If you’re a special needs parent, you know that springtime brings a lot more than April showers and May flowers. It brings renewed hope, but also sobering trepidation. I recently attended my sons’ IEP meetings to discuss their progress this year and set goals for the next one. Each year, I walk in with an open mind and a guarded heart, knowing that both are necessary when discussing my children’s futures. Because that is what these meetings represent to me: the future.
They also act as a mirror. As the SPED teams report on my sons’ progress, I cannot help but create mental side-by-side comparisons between my sons and myself.
I have been attending these meetings for Nico for seven years, and with each passing year it has become more clear that my son is profoundly autistic. His academic trajectory has become less certain as progress in traditional settings has slowed. There was a time when I believed that with proper engagement and responsive teaching, Nico would simply find his rhythm and the intellectual disability diagnosis would become less defining. After this year’s meeting—his seventh to date—I realized my husband and I must pivot more intentionally toward transition planning and what life may look like when he ages out of the school system.
What gave me peace, however, was knowing Nico is surrounded by incredible educators who have taken the time to learn how he learns best, what motivates him, and how to respond when he is struggling. As a parent, that is invaluable. I cannot be the only one who knows what is best for my child, especially when I am not with him for most of the day.
Maximo’s IEP meeting focused heavily on his emotional well-being and behavioral needs, as his diagnosis presents differently than Nico’s. Although Max and Nico share many of the same traits—flapping hands, difficulty with transitions, high anxiety, sensory sensitivities, and deep emotional sensitivity—Maximo is also a sophisticated communicator with advanced intelligence. Because of that, it can be easier for others to dismiss his special needs and unique behaviors as obstinance or disobedience.
Thankfully, he too has teachers who have taken the time to truly know him. They have listened to me and valued my recommendations. They have observed him closely, listened to him directly, and worked to understand how to best support him. They challenge him enough to help him grow, while also teaching him to advocate for himself and recognize his own limits.
What I found most refreshing in both IEP meetings was the clear thread of responsiveness woven through every conversation. My sons’ teachers and support teams understand that responsiveness is not optional—it is essential. It is the foundation of growth, progress, trust, and dignity. It strengthens relationships and builds empathy, two things every child deserves.
My question is this: why does that responsiveness so often disappear when autistic children become autistic adults?
Is it a generational gap? A lack of awareness? A lack of training? Or is it something harder to admit—disinterest, impatience, and a failure to empathize once accommodations are no longer legally mandated?
I ask because I have seen firsthand the inequities and lack of responsiveness shown toward neurodivergent adults in the workplace. I have watched incredibly brilliant, deeply feeling, and often misunderstood people be treated as though they are the problem. They are labeled resistant, overly dramatic, difficult, awkward, too intense, or as someone who makes others uncomfortable. I believe I recognize these inequities so clearly because I am deeply attuned to neurodivergence and have a natural ability to notice and understand the unique traits that others often overlook.
And as we roll right into Mental Health Awareness Month, I have been thinking a lot about the intersection between mental health and neurodivergence.
At times, neurodivergence can also be misunderstood or mischaracterized as solely a mental health issue, which makes these situations even more delicate in workplace settings. While anxiety, depression, and burnout can absolutely coexist with neurodivergence—especially after years of masking or feeling misunderstood—not every difference in communication style, emotional processing, sensory response, or social interaction should automatically be viewed through a pathological lens. When neurodivergent adults are mislabeled without deeper understanding, it can unintentionally create stigma, diminish credibility, and shift attention away from the real need: support, responsiveness, and awareness. This is why nuance matters so deeply. People deserve to be understood in context, not reduced to assumptions about behaviors that may simply reflect a different way of experiencing and navigating the world.
What if, instead of rushing to develop a biased narrative about someone, we first took the time to build a relationship and observe without judgment? What if we learned more about neurodiversity and what it can look like at work? What if we asked our neurodivergent colleagues how they work best and responded to that information with intention? What if we identified their strengths, recognized their triggers, and cultivated environments where they could contribute at a high level instead of merely survive?
Right now, there are generations of neurodivergent adults in the workforce who grew up without support, advocacy, therapy, medication, or language to explain their experience. There was less awareness, fewer screening tools, and far less understanding. Many were taught to mask, to overcompensate, to internalize shame, or to simply “try harder.”
Although I do not have an official diagnosis, I am almost certain that I am on the spectrum. Realizing that has brought relief, but it has also validated so many painful experiences and unanswered questions from my personal and professional life. It has helped me understand why certain environments felt unbearable, why ambiguity created intense anxiety, why social dynamics could feel exhausting, and why my strengths were not always recognized for what they were. It has also helped me understand why I have thrived tremendously in specific roles over the years, with those roles having the strongest impact and seeing the most success overall.
Research increasingly shows that neurodivergent individuals often bring tremendous value to organizations: pattern recognition, creativity, sustained focus, honesty, innovation, loyalty, and deep commitment to quality when supported appropriately. At the same time, studies show higher rates of unemployment, underemployment, burnout, and workplace exclusion among autistic adults—not because they lack talent, but because many systems were never designed with them in mind. Too often, employers see neurodivergence as a deficit and not an asset. In doing so, they overlook the very qualities they claim to value.
Responsiveness in the workplace does not require perfection or expensive overhauls. It does not require grand gestures for the sake of trying to better understand neurodivergence. It can look like direct feedback, reduced ambiguity, flexibility when possible, respect for sensory needs, thoughtful management, and a willingness to ask employees what helps them do their best work. It can look like choosing curiosity over judgment. It can look like understanding that professionalism is not one personality type, one communication style, or one narrow definition of success. It can look like clear communication, patience, flexibility, curiosity, and a willingness to understand how someone experiences the world. Responsiveness is the ability to extend grace and recognize that success, intelligence, and professionalism do not always come wrapped in the same package.
If we can create individualized plans, accommodations, and compassionate support systems for children, then surely we can extend that same humanity to adults. Neurodivergent people should not have to mask themselves into exhaustion just to be accepted. They should not have to prove their worth twice.
As a mother, I want a future for my sons where they are not merely tolerated, but valued. I want them to enter classrooms, workplaces, friendships, and communities where people seek to understand them rather than misunderstand them. I want their differences to be met with respect, their strengths to be nurtured, and their challenges to be met with compassion.
As an advocate, my hope is simple: that we keep growing in awareness, empathy, and responsiveness—not just for children, but for the adults they will become. Because every neurodivergent child is someone’s future adult. And every one of them deserves to walk into that future knowing they belong.
