthcare professionals have witnessed children thriving outside hospital walls. Donors have seen generosity transformed into lifechanging opportunities. The celebration isn’t simply about looking back. It’s about looking ahead. Community celebrations, open houses, fundraising events, and special anniversary activities are bringing together campers, alumni families, volunteers, donors, and friends to celebrate everything North Star Reach has accomplished while ensuring that future generations of children will

continue to experience the magic of camp. Upcoming events, including the annual MOOSE-ic Festival, open houses, and community celebrations, continue raising awareness while generating essential support for future programming. Every story shared reminds us why this work matters.

The Impact Lasts Long After Camp Ends Eventually, the campfires burn low. The songs grow quiet. The cabins empty. Families pack their cars and begin the drive home. But the impact remains. North Star Reach families consistently report increased confidence in their children, stronger family connections, reduced stress, expanded support networks, and greater optimism about the future. More importantly, they leave knowing they are not alone. Friendships continue. Support systems grow. Families discover new possibilities. As one parent reflected: “From shared laughter to brave steps outside our comfort zone, we left camp with more than memories. We left with confidence, belonging, and friendships to carry with us.”

Perhaps that’s North Star Reach’s greatest achievement. It creates a place where illness no longer becomes the defining characteristic of a child. Instead, children discover abilities they never knew they possessed while

building memories that remain with them long after camp concludes. For many families, North Star Reach represents hope during some of life’s most difficult seasons. It reminds parents that their children deserve joyful childhood experiences regardless of medical diagnoses. It reminds siblings that they, too, are part of a supportive community. Most importantly, it reminds every camper that they are capable of extraordinary things. As North Star Reach looks toward the future, its vision remains clear: to continue providing life-changing camp experiences that help children with serious health challenges build confidence, form meaningful relationships, and discover the joy of simply being kids. Through compassionate care, dedicated volunteers, generous donors, and an unwavering commitment to inclusion, the organization continues proving that every child deserves the chance to laugh around a campfire, paddle across a lake, and create memories that last a lifetime.

Join the Campily This Fall. North Star Reach will host three Family Camp Weekends at our fully accessible, medically supported camp in Pinckney, Michigan: September 11–13, 2026 October 9–11, 2026 October 23–25, 2026 Each weekend is offered completely free of charge and is designed to help families reconnect, build friendships, discover new possibilities, and create memories that last long after camp ends. Whether you are a family looking for support and community, a volunteer searching for a meaningful way to make a difference, or a donor interested in helping children and families thrive, there is a place for you at North Star Reach. If your family includes a child living with a serious medical condition, we encourage you to learn more and apply. If you’re looking for a meaningful way to give back, consider volunteering your time and talents.

If you’d like to help ensure every family can attend camp free of charge, consider making a gift or sponsoring a camper experience. We often say that camp is where strangers become friends, friends become family, and family becomes Campily. For ten years, that spirit has brought together thousands of children, siblings, parents, caregivers, volunteers, medical professionals, and supporters from across the Great Lakes region. Together, they have created a community built on belonging, resilience, joy, and hope. We would love for you to be part of it. And if you’ve ever wondered whether one weekend can truly change a family’s life, ask Ethan’s family. They arrived hoping for a fun weekend. They left with something much greater. They left knowing they belonged. They left with Mooseness. And once you’ve experienced Mooseness, you carry it with you wherever you go. To learn more about Family Camp Weekends, eligibility requirements, volunteer opportunities, or ways to support North Star Reach, visit www. northstarreach.org. Because every child deserves the chance to belong. Every family deserves the chance to reconnect. And everyone deserves a little more Mooseness in their life! For more information about North Star Reach, visit North Star Reach or follow the organization’s Facebook page @NorthStarReach for the latest camper stories, events, volunteer opportunities, and community updates.

North Star Reach 1200 University Camp Drive Pinckney, MI 48169 734-680-8744 northstarreach.org info@northstarreach.org Uniquely You Detroit Metro

Chapters of Change

“Breathe in deeply. And let it all go.” BY R E B E CC A PA RT E N

I FIRST READ Kendyl Arden’s The Art Therapy Way: A Self-Care Guide back in 2022. This review was mostly written after my initial reading but I did add some additional comments. This is a book that I would recommend to pretty much anyone. I really like how the book is organized into different sections based on the type of mood or emotion you are experiencing (happiness, pain, anger, grief etc.) and then with each activity there is a meditation / mantra, the actual activity instructions, and the follow up “processing” questions to think about. This is especially appealing for me because sometimes I’m better at writing than I am at creating something… so even if I decided not to do the art project specifically as described, I still have some amazing reflection questions to think about and use. This is still accurate years later. As I was looking through the activities again I was definitely more interested in the reflection questions. I initially envisioned adapting some of the activities to be part of my journal as opposed to separate pieces. But life happened and I got out of the habit of journaling. However, I can always try to get back into it and perhaps just write instead of doing the actual art activities. I was impressed with the variety of activities described. I will admit: creative journaling and self care are not new topics for me to explore. I have a Master of Social Work license (granted, not in clinical practice but still). So a lot of times I see the same activities suggested over and over. But this book has some that I think are very cool- “Get Your Anger Out” and “Chalk”. There are many relatable and meaningful mantras, things to think about, and even poems written by Arden herself interspersed throughout the book. The only “downside” of this book is that the meditation portions can be repetitive both within a single activity section and across the whole book. But, this feeling is likely because I sat and read the book straight through instead of on a activity by activity basis. All in all: I think this book is a great addition to the world of art therapy. Thank you to the author, Kendyl Arden, for an advanced reader copy. The opinions expressed are mine alone. 22

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NEXT MONTH

I’ll be reviewing the young adult novel All the Stars Align by Gretchen Schreiber.

Advocate Like A Mother

Understanding Present Levels of Performance (PLAAFP)

BY M A R IA G IA N COT T I , M . E D. - S T U D E N T A DVO C AC Y M I C H I G A N

AS THE NEW school year gets underway, IEP teams across Michigan are meeting, updating paperwork, and setting the stage for the year ahead. In the middle of all that paperwork sits one section that most parents skim right past, but it may be the most important part of the entire IEP: the Present Levels of Academic Achievement and Functional Performance, usually called PLAAFP. PLAAFP is exactly what it sounds like: a snapshot of where your child is right now. Academically, socially, emotionally, and behaviorally. It should answer a simple question, how is this student actually doing today, based on real, current data? Here’s why it matters so much. Every goal, every service, and every accommodation in the IEP is supposed to be built from the PLAAFP. If the PLAAFP is vague, outdated, or incomplete, everything built on top of it will be weak too. A goal that isn’t rooted in accurate present levels isn’t really measuring progress, it’s just a guess dressed up as a plan. Think of it this way: imagine a contractor building a house without ever measuring the lot. The blueprint might look great on paper, but if it doesn’t match reality, the house won’t fit. PLAAFP is the measurement. Everything else in the IEP is the blueprint built from it. A strong PLAAFP includes specific, measurable, data-based information: current grades, the most recent evaluation results, teacher input, benchmark or progress-monitoring scores, and a clear description of how the disability affects the student’s involvement and progress in the general curriculum. It should describe strengths, not just deficits, and it should reflect the whole child, including academics, behavior, communication, and social-emotional functioning, not just one subject area. Watch for red flags. Vague language like “doing fine” or “making progress” without any data attached tells you almost nothing. So does a PLAAFP that’s missing an entire area of need — social-emotional functioning, behavior, or communication — when you know, as the parent, that those needs exist. I’ve seen PLAAFPs that were copied and pasted from the year before with only the student’s age changed.

That’s not a snapshot of today; it’s an old photo mistaken for a current one. What can you do with this information? Ask the team directly: “What data supports this statement?” If a PLAAFP hasn’t changed much from last year, ask why. Compare this year’s present levels to last year’s to see whether your child is actually growing, staying flat, or losing ground. Bring your own observations, too. What you see at home is data the school may not have. It’s also worth asking whether the PLAAFP reflects any recent evaluations, outside reports, or provider notes you’ve shared with the school. If you’ve handed over a private evaluation or a letter from a therapist and it isn’t reflected anywhere in the present levels, that’s worth raising at the table. I also encourage parents to pay attention to how PLAAFP describes behavior and attention, even when the primary concern is academic. A student struggling with reading may also be struggling to sit still during instruction, and if that connection isn’t captured in the present levels, the team may end up addressing the wrong problem first. The most useful PLAAFPs paint a full picture, not a narrow one focused only on test scores. One practical habit that helps: keep your own running notes throughout the year, a few sentences after a rough week or a great one, so you have real, dated observations to bring to the annual meeting. Let’s look at the data because that’s where every good IEP conversation should start, and it’s the first place I look when I begin reviewing a family’s case. If you’re navigating an IEP or 504 Plan and want support making sense of it, Student Advocacy Michigan offers remote special education advocacy services to families throughout Michigan. Call (248) 372-9770 to schedule a consultation. You can also find more articles and resources at www. studentadvocacymi.com, or follow along @studentadvocacymi on Facebook and Instagram. Uniquely You Detroit Metro

See What’s Happening At STEP!

STEP Champions Inclusive Employment During National Disability Employment Awareness Month

his October, Services To Enhance Potential (STEP) proudly celebrates National Disability Employment Awareness Month (NDEAM) - a nationwide observance recognizing the contributions of workers with disabilities and promoting inclusive employment practices. While October shines a spotlight on this important message, at STEP inclusion and opportunity are at the heart of everything we do, all year long.

Employment Empowers Employment is about far more than earning a paycheck. It builds independence, confidence,

purpose, and connection. For individuals with disabilities, meaningful employment can be life-changing. Yet barriers still exist. At STEP, we are committed to expanding access to Competitive Integrated Employment (CIE) - where individuals with disabilities work in community settings alongside their peers, earn competitive wages, and contribute their unique talents. We believe everyone deserves the opportunity to pursue their goals and showcase their abilities in the workforce. 24

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Strong Partnerships, Stronger Communities Inclusive employment is made possible through collaboration. STEP is grateful for the many local businesses that partner with us to create welcoming, supportive workplaces. From retail and hospitality to healthcare, automotive, and manufacturing, these partnerships open doors for our members while providing employers with dedicated, dependable team members. When businesses invest in inclusive hiring, everyone benefits. Workplaces become more diverse, innovative, and reflective of the communities they serve.

Preparing for Success STEP continues to provide comprehensive job readiness training, vocational skill development, personalized employment planning, and ongoing support services. By focusing on each individual’s strengths and interests, we help remove barriers and build pathways toward long-term success.

Celebrate NDEAM With Us As we observe National Disability Employment Awareness Month this October, we invite the community to join us in advancing workplace inclusion. You can make a difference by: • Exploring inclusive hiring opportunities • Partnering with STEP as an employer • Volunteering your time or expertise • Sharing the message of equal opportunity Together, we can ensure individuals with disabilities have equitable access to meaningful careers - not just during NDEAM, but every day of the year. At STEP, we believe in potential. We see it, support it, and celebrate it. To learn more about our programs or how to partner with STEP, visit www.stepcentral.org.

10TH ANNUAL STEPS TO SUCCESS FUNDRAISER

Join us for our 10th Annual STEPS To Success fundraiser on Thursday, October 22, 2026 at SoHo Banquet & Event Center in Westland. Visit https:// stepcentral.org/10th-annual-steps-to-success/ for event information.

Uniquely You Detroit Metro

Making A Difference

D man with D Big Heart and D Plan The Unforgettable History of The DMAN Foundation { Danny’s Miracle Angel Network) BY C . J B U T T S THERE ARE MILLIONS of charities and organizations serving communities around the world. Some help families recover from natural disasters, such as the American Red Cross. Others support those facing serious illnesses, including St. Jude Children’s Research Hospital and the American Cancer Society. Still others focus on enriching lives and creating opportunities for individuals with disabilities. One such organization is the Danny’s Miracle Angel Network (DMAN) Foundation. Before exploring the programs and services they provide, it’s important to understand who they are, how they got started and the mission that continues to guide their work today.

The Mission Behind the DMAN Foundation On Jan. 26, 2026, I had the privilege of interviewing Ziad Kassab, the man behind the Danny’s Miracle Angel Network (DMAN) Foundation. 26

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The foundation’s story began in 2009 when Ziad’s brother, Danny, was tragically struck by a car. Three nurses who happened to be nearby helped save his life that day. While Danny survived the accident, his journey was far from easy. He spent the next 14 years dependent on a ventilator, limiting his ability to enjoy many of the experiences most of us take for granted. Wanting to improve the quality of life for individuals with disabilities and complex medical needs, Ziad and his family established the DMAN Foundation. Today, the organization’s mission focuses on helping people with disabilities live life to the fullest through three key programs: the DMAN Music Therapy Studio, the Travel Assistance Program and Dreams Come True on Woodward. After researching the many benefits of music therapy, the foundation launched the DMAN Music Therapy Studio. The program allows participants to work alongside accredited music therapists and audio engineers using

adaptive equipment to create, record and produce music. Clients can participate in one-on-one sessions where individualized goals are established and monitored, as well as group sessions that encourage collaboration, creativity and shared experiences. Another important initiative is the DMAN Travel Assistance Program. The program helps individuals with physical disabilities access travel opportunities that might otherwise be difficult or impossible. By providing support and resources, the program allows participants and their families to enjoy meaningful experiences and create lasting memories together.

Key Features:

Trip Support and Coordination: DMAN helps plan all aspects of travel, including accessible transportation, accommodations and medical equipment needs. Equipment Assistance: The organization helps coordinate the

transportation of necessary equipment, such as mobility devices. Medical and Accessibility Logistics: DMAN can arrange non-emergency medical transportation and help ensure access to needed medical resources at the destination. Event and Leisure Travel: The program goes beyond medical appointments. Participants can receive support for sporting events, concerts, vacations and unique experiences. Ticket Accessibility Coordination: DMAN may work with venues to exchange tickets for accessible seating when needed.

The purpose of the program is to reduce barriers to travel for individuals with significant physical disabilities and help them experience activities and destinations they may not have thought possible. Have you ever attended the Woodward Dream Cruise? One of DMAN’s signature events, Dreams Come True on Woodward, gives participants the opportunity to ride in the car of their dreams, whether that’s a Corvette or another favorite vehicle. Before the event begins, a NASCARstyle announcer welcomes participants and kicks off the festivities with the famous words, “Gentlemen, start your engines.” The event also includes great food, fellowship and an unforgettable experience. During my interview, I learned that the DMAN Foundation operates entirely through donations. Every program and event is funded by individuals and supporters who believe in the organization’s mission. One of the foundation’s greatest successes has been its move from Berkley to a larger facility in Southfield. At the same time, funding remains one of its biggest challenges because the organization relies solely on donations to continue its work. When asked what message he would like readers to take away, Ziad shared a simple but powerful reminder: no

matter what challenges you are facing, never give up. I have had the privilege of attending two spectacular events hosted by the DMAN Foundation: Dreams Come True on Woodward and the DMAN Christmas Party. It was at these events that I had the opportunity to meet Ziad himself. Let me tell you, they were some of the best events I have ever attended. Those experiences changed not only the way I see myself, but also the way I view disability as a whole. If you want to experience these amazing events for yourself, or know someone who could benefit from what the DMAN Foundation has to offer, I highly encourage you to learn more about the organization’s mission, programs and services. After attending two of their events myself, I can honestly say the impact they have on the disability community is something special. To learn more or get involved, visit the DMAN Foundation’s website at https://mydman.org/about/.

Uniquely You Detroit Metro

Healing Haven

Lighting matters, too. If bright lights are difficult, try lamps, curtains, or softer lighting when possible.

Notice the Sounds Around Your Child Noise can also affect regulation. Humming appliances, televisions, traffic, or nearby conversations may be hard for some children to ignore. Look for patterns: Does homework go better in a quieter space? Does your child need a break after loud activities? A calm corner, noise-reducing headphones, or moving a task to another room can help.

The Benefits of Organized Spaces for Children with Autism BY E M I LY C R A N E

ave you ever tried working in a cluttered area or been distracted by noise or lighting while trying to focus? Most of us would struggle in that environment. For children with autism, cluttered or overstimulating spaces can make it even harder to focus, learn new skills, and participate in daily routines. Everyday sights, sounds and clutter can feel overwhelming. A busy playroom, bright lighting or noisy room can make it harder to listen, learn and participate. The good news is that creating a more supportive space does not require a full home makeover. Small, intentional changes can reduce distractions, clarify expectations, and help your child feel more regulated.

Why the Environment Matters Children with autism often process sensory information differently. Visual clutter, unexpected noise, bright colors, 28

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Use Structure to Support Routines Organized spaces help reinforce expectations. A table can become a homework spot. A bin can hold bedtime books. A basket by the door can hold shoes or school items. These systems help children predict what happens in each space and what is expected. Visual schedules, first-then boards, or picture labels can add clarity. When children know what comes next, transitions may feel less stressful, and routines can become more manageable.

Tips for Your Home strong smells or harsh lighting can compete for attention and make daily tasks feel more difficult. Organized, predictable spaces give children fewer distractions to sort through and clearer cues about what comes next. This kind of structure can support focus, independence, smoother transitions, and routines that are easier to practice consistently at home. Here are a few thoughtful adjustments that can make everyday routines feel more manageable.

Begin with Visual Organization Start by looking at what your child sees. Clear surfaces in work or play areas, limit extra wall décor and use bins or drawers to keep unused materials out of sight. Picture labels, color-coded bins, or simple written labels can help children understand where items belong and encourage them to put things away more independently.

If your home feels overwhelming, start with one drawer, shelf, or corner. Remove items your child doesn’t need for that activity, group similar materials together, and add a simple label. Then observe how your child responds. Helpful first steps may include: • Use labeled bins for toys, art supplies, or school materials. • Reduce visual distractions when your child needs to focus. • Create a quiet space for breaks when your child feels overwhelmed. • Every child is different, so the goal is not a perfectly organized home. The goal is a space that helps your child feel calmer, more confident, and ready to participate in daily life. To learn more about Healing Haven’s comprehensive services—ABA, Speech and Occupational Therapies, Autism Evaluations and Developmental Testing, and Counseling—visit healinghavenaba.com.

Uniquely You Detroit Metro

This section is here to give our readers easier access when searching for a trusted neighborhood partner to use. Get to know the businesses that make this magazine possible. Please support them in return and thank them if you get the chance! ABA Services - In Home

Benevolent Behavior Therapy (947) 300-6700 www.benevolentbehaviortherapy.com

ABA/Autism Therapy Services

Print Solutions: Apparel & Beyond

Community Support

Private High School

Chalgian & Tripp Law Offices PLLC (248) 799-2711 www.Mielderlaw.com

Gateway Pediatric Therapy (248) 712-4266 gatewaypediatrictherapy.com

Best Buddies Michigan (517) 304-4959 www.bestbuddies.org/michigan

Healing Haven (248) 965-3916 www.healinghavenaba.com

Judson Center (248) 837-2020 www.JudsonCenter.org

ABA/Comprehensive Services

Disability Support Services

Total Spectrum ABA (844) 263-1613 totalspectrumcare.com

Adaptive Bike Program

Easterseals MORC (586) 303-6866 morc.easterseals.com/

Employment and Training Services

POSSiBiliTEEs, LLC (616) 613-0386 www.POSSiBiliTEEs.shop

AIM High School (248) 702-6922 www.aimhighschool.com

Recreational support

Rochester Avon Recreation Authority (RARA) (947) 886-0084 www.rararecreation.org

Recreational/ Music/ Art Therapy

Advanced Therapeutic Solutions (734) 352-3543 www.advancedtherapeauticsolutionsmi. com

The Agape Project (586) 388-2110 www.theagapeproject.com

Services To Enhance Potential (STEP) (734) 718-0483 www.stepcentral.org

Adaptive Custom Equipment

Family Support

My Relationships Project (313) 489-0043 www.myrelationshipsproject.com

Financial

Springhill Pooled Accounts Trust (248) 269-1319 springhillpooledtrust.org

3D3 Custom Solutions (248) 763-1367 3d3custom.com

Adaptive Sports Program

Healing Complex Kids (248) 370-8040 healingcomplexkids.org

CVLL Challenger Baseball (586) 781-5547 www.midistrict6.org

MIABLE (844) 656-7225 mi.savewithable.com

Advocacy

Photographer

Student Advocacy Michigan (248) 372-9770 www.studentadvocacymi.com

Art Studio

Paint a Miracle (248) 652-2702 www.paintamiracle.org

Attorney/Wills, Trusts, Estate Planning

September 2026

Footprints Photography ®️ (248) 922-1802 www.footprintsphotography.com

Podcast

On the Verge Blog & Podcast (734) 780-6795 www.VergeTalks.com

Relationship Support/Sexual Health

Special Needs Trust

Summer Camps & Programs North Star Reach (734) 680-8744 www.northstarreach.org

Uniquely You Detroit Metro

9151 Currency St. Irving, TX 75063 Celebrating the Disability Community in Detroit Metro counties

MUSIC THERAPY IS A TYPE OF THERAPY THAT USES MUSIC TO IMPROVE: physical | emotional | cognitive | and social functioning in individuals Effective in treating a variety of conditions, including:

depression

anxiety

autism

dementia

and chronic pain

CHECK US OUT ON SOCIAL MEDIA FOR INFORMATION, EVENTS, AND LOTS OF FUN

@AdvancedTherapeuticSolutionsMI @advancedtherapeuticsolutions @ats_mi

734.352.3543

advancedtherapeuticsolutionsmi.com